Variant report

Variant	rs59430864
Chromosome Location	chr17:59489008-59489009
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:158)
CpG islands
(count:61)
Chromatin interactive
region (count:75)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:158 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr17:59488940-59489090	HCFaa	heart:	n/a	n/a
2	CTCF	chr17:59488884-59489113	MCF-7	breast:	n/a	n/a
3	CTCF	chr17:59488824-59489122	MCF-7	breast:	n/a	chr17:59488875-59488883 chr17:59488868-59488886
4	CTCF	chr17:59488860-59489010	HCM	heart:	n/a	chr17:59488875-59488883 chr17:59488868-59488886
5	SIN3AK20	chr17:59486979-59489165	SK-N-SH	brain:	n/a	n/a
6	CTCF	chr17:59488940-59489090	AG04450	lung:	n/a	n/a
7	EBF1	chr17:59488900-59489151	GM12878	blood:	n/a	chr17:59489055-59489066
8	CTCF	chr17:59488960-59489110	BE2_C	brain:	n/a	n/a
9	YY1	chr17:59488637-59489186	SK-N-SH_RA	brain:	n/a	chr17:59489124-59489135
10	MEF2A	chr17:59485767-59490640	SK-N-SH	brain:	n/a	chr17:59489068-59489076
11	CTCF	chr17:59488940-59489090	Caco-2	colon:	n/a	n/a
12	MAX	chr17:59488561-59489135	H1-hESC	embryonic stem cell:	n/a	chr17:59488910-59488926
13	CTCF	chr17:59488920-59489070	AG04450	lung:	n/a	n/a
14	CTCF	chr17:59488860-59489010	GM12865	blood:	n/a	chr17:59488875-59488883 chr17:59488868-59488886
15	ZNF143	chr17:59488142-59490296	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr17:59488434-59489247	ECC-1	luminal epithelium:	n/a	n/a
17	CTCF	chr17:59488940-59489090	GM12872	blood:	n/a	n/a
18	CTCF	chr17:59488960-59489110	BJ	skin:	n/a	n/a
19	CTCF	chr17:59488920-59489070	HPF	lung:	n/a	n/a
20	CTCF	chr17:59488940-59489090	GM06990	blood:	n/a	n/a
21	ZBTB7A	chr17:59488540-59490591	ECC-1	luminal epithelium:	n/a	n/a
22	CTCF	chr17:59488920-59489070	NHLF	lung:	n/a	n/a
23	CTCF	chr17:59488980-59489130	NHDF-neo	bronchial:	n/a	n/a
24	EP300	chr17:59489007-59489355	T-47D	breast:	n/a	n/a
25	CTCF	chr17:59488813-59489124	GM19239	blood:	n/a	chr17:59488875-59488883 chr17:59488868-59488886
26	TCF7L2	chr17:59487998-59489013	HCT-116	colon:	n/a	n/a
27	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
28	CTCF	chr17:59489000-59489150	GM12869	blood:	n/a	n/a
29	CTCF	chr17:59488834-59489106	T-47D	breast:	n/a	chr17:59488875-59488883 chr17:59488868-59488886
30	POLR2A	chr17:59488779-59490150	HCT-116	colon:	n/a	n/a
31	MAX	chr17:59488599-59490228	ECC-1	luminal epithelium:	n/a	chr17:59488910-59488926
32	CTCF	chr17:59488880-59489030	AG04449	skin:	n/a	n/a
33	ELF1	chr17:59488648-59490160	GM12878	blood:	n/a	chr17:59489126-59489138 chr17:59489243-59489255
34	MYC	chr17:59488815-59489010	MCF-7	breast:	n/a	chr17:59488910-59488926
35	CTCF	chr17:59488940-59489090	HCPEpiC	choroid plexus:	n/a	n/a
36	MAX	chr17:59488627-59490510	SK-N-SH	brain:	n/a	chr17:59488910-59488926
37	GATA3	chr17:59488912-59489327	T-47D	breast:	n/a	chr17:59489068-59489078
38	POLR2A	chr17:59488778-59489658	MCF-7	breast:	n/a	n/a
39	CTCF	chr17:59489000-59489150	GM06990	blood:	n/a	n/a
40	CTCF	chr17:59488940-59489090	HFF	foreskin:	n/a	n/a
41	TEAD4	chr17:59484276-59495088	A549	lung:	n/a	n/a
42	CTCF	chr17:59488980-59489130	HVMF	connective:	n/a	n/a
43	TEAD4	chr17:59487963-59490539	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr17:59488900-59489050	SAEC	small airway:	n/a	n/a
45	RAD21	chr17:59488655-59490470	HCT-116	colon:	n/a	chr17:59488875-59488884
46	CTCF	chr17:59488940-59489090	HEK293	kidney:	n/a	n/a
47	CTCF	chr17:59488960-59489110	GM12871	blood:	n/a	n/a
48	CTCF	chr17:59488990-59489093	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr17:59488880-59489030	GM12864	blood:	n/a	n/a
50	RAD21	chr17:59488804-59489120	H1-hESC	embryonic stem cell:	n/a	chr17:59488875-59488884

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:59488988-59489038	HUVEC	blood vessel:	n/a
2	chr17:59488988-59489038	PANC-1	pancreas:	n/a
3	chr17:59488988-59489038	HRE	kidney:	n/a
4	chr17:59488988-59489038	CMK	blood:	n/a
5	chr17:59488988-59489038	MCF-7	breast:	n/a
6	chr17:59488988-59489038	HPAEpiC	pulmonary alveolar:	n/a
7	chr17:59488988-59489038	PFSK-1	brain:	n/a
