Variant report

Variant	rs730562
Chromosome Location	chr17:59488493-59488494
allele	A/C
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	SIN3AK20	chr17:59486979-59489165	SK-N-SH	brain:	n/a	n/a
2	MEF2A	chr17:59485767-59490640	SK-N-SH	brain:	n/a	chr17:59489068-59489076
3	ZNF143	chr17:59488142-59490296	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr17:59488434-59489247	ECC-1	luminal epithelium:	n/a	n/a
5	TCF7L2	chr17:59487998-59489013	HCT-116	colon:	n/a	n/a
6	RAD21	chr17:59487656-59491474	SK-N-SH	brain:	n/a	chr17:59488343-59488353 chr17:59488338-59488357 chr17:59491210-59491220 chr17:59488536-59488550 chr17:59488875-59488884 chr17:59488341-59488354 chr17:59487989-59487999 chr17:59488343-59488355
7	PBX3	chr17:59487113-59488862	SK-N-SH	brain:	n/a	n/a
8	TEAD4	chr17:59484276-59495088	A549	lung:	n/a	n/a
9	TEAD4	chr17:59487963-59490539	SK-N-SH	brain:	n/a	n/a
10	POLR2A	chr17:59488190-59488495	HUVEC	blood vessel:	n/a	n/a
11	ZBTB33	chr17:59487467-59488603	SK-N-SH	brain:	n/a	n/a
12	RAD21	chr17:59488044-59488566	H1-hESC	embryonic stem cell:	n/a	chr17:59488343-59488353 chr17:59488338-59488357 chr17:59488536-59488550 chr17:59488341-59488354 chr17:59488343-59488355
13	CTCF	chr17:59487481-59491170	SK-N-SH	brain:	n/a	chr17:59488340-59488353 chr17:59488339-59488360 chr17:59488875-59488883 chr17:59488337-59488355 chr17:59488587-59488600 chr17:59488868-59488886 chr17:59488590-59488603 chr17:59488342-59488352 chr17:59488534-59488547
14	RAD21	chr17:59483140-59491480	MCF-7	breast:	n/a	chr17:59488343-59488353 chr17:59488338-59488357 chr17:59491210-59491220 chr17:59488536-59488550 chr17:59488875-59488884 chr17:59488341-59488354 chr17:59487989-59487999 chr17:59488343-59488355
15	POLR2A	chr17:59486113-59491295	IMR90	lung:	n/a	n/a
16	MXI1	chr17:59487413-59490238	IMR90	lung:	n/a	n/a
17	POLR2A	chr17:59484175-59490331	ProgFib	skin:	n/a	n/a
18	POLR2A	chr17:59488270-59489110	HCT-116	colon:	n/a	n/a
19	MAX	chr17:59484138-59500997	MCF-7	breast:	n/a	chr17:59495541-59495552 chr17:59492978-59492987 chr17:59491213-59491223 chr17:59491485-59491495 chr17:59495570-59495581 chr17:59488910-59488926
20	RAD21	chr17:59488171-59488495	IMR90	lung:	n/a	chr17:59488343-59488353 chr17:59488338-59488357 chr17:59488341-59488354 chr17:59488343-59488355
21	POLR2A	chr17:59485546-59491030	SK-N-SH	brain:	n/a	n/a
22	SMC3	chr17:59485817-59492815	SK-N-SH	brain:	n/a	chr17:59488339-59488353 chr17:59491210-59491220 chr17:59488343-59488353
23	CTCF	chr17:59487959-59488549	IMR90	lung:	n/a	chr17:59488340-59488353 chr17:59488339-59488360 chr17:59488337-59488355 chr17:59488342-59488352 chr17:59488534-59488547
24	ZBTB7A	chr17:59488435-59490766	ECC-1	luminal epithelium:	n/a	n/a
25	CTCF	chr17:59488130-59489247	GM12878	blood:	n/a	chr17:59488340-59488353 chr17:59488339-59488360 chr17:59488875-59488883 chr17:59488337-59488355 chr17:59488587-59488600 chr17:59488868-59488886 chr17:59488590-59488603 chr17:59488342-59488352 chr17:59488534-59488547
26	NANOG	chr17:59488183-59488516	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr17:59488416-59490213	ECC-1	luminal epithelium:	n/a	n/a
28	MAX	chr17:59488137-59490396	SK-N-SH	brain:	n/a	chr17:59488910-59488926
29	CTCF	chr17:59488119-59488518	H1-hESC	embryonic stem cell:	n/a	chr17:59488340-59488353 chr17:59488339-59488360 chr17:59488337-59488355 chr17:59488342-59488352
30	HDAC2	chr17:59482687-59495676	MCF-7	breast:	n/a	chr17:59487075-59487094 chr17:59495598-59495612 chr17:59495596-59495610 chr17:59495599-59495613 chr17:59495595-59495609 chr17:59494256-59494265 chr17:59492574-59492588
31	MAZ	chr17:59486590-59490548	IMR90	lung:	n/a	chr17:59488910-59488926
