Variant report

Variant	rs626821
Chromosome Location	chr19:56633605-56633606
allele	A/G
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	MAX	chr19:56631362-56633713	HepG2	liver:	n/a	chr19:56631814-56631821 chr19:56631717-56631727 chr19:56631812-56631821 chr19:56631811-56631821 chr19:56632523-56632533
2	POLR2A	chr19:56632557-56633682	GM12891	blood:	n/a	n/a
3	MYC	chr19:56631571-56633698	K562	blood:	n/a	chr19:56631814-56631821 chr19:56631717-56631727 chr19:56631812-56631821 chr19:56631811-56631821 chr19:56632523-56632533
4	CUX1	chr19:56633180-56633772	K562	blood:	n/a	n/a
5	POLR2A	chr19:56627980-56633656	GM12878	blood:	n/a	n/a
6	MAFK	chr19:56632842-56633707	K562	blood:	n/a	n/a
7	RELA	chr19:56631782-56633610	GM15510	blood:	n/a	n/a
8	RCOR1	chr19:56633051-56633646	K562	blood:	n/a	n/a
9	TCF12	chr19:56631398-56633725	A549	lung:	n/a	chr19:56632499-56632509 chr19:56632914-56632921
10	POLR2A	chr19:56630150-56633674	GM12878	blood:	n/a	n/a
11	CHD1	chr19:56630697-56633691	IMR90	lung:	n/a	chr19:56632691-56632701 chr19:56632869-56632879 chr19:56632983-56632993
12	HCFC1	chr19:56631480-56633890	Hela-S3	cervix:	n/a	n/a
13	GABPA	chr19:56632383-56633668	A549	lung:	n/a	chr19:56632990-56632999 chr19:56632988-56633002 chr19:56632892-56632901 chr19:56632985-56632999 chr19:56632522-56632531 chr19:56632988-56632999
14	RCOR1	chr19:56632591-56633767	GM12878	blood:	n/a	n/a
15	MXI1	chr19:56630388-56633630	SK-N-SH	brain:	n/a	chr19:56632499-56632508
16	IRF1	chr19:56632591-56633656	K562	blood:	n/a	chr19:56632888-56632902
17	ZMIZ1	chr19:56632498-56633623	K562	blood:	n/a	n/a
18	POLR2A	chr19:56630760-56633631	Raji	blood:	n/a	n/a
19	POLR2A	chr19:56628080-56633666	PANC-1	pancreas:	n/a	n/a
20	MAZ	chr19:56630636-56633669	IMR90	lung:	n/a	chr19:56631814-56631821 chr19:56631717-56631727 chr19:56631812-56631821 chr19:56631811-56631821 chr19:56632523-56632533
21	MAX	chr19:56630383-56633643	A549	lung:	n/a	chr19:56631814-56631821 chr19:56631717-56631727 chr19:56631812-56631821 chr19:56631811-56631821 chr19:56632523-56632533
22	POLR2A	chr19:56632493-56633752	GM12878	blood:	n/a	n/a
23	MTA3	chr19:56632552-56633726	GM12878	blood:	n/a	n/a
24	MYC	chr19:56630868-56633820	A549	lung:	n/a	chr19:56631814-56631821 chr19:56631717-56631727 chr19:56631812-56631821 chr19:56631811-56631821 chr19:56632523-56632533
25	ARID3A	chr19:56632736-56633711	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56631390..56634909-chr19:56825062..56827444,3	MCF-7	breast:
2	chr19:56164264..56167135-chr19:56631802..56633967,4	K562	blood:
3	chr19:56627257..56634581-chr19:56650310..56656612,28	MCF-7	breast:
4	chr19:56629593..56636020-chr19:56650029..56654099,17	K562	blood:
5	chr19:56629593..56635165-chr19:56650391..56656450,20	K562	blood:
6	chr19:56154949..56157092-chr19:56632186..56634615,2	K562	blood:
7	chr19:56629015..56635457-chr19:56649954..56657591,25	MCF-7	breast:

Variant related genes	Relation type
ZNF787	TF binding region
ENSG00000267549	Chromatin interaction
ENSG00000167685	Chromatin interaction
ENSG00000131848	Chromatin interaction
ENSG00000063244	Chromatin interaction
ENSG00000171425	Chromatin interaction

