Variant report

Variant	rs73728965
Chromosome Location	chr6:31619535-31619536
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:31619517-31621306	K562	blood:	n/a	n/a
2	ETS1	chr6:31619325-31621283	K562	blood:	n/a	chr6:31620180-31620189 chr6:31620180-31620189 chr6:31620180-31620189 chr6:31620180-31620189 chr6:31620764-31620773 chr6:31620180-31620189 chr6:31620764-31620773 chr6:31620178-31620188 chr6:31620180-31620189 chr6:31621203-31621216 chr6:31620177-31620193 chr6:31620180-31620189 chr6:31620765-31620775
3	SIN3A	chr6:31619356-31621264	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr6:31619453-31621158	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr6:31619202-31621792	H1-hESC	embryonic stem cell:	n/a	n/a
6	PBX3	chr6:31619476-31621078	SK-N-SH	brain:	n/a	n/a
7	SIN3AK20	chr6:31619360-31619997	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr6:31619512-31621686	HCT-116	colon:	n/a	n/a
9	POLR2A	chr6:31619327-31621832	K562	blood:	n/a	n/a
10	CREB1	chr6:31619502-31621166	GM12878	blood:	n/a	n/a
11	SIN3AK20	chr6:31619452-31621142	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr6:31619509-31621043	SK-N-SH	brain:	n/a	chr6:31620481-31620491 chr6:31619768-31619778
13	POLR2A	chr6:31619393-31621867	PFSK-1	brain:	n/a	n/a
14	POU2F2	chr6:31619506-31621032	GM12878	blood:	n/a	n/a
15	POLR2A	chr6:31619422-31621702	PANC-1	pancreas:	n/a	n/a
16	SIN3AK20	chr6:31619433-31621214	K562	blood:	n/a	n/a
17	TAF1	chr6:31619510-31621289	K562	blood:	n/a	n/a
18	NR2F2	chr6:31619207-31622620	K562	blood:	n/a	n/a
19	POLR2A	chr6:31619356-31621374	GM12892	blood:	n/a	n/a
20	PML	chr6:31619202-31621612	K562	blood:	n/a	n/a
21	ELF1	chr6:31619483-31621234	GM12878	blood:	n/a	chr6:31620180-31620191 chr6:31620180-31620191 chr6:31620145-31620157
22	POLR2A	chr6:31619513-31621311	ECC-1	luminal epithelium:	n/a	n/a
23	MXI1	chr6:31619480-31621326	GM12878	blood:	n/a	n/a
24	POLR2A	chr6:31619351-31621694	GM12878	blood:	n/a	n/a
25	GABPA	chr6:31619456-31621139	MCF-7	breast:	n/a	chr6:31619949-31619963 chr6:31619946-31619960 chr6:31620423-31620437 chr6:31619949-31619960 chr6:31619949-31619958
26	SIN3AK20	chr6:31619323-31621273	MCF-7	breast:	n/a	n/a
27	MXI1	chr6:31619500-31621068	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr6:31619465-31621597	HepG2	liver:	n/a	n/a
29	POLR2A	chr6:31619494-31621078	HepG2	liver:	n/a	n/a
30	YY1	chr6:31619376-31621240	K562	blood:	n/a	n/a
31	POLR2A	chr6:31619341-31621771	K562	blood:	n/a	n/a
32	YY1	chr6:31619360-31621123	GM12878	blood:	n/a	n/a
33	EP300	chr6:31619481-31621195	ECC-1	luminal epithelium:	n/a	chr6:31620181-31620188 chr6:31620765-31620772
34	MAX	chr6:31619479-31621139	SK-N-SH	brain:	n/a	chr6:31620481-31620491 chr6:31619768-31619778
35	MBD4	chr6:31619417-31621133	HepG2	liver:	n/a	n/a
36	POLR2A	chr6:31619465-31621283	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr6:31619524-31621218	U87	brain:	n/a	n/a
38	POLR2A	chr6:31619362-31621412	IMR90	lung:	n/a	n/a
39	NR2F2	chr6:31619325-31621879	K562	blood:	n/a	n/a
40	MAX	chr6:31619436-31621339	HepG2	liver:	n/a	chr6:31620481-31620491 chr6:31619768-31619778
41	POLR2A	chr6:31619444-31621803	HepG2	liver:	n/a	n/a
42	PML	chr6:31619489-31621522	GM12878	blood:	n/a	n/a
43	GATA3	chr6:31619533-31621064	MCF-7	breast:	n/a	n/a
44	GABPA	chr6:31619408-31621169	K562	blood:	n/a	chr6:31619949-31619963 chr6:31619946-31619960 chr6:31620423-31620437 chr6:31619949-31619960 chr6:31619949-31619958
45	HDAC2	chr6:31619520-31621103	MCF-7	breast:	n/a	chr6:31619951-31619960 chr6:31619949-31619958
46	YY1	chr6:31619371-31619760	GM12892	blood:	n/a	n/a
47	POLR2A	chr6:31619511-31621635	K562	blood:	n/a	n/a
48	POLR2A	chr6:31619331-31621811	K562	blood:	n/a	n/a
49	NRF1	chr6:31619490-31621257	SK-N-SH	brain:	n/a	chr6:31619949-31619963 chr6:31619946-31619960 chr6:31620423-31620437 chr6:31619949-31619960 chr6:31619949-31619958
50	POLR2A	chr6:31619498-31621076	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31619513-31619563	HL-60	blood:	n/a
2	chr6:31619513-31619563	HepG2	liver:	n/a
3	chr6:31619513-31619563	AG10803	skin:	n/a
4	chr6:31619513-31619563	PrEC	prostate:	n/a
5	chr6:31619513-31619563	GM12878	blood:	n/a
6	chr6:31619513-31619563	HAEpiC	amniotic membrane:	n/a
7	chr6:31619513-31619563	AG09309	skin:	n/a
8	chr6:31619513-31619563	AoSMC	blood vessel:	n/a
9	chr6:31619513-31619563	NHDF-neo	bronchial:	n/a
10	chr6:31619513-31619563	NB4	blood:	n/a
