Variant report

Variant	rs534892
Chromosome Location	chr6:31763942-31763943
allele	C/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	chr6:31762842-31764771	HepG2	liver:	n/a	n/a
2	RCOR1	chr6:31763176-31764112	K562	blood:	n/a	n/a
3	POLR2A	chr6:31762366-31764289	MCF-7	breast:	n/a	n/a
4	MAX	chr6:31763037-31764061	K562	blood:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496 chr6:31763487-31763497
5	POLR2A	chr6:31762908-31764073	MCF10A-Er-Src	breast:	n/a	n/a
6	YY1	chr6:31763358-31763947	SK-N-SH_RA	brain:	n/a	chr6:31763754-31763763 chr6:31763468-31763482 chr6:31763467-31763481 chr6:31763754-31763768 chr6:31763748-31763762 chr6:31763368-31763382 chr6:31763539-31763548 chr6:31763371-31763385
7	GTF2F1	chr6:31762978-31763963	K562	blood:	n/a	n/a
8	POLR2A	chr6:31761995-31764710	K562	blood:	n/a	n/a
9	SRF	chr6:31763422-31763985	K562	blood:	n/a	chr6:31763540-31763550
10	MAX	chr6:31762191-31764152	HepG2	liver:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496 chr6:31763487-31763497
11	POLR2A	chr6:31762059-31764086	K562	blood:	n/a	n/a
12	ZBTB7A	chr6:31762354-31764110	ECC-1	luminal epithelium:	n/a	n/a
13	POLR2A	chr6:31762197-31764090	K562	blood:	n/a	n/a
14	MYC	chr6:31763139-31763980	MCF-7	breast:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496 chr6:31763487-31763497
15	TBP	chr6:31763403-31763949	HepG2	liver:	n/a	n/a
16	POLR2A	chr6:31762741-31764029	H1-hESC	embryonic stem cell:	n/a	n/a
17	TBP	chr6:31762866-31764101	K562	blood:	n/a	n/a
18	YY1	chr6:31762835-31763974	GM12878	blood:	n/a	chr6:31763754-31763763 chr6:31763468-31763482 chr6:31763467-31763481 chr6:31763754-31763768 chr6:31763748-31763762 chr6:31763368-31763382 chr6:31763539-31763548 chr6:31763371-31763385
19	ZNF143	chr6:31763487-31764031	K562	blood:	n/a	chr6:31763649-31763659
20	TBL1XR1	chr6:31763006-31764114	K562	blood:	n/a	n/a
21	CTCF	chr6:31763398-31764037	K562	blood:	n/a	chr6:31763806-31763822 chr6:31763474-31763487
22	POLR2A	chr6:31762085-31764245	HUVEC	blood vessel:	n/a	n/a
23	TAF1	chr6:31762265-31764119	K562	blood:	n/a	n/a
24	TAF1	chr6:31763090-31764020	HepG2	liver:	n/a	n/a
25	RUNX3	chr6:31763001-31764037	GM12878	blood:	n/a	n/a
26	POLR2A	chr6:31762954-31764081	K562	blood:	n/a	n/a
27	ZMIZ1	chr6:31762092-31764030	K562	blood:	n/a	n/a
28	POLR2A	chr6:31762842-31764116	HepG2	liver:	n/a	n/a
29	MXI1	chr6:31762943-31764057	K562	blood:	n/a	n/a
30	ETS1	chr6:31762362-31764134	K562	blood:	n/a	chr6:31763509-31763526 chr6:31762577-31762588 chr6:31763537-31763548 chr6:31763509-31763526
31	CTCF	chr6:31763619-31763944	MCF-7	breast:	n/a	chr6:31763806-31763822
32	POLR2A	chr6:31763104-31764035	GM19099	blood:	n/a	n/a
33	RAD21	chr6:31763256-31764155	HCT-116	colon:	n/a	chr6:31763371-31763384 chr6:31763760-31763773
34	POLR2A	chr6:31763054-31764095	GM12892	blood:	n/a	n/a
35	POLR2A	chr6:31763135-31763965	A549	lung:	n/a	n/a
36	ELF1	chr6:31763003-31764110	K562	blood:	n/a	chr6:31763540-31763552 chr6:31763370-31763382
37	CTCF	chr6:31763337-31764165	A549	lung:	n/a	chr6:31763806-31763822 chr6:31763474-31763487
38	E2F4	chr6:31763086-31763997	K562	blood:	n/a	chr6:31763365-31763375 chr6:31763540-31763550 chr6:31763477-31763487
39	RAD21	chr6:31763526-31764006	H1-hESC	embryonic stem cell:	n/a	chr6:31763760-31763773
40	POLR2A	chr6:31762274-31764763	K562	blood:	n/a	n/a
41	MAX	chr6:31763084-31763960	HUVEC	blood vessel:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496 chr6:31763487-31763497
42	USF1	chr6:31763178-31764030	K562	blood:	n/a	chr6:31763475-31763491 chr6:31763440-31763451 chr6:31763486-31763497 chr6:31763368-31763384 chr6:31763467-31763483
43	POLR2A	chr6:31762136-31765802	SK-N-MC	brain:	n/a	n/a
44	SPI1	chr6:31763669-31764019	K562	blood:	n/a	n/a
45	MAX	chr6:31761935-31764190	K562	blood:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496 chr6:31763487-31763497
46	GABPA	chr6:31762571-31764055	K562	blood:	n/a	chr6:31763555-31763564 chr6:31763644-31763653
47	RAD21	chr6:31763603-31763979	MCF-7	breast:	n/a	chr6:31763760-31763773
48	MAZ	chr6:31763180-31763987	Hela-S3	cervix:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496
