Variant report

Variant	rs28399553
Chromosome Location	chr8:95906794-95906795
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	POLR2A	chr8:95906312-95909423	H1-hESC	embryonic stem cell:	n/a	n/a
2	MAX	chr8:95906569-95909544	A549	lung:	n/a	chr8:95908461-95908468 chr8:95907052-95907061 chr8:95908035-95908044 chr8:95906818-95906827 chr8:95908582-95908592 chr8:95908460-95908469
3	UBTF	chr8:95906764-95908271	K562	blood:	n/a	n/a
4	E2F4	chr8:95906680-95909355	Hela-S3	cervix:	n/a	chr8:95908544-95908555 chr8:95908558-95908569 chr8:95907987-95907997 chr8:95906916-95906928 chr8:95907858-95907872 chr8:95907701-95907710 chr8:95906887-95906902 chr8:95907431-95907441 chr8:95907481-95907490 chr8:95908097-95908106 chr8:95907435-95907444 chr8:95909013-95909023
5	MYC	chr8:95906785-95906985	MCF-7	breast:	n/a	chr8:95906818-95906827
6	TCF12	chr8:95906638-95907685	ECC-1	luminal epithelium:	n/a	chr8:95907429-95907436 chr8:95906922-95906932 chr8:95906991-95907001
7	WRNIP1	chr8:95906636-95906813	GM12878	blood:	n/a	n/a
8	MXI1	chr8:95906481-95906830	GM12878	blood:	n/a	n/a
9	POLR2A	chr8:95906702-95909571	Hela-S3	cervix:	n/a	n/a
10	MXI1	chr8:95906523-95906955	Hela-S3	cervix:	n/a	n/a
11	SIN3A	chr8:95905721-95909315	H1-hESC	embryonic stem cell:	n/a	chr8:95908237-95908248 chr8:95907214-95907227 chr8:95906806-95906819 chr8:95906987-95906998 chr8:95908097-95908108 chr8:95908761-95908769
12	POLR2A	chr8:95906410-95906950	Hela-S3	cervix:	n/a	n/a
13	HCFC1	chr8:95905561-95909556	Hela-S3	cervix:	n/a	n/a
14	MAX	chr8:95906534-95909453	HepG2	liver:	n/a	chr8:95908461-95908468 chr8:95907052-95907061 chr8:95908035-95908044 chr8:95906818-95906827 chr8:95908582-95908592 chr8:95908460-95908469
15	POLR2A	chr8:95906600-95909154	Raji	blood:	n/a	n/a
16	MAX	chr8:95906404-95909411	MCF-7	breast:	n/a	chr8:95908461-95908468 chr8:95907052-95907061 chr8:95908035-95908044 chr8:95906818-95906827 chr8:95908582-95908592 chr8:95908460-95908469
17	SIN3AK20	chr8:95905630-95909476	MCF-7	breast:	n/a	n/a
18	MAZ	chr8:95906545-95906963	Hela-S3	cervix:	n/a	chr8:95906818-95906827
19	CTBP2	chr8:95906150-95908347	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:95906680-95906830	GM12873	blood:	n/a	n/a
21	SIN3AK20	chr8:95906458-95908990	MCF-7	breast:	n/a	n/a
22	ZBTB7A	chr8:95906706-95907244	K562	blood:	n/a	chr8:95906814-95906823
23	SIN3AK20	chr8:95906757-95909359	HCT-116	colon:	n/a	n/a
24	MAX	chr8:95906514-95909492	MCF-7	breast:	n/a	chr8:95908461-95908468 chr8:95907052-95907061 chr8:95908035-95908044 chr8:95906818-95906827 chr8:95908582-95908592 chr8:95908460-95908469
25	GATA1	chr8:95905339-95906912	PBDE	blood:	n/a	chr8:95905684-95905692
26	BACH1	chr8:95906321-95906874	H1-hESC	embryonic stem cell:	n/a	n/a
27	ELF1	chr8:95906557-95908456	GM12878	blood:	n/a	chr8:95907651-95907660
28	HMGN3	chr8:95906745-95909328	K562	blood:	n/a	n/a
29	TEAD4	chr8:95906529-95906959	K562	blood:	n/a	n/a
30	SMARCB1	chr8:95906357-95909312	Hela-S3	cervix:	n/a	n/a
31	E2F6	chr8:95906613-95909507	K562	blood:	n/a	chr8:95907987-95907997 chr8:95906916-95906928 chr8:95907858-95907872 chr8:95907701-95907710 chr8:95906887-95906902 chr8:95907431-95907441 chr8:95907481-95907490 chr8:95908097-95908106 chr8:95907435-95907444 chr8:95908954-95908965 chr8:95909013-95909023
32	EGR1	chr8:95906738-95907056	K562	blood:	n/a	n/a
33	UBTF	chr8:95906521-95909391	K562	blood:	n/a	n/a
34	MAZ	chr8:95906475-95909505	K562	blood:	n/a	chr8:95908461-95908468 chr8:95907052-95907061 chr8:95908035-95908044 chr8:95906818-95906827 chr8:95908582-95908592 chr8:95908460-95908469
35	CHD2	chr8:95906717-95909320	Hela-S3	cervix:	n/a	chr8:95908739-95908749
36	PML	chr8:95906606-95908290	MCF-7	breast:	n/a	chr8:95907184-95907192
37	POLR2A	chr8:95906492-95909263	K562	blood:	n/a	n/a
38	POLR2A	chr8:95906661-95909230	Hela-S3	cervix:	n/a	n/a
39	HA-E2F1	chr8:95906700-95909213	Hela-S3	cervix:	n/a	chr8:95907987-95907997 chr8:95906916-95906928 chr8:95907858-95907872 chr8:95907701-95907710 chr8:95906887-95906902 chr8:95907431-95907441 chr8:95907481-95907490 chr8:95908097-95908106 chr8:95907435-95907444 chr8:95909013-95909023
