Variant report

Variant	rs2049050
Chromosome Location	chr19:18315629-18315630
allele	C/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	BHLHE40	chr19:18313640-18316161	GM12878	blood:	n/a	chr19:18316105-18316121 chr19:18313961-18313977 chr19:18313862-18313878
2	POLR2A	chr19:18313893-18316689	K562	blood:	n/a	n/a
3	ZNF143	chr19:18314746-18315643	K562	blood:	n/a	chr19:18315610-18315628 chr19:18315555-18315574
4	POLR2A	chr19:18315038-18315863	HUVEC	blood vessel:	n/a	n/a
5	STAT3	chr19:18315514-18315714	MCF10A-Er-Src	breast:	n/a	chr19:18315609-18315621 chr19:18315567-18315575 chr19:18315678-18315698
6	JUND	chr19:18314330-18316098	H1-hESC	embryonic stem cell:	n/a	chr19:18315074-18315083 chr19:18315135-18315144
7	POLR2A	chr19:18315074-18316583	K562	blood:	n/a	n/a
8	POLR2A	chr19:18315077-18315759	SK-N-SH	brain:	n/a	n/a
9	GTF2F1	chr19:18315394-18315637	H1-hESC	embryonic stem cell:	n/a	n/a
10	SIN3AK20	chr19:18313627-18315638	MCF-7	breast:	n/a	n/a
11	POLR2A	chr19:18315174-18315720	K562	blood:	n/a	n/a
12	CREB1	chr19:18314395-18315744	H1-hESC	embryonic stem cell:	n/a	chr19:18314887-18314900
13	POLR2A	chr19:18315202-18316222	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr19:18315262-18315782	SK-N-MC	brain:	n/a	n/a
15	ZBTB7A	chr19:18315160-18315680	HepG2	liver:	n/a	n/a
16	CHD2	chr19:18314320-18315680	GM12878	blood:	n/a	n/a
17	ZNF143	chr19:18314728-18315672	GM12878	blood:	n/a	chr19:18315610-18315628 chr19:18315555-18315574
18	POLR2A	chr19:18315101-18315669	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr19:18315192-18315712	MCF10A-Er-Src	breast:	n/a	n/a
20	ELF1	chr19:18315486-18316292	GM12878	blood:	n/a	n/a
21	MAZ	chr19:18313254-18316673	IMR90	lung:	n/a	chr19:18315475-18315485 chr19:18313930-18313937 chr19:18316400-18316407 chr19:18315795-18315805 chr19:18313919-18313928 chr19:18316066-18316076 chr19:18313922-18313929 chr19:18316214-18316223 chr19:18316396-18316405
22	POLR2A	chr19:18315414-18315639	SK-N-SH	brain:	n/a	n/a
23	SP4	chr19:18314586-18315661	H1-hESC	embryonic stem cell:	n/a	chr19:18314984-18315000 chr19:18314856-18314872
24	POLR2A	chr19:18315472-18315631	HepG2	liver:	n/a	n/a
25	SIN3A	chr19:18313668-18316142	H1-hESC	embryonic stem cell:	n/a	chr19:18315296-18315310 chr19:18314487-18314498 chr19:18315302-18315310
26	POLR2A	chr19:18315069-18315789	PFSK-1	brain:	n/a	n/a
27	POLR2A	chr19:18315492-18315636	HepG2	liver:	n/a	n/a
28	POLR2A	chr19:18315463-18315710	H1-hESC	embryonic stem cell:	n/a	n/a
29	MYC	chr19:18313626-18315726	K562	blood:	n/a	chr19:18315475-18315485 chr19:18313930-18313937 chr19:18313919-18313928 chr19:18313922-18313929
30	BHLHE40	chr19:18313716-18316045	K562	blood:	n/a	chr19:18313961-18313977 chr19:18313862-18313878
31	POLR2A	chr19:18315183-18315697	MCF10A-Er-Src	breast:	n/a	n/a
32	TAF1	chr19:18315069-18316262	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr19:18315412-18316319	K562	blood:	n/a	n/a
34	POLR2A	chr19:18315438-18315682	HepG2	liver:	n/a	n/a
35	POLR2A	chr19:18315003-18315671	K562	blood:	n/a	n/a
36	NFIC	chr19:18314977-18315643	GM12878	blood:	n/a	n/a
37	TBP	chr19:18315129-18316282	H1-hESC	embryonic stem cell:	n/a	n/a
38	MXI1	chr19:18313159-18316795	SK-N-SH	brain:	n/a	n/a
39	TBP	chr19:18314750-18315683	GM12878	blood:	n/a	n/a
40	IRF1	chr19:18314705-18316172	K562	blood:	n/a	chr19:18314900-18314914 chr19:18314986-18315000 chr19:18315074-18315088 chr19:18315133-18315142 chr19:18315811-18315828 chr19:18316040-18316054 chr19:18315814-18315825 chr19:18314858-18314872
41	ZBTB7A	chr19:18314494-18316227	ECC-1	luminal epithelium:	n/a	n/a
42	ELK1	chr19:18315442-18315846	K562	blood:	n/a	n/a
43	POLR2A	chr19:18315148-18315686	HCT-116	colon:	n/a	n/a
44	ZBTB7A	chr19:18314393-18316375	ECC-1	luminal epithelium:	n/a	n/a
45	POLR2A	chr19:18315151-18315700	HepG2	liver:	n/a	n/a
46	SP1	chr19:18314766-18315630	GM12878	blood:	n/a	chr19:18314858-18314870 chr19:18314853-18314865 chr19:18314860-18314869 chr19:18314988-18314997 chr19:18314986-18314998 chr19:18315074-18315086 chr19:18314858-18314870 chr19:18315498-18315510 chr19:18315074-18315086 chr19:18315500-18315509 chr19:18315076-18315085 chr19:18314900-18314912 chr19:18314987-18314996 chr19:18315075-18315084 chr19:18314988-18314997 chr19:18315499-18315509 chr19:18315132-18315153 chr19:18315498-18315510 chr19:18314987-18314997 chr19:18315071-18315085 chr19:18315609-18315618 chr19:18314986-18314998
