Variant report

Variant	rs55650549
Chromosome Location	chr19:18303008-18303009
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:157)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:157 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:18302880-18303030	HEEpiC	esophagus:	n/a	n/a
2	RCOR1	chr19:18302940-18303183	K562	blood:	n/a	n/a
3	POLR2A	chr19:18302760-18304647	HepG2	liver:	n/a	n/a
4	STAT3	chr19:18302551-18303053	MCF10A-Er-Src	breast:	n/a	n/a
5	CTCF	chr19:18302860-18303010	HRE	kidney:	n/a	n/a
6	CTCF	chr19:18302860-18303010	HCFaa	heart:	n/a	n/a
7	CTCF	chr19:18302880-18303030	GM12871	blood:	n/a	n/a
8	FOS	chr19:18302533-18303114	MCF10A-Er-Src	breast:	n/a	n/a
9	MYC	chr19:18302472-18303092	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr19:18302797-18303261	HCT-116	colon:	n/a	n/a
11	RCOR1	chr19:18302740-18303967	GM12878	blood:	n/a	n/a
12	CTCF	chr19:18302880-18303030	AG04450	lung:	n/a	n/a
13	BCLAF1	chr19:18302700-18303326	GM12878	blood:	n/a	n/a
14	MTA3	chr19:18302476-18303035	GM12878	blood:	n/a	n/a
15	RUNX3	chr19:18302734-18304446	GM12878	blood:	n/a	n/a
16	CTCF	chr19:18302812-18303014	GM13977	blood:	n/a	n/a
17	RAD21	chr19:18302814-18303025	K562	blood:	n/a	n/a
18	POLR2A	chr19:18302724-18303797	U87	brain:	n/a	n/a
19	CTCF	chr19:18302920-18303070	SAEC	small airway:	n/a	n/a
20	FOXA1	chr19:18302659-18303139	HepG2	liver:	n/a	n/a
21	CTCF	chr19:18302860-18303010	A549	lung:	n/a	n/a
22	POLR2A	chr19:18302446-18304283	MCF10A-Er-Src	breast:	n/a	n/a
23	CTCF	chr19:18302880-18303030	BE2_C	brain:	n/a	n/a
24	FOS	chr19:18302547-18303056	MCF10A-Er-Src	breast:	n/a	n/a
25	CTCF	chr19:18302747-18303060	Spleen_OC	spleen:	n/a	n/a
26	RELA	chr19:18302584-18304668	GM18951	blood:	n/a	n/a
27	CTCF	chr19:18302712-18303109	GM12878	blood:	n/a	n/a
28	RAD21	chr19:18302679-18303200	MCF-7	breast:	n/a	n/a
29	TEAD4	chr19:18302527-18304262	K562	blood:	n/a	n/a
30	RAD21	chr19:18302469-18304830	SK-N-SH	brain:	n/a	chr19:18304495-18304509
31	RUNX3	chr19:18302667-18304183	GM12878	blood:	n/a	n/a
32	RAD21	chr19:18302618-18303150	ECC-1	luminal epithelium:	n/a	n/a
33	CTCF	chr19:18302860-18303010	GM12868	blood:	n/a	n/a
34	RAD21	chr19:18302801-18303057	HepG2	liver:	n/a	n/a
35	RCOR1	chr19:18302775-18304237	K562	blood:	n/a	n/a
36	MTA3	chr19:18302740-18303783	GM12878	blood:	n/a	n/a
37	MAZ	chr19:18302624-18304832	IMR90	lung:	n/a	n/a
38	CTCF	chr19:18302920-18303070	GM12866	blood:	n/a	n/a
39	MAZ	chr19:18302869-18303067	K562	blood:	n/a	n/a
40	FOXM1	chr19:18302774-18303312	GM12878	blood:	n/a	n/a
41	CTCF	chr19:18302880-18303030	GM12870	blood:	n/a	n/a
42	EBF1	chr19:18302734-18303136	GM12878	blood:	n/a	n/a
43	KAP1	chr19:18302708-18303831	HEK293	kidney:	n/a	n/a
44	RAD21	chr19:18302740-18303148	GM12878	blood:	n/a	n/a
45	CTCF	chr19:18302706-18303083	K562	blood:	n/a	n/a
46	RAD21	chr19:18302648-18303148	HepG2	liver:	n/a	n/a
47	RAD21	chr19:18302739-18303078	Hela-S3	cervix:	n/a	n/a
48	RAD21	chr19:18302720-18303122	IMR90	lung:	n/a	n/a
49	MYC	chr19:18302477-18303068	MCF10A-Er-Src	breast:	n/a	n/a
50	PRDM1	chr19:18302850-18303191	Hela-S3	cervix:	n/a	chr19:18302981-18302996

