Variant report

Variant	rs7816636
Chromosome Location	chr8:11205654-11205655
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F6	chr8:11205369-11205820	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr8:11204292-11205726	K562	blood:	n/a	n/a
3	MAX	chr8:11204451-11205720	A549	lung:	n/a	n/a
4	MXI1	chr8:11204116-11206215	SK-N-SH	brain:	n/a	chr8:11205597-11205606
5	POLR2A	chr8:11204505-11205734	MCF-7	breast:	n/a	n/a
6	HEY1	chr8:11205464-11205721	K562	blood:	n/a	n/a
7	ZBTB7A	chr8:11204901-11205859	ECC-1	luminal epithelium:	n/a	chr8:11205220-11205231
8	MYC	chr8:11205456-11205722	MCF-7	breast:	n/a	n/a
9	MXI1	chr8:11205382-11205866	IMR90	lung:	n/a	chr8:11205597-11205606
10	MAX	chr8:11205353-11205807	ECC-1	luminal epithelium:	n/a	n/a
11	MAX	chr8:11204414-11205871	A549	lung:	n/a	n/a
12	HDAC2	chr8:11205277-11205781	MCF-7	breast:	n/a	n/a
13	MYC	chr8:11204238-11205657	K562	blood:	n/a	n/a
14	MAX	chr8:11205488-11205770	K562	blood:	n/a	n/a
15	NRF1	chr8:11204810-11205787	SK-N-SH	brain:	n/a	n/a
16	ZBTB7A	chr8:11204410-11205819	ECC-1	luminal epithelium:	n/a	chr8:11204559-11204568 chr8:11205220-11205231
17	MAX	chr8:11204465-11205779	K562	blood:	n/a	n/a
18	POLR2A	chr8:11204468-11205705	MCF-7	breast:	n/a	n/a
19	ZBTB7A	chr8:11204209-11205803	K562	blood:	n/a	chr8:11204559-11204568 chr8:11205220-11205231
20	POLR2A	chr8:11204492-11205763	MCF-7	breast:	n/a	n/a
21	POLR2A	chr8:11203581-11205779	K562	blood:	n/a	n/a
22	UBTF	chr8:11204439-11205905	K562	blood:	n/a	n/a
23	MYC	chr8:11205362-11205743	MCF-7	breast:	n/a	n/a
24	MAX	chr8:11205354-11205808	H1-hESC	embryonic stem cell:	n/a	n/a
25	YY1	chr8:11205319-11205739	ECC-1	luminal epithelium:	n/a	n/a
26	E2F6	chr8:11204753-11205692	K562	blood:	n/a	chr8:11204973-11204983 chr8:11205135-11205142
27	ZNF384	chr8:11205652-11206030	K562	blood:	n/a	n/a
28	YY1	chr8:11205382-11205677	K562	blood:	n/a	n/a
29	E2F6	chr8:11204624-11205834	H1-hESC	embryonic stem cell:	n/a	chr8:11204973-11204983 chr8:11205135-11205142
30	HA-E2F1	chr8:11204294-11205852	MCF-7	breast:	n/a	chr8:11204560-11204569 chr8:11204973-11204983 chr8:11205135-11205142
31	E2F6	chr8:11204494-11205745	K562	blood:	n/a	chr8:11204560-11204569 chr8:11204973-11204983 chr8:11205135-11205142
32	MAX	chr8:11205290-11205810	MCF-7	breast:	n/a	n/a
33	BACH1	chr8:11204201-11206211	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAX	chr8:11205099-11205792	ECC-1	luminal epithelium:	n/a	n/a
35	SIN3A	chr8:11204264-11205807	H1-hESC	embryonic stem cell:	n/a	chr8:11204883-11204894
36	MYC	chr8:11204404-11205759	K562	blood:	n/a	n/a
37	YY1	chr8:11205372-11205664	ECC-1	luminal epithelium:	n/a	n/a
38	BHLHE40	chr8:11205469-11205676	K562	blood:	n/a	n/a
39	MAX	chr8:11204332-11205837	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11205619-11205669	AoSMC	blood vessel:	n/a
2	chr8:11205619-11205669	HL-60	blood:	n/a
3	chr8:11205619-11205669	MCF-7	breast:	n/a
4	chr8:11205619-11205669	AG10803	skin:	n/a
5	chr8:11205619-11205669	HepG2	liver:	n/a
6	chr8:11205619-11205669	Hepatocyte	liver:	n/a
7	chr8:11205619-11205669	PFSK-1	brain:	n/a
8	chr8:11205619-11205669	HCPEpiC	choroid plexus:	n/a
9	chr8:11205619-11205669	HCF	heart:	n/a
10	chr8:11205619-11205669	HRCEpiC	kidney:	n/a
11	chr8:11205619-11205669	Jurkat	blood:	n/a
12	chr8:11205619-11205669	HEK293	kidney:	embryo
13	chr8:11205619-11205669	HAEpiC	amniotic membrane:	n/a
14	chr8:11205619-11205669	Hela-S3	cervix:	n/a
15	chr8:11205619-11205669	HUVEC	blood vessel:	n/a
16	chr8:11205619-11205669	MCF10A-Er-Src	breast:	n/a
17	chr8:11205619-11205669	HEEpiC	esophagus:	n/a
18	chr8:11205619-11205669	HMEC	breast:	n/a
19	chr8:11205619-11205669	SK-N-SH	brain:	n/a
20	chr8:11205619-11205669	NT2-D1	testis:	n/a
21	chr8:11205619-11205669	PANC-1	pancreas:	n/a
22	chr8:11205619-11205669	K562	blood:	n/a
23	chr8:11205619-11205669	HIPEpiC	eye:	n/a
24	chr8:11205619-11205669	NB4	blood:	n/a
25	chr8:11205619-11205669	HCT-116	colon:	n/a
26	chr8:11205619-11205669	Caco-2	colon:	n/a
27	chr8:11205619-11205669	HNPCEpiC	eye:	n/a
28	chr8:11205619-11205669	GM06990	blood:	n/a
29	chr8:11205619-11205669	H1-hESC	embryonic stem cell:	embryo
30	chr8:11205619-11205669	T-47D	breast:	n/a
31	chr8:11205619-11205669	IMR90	lung:	fetal
32	chr8:11205619-11205669	PrEC	prostate:	n/a
33	chr8:11205619-11205669	NHDF-neo	bronchial:	n/a
34	chr8:11205619-11205669	ECC-1	luminal epithelium:	n/a
35	chr8:11205619-11205669	RPTEC	kidney:	n/a
36	chr8:11205619-11205669	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:11205619-11205669	U87	brain:	n/a
38	chr8:11205619-11205669	A549	lung:	n/a
39	chr8:11205619-11205669	SAEC	small airway:	n/a
40	chr8:11205619-11205669	LNCaP	prostate:	n/a
41	chr8:11205619-11205669	GM12878	blood:	n/a
42	chr8:11205619-11205669	SK-N-MC	brain:	n/a
