Variant report

Variant	rs35092817
Chromosome Location	chr6:31830882-31830883
allele	A/C
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	HEY1	chr6:31830298-31831020	K562	blood:	n/a	n/a
2	YY1	chr6:31830299-31831014	K562	blood:	n/a	n/a
3	SPI1	chr6:31830481-31830976	HL-60	blood:	n/a	n/a
4	ATF3	chr6:31830357-31831033	HepG2	liver:	n/a	chr6:31830879-31830892 chr6:31830648-31830657 chr6:31830881-31830901 chr6:31830717-31830737
5	E2F6	chr6:31830226-31831034	K562	blood:	n/a	chr6:31830862-31830871
6	RCOR1	chr6:31830291-31831058	K562	blood:	n/a	n/a
7	POLR2A	chr6:31830116-31831878	H1-hESC	embryonic stem cell:	n/a	n/a
8	FOSL1	chr6:31830153-31831079	K562	blood:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
9	RELA	chr6:31830314-31830917	GM15510	blood:	n/a	n/a
10	FOXM1	chr6:31830284-31831169	GM12878	blood:	n/a	n/a
11	CREB1	chr6:31830295-31831050	GM12878	blood:	n/a	chr6:31830879-31830892
12	TCF12	chr6:31830281-31831200	ECC-1	luminal epithelium:	n/a	n/a
13	SP2	chr6:31830405-31831004	HepG2	liver:	n/a	n/a
14	POLR2A	chr6:31830316-31830999	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr6:31830467-31831054	Hela-S3	cervix:	n/a	n/a
16	NFYA	chr6:31830511-31830902	GM12878	blood:	n/a	chr6:31830858-31830873 chr6:31830858-31830873 chr6:31830862-31830874 chr6:31830746-31830764 chr6:31830859-31830873
17	JUND	chr6:31830543-31831075	H1-hESC	embryonic stem cell:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830953-31830964 chr6:31830860-31830869
18	FOSL2	chr6:31830105-31831112	SK-N-SH	brain:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
19	SP1	chr6:31830399-31831106	A549	lung:	n/a	chr6:31830892-31830901 chr6:31830892-31830901 chr6:31830647-31830656 chr6:31830890-31830902 chr6:31830890-31830902 chr6:31830678-31830699 chr6:31830891-31830900 chr6:31830851-31830872 chr6:31830891-31830901 chr6:31830891-31830901
20	SP4	chr6:31830294-31831077	H1-hESC	embryonic stem cell:	n/a	chr6:31830888-31830904
21	EP300	chr6:31830351-31831019	HepG2	liver:	n/a	chr6:31830956-31830965
22	SIN3AK20	chr6:31830376-31831064	A549	lung:	n/a	n/a
23	USF1	chr6:31830334-31831018	SK-N-SH	brain:	n/a	chr6:31830715-31830728
24	GTF2F1	chr6:31830494-31831152	Hela-S3	cervix:	n/a	n/a
25	USF1	chr6:31830372-31830985	A549	lung:	n/a	chr6:31830715-31830728
26	E2F6	chr6:31830235-31830986	K562	blood:	n/a	chr6:31830862-31830871
27	GATA1	chr6:31830424-31832058	PBDE	blood:	n/a	chr6:31830604-31830611 chr6:31830955-31830964
28	JUND	chr6:31830244-31831121	H1-hESC	embryonic stem cell:	n/a	chr6:31830384-31830395 chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
29	TBP	chr6:31830315-31831083	HepG2	liver:	n/a	n/a
30	MAX	chr6:31829919-31830983	HepG2	liver:	n/a	chr6:31830956-31830965
31	USF1	chr6:31830371-31831000	A549	lung:	n/a	chr6:31830715-31830728
32	CREB1	chr6:31830090-31831928	K562	blood:	n/a	chr6:31830879-31830892
33	HDAC2	chr6:31830181-31830975	K562	blood:	n/a	n/a
34	EP300	chr6:31830616-31831082	K562	blood:	n/a	chr6:31830956-31830965
35	SIN3AK20	chr6:31830167-31831136	SK-N-SH	brain:	n/a	n/a
36	POLR2A	chr6:31830249-31830902	MCF-7	breast:	n/a	n/a
37	POLR2A	chr6:31830142-31830946	HUVEC	blood vessel:	n/a	n/a
38	BHLHE40	chr6:31830294-31830942	HepG2	liver:	n/a	chr6:31830715-31830728
39	TAF1	chr6:31830300-31830957	H1-neurons	neurons:	n/a	n/a
40	SIN3AK20	chr6:31830083-31831000	H1-hESC	embryonic stem cell:	n/a	n/a
41	MXI1	chr6:31830334-31831918	GM12878	blood:	n/a	chr6:31830718-31830727
42	PBX3	chr6:31830372-31831029	SK-N-SH	brain:	n/a	chr6:31830861-31830870
43	ZC3H11A	chr6:31830449-31831019	K562	blood:	n/a	n/a
44	FOS	chr6:31830302-31831130	K562	blood:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830955-31830966 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
45	ETS1	chr6:31830064-31830947	K562	blood:	n/a	chr6:31830804-31830815 chr6:31830197-31830211 chr6:31830673-31830684
46	MAX	chr6:31830282-31831116	SK-N-SH	brain:	n/a	chr6:31830956-31830965
47	HMGN3	chr6:31830240-31831012	K562	blood:	n/a	chr6:31830384-31830393
