Variant report

Variant	rs45493300
Chromosome Location	chr6:35465580-35465581
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	chr6:35464891-35466484	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr6:35464485-35466025	MCF-7	breast:	n/a	n/a
3	BHLHE40	chr6:35464925-35466949	K562	blood:	n/a	chr6:35465324-35465340 chr6:35466465-35466481
4	CHD2	chr6:35464391-35466037	Hela-S3	cervix:	n/a	chr6:35465063-35465073 chr6:35465017-35465027 chr6:35465585-35465595 chr6:35465520-35465530
5	HDAC2	chr6:35465110-35466099	MCF-7	breast:	n/a	n/a
6	POLR2A	chr6:35463981-35466364	MCF-7	breast:	n/a	n/a
7	JUND	chr6:35465146-35466301	MCF-7	breast:	n/a	chr6:35465289-35465298
8	PML	chr6:35465516-35466225	K562	blood:	n/a	n/a
9	YY1	chr6:35464756-35466361	K562	blood:	n/a	chr6:35465488-35465499 chr6:35466253-35466267 chr6:35465119-35465133 chr6:35464964-35464973 chr6:35465339-35465353
10	POLR2A	chr6:35465503-35465702	Gliobla	brain:	n/a	n/a
11	E2F1	chr6:35464788-35465933	Hela-S3	cervix:	n/a	chr6:35465546-35465556
12	POLR2A	chr6:35464907-35466790	K562	blood:	n/a	n/a
13	POLR2A	chr6:35464904-35466528	Hela-S3	cervix:	n/a	n/a
14	ZBTB7A	chr6:35463832-35466076	ECC-1	luminal epithelium:	n/a	chr6:35465457-35465465 chr6:35464366-35464377
15	TEAD4	chr6:35465429-35466054	K562	blood:	n/a	n/a
16	CTCF	chr6:35465500-35465650	HA-sp	spinal cord:	n/a	n/a
17	CTCF	chr6:35465397-35465797	K562	blood:	n/a	n/a
18	REST	chr6:35465440-35465942	K562	blood:	n/a	chr6:35465480-35465487
19	E2F6	chr6:35464871-35465875	K562	blood:	n/a	chr6:35465546-35465556
20	TCF12	chr6:35465558-35466063	H1-hESC	embryonic stem cell:	n/a	n/a
21	MAX	chr6:35464839-35465988	A549	lung:	n/a	chr6:35465374-35465383 chr6:35464965-35464975
22	MAX	chr6:35465030-35466050	MCF-7	breast:	n/a	chr6:35465374-35465383
23	E2F6	chr6:35465407-35465791	A549	lung:	n/a	chr6:35465546-35465556
24	E2F6	chr6:35464828-35466734	K562	blood:	n/a	chr6:35465546-35465556
25	GABPA	chr6:35465534-35466077	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr6:35465435-35465782	K562	blood:	n/a	n/a
27	RCOR1	chr6:35464964-35466052	K562	blood:	n/a	n/a
28	CTCF	chr6:35465580-35465635	H1-hESC	embryonic stem cell:	n/a	n/a
29	MYC	chr6:35465526-35466613	K562	blood:	n/a	chr6:35466408-35466421 chr6:35466413-35466421 chr6:35466410-35466419 chr6:35466410-35466419 chr6:35466409-35466420 chr6:35466410-35466419 chr6:35466408-35466421 chr6:35466410-35466420 chr6:35466405-35466424 chr6:35466410-35466420 chr6:35466409-35466420 chr6:35466408-35466421 chr6:35466409-35466420
30	MYC	chr6:35464935-35465641	MCF10A-Er-Src	breast:	n/a	chr6:35465374-35465383 chr6:35464965-35464975
31	MAZ	chr6:35463616-35466603	K562	blood:	n/a	chr6:35466408-35466421 chr6:35466413-35466421 chr6:35466410-35466419 chr6:35465374-35465383 chr6:35466410-35466419 chr6:35466409-35466420 chr6:35466410-35466419 chr6:35466408-35466421 chr6:35464965-35464975 chr6:35466410-35466420 chr6:35466405-35466424 chr6:35466410-35466420 chr6:35466409-35466420 chr6:35466408-35466421 chr6:35464473-35464483 chr6:35466409-35466420
32	POLR2A	chr6:35465558-35468992	K562	blood:	n/a	n/a
33	MYC	chr6:35464886-35466773	K562	blood:	n/a	chr6:35466408-35466421 chr6:35466413-35466421 chr6:35466410-35466419 chr6:35465374-35465383 chr6:35466410-35466419 chr6:35466409-35466420 chr6:35466410-35466419 chr6:35466408-35466421 chr6:35464965-35464975 chr6:35466410-35466420 chr6:35466405-35466424 chr6:35466410-35466420 chr6:35466409-35466420 chr6:35466408-35466421 chr6:35466409-35466420
34	CTCF	chr6:35465480-35465630	HCFaa	heart:	n/a	n/a
35	CTCF	chr6:35465404-35465660	K562	blood:	n/a	n/a
36	CTCF	chr6:35465528-35465695	MCF-7	breast:	n/a	n/a
37	RCOR1	chr6:35464987-35466091	Hela-S3	cervix:	n/a	n/a
38	MAX	chr6:35465427-35466609	NB4	blood:	n/a	chr6:35466408-35466421 chr6:35466413-35466421 chr6:35466410-35466419 chr6:35466410-35466419 chr6:35466409-35466420 chr6:35466410-35466419 chr6:35466408-35466421 chr6:35466410-35466420 chr6:35466405-35466424 chr6:35466410-35466420 chr6:35466409-35466420 chr6:35466408-35466421 chr6:35466409-35466420
39	CTCF	chr6:35465540-35465690	HCPEpiC	choroid plexus:	n/a	n/a
40	MAX	chr6:35465561-35465687	GM12878	blood:	n/a	n/a
41	HA-E2F1	chr6:35464761-35465943	Hela-S3	cervix:	n/a	chr6:35465546-35465556
42	HDAC2	chr6:35465376-35465978	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAX	chr6:35465367-35465982	A549	lung:	n/a	chr6:35465374-35465383
44	JUND	chr6:35465401-35465982	H1-hESC	embryonic stem cell:	n/a	n/a
45	SPI1	chr6:35465547-35466026	HL-60	blood:	n/a	n/a
46	SETDB1	chr6:35465029-35466382	K562	blood:	n/a	chr6:35465622-35465631
47	CTCF	chr6:35465460-35465610	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr6:35465500-35465650	HCM	heart:	n/a	n/a