49	YY1	chr6:31762588-31764031	K562	blood:	n/a	chr6:31763754-31763763 chr6:31763468-31763482 chr6:31763467-31763481 chr6:31763754-31763768 chr6:31763748-31763762 chr6:31763368-31763382 chr6:31763539-31763548 chr6:31763371-31763385
50	POLR2A	chr6:31762192-31764199	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31761672..31765296-chr6:31772847..31776146,6	MCF-7	breast:
2	chr6:31760815..31765798-chr6:31772413..31777523,17	MCF-7	breast:
3	chr6:31759482..31765185-chr6:31781824..31784897,13	MCF-7	breast:
4	chr6:31761659..31764051-chr6:31869423..31871582,3	K562	blood:
5	chr6:31763762..31765403-chr6:31864017..31865779,2	MCF-7	breast:
6	chr6:31619065..31621303-chr6:31762386..31764649,2	MCF-7	breast:
7	chr6:31626696..31628687-chr6:31762053..31764771,3	MCF-7	breast:
8	chr6:31429705..31431328-chr6:31762595..31764431,2	K562	blood:
9	chr6:31762561..31765176-chr6:31866590..31868817,2	MCF-7	breast:
10	chr17:56594989..56597705-chr6:31762274..31764941,2	MCF-7	breast:
11	chr6:31763546..31764167-chr6:31782631..31783559,2	K562	blood:
12	chr6:31758502..31767561-chr6:31786193..31804196,52	MCF-7	breast:
13	chr6:31762749..31764673-chr6:32143789..32146313,2	K562	blood:
14	chr6:31684792..31688095-chr6:31761930..31764765,3	MCF-7	breast:
15	chr6:31761047..31764270-chr6:31827785..31831725,4	MCF-7	breast:
16	chr6:31625699..31629901-chr6:31762894..31764968,3	MCF-7	breast:
17	chr6:31667922..31671961-chr6:31761581..31764967,5	MCF-7	breast:
18	chr6:31707530..31710458-chr6:31763602..31765832,2	MCF-7	breast:
19	chr6:31756951..31764627-chr6:31780500..31799197,32	MCF-7	breast:
20	chr6:31763649..31765429-chr6:31938517..31942129,4	K562	blood:
21	chr6:31760851..31764032-chr6:31800769..31804370,7	MCF-7	breast:
22	chr6:31761979..31764717-chr6:31829414..31832230,4	MCF-7	breast:
23	chr6:31763803..31765429-chr6:31940244..31942129,2	K562	blood:

Variant related genes	Relation type
VARS	TF binding region
ENSG00000204410	Chromatin interaction
ENSG00000108389	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204308	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204420	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000264672	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000227198	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000233902	Chromatin interaction
ENSG00000266776	Chromatin interaction
ENSG00000204310	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000206337	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs2021007	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs552412	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs613281	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs62395845	0.94[ASN][1000 genomes]
rs9267652	0.94[ASN][1000 genomes]
rs9267656	0.94[ASN][1000 genomes]
rs9267660	0.94[ASN][1000 genomes]
rs9267662	0.94[ASN][1000 genomes]
rs9267663	0.94[ASN][1000 genomes]
rs9267665	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
2	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
3	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
5	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
7	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
9	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
10	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
11	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
12	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
13	nsv884426	chr6:31728102-31800868	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
14	nsv884427	chr6:31728102-31802465	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
15	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
16	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
17	nsv884430	chr6:31731881-31800631	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
18	nsv884432	chr6:31734117-31777687	Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
19	nsv884433	chr6:31737701-31777687	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS 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	59 gene(s)	inside rSNPs	diseases
20	nsv884437	chr6:31739881-31777687	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