40	HA-E2F1	chr8:95906446-95909426	MCF-7	breast:	n/a	chr8:95907987-95907997 chr8:95906916-95906928 chr8:95907858-95907872 chr8:95907701-95907710 chr8:95906887-95906902 chr8:95907431-95907441 chr8:95907481-95907490 chr8:95908097-95908106 chr8:95907435-95907444 chr8:95909013-95909023
41	CTCF	chr8:95906720-95906870	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr8:95906780-95908473	MCF-7	breast:	n/a	n/a
43	E2F6	chr8:95906781-95907078	K562	blood:	n/a	chr8:95906916-95906928 chr8:95906887-95906902
44	MAX	chr8:95906785-95909404	HCT-116	colon:	n/a	chr8:95908461-95908468 chr8:95907052-95907061 chr8:95908035-95908044 chr8:95906818-95906827 chr8:95908582-95908592 chr8:95908460-95908469
45	SIN3AK20	chr8:95906590-95909162	PANC-1	pancreas:	n/a	n/a
46	MAX	chr8:95906627-95909403	ECC-1	luminal epithelium:	n/a	chr8:95908461-95908468 chr8:95907052-95907061 chr8:95908035-95908044 chr8:95906818-95906827 chr8:95908582-95908592 chr8:95908460-95908469
47	POLR2A	chr8:95906339-95909312	Hela-S3	cervix:	n/a	n/a
48	MXI1	chr8:95906447-95909476	IMR90	lung:	n/a	n/a
49	HDAC2	chr8:95906359-95909454	MCF-7	breast:	n/a	n/a
50	ZNF263	chr8:95906567-95908916	HEK293-T-REx	kidney:	n/a	chr8:95906978-95906987 chr8:95908579-95908588 chr8:95908400-95908409 chr8:95907942-95907951

No.	Distal block	Cell Line	Cell type
1	chr8:95839618..95841636-chr8:95906107..95908879,2	K562	blood:
2	chr8:95905635..95908338-chr8:95917636..95919532,2	MCF-7	breast:
3	chr8:95833645..95837522-chr8:95905761..95911691,14	MCF-7	breast:
4	chr8:95905969..95907155-chr8:96036661..96037534,3	MCF-7	breast:
5	chr8:95906396..95909110-chr8:96144664..96147276,2	MCF-7	breast:
6	chr8:95906455..95910081-chr8:96279389..96281894,5	K562	blood:
7	chr8:95833831..95839966-chr8:95906478..95910674,7	K562	blood:
8	chr8:95906302..95910709-chr8:96035472..96039639,10	MCF-7	breast:
9	chr8:95558228..95561115-chr8:95906355..95909204,2	K562	blood:
10	chr8:95833775..95836713-chr8:95905419..95909134,3	MCF-7	breast:
11	chr8:95905045..95910108-chr8:95959761..95963234,8	MCF-7	breast:
12	chr8:95906412..95908805-chr8:96098165..96100293,2	MCF-7	breast:
13	chr8:95905055..95911257-chr8:96032486..96039313,18	MCF-7	breast:
14	chr8:95906309..95909766-chr8:96145150..96148465,4	K562	blood:

Variant related genes	Relation type
CCNE2	TF binding region
NDUFAF6	TF binding region
ENSG00000254248	Chromatin interaction
ENSG00000175895	Chromatin interaction
ENSG00000253773	Chromatin interaction
ENSG00000253878	Chromatin interaction
ENSG00000164938	Chromatin interaction
ENSG00000238791	Chromatin interaction
ENSG00000212997	Chromatin interaction
ENSG00000156170	Chromatin interaction
ENSG00000164941	Chromatin interaction
ENSG00000156172	Chromatin interaction

Extended variants
information (count: 85 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10086541	0.81[CEU][hapmap]
rs10092003	0.81[CEU][hapmap];0.83[GIH][hapmap]
rs10093594	0.81[CEU][hapmap]
rs10096455	0.81[CEU][hapmap]
rs10097930	0.81[CEU][hapmap]
rs10098197	0.81[CEU][hapmap]
rs10098453	0.81[CEU][hapmap]
rs10111154	0.81[CEU][hapmap]
rs10504939	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs10956927	0.85[ASW][hapmap];0.83[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.85[MEX][hapmap];0.80[MKK][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11775475	0.94[CEU][hapmap];0.90[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11776189	0.81[CEU][hapmap]
rs11776489	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11776687	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11777132	0.81[EUR][1000 genomes]
rs11777353	0.83[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.83[EUR][1000 genomes]
rs11778553	0.87[CEU][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap]
rs11779282	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11779698	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs11780931	0.81[CEU][hapmap]
rs11781040	0.81[CEU][hapmap]
