Variant report

Variant	rs73617871
Chromosome Location	chr19:55896933-55896934
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:0)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EBF1	chr19:55896247-55897458	GM12878	blood:	n/a	chr19:55896623-55896634 chr19:55896625-55896634
2	POLR2A	chr19:55895189-55904986	PANC-1	pancreas:	n/a	n/a
3	POLR2A	chr19:55896221-55905168	PFSK-1	brain:	n/a	n/a
4	POLR2A	chr19:55894752-55898253	MCF-7	breast:	n/a	n/a
5	TAF1	chr19:55896556-55897789	ECC-1	luminal epithelium:	n/a	n/a
6	MAX	chr19:55896747-55898047	GM12878	blood:	n/a	n/a
7	NRF1	chr19:55896260-55897483	GM12878	blood:	n/a	chr19:55897249-55897256
8	SPI1	chr19:55896920-55897570	GM12878	blood:	n/a	chr19:55897296-55897303 chr19:55897244-55897251
9	POLR2A	chr19:55894809-55904996	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr19:55896284-55898300	ECC-1	luminal epithelium:	n/a	n/a
11	TCF7L2	chr19:55895454-55897550	Hela-S3	cervix:	n/a	n/a
12	RELA	chr19:55896254-55897708	GM18505	blood:	n/a	n/a
13	YY1	chr19:55896584-55897898	SK-N-SH	brain:	n/a	chr19:55897711-55897725 chr19:55897719-55897731 chr19:55897710-55897721
14	RFX5	chr19:55896299-55897845	Hela-S3	cervix:	n/a	chr19:55896849-55896858
15	ELK1	chr19:55896566-55897506	GM12878	blood:	n/a	chr19:55896881-55896890 chr19:55896881-55896890
16	HEY1	chr19:55896494-55897600	HepG2	liver:	n/a	n/a
17	CREB1	chr19:55896933-55897516	A549	lung:	n/a	n/a
18	POLR2A	chr19:55896379-55898180	GM10847	blood:	n/a	n/a
19	RFX5	chr19:55896582-55897373	K562	blood:	n/a	chr19:55896849-55896858
20	CEBPB	chr19:55896868-55897392	HepG2	liver:	n/a	n/a
21	ELF1	chr19:55895215-55898290	GM12878	blood:	n/a	n/a
22	MXI1	chr19:55895228-55897931	GM12878	blood:	n/a	chr19:55896434-55896449
23	IRF1	chr19:55896411-55897670	K562	blood:	n/a	chr19:55897626-55897635
24	CREB1	chr19:55896297-55897876	HepG2	liver:	n/a	n/a
25	MAFK	chr19:55896068-55897631	Hela-S3	cervix:	n/a	n/a
26	E2F4	chr19:55896466-55897340	MCF10A-Er-Src	breast:	n/a	n/a
27	FOXP2	chr19:55896933-55897431	SK-N-MC	brain:	n/a	n/a
28	CHD1	chr19:55895365-55898225	GM12878	blood:	n/a	chr19:55897281-55897291
29	CEBPB	chr19:55896442-55897509	Hela-S3	cervix:	n/a	n/a
30	BCL3	chr19:55896698-55898611	A549	lung:	n/a	chr19:55897712-55897725
31	GABPA	chr19:55896747-55897544	Hela-S3	cervix:	n/a	chr19:55897249-55897256
32	POLR2A	chr19:55896876-55897945	HL-60	blood:	n/a	n/a
33	TAF1	chr19:55896511-55898107	PFSK-1	brain:	n/a	n/a
34	CUX1	chr19:55896894-55897044	K562	blood:	n/a	n/a
35	MAZ	chr19:55896040-55899400	IMR90	lung:	n/a	n/a
36	MAX	chr19:55896156-55897062	ECC-1	luminal epithelium:	n/a	n/a
37	CREB1	chr19:55896679-55897703	GM12878	blood:	n/a	n/a
38	KAP1	chr19:55896398-55897657	U2OS	brain:	n/a	chr19:55896564-55896572
39	ELF1	chr19:55896689-55897928	MCF-7	breast:	n/a	n/a
40	STAT1	chr19:55896509-55897503	GM12878	blood:	n/a	chr19:55897104-55897112 chr19:55896517-55896529 chr19:55897104-55897113 chr19:55897101-55897115 chr19:55897098-55897118 chr19:55897103-55897112
41	CREB1	chr19:55896592-55897570	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr19:55894933-55899226	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr19:55894841-55904473	GM12878	blood:	n/a	n/a
44	MAFF	chr19:55896586-55897131	K562	blood:	n/a	chr19:55896988-55897006
45	POLR2A	chr19:55894888-55898899	HCT-116	colon:	n/a	n/a
46	STAT5A	chr19:55896901-55897521	K562	blood:	n/a	chr19:55897104-55897112 chr19:55897104-55897113 chr19:55897101-55897115 chr19:55897098-55897118 chr19:55897103-55897112
47	TAF1	chr19:55896811-55897911	H1-hESC	embryonic stem cell:	n/a	n/a
48	SIN3AK20	chr19:55895878-55897971	A549	lung:	n/a	n/a
49	EP300	chr19:55896302-55898078	A549	lung:	n/a	chr19:55897377-55897390
50	FOXM1	chr19:55896807-55897785	GM12878	blood:	n/a	n/a

No data

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:55896877..55897816-chr5:40679285..40679925,2	Hela-S3	cervix:
2	chr1:207226289..207227212-chr19:55896531..55897368,2	Hela-S3	cervix:
3	chr19:55823464..55826330-chr19:55895839..55897865,2	K562	blood:
4	chr19:55895254..55897852-chr19:55973441..55975937,2	K562	blood:
5	chr19:55676207..55678218-chr19:55894877..55897476,2	MCF-7	breast:
6	chr19:55896238..55898809-chr19:55984514..55989160,4	K562	blood:
7	chr19:55894730..55901388-chr19:55970612..55975937,9	K562	blood:
8	chr19:55896857..55897425-chr5:156569724..156570322,2	Hela-S3	cervix:
9	chr19:55787879..55795650-chr19:55893762..55898931,9	MCF-7	breast:
10	chr19:55811782..55819446-chr19:55894353..55900958,7	K562	blood:
11	chr19:55811558..55817329-chr19:55895333..55899907,9	MCF-7	breast:
12	chr19:55894504..55900051-chr19:55962971..55968155,6	K562	blood:
13	chr19:55677411..55679148-chr19:55895317..55896952,2	MCF-7	breast:
14	chr19:55894386..55898784-chr19:55971378..55974677,5	MCF-7	breast:
15	chr19:55862642..55868480-chr19:55895176..55899926,10	K562	blood:
16	chr19:55764902..55773441-chr19:55891413..55900303,21	K562	blood:
17	chr19:55863699..55867009-chr19:55895864..55899065,4	MCF-7	breast:
18	chr19:55724006..55730191-chr19:55893749..55903961,17	K562	blood:
19	chr19:55627804..55630494-chr19:55895380..55898353,2	K562	blood:
20	chr12:57984859..57985397-chr19:55896847..55897561,2	HCT-116	colon:
21	chr19:55767441..55773483-chr19:55893952..55900251,14	MCF-7	breast:
22	chr19:55869722..55871844-chr19:55895437..55897216,2	MCF-7	breast:
23	chr19:55895074..55897174-chr19:56145786..56148520,2	MCF-7	breast:
24	chr14:53257754..53258322-chr19:55896921..55897500,2	Hela-S3	cervix:
25	chr19:55848515..55857343-chr19:55894079..55900232,19	MCF-7	breast:
26	chr19:55673897..55675427-chr19:55894913..55897394,2	MCF-7	breast:
27	chr19:55654842..55658352-chr19:55895153..55898113,3	MCF-7	breast:
28	chr19:55896909..55897465-chr2:27886092..27886795,2	Hela-S3	cervix:
29	chr19:55854922..55862011-chr19:55892906..55898744,13	MCF-7	breast:
30	chr19:55864065..55867080-chr19:55895058..55897568,4	K562	blood:
31	chr19:55790067..55793851-chr19:55895113..55900809,14	K562	blood:
32	chr19:55669739..55671839-chr19:55895942..55898733,2	K562	blood:
33	chr19:55687032..55688994-chr19:55895402..55898104,2	K562	blood:
34	chr19:55895123..55898992-chr19:55986838..55992189,7	MCF-7	breast:
35	chr19:55763551..55774813-chr19:55891413..55900376,23	K562	blood:
36	chr19:55592169..55594034-chr19:55895749..55898728,2	K562	blood:
37	chr19:55790016..55797764-chr19:55893451..55899813,15	MCF-7	breast:
38	chr19:55723991..55730191-chr19:55895529..55902666,13	K562	blood:
39	chr19:55896562..55898629-chr19:55953119..55955892,2	MCF-7	breast:
40	chr19:55894932..55897598-chr19:56114798..56116891,2	MCF-7	breast:
41	chr19:55848915..55854876-chr19:55892600..55899757,13	MCF-7	breast:
42	chr19:55896752..55897315-chr2:28614607..28615482,2	Hela-S3	cervix:
43	chr19:55896596..55898990-chr19:55971446..55973469,2	MCF-7	breast:
44	chr19:55869009..55871101-chr19:55896395..55898279,2	K562	blood:
45	chr19:55811657..55813944-chr19:55896154..55898811,3	K562	blood:
46	chr19:55743829..55748910-chr19:55895144..55898736,4	K562	blood:
47	chr19:55675848..55678136-chr19:55894504..55899983,4	K562	blood:
48	chr16:89641748..89642663-chr19:55896888..55897643,2	HCT-116	colon:
49	chr19:55769552..55771558-chr19:55896824..55899608,3	MCF-7	breast:
50	chr19:55895254..55899821-chr19:55961359..55968155,8	K562	blood:

No data

Variant related genes	Relation type
RPL28	TF binding region
TMEM238	TF binding region
ENSG00000113263	Chromatin interaction
ENSG00000179943	Chromatin interaction
ENSG00000173581	Chromatin interaction
ENSG00000075426	Chromatin interaction
ENSG00000180667	Chromatin interaction
ENSG00000117289	Chromatin interaction
ENSG00000123836	Chromatin interaction
ENSG00000163798	Chromatin interaction
ENSG00000134824	Chromatin interaction
ENSG00000267706	Chromatin interaction
ENSG00000268729	Chromatin interaction
ENSG00000129990	Chromatin interaction
ENSG00000135077	Chromatin interaction
ENSG00000267577	Chromatin interaction
ENSG00000171522	Chromatin interaction
ENSG00000267110	Chromatin interaction
ENSG00000100442	Chromatin interaction
ENSG00000213015	Chromatin interaction
ENSG00000239137	Chromatin interaction
ENSG00000197483	Chromatin interaction
ENSG00000133265	Chromatin interaction
ENSG00000155868	Chromatin interaction
ENSG00000166908	Chromatin interaction
ENSG00000119760	Chromatin interaction