47	POLR2A	chr19:18313854-18316102	H1-neurons	neurons:	n/a	n/a
48	YY1	chr19:18315381-18315835	K562	blood:	n/a	chr19:18315498-18315509
49	MAZ	chr19:18314610-18316132	HepG2	liver:	n/a	chr19:18315475-18315485 chr19:18315795-18315805 chr19:18316066-18316076
50	POLR2A	chr19:18313917-18317009	IMR90	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18265635..18269832-chr19:18313306..18316630,4	K562	blood:
2	chr19:18313264..18315629-chr19:18528906..18531425,2	MCF-7	breast:
3	chr19:18312530..18316975-chr19:18331566..18338113,9	K562	blood:
4	chr19:18311216..18316508-chr19:18389022..18394678,9	MCF-7	breast:
5	chr19:18207464..18209881-chr19:18313864..18315972,2	MCF-7	breast:
6	chr19:18313659..18316582-chr19:18386529..18393683,9	K562	blood:
7	chr19:18311642..18316628-chr19:18388957..18392513,10	K562	blood:
8	chr19:18312530..18319182-chr19:18329520..18338113,19	K562	blood:
9	chr19:18302057..18307216-chr19:18311605..18315914,14	MCF-7	breast:
10	chr19:18313916..18318092-chr19:18528402..18531529,5	K562	blood:
11	chr19:18265822..18267690-chr19:18314234..18316588,2	MCF-7	breast:
12	chr19:18314296..18317431-chr19:18383748..18386421,3	K562	blood:
13	chr19:18264824..18267615-chr19:18313161..18315862,2	MCF-7	breast:
14	chr19:18314746..18317215-chr19:18546753..18549806,3	K562	blood:
15	chr19:18314629..18316965-chr19:18497132..18498761,2	K562	blood:
16	chr19:18272069..18275031-chr19:18313759..18316428,2	K562	blood:
17	chr19:18302289..18309850-chr19:18311214..18320810,23	K562	blood:
18	chr19:18312925..18315923-chr20:55967993..55969596,2	MCF-7	breast:
19	chr19:18270643..18273104-chr19:18313490..18316053,2	K562	blood:
20	chr19:18314296..18317366-chr19:18383748..18385809,3	K562	blood:
21	chr19:18313702..18316146-chr19:18389721..18392001,2	MCF-7	breast:
22	chr19:18315560..18317882-chr19:18321449..18323321,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPV17L2-1	chr19:18315535-18315709	XLOC_012991
2	lnc-MPV17L2-1	chr19:18315540-18315709	NONHSAT062942
3	lnc-MPV17L2-1	chr19:18315540-18315709	ENSG00000268650.3
4	lnc-MPV17L2-1	chr19:18315551-18315709	ENSG00000268650.3
5	lnc-MPV17L2-1	chr19:18315544-18315709	ENSG00000268650.3
6	lnc-MPV17L2-1	chr19:18315546-18315709	NONHSAT062944
7	lnc-MPV17L2-1	chr19:18315540-18315709	NONHSAT062943

Variant related genes	Relation type
RAB3A	TF binding region
ENSG00000105650	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000105647	Chromatin interaction
ENSG00000099308	Chromatin interaction
ENSG00000218018	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000096996	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000254858	Chromatin interaction
ENSG00000130518	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1045747	0.89[JPT][hapmap]
rs1046565	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11881258	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12460619	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12461021	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12462801	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17683509	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17683539	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2229228	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2271882	0.86[CHB][hapmap]
rs3803919	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4458132	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4808118	0.89[JPT][hapmap]
rs4808768	0.92[EUR][1000 genomes]
rs55650549	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62120367	0.85[EUR][1000 genomes]
rs62120368	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62120382	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62120383	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62120385	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62120388	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62120393	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7245576	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7246274	0.93[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7249773	0.83[ASN][1000 genomes]
