Variant report

Variant	rs10421857
Chromosome Location	chr19:42927362-42927363
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	RELA	chr19:42926970-42927511	GM19099	blood:	n/a	n/a
2	JUND	chr19:42927258-42927608	H1-hESC	embryonic stem cell:	n/a	n/a
3	SIX5	chr19:42927289-42927548	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr19:42926830-42928192	GM12878	blood:	n/a	n/a
5	SP1	chr19:42926984-42928287	HCT-116	colon:	n/a	chr19:42927854-42927866 chr19:42927116-42927130 chr19:42928163-42928172 chr19:42927855-42927869 chr19:42927887-42927898 chr19:42928162-42928171 chr19:42928194-42928206 chr19:42928196-42928205 chr19:42928239-42928253 chr19:42927854-42927866 chr19:42927887-42927899 chr19:42927854-42927865 chr19:42928215-42928225 chr19:42927889-42927898 chr19:42927856-42927865 chr19:42927888-42927897 chr19:42927888-42927902 chr19:42927855-42927864 chr19:42927887-42927899
6	CHD1	chr19:42926733-42928070	GM12878	blood:	n/a	n/a
7	SP1	chr19:42927160-42928603	H1-hESC	embryonic stem cell:	n/a	chr19:42927854-42927866 chr19:42928323-42928332 chr19:42928163-42928172 chr19:42927855-42927869 chr19:42927887-42927898 chr19:42928162-42928171 chr19:42928194-42928206 chr19:42928196-42928205 chr19:42928239-42928253 chr19:42927854-42927866 chr19:42927887-42927899 chr19:42927854-42927865 chr19:42928321-42928333 chr19:42928215-42928225 chr19:42927889-42927898 chr19:42927856-42927865 chr19:42927888-42927897 chr19:42927888-42927902 chr19:42927855-42927864 chr19:42927887-42927899
8	MAZ	chr19:42927073-42928214	GM12878	blood:	n/a	chr19:42928020-42928035 chr19:42928021-42928032 chr19:42928022-42928031 chr19:42928160-42928170 chr19:42928023-42928030 chr19:42927636-42927646 chr19:42928021-42928032
9	SIN3AK20	chr19:42927270-42927857	SK-N-SH	brain:	n/a	n/a
10	BACH1	chr19:42927187-42927770	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr19:42926774-42928253	GM12892	blood:	n/a	n/a
12	SIN3A	chr19:42926983-42928494	H1-hESC	embryonic stem cell:	n/a	chr19:42927986-42927999
13	SIN3A	chr19:42926858-42928026	GM12878	blood:	n/a	chr19:42927986-42927999
14	POLR2A	chr19:42926472-42928276	Raji	blood:	n/a	n/a
15	POLR2A	chr19:42927297-42928091	HCT-116	colon:	n/a	n/a
16	RCOR1	chr19:42927202-42928111	GM12878	blood:	n/a	n/a
17	EP300	chr19:42927263-42927463	HepG2	liver:	n/a	n/a
18	USF1	chr19:42927301-42927557	SK-N-SH_RA	brain:	n/a	n/a
19	POLR2A	chr19:42926811-42928161	GM12878	blood:	n/a	n/a
20	MXI1	chr19:42927090-42928813	IMR90	lung:	n/a	n/a
21	REST	chr19:42926649-42928673	H1-neurons	neurons:	n/a	chr19:42927980-42927998 chr19:42927655-42927668 chr19:42927979-42927999 chr19:42927541-42927551
22	CHD1	chr19:42926653-42928296	IMR90	lung:	n/a	n/a
23	ATF2	chr19:42927036-42927474	GM12878	blood:	n/a	n/a
24	ZEB1	chr19:42926851-42927757	GM12878	blood:	n/a	n/a
25	POLR2A	chr19:42926820-42928184	GM12891	blood:	n/a	n/a
26	TBP	chr19:42927330-42928539	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr19:42927123-42927699	H1-hESC	embryonic stem cell:	n/a	n/a
28	ELF1	chr19:42926690-42928210	GM12878	blood:	n/a	chr19:42927978-42927990
29	POLR2A	chr19:42926892-42928209	GM12878	blood:	n/a	n/a
30	SIX5	chr19:42927280-42927644	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr19:42926829-42928284	GM12878	blood:	n/a	n/a
32	ELF1	chr19:42926489-42928635	GM12878	blood:	n/a	chr19:42927978-42927990
33	POLR2A	chr19:42926875-42928366	GM19193	blood:	n/a	n/a
34	MTA3	chr19:42926179-42928574	GM12878	blood:	n/a	n/a
35	SP1	chr19:42927207-42928512	H1-hESC	embryonic stem cell:	n/a	chr19:42927854-42927866 chr19:42928323-42928332 chr19:42928163-42928172 chr19:42927855-42927869 chr19:42927887-42927898 chr19:42928162-42928171 chr19:42928194-42928206 chr19:42928196-42928205 chr19:42928239-42928253 chr19:42927854-42927866 chr19:42927887-42927899 chr19:42927854-42927865 chr19:42928321-42928333 chr19:42928215-42928225 chr19:42927889-42927898 chr19:42927856-42927865 chr19:42927888-42927897 chr19:42927888-42927902 chr19:42927855-42927864 chr19:42927887-42927899
36	POLR2A	chr19:42926890-42928288	GM18951	blood:	n/a	n/a
37	POLR2A	chr19:42926940-42928261	GM15510	blood:	n/a	n/a
38	NFATC1	chr19:42927202-42927789	GM12878	blood:	n/a	n/a
39	EP300	chr19:42927172-42927632	GM12878	blood:	n/a	n/a
40	POLR2A	chr19:42927324-42928039	U87	brain:	n/a	n/a
41	SREBP1	chr19:42926508-42928071	GM12878	blood:	n/a	n/a
42	SP1	chr19:42927120-42928383	GM12878	blood:	n/a	chr19:42927854-42927866 chr19:42928323-42928332 chr19:42928163-42928172 chr19:42927855-42927869 chr19:42927887-42927898 chr19:42928162-42928171 chr19:42928194-42928206 chr19:42928196-42928205 chr19:42928239-42928253 chr19:42927854-42927866 chr19:42927887-42927899 chr19:42927854-42927865 chr19:42928321-42928333 chr19:42928215-42928225 chr19:42927889-42927898 chr19:42927856-42927865 chr19:42927888-42927897 chr19:42927888-42927902 chr19:42927855-42927864 chr19:42927887-42927899