11	chr6:31619513-31619563	Hepatocyte	liver:	n/a
12	chr6:31619513-31619563	HIPEpiC	eye:	n/a
13	chr6:31619513-31619563	ovcar-3	ovarian:	n/a
14	chr6:31619513-31619563	AG04450	lung:	fetal
15	chr6:31619513-31619563	BJ	skin:	n/a
16	chr6:31619513-31619563	BE2_C	brain:	n/a
17	chr6:31619513-31619563	H1-hESC	embryonic stem cell:	embryo
18	chr6:31619513-31619563	Hela-S3	cervix:	n/a
19	chr6:31619513-31619563	SKMC	muscle:	n/a
20	chr6:31619513-31619563	GM19239	blood:	n/a
21	chr6:31619513-31619563	HCF	heart:	n/a
22	chr6:31619513-31619563	PFSK-1	brain:	n/a
23	chr6:31619513-31619563	A549	lung:	n/a
24	chr6:31619513-31619563	HEK293	kidney:	embryo
25	chr6:31619513-31619563	LNCaP	prostate:	n/a
26	chr6:31619513-31619563	ProgFib	skin:	n/a
27	chr6:31619513-31619563	SK-N-SH	brain:	n/a
28	chr6:31619513-31619563	AG04449	skin:	fetal
29	chr6:31619513-31619563	HEEpiC	esophagus:	n/a
30	chr6:31619513-31619563	GM06990	blood:	n/a
31	chr6:31619513-31619563	MCF-7	breast:	n/a
32	chr6:31619513-31619563	CMK	blood:	n/a
33	chr6:31619513-31619563	Caco-2	colon:	n/a
34	chr6:31619513-31619563	PANC-1	pancreas:	n/a
35	chr6:31619513-31619563	HRCEpiC	kidney:	n/a
36	chr6:31619513-31619563	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:31619513-31619563	ECC-1	luminal epithelium:	n/a
38	chr6:31619513-31619563	U87	brain:	n/a
39	chr6:31619513-31619563	NHBE	bronchial:	n/a
40	chr6:31619513-31619563	HMEC	breast:	n/a
41	chr6:31619513-31619563	NT2-D1	testis:	n/a
42	chr6:31619513-31619563	HRPEpiC	eye:	n/a
43	chr6:31619513-31619563	HUVEC	blood vessel:	n/a
44	chr6:31619513-31619563	NH-A	brain:	n/a
45	chr6:31619513-31619563	MCF10A-Er-Src	breast:	n/a
46	chr6:31619513-31619563	HCM	heart:	n/a
47	chr6:31619513-31619563	GM12892	blood:	n/a
48	chr6:31619513-31619563	Jurkat	blood:	n/a
49	chr6:31619513-31619563	HCPEpiC	choroid plexus:	n/a
50	chr6:31619513-31619563	HCT-116	colon:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:
2	chr6:31617977..31621822-chr6:31647367..31651078,5	MCF-7	breast:
3	chr6:31618484..31622073-chr6:31864833..31868659,4	K562	blood:
4	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
5	chr1:45987012..45987529-chr6:31619119..31619881,2	Hela-S3	cervix:
6	chr6:31619534..31622102-chr6:31706429..31708950,2	MCF-7	breast:
7	chr6:31619085..31621370-chr6:31801083..31803892,2	MCF-7	breast:
8	chr6:31586197..31590294-chr6:31618213..31621899,10	MCF-7	breast:
9	chr6:31590485..31592545-chr6:31618288..31620102,2	MCF-7	breast:
10	chr6:31618191..31620672-chr6:31669780..31672189,2	MCF-7	breast:
11	chr6:31618325..31621676-chr6:31863690..31867276,5	K562	blood:
12	chr6:31507205..31511686-chr6:31618024..31622039,13	K562	blood:
13	chr6:31594287..31597004-chr6:31618520..31620536,2	MCF-7	breast:
14	chr6:31618645..31621732-chr6:31914935..31918984,4	K562	blood:
15	chr6:31618887..31620702-chr6:31843664..31845751,2	MCF-7	breast:
16	chr6:31619043..31621335-chr6:31782938..31784758,2	MCF-7	breast:
17	chr6:31619018..31621668-chr6:31828535..31831298,4	MCF-7	breast:
18	chr6:31507451..31516055-chr6:31617949..31624791,11	MCF-7	breast:
19	chr6:31619065..31621303-chr6:31762386..31764649,2	MCF-7	breast:
20	chr6:31619174..31622035-chr6:31794476..31797735,3	MCF-7	breast:
21	chr17:59488570..59491510-chr6:31618990..31620979,2	MCF-7	breast:
22	chr6:31461147..31462941-chr6:31618531..31620077,2	K562	blood:
23	chr6:31619280..31620873-chr6:31935756..31938534,2	K562	blood:
24	chr6:31618346..31620951-chr6:31659194..31661993,2	MCF-7	breast:
25	chr6:31619268..31620861-chr6:31687198..31689564,2	MCF-7	breast:
26	chr6:31507406..31516955-chr6:31615847..31623354,26	K562	blood:
27	chr6:31512553..31516955-chr6:31618753..31622292,7	K562	blood:
28	chr1:28832657..28835568-chr6:31619197..31620853,2	K562	blood:

No data

Variant related genes	Relation type
APOM	TF binding region
APOM	CpG island
ENSG00000243649	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000187013	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204421	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000242125	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000200087	Chromatin interaction
ENSG00000204516	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000267280	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs57541574	1.00[AFR][1000 genomes]
rs73728952	1.00[AFR][1000 genomes]
rs73728969	1.00[AFR][1000 genomes]
rs73728972	1.00[AFR][1000 genomes]
