Variant report

Variant	rs440454
Chromosome Location	chr6:31927342-31927343
allele	C/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	ELF1	chr6:31926369-31927344	K562	blood:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
2	POLR2A	chr6:31926273-31927396	HUVEC	blood vessel:	n/a	n/a
3	GABPA	chr6:31926167-31927372	A549	lung:	n/a	n/a
4	POLR2A	chr6:31926482-31927344	HepG2	liver:	n/a	n/a
5	ELF1	chr6:31926526-31927397	HepG2	liver:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
6	CREB1	chr6:31926122-31927508	HepG2	liver:	n/a	n/a
7	WRNIP1	chr6:31926759-31927484	GM12878	blood:	n/a	n/a
8	CREB1	chr6:31926206-31927349	GM12878	blood:	n/a	n/a
9	POLR2A	chr6:31926364-31927460	K562	blood:	n/a	n/a
10	STAT5A	chr6:31926186-31927457	GM12878	blood:	n/a	chr6:31926997-31927009
11	EP300	chr6:31926560-31927480	HepG2	liver:	n/a	chr6:31926869-31926876
12	ELF1	chr6:31926307-31927548	HCT-116	colon:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
13	CREB1	chr6:31926068-31927469	HepG2	liver:	n/a	n/a
14	GABPA	chr6:31926124-31927388	SK-N-SH	brain:	n/a	n/a
15	NR2C2	chr6:31926671-31927463	HepG2	liver:	n/a	chr6:31927036-31927051 chr6:31927037-31927050 chr6:31927057-31927072 chr6:31927051-31927064
16	NR2F2	chr6:31926654-31927367	MCF-7	breast:	n/a	chr6:31927054-31927069 chr6:31927036-31927051 chr6:31927057-31927072
17	ZC3H11A	chr6:31926441-31927385	K562	blood:	n/a	n/a
18	NR2F2	chr6:31926331-31927666	K562	blood:	n/a	chr6:31927054-31927069 chr6:31927036-31927051 chr6:31927057-31927072
19	HNF4A	chr6:31926545-31927360	HepG2	liver:	n/a	chr6:31927036-31927050 chr6:31927048-31927066 chr6:31927036-31927050 chr6:31927037-31927049 chr6:31927035-31927050 chr6:31927037-31927049 chr6:31927037-31927050 chr6:31927036-31927049 chr6:31927039-31927055 chr6:31927043-31927050 chr6:31927051-31927064 chr6:31927035-31927050 chr6:31927035-31927050 chr6:31927032-31927054 chr6:31927043-31927057 chr6:31927037-31927049 chr6:31927035-31927050 chr6:31927037-31927050 chr6:31927034-31927052 chr6:31927051-31927063 chr6:31927037-31927049 chr6:31927036-31927048 chr6:31927035-31927050 chr6:31927035-31927050 chr6:31927054-31927066 chr6:31927050-31927064 chr6:31927036-31927050 chr6:31927037-31927050
20	MXI1	chr6:31926047-31927579	SK-N-SH	brain:	n/a	n/a
21	MBD4	chr6:31926296-31927438	HepG2	liver:	n/a	n/a
22	HDAC2	chr6:31926362-31927405	MCF-7	breast:	n/a	n/a
23	GABPA	chr6:31926391-31927453	A549	lung:	n/a	n/a
24	HNF4G	chr6:31926669-31927479	HepG2	liver:	n/a	chr6:31927036-31927050 chr6:31927048-31927066 chr6:31927036-31927050 chr6:31927037-31927049 chr6:31927035-31927050 chr6:31927037-31927049 chr6:31927037-31927050 chr6:31927036-31927049 chr6:31927039-31927055 chr6:31927043-31927050 chr6:31927051-31927064 chr6:31927035-31927050 chr6:31927035-31927050 chr6:31927032-31927054 chr6:31927043-31927057 chr6:31927037-31927049 chr6:31927035-31927050 chr6:31927037-31927050 chr6:31927034-31927052 chr6:31927051-31927063 chr6:31927037-31927049 chr6:31927036-31927048 chr6:31927035-31927050 chr6:31927054-31927066 chr6:31927050-31927064 chr6:31927036-31927050 chr6:31927037-31927050
25	NR2F2	chr6:31926450-31927533	MCF-7	breast:	n/a	chr6:31927054-31927069 chr6:31927036-31927051 chr6:31927057-31927072
26	HEY1	chr6:31926893-31927344	K562	blood:	n/a	n/a
27	GABPA	chr6:31926139-31927411	K562	blood:	n/a	n/a
28	CHD2	chr6:31926554-31927446	K562	blood:	n/a	n/a
29	REST	chr6:31926118-31927391	H1-neurons	neurons:	n/a	chr6:31926851-31926864
30	POLR2A	chr6:31926404-31927412	GM12878	blood:	n/a	n/a
31	NR2C2	chr6:31926659-31927515	Hela-S3	cervix:	n/a	chr6:31927036-31927051 chr6:31927037-31927050 chr6:31927057-31927072 chr6:31927051-31927064
32	SMC3	chr6:31926527-31927357	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr6:31925933-31927989	HepG2	liver:	n/a	n/a
34	SP1	chr6:31926259-31927447	HCT-116	colon:	n/a	chr6:31926996-31927005 chr6:31926995-31927007 chr6:31926897-31926908 chr6:31926992-31927006
35	RAD21	chr6:31926515-31927447	HepG2	liver:	n/a	n/a
36	HCFC1	chr6:31925525-31927640	Hela-S3	cervix:	n/a	n/a
37	RCOR1	chr6:31926518-31927348	K562	blood:	n/a	n/a
38	TAF1	chr6:31926344-31927372	ECC-1	luminal epithelium:	n/a	n/a
39	NFIC	chr6:31926478-31927379	HepG2	liver:	n/a	n/a
40	ATF3	chr6:31926263-31927384	K562	blood:	n/a	n/a
41	MAZ	chr6:31926085-31928360	IMR90	lung:	n/a	n/a
42	SRF	chr6:31926367-31927415	HCT-116	colon:	n/a	n/a
43	NR2C2	chr6:31926797-31927465	GM12878	blood:	n/a	chr6:31927036-31927051 chr6:31927037-31927050 chr6:31927057-31927072 chr6:31927051-31927064
44	MYBL2	chr6:31926125-31927632	HepG2	liver:	n/a	n/a
45	ELF1	chr6:31926230-31927520	MCF-7	breast:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
46	JUN	chr6:31925824-31927905	K562	blood:	n/a	n/a
47	POLR2A	chr6:31926309-31927410	PFSK-1	brain:	n/a	n/a
48	POLR2A	chr6:31926395-31927420	HepG2	liver:	n/a	n/a
49	GABPA	chr6:31926236-31927369	SK-N-SH	brain:	n/a	n/a
50	ELF1	chr6:31926195-31927567	HCT-116	colon:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876