48	ARID3A	chr6:31830632-31831050	K562	blood:	n/a	n/a
49	SREBP2	chr6:31830553-31831005	HepG2	liver:	n/a	n/a
50	E2F6	chr6:31830386-31831129	H1-hESC	embryonic stem cell:	n/a	chr6:31830862-31830871

No.	Distal block	Cell Line	Cell type
1	chr6:31619018..31621668-chr6:31828535..31831298,4	MCF-7	breast:
2	chr6:31761047..31764270-chr6:31827785..31831725,4	MCF-7	breast:
3	chr6:31514420..31518271-chr6:31830053..31832008,3	K562	blood:
4	chr6:31748274..31750464-chr6:31829000..31831442,2	MCF-7	breast:
5	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
6	chr6:31828758..31831666-chr6:31853611..31856072,2	MCF-7	breast:
7	chr6:31734752..31736298-chr6:31828518..31831343,2	K562	blood:
8	chr6:31758631..31763066-chr6:31827655..31831615,4	K562	blood:
9	chr6:31745070..31746845-chr6:31830028..31832915,2	MCF-7	breast:
10	chr6:31774091..31776344-chr6:31828893..31831277,2	K562	blood:
11	chr6:31827799..31831011-chr6:31868395..31870845,5	MCF-7	breast:
12	chr6:31830673..31832900-chr6:31938643..31940364,3	MCF-7	breast:
13	chr6:31830409..31832412-chr6:32014093..32016041,2	K562	blood:
14	chr6:31509002..31510673-chr6:31830602..31832330,2	K562	blood:
15	chr6:31761979..31764717-chr6:31829414..31832230,4	MCF-7	breast:
16	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
17	chr6:31750326..31751829-chr6:31829443..31831754,2	MCF-7	breast:
18	chr6:31781780..31785433-chr6:31828310..31832689,5	K562	blood:
19	chr6:31772422..31776496-chr6:31829254..31834757,6	K562	blood:
20	chr6:31828023..31833065-chr6:31863439..31869544,9	K562	blood:
21	chr6:31703656..31706945-chr6:31827756..31831598,5	MCF-7	breast:
22	chr6:31630209..31635577-chr6:31828786..31834874,28	K562	blood:
23	chr6:31830083..31833987-chr6:31862759..31865610,4	MCF-7	breast:
24	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
25	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
26	chr6:31794817..31797801-chr6:31829779..31831981,3	K562	blood:
27	chr6:31706534..31708652-chr6:31828813..31831366,2	K562	blood:
28	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
29	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
30	chr6:31829731..31832430-chr6:31863949..31866099,3	K562	blood:
31	chr6:31781780..31785433-chr6:31829263..31832689,6	K562	blood:
32	chr6:31830500..31832979-chr6:31939876..31941891,3	K562	blood:
33	chr6:31828952..31831553-chr6:31912715..31914981,2	K562	blood:
34	chr6:31706755..31708433-chr6:31830637..31832576,2	K562	blood:
35	chr6:31694918..31699964-chr6:31826467..31832957,9	K562	blood:
36	chr6:31828958..31833712-chr6:31836982..31839801,4	MCF-7	breast:
37	chr6:31711834..31714451-chr6:31829809..31833042,3	K562	blood:
38	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
39	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
40	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
41	chr6:31586339..31592286-chr6:31830032..31833457,6	K562	blood:
42	chr6:31701938..31704638-chr6:31828885..31832061,3	K562	blood:
43	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:
44	chr6:31630330..31634433-chr6:31829449..31833019,5	MCF-7	breast:
45	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
46	chr6:31694971..31696688-chr6:31829211..31832001,2	MCF-7	breast:
47	chr6:31780296..31786175-chr6:31828333..31833086,7	MCF-7	breast:
48	chr6:31829193..31831687-chr6:31925120..31927788,2	MCF-7	breast:
49	chr6:31794986..31795591-chr6:31830132..31830996,2	K562	blood:
50	chr6:31626270..31630199-chr6:31829030..31832230,7	K562	blood:

Variant related genes	Relation type
NEU1	TF binding region
ENSG00000200816	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000227198	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000201754	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11548074	0.81[EUR][1000 genomes]
rs13192107	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13194698	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17201319	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34287387	0.90[EUR][1000 genomes]