rs7769899	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 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	nsv462871	chr6:31575276-31632134	Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
15	nsv601942	chr6:31575276-31632134	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
16	nsv884419	chr6:31585000-31632651	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
17	nsv884420	chr6:31586827-31632651	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
18	nsv884421	chr6:31588151-31631907	Active TSS Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	129 gene(s)	inside rSNPs	diseases
19	nsv884422	chr6:31592524-31631907	Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
20	nsv884424	chr6:31593729-31632651	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
21	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
22	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	chr6:31617600-31619600	Weak transcription	Aorta	Aorta
2	chr6:31618600-31619600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:31618600-31619600	Flanking Active TSS	Duodenum Mucosa	Duodenum
4	chr6:31618600-31619800	Flanking Active TSS	Fetal Brain Male	brain
5	chr6:31618600-31619800	Transcr. at gene 5' and 3'	Dnd41	blood
6	chr6:31618600-31620000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:31618600-31620000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr6:31618800-31619600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:31618800-31619600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
10	chr6:31618800-31619600	Flanking Active TSS	Fetal Lung	lung
11	chr6:31618800-31619600	Flanking Active TSS	Rectal Smooth Muscle	rectum
12	chr6:31618800-31619800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr6:31618800-31619800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:31618800-31619800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:31618800-31619800	Flanking Active TSS	Colon Smooth Muscle	Colon
16	chr6:31618800-31619800	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
17	chr6:31618800-31619800	Transcr. at gene 5' and 3'	K562	blood
18	chr6:31618800-31619800	Flanking Active TSS	NH-A	brain
19	chr6:31618800-31621600	Active TSS	A549	lung
20	chr6:31619000-31619600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
21	chr6:31619000-31619600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:31619000-31619600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:31619000-31619600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:31619000-31619600	Flanking Active TSS	Hela-S3	cervix
25	chr6:31619000-31619600	Flanking Active TSS	NHEK	skin
26	chr6:31619000-31619600	Flanking Active TSS	Osteobl	bone
27	chr6:31619000-31619800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:31619000-31619800	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr6:31619000-31619800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr6:31619000-31619800	Flanking Active TSS	Liver	Liver
31	chr6:31619000-31620000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
32	chr6:31619000-31621000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:31619000-31621400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:31619000-31621400	Active TSS	NHDF-Ad	bronchial
35	chr6:31619000-31621400	Active TSS	NHLF	lung
36	chr6:31619000-31621600	Active TSS	H9 Cell Line	embryonic stem cell
37	chr6:31619000-31621600	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr6:31619000-31621600	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr6:31619000-31621600	Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr6:31619000-31621600	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr6:31619200-31619600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
42	chr6:31619200-31619600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:31619200-31619600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:31619200-31619600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr6:31619200-31619600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr6:31619200-31619600	Transcr. at gene 5' and 3'	Colonic Mucosa	Colon
47	chr6:31619200-31619600	Flanking Active TSS	Fetal Heart	heart
48	chr6:31619200-31619600	Flanking Active TSS	Fetal Intestine Large	intestine
49	chr6:31619200-31619600	Flanking Active TSS	Fetal Kidney	kidney
50	chr6:31619200-31619600	Flanking Active TSS	Fetal Muscle Trunk	muscle

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