Variant report

Variant	rs62440490
Chromosome Location	chr6:74363882-74363883
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	MYC	chr6:74363561-74364897	K562	blood:	n/a	n/a
2	ZNF143	chr6:74363467-74364325	H1-hESC	embryonic stem cell:	n/a	chr6:74363880-74363890
3	CREB1	chr6:74363413-74364265	GM12878	blood:	n/a	n/a
4	HA-E2F1	chr6:74363501-74364388	MCF-7	breast:	n/a	chr6:74363878-74363887 chr6:74363784-74363793
5	YY1	chr6:74363501-74364316	ECC-1	luminal epithelium:	n/a	chr6:74363788-74363810 chr6:74363781-74363790 chr6:74363781-74363792 chr6:74363788-74363798 chr6:74363726-74363735 chr6:74363705-74363716 chr6:74363707-74363716 chr6:74363767-74363781 chr6:74363787-74363799 chr6:74363784-74363793 chr6:74363789-74363797
6	POLR2A	chr6:74363520-74364168	K562	blood:	n/a	n/a
7	POLR2A	chr6:74362871-74364176	H1-neurons	neurons:	n/a	n/a
8	POU2F2	chr6:74363676-74364178	GM12891	blood:	n/a	n/a
9	RFX5	chr6:74363706-74364147	GM12878	blood:	n/a	n/a
10	ZBTB33	chr6:74363640-74364142	SK-N-SH	brain:	n/a	n/a
11	SIN3A	chr6:74362390-74364417	H1-hESC	embryonic stem cell:	n/a	n/a
12	MYC	chr6:74363558-74364139	MCF-7	breast:	n/a	n/a
13	MAX	chr6:74363403-74364262	HepG2	liver:	n/a	n/a
14	MYC	chr6:74363484-74364519	K562	blood:	n/a	n/a
15	MYC	chr6:74363541-74364910	MCF10A-Er-Src	breast:	n/a	n/a
16	ETS1	chr6:74363652-74364194	GM12878	blood:	n/a	chr6:74363705-74363716 chr6:74363781-74363792 chr6:74363778-74363789 chr6:74363881-74363892
17	CHD2	chr6:74363487-74364149	K562	blood:	n/a	n/a
18	POLR2A	chr6:74363502-74364131	HepG2	liver:	n/a	n/a
19	TAF1	chr6:74363614-74364278	K562	blood:	n/a	n/a
20	MXI1	chr6:74362128-74364844	IMR90	lung:	n/a	n/a
21	MYC	chr6:74363650-74364913	K562	blood:	n/a	n/a
22	SETDB1	chr6:74363845-74364281	U2OS	brain:	n/a	n/a
23	SP4	chr6:74363625-74364054	H1-hESC	embryonic stem cell:	n/a	chr6:74363703-74363714 chr6:74363776-74363792
24	TCF3	chr6:74363150-74364108	GM12878	blood:	n/a	chr6:74363619-74363634 chr6:74363262-74363272 chr6:74363622-74363631
25	MXI1	chr6:74363492-74364159	H1-hESC	embryonic stem cell:	n/a	n/a
26	TAF1	chr6:74363494-74364143	H1-hESC	embryonic stem cell:	n/a	n/a
27	YY1	chr6:74363200-74364406	GM12878	blood:	n/a	chr6:74363788-74363810 chr6:74363781-74363790 chr6:74363414-74363428 chr6:74363781-74363792 chr6:74363788-74363798 chr6:74363417-74363431 chr6:74363726-74363735 chr6:74363453-74363467 chr6:74363705-74363716 chr6:74363707-74363716 chr6:74363767-74363781 chr6:74363787-74363799 chr6:74363784-74363793 chr6:74363461-74363470 chr6:74363789-74363797
28	HCFC1	chr6:74363256-74365359	Hela-S3	cervix:	n/a	n/a
29	CCNT2	chr6:74362748-74364091	K562	blood:	n/a	n/a
30	SPI1	chr6:74363826-74364294	GM12891	blood:	n/a	n/a
31	ZNF143	chr6:74363554-74364048	Hela-S3	cervix:	n/a	chr6:74363880-74363890
32	MXI1	chr6:74362158-74364581	SK-N-SH	brain:	n/a	n/a
33	EGR1	chr6:74362844-74364174	K562	blood:	n/a	chr6:74363708-74363717 chr6:74363779-74363792 chr6:74363783-74363793 chr6:74363779-74363792 chr6:74363778-74363792 chr6:74363779-74363789 chr6:74363779-74363792 chr6:74363780-74363789 chr6:74363705-74363718 chr6:74363706-74363720 chr6:74363778-74363793
34	TBL1XR1	chr6:74363689-74364001	K562	blood:	n/a	n/a
35	FOXP2	chr6:74363453-74364052	PFSK-1	brain:	n/a	n/a
36	HEY1	chr6:74363425-74364509	HepG2	liver:	n/a	n/a
37	ARID3A	chr6:74363545-74364274	HepG2	liver:	n/a	n/a
38	BRCA1	chr6:74363669-74364007	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr6:74363314-74364208	MCF-7	breast:	n/a	n/a
40	TCF12	chr6:74363588-74364610	A549	lung:	n/a	n/a
41	SMARCC1	chr6:74362749-74364416	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr6:74363619-74363901	A549	lung:	n/a	n/a
43	MAX	chr6:74363723-74364277	H1-hESC	embryonic stem cell:	n/a	n/a
44	SIX5	chr6:74363641-74364040	GM12878	blood:	n/a	n/a
