Variant report

Variant	rs62422236
Chromosome Location	chr6:118972633-118972634
allele	G/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	YY1	chr6:118972095-118972843	K562	blood:	n/a	chr6:118972800-118972809 chr6:118972232-118972241 chr6:118972304-118972318 chr6:118972797-118972811 chr6:118972759-118972768 chr6:118972275-118972286
2	HEY1	chr6:118972396-118972824	K562	blood:	n/a	chr6:118972435-118972450 chr6:118972643-118972658
3	MAX	chr6:118972052-118973201	HepG2	liver:	n/a	chr6:118972272-118972282 chr6:118973072-118973083 chr6:118972798-118972808
4	POLR2A	chr6:118971590-118973146	K562	blood:	n/a	n/a
5	POLR2A	chr6:118972148-118973524	K562	blood:	n/a	n/a
6	POU2F2	chr6:118972476-118972792	GM12891	blood:	n/a	n/a
7	PML	chr6:118972263-118972856	K562	blood:	n/a	n/a
8	CREB1	chr6:118972434-118973207	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAX	chr6:118971665-118973332	H1-hESC	embryonic stem cell:	n/a	chr6:118973262-118973271 chr6:118972272-118972282 chr6:118973072-118973083 chr6:118972798-118972808
10	TAF1	chr6:118972297-118973223	ECC-1	luminal epithelium:	n/a	n/a
11	RFX5	chr6:118972629-118972945	Hela-S3	cervix:	n/a	n/a
12	EP300	chr6:118971882-118973273	SK-N-SH	brain:	n/a	chr6:118971946-118971962 chr6:118971949-118971958 chr6:118972755-118972771 chr6:118972236-118972252 chr6:118972200-118972216
13	MYC	chr6:118972072-118973280	MCF10A-Er-Src	breast:	n/a	chr6:118973262-118973271 chr6:118972272-118972282 chr6:118973072-118973083 chr6:118972798-118972808
14	TBP	chr6:118972229-118972920	K562	blood:	n/a	n/a
15	POLR2A	chr6:118971546-118973280	GM19099	blood:	n/a	n/a
16	TAF1	chr6:118972558-118972769	GM12892	blood:	n/a	n/a
17	POLR2A	chr6:118972456-118973291	HEK293	kidney:	n/a	n/a
18	POLR2A	chr6:118971844-118973096	MCF10A-Er-Src	breast:	n/a	n/a
19	RAD21	chr6:118972582-118972813	K562	blood:	n/a	n/a
20	POLR2A	chr6:118972477-118973160	GM12878	blood:	n/a	n/a
21	POLR2A	chr6:118971567-118973212	ProgFib	skin:	n/a	n/a
22	POU2F2	chr6:118972520-118973144	GM12878	blood:	n/a	n/a
23	MXI1	chr6:118970121-118973661	SK-N-SH	brain:	n/a	chr6:118973072-118973081
24	TAF1	chr6:118972481-118972898	GM12878	blood:	n/a	n/a
25	IRF1	chr6:118972500-118973144	K562	blood:	n/a	chr6:118972749-118972763 chr6:118972799-118972813
26	YY1	chr6:118972467-118972848	ECC-1	luminal epithelium:	n/a	chr6:118972800-118972809 chr6:118972797-118972811 chr6:118972759-118972768
27	POLR2A	chr6:118972454-118973172	MCF-7	breast:	n/a	n/a
28	SIN3AK20	chr6:118971954-118972803	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr6:118971796-118973334	HepG2	liver:	n/a	chr6:118973262-118973271 chr6:118972272-118972282 chr6:118973072-118973083 chr6:118972798-118972808
30	EP300	chr6:118972590-118972784	K562	blood:	n/a	chr6:118972755-118972771
31	POLR2A	chr6:118971544-118973210	H1-neurons	neurons:	n/a	n/a
32	MYC	chr6:118972058-118972724	MCF-7	breast:	n/a	chr6:118972272-118972282
33	EGR1	chr6:118972630-118972968	K562	blood:	n/a	chr6:118972795-118972808 chr6:118972800-118972810 chr6:118972754-118972767 chr6:118972796-118972810 chr6:118972795-118972808 chr6:118972753-118972768 chr6:118972755-118972765 chr6:118972751-118972765
34	MAX	chr6:118971686-118973351	GM12878	blood:	n/a	chr6:118973262-118973271 chr6:118972272-118972282 chr6:118973072-118973083 chr6:118972798-118972808
35	MYC	chr6:118971600-118973237	K562	blood:	n/a	chr6:118972272-118972282 chr6:118973072-118973083 chr6:118972798-118972808
36	RAD21	chr6:118972443-118973021	SK-N-SH_RA	brain:	n/a	chr6:118972986-118972998
37	POLR2A	chr6:118971483-118973331	IMR90	lung:	n/a	n/a
38	KAP1	chr6:118972442-118972662	U2OS	brain:	n/a	n/a
39	REST	chr6:118971563-118973518	H1-neurons	neurons:	n/a	chr6:118972340-118972349 chr6:118972199-118972209 chr6:118972336-118972346 chr6:118972197-118972211
40	ETS1	chr6:118972487-118972867	K562	blood:	n/a	chr6:118972798-118972809 chr6:118972753-118972764
41	TAL1	chr6:118972274-118972800	K562	blood:	n/a	n/a
42	MXI1	chr6:118972180-118973206	HepG2	liver:	n/a	chr6:118973072-118973081
43	PML	chr6:118971382-118973332	GM12878	blood:	n/a	n/a
44	E2F6	chr6:118971779-118973168	K562	blood:	n/a	chr6:118972619-118972629 chr6:118971912-118971927 chr6:118971976-118971988 chr6:118972965-118972977 chr6:118972800-118972809 chr6:118971949-118971959 chr6:118972930-118972942 chr6:118972272-118972283 chr6:118971837-118971854
45	TAF1	chr6:118972505-118972877	SK-N-SH	brain:	n/a	n/a
46	CREB1	chr6:118971570-118973287	HepG2	liver:	n/a	n/a