32	POLR2A	chr17:59486508-59490170	SK-N-SH	brain:	n/a	n/a
33	SIN3A	chr17:59488165-59490819	H1-hESC	embryonic stem cell:	n/a	chr17:59488796-59488809 chr17:59489191-59489200 chr17:59488625-59488638 chr17:59488577-59488590
34	PBX3	chr17:59486670-59490297	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:59488443-59488493	A549	lung:	n/a
2	chr17:59488443-59488493	Hepatocyte	liver:	n/a
3	chr17:59488443-59488493	Caco-2	colon:	n/a
4	chr17:59488443-59488493	AG04450	lung:	fetal
5	chr17:59488443-59488493	PrEC	prostate:	n/a
6	chr17:59488443-59488493	NHBE	bronchial:	n/a
7	chr17:59488443-59488493	HPAEpiC	pulmonary alveolar:	n/a
8	chr17:59488443-59488493	PANC-1	pancreas:	n/a
9	chr17:59488443-59488493	GM12891	blood:	n/a
10	chr17:59488443-59488493	HCT-116	colon:	n/a
11	chr17:59488443-59488493	BE2_C	brain:	n/a
12	chr17:59488443-59488493	SK-N-SH	brain:	n/a
13	chr17:59488443-59488493	AG09309	skin:	n/a
14	chr17:59488443-59488493	IMR90	lung:	fetal
15	chr17:59488443-59488493	HNPCEpiC	eye:	n/a
16	chr17:59488443-59488493	HEK293	kidney:	embryo
17	chr17:59488443-59488493	BJ	skin:	n/a
18	chr17:59488443-59488493	AG10803	skin:	n/a
19	chr17:59488443-59488493	ECC-1	luminal epithelium:	n/a
20	chr17:59488443-59488493	MCF-7	breast:	n/a
21	chr17:59488443-59488493	HRPEpiC	eye:	n/a
22	chr17:59488443-59488493	SK-N-SH_RA	brain:	n/a
23	chr17:59488443-59488493	HepG2	liver:	n/a
24	chr17:59488443-59488493	GM06990	blood:	n/a
25	chr17:59488443-59488493	LNCaP	prostate:	n/a
26	chr17:59488443-59488493	AoSMC	blood vessel:	n/a
27	chr17:59488443-59488493	HMEC	breast:	n/a
28	chr17:59488443-59488493	HRE	kidney:	n/a
29	chr17:59488443-59488493	GM12878	blood:	n/a
30	chr17:59488443-59488493	ovcar-3	ovarian:	n/a
31	chr17:59488443-59488493	HCF	heart:	n/a
32	chr17:59488443-59488493	HCM	heart:	n/a
33	chr17:59488443-59488493	HEEpiC	esophagus:	n/a
34	chr17:59488443-59488493	HAEpiC	amniotic membrane:	n/a
35	chr17:59488443-59488493	NHDF-neo	bronchial:	n/a
36	chr17:59488443-59488493	SK-N-MC	brain:	n/a
37	chr17:59488443-59488493	CMK	blood:	n/a
38	chr17:59488443-59488493	HIPEpiC	eye:	n/a
39	chr17:59488443-59488493	SKMC	muscle:	n/a
40	chr17:59488443-59488493	NH-A	brain:	n/a
41	chr17:59488443-59488493	GM19239	blood:	n/a
42	chr17:59488443-59488493	MCF10A-Er-Src	breast:	n/a
43	chr17:59488443-59488493	Jurkat	blood:	n/a
44	chr17:59488443-59488493	HL-60	blood:	n/a
45	chr17:59488443-59488493	AG04449	skin:	fetal
46	chr17:59488443-59488493	ProgFib	skin:	n/a
47	chr17:59488443-59488493	GM12892	blood:	n/a
48	chr17:59488443-59488493	NB4	blood:	n/a
49	chr17:59488443-59488493	HRCEpiC	kidney:	n/a
50	chr17:59488443-59488493	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:59488009..59490784-chr17:78119613..78122104,2	MCF-7	breast:
2	chr17:59470525..59474011-chr17:59486288..59490375,89	MCF-7	breast:
3	chr17:59487822..59491370-chr20:49345755..49351152,8	MCF-7	breast:
4	chr17:59486475..59488762-chr20:45887507..45889647,2	MCF-7	breast:
5	chr17:57064353..57067451-chr17:59486567..59489337,3	MCF-7	breast:
6	chr17:59415713..59496229-chr20:49401322..49431802,760	MCF-7	breast:
7	chr17:59079366..59079901-chr17:59488032..59488748,2	MCF-7	breast:
8	chr17:59488147..59491206-chr17:73773645..73776030,4	MCF-7	breast:
9	chr16:85588910..85591052-chr17:59486534..59488510,2	MCF-7	breast:
10	chr17:59487742..59490467-chr20:52208536..52212416,5	MCF-7	breast:
11	chr17:59488387..59491331-chr17:73367342..73369969,2	MCF-7	breast:
12	chr12:14922167..14924156-chr17:59485855..59488624,2	MCF-7	breast:
13	chr17:59486721..59489555-chr19:54973484..54975427,2	MCF-7	breast:
14	chr17:59485117..59489801-chr22:29195073..29197990,4	MCF-7	breast:
15	chr1:41155776..41157819-chr17:59487564..59490052,2	MCF-7	breast:
16	chr17:59485603..59490421-chr20:49409438..49412592,198	MCF-7	breast:
17	chr17:57076071..57077783-chr17:59486729..59488516,2	MCF-7	breast:
18	chr17:59487230..59489642-chr5:6632867..6634401,2	MCF-7	breast:
19	chr17:59487144..59488865-chr3:64487071..64489605,2	MCF-7	breast:
20	chr17:59487872..59488837-chr17:59628277..59629342,5	MCF-7	breast:
21	chr1:219876789..219878405-chr17:59486605..59488633,2	MCF-7	breast:
22	chr17:59487584..59490320-chr17:60003961..60006356,2	MCF-7	breast:
23	chr14:38063644..38065305-chr17:59487657..59489465,2	MCF-7	breast:
24	chr17:59486098..59489964-chr20:45947329..45951517,6	MCF-7	breast:
25	chr17:59488052..59488861-chr17:59628476..59629187,2	MCF-7	breast:
26	chr17:59488344..59489973-chr17:73719352..73722145,2	MCF-7	breast:
27	chr17:59079471..59082667-chr17:59485930..59489124,3	MCF-7	breast:
28	chr17:59486789..59493376-chr20:46130669..46135131,5	MCF-7	breast:
29	chr17:59488402..59491332-chr5:170814071..170816184,2	MCF-7	breast:
30	chr17:59485646..59489353-chr20:52553682..52557868,4	MCF-7	breast:
31	chr17:59486878..59488888-chr20:52405963..52408731,2	MCF-7	breast:
32	chr17:59486940..59488565-chr20:49345606..49347486,2	MCF-7	breast:
33	chr17:59488351..59489947-chr8:101320286..101322497,2	MCF-7	breast:
34	chr17:59487737..59488821-chr17:59651765..59652893,4	MCF-7	breast:
35	chr1:112489519..112492004-chr17:59487264..59488851,2	MCF-7	breast:
36	chr1:121483602..121485397-chr17:59486737..59488712,2	MCF-7	breast:
37	chr17:59487879..59490260-chr20:55840268..55844036,3	MCF-7	breast:
38	chr17:59487495..59490414-chr2:220361426..220363256,2	MCF-7	breast:
39	chr17:59486762..59488545-chr20:49347784..49350072,2	MCF-7	breast:
40	chr17:57861160..57863240-chr17:59486550..59489513,2	MCF-7	breast:
41	chr12:120728256..120729969-chr17:59488403..59490292,2	MCF-7	breast:
42	chr1:152018576..152021368-chr17:59488179..59489785,2	MCF-7	breast:
43	chr17:59477427..59479626-chr17:59488065..59490134,11	MCF-7	breast:
44	chr17:59476401..59478732-chr17:59488339..59490282,10	MCF-7	breast:
45	chr17:59486998..59489266-chr20:45978277..45980916,2	MCF-7	breast:
46	chr15:51570778..51573248-chr17:59486536..59489007,2	MCF-7	breast:
47	chr17:59488148..59489737-chr7:158619933..158622291,2	MCF-7	breast:
48	chr1:153584110..153586999-chr17:59487265..59488769,2	MCF-7	breast:
49	chr17:59487467..59489683-chr20:55680392..55683930,3	MCF-7	breast:
50	chr17:56734938..56737169-chr17:59487119..59490178,3	MCF-7	breast:

Variant related genes	Relation type
C17orf82	TF binding region
C17orf82	CpG island
ENSG00000171385	Chromatin interaction
ENSG00000155130	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000108506	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000085433	Chromatin interaction
ENSG00000136603	Chromatin interaction
ENSG00000103326	Chromatin interaction
ENSG00000034677	Chromatin interaction
ENSG00000206652	Chromatin interaction
ENSG00000132481	Chromatin interaction
ENSG00000129514	Chromatin interaction
ENSG00000108423	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000226471	Chromatin interaction
ENSG00000072195	Chromatin interaction
ENSG00000231078	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000267801	Chromatin interaction
ENSG00000264853	Chromatin interaction
ENSG00000066136	Chromatin interaction
ENSG00000089157	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000102225	Chromatin interaction
ENSG00000141376	Chromatin interaction
ENSG00000100219	Chromatin interaction
ENSG00000037474	Chromatin interaction