8	chr17:59488988-59489038	H1-hESC	embryonic stem cell:	embryo
9	chr17:59488988-59489038	K562	blood:	n/a
10	chr17:59488988-59489038	SKMC	muscle:	n/a
11	chr17:59488988-59489038	GM12892	blood:	n/a
12	chr17:59488988-59489038	PrEC	prostate:	n/a
13	chr17:59488988-59489038	SAEC	small airway:	n/a
14	chr17:59488988-59489038	HCT-116	colon:	n/a
15	chr17:59488988-59489038	AG09309	skin:	n/a
16	chr17:59488988-59489038	ProgFib	skin:	n/a
17	chr17:59488988-59489038	AoSMC	blood vessel:	n/a
18	chr17:59488988-59489038	T-47D	breast:	n/a
19	chr17:59488988-59489038	MCF10A-Er-Src	breast:	n/a
20	chr17:59488988-59489038	ECC-1	luminal epithelium:	n/a
21	chr17:59488988-59489038	NHDF-neo	bronchial:	n/a
22	chr17:59488988-59489038	NT2-D1	testis:	n/a
23	chr17:59488988-59489038	GM19239	blood:	n/a
24	chr17:59488988-59489038	HCF	heart:	n/a
25	chr17:59488988-59489038	AG04449	skin:	fetal
26	chr17:59488988-59489038	Hepatocyte	liver:	n/a
27	chr17:59488988-59489038	NHBE	bronchial:	n/a
28	chr17:59488988-59489038	GM06990	blood:	n/a
29	chr17:59488988-59489038	HCM	heart:	n/a
30	chr17:59488988-59489038	Caco-2	colon:	n/a
31	chr17:59488988-59489038	LNCaP	prostate:	n/a
32	chr17:59488988-59489038	HL-60	blood:	n/a
33	chr17:59488988-59489038	NH-A	brain:	n/a
34	chr17:59488988-59489038	HEK293	kidney:	embryo
35	chr17:59488988-59489038	HEEpiC	esophagus:	n/a
36	chr17:59488988-59489038	AG04450	lung:	fetal
37	chr17:59488988-59489038	HNPCEpiC	eye:	n/a
38	chr17:59488988-59489038	HRCEpiC	kidney:	n/a
39	chr17:59488988-59489038	A549	lung:	n/a
40	chr17:59488988-59489038	Hela-S3	cervix:	n/a
41	chr17:59488988-59489038	HIPEpiC	eye:	n/a
42	chr17:59488988-59489038	Jurkat	blood:	n/a
43	chr17:59488988-59489038	AG10803	skin:	n/a
44	chr17:59488988-59489038	HepG2	liver:	n/a
45	chr17:59488988-59489038	HAEpiC	amniotic membrane:	n/a
46	chr17:59488988-59489038	HRPEpiC	eye:	n/a
47	chr17:59488988-59489038	GM12878	blood:	n/a
48	chr17:59488988-59489038	SK-N-SH	brain:	n/a
49	chr17:59488988-59489038	BJ	skin:	n/a
50	chr17:59488988-59489038	ovcar-3	ovarian:	n/a

(count:75 , 50 per page) page: 1 2

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	chr12:116713817..116716728-chr17:59488795..59490962,2	MCF-7	breast:
5	chr17:59488630..59491909-chr20:52682988..52685576,3	MCF-7	breast:
6	chr17:57064353..57067451-chr17:59486567..59489337,3	MCF-7	breast:
7	chr17:59415713..59496229-chr20:49401322..49431802,760	MCF-7	breast:
8	chr17:59488147..59491206-chr17:73773645..73776030,4	MCF-7	breast:
9	chr17:59487742..59490467-chr20:52208536..52212416,5	MCF-7	breast:
10	chr17:59488387..59491331-chr17:73367342..73369969,2	MCF-7	breast:
11	chr17:59486721..59489555-chr19:54973484..54975427,2	MCF-7	breast:
12	chr17:59485117..59489801-chr22:29195073..29197990,4	MCF-7	breast:
13	chr1:41155776..41157819-chr17:59487564..59490052,2	MCF-7	breast:
14	chr17:59485603..59490421-chr20:49409438..49412592,198	MCF-7	breast:
15	chr17:59487230..59489642-chr5:6632867..6634401,2	MCF-7	breast:
16	chr17:57181543..57184200-chr17:59488935..59490643,2	MCF-7	breast:
17	chr17:59488984..59491525-chr17:73774194..73776083,3	MCF-7	breast:
18	chr17:59488637..59490196-chr17:73813357..73815941,2	MCF-7	breast:
19	chr17:59470667..59471725-chr17:59488553..59489465,8	MCF-7	breast:
20	chr17:59487584..59490320-chr17:60003961..60006356,2	MCF-7	breast:
21	chr17:59488570..59491510-chr6:31618990..31620979,2	MCF-7	breast:
22	chr14:38063644..38065305-chr17:59487657..59489465,2	MCF-7	breast:
23	chr17:59486098..59489964-chr20:45947329..45951517,6	MCF-7	breast:
24	chr17:56707849..56710455-chr17:59488567..59490591,3	MCF-7	breast:
25	chr17:59488344..59489973-chr17:73719352..73722145,2	MCF-7	breast:
26	chr17:59079471..59082667-chr17:59485930..59489124,3	MCF-7	breast:
27	chr17:59486789..59493376-chr20:46130669..46135131,5	MCF-7	breast:
28	chr17:59488402..59491332-chr5:170814071..170816184,2	MCF-7	breast:
29	chr17:59485646..59489353-chr20:52553682..52557868,4	MCF-7	breast:
30	chr17:59488351..59489947-chr8:101320286..101322497,2	MCF-7	breast:
31	chr17:59488616..59494924-chr20:52554630..52559372,9	MCF-7	breast:
32	chr17:59487879..59490260-chr20:55840268..55844036,3	MCF-7	breast:
33	chr17:59487495..59490414-chr2:220361426..220363256,2	MCF-7	breast:
34	chr17:57861160..57863240-chr17:59486550..59489513,2	MCF-7	breast:
35	chr12:120728256..120729969-chr17:59488403..59490292,2	MCF-7	breast:
36	chr1:152018576..152021368-chr17:59488179..59489785,2	MCF-7	breast:
37	chr17:59488661..59490672-chr20:48729350..48731210,2	MCF-7	breast:
38	chr17:59079506..59080341-chr17:59488921..59489759,2	MCF-7	breast:
39	chr17:59477427..59479626-chr17:59488065..59490134,11	MCF-7	breast:
40	chr17:59476401..59478732-chr17:59488339..59490282,10	MCF-7	breast:
41	chr17:59486998..59489266-chr20:45978277..45980916,2	MCF-7	breast:
42	chr17:59488148..59489737-chr7:158619933..158622291,2	MCF-7	breast:
43	chr17:59487467..59489683-chr20:55680392..55683930,3	MCF-7	breast:
44	chr17:56734938..56737169-chr17:59487119..59490178,3	MCF-7	breast:
45	chr17:59488495..59490414-chr20:49410870..49412182,25	MCF-7	breast:
46	chr1:112527808..112533804-chr17:59487383..59491538,7	MCF-7	breast:
47	chr17:59488637..59491687-chr20:49346765..49351004,5	MCF-7	breast:
48	chr12:120636290..120639093-chr17:59486664..59489640,2	MCF-7	breast:
49	chr17:56707801..56710950-chr17:59485321..59490857,5	MCF-7	breast:
50	chr17:59484671..59491871-chr20:55837745..55844407,10	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267280	TF binding region
C17orf82	TF binding region
ENSG00000267280	CpG island
C17orf82	CpG island
ENSG00000202077	Chromatin interaction
ENSG00000267637	Chromatin interaction
ENSG00000129514	Chromatin interaction
ENSG00000139865	Chromatin interaction
ENSG00000181163	Chromatin interaction
ENSG00000264853	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000164180	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000231437	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000206652	Chromatin interaction
ENSG00000226471	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000117868	Chromatin interaction
ENSG00000089157	Chromatin interaction
ENSG00000108443	Chromatin interaction
ENSG00000108395	Chromatin interaction
ENSG00000231078	Chromatin interaction
ENSG00000100219	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000072195	Chromatin interaction
ENSG00000265595	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000224738	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000085433	Chromatin interaction
ENSG00000272145	Chromatin interaction
ENSG00000212694	Chromatin interaction
ENSG00000268603	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000139725	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000236352	Chromatin interaction
ENSG00000141376	Chromatin interaction
ENSG00000132478	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000108506	Chromatin interaction
ENSG00000066136	Chromatin interaction
ENSG00000037474	Chromatin interaction
ENSG00000182909	Chromatin interaction
ENSG00000123066	Chromatin interaction
ENSG00000102225	Chromatin interaction
ENSG00000141543	Chromatin interaction
ENSG00000244687	Chromatin interaction
ENSG00000171385	Chromatin interaction
ENSG00000206573	Chromatin interaction
ENSG00000231128	Chromatin interaction
ENSG00000008513	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000145545	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000163191	Chromatin interaction
ENSG00000103326	Chromatin interaction
ENSG00000168137	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000034677	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000108479	Chromatin interaction
ENSG00000108423	Chromatin interaction
ENSG00000155130	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000124243	Chromatin interaction
ENSG00000132470	Chromatin interaction
ENSG00000247828	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000216168	Chromatin interaction
ENSG00000081019	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs4459608	1.00[ASN][1000 genomes]
rs57045595	1.00[ASN][1000 genomes]
rs58036240	1.00[ASN][1000 genomes]
rs58832799	1.00[ASN][1000 genomes]
rs59382073	1.00[ASN][1000 genomes]
rs60549606	1.00[ASN][1000 genomes]