45	SMC3	chr6:74363843-74363969	K562	blood:	n/a	n/a
46	STAT5A	chr6:74363297-74364235	GM12878	blood:	n/a	chr6:74363701-74363713
47	RCOR1	chr6:74362329-74364399	Hela-S3	cervix:	n/a	n/a
48	YY1	chr6:74363205-74364397	K562	blood:	n/a	chr6:74363788-74363810 chr6:74363781-74363790 chr6:74363414-74363428 chr6:74363781-74363792 chr6:74363788-74363798 chr6:74363417-74363431 chr6:74363726-74363735 chr6:74363453-74363467 chr6:74363705-74363716 chr6:74363707-74363716 chr6:74363767-74363781 chr6:74363787-74363799 chr6:74363784-74363793 chr6:74363461-74363470 chr6:74363789-74363797
49	E2F4	chr6:74363598-74364102	MCF10A-Er-Src	breast:	n/a	chr6:74363878-74363887 chr6:74363784-74363793
50	MXI1	chr6:74363541-74364280	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74363879-74363929	AG04449	skin:	fetal
2	chr6:74363837-74363887	CMK	blood:	n/a
3	chr6:74363837-74363887	AoSMC	blood vessel:	n/a
4	chr6:74363879-74363929	SK-N-MC	brain:	n/a
5	chr6:74363837-74363887	HMEC	breast:	n/a
6	chr6:74363837-74363887	Hela-S3	cervix:	n/a
7	chr6:74363837-74363887	LNCaP	prostate:	n/a
8	chr6:74363879-74363929	HCT-116	colon:	n/a
9	chr6:74363837-74363887	SKMC	muscle:	n/a
10	chr6:74363879-74363929	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:74363879-74363929	HCF	heart:	n/a
12	chr6:74363879-74363929	ECC-1	luminal epithelium:	n/a
13	chr6:74363837-74363887	Caco-2	colon:	n/a
14	chr6:74363879-74363929	PFSK-1	brain:	n/a
15	chr6:74363837-74363887	T-47D	breast:	n/a
16	chr6:74363837-74363887	Jurkat	blood:	n/a
17	chr6:74363837-74363887	HRE	kidney:	n/a
18	chr6:74363837-74363887	HCT-116	colon:	n/a
19	chr6:74363879-74363929	MCF10A-Er-Src	breast:	n/a
20	chr6:74363837-74363887	AG10803	skin:	n/a
21	chr6:74363879-74363929	Jurkat	blood:	n/a
22	chr6:74363837-74363887	HNPCEpiC	eye:	n/a
23	chr6:74363837-74363887	NH-A	brain:	n/a
24	chr6:74363837-74363887	SK-N-SH_RA	brain:	n/a
25	chr6:74363837-74363887	HEK293	kidney:	embryo
26	chr6:74363879-74363929	BE2_C	brain:	n/a
27	chr6:74363837-74363887	NB4	blood:	n/a
28	chr6:74363879-74363929	HIPEpiC	eye:	n/a
29	chr6:74363837-74363887	IMR90	lung:	fetal
30	chr6:74363879-74363929	HEEpiC	esophagus:	n/a
31	chr6:74363879-74363929	BJ	skin:	n/a
32	chr6:74363879-74363929	GM12878	blood:	n/a
33	chr6:74363837-74363887	HepG2	liver:	n/a
34	chr6:74363879-74363929	ovcar-3	ovarian:	n/a
35	chr6:74363879-74363929	GM12891	blood:	n/a
36	chr6:74363837-74363887	AG09309	skin:	n/a
37	chr6:74363837-74363887	SAEC	small airway:	n/a
38	chr6:74363837-74363887	NHBE	bronchial:	n/a
39	chr6:74363879-74363929	HEK293	kidney:	embryo
40	chr6:74363879-74363929	MCF-7	breast:	n/a
41	chr6:74363837-74363887	HIPEpiC	eye:	n/a
42	chr6:74363837-74363887	HCM	heart:	n/a
43	chr6:74363879-74363929	AG04450	lung:	fetal
44	chr6:74363837-74363887	HEEpiC	esophagus:	n/a
45	chr6:74363879-74363929	HCPEpiC	choroid plexus:	n/a
46	chr6:74363879-74363929	H1-hESC	embryonic stem cell:	embryo
47	chr6:74363837-74363887	MCF10A-Er-Src	breast:	n/a
48	chr6:74363879-74363929	HRPEpiC	eye:	n/a
49	chr6:74363879-74363929	RPTEC	kidney:	n/a
50	chr6:74363879-74363929	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:74353596..74359738-chr6:74361541..74364786,8	MCF-7	breast:
2	chr6:74170014..74172890-chr6:74363161..74365164,3	K562	blood:
3	chr19:1591885..1592846-chr6:74363577..74364084,2	Hela-S3	cervix:
4	chr6:74228702..74232744-chr6:74360665..74366385,13	MCF-7	breast:
5	chr14:74180498..74181170-chr6:74363307..74364061,2	Hela-S3	cervix:
6	chr6:74220976..74234980-chr6:74352572..74366941,62	K562	blood:
7	chr5:39073740..39074512-chr6:74363188..74364025,2	Hela-S3	cervix:
8	chr6:74169971..74171514-chr6:74363161..74365275,2	K562	blood:
9	chr6:74219718..74234750-chr6:74354945..74369231,56	K562	blood:
10	chr6:74103315..74106293-chr6:74362194..74365078,3	MCF-7	breast:
11	chr6:74363322..74365404-chr6:75950708..75953547,2	MCF-7	breast:
12	chr14:35871636..35873724-chr6:74363774..74365365,2	MCF-7	breast:
13	chr6:74228067..74234767-chr6:74357105..74365312,16	MCF-7	breast:
14	chr6:74354143..74358709-chr6:74361254..74364709,5	MCF-7	breast:

Variant related genes	Relation type
SLC17A5	TF binding region
SLC17A5	CpG island
ENSG00000135297	Chromatin interaction
ENSG00000156508	Chromatin interaction
ENSG00000119899	Chromatin interaction
ENSG00000080007	Chromatin interaction
ENSG00000203907	Chromatin interaction
ENSG00000229862	Chromatin interaction
ENSG00000100906	Chromatin interaction
ENSG00000238464	Chromatin interaction
ENSG00000071655	Chromatin interaction
ENSG00000164327	Chromatin interaction
ENSG00000112695	Chromatin interaction
ENSG00000176903	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10455093	0.84[AMR][1000 genomes]
rs10455094	0.89[AMR][1000 genomes]
rs10455095	0.92[AMR][1000 genomes]
rs10455279	0.89[AMR][1000 genomes]
rs10455280	0.89[AMR][1000 genomes]
rs10943107	0.82[AMR][1000 genomes]
rs10943108	0.86[AMR][1000 genomes]
rs10943111	0.89[AMR][1000 genomes]
rs10943114	0.86[AMR][1000 genomes]
rs10943115	0.89[AMR][1000 genomes]
rs10943118	0.92[AMR][1000 genomes]
rs10943119	0.92[AMR][1000 genomes]
rs11750970	0.81[AMR][1000 genomes]
rs11751984	0.86[AMR][1000 genomes]
rs11758258	0.92[AMR][1000 genomes]
rs11969324	0.82[AMR][1000 genomes]
rs12154139	0.89[AMR][1000 genomes]
rs12189643	0.92[AMR][1000 genomes]
rs12189647	0.92[AMR][1000 genomes]
rs12190442	0.89[AMR][1000 genomes]
rs12190753	0.89[AMR][1000 genomes]
rs12191213	0.86[AMR][1000 genomes]
rs12192476	0.92[AMR][1000 genomes]
rs12199348	0.89[AMR][1000 genomes]
rs12199822	0.89[AMR][1000 genomes]
rs12199937	0.87[AMR][1000 genomes]
rs12201702	0.89[AMR][1000 genomes]
rs12201746	0.89[AMR][1000 genomes]
rs12202024	0.82[AMR][1000 genomes]
rs12206001	0.92[AMR][1000 genomes]
rs12207204	0.87[AMR][1000 genomes]
rs12207961	0.89[AMR][1000 genomes]
rs12210690	0.89[AMR][1000 genomes]
rs12212339	0.92[AMR][1000 genomes]
rs12214293	0.90[AMR][1000 genomes]
rs12214539	0.86[AMR][1000 genomes]
rs17758926	0.89[AMR][1000 genomes]
rs3734517	0.86[AMR][1000 genomes]
rs3757112	0.89[AMR][1000 genomes]
rs3799289	0.92[AMR][1000 genomes]
rs3799290	0.92[AMR][1000 genomes]
rs3799293	0.92[AMR][1000 genomes]
rs3799295	0.89[AMR][1000 genomes]
rs3823122	0.92[AMR][1000 genomes]
rs3928609	0.92[AMR][1000 genomes]
rs4706544	0.92[AMR][1000 genomes]
rs4706545	0.90[AMR][1000 genomes]
rs4706546	0.92[AMR][1000 genomes]
rs4706547	0.92[AMR][1000 genomes]
rs4706548	0.92[AMR][1000 genomes]
rs4706549	0.92[AMR][1000 genomes]
rs4706550	0.92[AMR][1000 genomes]
rs4708068	0.89[AMR][1000 genomes]
rs4708070	0.92[AMR][1000 genomes]
rs55698483	0.87[AMR][1000 genomes]
rs56004619	0.81[AMR][1000 genomes]
rs56390246	0.89[AMR][1000 genomes]
rs62438423	0.81[AMR][1000 genomes]
rs62438424	0.82[AMR][1000 genomes]
rs62438426	0.81[AMR][1000 genomes]
rs62438431	0.86[AMR][1000 genomes]
rs62440461	0.89[AMR][1000 genomes]
rs62440465	0.89[AMR][1000 genomes]
rs62440489	0.92[AMR][1000 genomes]
rs72947490	0.84[AMR][1000 genomes]
rs9352013	0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv886158	chr6:74126084-74436825	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
3	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
5	nsv1017716	chr6:74173173-74401162	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS 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	170 gene(s)	inside rSNPs	diseases
6	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS 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 miRNA target site	172 gene(s)	inside rSNPs	diseases
7	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