ENSG00000125503	Chromatin interaction
ENSG00000171443	Chromatin interaction
ENSG00000267649	Chromatin interaction
ENSG00000269859	Chromatin interaction
ENSG00000163874	Chromatin interaction
ENSG00000105063	Chromatin interaction
ENSG00000171425	Chromatin interaction
ENSG00000063241	Chromatin interaction
ENSG00000160469	Chromatin interaction
ENSG00000160471	Chromatin interaction
ENSG00000149485	Chromatin interaction
ENSG00000105048	Chromatin interaction
ENSG00000267531	Chromatin interaction
ENSG00000187902	Chromatin interaction
ENSG00000133247	Chromatin interaction
ENSG00000261221	Chromatin interaction
ENSG00000233621	Chromatin interaction
ENSG00000111530	Chromatin interaction
ENSG00000178773	Chromatin interaction
ENSG00000167646	Chromatin interaction
ENSG00000131037	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000090971	Chromatin interaction
ENSG00000266462	Chromatin interaction
ENSG00000100522	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10403564	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10403989	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10404049	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10404370	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10405802	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10407066	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10408088	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10408448	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10408525	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10408540	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10410269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10411984	0.88[AFR][1000 genomes]
rs10415365	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10416908	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10420818	1.00[AFR][1000 genomes]
rs10421889	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10423589	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10424289	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10424652	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10425107	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10425362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10425596	0.88[AFR][1000 genomes]
rs28408730	1.00[AFR][1000 genomes]
rs28536711	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28540780	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28797308	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59698058	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61468173	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73617888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73617896	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73619606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73619611	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73619651	0.93[AFR][1000 genomes];0.85[AMR][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	esv1816335	chr19:55683977-55901099	Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv1065760	chr19:55721521-55929740	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
3	nsv912456	chr19:55725410-55925500	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
4	nsv912457	chr19:55725410-56019597	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	228 gene(s)	inside rSNPs	diseases
5	nsv432086	chr19:55807586-56050844	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	220 gene(s)	inside rSNPs	diseases
6	nsv912460	chr19:55814881-55897327	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
7	nsv912461	chr19:55845386-55897327	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv470162	chr19:55845386-55902257	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
9	nsv912462	chr19:55845386-55925500	Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
10	nsv912463	chr19:55845386-56004901	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
11	nsv912464	chr19:55850269-55921164	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer 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 miRNA target site	203 gene(s)	inside rSNPs	diseases
