Variant report

Variant	rs61468173
Chromosome Location	chr19:55898455-55898456
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:65)
CpG islands
(count:0)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:65 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:55895189-55904986	PANC-1	pancreas:	n/a	n/a
2	POLR2A	chr19:55896221-55905168	PFSK-1	brain:	n/a	n/a
3	POLR2A	chr19:55894809-55904996	Hela-S3	cervix:	n/a	n/a
4	BCL3	chr19:55896698-55898611	A549	lung:	n/a	chr19:55897712-55897725
5	MAZ	chr19:55896040-55899400	IMR90	lung:	n/a	n/a
6	POLR2A	chr19:55894933-55899226	MCF10A-Er-Src	breast:	n/a	n/a
7	POLR2A	chr19:55894841-55904473	GM12878	blood:	n/a	n/a
8	POLR2A	chr19:55894888-55898899	HCT-116	colon:	n/a	n/a
9	SIN3AK20	chr19:55897093-55898498	K562	blood:	n/a	n/a
10	POLR2A	chr19:55895220-55903350	K562	blood:	n/a	n/a
11	POLR2A	chr19:55895580-55900320	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr19:55894856-55898584	GM19099	blood:	n/a	n/a
13	POLR2A	chr19:55895906-55903362	K562	blood:	n/a	n/a
14	POLR2A	chr19:55896728-55903901	GM12892	blood:	n/a	n/a
15	SIN3AK20	chr19:55896835-55898540	A549	lung:	n/a	n/a
16	POLR2A	chr19:55894941-55898566	GM19193	blood:	n/a	n/a
17	POLR2A	chr19:55898325-55899679	ECC-1	luminal epithelium:	n/a	n/a
18	POLR2A	chr19:55898313-55898501	ProgFib	skin:	n/a	n/a
19	POLR2A	chr19:55896275-55903749	PFSK-1	brain:	n/a	n/a
20	POLR2A	chr19:55894981-55899557	GM18951	blood:	n/a	n/a
21	POLR2A	chr19:55898335-55898607	GM12878	blood:	n/a	n/a
22	POLR2A	chr19:55897004-55902318	HL-60	blood:	n/a	n/a
23	POLR2A	chr19:55896736-55898692	GM12892	blood:	n/a	n/a
24	POLR2A	chr19:55895851-55899139	K562	blood:	n/a	n/a
25	POLR2A	chr19:55896334-55903301	GM12878	blood:	n/a	n/a
26	MTA3	chr19:55898370-55898681	GM12878	blood:	n/a	n/a
27	HCFC1	chr19:55894746-55898950	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr19:55896526-55899423	GM12878	blood:	n/a	n/a
29	WRNIP1	chr19:55898354-55898916	GM12878	blood:	n/a	n/a
30	POLR2A	chr19:55894561-55904659	K562	blood:	n/a	n/a
31	POLR2A	chr19:55896138-55903881	GM12892	blood:	n/a	n/a
32	POLR2A	chr19:55894840-55903086	K562	blood:	n/a	n/a
33	POLR2A	chr19:55894680-55903724	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr19:55896739-55898693	GM12891	blood:	n/a	n/a
35	CHD1	chr19:55896302-55901705	IMR90	lung:	n/a	chr19:55897281-55897291
36	POLR2A	chr19:55895228-55904984	GM12891	blood:	n/a	n/a
37	SIN3A	chr19:55895198-55898636	H1-hESC	embryonic stem cell:	n/a	chr19:55897710-55897721 chr19:55895743-55895754
38	POLR2A	chr19:55896525-55899245	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr19:55896380-55904806	U87	brain:	n/a	n/a
40	POLR2A	chr19:55896556-55899440	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr19:55898328-55898614	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr19:55896254-55899626	IMR90	lung:	n/a	n/a
43	POLR2A	chr19:55898455-55898550	HepG2	liver:	n/a	n/a
44	POLR2A	chr19:55894992-55899234	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr19:55896741-55903157	GM12878	blood:	n/a	n/a
46	POLR2A	chr19:55895466-55904599	HepG2	liver:	n/a	n/a
47	TCF12	chr19:55895463-55898824	A549	lung:	n/a	chr19:55895708-55895715
48	SIN3AK20	chr19:55898444-55898788	SK-N-SH	brain:	n/a	n/a
49	POLR2A	chr19:55896365-55903981	K562	blood:	n/a	n/a
50	POLR2A	chr19:55898399-55898878	Hela-S3	cervix:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr19:55864329..55868013-chr19:55897841..55899933,3	K562	blood:
