Variant report

Variant	rs13204572
Chromosome Location	chr6:26189356-26189357
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:634)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RXRA	chr6:26189238-26189465	GM12878	blood:	n/a	n/a
2	REST	chr6:26189168-26189477	H1-hESC	embryonic stem cell:	n/a	n/a
3	ZC3H11A	chr6:26188729-26189535	K562	blood:	n/a	n/a
4	TEAD4	chr6:26188981-26189679	SK-N-SH	brain:	n/a	n/a
5	ZBTB33	chr6:26188867-26189532	HepG2	liver:	n/a	n/a
6	MAFK	chr6:26188727-26189552	K562	blood:	n/a	n/a
7	POLR2A	chr6:26188197-26189518	HCT-116	colon:	n/a	n/a
8	CEBPD	chr6:26188043-26189749	K562	blood:	n/a	n/a
9	SIN3AK20	chr6:26188361-26189692	K562	blood:	n/a	n/a
10	SIN3AK20	chr6:26189044-26189517	H1-hESC	embryonic stem cell:	n/a	n/a
11	RCOR1	chr6:26188725-26189520	HepG2	liver:	n/a	n/a
12	FOSL2	chr6:26189115-26189464	A549	lung:	n/a	n/a
13	ELF1	chr6:26188677-26189471	HepG2	liver:	n/a	n/a
14	POLR2A	chr6:26188390-26189498	GM19193	blood:	n/a	n/a
15	POLR2A	chr6:26186579-26189799	H1-hESC	embryonic stem cell:	n/a	n/a
16	ZBTB33	chr6:26188018-26189693	SK-N-SH	brain:	n/a	n/a
17	CTCF	chr6:26189220-26189370	GM12873	blood:	n/a	n/a
18	SIN3A	chr6:26188737-26189590	GM12878	blood:	n/a	n/a
19	POLR2A	chr6:26188387-26189498	GM12892	blood:	n/a	n/a
20	POLR2A	chr6:26187922-26189658	PANC-1	pancreas:	n/a	n/a
21	ELF1	chr6:26188681-26189510	A549	lung:	n/a	n/a
22	MYC	chr6:26188389-26189562	K562	blood:	n/a	chr6:26188885-26188892 chr6:26188884-26188893
23	MAX	chr6:26189182-26189537	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:26189220-26189370	GM12870	blood:	n/a	n/a
25	MYBL2	chr6:26188167-26189684	HepG2	liver:	n/a	n/a
26	NFE2	chr6:26189131-26189467	GM12878	blood:	n/a	n/a
27	EP300	chr6:26189191-26189536	GM12878	blood:	n/a	n/a
28	MAX	chr6:26188507-26189536	K562	blood:	n/a	chr6:26188885-26188892 chr6:26188884-26188893
29	STAT3	chr6:26189041-26189566	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr6:26188194-26189635	ProgFib	skin:	n/a	n/a
31	PML	chr6:26188071-26189691	GM12878	blood:	n/a	n/a
32	POLR2A	chr6:26188120-26190099	K562	blood:	n/a	n/a
33	CREB1	chr6:26188406-26189685	GM12878	blood:	n/a	n/a
34	YY1	chr6:26188090-26189520	GM12891	blood:	n/a	chr6:26188283-26188291 chr6:26188482-26188491 chr6:26188334-26188344
35	SIN3AK20	chr6:26188281-26189614	SK-N-SH	brain:	n/a	n/a
36	ATF2	chr6:26188538-26189598	GM12878	blood:	n/a	n/a
37	YY1	chr6:26188921-26189502	HCT-116	colon:	n/a	n/a
38	POLR2A	chr6:26187684-26208312	K562	blood:	n/a	n/a
39	POLR2A	chr6:26188147-26189609	GM12878	blood:	n/a	n/a
40	POLR2A	chr6:26188308-26189521	Raji	blood:	n/a	n/a
41	TRIM28	chr6:26188088-26189734	K562	blood:	n/a	n/a
42	CEBPB	chr6:26188134-26189685	HCT-116	colon:	n/a	n/a
43	YY1	chr6:26189223-26189372	K562	blood:	n/a	n/a
44	REST	chr6:26189173-26189477	GM12878	blood:	n/a	n/a
45	MAX	chr6:26188493-26189499	K562	blood:	n/a	chr6:26188885-26188892 chr6:26188884-26188893
46	REST	chr6:26189028-26189513	PANC-1	pancreas:	n/a	n/a
47	JUND	chr6:26188956-26189695	SK-N-SH	brain:	n/a	n/a
48	UBTF	chr6:26188571-26189463	K562	blood:	n/a	n/a
49	POLR2A	chr6:26188477-26189578	K562	blood:	n/a	n/a
50	IRF1	chr6:26188652-26189561	K562	blood:	n/a	chr6:26189404-26189418