No.	Distal block	Cell Line	Cell type
1	chr6:31631207..31634109-chr6:31926807..31929140,3	K562	blood:
2	chr6:31844767..31847605-chr6:31925658..31928567,2	MCF-7	breast:
3	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
4	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
5	chr6:31864040..31872511-chr6:31917614..31930102,27	MCF-7	breast:
6	chr6:31864712..31866806-chr6:31924793..31927734,3	K562	blood:
7	chr6:31894560..31897888-chr6:31924484..31928410,3	K562	blood:
8	chr6:31867075..31869848-chr6:31926953..31928795,2	K562	blood:
9	chr6:31829193..31831687-chr6:31925120..31927788,2	MCF-7	breast:
10	chr6:31799457..31804164-chr6:31924693..31928301,4	K562	blood:
11	chr6:31632061..31634821-chr6:31925160..31927798,3	MCF-7	breast:
12	chr6:31654964..31657960-chr6:31926410..31928172,2	K562	blood:
13	chr6:31867895..31873109-chr6:31925613..31930389,7	K562	blood:
14	chr6:31886651..31888947-chr6:31926731..31929141,2	MCF-7	breast:
15	chr6:31742931..31744824-chr6:31926408..31928564,2	K562	blood:

Variant related genes	Relation type
NELFE	TF binding region
SKIV2L	TF binding region
MIR1236	TF binding region
ENSG00000204435	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000244255	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204385	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 11 )

