Variant report

Variant	rs34568880
Chromosome Location	chr6:31514448-31514449
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:31514204-31515545	A549	lung:	n/a	n/a
2	GABPA	chr6:31514250-31514745	H1-hESC	embryonic stem cell:	n/a	n/a
3	SIN3A	chr6:31514363-31515538	GM12878	blood:	n/a	n/a
4	FOSL1	chr6:31514315-31514744	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr6:31514304-31515734	H1-hESC	embryonic stem cell:	n/a	n/a
6	HDAC2	chr6:31514307-31514858	K562	blood:	n/a	n/a
7	GABPA	chr6:31514366-31514665	GM12878	blood:	n/a	n/a
8	CTCF	chr6:31514315-31514765	A549	lung:	n/a	n/a
9	MAX	chr6:31514244-31514724	H1-hESC	embryonic stem cell:	n/a	chr6:31514653-31514663
10	TCF12	chr6:31514200-31514687	H1-hESC	embryonic stem cell:	n/a	n/a
11	PAX5	chr6:31514345-31514693	GM12878	blood:	n/a	n/a
12	CTCF	chr6:31514416-31514746	T-47D	breast:	n/a	n/a
13	SIN3A	chr6:31513957-31515569	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr6:31514359-31514708	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr6:31514257-31514786	H1-hESC	embryonic stem cell:	n/a	n/a
16	EP300	chr6:31514338-31514683	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr6:31514446-31514676	GM20000	blood:	n/a	n/a
18	PBX3	chr6:31514246-31514807	SK-N-SH	brain:	n/a	n/a
19	POLR2A	chr6:31514171-31516364	HUVEC	blood vessel:	n/a	n/a
20	NR2F2	chr6:31514394-31514825	K562	blood:	n/a	n/a
21	CREB1	chr6:31514351-31514720	A549	lung:	n/a	n/a
22	HCFC1	chr6:31514267-31517032	Hela-S3	cervix:	n/a	n/a
23	FOS	chr6:31514414-31514730	MCF10A-Er-Src	breast:	n/a	n/a
24	MAX	chr6:31514259-31514778	NB4	blood:	n/a	chr6:31514653-31514663
25	ZEB1	chr6:31514292-31514637	GM12878	blood:	n/a	n/a
26	ATF2	chr6:31514162-31515523	H1-hESC	embryonic stem cell:	n/a	n/a
27	EBF1	chr6:31514351-31515500	GM12878	blood:	n/a	chr6:31515251-31515264 chr6:31515252-31515262 chr6:31515251-31515262 chr6:31515253-31515262
28	SMC3	chr6:31514395-31515446	K562	blood:	n/a	n/a
29	MAZ	chr6:31514332-31515574	HepG2	liver:	n/a	chr6:31514843-31514853 chr6:31514653-31514663
30	SP1	chr6:31514116-31515620	HCT-116	colon:	n/a	chr6:31514526-31514537 chr6:31515171-31515185 chr6:31514846-31514858 chr6:31514202-31514211 chr6:31514840-31514852 chr6:31514848-31514857 chr6:31514842-31514851 chr6:31515227-31515234 chr6:31514565-31514572 chr6:31514841-31514855 chr6:31514201-31514211 chr6:31514388-31514402 chr6:31515172-31515181 chr6:31515285-31515296 chr6:31515166-31515180 chr6:31514840-31514852
31	BCLAF1	chr6:31514205-31514932	GM12878	blood:	n/a	n/a
32	RUNX3	chr6:31514281-31515568	GM12878	blood:	n/a	n/a
33	MXI1	chr6:31514307-31514813	HepG2	liver:	n/a	n/a
34	POLR2A	chr6:31514153-31515692	H1-neurons	neurons:	n/a	n/a
35	RAD21	chr6:31514354-31514902	A549	lung:	n/a	n/a
36	USF2	chr6:31514400-31515338	H1-hESC	embryonic stem cell:	n/a	n/a
37	NR2F2	chr6:31514167-31516638	K562	blood:	n/a	n/a
38	CTCF	chr6:31514429-31514717	Fibrobl	skin:	n/a	n/a
39	RAD21	chr6:31514354-31514868	HepG2	liver:	n/a	n/a
40	GTF2F1	chr6:31514318-31514818	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr6:31514417-31514739	GM19239	blood:	n/a	n/a
42	CTCF	chr6:31514419-31514676	ECC-1	luminal epithelium:	n/a	n/a
43	REST	chr6:31514211-31514699	SK-N-SH	brain:	n/a	chr6:31514391-31514404
44	CTCF	chr6:31514335-31514755	K562	blood:	n/a	n/a
45	RAD21	chr6:31514302-31514742	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:31514408-31514717	ECC-1	luminal epithelium:	n/a	n/a
47	NFIC	chr6:31514372-31514908	HepG2	liver:	n/a	n/a
48	CREB1	chr6:31514189-31515729	GM12878	blood:	n/a	n/a
49	CTCF	chr6:31514426-31514722	A549	lung:	n/a	n/a