12	nsv516199	chr19:55854313-55901099	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
13	nsv912465	chr19:55854313-55935184	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS 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 miRNA target site	196 gene(s)	inside rSNPs	diseases
14	nsv912470	chr19:55872591-55897170	Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	79 gene(s)	inside rSNPs	diseases
15	nsv912473	chr19:55874642-56145428	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
16	nsv544085	chr19:55875808-55911275	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
17	nsv912476	chr19:55876747-55897327	Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	91 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55894400-55897400	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr19:55894600-55898200	Active TSS	H9 Cell Line	embryonic stem cell
3	chr19:55894600-55898600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr19:55894800-55897800	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr19:55894800-55897800	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr19:55894800-55899000	Active TSS	Small Intestine	intestine
7	chr19:55894800-55899200	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr19:55894800-55899600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr19:55895000-55897800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr19:55895000-55898000	Active TSS	Psoas Muscle	Psoas
11	chr19:55895000-55898400	Active TSS	Aorta	Aorta
12	chr19:55895200-55898400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:55895400-55897000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr19:55895600-55897000	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr19:55895600-55897000	Flanking Active TSS	Primary B cells from peripheral blood	blood
16	chr19:55895600-55897000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr19:55896000-55898000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr19:55896400-55898200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr19:55896400-55898400	Active TSS	Gastric	stomach
20	chr19:55896600-55897000	Active TSS	Right Atrium	heart
21	chr19:55896600-55897400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:55896600-55897400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr19:55896600-55897400	Active TSS	Dnd41	blood
24	chr19:55896600-55897400	Active TSS	HepG2	liver
25	chr19:55896600-55897600	Active TSS	Adipose Nuclei	Adipose
26	chr19:55896600-55897600	Active TSS	A549	lung
27	chr19:55896600-55897600	Active TSS	NHEK	skin
28	chr19:55896600-55897800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr19:55896600-55897800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr19:55896600-55897800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:55896600-55897800	Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr19:55896600-55897800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr19:55896600-55897800	Active TSS	Fetal Brain Female	brain
34	chr19:55896600-55897800	Active TSS	Fetal Intestine Small	intestine
35	chr19:55896600-55897800	Active TSS	Hela-S3	cervix
36	chr19:55896600-55897800	Active TSS	HMEC	breast
37	chr19:55896600-55898000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr19:55896600-55898000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr19:55896600-55898000	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr19:55896600-55898000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr19:55896600-55898000	Active TSS	Brain Cingulate Gyrus	brain
42	chr19:55896600-55898000	Active TSS	Brain Hippocampus Middle	brain
43	chr19:55896600-55898000	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr19:55896600-55898000	Active TSS	Brain Substantia Nigra	brain
45	chr19:55896600-55898000	Active TSS	Colonic Mucosa	Colon
46	chr19:55896600-55898000	Active TSS	Duodenum Mucosa	Duodenum
47	chr19:55896600-55898000	Active TSS	Esophagus	oesophagus
48	chr19:55896600-55898000	Active TSS	Lung	lung
49	chr19:55896600-55898000	Active TSS	Right Ventricle	heart
50	chr19:55896600-55898000	Active TSS	GM12878-XiMat	blood

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