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs11673628	0.84[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs12459102	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12981138	0.85[ASN][1000 genomes]
rs12983086	0.89[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs2450439	0.96[ASN][1000 genomes]
rs2631625	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2631627	0.95[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2631628	0.93[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2631631	1.00[CEU][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2631637	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2631640	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2637088	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2637092	0.94[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2637094	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2637097	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2637114	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2932757	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs473953	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs478402	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4801676	0.84[CHB][hapmap];0.89[CHD][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs481936	0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs490345	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs492078	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs497453	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs501798	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs504350	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs506547	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs509897	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs517021	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs517582	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs521092	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs522980	0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs524778	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs524829	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs524988	0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs525827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.90[MEX][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs527715	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs530102	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs533640	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs533734	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs535393	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs536342	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs536414	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs537425	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs540900	1.00[CEU][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.90[MEX][hapmap]
rs544365	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs545570	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs547002	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs547945	1.00[CEU][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs564050	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs564973	0.90[ASN][1000 genomes]
rs565879	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs569310	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs572851	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs578990	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs578991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs582271	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs583330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs587702	0.86[ASN][1000 genomes]
rs588574	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs592827	0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs599405	1.00[CEU][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.85[MEX][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs609736	0.97[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.85[MEX][hapmap];0.81[ASN][1000 genomes]
rs609755	0.81[ASN][1000 genomes]
rs619934	0.83[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs628090	0.86[ASN][1000 genomes]
rs629544	1.00[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs630704	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs640654	0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs642776	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs643133	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.90[MEX][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs643174	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs648352	0.84[AMR][1000 genomes]
rs659424	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs662308	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs662763	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs665082	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs665846	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs665857	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs667438	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs667523	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs667974	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs669866	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs677127	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs677142	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs678540	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs684653	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs685117	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap];0.82[MEX][hapmap];0.91[ASN][1000 genomes]
rs8103672	0.84[CHB][hapmap];0.86[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs8108818	0.80[ASN][1000 genomes]
rs9676765	0.95[JPT][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056598	chr19:56331762-56703428	Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
2	nsv1064371	chr19:56418215-56842450	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
3	nsv1057316	chr19:56418215-56849458	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv580354	chr19:56505685-56723492	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
5	nsv833883	chr19:56512601-56640089	Strong transcription Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS 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	41 gene(s)	inside rSNPs	diseases
6	nsv523651	chr19:56537528-56707048	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1057820	chr19:56555942-56720262	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv528998	chr19:56578238-56707048	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
9	nsv912512	chr19:56592286-56636759	Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
10	nsv517365	chr19:56592286-56674548	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv912513	chr19:56592286-56685463	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
12	nsv521744	chr19:56592286-56686953	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
13	nsv912514	chr19:56596815-56636759	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
14	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
15	esv1809307	chr19:56604027-56633623	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
16	esv1824038	chr19:56610449-56636632	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
17	esv3331653	chr19:56631165-56634013	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	n/a
18	esv3409452	chr19:56631390-56633688	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56631200-56633800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr19:56633000-56633800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
3	chr19:56633000-56633800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
4	chr19:56633000-56633800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr19:56633200-56633800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
6	chr19:56633200-56633800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
7	chr19:56633200-56633800	Flanking Active TSS	A549	lung
8	chr19:56633400-56633800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr19:56633400-56633800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr19:56633400-56634600	Weak transcription	Ovary	ovary
11	chr19:56633400-56634800	Enhancers	Fetal Stomach	stomach
12	chr19:56633400-56635200	Enhancers	Fetal Muscle Leg	muscle
13	chr19:56633400-56636800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:56633400-56636800	Weak transcription	HSMM	muscle
15	chr19:56633400-56637000	Weak transcription	Left Ventricle	heart
16	chr19:56633600-56633800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:56633600-56633800	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr19:56633600-56633800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr19:56633600-56633800	Enhancers	Primary B cells from cord blood	blood
20	chr19:56633600-56633800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr19:56633600-56633800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr19:56633600-56633800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr19:56633600-56633800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr19:56633600-56633800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr19:56633600-56633800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr19:56633600-56633800	Enhancers	Brain Anterior Caudate	brain
27	chr19:56633600-56633800	Enhancers	Colon Smooth Muscle	Colon
28	chr19:56633600-56633800	Enhancers	Fetal Kidney	kidney
29	chr19:56633600-56633800	Enhancers	Fetal Lung	lung
30	chr19:56633600-56633800	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr19:56633600-56633800	Enhancers	Dnd41	blood
32	chr19:56633600-56633800	Active TSS	GM12878-XiMat	blood
33	chr19:56633600-56633800	Enhancers	Hela-S3	cervix
34	chr19:56633600-56633800	Enhancers	K562	blood
35	chr19:56633600-56634000	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr19:56633600-56634000	Enhancers	Primary hematopoietic stem cells	blood
37	chr19:56633600-56634000	Enhancers	Fetal Thymus	thymus
38	chr19:56633600-56634000	Enhancers	HepG2	liver
39	chr19:56633600-56634800	Weak transcription	Thymus	Thymus
40	chr19:56633600-56636200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr19:56633600-56636800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr19:56633600-56636800	Weak transcription	Colonic Mucosa	Colon
43	chr19:56633600-56636800	Weak transcription	Placenta	Placenta
44	chr19:56633600-56636800	Weak transcription	Pancreas	Pancrea
45	chr19:56633600-56636800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr19:56633600-56636800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr19:56633600-56636800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr19:56633600-56636800	Weak transcription	HSMMtube	muscle
49	chr19:56633600-56637000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr19:56633600-56637000	Weak transcription	Psoas Muscle	Psoas

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