Variant report

Variant	rs2260164
Chromosome Location	chr19:43968312-43968313
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	POLR2A	chr19:43967208-43968443	H1-neurons	neurons:	n/a	n/a
2	POLR2A	chr19:43967490-43968600	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr19:43967436-43968508	MCF10A-Er-Src	breast:	n/a	n/a
4	CEBPB	chr19:43967416-43968347	Hela-S3	cervix:	n/a	n/a
5	SP1	chr19:43966841-43968561	H1-hESC	embryonic stem cell:	n/a	chr19:43967505-43967515 chr19:43967621-43967630 chr19:43968002-43968011 chr19:43967622-43967635 chr19:43968382-43968394 chr19:43968003-43968012 chr19:43968364-43968374 chr19:43967505-43967514 chr19:43967714-43967723 chr19:43967664-43967675 chr19:43968415-43968424 chr19:43968414-43968426 chr19:43967621-43967631 chr19:43967969-43967979 chr19:43967505-43967519 chr19:43967639-43967649 chr19:43967713-43967724 chr19:43967557-43967569 chr19:43967505-43967515 chr19:43967622-43967631 chr19:43967621-43967630 chr19:43967998-43968012 chr19:43967557-43967569 chr19:43967952-43967962 chr19:43967640-43967649 chr19:43968002-43968012 chr19:43967558-43967567 chr19:43967506-43967515 chr19:43967620-43967632 chr19:43968363-43968375 chr19:43967638-43967650 chr19:43968383-43968393 chr19:43967715-43967724 chr19:43967638-43967650 chr19:43968382-43968394 chr19:43967713-43967725 chr19:43968001-43968013 chr19:43968411-43968425 chr19:43967559-43967568 chr19:43967639-43967653 chr19:43967558-43967567 chr19:43968001-43968013 chr19:43967713-43967725 chr19:43967504-43967516 chr19:43968003-43968012 chr19:43968383-43968393 chr19:43967620-43967632 chr19:43968127-43968139 chr19:43968381-43968388 chr19:43967969-43967979 chr19:43968365-43968374 chr19:43968363-43968375 chr19:43968002-43968012 chr19:43967504-43967516 chr19:43968414-43968426 chr19:43967505-43967514 chr19:43967952-43967962 chr19:43967558-43967568 chr19:43968416-43968425 chr19:43967681-43967692
6	ZNF384	chr19:43968140-43968397	K562	blood:	n/a	n/a
7	REST	chr19:43966874-43968994	H1-neurons	neurons:	n/a	chr19:43967994-43968007
8	MAX	chr19:43967297-43968357	GM12878	blood:	n/a	n/a
9	MAX	chr19:43966965-43968642	ECC-1	luminal epithelium:	n/a	n/a
10	SP1	chr19:43967404-43968441	K562	blood:	n/a	chr19:43967505-43967515 chr19:43967621-43967630 chr19:43968002-43968011 chr19:43967622-43967635 chr19:43968382-43968394 chr19:43968003-43968012 chr19:43968364-43968374 chr19:43967505-43967514 chr19:43967714-43967723 chr19:43967664-43967675 chr19:43968415-43968424 chr19:43968414-43968426 chr19:43967621-43967631 chr19:43967969-43967979 chr19:43967505-43967519 chr19:43967639-43967649 chr19:43967713-43967724 chr19:43967557-43967569 chr19:43967505-43967515 chr19:43967622-43967631 chr19:43967621-43967630 chr19:43967998-43968012 chr19:43967557-43967569 chr19:43967952-43967962 chr19:43967640-43967649 chr19:43968002-43968012 chr19:43967558-43967567 chr19:43967506-43967515 chr19:43967620-43967632 chr19:43968363-43968375 chr19:43967638-43967650 chr19:43968383-43968393 chr19:43967715-43967724 chr19:43967638-43967650 chr19:43968382-43968394 chr19:43967713-43967725 chr19:43968001-43968013 chr19:43968411-43968425 chr19:43967559-43967568 chr19:43967639-43967653 chr19:43967558-43967567 chr19:43968001-43968013 chr19:43967713-43967725 chr19:43967504-43967516 chr19:43968003-43968012 chr19:43968383-43968393 chr19:43967620-43967632 chr19:43968127-43968139 chr19:43968381-43968388 chr19:43967969-43967979 chr19:43968365-43968374 chr19:43968363-43968375 chr19:43968002-43968012 chr19:43967504-43967516 chr19:43968414-43968426 chr19:43967505-43967514 chr19:43967952-43967962 chr19:43967558-43967568 chr19:43968416-43968425 chr19:43967681-43967692
11	POLR2A	chr19:43967699-43968625	K562	blood:	n/a	n/a
12	MAX	chr19:43966917-43968790	A549	lung:	n/a	n/a
13	TCF12	chr19:43967689-43968447	A549	lung:	n/a	n/a
14	HCFC1	chr19:43967853-43968451	K562	blood:	n/a	n/a
15	POLR2A	chr19:43966859-43968477	H1-hESC	embryonic stem cell:	n/a	n/a
