Variant report

Variant	rs805299
Chromosome Location	chr6:31619652-31619653
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	MAX	chr6:31619552-31621260	MCF-7	breast:	n/a	chr6:31620481-31620491 chr6:31619768-31619778
2	MAX	chr6:31619581-31621234	ECC-1	luminal epithelium:	n/a	chr6:31620481-31620491 chr6:31619768-31619778
3	BHLHE40	chr6:31619517-31621306	K562	blood:	n/a	n/a
4	ATF2	chr6:31619544-31621131	GM12878	blood:	n/a	n/a
5	BRCA1	chr6:31619612-31619851	GM12878	blood:	n/a	n/a
6	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
7	POLR2A	chr6:31619601-31621730	K562	blood:	n/a	n/a
8	POLR2A	chr6:31619552-31621106	HCT-116	colon:	n/a	n/a
9	SIN3A	chr6:31619356-31621264	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPD	chr6:31619552-31621768	K562	blood:	n/a	n/a
11	POLR2A	chr6:31619453-31621158	H1-hESC	embryonic stem cell:	n/a	n/a
12	GABPA	chr6:31619545-31621056	K562	blood:	n/a	chr6:31619949-31619963 chr6:31619946-31619960 chr6:31620423-31620437 chr6:31619949-31619960 chr6:31619949-31619958
13	GTF2F1	chr6:31619605-31619882	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr6:31619202-31621792	H1-hESC	embryonic stem cell:	n/a	n/a
15	PBX3	chr6:31619476-31621078	SK-N-SH	brain:	n/a	n/a
16	NFYA	chr6:31619625-31620857	K562	blood:	n/a	n/a
17	SIN3AK20	chr6:31619360-31619997	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr6:31619512-31621686	HCT-116	colon:	n/a	n/a
19	POLR2A	chr6:31619327-31621832	K562	blood:	n/a	n/a
20	MYC	chr6:31619617-31621303	K562	blood:	n/a	chr6:31620481-31620491 chr6:31619768-31619778
21	TBP	chr6:31619568-31621182	K562	blood:	n/a	n/a
22	PBX3	chr6:31619646-31619945	GM12878	blood:	n/a	n/a
23	CREB1	chr6:31619502-31621166	GM12878	blood:	n/a	n/a
24	MXI1	chr6:31619611-31621488	K562	blood:	n/a	n/a
25	SIN3AK20	chr6:31619452-31621142	H1-hESC	embryonic stem cell:	n/a	n/a
26	TBP	chr6:31619590-31621131	HepG2	liver:	n/a	n/a
27	E2F6	chr6:31619632-31620190	K562	blood:	n/a	chr6:31619945-31619953 chr6:31619946-31619953 chr6:31619950-31619959 chr6:31619946-31619953 chr6:31619946-31619953
28	CHD1	chr6:31619553-31620108	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr6:31619509-31621043	SK-N-SH	brain:	n/a	chr6:31620481-31620491 chr6:31619768-31619778
30	CEBPB	chr6:31619609-31621828	K562	blood:	n/a	chr6:31621514-31621525
31	ZNF384	chr6:31619546-31621003	K562	blood:	n/a	n/a
32	TAF1	chr6:31619592-31621271	HepG2	liver:	n/a	n/a
33	HEY1	chr6:31619539-31621161	HepG2	liver:	n/a	n/a
34	POLR2A	chr6:31619393-31621867	PFSK-1	brain:	n/a	n/a
35	POU2F2	chr6:31619506-31621032	GM12878	blood:	n/a	n/a
36	POLR2A	chr6:31619558-31621409	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr6:31619422-31621702	PANC-1	pancreas:	n/a	n/a
38	POLR2A	chr6:31619595-31621200	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr6:31619610-31621147	GM12892	blood:	n/a	n/a
40	POLR2A	chr6:31619632-31621142	GM18505	blood:	n/a	n/a
41	SIN3AK20	chr6:31619433-31621214	K562	blood:	n/a	n/a
42	TAF1	chr6:31619510-31621289	K562	blood:	n/a	n/a
43	NR2F2	chr6:31619207-31622620	K562	blood:	n/a	n/a
44	POLR2A	chr6:31619356-31621374	GM12892	blood:	n/a	n/a
45	EP300	chr6:31619562-31621215	K562	blood:	n/a	chr6:31620181-31620188 chr6:31620765-31620772
46	PML	chr6:31619202-31621612	K562	blood:	n/a	n/a
47	ELF1	chr6:31619483-31621234	GM12878	blood:	n/a	chr6:31620180-31620191 chr6:31620180-31620191 chr6:31620145-31620157
48	POLR2A	chr6:31619513-31621311	ECC-1	luminal epithelium:	n/a	n/a
49	NFYB	chr6:31619627-31619998	Hela-S3	cervix:	n/a	n/a
50	GABPA	chr6:31619635-31621027	A549	lung:	n/a	chr6:31619949-31619963 chr6:31619946-31619960 chr6:31620423-31620437 chr6:31619949-31619960 chr6:31619949-31619958