47	TAF1	chr6:118972435-118972835	H1-neurons	neurons:	n/a	n/a
48	RCOR1	chr6:118971443-118973311	K562	blood:	n/a	n/a
49	HCFC1	chr6:118971912-118973173	K562	blood:	n/a	n/a
50	MAZ	chr6:118971414-118973387	IMR90	lung:	n/a	chr6:118973262-118973271 chr6:118972272-118972282 chr6:118973072-118973083 chr6:118972798-118972808

No.	Distal block	Cell Line	Cell type
1	chr6:118966044..118969834-chr6:118971302..118974528,3	MCF-7	breast:
2	chr6:118972255..118975649-chr6:119030496..119033791,4	K562	blood:
3	chr6:118951505..118954170-chr6:118971073..118972988,2	K562	blood:
4	chr6:118965633..118969017-chr6:118971135..118973717,5	K562	blood:
5	chr6:118969568..118974185-chr6:119029207..119033276,8	K562	blood:

Variant related genes	Relation type
CEP85L	TF binding region
ENSG00000111860	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10484286	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484289	0.83[ASN][1000 genomes]
rs13437605	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17080456	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17349133	0.95[ASN][1000 genomes]
rs17349301	0.95[ASN][1000 genomes]
rs17424234	0.83[ASN][1000 genomes]
rs17427284	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1891715	0.95[ASN][1000 genomes]
rs2356501	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28605789	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3902035	0.95[ASN][1000 genomes]
rs4416700	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55697388	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55850368	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55894300	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56082110	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56406560	0.95[ASN][1000 genomes]
rs62422189	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422190	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422193	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422195	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62422220	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62422221	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62422223	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62422224	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422227	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62422228	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62422229	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62422230	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422234	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422235	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422247	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62422248	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62422250	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62422253	0.91[ASN][1000 genomes]
rs62422254	0.95[ASN][1000 genomes]
rs62424175	0.83[ASN][1000 genomes]
rs62424202	0.83[ASN][1000 genomes]
rs724868	0.83[ASN][1000 genomes]
rs72952733	0.83[ASN][1000 genomes]
rs72952793	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72954806	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72956993	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9320656	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9320660	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9320666	0.84[ASN][1000 genomes]
rs9481825	0.80[ASN][1000 genomes]
rs9481826	0.80[ASN][1000 genomes]
rs9481833	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9481844	0.84[ASN][1000 genomes]
rs9489442	0.80[ASN][1000 genomes]
rs9489447	0.88[ASN][1000 genomes]
rs9489450	0.88[ASN][1000 genomes]
rs9489452	0.88[ASN][1000 genomes]
rs9489457	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9489458	0.88[ASN][1000 genomes]
rs9489460	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9489462	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9489463	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9489467	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9489477	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9489493	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats 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 miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv1034448	chr6:118698169-119016383	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv1025097	chr6:118699752-119058789	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
