Variant report

Variant	rs73675449
Chromosome Location	chr8:42911335-42911336
allele	A/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	SP1	chr8:42910883-42911843	HCT-116	colon:	n/a	chr8:42911444-42911456 chr8:42911446-42911455 chr8:42911441-42911455 chr8:42911436-42911450 chr8:42911446-42911455 chr8:42911445-42911455 chr8:42911445-42911455 chr8:42911444-42911455 chr8:42911445-42911454 chr8:42911444-42911456
2	EGR1	chr8:42911198-42911545	GM12878	blood:	n/a	chr8:42911416-42911425
3	ELF1	chr8:42911040-42911656	SK-N-SH	brain:	n/a	chr8:42911414-42911425 chr8:42911413-42911424
4	POLR2A	chr8:42910727-42911772	SK-N-SH	brain:	n/a	n/a
5	EP300	chr8:42911157-42911607	GM12878	blood:	n/a	chr8:42911415-42911424
6	JUND	chr8:42910913-42912068	K562	blood:	n/a	n/a
7	CTCF	chr8:42911240-42911390	SAEC	small airway:	n/a	n/a
8	PAX5	chr8:42911054-42912117	GM12878	blood:	n/a	chr8:42911416-42911425 chr8:42911867-42911876
9	CEBPD	chr8:42910977-42911736	K562	blood:	n/a	n/a
10	ZBTB33	chr8:42911074-42911538	K562	blood:	n/a	n/a
11	ZMIZ1	chr8:42910843-42911953	K562	blood:	n/a	n/a
12	POLR2A	chr8:42910712-42912758	Hela-S3	cervix:	n/a	n/a
13	E2F4	chr8:42911014-42911932	K562	blood:	n/a	chr8:42911831-42911841 chr8:42911864-42911874 chr8:42911867-42911876
14	SP1	chr8:42911119-42911937	GM12878	blood:	n/a	chr8:42911444-42911456 chr8:42911446-42911455 chr8:42911441-42911455 chr8:42911436-42911450 chr8:42911446-42911455 chr8:42911445-42911455 chr8:42911445-42911455 chr8:42911444-42911455 chr8:42911445-42911454 chr8:42911444-42911456
15	NR3C1	chr8:42911117-42911946	A549	lung:	n/a	n/a
16	TCF12	chr8:42911067-42911922	GM12878	blood:	n/a	chr8:42911735-42911745 chr8:42911387-42911394
17	TAF1	chr8:42911073-42912122	GM12878	blood:	n/a	n/a
18	YY1	chr8:42910746-42912240	SK-N-SH	brain:	n/a	chr8:42911485-42911497 chr8:42911834-42911845 chr8:42911863-42911877 chr8:42911863-42911872
19	POLR2A	chr8:42910833-42911962	HEK293	kidney:	n/a	n/a
20	TAF1	chr8:42910750-42911821	ECC-1	luminal epithelium:	n/a	n/a
21	POLR2A	chr8:42910977-42912001	MCF-7	breast:	n/a	n/a
22	GATA3	chr8:42911073-42911577	T-47D	breast:	n/a	chr8:42911411-42911422 chr8:42911416-42911426
23	MXI1	chr8:42911066-42912708	HepG2	liver:	n/a	n/a
24	PML	chr8:42911083-42911546	GM12878	blood:	n/a	n/a
25	MAX	chr8:42911015-42911999	HepG2	liver:	n/a	chr8:42911803-42911812
26	GABPA	chr8:42910945-42911681	MCF-7	breast:	n/a	n/a
27	BCLAF1	chr8:42910710-42912103	GM12878	blood:	n/a	chr8:42911416-42911425 chr8:42911832-42911845 chr8:42911360-42911373 chr8:42911761-42911770
28	CBX3	chr8:42910729-42911547	K562	blood:	n/a	n/a
29	REST	chr8:42911043-42911837	PFSK-1	brain:	n/a	chr8:42911472-42911485
30	RAD21	chr8:42911110-42911575	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr8:42910663-42912107	GM12891	blood:	n/a	n/a
32	TCF12	chr8:42910945-42911640	A549	lung:	n/a	chr8:42911387-42911394
33	POU2F2	chr8:42911135-42911657	GM12878	blood:	n/a	n/a
34	SP2	chr8:42911066-42911595	H1-hESC	embryonic stem cell:	n/a	chr8:42911346-42911361
35	RELA	chr8:42911078-42912789	GM15510	blood:	n/a	n/a
36	BRCA1	chr8:42911125-42911486	HepG2	liver:	n/a	n/a
37	GABPA	chr8:42911110-42911940	HepG2	liver:	n/a	n/a
38	PML	chr8:42910956-42911910	K562	blood:	n/a	n/a
39	POLR2A	chr8:42910839-42912032	A549	lung:	n/a	n/a
40	SIN3AK20	chr8:42910786-42911799	HCT-116	colon:	n/a	n/a
41	FOXA1	chr8:42911031-42911589	HepG2	liver:	n/a	n/a
42	TCF12	chr8:42911154-42911531	GM12878	blood:	n/a	chr8:42911387-42911394
43	FOXP2	chr8:42911022-42911672	SK-N-MC	brain:	n/a	n/a
44	YY1	chr8:42911244-42911620	HCT-116	colon:	n/a	chr8:42911485-42911497
45	ZBTB33	chr8:42911046-42911496	HCT-116	colon:	n/a	n/a
46	FOXM1	chr8:42910994-42911673	ECC-1	luminal epithelium:	n/a	n/a
47	IRF4	chr8:42911047-42911625	GM12878	blood:	n/a	n/a
48	YY1	chr8:42910939-42912119	GM12878	blood:	n/a	chr8:42911485-42911497 chr8:42911834-42911845 chr8:42911863-42911877 chr8:42911863-42911872