50	POLR2A	chr6:31514218-31514781	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31514402-31514452	NHBE	bronchial:	n/a
2	chr6:31514402-31514452	A549	lung:	n/a
3	chr6:31514402-31514452	HEK293	kidney:	embryo
4	chr6:31514402-31514452	HCF	heart:	n/a
5	chr6:31514402-31514452	MCF-7	breast:	n/a
6	chr6:31514402-31514452	Caco-2	colon:	n/a
7	chr6:31514402-31514452	HUVEC	blood vessel:	n/a
8	chr6:31514402-31514452	Hela-S3	cervix:	n/a
9	chr6:31514402-31514452	SKMC	muscle:	n/a
10	chr6:31514402-31514452	AG10803	skin:	n/a
11	chr6:31514402-31514452	HRCEpiC	kidney:	n/a
12	chr6:31514402-31514452	SK-N-SH	brain:	n/a
13	chr6:31514402-31514452	GM12878	blood:	n/a
14	chr6:31514402-31514452	T-47D	breast:	n/a
15	chr6:31514402-31514452	K562	blood:	n/a
16	chr6:31514402-31514452	HEEpiC	esophagus:	n/a
17	chr6:31514402-31514452	BE2_C	brain:	n/a
18	chr6:31514402-31514452	HNPCEpiC	eye:	n/a
19	chr6:31514402-31514452	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:31514402-31514452	NH-A	brain:	n/a
21	chr6:31514402-31514452	Jurkat	blood:	n/a
22	chr6:31514402-31514452	AG09319	gingival:	n/a
23	chr6:31514402-31514452	HRPEpiC	eye:	n/a
24	chr6:31514402-31514452	HepG2	liver:	n/a
25	chr6:31514402-31514452	LNCaP	prostate:	n/a
26	chr6:31514402-31514452	HIPEpiC	eye:	n/a
27	chr6:31514402-31514452	RPTEC	kidney:	n/a
28	chr6:31514402-31514452	HL-60	blood:	n/a
29	chr6:31514402-31514452	ProgFib	skin:	n/a
30	chr6:31514402-31514452	Hepatocyte	liver:	n/a
31	chr6:31514402-31514452	NB4	blood:	n/a
32	chr6:31514402-31514452	HCPEpiC	choroid plexus:	n/a
33	chr6:31514402-31514452	BJ	skin:	n/a
34	chr6:31514402-31514452	GM12892	blood:	n/a
35	chr6:31514402-31514452	H1-hESC	embryonic stem cell:	embryo
36	chr6:31514402-31514452	GM12891	blood:	n/a
37	chr6:31514402-31514452	SAEC	small airway:	n/a
38	chr6:31514402-31514452	HCT-116	colon:	n/a
39	chr6:31514402-31514452	GM06990	blood:	n/a
40	chr6:31514402-31514452	HRE	kidney:	n/a
41	chr6:31514402-31514452	NHDF-neo	bronchial:	n/a
42	chr6:31514402-31514452	AG04449	skin:	fetal
43	chr6:31514402-31514452	HCM	heart:	n/a
44	chr6:31514402-31514452	AG09309	skin:	n/a
45	chr6:31514402-31514452	SK-N-SH_RA	brain:	n/a
46	chr6:31514402-31514452	AoSMC	blood vessel:	n/a
47	chr6:31514402-31514452	PFSK-1	brain:	n/a
48	chr6:31514402-31514452	GM19239	blood:	n/a
49	chr6:31514402-31514452	IMR90	lung:	fetal
50	chr6:31514402-31514452	PANC-1	pancreas:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31512487..31517874-chr6:31628889..31634381,12	K562	blood:
2	chr6:31464396..31467286-chr6:31513352..31515783,2	MCF-7	breast:
3	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
4	chr6:31461866..31464235-chr6:31513189..31515982,2	K562	blood:
5	chr6:31507451..31516055-chr6:31617949..31624791,11	MCF-7	breast:
6	chr6:31511781..31517209-chr6:31545410..31553496,14	K562	blood:
7	chr6:31513227..31514963-chr6:31602419..31605642,3	K562	blood:
8	chr6:31513206..31515445-chr6:31647940..31649568,2	MCF-7	breast:
9	chr6:31513047..31514729-chr6:31802148..31804053,2	MCF-7	breast:
10	chr6:31513724..31516419-chr6:31731123..31734011,2	K562	blood:
11	chr6:31462227..31464927-chr6:31513555..31516059,3	MCF-7	breast:
12	chr6:31465192..31467276-chr6:31514353..31517870,3	K562	blood:
13	chr6:31460255..31464524-chr6:31513189..31516444,5	K562	blood:
14	chr6:31512960..31516876-chr6:31549415..31551752,3	MCF-7	breast:
15	chr6:31512174..31516924-chr6:31632110..31634699,4	MCF-7	breast:
16	chr6:31512553..31516955-chr6:31618753..31622292,7	K562	blood:
17	chr6:31511829..31516829-chr6:31586761..31590434,8	MCF-7	breast:
18	chr6:31513113..31516557-chr6:31559255..31561759,3	K562	blood:
19	chr6:31513116..31516827-chr6:31558104..31561639,4	K562	blood:
20	chr6:31513053..31519210-chr6:31585987..31595406,29	K562	blood:
21	chr6:31513771..31519008-chr6:31582734..31585702,4	K562	blood:
22	chr6:31465192..31467253-chr6:31513874..31515853,2	K562	blood:
23	chr6:31514420..31518271-chr6:31830053..31832008,3	K562	blood:
24	chr6:31513726..31516111-chr6:31705969..31708009,2	MCF-7	breast:
25	chr6:31507406..31516955-chr6:31615847..31623354,26	K562	blood:
26	chr6:31513237..31516038-chr6:31696007..31697508,2	K562	blood:
27	chr6:31513245..31516542-chr6:31782394..31785632,3	MCF-7	breast:
28	chr6:31514014..31516004-chr6:31637492..31640233,2	MCF-7	breast:
29	chr6:31512646..31517552-chr6:31586243..31590655,20	K562	blood:
30	chr6:31513697..31516891-chr6:31590663..31594798,6	K562	blood:
31	chr6:31513816..31516540-chr6:31705988..31708603,3	K562	blood:
32	chr6:31513842..31516738-chr6:31801353..31804200,3	K562	blood:
33	chr6:31514283..31516079-chr6:31548550..31550492,2	MCF-7	breast:
34	chr6:31512487..31516692-chr6:31630820..31634965,11	K562	blood:
35	chr6:31514041..31516822-chr6:31607895..31609599,2	K562	blood:
36	chr6:31513234..31515924-chr6:31582326..31585070,2	K562	blood:

No data

Variant related genes	Relation type
DDX39B	TF binding region
ATP6V1G2	TF binding region
ATP6V1G2-DDX39B	TF binding region
NFKBIL1	TF binding region
DDX39B	CpG island
ATP6V1G2-DDX39B	CpG island
ATP6V1G2	CpG island
NFKBIL1	CpG island
ENSG00000235663	Chromatin interaction
ENSG00000204475	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000240053	Chromatin interaction
ENSG00000201680	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000228727	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204516	Chromatin interaction
ENSG00000204472	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000227507	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204389	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11552113	0.83[ASN][1000 genomes]
rs13194402	0.83[ASN][1000 genomes]
rs13197153	0.86[ASN][1000 genomes]
rs13204983	0.83[ASN][1000 genomes]
rs13211189	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13211368	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13217049	0.86[ASN][1000 genomes]
rs17200810	1.00[ASN][1000 genomes]
rs3093672	1.00[ASN][1000 genomes]
rs34038095	0.83[ASN][1000 genomes]
rs34346286	0.86[ASN][1000 genomes]
rs34422607	0.83[ASN][1000 genomes]
rs34451538	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35012663	0.83[ASN][1000 genomes]
rs35309880	0.86[ASN][1000 genomes]
rs35340190	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35700586	0.83[ASN][1000 genomes]
rs35963002	1.00[ASN][1000 genomes]
rs35969216	1.00[ASN][1000 genomes]
rs41267058	0.83[ASN][1000 genomes]
rs41273252	1.00[ASN][1000 genomes]
rs4647191	1.00[ASN][1000 genomes]
rs71563338	0.86[ASN][1000 genomes]
rs71563350	0.86[ASN][1000 genomes]
rs71563354	0.83[ASN][1000 genomes]
rs71563359	0.83[ASN][1000 genomes]
rs71563361	0.83[ASN][1000 genomes]
rs71563362	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
2	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
3	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	nsv1018463	chr6:31337336-31525275	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
13	nsv538189	chr6:31337336-31525275	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
14	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
15	esv2757162	chr6:31353329-31542308	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
16	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
17	nsv432877	chr6:31412961-31528690	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