2	chr19:55822211..55824840-chr19:55897185..55900181,3	MCF-7	breast:
3	chr19:55896238..55898809-chr19:55984514..55989160,4	K562	blood:
4	chr19:55894730..55901388-chr19:55970612..55975937,9	K562	blood:
5	chr19:55787879..55795650-chr19:55893762..55898931,9	MCF-7	breast:
6	chr19:55811782..55819446-chr19:55894353..55900958,7	K562	blood:
7	chr19:55811558..55817329-chr19:55895333..55899907,9	MCF-7	breast:
8	chr19:55894504..55900051-chr19:55962971..55968155,6	K562	blood:
9	chr19:55897327..55899035-chr19:56164311..56166921,2	K562	blood:
10	chr19:55894386..55898784-chr19:55971378..55974677,5	MCF-7	breast:
11	chr19:55862642..55868480-chr19:55895176..55899926,10	K562	blood:
12	chr19:55764902..55773441-chr19:55891413..55900303,21	K562	blood:
13	chr19:55863699..55867009-chr19:55895864..55899065,4	MCF-7	breast:
14	chr19:55724006..55730191-chr19:55893749..55903961,17	K562	blood:
15	chr19:55736940..55740249-chr19:55897225..55900387,3	K562	blood:
16	chr19:55767441..55773483-chr19:55893952..55900251,14	MCF-7	breast:
17	chr19:55848515..55857343-chr19:55894079..55900232,19	MCF-7	breast:
18	chr19:55897327..55900767-chr19:56164045..56167151,4	K562	blood:
19	chr19:55854922..55862011-chr19:55892906..55898744,13	MCF-7	breast:
20	chr19:55790067..55793851-chr19:55895113..55900809,14	K562	blood:
21	chr19:55669739..55671839-chr19:55895942..55898733,2	K562	blood:
22	chr19:55897240..55898959-chr7:104651761..104654641,2	K562	blood:
23	chr19:55895123..55898992-chr19:55986838..55992189,7	MCF-7	breast:
24	chr19:55763551..55774813-chr19:55891413..55900376,23	K562	blood:
25	chr19:55592169..55594034-chr19:55895749..55898728,2	K562	blood:
26	chr19:18390778..18393256-chr19:55897402..55899140,2	MCF-7	breast:
27	chr19:55790016..55797764-chr19:55893451..55899813,15	MCF-7	breast:
28	chr19:55723991..55730191-chr19:55895529..55902666,13	K562	blood:
29	chr19:55896562..55898629-chr19:55953119..55955892,2	MCF-7	breast:
30	chr19:55848915..55854876-chr19:55892600..55899757,13	MCF-7	breast:
31	chr19:55896596..55898990-chr19:55971446..55973469,2	MCF-7	breast:
32	chr19:55811657..55813944-chr19:55896154..55898811,3	K562	blood:
33	chr19:55743829..55748910-chr19:55895144..55898736,4	K562	blood:
34	chr19:55675848..55678136-chr19:55894504..55899983,4	K562	blood:
35	chr19:55769552..55771558-chr19:55896824..55899608,3	MCF-7	breast:
36	chr19:55895254..55899821-chr19:55961359..55968155,8	K562	blood:
37	chr19:55847527..55853936-chr19:55895162..55898950,13	K562	blood:
38	chr19:55895470..55898612-chr19:55996647..55999091,3	MCF-7	breast:
39	chr19:55670339..55672194-chr19:55895106..55898791,3	K562	blood:
40	chr19:55790075..55793363-chr19:55895323..55900809,10	K562	blood:
41	chr19:55896562..55899346-chr19:56111616..56113771,2	MCF-7	breast:
42	chr19:55717069..55718690-chr19:55897128..55899524,2	K562	blood:
43	chr19:55897252..55900237-chr19:55952546..55954535,2	K562	blood:
44	chr19:55896816..55898587-chr19:56153997..56156129,2	MCF-7	breast:
45	chr19:55814396..55817267-chr19:55897234..55899790,3	K562	blood:
46	chr19:55723904..55730206-chr19:55894141..55899052,9	MCF-7	breast:
47	chr19:55808885..55818962-chr19:55893792..55900928,16	MCF-7	breast:
48	chr19:55847613..55856135-chr19:55893756..55900268,15	K562	blood:
49	chr19:55794940..55798200-chr19:55895681..55898839,3	K562	blood:
50	chr19:55677235..55679036-chr19:55897209..55898733,2	K562	blood:

No data

Variant related genes	Relation type
TMEM238	TF binding region
ENSG00000268729	Chromatin interaction
ENSG00000269808	Chromatin interaction
ENSG00000187902	Chromatin interaction
ENSG00000269859	Chromatin interaction
ENSG00000090971	Chromatin interaction
ENSG00000239137	Chromatin interaction
ENSG00000160471	Chromatin interaction
ENSG00000171425	Chromatin interaction
ENSG00000005483	Chromatin interaction
ENSG00000267577	Chromatin interaction
ENSG00000197483	Chromatin interaction
ENSG00000171443	Chromatin interaction
ENSG00000167646	Chromatin interaction
ENSG00000267110	Chromatin interaction
ENSG00000063241	Chromatin interaction
ENSG00000063244	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000133265	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000105063	Chromatin interaction
ENSG00000267649	Chromatin interaction
ENSG00000179943	Chromatin interaction
ENSG00000133247	Chromatin interaction
ENSG00000160469	Chromatin interaction
ENSG00000080031	Chromatin interaction
ENSG00000180089	Chromatin interaction
ENSG00000267531	Chromatin interaction
ENSG00000228393	Chromatin interaction
ENSG00000266462	Chromatin interaction
ENSG00000131037	Chromatin interaction

Extended variants
information (count: 46 )
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]
rs73617871	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:13 , 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	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55894600-55898600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:55894800-55899000	Active TSS	Small Intestine	intestine
3	chr19:55894800-55899200	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr19:55894800-55899600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr19:55896800-55899000	Active TSS	HSMMtube	muscle
6	chr19:55897400-55898600	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr19:55897400-55899400	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr19:55897400-55899800	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
9	chr19:55897400-55900200	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
10	chr19:55897400-55900200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
11	chr19:55897400-55900400	Transcr. at gene 5' and 3'	Dnd41	blood
12	chr19:55897600-55899800	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
13	chr19:55897600-55900200	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
14	chr19:55897600-55900400	Transcr. at gene 5' and 3'	NHEK	skin
15	chr19:55897600-55901000	Transcr. at gene 5' and 3'	A549	lung
16	chr19:55897600-55903000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr19:55897800-55898600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr19:55897800-55898600	Flanking Active TSS	Liver	Liver
19	chr19:55897800-55899200	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
20	chr19:55897800-55899400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
21	chr19:55897800-55899600	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr19:55897800-55899600	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr19:55897800-55899600	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr19:55897800-55899800	Transcr. at gene 5' and 3'	HMEC	breast
25	chr19:55897800-55900200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
26	chr19:55897800-55900600	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
27	chr19:55897800-55900800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr19:55897800-55901400	Transcr. at gene 5' and 3'	Hela-S3	cervix
29	chr19:55897800-55902200	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr19:55897800-55903000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr19:55898000-55898600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr19:55898000-55898800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr19:55898000-55898800	Flanking Active TSS	Fetal Heart	heart
34	chr19:55898000-55899000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr19:55898000-55899000	Transcr. at gene 5' and 3'	Cortex derived primary cultured neurospheres	brain
36	chr19:55898000-55899000	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
37	chr19:55898000-55899000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
38	chr19:55898000-55899200	Flanking Active TSS	Psoas Muscle	Psoas
39	chr19:55898000-55899200	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
40	chr19:55898000-55899400	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
41	chr19:55898000-55899400	Transcr. at gene 5' and 3'	Thymus	Thymus
42	chr19:55898000-55899600	Transcr. at gene 5' and 3'	Lung	lung
43	chr19:55898000-55900000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr19:55898000-55900000	Transcr. at gene 5' and 3'	Brain Hippocampus Middle	brain
45	chr19:55898000-55900000	Transcr. at gene 5' and 3'	Esophagus	oesophagus
46	chr19:55898000-55900200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr19:55898000-55900200	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:55898000-55900200	Transcr. at gene 5' and 3'	Brain Cingulate Gyrus	brain
49	chr19:55898000-55900400	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
50	chr19:55898000-55900400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--

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