49	CUX1	chr8:42911156-42911462	GM12878	blood:	n/a	n/a
50	REST	chr8:42910577-42912408	H1-neurons	neurons:	n/a	chr8:42911472-42911485 chr8:42912154-42912167

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:42911308-42911358	U87	brain:	n/a
2	chr8:42911308-42911358	HRE	kidney:	n/a
3	chr8:42911287-42911337	AoSMC	blood vessel:	n/a
4	chr8:42911315-42911365	CMK	blood:	n/a
5	chr8:42911315-42911365	U87	brain:	n/a
6	chr8:42911287-42911337	PFSK-1	brain:	n/a
7	chr8:42911308-42911358	GM19239	blood:	n/a
8	chr8:42911315-42911365	GM19239	blood:	n/a
9	chr8:42911315-42911365	MCF10A-Er-Src	breast:	n/a
10	chr8:42911308-42911358	NHDF-neo	bronchial:	n/a
11	chr8:42911308-42911358	A549	lung:	n/a
12	chr8:42911287-42911337	SK-N-SH_RA	brain:	n/a
13	chr8:42911287-42911337	HL-60	blood:	n/a
14	chr8:42911308-42911358	HEK293	kidney:	embryo
15	chr8:42911287-42911337	GM19239	blood:	n/a
16	chr8:42911308-42911358	PANC-1	pancreas:	n/a
17	chr8:42911287-42911337	NB4	blood:	n/a
18	chr8:42911287-42911337	ProgFib	skin:	n/a
19	chr8:42911315-42911365	BJ	skin:	n/a
20	chr8:42911308-42911358	T-47D	breast:	n/a
21	chr8:42911315-42911365	AoSMC	blood vessel:	n/a
22	chr8:42911308-42911358	HCF	heart:	n/a
23	chr8:42911308-42911358	ovcar-3	ovarian:	n/a
24	chr8:42911315-42911365	HRCEpiC	kidney:	n/a
25	chr8:42911315-42911365	PANC-1	pancreas:	n/a
26	chr8:42911287-42911337	SAEC	small airway:	n/a
27	chr8:42911315-42911365	HEK293	kidney:	embryo
28	chr8:42911287-42911337	Jurkat	blood:	n/a
29	chr8:42911287-42911337	HepG2	liver:	n/a
30	chr8:42911287-42911337	NHBE	bronchial:	n/a
31	chr8:42911308-42911358	Caco-2	colon:	n/a
32	chr8:42911287-42911337	SK-N-SH	brain:	n/a
33	chr8:42911308-42911358	NHBE	bronchial:	n/a
34	chr8:42911287-42911337	PrEC	prostate:	n/a
35	chr8:42911308-42911358	IMR90	lung:	fetal
36	chr8:42911308-42911358	GM06990	blood:	n/a
37	chr8:42911287-42911337	T-47D	breast:	n/a
38	chr8:42911315-42911365	GM12878	blood:	n/a
39	chr8:42911287-42911337	SK-N-MC	brain:	n/a
40	chr8:42911308-42911358	PrEC	prostate:	n/a
41	chr8:42911315-42911365	AG04450	lung:	fetal
42	chr8:42911287-42911337	HEEpiC	esophagus:	n/a
43	chr8:42911308-42911358	SK-N-SH_RA	brain:	n/a
44	chr8:42911308-42911358	Hepatocyte	liver:	n/a
45	chr8:42911315-42911365	T-47D	breast:	n/a
46	chr8:42911287-42911337	HRPEpiC	eye:	n/a
47	chr8:42911315-42911365	HRE	kidney:	n/a
48	chr8:42911287-42911337	RPTEC	kidney:	n/a
49	chr8:42911315-42911365	AG10803	skin:	n/a
50	chr8:42911287-42911337	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:42697938..42699584-chr8:42910062..42912645,3	K562	blood:
2	chr17:57913947..57916769-chr8:42908901..42912808,3	MCF-7	breast:
3	chr11:18656195..18656698-chr8:42911083..42911641,2	HCT-116	colon:
4	chr8:42749450..42753570-chr8:42908450..42913824,10	K562	blood:
5	chr16:69362649..69364696-chr8:42910150..42912284,2	MCF-7	breast:
6	chr8:42696480..42700026-chr8:42910062..42913362,8	K562	blood:
7	chr8:42749514..42753230-chr8:42909984..42914905,15	K562	blood:
8	chr1:149223731..149224401-chr8:42910787..42911478,3	HCT-116	colon:
9	chr8:42909717..42915258-chr8:42945286..42950388,10	K562	blood:
10	chr6:27113962..27114911-chr8:42910971..42911696,2	Hela-S3	cervix:
11	chr8:42910109..42913983-chr8:42935455..42940036,4	K562	blood:
12	chr22:50689435..50690174-chr8:42910972..42911646,2	HCT-116	colon:
13	chr8:42747025..42751990-chr8:42908756..42912609,5	MCF-7	breast:
14	chr8:42910668..42913653-chr8:42931061..42934093,3	K562	blood:
15	chr2:128458367..128459242-chr8:42911232..42912127,2	Hela-S3	cervix:
16	chr1:43833271..43833905-chr8:42911170..42911952,2	Hela-S3	cervix:
17	chr8:42749163..42753793-chr8:42909851..42913083,6	MCF-7	breast:
18	chr8:42911182..42911990-chr9:88897072..88897738,2	Hela-S3	cervix:

Variant related genes	Relation type
FNTA	TF binding region
FNTA	CpG island