43	CTCF	chr19:42927240-42927390	GM12874	blood:	n/a	n/a
44	SIX5	chr19:42927245-42927613	GM12878	blood:	n/a	n/a
45	POLR2A	chr19:42926745-42928431	H1-neurons	neurons:	n/a	n/a
46	SPI1	chr19:42926722-42927535	GM12878	blood:	n/a	chr19:42927152-42927159 chr19:42927149-42927162 chr19:42927151-42927160 chr19:42927150-42927163
47	POLR2A	chr19:42927067-42927749	GM12892	blood:	n/a	n/a
48	POLR2A	chr19:42927309-42928111	SK-N-SH	brain:	n/a	n/a
49	MAZ	chr19:42926407-42928545	IMR90	lung:	n/a	chr19:42928020-42928035 chr19:42928021-42928032 chr19:42928022-42928031 chr19:42928353-42928363 chr19:42928160-42928170 chr19:42928023-42928030 chr19:42927636-42927646 chr19:42928021-42928032
50	POLR2A	chr19:42926691-42928128	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:42927142..42929606-chr19:42930289..42932952,2	MCF-7	breast:

Variant related genes	Relation type
LIPE	TF binding region
LIPE-AS1	TF binding region
ENSG00000079435	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10401224	0.93[YRI][hapmap];1.00[EUR][1000 genomes]
rs10402438	1.00[EUR][1000 genomes]
rs10403856	1.00[AMR][1000 genomes]
rs10404650	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10406800	0.93[YRI][hapmap];0.83[AFR][1000 genomes];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]
rs10408258	1.00[EUR][1000 genomes]
rs10408986	1.00[AMR][1000 genomes]
rs10409428	0.93[YRI][hapmap];1.00[EUR][1000 genomes]
rs10409433	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10409939	1.00[EUR][1000 genomes]
rs10410129	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10410174	1.00[AMR][1000 genomes]
rs10410653	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10411498	0.86[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10411908	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10413484	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10414695	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10415759	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10415999	1.00[EUR][1000 genomes]
rs10416535	0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10417606	1.00[AMR][1000 genomes]
rs10418102	1.00[AMR][1000 genomes]
rs10418312	0.93[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10418988	0.93[YRI][hapmap];1.00[AMR][1000 genomes]
rs10420327	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10421331	1.00[AMR][1000 genomes]
rs10421409	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10421510	0.86[YRI][hapmap];1.00[EUR][1000 genomes]
rs10421902	0.83[AFR][1000 genomes];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[YRI][hapmap];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	0.93[YRI][hapmap];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	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13343388	0.93[AFR][1000 genomes];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	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13346831	1.00[AMR][1000 genomes]
rs13346837	1.00[EUR][1000 genomes]
rs13346879	1.00[AMR][1000 genomes]
rs2229614	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28402882	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28463673	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28469564	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[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28657829	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28663042	0.88[AFR][1000 genomes];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]
rs28686771	1.00[AMR][1000 genomes]
rs28699037	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28711448	1.00[EUR][1000 genomes]
rs28715574	1.00[EUR][1000 genomes]
rs33919763	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35707383	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36089262	0.93[AFR][1000 genomes];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	0.93[AFR][1000 genomes];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	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73552879	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73554520	1.00[EUR][1000 genomes]
rs73554531	1.00[EUR][1000 genomes]
rs73558432	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73560411	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8099885	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8109258	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9304602	0.80[YRI][hapmap];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	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
4	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
5	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
6	nsv911788	chr19:42887492-42930652	Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv911792	chr19:42901430-42929254	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv911793	chr19:42901430-42929502	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