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18302642..18303148-chr19:18362353..18362883,2	MCF-7	breast:
2	chr19:18301148..18305001-chr19:18389528..18394862,10	MCF-7	breast:
3	chr19:18262556..18266763-chr19:18301801..18307197,7	K562	blood:
4	chr19:18302787..18307396-chr19:18383842..18390051,8	K562	blood:
5	chr19:18263401..18266218-chr19:18302169..18305024,2	MCF-7	breast:
6	chr19:18301873..18308921-chr19:18309874..18315133,13	MCF-7	breast:
7	chr19:18302931..18304464-chr19:18547111..18549483,2	K562	blood:
8	chr19:18302575..18305285-chr19:18390568..18392250,2	MCF-7	breast:
9	chr19:18302080..18305763-chr19:18333769..18336252,4	K562	blood:
10	chr19:18223936..18224487-chr19:18302381..18303176,2	K562	blood:
11	chr19:18302289..18309850-chr19:18311214..18320810,23	K562	blood:
12	chr19:18278665..18280705-chr19:18302559..18305155,2	K562	blood:
13	chr19:18283035..18288338-chr19:18301660..18307351,8	K562	blood:
14	chr19:18302942..18305811-chr19:18331893..18333423,2	MCF-7	breast:
15	chr19:18302057..18307216-chr19:18311605..18315914,14	MCF-7	breast:
16	chr19:18302376..18304166-chr19:18432954..18434966,2	K562	blood:
17	chr19:18301435..18303273-chr19:18392277..18393876,2	K562	blood:
18	chr19:18282952..18288338-chr19:18301660..18306832,7	K562	blood:
19	chr19:18261707..18265058-chr19:18302365..18306548,5	K562	blood:
20	chr19:18275085..18277218-chr19:18301566..18304039,2	K562	blood:
21	chr19:18301633..18303907-chr19:18432550..18435095,2	MCF-7	breast:
22	chr19:18268586..18275019-chr19:18302013..18308723,7	MCF-7	breast:

No data

Variant related genes	Relation type
MPV17L2	TF binding region
ENSG00000269145	Chromatin interaction
ENSG00000105649	Chromatin interaction
ENSG00000130520	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000216490	Chromatin interaction
ENSG00000105650	Chromatin interaction
ENSG00000268173	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000268650	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000105647	Chromatin interaction
ENSG00000267959	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1046565	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11881258	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12460619	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12461021	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12462801	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17683509	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17683539	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2049050	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2229228	0.91[EUR][1000 genomes]
rs3803919	0.93[EUR][1000 genomes]
rs4458132	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4808768	0.86[EUR][1000 genomes]
rs62120367	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62120368	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62120382	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62120383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62120385	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62120388	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62120393	0.90[EUR][1000 genomes]
rs6512247	0.86[ASN][1000 genomes]
rs7245576	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7246274	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7249773	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7259695	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8100626	0.91[EUR][1000 genomes]
rs8104010	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8109807	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055932	chr19:17923918-18369944	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv543923	chr19:17923918-18369944	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
3	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
4	esv1837595	chr19:18085428-18393682	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
5	nsv911241	chr19:18193191-18304700	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv911242	chr19:18201757-18304700	Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv911244	chr19:18206681-18304700	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	nsv911245	chr19:18206681-18338101	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription 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 miRNA target site	37 gene(s)	inside rSNPs	diseases
9	nsv833775	chr19:18213761-18390074	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
10	nsv911248	chr19:18224729-18338101	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
11	nsv911249	chr19:18224729-18375846	Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
12	nsv911250	chr19:18224729-18376522	Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription 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 target site	37 gene(s)	inside rSNPs	diseases
13	nsv911251	chr19:18224729-18422364	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats 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	136 gene(s)	inside rSNPs	diseases
14	nsv911252	chr19:18234588-18338101	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
15	nsv911253	chr19:18240127-18418044	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
16	nsv916325	chr19:18244780-18534927	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Strong transcription 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 miRNA target site	167 gene(s)	inside rSNPs	diseases
17	nsv911254	chr19:18248146-18310678	Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
18	nsv911256	chr19:18255359-18338101	Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription 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 target site	37 gene(s)	inside rSNPs	diseases
19	nsv911260	chr19:18288069-18386798	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
20	nsv911261	chr19:18288947-18311199	Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
21	nsv911262	chr19:18288947-18312453	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
22	nsv828470	chr19:18289598-18311602	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
23	nsv828471	chr19:18293567-18311602	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
24	nsv819691	chr19:18294153-18312275	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18302400-18303200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:18302400-18303400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr19:18302400-18304200	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr19:18302600-18303200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr19:18302600-18303200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:18302600-18303200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr19:18302600-18303200	Flanking Active TSS	Liver	Liver
8	chr19:18302600-18303200	Flanking Active TSS	Colon Smooth Muscle	Colon
9	chr19:18302600-18303200	Flanking Active TSS	NHEK	skin
10	chr19:18302600-18303400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
11	chr19:18302600-18303400	Flanking Active TSS	HMEC	breast
12	chr19:18302600-18303400	Flanking Active TSS	HUVEC	blood vessel
13	chr19:18302600-18303600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr19:18302600-18303600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr19:18302600-18303600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr19:18302600-18303600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr19:18302600-18304000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr19:18302600-18304400	Active TSS	Brain Cingulate Gyrus	brain
19	chr19:18302600-18304400	Active TSS	Fetal Lung	lung
20	chr19:18302600-18304600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr19:18302600-18304600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr19:18302600-18304600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr19:18302600-18304600	Active TSS	Brain Anterior Caudate	brain
24	chr19:18302600-18304600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr19:18302600-18304600	Active TSS	Lung	lung
26	chr19:18302600-18304600	Active TSS	Rectal Smooth Muscle	rectum
27	chr19:18302600-18304600	Active TSS	HSMM	muscle
28	chr19:18302600-18304800	Active TSS	Right Atrium	heart
29	chr19:18302600-18304800	Active TSS	A549	lung
30	chr19:18302600-18304800	Active TSS	NHDF-Ad	bronchial
31	chr19:18302600-18304800	Active TSS	NHLF	lung
32	chr19:18302600-18305000	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr19:18302600-18305000	Active TSS	HSMMtube	muscle
34	chr19:18302600-18305200	Active TSS	Fetal Kidney	kidney
35	chr19:18302800-18303200	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr19:18302800-18303200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr19:18302800-18303200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
38	chr19:18302800-18303200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr19:18302800-18303200	Flanking Active TSS	Fetal Intestine Large	intestine
40	chr19:18302800-18303200	Active TSS	Thymus	Thymus
41	chr19:18302800-18303400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr19:18302800-18303400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr19:18302800-18303400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr19:18302800-18303400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
45	chr19:18302800-18303400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr19:18302800-18303400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr19:18302800-18303400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr19:18302800-18303400	Flanking Active TSS	Fetal Heart	heart
49	chr19:18302800-18303400	Flanking Active TSS	Fetal Muscle Leg	muscle
50	chr19:18302800-18303400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum

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