Variant report

Variant	rs58036240
Chromosome Location	chr17:59489787-59489788
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:279)
CpG islands
(count:61)
Chromatin interactive
region (count:134)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PAX5	chr17:59489711-59490060	GM12878	blood:	n/a	n/a
2	CTCF	chr17:59489753-59490043	ECC-1	luminal epithelium:	n/a	n/a
3	CTCF	chr17:59489755-59490057	GM10266	blood:	n/a	n/a
4	CTCF	chr17:59489726-59490106	Spleen_OC	spleen:	n/a	n/a
5	SIX5	chr17:59489498-59490193	A549	lung:	n/a	n/a
6	RXRA	chr17:59489732-59490028	GM12878	blood:	n/a	n/a
7	YY1	chr17:59489559-59490181	SK-N-SH_RA	brain:	n/a	n/a
8	MBD4	chr17:59489670-59490180	HepG2	liver:	n/a	n/a
9	CTCF	chr17:59489768-59490010	MCF-7	breast:	n/a	n/a
10	RAD21	chr17:59489728-59490109	GM12878	blood:	n/a	n/a
11	MAX	chr17:59489358-59490419	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr17:59489694-59490065	SK-N-SH_RA	brain:	n/a	n/a
13	POLR2A	chr17:59489427-59490128	MCF10A-Er-Src	breast:	n/a	n/a
14	NFIC	chr17:59489653-59490526	HepG2	liver:	n/a	n/a
15	TCF12	chr17:59489128-59490537	A549	lung:	n/a	n/a
16	POU2F2	chr17:59489765-59490101	GM12878	blood:	n/a	n/a
17	TFAP2C	chr17:59489352-59490198	Hela-S3	cervix:	n/a	n/a
18	MAZ	chr17:59489750-59490439	HepG2	liver:	n/a	n/a
19	MEF2A	chr17:59485767-59490640	SK-N-SH	brain:	n/a	chr17:59489068-59489076
20	JUND	chr17:59489446-59490185	A549	lung:	n/a	n/a
21	CTCF	chr17:59489640-59490088	T-47D	breast:	n/a	n/a
22	GATA3	chr17:59489693-59490109	T-47D	breast:	n/a	n/a
23	MAX	chr17:59489260-59491073	HepG2	liver:	n/a	n/a
24	GABPA	chr17:59489692-59490455	H1-hESC	embryonic stem cell:	n/a	n/a
25	SP1	chr17:59489697-59490030	GM12878	blood:	n/a	n/a
26	MAX	chr17:59489737-59490526	H1-hESC	embryonic stem cell:	n/a	n/a
27	BHLHE40	chr17:59489500-59490043	GM12878	blood:	n/a	n/a
28	CTCF	chr17:59489775-59490040	LNCaP	prostate:	n/a	n/a
29	ZNF143	chr17:59488142-59490296	H1-hESC	embryonic stem cell:	n/a	n/a
30	RAD21	chr17:59489382-59490427	H1-hESC	embryonic stem cell:	n/a	n/a
31	TAF1	chr17:59489397-59490026	A549	lung:	n/a	n/a
32	CHD2	chr17:59489746-59490497	H1-hESC	embryonic stem cell:	n/a	n/a
33	MTA3	chr17:59489603-59490147	GM12878	blood:	n/a	n/a
34	RAD21	chr17:59489446-59490386	A549	lung:	n/a	n/a
35	ZBTB7A	chr17:59488540-59490591	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr17:59489465-59490076	HUVEC	blood vessel:	n/a	n/a
37	RAD21	chr17:59489579-59490265	ECC-1	luminal epithelium:	n/a	n/a
38	POLR2A	chr17:59489768-59490903	HepG2	liver:	n/a	n/a
39	EBF1	chr17:59489733-59489931	GM12878	blood:	n/a	n/a
40	SIN3AK20	chr17:59489260-59490566	SK-N-SH	brain:	n/a	n/a
41	YY1	chr17:59489730-59490032	A549	lung:	n/a	n/a
42	HDAC2	chr17:59489543-59490414	HepG2	liver:	n/a	n/a
43	YY1	chr17:59489418-59490162	SK-N-SH	brain:	n/a	n/a
44	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
45	CTCF	chr17:59489751-59490043	Lung_OC	lung:	n/a	n/a
46	ARID3A	chr17:59489747-59490228	HepG2	liver:	n/a	n/a
47	TCF12	chr17:59489565-59490252	ECC-1	luminal epithelium:	n/a	n/a
48	MYC	chr17:59489458-59490045	MCF10A-Er-Src	breast:	n/a	n/a
49	FOXM1	chr17:59489686-59490004	GM12878	blood:	n/a	n/a