16	SIN3A	chr19:43966942-43968630	H1-hESC	embryonic stem cell:	n/a	n/a
17	TBP	chr19:43967018-43968658	H1-hESC	embryonic stem cell:	n/a	n/a
18	IRF1	chr19:43967118-43968636	K562	blood:	n/a	chr19:43967502-43967516 chr19:43967711-43967725 chr19:43967618-43967632 chr19:43968127-43968141 chr19:43967968-43967982 chr19:43967555-43967569 chr19:43968414-43968428 chr19:43968001-43968015 chr19:43968382-43968396 chr19:43968363-43968377
19	CCNT2	chr19:43967219-43968539	K562	blood:	n/a	chr19:43968364-43968373 chr19:43967506-43967515 chr19:43968002-43968011 chr19:43967640-43967649
20	SP1	chr19:43967748-43968369	GM12878	blood:	n/a	chr19:43968002-43968011 chr19:43968003-43968012 chr19:43967969-43967979 chr19:43967998-43968012 chr19:43967952-43967962 chr19:43968002-43968012 chr19:43968001-43968013 chr19:43968001-43968013 chr19:43968003-43968012 chr19:43968127-43968139 chr19:43967969-43967979 chr19:43968002-43968012 chr19:43967952-43967962
21	SP1	chr19:43967179-43968510	GM12878	blood:	n/a	chr19:43967505-43967515 chr19:43967621-43967630 chr19:43968002-43968011 chr19:43967622-43967635 chr19:43968382-43968394 chr19:43968003-43968012 chr19:43968364-43968374 chr19:43967505-43967514 chr19:43967714-43967723 chr19:43967664-43967675 chr19:43968415-43968424 chr19:43968414-43968426 chr19:43967621-43967631 chr19:43967969-43967979 chr19:43967505-43967519 chr19:43967639-43967649 chr19:43967713-43967724 chr19:43967557-43967569 chr19:43967505-43967515 chr19:43967622-43967631 chr19:43967621-43967630 chr19:43967998-43968012 chr19:43967557-43967569 chr19:43967952-43967962 chr19:43967640-43967649 chr19:43968002-43968012 chr19:43967558-43967567 chr19:43967506-43967515 chr19:43967620-43967632 chr19:43968363-43968375 chr19:43967638-43967650 chr19:43968383-43968393 chr19:43967715-43967724 chr19:43967638-43967650 chr19:43968382-43968394 chr19:43967713-43967725 chr19:43968001-43968013 chr19:43968411-43968425 chr19:43967559-43967568 chr19:43967639-43967653 chr19:43967558-43967567 chr19:43968001-43968013 chr19:43967713-43967725 chr19:43967504-43967516 chr19:43968003-43968012 chr19:43968383-43968393 chr19:43967620-43967632 chr19:43968127-43968139 chr19:43968381-43968388 chr19:43967969-43967979 chr19:43968365-43968374 chr19:43968363-43968375 chr19:43968002-43968012 chr19:43967504-43967516 chr19:43968414-43968426 chr19:43967505-43967514 chr19:43967952-43967962 chr19:43967558-43967568 chr19:43968416-43968425 chr19:43967681-43967692
22	NFYB	chr19:43968017-43968321	GM12878	blood:	n/a	chr19:43968194-43968204
23	SMC3	chr19:43968225-43968321	GM12878	blood:	n/a	n/a
24	RCOR1	chr19:43968142-43968335	HepG2	liver:	n/a	n/a
25	ELF1	chr19:43967070-43968686	GM12878	blood:	n/a	chr19:43967665-43967677 chr19:43967558-43967570
26	MAX	chr19:43967112-43968573	K562	blood:	n/a	n/a
27	MYC	chr19:43967350-43968418	MCF10A-Er-Src	breast:	n/a	n/a
28	STAT1	chr19:43967443-43968533	GM12878	blood:	n/a	chr19:43967999-43968011 chr19:43968042-43968050
29	MAX	chr19:43967144-43968539	K562	blood:	n/a	n/a
30	TBL1XR1	chr19:43968125-43968312	K562	blood:	n/a	n/a
31	SP1	chr19:43967158-43968529	A549	lung:	n/a	chr19:43967505-43967515 chr19:43967621-43967630 chr19:43968002-43968011 chr19:43967622-43967635 chr19:43968382-43968394 chr19:43968003-43968012 chr19:43968364-43968374 chr19:43967505-43967514 chr19:43967714-43967723 chr19:43967664-43967675 chr19:43968415-43968424 chr19:43968414-43968426 chr19:43967621-43967631 chr19:43967969-43967979 chr19:43967505-43967519 chr19:43967639-43967649 chr19:43967713-43967724 chr19:43967557-43967569 chr19:43967505-43967515 chr19:43967622-43967631 chr19:43967621-43967630 chr19:43967998-43968012 chr19:43967557-43967569 chr19:43967952-43967962 chr19:43967640-43967649 chr19:43968002-43968012 chr19:43967558-43967567 chr19:43967506-43967515 chr19:43967620-43967632 chr19:43968363-43968375 chr19:43967638-43967650 chr19:43968383-43968393 chr19:43967715-43967724 chr19:43967638-43967650 chr19:43968382-43968394 chr19:43967713-43967725 chr19:43968001-43968013 chr19:43968411-43968425 chr19:43967559-43967568 chr19:43967639-43967653 chr19:43967558-43967567 chr19:43968001-43968013 chr19:43967713-43967725 chr19:43967504-43967516 chr19:43968003-43968012 chr19:43968383-43968393 chr19:43967620-43967632 chr19:43968127-43968139 chr19:43968381-43968388 chr19:43967969-43967979 chr19:43968365-43968374 chr19:43968363-43968375 chr19:43968002-43968012 chr19:43967504-43967516 chr19:43968414-43968426 chr19:43967505-43967514 chr19:43967952-43967962 chr19:43967558-43967568 chr19:43968416-43968425 chr19:43967681-43967692