ENSG00000197903	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000206737	Chromatin interaction
ENSG00000100429	Chromatin interaction
ENSG00000168522	Chromatin interaction
ENSG00000120925	Chromatin interaction
ENSG00000173349	Chromatin interaction
ENSG00000179119	Chromatin interaction
ENSG00000135070	Chromatin interaction
ENSG00000131931	Chromatin interaction
ENSG00000258429	Chromatin interaction
ENSG00000066322	Chromatin interaction
ENSG00000266044	Chromatin interaction
ENSG00000185900	Chromatin interaction
ENSG00000168172	Chromatin interaction
ENSG00000062716	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs16891648	1.00[AMR][1000 genomes]
rs16891652	1.00[AMR][1000 genomes]
rs16891654	1.00[AMR][1000 genomes]
rs16891682	1.00[AMR][1000 genomes]
rs16891686	1.00[AMR][1000 genomes]
rs16891699	1.00[AMR][1000 genomes]
rs16891701	1.00[AMR][1000 genomes]
rs16891704	1.00[AMR][1000 genomes]
rs55636430	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55745135	1.00[AMR][1000 genomes]
rs55870161	1.00[AMR][1000 genomes]
rs55908519	1.00[AMR][1000 genomes]
rs55959405	1.00[AMR][1000 genomes]
rs56313744	1.00[AMR][1000 genomes]
rs56384848	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56789342	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57012672	1.00[AMR][1000 genomes]
rs57180588	1.00[AMR][1000 genomes]
rs57279972	1.00[AMR][1000 genomes]
rs57354259	1.00[AMR][1000 genomes]
rs57713224	1.00[AMR][1000 genomes]
rs57746820	1.00[AMR][1000 genomes]
rs57798571	1.00[AMR][1000 genomes]
rs58729340	1.00[AMR][1000 genomes]
rs59139251	1.00[AMR][1000 genomes]
rs59320956	1.00[AMR][1000 genomes]
rs60259766	1.00[AMR][1000 genomes]
rs60491458	1.00[AMR][1000 genomes]
rs60748981	1.00[AMR][1000 genomes]
rs60960611	1.00[AMR][1000 genomes]
rs61356971	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61468554	1.00[AMR][1000 genomes]
rs73675437	1.00[AMR][1000 genomes]
rs73675439	1.00[AMR][1000 genomes]
rs73675443	1.00[AMR][1000 genomes]
rs73675448	1.00[AMR][1000 genomes]
rs73675450	1.00[AMR][1000 genomes]
rs73675452	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73675454	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73675457	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73675458	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73675460	1.00[AMR][1000 genomes]
rs73675461	1.00[AMR][1000 genomes]
rs73675463	1.00[AMR][1000 genomes]
rs73675464	1.00[AMR][1000 genomes]
rs73675466	1.00[AMR][1000 genomes]
rs73675467	1.00[AMR][1000 genomes]
rs73675468	1.00[AMR][1000 genomes]
rs73675469	1.00[AMR][1000 genomes]
rs73675470	1.00[AMR][1000 genomes]
rs73675473	1.00[AMR][1000 genomes]
rs73675475	1.00[AMR][1000 genomes]
rs73675476	1.00[AMR][1000 genomes]
rs73675478	1.00[AMR][1000 genomes]
rs73675493	1.00[AMR][1000 genomes]
rs73675496	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890846	chr8:42625663-43240123	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers 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	86 gene(s)	inside rSNPs	diseases
2	nsv1024688	chr8:42709414-43333639	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers 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	78 gene(s)	inside rSNPs	diseases
3	nsv539563	chr8:42709414-43333639	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
4	nsv1033927	chr8:42748842-43575771	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
5	nsv533812	chr8:42755447-43528350	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
6	nsv1032781	chr8:42772394-43461484	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
7	nsv1021281	chr8:42807619-43472678	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
8	nsv429912	chr8:42852444-43701143	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
9	nsv869499	chr8:42858608-43541986	Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