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26189355-26189405	HEEpiC	esophagus:	n/a
2	chr6:26189340-26189390	PFSK-1	brain:	n/a
3	chr6:26189333-26189383	NHDF-neo	bronchial:	n/a
4	chr6:26189340-26189390	SAEC	small airway:	n/a
5	chr6:26189340-26189390	AG04449	skin:	fetal
6	chr6:26189333-26189383	HRE	kidney:	n/a
7	chr6:26189355-26189405	GM12891	blood:	n/a
8	chr6:26189333-26189383	SK-N-SH_RA	brain:	n/a
9	chr6:26189340-26189390	AoSMC	blood vessel:	n/a
10	chr6:26189333-26189383	HCM	heart:	n/a
11	chr6:26189355-26189405	AG09319	gingival:	n/a
12	chr6:26189340-26189390	Caco-2	colon:	n/a
13	chr6:26189355-26189405	PrEC	prostate:	n/a
14	chr6:26189340-26189390	HEK293	kidney:	embryo
15	chr6:26189340-26189390	PANC-1	pancreas:	n/a
16	chr6:26189355-26189405	HCF	heart:	n/a
17	chr6:26189333-26189383	HCF	heart:	n/a
18	chr6:26189355-26189405	AG04450	lung:	fetal
19	chr6:26189340-26189390	U87	brain:	n/a
20	chr6:26189333-26189383	SK-N-SH	brain:	n/a
21	chr6:26189333-26189383	HMEC	breast:	n/a
22	chr6:26189340-26189390	AG09309	skin:	n/a
23	chr6:26189333-26189383	IMR90	lung:	fetal
24	chr6:26189340-26189390	AG10803	skin:	n/a
25	chr6:26189340-26189390	GM12892	blood:	n/a
26	chr6:26189340-26189390	HRCEpiC	kidney:	n/a
27	chr6:26189355-26189405	HUVEC	blood vessel:	n/a
28	chr6:26189340-26189390	BJ	skin:	n/a
29	chr6:26189355-26189405	SKMC	muscle:	n/a
30	chr6:26189340-26189390	GM06990	blood:	n/a
31	chr6:26189333-26189383	K562	blood:	n/a
32	chr6:26189355-26189405	GM06990	blood:	n/a
33	chr6:26189340-26189390	NH-A	brain:	n/a
34	chr6:26189333-26189383	ECC-1	luminal epithelium:	n/a
35	chr6:26189333-26189383	HepG2	liver:	n/a
36	chr6:26189355-26189405	HEK293	kidney:	embryo
37	chr6:26189355-26189405	Jurkat	blood:	n/a
38	chr6:26189355-26189405	ovcar-3	ovarian:	n/a
39	chr6:26189340-26189390	GM12878	blood:	n/a
40	chr6:26189355-26189405	CMK	blood:	n/a
41	chr6:26189340-26189390	A549	lung:	n/a
42	chr6:26189355-26189405	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:26189340-26189390	GM19239	blood:	n/a
44	chr6:26189340-26189390	Hela-S3	cervix:	n/a
45	chr6:26189340-26189390	HUVEC	blood vessel:	n/a
46	chr6:26189333-26189383	HRPEpiC	eye:	n/a
47	chr6:26189340-26189390	AG09319	gingival:	n/a
48	chr6:26189355-26189405	LNCaP	prostate:	n/a
49	chr6:26189340-26189390	NT2-D1	testis:	n/a
50	chr6:26189355-26189405	A549	lung:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26187375..26189880-chr6:27097420..27103446,8	K562	blood:
2	chr6:26026488..26028214-chr6:26187877..26190582,2	MCF-7	breast:
3	chr6:26187666..26189518-chr6:27113172..27116022,2	K562	blood:
4	chr6:26188276..26190980-chr6:26381179..26383865,2	K562	blood:
5	chr12:14923443..14923997-chr6:26189034..26189552,2	Hela-S3	cervix:
6	chr6:26187831..26190328-chr6:26520761..26523308,3	K562	blood:
7	chr20:45985042..45987861-chr6:26187518..26190404,2	MCF-7	breast:
8	chr6:26186794..26189358-chr6:31620269..31622161,2	K562	blood:
9	chr20:45946934..45948721-chr6:26187460..26189377,3	MCF-7	breast:
10	chr5:180659417..180661225-chr6:26188646..26190614,2	K562	blood:
11	chr6:26188869..26191553-chr6:26538652..26541093,2	K562	blood:
12	chr6:26158179..26158704-chr6:26188866..26189377,2	HCT-116	colon:
13	chr6:26187875..26189403-chr6:27797113..27800006,2	MCF-7	breast:
14	chr6:26187687..26190163-chr6:27098059..27101507,5	K562	blood:
15	chr6:26187662..26190884-chr6:27112568..27116666,4	MCF-7	breast:
16	chr12:122150220..122151057-chr6:26188979..26189750,2	NB4	blood:
17	chr6:26054932..26056773-chr6:26188728..26190968,2	MCF-7	breast:
18	chr1:25573445..25574165-chr6:26188934..26189726,2	NB4	blood:
19	chr6:26187257..26192079-chr6:27098954..27103250,7	MCF-7	breast:
20	chr6:26187432..26189405-chr7:158620973..158622710,2	MCF-7	breast:
21	chr6:26032288..26035408-chr6:26183846..26189517,7	MCF-7	breast:
22	chr6:26187760..26190799-chr6:26518890..26523308,5	K562	blood:
23	chr6:26187507..26190261-chr6:27099153..27102365,6	MCF-7	breast:
24	chr17:7387332..7388065-chr6:26189234..26189746,2	NB4	blood:

