Variant report

Variant	rs3869144
Chromosome Location	chr6:31831159-31831160
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	chr6:31830116-31831878	H1-hESC	embryonic stem cell:	n/a	n/a
2	FOXM1	chr6:31830284-31831169	GM12878	blood:	n/a	n/a
3	TCF12	chr6:31830281-31831200	ECC-1	luminal epithelium:	n/a	n/a
4	YY1	chr6:31830997-31832002	H1-hESC	embryonic stem cell:	n/a	n/a
5	SP1	chr6:31831127-31831966	A549	lung:	n/a	n/a
6	GATA1	chr6:31830424-31832058	PBDE	blood:	n/a	chr6:31830604-31830611 chr6:31830955-31830964
7	YY1	chr6:31831158-31831784	HepG2	liver:	n/a	n/a
8	CREB1	chr6:31830090-31831928	K562	blood:	n/a	chr6:31830879-31830892
9	MXI1	chr6:31830334-31831918	GM12878	blood:	n/a	chr6:31830718-31830727
10	POLR2A	chr6:31829373-31832286	HepG2	liver:	n/a	n/a
11	JUND	chr6:31830207-31831896	K562	blood:	n/a	chr6:31830384-31830395 chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
12	POLR2A	chr6:31831102-31832010	PFSK-1	brain:	n/a	n/a
13	MAX	chr6:31830311-31831945	ECC-1	luminal epithelium:	n/a	chr6:31830956-31830965
14	MAX	chr6:31830301-31831977	A549	lung:	n/a	chr6:31830956-31830965
15	NFIC	chr6:31830234-31831903	GM12878	blood:	n/a	n/a
16	SP1	chr6:31830342-31831977	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
17	PML	chr6:31830232-31831968	K562	blood:	n/a	n/a
18	FOSL2	chr6:31830127-31831202	MCF-7	breast:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
19	POLR2A	chr6:31829794-31831853	K562	blood:	n/a	n/a
20	JUND	chr6:31830022-31831866	MCF-7	breast:	n/a	chr6:31830384-31830395 chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
21	MAX	chr6:31830091-31831957	K562	blood:	n/a	chr6:31830956-31830965
22	SIN3AK20	chr6:31831158-31831882	H1-hESC	embryonic stem cell:	n/a	n/a
23	SIN3AK20	chr6:31829716-31832030	MCF-7	breast:	n/a	n/a
24	SRF	chr6:31831147-31831790	MCF-7	breast:	n/a	n/a
25	ZNF384	chr6:31830271-31832025	K562	blood:	n/a	n/a
26	CREB1	chr6:31830305-31831967	GM12878	blood:	n/a	chr6:31830879-31830892
27	FOSL2	chr6:31830709-31831164	A549	lung:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830953-31830964 chr6:31830860-31830869
28	SP1	chr6:31831153-31831975	H1-hESC	embryonic stem cell:	n/a	n/a
29	SIN3A	chr6:31829897-31831866	H1-hESC	embryonic stem cell:	n/a	chr6:31830310-31830321 chr6:31830718-31830727
30	GTF3C2	chr6:31830962-31832065	Hela-S3	cervix:	n/a	n/a
31	SP2	chr6:31831158-31831686	K562	blood:	n/a	n/a
32	FOS	chr6:31830193-31831886	HUVEC	blood vessel:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830955-31830966 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
33	MAX	chr6:31831108-31831953	H1-hESC	embryonic stem cell:	n/a	n/a
34	YY1	chr6:31831030-31831952	K562	blood:	n/a	n/a
35	E2F4	chr6:31830343-31831844	MCF10A-Er-Src	breast:	n/a	chr6:31830862-31830871 chr6:31830918-31830929
36	FOSL1	chr6:31829957-31831836	K562	blood:	n/a	chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
37	SIN3A	chr6:31830272-31831777	GM12878	blood:	n/a	chr6:31830310-31830321 chr6:31830718-31830727
38	TRIM28	chr6:31830211-31832026	K562	blood:	n/a	n/a
39	YY1	chr6:31831146-31831722	ECC-1	luminal epithelium:	n/a	n/a
40	TAF1	chr6:31831128-31831898	H1-hESC	embryonic stem cell:	n/a	n/a
41	EP300	chr6:31830398-31831936	ECC-1	luminal epithelium:	n/a	chr6:31830956-31830965
42	MYBL2	chr6:31830251-31832006	HepG2	liver:	n/a	n/a
43	POLR2A	chr6:31831137-31831881	HL-60	blood:	n/a	n/a
44	JUN	chr6:31829065-31833596	K562	blood:	n/a	chr6:31833071-31833080 chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
45	POLR2A	chr6:31829585-31831955	K562	blood:	n/a	n/a