8	nsv603694	chr6:74275405-74365807	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv1029927	chr6:74300496-74424355	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
10	nsv1027691	chr6:74302980-74417450	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	21 gene(s)	inside rSNPs	diseases
11	esv3408073	chr6:74362256-74364804	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr6:74361800-74364200	Active TSS	NH-A	brain
2	chr6:74361800-74364400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:74361800-74364600	Active TSS	Fetal Intestine Large	intestine
4	chr6:74361800-74364800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:74361800-74364800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:74361800-74364800	Active TSS	K562	blood
7	chr6:74361800-74365200	Active TSS	NHDF-Ad	bronchial
8	chr6:74362000-74364400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:74362000-74364400	Active TSS	Brain Anterior Caudate	brain
10	chr6:74362000-74364400	Active TSS	Fetal Muscle Leg	muscle
11	chr6:74362000-74364600	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr6:74362000-74364600	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr6:74362000-74364600	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr6:74362200-74364400	Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr6:74362200-74364400	Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr6:74362200-74364400	Active TSS	Fetal Intestine Small	intestine
17	chr6:74362200-74364400	Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr6:74362200-74364400	Active TSS	GM12878-XiMat	blood
19	chr6:74362200-74364400	Active TSS	Hela-S3	cervix
20	chr6:74362200-74364400	Active TSS	Monocytes-CD14+_RO01746	blood
21	chr6:74362200-74364600	Active TSS	NHLF	lung
22	chr6:74362200-74364800	Active TSS	Duodenum Mucosa	Duodenum
23	chr6:74362200-74365000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:74362200-74365000	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr6:74362200-74365000	Active TSS	HSMMtube	muscle
26	chr6:74362400-74364000	Active TSS	Primary T cells fromperipheralblood	blood
27	chr6:74362400-74364000	Active TSS	Fetal Thymus	thymus
28	chr6:74362400-74364200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr6:74362400-74364200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:74362400-74364200	Active TSS	Fetal Muscle Trunk	muscle
31	chr6:74362400-74364400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr6:74362400-74364400	Active TSS	Muscle Satellite Cultured Cells	--
33	chr6:74362400-74364400	Active TSS	Brain Angular Gyrus	brain
34	chr6:74362400-74364400	Active TSS	Brain Cingulate Gyrus	brain
35	chr6:74362400-74364400	Active TSS	Fetal Kidney	kidney
36	chr6:74362400-74364400	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr6:74362400-74364400	Active TSS	Thymus	Thymus
38	chr6:74362400-74364400	Active TSS	HMEC	breast
39	chr6:74362400-74364600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr6:74362400-74364600	Active TSS	H1 Cell Line	embryonic stem cell
41	chr6:74362400-74364600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:74362400-74364600	Active TSS	Brain Hippocampus Middle	brain
43	chr6:74362400-74364600	Active TSS	Fetal Lung	lung
44	chr6:74362400-74364600	Active TSS	Psoas Muscle	Psoas
45	chr6:74362400-74364800	Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr6:74362400-74364800	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr6:74362400-74364800	Active TSS	Right Atrium	heart
48	chr6:74362400-74364800	Active TSS	Right Ventricle	heart
49	chr6:74362400-74364800	Active TSS	Stomach Smooth Muscle	stomach
50	chr6:74362600-74364200	Active TSS	Cortex derived primary cultured neurospheres	brain

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