43	chr8:11205619-11205669	AG04450	lung:	fetal
44	chr8:11205619-11205669	GM12891	blood:	n/a
45	chr8:11205619-11205669	BE2_C	brain:	n/a
46	chr8:11205619-11205669	CMK	blood:	n/a
47	chr8:11205619-11205669	HRPEpiC	eye:	n/a
48	chr8:11205619-11205669	AG04449	skin:	fetal
49	chr8:11205619-11205669	HCM	heart:	n/a
50	chr8:11205619-11205669	ProgFib	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11195675..11197986-chr8:11203854..11205997,2	MCF-7	breast:
2	chr8:11141950..11143471-chr8:11205387..11207796,2	K562	blood:
3	chr8:11202670..11208385-chr8:11211112..11215163,10	K562	blood:
4	chr8:11205483..11207435-chr8:11216914..11218469,2	MCF-7	breast:
5	chr8:11204525..11206554-chr8:11212652..11215291,3	MCF-7	breast:
6	chr8:11141452..11143588-chr8:11203845..11206287,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000255020	TF binding region
ENSG00000255020	CpG island
ENSG00000154316	Chromatin interaction
ENSG00000104643	Chromatin interaction

Extended variants
information (count: 84 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10096194	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10098322	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10110557	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11250129	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11774673	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11775635	0.81[AFR][1000 genomes]
rs11781375	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11782706	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11784458	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11784544	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11991153	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11994376	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13248147	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13250270	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13253016	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13253735	0.80[AMR][1000 genomes]
rs13263127	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13266233	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13270679	0.83[AFR][1000 genomes]
rs1435273	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17741537	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17797894	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1897950	0.81[AFR][1000 genomes]
rs1897951	0.81[AFR][1000 genomes]
rs1962656	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2060456	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2060457	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2060459	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2293855	0.87[AFR][1000 genomes]
rs2293856	0.87[AFR][1000 genomes]
rs2293858	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2293859	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2293860	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2736277	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28507159	0.82[AFR][1000 genomes]
rs3174048	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34237267	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35392635	0.84[AFR][1000 genomes]
rs35631424	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35687566	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35747588	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3779891	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3808509	0.83[AFR][1000 genomes]
rs3808518	0.81[AFR][1000 genomes]
rs4394351	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4413734	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4568582	0.83[AFR][1000 genomes]
rs5029571	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs58283816	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62488721	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6601580	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6988922	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6995404	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6996368	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7003241	0.82[AFR][1000 genomes]
rs7005469	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7008205	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7016671	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7815463	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7815802	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7815804	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7816601	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7817658	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7819395	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7820895	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7828711	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7831346	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7833966	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7834139	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7837036	0.84[AFR][1000 genomes]