ENSG00000081019	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000108479	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000231437	Chromatin interaction
ENSG00000272145	Chromatin interaction
ENSG00000108443	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000259701	Chromatin interaction
ENSG00000231128	Chromatin interaction
ENSG00000163191	Chromatin interaction
ENSG00000141543	Chromatin interaction
ENSG00000267637	Chromatin interaction
ENSG00000268603	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000197837	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000124243	Chromatin interaction
ENSG00000168137	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000236352	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000132470	Chromatin interaction
ENSG00000139725	Chromatin interaction
ENSG00000181163	Chromatin interaction
ENSG00000212694	Chromatin interaction
ENSG00000216168	Chromatin interaction
ENSG00000182909	Chromatin interaction
ENSG00000188643	Chromatin interaction
ENSG00000008513	Chromatin interaction
ENSG00000206573	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000117868	Chromatin interaction
ENSG00000145545	Chromatin interaction
ENSG00000139865	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs4459608	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs57045595	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs58036240	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs58832799	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs59382073	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs59430864	0.85[ASN][1000 genomes]
rs60549606	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61764069	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs734375	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73991913	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73991919	0.90[AMR][1000 genomes]
rs758600	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065939	chr17:59283350-59517730	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	331 gene(s)	inside rSNPs	diseases
2	nsv833505	chr17:59323466-59518007	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	326 gene(s)	inside rSNPs	diseases
3	nsv833506	chr17:59362377-59562984	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
4	nsv518130	chr17:59456589-59491281	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	265 gene(s)	inside rSNPs	diseases
5	esv1796927	chr17:59460119-59495319	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	270 gene(s)	inside rSNPs	diseases
6	nsv908663	chr17:59464069-59521310	Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	278 gene(s)	inside rSNPs	diseases
7	nsv908664	chr17:59465697-59491030	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	261 gene(s)	inside rSNPs	diseases
8	nsv908665	chr17:59470193-59494574	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	264 gene(s)	inside rSNPs	diseases
9	nsv908666	chr17:59470842-59489822	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	253 gene(s)	inside rSNPs	diseases
10	nsv908667	chr17:59471151-59491030	Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	256 gene(s)	inside rSNPs	diseases
11	nsv908668	chr17:59471151-59494574	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	263 gene(s)	inside rSNPs	diseases
12	nsv908669	chr17:59471372-59491030	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
13	nsv908670	chr17:59471372-59494574	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	262 gene(s)	inside rSNPs	diseases
14	nsv908671	chr17:59475888-59494574	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