rs35421785	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36097221	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563386	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
16	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' 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	197 gene(s)	inside rSNPs	diseases
18	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
19	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
20	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
21	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
22	nsv884472	chr6:31813898-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
23	nsv508399	chr6:31829474-31902423	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31829200-31831200	Active TSS	NHLF	lung
2	chr6:31829200-31832000	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr6:31829200-31832400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:31829400-31832200	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr6:31829400-31832400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:31829600-31831000	Active TSS	NH-A	brain
7	chr6:31829600-31832200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr6:31829600-31832200	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr6:31829600-31832200	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr6:31829600-31832200	Active TSS	HSMM	muscle
11	chr6:31829600-31832200	Active TSS	HSMMtube	muscle
12	chr6:31829600-31832200	Active TSS	NHDF-Ad	bronchial
13	chr6:31829600-31832400	Active TSS	H9 Cell Line	embryonic stem cell
14	chr6:31829800-31831000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:31829800-31831800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr6:31829800-31832200	Active TSS	Fetal Kidney	kidney
17	chr6:31829800-31832400	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr6:31829800-31832400	Active TSS	A549	lung
19	chr6:31830000-31831000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:31830000-31831000	Active TSS	Pancreas	Pancrea
21	chr6:31830000-31831200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:31830000-31831200	Active TSS	Lung	lung
23	chr6:31830000-31831200	Active TSS	HMEC	breast
24	chr6:31830000-31832000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:31830000-31832000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:31830000-31832000	Active TSS	Ovary	ovary
27	chr6:31830000-31832000	Active TSS	Right Atrium	heart
28	chr6:31830000-31832200	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr6:31830000-31832200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:31830000-31832200	Active TSS	Right Ventricle	heart
31	chr6:31830000-31832400	Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr6:31830000-31832400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr6:31830000-31832400	Bivalent/Poised TSS	HepG2	liver
34	chr6:31830200-31831000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:31830200-31831000	Active TSS	Primary B cells from cord blood	blood
36	chr6:31830200-31831000	Active TSS	Muscle Satellite Cultured Cells	--
37	chr6:31830200-31831000	Active TSS	Brain Anterior Caudate	brain
38	chr6:31830200-31831000	Active TSS	Brain Hippocampus Middle	brain
39	chr6:31830200-31831000	Active TSS	Colonic Mucosa	Colon
40	chr6:31830200-31831000	Active TSS	Fetal Intestine Large	intestine
41	chr6:31830200-31831000	Active TSS	Fetal Intestine Small	intestine
42	chr6:31830200-31831000	Active TSS	Fetal Stomach	stomach
43	chr6:31830200-31831000	Active TSS	K562	blood
44	chr6:31830200-31831000	Active TSS	Monocytes-CD14+_RO01746	blood
45	chr6:31830200-31831000	Active TSS	NHEK	skin
46	chr6:31830200-31831200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr6:31830200-31831200	Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr6:31830200-31831200	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr6:31830200-31831200	Active TSS	Esophagus	oesophagus
50	chr6:31830200-31831200	Active TSS	Skeletal Muscle Female	skeletal muscle

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