9	nsv911794	chr19:42901430-42930652	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv911795	chr19:42901430-42932699	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
11	nsv911798	chr19:42904653-42930652	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer 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	9 gene(s)	inside rSNPs	diseases
12	nsv911799	chr19:42905645-42930652	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv911800	chr19:42906914-42930652	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv911801	chr19:42910416-42929502	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
15	nsv911802	chr19:42915110-42929254	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv911804	chr19:42916841-42932699	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	nsv911806	chr19:42919405-42928397	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
18	nsv911807	chr19:42920555-42929254	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv579633	chr19:42925636-42929254	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	nsv911808	chr19:42925636-42930652	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42925400-42927400	Flanking Active TSS	NHEK	skin
2	chr19:42925400-42928400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr19:42925600-42927400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr19:42925800-42928400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr19:42926000-42928600	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr19:42926200-42927400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
7	chr19:42926200-42927600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr19:42926200-42927600	Flanking Active TSS	GM12878-XiMat	blood
9	chr19:42926200-42928400	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr19:42926200-42929200	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr19:42926400-42927400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr19:42926400-42927400	Flanking Active TSS	Primary B cells from peripheral blood	blood
13	chr19:42926400-42927400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
14	chr19:42926400-42927400	Flanking Active TSS	Duodenum Mucosa	Duodenum
15	chr19:42926400-42927600	Flanking Active TSS	Primary hematopoietic stem cells	blood
16	chr19:42926400-42927600	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
17	chr19:42926400-42928200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:42926400-42928200	Flanking Active TSS	HUVEC	blood vessel
19	chr19:42926400-42928400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
20	chr19:42926400-42928400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr19:42926600-42927400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
22	chr19:42926600-42927400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
23	chr19:42926600-42927400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
24	chr19:42926600-42927400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr19:42926600-42927600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr19:42926600-42927600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr19:42926600-42927600	Flanking Active TSS	Fetal Thymus	thymus
28	chr19:42926600-42927600	Flanking Active TSS	Spleen	Spleen
29	chr19:42926600-42928400	Flanking Active TSS	Colonic Mucosa	Colon
30	chr19:42926600-42928400	Active TSS	Fetal Kidney	kidney
31	chr19:42926600-42928600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
32	chr19:42926600-42928600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr19:42926600-42928600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr19:42926600-42928600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
35	chr19:42926600-42928600	Flanking Active TSS	HMEC	breast
36	chr19:42926800-42927400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
37	chr19:42926800-42927400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:42926800-42927400	Flanking Active TSS	Fetal Stomach	stomach
39	chr19:42926800-42927400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr19:42926800-42927400	Flanking Active TSS	NH-A	brain
41	chr19:42926800-42927400	Flanking Active TSS	NHDF-Ad	bronchial
42	chr19:42926800-42927400	Flanking Active TSS	Osteobl	bone
43	chr19:42926800-42927600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr19:42926800-42927600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr19:42926800-42927600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr19:42926800-42927600	Flanking Active TSS	Lung	lung
47	chr19:42926800-42927600	Flanking Active TSS	NHLF	lung
48	chr19:42926800-42928400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr19:42926800-42928400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
50	chr19:42926800-42928400	Active TSS	Pancreatic Islets	Pancreatic Islet

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