32	MAX	chr19:43967296-43968365	NB4	blood:	n/a	n/a
33	MYC	chr19:43967614-43968328	NB4	blood:	n/a	n/a
34	NRF1	chr19:43967270-43968684	SK-N-SH	brain:	n/a	chr19:43967569-43967580
35	RFX5	chr19:43967485-43968387	Hela-S3	cervix:	n/a	chr19:43968166-43968181
36	PBX3	chr19:43967794-43968450	SK-N-SH	brain:	n/a	n/a
37	NFYA	chr19:43967680-43968361	Hela-S3	cervix:	n/a	chr19:43968194-43968204
38	CHD2	chr19:43968301-43968494	HepG2	liver:	n/a	n/a
39	STAT3	chr19:43968299-43968420	MCF10A-Er-Src	breast:	n/a	n/a
40	RCOR1	chr19:43967727-43968553	K562	blood:	n/a	n/a
41	E2F6	chr19:43966912-43968319	A549	lung:	n/a	n/a
42	MAX	chr19:43967100-43968707	MCF-7	breast:	n/a	n/a
43	POLR2A	chr19:43967600-43968378	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr19:43967159-43968730	MCF-7	breast:	n/a	n/a
45	BACH1	chr19:43967922-43968333	K562	blood:	n/a	n/a
46	POLR2A	chr19:43967659-43968326	SK-N-MC	brain:	n/a	n/a
47	MXI1	chr19:43967092-43968672	HepG2	liver:	n/a	n/a
48	CHD2	chr19:43967340-43968608	GM12878	blood:	n/a	n/a
49	POLR2A	chr19:43967608-43968549	PFSK-1	brain:	n/a	n/a
50	MYC	chr19:43967305-43968521	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:43965066..43971111-chr19:44006791..44009897,14	MCF-7	breast:
2	chr19:43967204..43969877-chr19:44006593..44010322,9	MCF-7	breast:
3	chr19:43966525..43969059-chr19:44008556..44010178,2	K562	blood:
4	chr19:43967559..43969177-chr19:44122484..44124753,2	K562	blood:
5	chr19:43857729..43859549-chr19:43967499..43969532,2	MCF-7	breast:
6	chr19:43967717..43971076-chr19:44036987..44039699,3	MCF-7	breast:
7	chr19:43966113..43971089-chr19:44005040..44010546,6	K562	blood:

Variant related genes	Relation type
LYPD3	TF binding region
ENSG00000131116	Chromatin interaction
ENSG00000176531	Chromatin interaction
ENSG00000204936	Chromatin interaction
ENSG00000176472	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11668793	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2599433	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2599434	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2599437	0.81[CEU][hapmap]
rs2599438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2599441	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2599442	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2682568	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2682582	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2682583	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35107209	0.91[ASN][1000 genomes]
rs57029828	0.89[ASN][1000 genomes]
rs60027199	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055872	chr19:43173614-44075193	Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv544009	chr19:43173614-44075193	Enhancers ZNF genes & repeats Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1067126	chr19:43260649-44075194	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv544015	chr19:43260649-44075194	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv1057657	chr19:43302497-44076564	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv1059631	chr19:43316978-44075054	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv544030	chr19:43316978-44075054	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	nsv532820	chr19:43807486-44080610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv1056721	chr19:43808474-44095077	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv532821	chr19:43842383-44357315	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer 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	62 gene(s)	inside rSNPs	diseases
