Variant report

Variant	rs62395807
Chromosome Location	chr6:31632808-31632809
allele	A/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	JUND	chr6:31632604-31633218	HepG2	liver:	n/a	n/a
2	ZNF143	chr6:31632615-31634450	K562	blood:	n/a	chr6:31633784-31633802 chr6:31633614-31633632 chr6:31633725-31633743
3	FOS	chr6:31632579-31632938	MCF10A-Er-Src	breast:	n/a	n/a
4	HCFC1	chr6:31632027-31634910	Hela-S3	cervix:	n/a	n/a
5	MAFK	chr6:31632292-31634152	K562	blood:	n/a	n/a
6	E2F6	chr6:31632653-31633118	H1-hESC	embryonic stem cell:	n/a	chr6:31632907-31632915 chr6:31632907-31632919 chr6:31632908-31632915 chr6:31632769-31632780 chr6:31632906-31632917 chr6:31632826-31632835 chr6:31632769-31632780 chr6:31632769-31632780 chr6:31632766-31632783 chr6:31632908-31632915 chr6:31632908-31632915 chr6:31632769-31632780 chr6:31632766-31632783
7	SIN3AK20	chr6:31632551-31633150	SK-N-SH	brain:	n/a	n/a
8	REST	chr6:31632754-31633054	A549	lung:	n/a	n/a
9	YY1	chr6:31632653-31633048	K562	blood:	n/a	chr6:31632755-31632777 chr6:31632766-31632774
10	REST	chr6:31632240-31634048	H1-neurons	neurons:	n/a	chr6:31633472-31633492 chr6:31633479-31633492
11	CUX1	chr6:31631866-31634258	K562	blood:	n/a	chr6:31633594-31633608
12	MYC	chr6:31632654-31634155	K562	blood:	n/a	chr6:31634058-31634068
13	BCLAF1	chr6:31632487-31634355	K562	blood:	n/a	chr6:31633646-31633655 chr6:31634115-31634124 chr6:31634061-31634070
14	YY1	chr6:31632356-31634157	GM12892	blood:	n/a	chr6:31634060-31634069 chr6:31632755-31632777 chr6:31634061-31634072 chr6:31632766-31632774 chr6:31633161-31633172
15	ELF1	chr6:31632621-31634150	MCF-7	breast:	n/a	chr6:31632674-31632685 chr6:31633639-31633652
16	SP1	chr6:31632548-31633912	HepG2	liver:	n/a	chr6:31633308-31633318 chr6:31633669-31633678
17	GABPA	chr6:31632734-31634101	K562	blood:	n/a	chr6:31633670-31633679 chr6:31632825-31632836 chr6:31632948-31632957 chr6:31634060-31634069 chr6:31633643-31633650
18	POLR2A	chr6:31632705-31634221	MCF-7	breast:	n/a	n/a
19	POLR2A	chr6:31632353-31634300	SK-N-MC	brain:	n/a	n/a
20	ELK1	chr6:31631742-31634144	K562	blood:	n/a	chr6:31633646-31633655 chr6:31633646-31633655
21	RAD21	chr6:31632609-31632963	Hela-S3	cervix:	n/a	n/a
22	STAT5A	chr6:31632431-31634415	GM12878	blood:	n/a	chr6:31634066-31634078 chr6:31633551-31633563 chr6:31633839-31633851 chr6:31633070-31633078
23	POLR2A	chr6:31632724-31633727	U87	brain:	n/a	n/a
24	MAX	chr6:31632427-31634207	SK-N-SH	brain:	n/a	chr6:31634058-31634068
25	POLR2A	chr6:31632451-31634149	SK-N-SH	brain:	n/a	n/a
26	POLR2A	chr6:31632506-31634185	PANC-1	pancreas:	n/a	n/a
27	ATF3	chr6:31631679-31633915	K562	blood:	n/a	chr6:31633492-31633501 chr6:31632951-31632971 chr6:31632950-31632959
28	TRIM28	chr6:31631410-31634096	K562	blood:	n/a	chr6:31633746-31633754
29	TCF7L2	chr6:31632379-31632988	HEK293	kidney:	n/a	n/a
30	YY1	chr6:31632381-31633935	H1-hESC	embryonic stem cell:	n/a	chr6:31632755-31632777 chr6:31632766-31632774 chr6:31633161-31633172
31	NFIC	chr6:31632701-31633377	ECC-1	luminal epithelium:	n/a	n/a
32	RCOR1	chr6:31632635-31633806	GM12878	blood:	n/a	n/a
33	HNF4G	chr6:31632495-31634203	HepG2	liver:	n/a	chr6:31633191-31633205 chr6:31633814-31633827 chr6:31633810-31633822 chr6:31633814-31633827 chr6:31633809-31633831 chr6:31633191-31633205 chr6:31633193-31633205 chr6:31633191-31633204
34	YY1	chr6:31631619-31634169	K562	blood:	n/a	chr6:31634060-31634069 chr6:31632755-31632777 chr6:31634061-31634072 chr6:31632766-31632774 chr6:31633161-31633172
35	CHD2	chr6:31632789-31634181	HepG2	liver:	n/a	n/a
36	MTA3	chr6:31632175-31634692	GM12878	blood:	n/a	n/a
37	REST	chr6:31632567-31633374	HepG2	liver:	n/a	n/a
38	ATF2	chr6:31632493-31633150	GM12878	blood:	n/a	n/a
39	TEAD4	chr6:31631617-31634618	K562	blood:	n/a	n/a
40	HCFC1	chr6:31631398-31634556	K562	blood:	n/a	n/a
41	STAT3	chr6:31632663-31633176	MCF10A-Er-Src	breast:	n/a	chr6:31633070-31633078