46	REST	chr6:31831142-31832135	H1-neurons	neurons:	n/a	chr6:31831552-31831565
47	SP1	chr6:31831152-31832000	HCT-116	colon:	n/a	n/a
48	MXI1	chr6:31829645-31832562	SK-N-SH	brain:	n/a	chr6:31830718-31830727
49	POLR2A	chr6:31831139-31831846	HL-60	blood:	n/a	n/a
50	POLR2A	chr6:31831156-31831886	K562	blood:	n/a	n/a

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	chr6:31830912..31833686-chr6:32013315..32015593,2	K562	blood:
4	chr6:31514420..31518271-chr6:31830053..31832008,3	K562	blood:
5	chr6:31748274..31750464-chr6:31829000..31831442,2	MCF-7	breast:
6	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
7	chr6:31828758..31831666-chr6:31853611..31856072,2	MCF-7	breast:
8	chr6:31734752..31736298-chr6:31828518..31831343,2	K562	blood:
9	chr6:31758631..31763066-chr6:31827655..31831615,4	K562	blood:
10	chr6:31745070..31746845-chr6:31830028..31832915,2	MCF-7	breast:
11	chr6:31774091..31776344-chr6:31828893..31831277,2	K562	blood:
12	chr6:31670174..31672313-chr6:31830988..31833810,3	K562	blood:
13	chr6:31830673..31832900-chr6:31938643..31940364,3	MCF-7	breast:
14	chr6:31830409..31832412-chr6:32014093..32016041,2	K562	blood:
15	chr6:31509002..31510673-chr6:31830602..31832330,2	K562	blood:
16	chr6:31761979..31764717-chr6:31829414..31832230,4	MCF-7	breast:
17	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
18	chr6:31750326..31751829-chr6:31829443..31831754,2	MCF-7	breast:
19	chr6:31781780..31785433-chr6:31828310..31832689,5	K562	blood:
20	chr6:31772422..31776496-chr6:31829254..31834757,6	K562	blood:
21	chr6:31828023..31833065-chr6:31863439..31869544,9	K562	blood:
22	chr6:31703656..31706945-chr6:31827756..31831598,5	MCF-7	breast:
23	chr6:31630209..31635577-chr6:31828786..31834874,28	K562	blood:
24	chr6:31830083..31833987-chr6:31862759..31865610,4	MCF-7	breast:
25	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
26	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
27	chr6:31794817..31797801-chr6:31829779..31831981,3	K562	blood:
28	chr6:31706534..31708652-chr6:31828813..31831366,2	K562	blood:
29	chr6:31830894..31832674-chr6:31912375..31914374,2	MCF-7	breast:
30	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
31	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
32	chr6:31829731..31832430-chr6:31863949..31866099,3	K562	blood:
33	chr6:31781780..31785433-chr6:31829263..31832689,6	K562	blood:
34	chr6:31830500..31832979-chr6:31939876..31941891,3	K562	blood:
35	chr6:31828952..31831553-chr6:31912715..31914981,2	K562	blood:
36	chr6:31706755..31708433-chr6:31830637..31832576,2	K562	blood:
37	chr6:31694918..31699964-chr6:31826467..31832957,9	K562	blood:
38	chr6:31828958..31833712-chr6:31836982..31839801,4	MCF-7	breast:
39	chr6:31711834..31714451-chr6:31829809..31833042,3	K562	blood:
40	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
41	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
42	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
43	chr6:31586339..31592286-chr6:31830032..31833457,6	K562	blood:
44	chr6:31701938..31704638-chr6:31828885..31832061,3	K562	blood:
45	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:
46	chr6:31630330..31634433-chr6:31829449..31833019,5	MCF-7	breast:
47	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
48	chr6:31694971..31696688-chr6:31829211..31832001,2	MCF-7	breast:
49	chr6:31780296..31786175-chr6:31828333..31833086,7	MCF-7	breast:
50	chr6:31829193..31831687-chr6:31925120..31927788,2	MCF-7	breast:

Variant related genes	Relation type
NEU1	TF binding region