No data

Variant related genes	Relation type
HIST1H4D	TF binding region
HIST1H4D	CpG island
ENSG00000117616	Chromatin interaction
ENSG00000182952	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000197914	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000117868	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000188735	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000146063	Chromatin interaction
ENSG00000197837	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000174282	Chromatin interaction
ENSG00000181222	Chromatin interaction
ENSG00000124508	Chromatin interaction
ENSG00000267882	Chromatin interaction
ENSG00000158373	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 14 )

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

rs_ID	r²[population]
rs10484439	0.85[EUR][1000 genomes]
rs13220522	0.81[EUR][1000 genomes]
rs17598658	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34107459	0.81[EUR][1000 genomes]
rs34158769	0.81[EUR][1000 genomes]
rs34961555	0.98[EUR][1000 genomes]
rs35162296	0.81[EUR][1000 genomes]
rs55706012	0.87[EUR][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	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
8	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
9	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
10	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
11	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
12	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
13	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
14	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
15	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
16	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
17	nsv518431	chr6:26148311-26211368	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
18	nsv526456	chr6:26148311-26211368	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
19	nsv883490	chr6:26172219-26231608	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	316 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs13204572	BTN3A2	cis	Thyroid	GTEx
rs13204572	BTN3A2	cis	Skin Sun Exposed Lower leg	GTEx
rs13204572	BTN3A2	cis	Artery Aorta	GTEx
rs13204572	BTN3A2///BTN3A3	Cis_1M	lymphoblastoid	RTeQTL
rs13204572	BTN3A2	cis	Muscle Skeletal	GTEx
rs13204572	BTN3A2	cis	Adipose Subcutaneous	GTEx
rs13204572	BTN3A2	cis	Esophagus Muscularis	GTEx
rs13204572	BTN3A2	cis	Artery Tibial	GTEx
rs13204572	BTN3A1	Cis_1M	lymphoblastoid	RTeQTL
rs13204572	BTN3A2	cis	Nerve Tibial	GTEx
rs13204572	BTN3A2	cis	Heart Left Ventricle	GTEx
rs13204572	BTN3A2	cis	Esophagus Mucosa	GTEx
rs13204572	BTN3A2	Cis_1M	lymphoblastoid	RTeQTL
rs13204572	BTN3A2	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26182000-26193000	Weak transcription	Dnd41	blood
2	chr6:26187400-26189400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:26187800-26189600	Flanking Active TSS	Fetal Thymus	thymus
4	chr6:26188000-26189400	Active TSS	H9 Cell Line	embryonic stem cell
5	chr6:26188000-26189400	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr6:26188000-26189400	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr6:26188000-26189400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:26188000-26189400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:26188000-26189600	Active TSS	H1 Cell Line	embryonic stem cell
10	chr6:26188000-26189600	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr6:26188000-26189600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:26188000-26189600	Active TSS	A549	lung
13	chr6:26188000-26189800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr6:26188000-26189800	Active TSS	Fetal Brain Female	brain
15	chr6:26188000-26189800	Active TSS	Fetal Kidney	kidney
16	chr6:26188200-26189400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:26188200-26189400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:26188200-26189400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:26188200-26189400	Active TSS	Colonic Mucosa	Colon
20	chr6:26188200-26189600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr6:26188200-26189600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:26188200-26189600	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr6:26188200-26189600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr6:26188200-26189600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:26188200-26189600	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr6:26188200-26189600	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr6:26188200-26189600	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr6:26188200-26189600	Active TSS	Fetal Lung	lung
29	chr6:26188200-26189600	Flanking Active TSS	NHEK	skin
30	chr6:26188200-26189600	Active TSS	Osteobl	bone
31	chr6:26188200-26189800	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr6:26188200-26189800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr6:26188200-26190000	Active TSS	Rectal Smooth Muscle	rectum
34	chr6:26188400-26189400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:26188400-26189400	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr6:26188400-26189400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:26188400-26189400	Flanking Active TSS	Primary B cells from peripheral blood	blood
38	chr6:26188400-26189400	Flanking Active TSS	Liver	Liver
39	chr6:26188400-26189400	Active TSS	Brain Angular Gyrus	brain
40	chr6:26188400-26189400	Active TSS	Brain Substantia Nigra	brain
41	chr6:26188400-26189400	Active TSS	Esophagus	oesophagus
42	chr6:26188400-26189400	Active TSS	NHDF-Ad	bronchial
43	chr6:26188400-26189600	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr6:26188400-26189600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr6:26188400-26189600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr6:26188400-26189600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr6:26188400-26189600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr6:26188400-26189600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:26188400-26189600	Flanking Active TSS	Fetal Muscle Leg	muscle
50	chr6:26188400-26189600	Active TSS	Fetal Stomach	stomach

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