42	USF2	chr6:31632665-31633944	Hela-S3	cervix:	n/a	n/a
43	NFIC	chr6:31632533-31634013	HepG2	liver:	n/a	n/a
44	JUND	chr6:31632645-31633986	HepG2	liver:	n/a	n/a
45	SP1	chr6:31632600-31633017	GM12878	blood:	n/a	n/a
46	CCNT2	chr6:31632705-31634099	K562	blood:	n/a	chr6:31634060-31634069 chr6:31633309-31633318
47	CBX3	chr6:31631090-31634828	K562	blood:	n/a	chr6:31632567-31632578
48	POLR2A	chr6:31632574-31634109	GM12878	blood:	n/a	n/a
49	GATA3	chr6:31632775-31633557	A549	lung:	n/a	chr6:31633338-31633346
50	POLR2A	chr6:31632511-31634079	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31632764-31632814	GM12891	blood:	n/a
2	chr6:31632759-31632809	GM12878	blood:	n/a
3	chr6:31632764-31632814	NT2-D1	testis:	n/a
4	chr6:31632774-31632824	HL-60	blood:	n/a
5	chr6:31632759-31632809	GM06990	blood:	n/a
6	chr6:31632759-31632809	GM12891	blood:	n/a
7	chr6:31632759-31632809	HCF	heart:	n/a
8	chr6:31632759-31632809	PANC-1	pancreas:	n/a
9	chr6:31632764-31632814	SAEC	small airway:	n/a
10	chr6:31632759-31632809	Caco-2	colon:	n/a
11	chr6:31632774-31632824	HCM	heart:	n/a
12	chr6:31632774-31632824	SAEC	small airway:	n/a
13	chr6:31632759-31632809	HCT-116	colon:	n/a
14	chr6:31632774-31632824	PANC-1	pancreas:	n/a
15	chr6:31632759-31632809	AG09319	gingival:	n/a
16	chr6:31632764-31632814	HCT-116	colon:	n/a
17	chr6:31632759-31632809	HIPEpiC	eye:	n/a
18	chr6:31632764-31632814	NHDF-neo	bronchial:	n/a
19	chr6:31632759-31632809	HL-60	blood:	n/a
20	chr6:31632759-31632809	H1-hESC	embryonic stem cell:	embryo
21	chr6:31632759-31632809	HepG2	liver:	n/a
22	chr6:31632759-31632809	HAEpiC	amniotic membrane:	n/a
23	chr6:31632774-31632824	HMEC	breast:	n/a
24	chr6:31632774-31632824	Hela-S3	cervix:	n/a
25	chr6:31632774-31632824	HUVEC	blood vessel:	n/a
26	chr6:31632764-31632814	T-47D	breast:	n/a
27	chr6:31632764-31632814	SK-N-SH	brain:	n/a
28	chr6:31632774-31632824	A549	lung:	n/a
29	chr6:31632774-31632824	LNCaP	prostate:	n/a
30	chr6:31632759-31632809	GM12892	blood:	n/a
31	chr6:31632759-31632809	AoSMC	blood vessel:	n/a
32	chr6:31632759-31632809	HCPEpiC	choroid plexus:	n/a
33	chr6:31632774-31632824	PFSK-1	brain:	n/a
34	chr6:31632764-31632814	GM19239	blood:	n/a
35	chr6:31632764-31632814	H1-hESC	embryonic stem cell:	embryo
36	chr6:31632759-31632809	Jurkat	blood:	n/a
37	chr6:31632759-31632809	HMEC	breast:	n/a
38	chr6:31632759-31632809	CMK	blood:	n/a
39	chr6:31632774-31632824	HepG2	liver:	n/a
40	chr6:31632774-31632824	NH-A	brain:	n/a
41	chr6:31632764-31632814	GM06990	blood:	n/a
42	chr6:31632764-31632814	HAEpiC	amniotic membrane:	n/a
43	chr6:31632774-31632824	T-47D	breast:	n/a
44	chr6:31632759-31632809	HEK293	kidney:	embryo
45	chr6:31632764-31632814	PFSK-1	brain:	n/a
46	chr6:31632764-31632814	CMK	blood:	n/a
47	chr6:31632774-31632824	Hepatocyte	liver:	n/a
48	chr6:31632764-31632814	HCPEpiC	choroid plexus:	n/a
49	chr6:31632774-31632824	AG04450	lung:	fetal
50	chr6:31632764-31632814	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31630330..31634433-chr6:31829449..31833019,5	MCF-7	breast:
2	chr6:31630209..31635577-chr6:31828786..31834874,28	K562	blood:
3	chr6:31631113..31634365-chr6:31867924..31871902,6	K562	blood:
4	chr6:31506496..31512275-chr6:31630248..31634828,11	K562	blood:
5	chr10:33247123..33247949-chr6:31632509..31633366,2	Hela-S3	cervix:
6	chr16:21610180..21611076-chr6:31632628..31633471,2	Hela-S3	cervix:
7	chr6:31631384..31635745-chr6:32161942..32163949,3	K562	blood:
8	chr6:31630940..31635916-chr6:31782579..31784659,6	MCF-7	breast:
9	chr6:31632734..31637057-chr6:31703384..31706202,6	MCF-7	breast:
10	chr6:31632296..31634965-chr6:31685541..31687886,2	MCF-7	breast:
11	chr6:31631824..31634552-chr6:31668867..31671892,6	MCF-7	breast:
12	chr6:31547676..31550388-chr6:31631712..31633963,2	K562	blood:
13	chr6:31632664..31635327-chr6:31741807..31745187,4	MCF-7	breast:
14	chr6:31631207..31634109-chr6:31926807..31929140,3	K562	blood:
15	chr6:31630921..31635353-chr6:31802314..31807064,6	MCF-7	breast:
16	chr6:31505350..31512312-chr6:31630543..31635379,11	K562	blood:
17	chr6:31632546..31633385-chr7:75988056..75988692,2	NB4	blood:
18	chr6:31631384..31634257-chr6:32162297..32163949,2	K562	blood:
19	chr12:54019755..54020430-chr6:31632722..31633291,2	Hela-S3	cervix:
20	chr6:31588013..31588629-chr6:31632757..31633652,2	MCF-7	breast:
21	chr6:31630896..31633436-chr6:31799776..31802391,2	MCF-7	breast:
22	chr6:31586074..31595285-chr6:31626460..31635395,11	MCF-7	breast:
23	chr6:31632061..31634821-chr6:31925160..31927798,3	MCF-7	breast:
24	chr6:31632509..31634236-chr6:31853959..31856343,2	K562	blood:
25	chr6:31627970..31635325-chr6:31864036..31871429,12	K562	blood:
26	chr6:31628509..31634075-chr6:31935054..31938547,6	K562	blood:
27	chr6:31632488..31634160-chr6:31845506..31848503,2	MCF-7	breast:
28	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
29	chr6:31632318..31634134-chr6:31707864..31709911,2	MCF-7	breast:
30	chr6:31512487..31517874-chr6:31628889..31634381,12	K562	blood:
31	chr6:31632224..31633782-chr6:32938836..32940645,2	K562	blood:
32	chr6:31630138..31633537-chr6:31702184..31707226,4	MCF-7	breast:
33	chr6:31512174..31516924-chr6:31632110..31634699,4	MCF-7	breast:
34	chr6:31548503..31550806-chr6:31631619..31633429,4	MCF-7	breast:
35	chr6:31631741..31634123-chr6:32936470..32938783,3	MCF-7	breast:
36	chr6:31631447..31633355-chr6:32013677..32016476,2	K562	blood:
37	chr6:31632509..31634091-chr6:31794981..31797016,2	MCF-7	breast:
38	chr6:31632206..31634072-chr6:31697899..31700595,2	MCF-7	breast:
39	chr6:31632223..31634660-chr6:31938839..31941215,3	K562	blood:
40	chr6:30585114..30586870-chr6:31632529..31634643,2	K562	blood:
41	chr6:31632360..31634286-chr7:148580319..148582667,2	K562	blood:
42	chr6:31631608..31633822-chr6:31656164..31658364,2	MCF-7	breast:
43	chr6:31632122..31634257-chr7:1497327..1499894,2	K562	blood:
44	chr6:31631495..31634660-chr6:31935613..31943206,9	K562	blood:
45	chr6:31512487..31516692-chr6:31630820..31634965,11	K562	blood:
46	chr6:31619844..31620713-chr6:31632640..31633445,3	HCT-116	colon:

Variant related genes	Relation type
CSNK2B	TF binding region
C6orf47	TF binding region
ENSG00000263020	TF binding region
ENSG00000263020	CpG island
C6orf47	CpG island
CSNK2B	CpG island
ENSG00000204387	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000150093	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000266776	Chromatin interaction
ENSG00000229656	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000227507	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204568	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000263756	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000170653	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204257	Chromatin interaction
ENSG00000164877	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000213654	Chromatin interaction
ENSG00000106462	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000197006	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000170027	Chromatin interaction
ENSG00000225981	Chromatin interaction
ENSG00000204420	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs17207706	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs35444838	1.00[EUR][1000 genomes]
rs62395765	1.00[AFR][1000 genomes]
rs62395768	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 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	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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	250 gene(s)	inside rSNPs	diseases
10	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
11	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