rs61068714	0.83[ASN][1000 genomes]
rs61764069	1.00[ASN][1000 genomes]
rs730562	0.85[ASN][1000 genomes]
rs734375	1.00[ASN][1000 genomes]
rs73991913	1.00[ASN][1000 genomes]
rs73991919	0.85[ASN][1000 genomes]
rs758600	1.00[AMR][1000 genomes];1.00[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:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59486200-59489800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr17:59486400-59490600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr17:59486400-59490800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr17:59486600-59489200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
5	chr17:59486600-59491000	Active TSS	Aorta	Aorta
6	chr17:59487000-59489400	Weak transcription	K562	blood
7	chr17:59487000-59489800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
8	chr17:59487200-59489400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
9	chr17:59487400-59490400	Bivalent Enhancer	Fetal Brain Male	brain
10	chr17:59487600-59489400	Weak transcription	HepG2	liver
11	chr17:59487600-59490800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
12	chr17:59487800-59489200	Bivalent/Poised TSS	Psoas Muscle	Psoas
13	chr17:59487800-59489800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
14	chr17:59487800-59489800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
15	chr17:59487800-59489800	Active TSS	Right Atrium	heart
16	chr17:59487800-59490400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr17:59487800-59490600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
18	chr17:59487800-59490600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
19	chr17:59487800-59490800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
20	chr17:59488000-59489200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr17:59488000-59489600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:59488000-59489600	Flanking Bivalent TSS/Enh	Thymus	Thymus
23	chr17:59488000-59489800	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
24	chr17:59488000-59489800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr17:59488000-59489800	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
26	chr17:59488000-59490200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
27	chr17:59488000-59490200	Active TSS	Muscle Satellite Cultured Cells	--
28	chr17:59488000-59490400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
29	chr17:59488000-59490600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
30	chr17:59488000-59490600	Active TSS	Fetal Lung	lung
31	chr17:59488000-59490800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
32	chr17:59488000-59490800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr17:59488200-59489200	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr17:59488200-59489200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr17:59488200-59489200	Active TSS	Right Ventricle	heart
36	chr17:59488200-59489200	Bivalent/Poised TSS	NHEK	skin
37	chr17:59488200-59489400	Bivalent/Poised TSS	Primary T helper naive cells from peripheral blood	blood
38	chr17:59488200-59489400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr17:59488200-59489400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
40	chr17:59488200-59489800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
41	chr17:59488200-59490200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr17:59488200-59490200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr17:59488200-59490200	Active TSS	Left Ventricle	heart
44	chr17:59488200-59490400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr17:59488200-59490400	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr17:59488200-59490400	Active TSS	NHLF	lung
47	chr17:59488200-59490600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
48	chr17:59488200-59490600	Active TSS	Brain Angular Gyrus	brain
49	chr17:59488200-59490600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
50	chr17:59488200-59490600	Active TSS	Esophagus	oesophagus

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