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	chr14:75745180..75745877-chr6:31619624..31620407,2	Hela-S3	cervix:
13	chr6:31507205..31511686-chr6:31618024..31622039,13	K562	blood:
14	chr6:31594287..31597004-chr6:31618520..31620536,2	MCF-7	breast:
15	chr6:31618645..31621732-chr6:31914935..31918984,4	K562	blood:
16	chr6:31618887..31620702-chr6:31843664..31845751,2	MCF-7	breast:
17	chr6:31619043..31621335-chr6:31782938..31784758,2	MCF-7	breast:
18	chr6:31619018..31621668-chr6:31828535..31831298,4	MCF-7	breast:
19	chr6:31507451..31516055-chr6:31617949..31624791,11	MCF-7	breast:
20	chr6:31619065..31621303-chr6:31762386..31764649,2	MCF-7	breast:
21	chr6:31619174..31622035-chr6:31794476..31797735,3	MCF-7	breast:
22	chr17:59488570..59491510-chr6:31618990..31620979,2	MCF-7	breast:
23	chr6:31461147..31462941-chr6:31618531..31620077,2	K562	blood:
24	chr6:31619280..31620873-chr6:31935756..31938534,2	K562	blood:
25	chr6:31618346..31620951-chr6:31659194..31661993,2	MCF-7	breast:
26	chr6:31587877..31588813-chr6:31619626..31620207,2	MCF-7	breast:
27	chr6:31619268..31620861-chr6:31687198..31689564,2	MCF-7	breast:
28	chr6:31507406..31516955-chr6:31615847..31623354,26	K562	blood:
29	chr6:31512553..31516955-chr6:31618753..31622292,7	K562	blood:
30	chr1:28832657..28835568-chr6:31619197..31620853,2	K562	blood:

Variant related genes	Relation type
APOM	TF binding region
ENSG00000204389	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000170345	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000242125	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000187013	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000200087	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000204421	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204516	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000254870	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs13716	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2051552	0.80[AMR][1000 genomes]
rs2259571	0.82[AMR][1000 genomes]
rs2260000	0.84[AMR][1000 genomes]
rs2260050	0.87[AMR][1000 genomes]
rs2507957	0.81[AMR][1000 genomes]
rs2736172	0.83[AMR][1000 genomes]
rs2736176	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2844472	0.84[AMR][1000 genomes]
rs2857698	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3091280	0.80[AMR][1000 genomes]
rs5872	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs707919	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs707939	0.81[AMR][1000 genomes]
rs755714	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][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

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs805299	HLA-DQB1	Cis_chr	lymphoblastoid	RTeQTL
rs805299	CSNK2B	cis	multi-tissue	Pritchard
rs805299	AIF1	Cis_1M	lymphoblastoid	RTeQTL
rs805299	CSNK2B	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31618600-31619800	Flanking Active TSS	Fetal Brain Male	brain
2	chr6:31618600-31619800	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr6:31618600-31620000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:31618600-31620000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:31618800-31619800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
6	chr6:31618800-31619800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:31618800-31619800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:31618800-31619800	Flanking Active TSS	Colon Smooth Muscle	Colon
9	chr6:31618800-31619800	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
10	chr6:31618800-31619800	Transcr. at gene 5' and 3'	K562	blood
11	chr6:31618800-31619800	Flanking Active TSS	NH-A	brain
12	chr6:31618800-31621600	Active TSS	A549	lung
13	chr6:31619000-31619800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:31619000-31619800	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr6:31619000-31619800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr6:31619000-31619800	Flanking Active TSS	Liver	Liver
17	chr6:31619000-31620000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr6:31619000-31621000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:31619000-31621400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr6:31619000-31621400	Active TSS	NHDF-Ad	bronchial
21	chr6:31619000-31621400	Active TSS	NHLF	lung
22	chr6:31619000-31621600	Active TSS	H9 Cell Line	embryonic stem cell
23	chr6:31619000-31621600	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr6:31619000-31621600	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr6:31619000-31621600	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr6:31619000-31621600	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr6:31619200-31619800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:31619200-31619800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
29	chr6:31619200-31619800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
30	chr6:31619200-31619800	Flanking Active TSS	Primary T cells from cord blood	blood
31	chr6:31619200-31619800	Flanking Active TSS	Primary hematopoietic stem cells	blood
32	chr6:31619200-31619800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr6:31619200-31619800	Flanking Active TSS	Fetal Muscle Leg	muscle
34	chr6:31619200-31619800	Flanking Active TSS	Fetal Thymus	thymus
35	chr6:31619200-31619800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr6:31619200-31620000	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr6:31619200-31620000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr6:31619200-31620400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:31619200-31621000	Active TSS	GM12878-XiMat	blood
40	chr6:31619200-31621400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr6:31619200-31621400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:31619200-31621400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:31619200-31621400	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr6:31619200-31621600	Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr6:31619200-31621600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:31619200-31621600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr6:31619200-31621600	Active TSS	Psoas Muscle	Psoas
48	chr6:31619400-31619800	Flanking Active TSS	Primary B cells from peripheral blood	blood
49	chr6:31619400-31619800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr6:31619400-31619800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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