Variant report

Variant	rs28722756
Chromosome Location	chr8:6604828-6604829
allele	A/G
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	BHLHE40	chr8:6604602-6604987	K562	blood:	n/a	n/a
2	GATA3	chr8:6604675-6605033	SK-N-SH	brain:	n/a	n/a
3	EP300	chr8:6604623-6605044	K562	blood:	n/a	n/a
4	BCL3	chr8:6604603-6605014	GM12878	blood:	n/a	n/a
5	MAX	chr8:6604654-6604949	NB4	blood:	n/a	chr8:6604800-6604810
6	POLR2A	chr8:6604556-6605047	GM12891	blood:	n/a	n/a
7	JUND	chr8:6604467-6605077	K562	blood:	n/a	chr8:6604834-6604842
8	STAT3	chr8:6604750-6604862	MCF10A-Er-Src	breast:	n/a	n/a
9	MAX	chr8:6604639-6604981	K562	blood:	n/a	chr8:6604800-6604810
10	YY1	chr8:6604708-6604847	K562	blood:	n/a	n/a
11	MTA3	chr8:6602677-6604839	GM12878	blood:	n/a	n/a
12	IRF1	chr8:6603500-6605002	K562	blood:	n/a	chr8:6604005-6604012 chr8:6603611-6603620
13	MAX	chr8:6604669-6604957	K562	blood:	n/a	chr8:6604800-6604810
14	MYC	chr8:6604700-6604862	K562	blood:	n/a	chr8:6604800-6604810
15	ATF1	chr8:6604663-6604977	K562	blood:	n/a	n/a
16	POLR2A	chr8:6604691-6604908	GM12878	blood:	n/a	n/a
17	WRNIP1	chr8:6604689-6604905	GM12878	blood:	n/a	n/a
18	POLR2A	chr8:6603232-6606791	GM12891	blood:	n/a	n/a
19	NFIC	chr8:6603428-6604892	GM12878	blood:	n/a	n/a
20	JUN	chr8:6604619-6605033	K562	blood:	n/a	chr8:6604834-6604842
21	JUN	chr8:6602235-6605293	K562	blood:	n/a	chr8:6603936-6603945 chr8:6602523-6602535 chr8:6604834-6604842 chr8:6603896-6603905
22	STAT5A	chr8:6604559-6605070	K562	blood:	n/a	n/a
23	POLR2A	chr8:6603468-6605423	PBDE	blood:	n/a	n/a
24	POLR2A	chr8:6604564-6605066	GM12878	blood:	n/a	n/a
25	FOSL1	chr8:6604630-6604973	K562	blood:	n/a	chr8:6604834-6604842
26	MAX	chr8:6604629-6604985	K562	blood:	n/a	chr8:6604800-6604810
27	RCOR1	chr8:6604619-6605015	K562	blood:	n/a	n/a
28	STAT3	chr8:6604763-6604849	MCF10A-Er-Src	breast:	n/a	n/a
29	NFATC1	chr8:6602515-6605375	GM12878	blood:	n/a	n/a
30	CUX1	chr8:6604517-6605283	K562	blood:	n/a	n/a
31	TEAD4	chr8:6604553-6605070	K562	blood:	n/a	n/a
32	NFIC	chr8:6602552-6604940	GM12878	blood:	n/a	n/a
33	MYC	chr8:6604582-6605071	K562	blood:	n/a	chr8:6604800-6604810
34	JUN	chr8:6604608-6605024	K562	blood:	n/a	chr8:6604834-6604842
35	MYC	chr8:6604591-6605036	K562	blood:	n/a	chr8:6604800-6604810
36	EBF1	chr8:6603593-6604871	GM12878	blood:	n/a	chr8:6604149-6604160
37	GATA1	chr8:6603374-6605437	PBDE	blood:	n/a	chr8:6603896-6603906 chr8:6603744-6603753 chr8:6603745-6603762
38	STAT5A	chr8:6604572-6605016	K562	blood:	n/a	n/a
39	POLR2A	chr8:6601783-6608310	GM12878	blood:	n/a	n/a
40	MYC	chr8:6604433-6605223	K562	blood:	n/a	chr8:6604800-6604810
41	TBL1XR1	chr8:6603551-6605027	K562	blood:	n/a	n/a
42	ZC3H11A	chr8:6604743-6605211	K562	blood:	n/a	n/a
43	POLR2A	chr8:6604500-6605069	GM12878	blood:	n/a	n/a
44	MAFK	chr8:6604081-6604986	K562	blood:	n/a	n/a
45	NFATC1	chr8:6603609-6604969	GM12878	blood:	n/a	n/a
46	POLR2A	chr8:6604771-6606768	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:6564149..6568457-chr8:6601682..6605924,8	K562	blood:
2	chr8:6564149..6568070-chr8:6601682..6607895,12	K562	blood:

Variant related genes	Relation type
AGPAT5	TF binding region
ENSG00000249898	Chromatin interaction
ENSG00000155189	Chromatin interaction