18	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
19	nsv470809	chr6:31496915-31544189	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31510600-31514600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:31510600-31514600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr6:31510600-31515800	Weak transcription	Gastric	stomach
4	chr6:31510800-31514600	Weak transcription	Small Intestine	intestine
5	chr6:31510800-31515400	Weak transcription	Lung	lung
6	chr6:31511000-31514600	Weak transcription	Right Ventricle	heart
7	chr6:31511200-31514600	Weak transcription	Pancreas	Pancrea
8	chr6:31511600-31514600	Weak transcription	Psoas Muscle	Psoas
9	chr6:31513200-31514800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:31513200-31515800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:31513400-31514600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:31513400-31515000	Flanking Active TSS	Brain Germinal Matrix	brain
13	chr6:31513400-31515800	Active TSS	Brain Angular Gyrus	brain
14	chr6:31513600-31514600	Flanking Active TSS	Brain Anterior Caudate	brain
15	chr6:31513600-31514600	Flanking Active TSS	Brain Substantia Nigra	brain
16	chr6:31513600-31515800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:31513600-31515800	Active TSS	NHDF-Ad	bronchial
18	chr6:31513600-31516000	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr6:31513600-31516000	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr6:31513600-31516200	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr6:31513800-31514600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:31513800-31514600	Flanking Active TSS	Brain Cingulate Gyrus	brain
23	chr6:31513800-31514600	Flanking Active TSS	Fetal Muscle Trunk	muscle
24	chr6:31513800-31514600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr6:31513800-31514600	Enhancers	NHEK	skin
26	chr6:31513800-31514800	Flanking Active TSS	Fetal Muscle Leg	muscle
27	chr6:31513800-31514800	Flanking Active TSS	Fetal Stomach	stomach
28	chr6:31513800-31515000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:31513800-31515000	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr6:31513800-31515200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:31513800-31515200	Flanking Active TSS	Dnd41	blood
32	chr6:31513800-31515600	Active TSS	H9 Cell Line	embryonic stem cell
33	chr6:31514000-31514600	Enhancers	Primary T cells from cord blood	blood
34	chr6:31514000-31514600	Enhancers	Primary T cells fromperipheralblood	blood
35	chr6:31514000-31514600	Enhancers	Primary hematopoietic stem cells	blood
36	chr6:31514000-31514600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:31514000-31514600	Enhancers	Liver	Liver
38	chr6:31514000-31515000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr6:31514000-31515200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:31514000-31515200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr6:31514000-31515600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr6:31514000-31515800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:31514000-31515800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:31514000-31515800	Active TSS	Fetal Intestine Small	intestine
45	chr6:31514000-31515800	Active TSS	Fetal Lung	lung
46	chr6:31514000-31515800	Active TSS	HSMMtube	muscle
47	chr6:31514000-31516000	Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr6:31514000-31516000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr6:31514000-31516000	Flanking Active TSS	Fetal Thymus	thymus
50	chr6:31514000-31516400	Active TSS	Fetal Kidney	kidney

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