ENSG00000198563	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000227198	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000234006	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11968400	0.90[ASN][1000 genomes]
rs12193504	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12210887	0.97[ASN][1000 genomes]
rs12212242	0.97[ASN][1000 genomes]
rs13191375	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34249798	0.90[EUR][1000 genomes]
rs693906	1.00[ASN][1000 genomes]
rs73400280	0.93[ASN][1000 genomes]
rs7765136	0.97[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	chr6:31829600-31832200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:31829600-31832200	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr6:31829600-31832200	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr6:31829600-31832200	Active TSS	HSMM	muscle
10	chr6:31829600-31832200	Active TSS	HSMMtube	muscle
11	chr6:31829600-31832200	Active TSS	NHDF-Ad	bronchial
12	chr6:31829600-31832400	Active TSS	H9 Cell Line	embryonic stem cell
13	chr6:31829800-31831800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr6:31829800-31832200	Active TSS	Fetal Kidney	kidney
15	chr6:31829800-31832400	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr6:31829800-31832400	Active TSS	A549	lung
17	chr6:31830000-31831200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:31830000-31831200	Active TSS	Lung	lung
19	chr6:31830000-31831200	Active TSS	HMEC	breast
20	chr6:31830000-31832000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:31830000-31832000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:31830000-31832000	Active TSS	Ovary	ovary
23	chr6:31830000-31832000	Active TSS	Right Atrium	heart
24	chr6:31830000-31832200	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr6:31830000-31832200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr6:31830000-31832200	Active TSS	Right Ventricle	heart
27	chr6:31830000-31832400	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr6:31830000-31832400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr6:31830000-31832400	Bivalent/Poised TSS	HepG2	liver
30	chr6:31830200-31831200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr6:31830200-31831200	Active TSS	Primary T killer memory cells from peripheral blood	blood
32	chr6:31830200-31831200	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr6:31830200-31831200	Active TSS	Esophagus	oesophagus
34	chr6:31830200-31831200	Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr6:31830200-31831200	Active TSS	Stomach Smooth Muscle	stomach
36	chr6:31830200-31831400	Active TSS	Placenta Amnion	Placenta Amnion
37	chr6:31830200-31831800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:31830200-31831800	Active TSS	Spleen	Spleen
39	chr6:31830200-31832000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr6:31830200-31832000	Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr6:31830200-31832000	Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr6:31830200-31832000	Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr6:31830200-31832000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:31830200-31832000	Active TSS	Brain Cingulate Gyrus	brain
45	chr6:31830200-31832000	Active TSS	Psoas Muscle	Psoas
46	chr6:31830200-31832000	Active TSS	Rectal Smooth Muscle	rectum
47	chr6:31830200-31832200	Active TSS	H1 Cell Line	embryonic stem cell
48	chr6:31830200-31832200	Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr6:31830200-31832200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:31830200-31832200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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