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10086543	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10088817	0.92[AFR][1000 genomes]
rs10090110	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10091758	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10091854	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10093190	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10095639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10095736	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10099645	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10100374	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10102003	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10102783	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10104430	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10104813	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10105115	0.92[AFR][1000 genomes]
rs10105620	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10107056	1.00[AMR][1000 genomes]
rs10108416	0.92[AFR][1000 genomes]
rs10112451	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10113271	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10481363	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10481382	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10481383	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13439495	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17077743	1.00[AMR][1000 genomes]
rs17077753	1.00[AMR][1000 genomes]
rs17077756	1.00[AMR][1000 genomes]
rs17317651	1.00[AMR][1000 genomes]
rs28406664	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28440106	1.00[AMR][1000 genomes]
rs28457858	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28470869	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28604439	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28607557	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28640978	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28659886	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28665136	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28680736	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28685103	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28688598	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28692721	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28742927	1.00[AMR][1000 genomes]
rs28744398	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28759314	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28797585	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55688364	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55696710	1.00[AMR][1000 genomes]
rs56030398	0.92[AFR][1000 genomes]
rs56284142	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56777140	1.00[AMR][1000 genomes]
rs57584984	1.00[AMR][1000 genomes]
rs58032777	0.92[AFR][1000 genomes]
rs58394237	1.00[AMR][1000 genomes]
rs58786722	1.00[AMR][1000 genomes]
rs59731299	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59852951	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6986579	1.00[AMR][1000 genomes]
rs6987742	1.00[AMR][1000 genomes]
rs73508233	1.00[AMR][1000 genomes]
rs73508250	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73508251	0.88[AFR][1000 genomes]
rs73508276	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73508282	1.00[AMR][1000 genomes]
rs73509817	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73511991	1.00[AMR][1000 genomes]
rs73524926	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73524938	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73524939	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73524949	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7357377	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7357402	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73661460	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73661462	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73661463	1.00[AMR][1000 genomes]
rs73661465	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021175	chr8:5965453-6880364	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1027682	chr8:6018123-6920312	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv1027313	chr8:6286575-6920312	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1021684	chr8:6350091-6809455	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv2422383	chr8:6362389-6781593	Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv610004	chr8:6402366-6772913	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv1029241	chr8:6411300-6761720	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv933075	chr8:6456475-7366650	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
9	nsv1025976	chr8:6472948-6686972	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription 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	15 gene(s)	inside rSNPs	diseases
10	nsv933768	chr8:6482944-6618221	Strong transcription Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv831220	chr8:6527845-6728491	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv1030637	chr8:6545498-6669949	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
13	nsv1034115	chr8:6546984-6665832	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers 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	13 gene(s)	inside rSNPs	diseases
14	nsv465436	chr8:6568201-6921404	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	nsv610006	chr8:6568201-6921404	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
16	nsv1031063	chr8:6570354-6622685	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
17	nsv1027883	chr8:6570354-7250368	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
18	nsv1024685	chr8:6575334-6622685	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
19	nsv1034812	chr8:6578390-6920312	Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
20	nsv949532	chr8:6579563-6999220	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
21	nsv482865	chr8:6585920-6765111	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription 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	12 gene(s)	inside rSNPs	diseases
22	nsv1015563	chr8:6596171-6730826	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
23	nsv539432	chr8:6596171-6730826	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6585800-6615800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:6587200-6617000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:6587600-6608000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr8:6587800-6605200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr8:6587800-6607400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr8:6587800-6612000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr8:6587800-6617000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr8:6588600-6607400	Weak transcription	Spleen	Spleen
9	chr8:6591000-6605200	Weak transcription	Fetal Brain Female	brain
10	chr8:6591000-6614200	Weak transcription	Left Ventricle	heart
11	chr8:6591000-6617400	Weak transcription	Psoas Muscle	Psoas
12	chr8:6591200-6607200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr8:6591200-6607200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr8:6591200-6614600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:6591200-6625400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:6591400-6607200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr8:6591400-6607400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr8:6591400-6618200	Weak transcription	NHDF-Ad	bronchial
19	chr8:6591400-6625000	Weak transcription	NH-A	brain
20	chr8:6591400-6633200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:6591600-6614200	Weak transcription	NHLF	lung
22	chr8:6591600-6616600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr8:6591600-6618200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:6592600-6625000	Weak transcription	Osteobl	bone
25	chr8:6593000-6605200	Weak transcription	Brain Germinal Matrix	brain
26	chr8:6593000-6605800	Weak transcription	Thymus	Thymus
27	chr8:6593000-6607400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:6593000-6607400	Weak transcription	Pancreas	Pancrea
29	chr8:6593000-6622800	Weak transcription	Esophagus	oesophagus
30	chr8:6593200-6607400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr8:6593400-6612200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr8:6594400-6617400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr8:6594400-6625200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr8:6594800-6607400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr8:6594800-6607400	Weak transcription	Aorta	Aorta
36	chr8:6595400-6629600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr8:6596000-6607400	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr8:6597000-6607200	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr8:6597800-6611600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr8:6597800-6616200	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr8:6598000-6607000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr8:6598000-6617000	Strong transcription	Dnd41	blood
43	chr8:6599800-6607400	Weak transcription	HMEC	breast
44	chr8:6600200-6605600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:6600600-6610800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:6601400-6607000	Weak transcription	HSMMtube	muscle
47	chr8:6601800-6608400	Enhancers	Stomach Mucosa	stomach
48	chr8:6602000-6611200	Strong transcription	Fetal Thymus	thymus
49	chr8:6602200-6605400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr8:6602200-6605600	Enhancers	Liver	Liver

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