49	ZC3H11A	chr6:35465558-35465813	K562	blood:	n/a	n/a
50	FOXP2	chr6:35465453-35466193	PFSK-1	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:35423795..35426623-chr6:35465037..35468781,3	K562	blood:
2	chr17:36905700..36906366-chr6:35464667..35465593,2	Hela-S3	cervix:
3	chr6:35260813..35263112-chr6:35464822..35466518,2	K562	blood:
4	chr6:35270724..35273111-chr6:35465041..35467348,2	K562	blood:
5	chr6:35464935..35465692-chr7:44835784..44836776,2	Hela-S3	cervix:
6	chr6:35419956..35422517-chr6:35464991..35466898,2	MCF-7	breast:
7	chr6:35465446..35468035-chr6:35607430..35610345,2	K562	blood:
8	chr6:35465223..35467694-chr6:35696445..35698937,2	K562	blood:
9	chr6:35225785..35227535-chr6:35464894..35467017,2	K562	blood:
10	chr6:35465082..35466862-chr6:35699908..35701462,2	MCF-7	breast:
11	chr1:153699734..153700587-chr6:35465219..35465916,2	Hela-S3	cervix:
12	chr6:35463571..35465690-chr6:35654249..35656915,2	K562	blood:
13	chr6:35264944..35267460-chr6:35465302..35468823,3	MCF-7	breast:
14	chr6:35464312..35466499-chr6:35694204..35696742,2	MCF-7	breast:
15	chr5:130531404..130532060-chr6:35465194..35466059,2	Hela-S3	cervix:
16	chr6:35464601..35467910-chr6:35655207..35659461,3	K562	blood:
17	chr19:11198114..11200950-chr6:35464173..35466447,2	K562	blood:
18	chr6:35376688..35379327-chr6:35465068..35467470,3	K562	blood:
19	chr6:35289938..35291662-chr6:35465459..35467668,2	K562	blood:
20	chr6:35310112..35312932-chr6:35464368..35466518,2	K562	blood:
21	chr6:35227208..35228940-chr6:35464081..35465836,2	K562	blood:
22	chr6:35464241..35466956-chr6:35695881..35700309,4	MCF-7	breast:
23	chr1:210547375..210547960-chr6:35465386..35466203,2	Hela-S3	cervix:
24	chr2:176033099..176033744-chr6:35465562..35466338,2	Hela-S3	cervix:
25	chr20:15349649..15350459-chr6:35465170..35465747,2	MCF-7	breast:
26	chr6:35465054..35467000-chr6:36192851..36194879,2	MCF-7	breast:
27	chr5:43514826..43515720-chr6:35464905..35465668,2	Hela-S3	cervix:
28	chr6:35418643..35423313-chr6:35462563..35468017,10	K562	blood:
29	chr6:35263661..35265616-chr6:35463054..35466039,2	MCF-7	breast:
30	chr6:35465083..35467815-chr6:35613967..35615894,2	MCF-7	breast:
31	chr11:33757381..33758237-chr6:35465059..35466295,3	Hela-S3	cervix:

Variant related genes	Relation type
TEAD3	TF binding region
ENSG00000085063	Chromatin interaction
ENSG00000172244	Chromatin interaction
ENSG00000056661	Chromatin interaction
ENSG00000143624	Chromatin interaction
ENSG00000130164	Chromatin interaction
ENSG00000096060	Chromatin interaction
ENSG00000112033	Chromatin interaction
ENSG00000115966	Chromatin interaction
ENSG00000023892	Chromatin interaction
ENSG00000112039	Chromatin interaction
ENSG00000065029	Chromatin interaction
ENSG00000200972	Chromatin interaction
ENSG00000248240	Chromatin interaction
ENSG00000196262	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1883636	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2067997	0.80[EUR][1000 genomes]
rs3777746	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3798344	0.80[EUR][1000 genomes]
rs6928735	0.80[EUR][1000 genomes]
rs6929353	0.81[EUR][1000 genomes]
rs7738975	0.96[ASN][1000 genomes]
rs7768844	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9689798	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528351	chr6:35377922-35465786	Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
2	nsv519370	chr6:35378778-35537406	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
3	nsv984463	chr6:35432948-35477634	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	67 gene(s)	inside rSNPs	diseases
4	esv1843819	chr6:35457396-35465749	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
5	esv1851060	chr6:35457396-35465749	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
6	esv1794339	chr6:35457396-35465786	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
7	esv1800978	chr6:35457396-35465786	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
8	esv1803037	chr6:35457396-35465786	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak 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	23 gene(s)	inside rSNPs	diseases
9	esv1837448	chr6:35457396-35465786	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
10	nsv462909	chr6:35457396-35502202	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
11	nsv602912	chr6:35457396-35502202	Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
12	esv3384067	chr6:35462874-35466272	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
13	esv3507609	chr6:35463474-35466122	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
14	esv3507610	chr6:35463474-35466122	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