rs7259695	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8100626	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8104010	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8109807	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][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	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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	nsv911263	chr19:18309365-18324329	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv911264	chr19:18309365-18369644	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2049050	ZNF738	cis	parietal	SCAN
rs2049050	OR7A10	cis	cerebellum	SCAN
rs2049050	ZNF429	cis	cerebellum	SCAN
rs2049050	KIAA1683	cis	cerebellum	SCAN
rs2049050	UBA52	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18313400-18316800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr19:18313600-18316400	Active TSS	Colon Smooth Muscle	Colon
3	chr19:18313600-18317000	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr19:18313800-18316200	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr19:18313800-18316400	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr19:18313800-18316800	Active TSS	H9 Cell Line	embryonic stem cell
7	chr19:18314000-18316600	Active TSS	Fetal Kidney	kidney
8	chr19:18314000-18316800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr19:18314000-18317000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr19:18314200-18316000	Active TSS	Lung	lung
11	chr19:18314200-18316000	Active TSS	Small Intestine	intestine
12	chr19:18314200-18316200	Active TSS	HepG2	liver
13	chr19:18314200-18316400	Active TSS	Brain Anterior Caudate	brain
14	chr19:18314200-18316400	Active TSS	Psoas Muscle	Psoas
15	chr19:18314200-18316600	Active TSS	Ovary	ovary
16	chr19:18314200-18317200	Active TSS	Fetal Brain Female	brain
17	chr19:18314400-18315800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr19:18314400-18316000	Active TSS	Sigmoid Colon	Sigmoid Colon
19	chr19:18314400-18316200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr19:18314400-18316200	Active TSS	Aorta	Aorta
21	chr19:18314400-18316200	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr19:18314400-18316200	Active TSS	Brain Substantia Nigra	brain
23	chr19:18314400-18316200	Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr19:18314400-18316200	Active TSS	A549	lung
25	chr19:18314400-18316200	Active TSS	Hela-S3	cervix
26	chr19:18314400-18316200	Active TSS	NHDF-Ad	bronchial
27	chr19:18314400-18316400	Active TSS	H1 Cell Line	embryonic stem cell
28	chr19:18314400-18316400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:18314400-18316400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr19:18314400-18316400	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr19:18314400-18316400	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr19:18314400-18316400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr19:18314400-18316400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr19:18314400-18316400	Active TSS	Brain Cingulate Gyrus	brain
35	chr19:18314400-18316400	Active TSS	Fetal Lung	lung
36	chr19:18314400-18316400	Active TSS	Right Ventricle	heart
37	chr19:18314400-18316400	Active TSS	K562	blood
38	chr19:18314400-18316600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr19:18314400-18316600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr19:18314400-18316600	Active TSS	Right Atrium	heart
41	chr19:18314400-18317000	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr19:18314400-18317600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr19:18314600-18315800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr19:18314600-18316000	Active TSS	Gastric	stomach
45	chr19:18314600-18316200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr19:18314600-18316200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:18314600-18316200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr19:18314600-18316200	Active TSS	Colonic Mucosa	Colon
49	chr19:18314600-18316200	Active TSS	Esophagus	oesophagus
50	chr19:18314600-18316200	Active TSS	Pancreas	Pancrea

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