rs11781429	0.83[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs11781757	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs11782617	0.92[ASW][hapmap];0.83[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11782818	0.87[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap]
rs11783522	0.94[CEU][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11783589	0.83[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11783878	0.87[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap]
rs11783941	1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs11784299	0.85[ASW][hapmap];0.83[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.85[MEX][hapmap];0.80[MKK][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11786021	0.89[CHD][hapmap];1.00[JPT][hapmap]
rs11786088	0.83[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11786389	0.83[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11786451	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11787377	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12056517	0.83[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12056808	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13250762	1.00[JPT][hapmap]
rs16893774	0.94[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.84[TSI][hapmap];0.84[YRI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16917079	0.84[ASW][hapmap];0.83[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16917081	1.00[JPT][hapmap]
rs16917082	0.82[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs16917093	0.83[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16917102	1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs16917106	0.86[ASW][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs16917117	0.94[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.84[YRI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16917233	0.81[CEU][hapmap]
rs17359493	0.83[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17665737	0.86[CEU][hapmap];1.00[JPT][hapmap]
rs28399563	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28399571	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2904889	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3802191	0.87[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap]
rs4075834	0.85[ASW][hapmap];0.82[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.82[MEX][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4323442	0.81[CEU][hapmap]
rs4345531	1.00[JPT][hapmap]
rs4355737	0.84[EUR][1000 genomes]
rs57063661	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58675831	0.83[EUR][1000 genomes]
rs59091366	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59265059	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59521030	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs60171840	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6471505	0.81[CEU][hapmap]
rs6651271	0.81[CEU][hapmap]
rs6651272	0.81[CEU][hapmap]
rs6986418	0.82[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs6989591	0.92[ASW][hapmap];0.83[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7009940	0.86[ASW][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.86[MKK][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs716733	0.86[ASW][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];0.81[YRI][hapmap];0.91[ASN][1000 genomes]
rs73269188	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73269198	0.83[EUR][1000 genomes]
rs73269199	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73271148	0.85[EUR][1000 genomes]
rs73271178	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7812312	0.81[CEU][hapmap]
rs7826196	0.81[CEU][hapmap]
rs7834966	0.84[ASW][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7844932	0.92[GIH][hapmap]