rs7838897	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7839053	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv831233	chr8:11046854-11234384	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1033312	chr8:11126800-11252170	Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	esv1821756	chr8:11169178-11217587	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv890354	chr8:11176147-11266131	Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
10	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
11	nsv890355	chr8:11202154-11219334	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv890356	chr8:11202154-11223022	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7816636	MTMR9	Cis_1M	lymphoblastoid	RTeQTL
rs7816636	C8orf5	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11202800-11206200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
2	chr8:11202800-11207200	Active TSS	Pancreas	Pancrea
3	chr8:11203800-11206200	Bivalent Enhancer	Placenta	Placenta
4	chr8:11204000-11205800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
5	chr8:11204000-11206400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
6	chr8:11204200-11205800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
7	chr8:11204200-11205800	Active TSS	Brain Substantia Nigra	brain
8	chr8:11204200-11206000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
9	chr8:11204200-11206200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr8:11204200-11206200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
11	chr8:11204200-11206400	Active TSS	Brain Anterior Caudate	brain
12	chr8:11204400-11205800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:11204400-11205800	Bivalent/Poised TSS	Left Ventricle	heart
14	chr8:11204400-11206000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:11204400-11206200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:11204400-11206200	Bivalent/Poised TSS	HSMM	muscle
17	chr8:11204400-11206400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
18	chr8:11204600-11205800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:11204600-11205800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr8:11204600-11205800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:11204600-11205800	Bivalent Enhancer	Small Intestine	intestine
22	chr8:11204600-11205800	Bivalent/Poised TSS	HSMMtube	muscle
23	chr8:11204600-11206000	Bivalent/Poised TSS	Fetal Kidney	kidney
24	chr8:11204600-11206000	Active TSS	Gastric	stomach
25	chr8:11204600-11206200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
26	chr8:11204800-11205800	Flanking Bivalent TSS/Enh	Ovary	ovary
27	chr8:11204800-11206000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:11204800-11206000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
29	chr8:11204800-11206000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:11204800-11206000	Active TSS	Placenta Amnion	Placenta Amnion
31	chr8:11204800-11206000	Bivalent/Poised TSS	Stomach Mucosa	stomach
32	chr8:11204800-11206200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr8:11205000-11205800	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:11205000-11205800	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:11205000-11205800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
36	chr8:11205000-11205800	Bivalent Enhancer	Fetal Brain Male	brain
37	chr8:11205000-11206000	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:11205000-11206000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:11205000-11206000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
40	chr8:11205000-11206000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
41	chr8:11205000-11206000	Bivalent/Poised TSS	Fetal Thymus	thymus
42	chr8:11205000-11206000	Active TSS	Right Ventricle	heart
43	chr8:11205000-11206000	Active TSS	NHDF-Ad	bronchial
44	chr8:11205000-11206200	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr8:11205000-11206200	Bivalent Enhancer	Lung	lung
46	chr8:11205200-11205800	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
47	chr8:11205200-11205800	Bivalent/Poised TSS	A549	lung
48	chr8:11205200-11206000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
49	chr8:11205200-11206000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
50	chr8:11205200-11206000	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach

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