12	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription 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 miRNA target site	206 gene(s)	inside rSNPs	diseases
13	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
14	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
15	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

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31631000-31633200	Flanking Active TSS	Adipose Nuclei	Adipose
2	chr6:31631200-31633200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:31631200-31633400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:31631200-31634800	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr6:31631400-31633200	Flanking Active TSS	Primary hematopoietic stem cells	blood
6	chr6:31631400-31634200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
7	chr6:31631400-31634400	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr6:31631400-31634600	Active TSS	H9 Cell Line	embryonic stem cell
9	chr6:31631400-31634600	Active TSS	Aorta	Aorta
10	chr6:31631600-31633200	Flanking Active TSS	HUVEC	blood vessel
11	chr6:31631600-31634400	Active TSS	Fetal Kidney	kidney
12	chr6:31631600-31634600	Active TSS	Ovary	ovary
13	chr6:31631600-31634800	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr6:31631800-31633000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr6:31631800-31633200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr6:31631800-31634600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr6:31631800-31634600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:31631800-31634600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:31631800-31634600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
20	chr6:31631800-31634800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:31632000-31633000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:31632000-31633200	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr6:31632000-31634200	Active TSS	Fetal Lung	lung
24	chr6:31632000-31634400	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr6:31632000-31634400	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr6:31632000-31634400	Active TSS	Colon Smooth Muscle	Colon
27	chr6:31632000-31634400	Active TSS	Fetal Heart	heart
28	chr6:31632000-31634400	Active TSS	Fetal Intestine Large	intestine
29	chr6:31632000-31634400	Active TSS	Small Intestine	intestine
30	chr6:31632000-31634600	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr6:31632000-31634800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:31632200-31634000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:31632200-31634200	Active TSS	Brain Germinal Matrix	brain
34	chr6:31632200-31634200	Active TSS	Thymus	Thymus
35	chr6:31632200-31634400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:31632200-31634400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr6:31632200-31634400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:31632200-31634400	Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr6:31632200-31634400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr6:31632200-31634600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:31632200-31634600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:31632200-31634600	Active TSS	Sigmoid Colon	Sigmoid Colon
43	chr6:31632200-31634600	Active TSS	NHDF-Ad	bronchial
44	chr6:31632200-31635400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr6:31632400-31633000	Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr6:31632400-31633000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:31632400-31633200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr6:31632400-31633400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:31632400-31634000	Active TSS	Placenta	Placenta
50	chr6:31632400-31634000	Active TSS	Dnd41	blood

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