rs9297950	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised 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	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv532338	chr8:95296118-95971825	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv891203	chr8:95883232-95948202	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv891204	chr8:95883232-95965135	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Genic enhancers 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 target site	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs28399553	C8orf38	cis	cerebellum	SCAN
rs28399553	INTS8	cis	lymphoblastoid	seeQTL
rs28399553	MATN2	cis	parietal	SCAN
rs28399553	INTS8	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95890600-95906800	Weak transcription	Aorta	Aorta
2	chr8:95905400-95907400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:95905400-95907400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:95905600-95906800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:95905600-95906800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr8:95905600-95907000	Flanking Active TSS	HUVEC	blood vessel
7	chr8:95905600-95907200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr8:95905600-95907400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:95905600-95907400	Flanking Active TSS	Fetal Thymus	thymus
10	chr8:95905600-95907400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
11	chr8:95905600-95909200	Active TSS	Brain Substantia Nigra	brain
12	chr8:95905600-95909200	Active TSS	Fetal Brain Female	brain
13	chr8:95905600-95909600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr8:95905800-95906800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr8:95905800-95906800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:95905800-95906800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:95905800-95906800	Flanking Active TSS	Duodenum Mucosa	Duodenum
18	chr8:95905800-95906800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
19	chr8:95905800-95906800	Enhancers	Spleen	Spleen
20	chr8:95905800-95907000	Flanking Active TSS	Thymus	Thymus
21	chr8:95905800-95907200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:95905800-95907400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr8:95905800-95907400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr8:95905800-95909600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:95905800-95909600	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr8:95905800-95909600	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr8:95906000-95906800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:95906000-95906800	Flanking Active TSS	Dnd41	blood
29	chr8:95906000-95906800	Flanking Active TSS	NHEK	skin
30	chr8:95906000-95907400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr8:95906000-95907600	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr8:95906000-95909200	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr8:95906000-95909200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr8:95906000-95909200	Active TSS	Right Atrium	heart
35	chr8:95906200-95906800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:95906200-95906800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
37	chr8:95906200-95906800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
38	chr8:95906200-95906800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr8:95906200-95906800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
40	chr8:95906200-95906800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:95906200-95906800	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr8:95906200-95906800	Flanking Active TSS	Fetal Heart	heart
43	chr8:95906200-95906800	Flanking Active TSS	Fetal Lung	lung
44	chr8:95906200-95906800	Flanking Active TSS	A549	lung
45	chr8:95906200-95906800	Flanking Active TSS	GM12878-XiMat	blood
46	chr8:95906200-95906800	Flanking Active TSS	HMEC	breast
47	chr8:95906200-95906800	Flanking Active TSS	K562	blood
48	chr8:95906200-95906800	Flanking Active TSS	Osteobl	bone
49	chr8:95906200-95907000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr8:95906200-95907200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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