15	nsv908672	chr17:59476062-59494574	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59485400-59488600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:59485800-59489000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
3	chr17:59486200-59489800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr17:59486400-59490600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
5	chr17:59486400-59490800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr17:59486600-59489200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
7	chr17:59486600-59491000	Active TSS	Aorta	Aorta
8	chr17:59487000-59488600	Enhancers	Pancreas	Pancrea
9	chr17:59487000-59488600	Enhancers	Spleen	Spleen
10	chr17:59487000-59488800	Bivalent Enhancer	HUVEC	blood vessel
11	chr17:59487000-59489400	Weak transcription	K562	blood
12	chr17:59487000-59489800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
13	chr17:59487200-59489400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
14	chr17:59487400-59488800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr17:59487400-59489000	Bivalent Enhancer	Fetal Thymus	thymus
16	chr17:59487400-59489000	Bivalent Enhancer	GM12878-XiMat	blood
17	chr17:59487400-59490400	Bivalent Enhancer	Fetal Brain Male	brain
18	chr17:59487600-59488600	Enhancers	Lung	lung
19	chr17:59487600-59488800	Weak transcription	A549	lung
20	chr17:59487600-59488800	Weak transcription	HMEC	breast
21	chr17:59487600-59488800	Weak transcription	HSMM	muscle
22	chr17:59487600-59489000	Weak transcription	Hela-S3	cervix
23	chr17:59487600-59489400	Weak transcription	HepG2	liver
24	chr17:59487600-59490800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
25	chr17:59487800-59489200	Bivalent/Poised TSS	Psoas Muscle	Psoas
26	chr17:59487800-59489800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
27	chr17:59487800-59489800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
28	chr17:59487800-59489800	Active TSS	Right Atrium	heart
29	chr17:59487800-59490400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr17:59487800-59490600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
31	chr17:59487800-59490600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
32	chr17:59487800-59490800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
33	chr17:59488000-59488600	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr17:59488000-59489000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr17:59488000-59489000	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
36	chr17:59488000-59489200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr17:59488000-59489600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:59488000-59489600	Flanking Bivalent TSS/Enh	Thymus	Thymus
39	chr17:59488000-59489800	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
40	chr17:59488000-59489800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr17:59488000-59489800	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
42	chr17:59488000-59490200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
43	chr17:59488000-59490200	Active TSS	Muscle Satellite Cultured Cells	--
44	chr17:59488000-59490400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
45	chr17:59488000-59490600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
46	chr17:59488000-59490600	Active TSS	Fetal Lung	lung
47	chr17:59488000-59490800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
48	chr17:59488000-59490800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr17:59488200-59488600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr17:59488200-59488600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

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