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

rs_ID	r²[population]
rs1048709	0.81[AMR][1000 genomes]
rs386480	0.98[EUR][1000 genomes]
rs389883	0.98[EUR][1000 genomes]
rs410851	0.98[EUR][1000 genomes]
rs419788	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs437179	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs537160	0.81[EUR][1000 genomes]
rs630379	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 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	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
9	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
10	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
11	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
12	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
13	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
14	nsv601961	chr6:31868322-32484368	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
15	nsv427751	chr6:31871512-32092843	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
16	nsv428141	chr6:31871512-32092843	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
17	esv2758043	chr6:31871512-32209113	Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	esv2759415	chr6:31871512-32209113	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
19	nsv830628	chr6:31887554-31947600	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
20	nsv933250	chr6:31905060-32008005	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
21	nsv934279	chr6:31905060-32013902	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv884512	chr6:31908470-31933161	Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
23	nsv884513	chr6:31922575-32066025	Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
24	nsv884514	chr6:31923052-31958960	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
25	nsv932869	chr6:31924496-32013902	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
26	nsv933913	chr6:31924682-32009282	Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
27	nsv284	chr6:31925739-31996721	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
28	nsv5247	chr6:31925739-32023216	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs440454	HLA-DRB1	cis	lymphoblastoid	seeQTL
rs440454	HMGA1	cis	cerebellum	SCAN
rs440454	HLA-DRB5	cis	lymphoblastoid	seeQTL
rs440454	SKIV2L	cis	lymphoblastoid	seeQTL
rs440454	HLA-C	cis	multi-tissue	Pritchard
rs440454	HLA-DRB5	cis	cerebellum	SCAN
rs440454	HLA-DRB5	cis	multi-tissue	Pritchard
rs440454	HLA-DRA	cis	multi-tissue	Pritchard
rs440454	HLA-DRB1	cis	multi-tissue	Pritchard
rs440454	ERG	trans	multi-tissue	Pritchard
rs440454	HLA-C	cis	lymphoblastoid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31925600-31927800	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr6:31925800-31927400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr6:31925800-31927400	Active TSS	Psoas Muscle	Psoas
4	chr6:31926000-31927400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:31926000-31927600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:31926000-31927600	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr6:31926000-31927800	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr6:31926000-31927800	Active TSS	A549	lung
9	chr6:31926200-31927400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:31926200-31927400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:31926200-31927400	Active TSS	Muscle Satellite Cultured Cells	--
12	chr6:31926200-31927400	Active TSS	Aorta	Aorta
13	chr6:31926200-31927400	Active TSS	Brain Hippocampus Middle	brain
14	chr6:31926200-31927400	Active TSS	Small Intestine	intestine
15	chr6:31926200-31927400	Bivalent/Poised TSS	HepG2	liver
16	chr6:31926200-31927400	Active TSS	HSMM	muscle
17	chr6:31926200-31927600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr6:31926200-31927600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:31926200-31927600	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr6:31926200-31927600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:31926200-31927600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr6:31926200-31927800	Active TSS	H1 Cell Line	embryonic stem cell
23	chr6:31926200-31927800	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr6:31926200-31927800	Active TSS	NHLF	lung
25	chr6:31926200-31928000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr6:31926400-31927400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr6:31926400-31927400	Active TSS	Gastric	stomach
28	chr6:31926600-31927400	Active TSS	Lung	lung
29	chr6:31926600-31927400	Active TSS	Sigmoid Colon	Sigmoid Colon
30	chr6:31927000-31927400	Flanking Active TSS	Primary B cells from peripheral blood	blood
31	chr6:31927000-31927400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:31927000-31927400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr6:31927000-31927400	Flanking Active TSS	Colonic Mucosa	Colon
34	chr6:31927000-31927400	Flanking Active TSS	Fetal Brain Male	brain
35	chr6:31927000-31927400	Flanking Active TSS	Placenta	Placenta
36	chr6:31927000-31927400	Flanking Active TSS	Fetal Stomach	stomach
37	chr6:31927000-31927600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
38	chr6:31927000-31927600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr6:31927000-31927600	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr6:31927000-31927600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
41	chr6:31927000-31927600	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr6:31927000-31927600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr6:31927000-31927600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
44	chr6:31927000-31927600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr6:31927000-31927600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr6:31927000-31927600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr6:31927000-31927600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr6:31927000-31927600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
49	chr6:31927000-31927600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr6:31927000-31927600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood

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