21	nsv884440	chr6:31743882-31775984	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
22	nsv884442	chr6:31745518-31764899	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	43 gene(s)	inside rSNPs	diseases
23	nsv884443	chr6:31745518-31777687	Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
24	nsv884444	chr6:31756670-31768217	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases
25	nsv884445	chr6:31756907-31769250	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases
26	nsv884446	chr6:31760309-31768971	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases
27	nsv884447	chr6:31760654-31770770	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 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	chr6:31761000-31764000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:31761000-31764600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:31761200-31764000	Active TSS	GM12878-XiMat	blood
4	chr6:31761400-31764200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:31761400-31764400	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr6:31761800-31764000	Active TSS	HSMMtube	muscle
7	chr6:31761800-31764000	Active TSS	NHLF	lung
8	chr6:31761800-31764200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:31761800-31764200	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr6:31761800-31764200	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr6:31761800-31764400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:31762000-31764000	Active TSS	H1 Cell Line	embryonic stem cell
13	chr6:31762000-31764000	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr6:31762000-31764200	Active TSS	H9 Cell Line	embryonic stem cell
15	chr6:31762000-31764200	Active TSS	Psoas Muscle	Psoas
16	chr6:31762200-31764000	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr6:31762200-31764000	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr6:31762200-31764000	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr6:31762200-31764000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr6:31762200-31764000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:31762200-31764000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:31762200-31764000	Active TSS	NHDF-Ad	bronchial
23	chr6:31762200-31764200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:31762200-31764200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:31762200-31764200	Active TSS	Brain Hippocampus Middle	brain
26	chr6:31762200-31764200	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr6:31762200-31764200	Active TSS	A549	lung
28	chr6:31762200-31764200	Active TSS	HSMM	muscle
29	chr6:31762400-31764000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:31762400-31764000	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr6:31762400-31764000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
32	chr6:31762400-31764000	Active TSS	Aorta	Aorta
33	chr6:31762400-31764000	Active TSS	Ovary	ovary
34	chr6:31762400-31764200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:31762400-31764200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr6:31762400-31764200	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr6:31762400-31764200	Active TSS	Left Ventricle	heart
38	chr6:31762400-31764200	Active TSS	Sigmoid Colon	Sigmoid Colon
39	chr6:31762400-31764400	Active TSS	Hela-S3	cervix
40	chr6:31762600-31764000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:31762600-31764000	Active TSS	Colon Smooth Muscle	Colon
42	chr6:31762600-31764000	Active TSS	Esophagus	oesophagus
43	chr6:31762600-31764000	Active TSS	Fetal Kidney	kidney
44	chr6:31762600-31764000	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr6:31762600-31764000	Active TSS	Rectal Smooth Muscle	rectum
46	chr6:31762600-31764000	Transcr. at gene 5' and 3'	Right Atrium	heart
47	chr6:31762600-31764200	Active TSS	Primary T cells from cord blood	blood
48	chr6:31762600-31764200	Active TSS	Osteobl	bone
49	chr6:31762600-31764400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:31762800-31764000	Active TSS	Brain Inferior Temporal Lobe	brain

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