10	nsv916847	chr8:42858611-43541984	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
11	nsv1027779	chr8:42863024-43729296	Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
12	nsv1025336	chr8:42905623-43333638	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
13	nsv539564	chr8:42905623-43333638	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
14	nsv831302	chr8:42909483-43105520	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:42910200-42913200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:42910400-42912000	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr8:42910400-42912200	Active TSS	HSMMtube	muscle
4	chr8:42910400-42912600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:42910400-42912600	Active TSS	Duodenum Smooth Muscle	Duodenum
6	chr8:42910400-42912600	Active TSS	A549	lung
7	chr8:42910400-42912600	Active TSS	Monocytes-CD14+_RO01746	blood
8	chr8:42910400-42912800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr8:42910400-42913000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr8:42910400-42913200	Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr8:42910400-42913200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:42910400-42913200	Active TSS	HSMM	muscle
13	chr8:42910400-42913200	Active TSS	K562	blood
14	chr8:42910400-42913400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:42910600-42911600	Active TSS	Brain Germinal Matrix	brain
16	chr8:42910600-42912000	Active TSS	Colonic Mucosa	Colon
17	chr8:42910600-42912200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr8:42910600-42912200	Active TSS	Brain Inferior Temporal Lobe	brain
19	chr8:42910600-42912200	Active TSS	Duodenum Mucosa	Duodenum
20	chr8:42910600-42912200	Active TSS	Stomach Smooth Muscle	stomach
21	chr8:42910600-42912400	Active TSS	Aorta	Aorta
22	chr8:42910600-42912400	Active TSS	Brain Anterior Caudate	brain
23	chr8:42910600-42912400	Active TSS	Colon Smooth Muscle	Colon
24	chr8:42910600-42912400	Active TSS	Fetal Brain Female	brain
25	chr8:42910600-42912400	Active TSS	Fetal Intestine Large	intestine
26	chr8:42910600-42912600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr8:42910600-42912600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:42910600-42912600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr8:42910600-42912600	Active TSS	Brain Angular Gyrus	brain
30	chr8:42910600-42912600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr8:42910600-42912600	Active TSS	Fetal Kidney	kidney
32	chr8:42910600-42912600	Active TSS	Psoas Muscle	Psoas
33	chr8:42910600-42912800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:42910600-42912800	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr8:42910600-42912800	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr8:42910600-42912800	Active TSS	Ovary	ovary
37	chr8:42910600-42912800	Active TSS	Right Ventricle	heart
38	chr8:42910600-42913000	Active TSS	H1 Cell Line	embryonic stem cell
39	chr8:42910600-42913000	Active TSS	H9 Cell Line	embryonic stem cell
40	chr8:42910600-42913000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr8:42910600-42913000	Active TSS	GM12878-XiMat	blood
42	chr8:42910600-42913200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:42910600-42913200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:42910600-42913200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:42910800-42911400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:42910800-42911400	ZNF genes & repeats	Fetal Brain Male	brain
47	chr8:42910800-42912000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr8:42910800-42912000	Active TSS	Cortex derived primary cultured neurospheres	brain
49	chr8:42910800-42912200	Active TSS	Brain Cingulate Gyrus	brain
50	chr8:42910800-42912200	Active TSS	Brain Hippocampus Middle	brain

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