11	nsv1058162	chr19:43846238-44055058	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv2501	chr19:43942581-43978424	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	8 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	chr19:43966600-43968600	Active TSS	H9 Cell Line	embryonic stem cell
2	chr19:43966600-43968600	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr19:43966800-43968600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr19:43966800-43968600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:43966800-43969000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
6	chr19:43967000-43968400	Active TSS	NHLF	lung
7	chr19:43967000-43968600	Active TSS	H1 Cell Line	embryonic stem cell
8	chr19:43967000-43968600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr19:43967000-43968600	Active TSS	Brain Cingulate Gyrus	brain
10	chr19:43967000-43968600	Active TSS	Fetal Kidney	kidney
11	chr19:43967000-43968600	Active TSS	Rectal Smooth Muscle	rectum
12	chr19:43967000-43968600	Active TSS	A549	lung
13	chr19:43967000-43968800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr19:43967000-43968800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr19:43967000-43968800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
16	chr19:43967000-43968800	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr19:43967000-43969000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr19:43967000-43969000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr19:43967000-43969000	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr19:43967200-43968400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr19:43967200-43968400	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr19:43967200-43968400	Active TSS	Gastric	stomach
23	chr19:43967200-43968400	Active TSS	Right Atrium	heart
24	chr19:43967200-43968600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr19:43967200-43968600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:43967200-43968600	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr19:43967200-43968600	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr19:43967200-43968600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr19:43967200-43968600	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr19:43967200-43968600	Active TSS	Aorta	Aorta
31	chr19:43967200-43968600	Active TSS	Colon Smooth Muscle	Colon
32	chr19:43967200-43968600	Active TSS	Fetal Lung	lung
33	chr19:43967200-43968600	Flanking Active TSS	Fetal Thymus	thymus
34	chr19:43967200-43968600	Active TSS	HSMM	muscle
35	chr19:43967200-43968600	Active TSS	HSMMtube	muscle
36	chr19:43967200-43968800	Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr19:43967200-43968800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr19:43967200-43968800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr19:43967200-43968800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
40	chr19:43967200-43968800	Flanking Active TSS	Liver	Liver
41	chr19:43967200-43968800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
42	chr19:43967200-43968800	Active TSS	Ovary	ovary
43	chr19:43967200-43968800	Active TSS	Psoas Muscle	Psoas
44	chr19:43967200-43969000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
45	chr19:43967400-43968400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr19:43967400-43968400	Active TSS	Primary B cells from peripheral blood	blood
47	chr19:43967400-43968400	Active TSS	Primary T cells from cord blood	blood
48	chr19:43967400-43968400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr19:43967400-43968400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr19:43967400-43968400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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