15	esv3440600	chr6:35463499-35466347	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
16	esv2758048	chr6:35463741-35806504	Genic enhancers Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
17	esv2759420	chr6:35463741-35806504	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Strong transcription 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	52 gene(s)	inside rSNPs	diseases
18	esv3323555	chr6:35464074-35465922	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
19	esv13071	chr6:35464170-35465801	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
20	esv1792492	chr6:35464197-35465786	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
21	esv1820663	chr6:35464197-35471362	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
22	nsv602915	chr6:35464327-35465594	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
23	nsv602918	chr6:35464698-35465594	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases
24	esv1835988	chr6:35464698-35465749	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases
25	nsv602919	chr6:35464698-35465749	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases
26	nsv602920	chr6:35464773-35465594	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	22 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	chr6:35463200-35466000	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr6:35463200-35466200	Active TSS	Fetal Kidney	kidney
3	chr6:35463400-35465600	Active TSS	Sigmoid Colon	Sigmoid Colon
4	chr6:35463400-35465800	Active TSS	Small Intestine	intestine
5	chr6:35463400-35466000	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr6:35463600-35465600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:35463600-35465600	Active TSS	Fetal Intestine Large	intestine
8	chr6:35463600-35465600	Active TSS	Placenta	Placenta
9	chr6:35463600-35465600	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr6:35463600-35465600	Active TSS	Right Ventricle	heart
11	chr6:35463600-35465600	Bivalent/Poised TSS	Thymus	Thymus
12	chr6:35463600-35465800	Active TSS	Gastric	stomach
13	chr6:35463600-35466000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:35463600-35466000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:35463600-35466000	Active TSS	Colon Smooth Muscle	Colon
16	chr6:35463600-35466000	Active TSS	Esophagus	oesophagus
17	chr6:35463600-35466000	Active TSS	Ovary	ovary
18	chr6:35463600-35466000	Active TSS	A549	lung
19	chr6:35463600-35466000	Active TSS	NHLF	lung
20	chr6:35463600-35466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr6:35463600-35466200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:35463600-35466200	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr6:35463600-35466200	Active TSS	Aorta	Aorta
24	chr6:35463600-35466200	Active TSS	Placenta Amnion	Placenta Amnion
25	chr6:35463600-35466200	Active TSS	Rectal Smooth Muscle	rectum
26	chr6:35463600-35466200	Active TSS	HSMMtube	muscle
27	chr6:35463600-35466800	Active TSS	H9 Cell Line	embryonic stem cell
28	chr6:35463800-35465600	Active TSS	Brain Anterior Caudate	brain
29	chr6:35463800-35465600	Active TSS	Brain Hippocampus Middle	brain
30	chr6:35463800-35465600	Active TSS	Left Ventricle	heart
31	chr6:35463800-35465600	Active TSS	Stomach Smooth Muscle	stomach
32	chr6:35463800-35465800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:35463800-35465800	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr6:35463800-35466000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:35463800-35466000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr6:35463800-35466000	Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr6:35463800-35466000	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr6:35463800-35466000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr6:35463800-35466000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:35463800-35466000	Bivalent/Poised TSS	Fetal Brain Female	brain
41	chr6:35463800-35466000	Active TSS	NHDF-Ad	bronchial
42	chr6:35463800-35466400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:35463800-35466400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr6:35464000-35465600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr6:35464000-35465600	Active TSS	Fetal Muscle Leg	muscle
46	chr6:35464000-35465800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:35464000-35465800	Active TSS	K562	blood
48	chr6:35464000-35466000	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr6:35464000-35466000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:35464000-35466000	Active TSS	Psoas Muscle	Psoas

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