11	nsv532052	chr6:118711850-119057295	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer 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	9 gene(s)	inside rSNPs	diseases
12	nsv432959	chr6:118716318-119010307	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
13	nsv604556	chr6:118722589-119065365	Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
14	nsv949416	chr6:118772508-119033063	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv948980	chr6:118772508-119137658	Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
16	nsv604559	chr6:118786486-119113317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
17	nsv1022865	chr6:118786586-119058789	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
18	nsv1020405	chr6:118786586-119241006	ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
19	nsv1030331	chr6:118874345-118975680	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 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	chr6:118970000-118973000	Active TSS	GM12878-XiMat	blood
2	chr6:118970000-118973200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:118970000-118973200	Active TSS	Fetal Brain Male	brain
4	chr6:118970200-118973000	Active TSS	Cortex derived primary cultured neurospheres	brain
5	chr6:118970200-118973000	Active TSS	HMEC	breast
6	chr6:118970200-118973200	Active TSS	NHLF	lung
7	chr6:118970400-118973000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:118970400-118973000	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr6:118970400-118973000	Active TSS	Fetal Muscle Leg	muscle
10	chr6:118970400-118973400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:118970400-118973400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:118970400-118973400	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr6:118970600-118973000	Active TSS	Stomach Smooth Muscle	stomach
14	chr6:118970600-118973200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:118970600-118973200	Active TSS	Psoas Muscle	Psoas
16	chr6:118970600-118973400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr6:118970600-118973400	Active TSS	Ovary	ovary
18	chr6:118970600-118973400	Active TSS	Right Atrium	heart
19	chr6:118970600-118973400	Active TSS	HSMM	muscle
20	chr6:118970600-118973600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr6:118970600-118973600	Active TSS	A549	lung
22	chr6:118970600-118973600	Active TSS	NHDF-Ad	bronchial
23	chr6:118970800-118973000	Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr6:118970800-118973200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
25	chr6:118970800-118973200	Active TSS	Fetal Stomach	stomach
26	chr6:118970800-118973200	Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr6:118970800-118973400	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr6:118970800-118973400	Active TSS	HSMMtube	muscle
29	chr6:118970800-118973600	Active TSS	Muscle Satellite Cultured Cells	--
30	chr6:118970800-118973800	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr6:118970800-118974000	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr6:118971000-118973200	Active TSS	H1 Cell Line	embryonic stem cell
33	chr6:118971000-118973200	Active TSS	Fetal Brain Female	brain
34	chr6:118971000-118973400	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr6:118971000-118973600	Active TSS	Brain Angular Gyrus	brain
36	chr6:118971200-118972800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr6:118971200-118973000	Active TSS	Fetal Muscle Trunk	muscle
38	chr6:118971200-118973000	Active TSS	Fetal Thymus	thymus
39	chr6:118971200-118973200	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr6:118971200-118973200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
41	chr6:118971200-118973200	Active TSS	Sigmoid Colon	Sigmoid Colon
42	chr6:118971200-118973200	Active TSS	Osteobl	bone
43	chr6:118971200-118973400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr6:118971200-118973400	Active TSS	H9 Cell Line	embryonic stem cell
45	chr6:118971200-118973400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr6:118971200-118973400	Active TSS	Right Ventricle	heart
47	chr6:118971200-118973600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:118971200-118973600	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr6:118971200-118973800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr6:118971400-118973000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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