50	GABPA	chr17:59489726-59490331	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:59489784-59489834	HRPEpiC	eye:	n/a
2	chr17:59489784-59489834	GM12891	blood:	n/a
3	chr17:59489784-59489834	HEEpiC	esophagus:	n/a
4	chr17:59489784-59489834	HRCEpiC	kidney:	n/a
5	chr17:59489784-59489834	BE2_C	brain:	n/a
6	chr17:59489784-59489834	U87	brain:	n/a
7	chr17:59489784-59489834	AG10803	skin:	n/a
8	chr17:59489784-59489834	GM12878	blood:	n/a
9	chr17:59489784-59489834	T-47D	breast:	n/a
10	chr17:59489784-59489834	ovcar-3	ovarian:	n/a
11	chr17:59489784-59489834	SK-N-SH	brain:	n/a
12	chr17:59489784-59489834	SKMC	muscle:	n/a
13	chr17:59489784-59489834	HCT-116	colon:	n/a
14	chr17:59489784-59489834	HEK293	kidney:	embryo
15	chr17:59489784-59489834	AG04450	lung:	fetal
16	chr17:59489784-59489834	NT2-D1	testis:	n/a
17	chr17:59489784-59489834	Jurkat	blood:	n/a
18	chr17:59489784-59489834	Hepatocyte	liver:	n/a
19	chr17:59489784-59489834	ProgFib	skin:	n/a
20	chr17:59489784-59489834	HRE	kidney:	n/a
21	chr17:59489784-59489834	PFSK-1	brain:	n/a
22	chr17:59489784-59489834	HMEC	breast:	n/a
23	chr17:59489784-59489834	GM12892	blood:	n/a
24	chr17:59489784-59489834	HCM	heart:	n/a
25	chr17:59489784-59489834	HAEpiC	amniotic membrane:	n/a
26	chr17:59489784-59489834	K562	blood:	n/a
27	chr17:59489784-59489834	Hela-S3	cervix:	n/a
28	chr17:59489784-59489834	HPAEpiC	pulmonary alveolar:	n/a
29	chr17:59489784-59489834	HIPEpiC	eye:	n/a
30	chr17:59489784-59489834	HUVEC	blood vessel:	n/a
31	chr17:59489784-59489834	CMK	blood:	n/a
32	chr17:59489784-59489834	SK-N-MC	brain:	n/a
33	chr17:59489784-59489834	NB4	blood:	n/a
34	chr17:59489784-59489834	ECC-1	luminal epithelium:	n/a
35	chr17:59489784-59489834	GM19239	blood:	n/a
36	chr17:59489784-59489834	IMR90	lung:	fetal
37	chr17:59489784-59489834	PrEC	prostate:	n/a
38	chr17:59489784-59489834	PANC-1	pancreas:	n/a
39	chr17:59489784-59489834	HL-60	blood:	n/a
40	chr17:59489784-59489834	HCF	heart:	n/a
41	chr17:59489784-59489834	NHBE	bronchial:	n/a
42	chr17:59489784-59489834	BJ	skin:	n/a
43	chr17:59489784-59489834	NH-A	brain:	n/a
44	chr17:59489784-59489834	MCF10A-Er-Src	breast:	n/a
45	chr17:59489784-59489834	SK-N-SH_RA	brain:	n/a
46	chr17:59489784-59489834	HCPEpiC	choroid plexus:	n/a
47	chr17:59489784-59489834	LNCaP	prostate:	n/a
48	chr17:59489784-59489834	RPTEC	kidney:	n/a
49	chr17:59489784-59489834	GM06990	blood:	n/a
50	chr17:59489784-59489834	SAEC	small airway:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:59489469..59490241-chr20:55845005..55845901,3	MCF-7	breast:
2	chr17:59489404..59490020-chr3:111410090..111410766,2	MCF-7	breast:
3	chr17:59488009..59490784-chr17:78119613..78122104,2	MCF-7	breast:
4	chr17:59489661..59490440-chr17:59653693..59654566,2	MCF-7	breast:
5	chr17:59489694..59490861-chr17:59502803..59503675,3	MCF-7	breast:
6	chr17:59470525..59474011-chr17:59486288..59490375,89	MCF-7	breast:
7	chr17:59487822..59491370-chr20:49345755..49351152,8	MCF-7	breast:
8	chr12:116713817..116716728-chr17:59488795..59490962,2	MCF-7	breast:
9	chr17:59489649..59492493-chr3:119811877..119814556,2	MCF-7	breast:
10	chr17:59489520..59490149-chr20:55827449..55828309,2	MCF-7	breast:
11	chr17:59489463..59489973-chr17:59661262..59662077,2	MCF-7	breast:
12	chr17:59488630..59491909-chr20:52682988..52685576,3	MCF-7	breast:
13	chr17:59489126..59490399-chr17:59644784..59645856,3	MCF-7	breast:
14	chr17:59415713..59496229-chr20:49401322..49431802,760	MCF-7	breast:
15	chr17:59488147..59491206-chr17:73773645..73776030,4	MCF-7	breast:
16	chr17:59489674..59490313-chr17:59564952..59565665,2	MCF-7	breast:
17	chr17:59487742..59490467-chr20:52208536..52212416,5	MCF-7	breast:
18	chr17:59489585..59490693-chr20:49409810..49410733,3	MCF-7	breast:
19	chr17:57936511..57937414-chr17:59489781..59490328,2	MCF-7	breast:
20	chr17:59488387..59491331-chr17:73367342..73369969,2	MCF-7	breast:
21	chr1:202779094..202781986-chr17:59489238..59490887,2	MCF-7	breast:
22	chr17:59312551..59313435-chr17:59489579..59490104,2	MCF-7	breast:
23	chr17:59489293..59491949-chr8:125051873..125054864,2	MCF-7	breast:
24	chr17:59489613..59491206-chr17:59800419..59803266,2	MCF-7	breast:
25	chr17:59485117..59489801-chr22:29195073..29197990,4	MCF-7	breast:
26	chr17:59466830..59467981-chr17:59489440..59490777,4	MCF-7	breast:
27	chr1:41155776..41157819-chr17:59487564..59490052,2	MCF-7	breast:
28	chr17:59485603..59490421-chr20:49409438..49412592,198	MCF-7	breast:
29	chr14:68763338..68764227-chr17:59489430..59490294,2	MCF-7	breast:
30	chr17:59489419..59490363-chr20:52531972..52532900,2	MCF-7	breast:
31	chr17:59489592..59490427-chr21:38317002..38317522,3	MCF-7	breast:
32	chr17:59489569..59490613-chr17:59806350..59807273,3	MCF-7	breast:
33	chr17:59489678..59490370-chr20:45848502..45849271,2	MCF-7	breast:
34	chr17:59489492..59490051-chr17:59547690..59548679,2	MCF-7	breast:
35	chr17:57181543..57184200-chr17:59488935..59490643,2	MCF-7	breast:
36	chr17:57081949..57082809-chr17:59489487..59490386,4	MCF-7	breast:
37	chr17:59489184..59491261-chr17:59650345..59653673,119	MCF-7	breast:
38	chr17:59489445..59491262-chr17:59628200..59629244,34	MCF-7	breast:
39	chr17:59488984..59491525-chr17:73774194..73776083,3	MCF-7	breast:
40	chr17:59489384..59491650-chr6:42749691..42752599,2	MCF-7	breast:
41	chr17:59489460..59490356-chr17:59656181..59656834,2	MCF-7	breast:
42	chr17:59488637..59490196-chr17:73813357..73815941,2	MCF-7	breast:
43	chr11:72144872..72145710-chr17:59489412..59490113,2	MCF-7	breast:
44	chr17:59489431..59490207-chr20:45838071..45838594,2	MCF-7	breast:
45	chr17:59475999..59476687-chr17:59489352..59490506,3	MCF-7	breast:
46	chr17:59487584..59490320-chr17:60003961..60006356,2	MCF-7	breast:
47	chr17:59489572..59490208-chr17:59646822..59647354,2	MCF-7	breast:
48	chr17:59488570..59491510-chr6:31618990..31620979,2	MCF-7	breast:
49	chr17:59489145..59490826-chr17:59913944..59915515,20	MCF-7	breast:
50	chr17:59489517..59490423-chr5:139348063..139348948,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267280	TF binding region
ENSG00000267280	CpG island
ENSG00000254249	Chromatin interaction
ENSG00000103326	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000124243	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000139725	Chromatin interaction
ENSG00000181171	Chromatin interaction
ENSG00000072195	Chromatin interaction
ENSG00000100219	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000141543	Chromatin interaction
ENSG00000212694	Chromatin interaction
ENSG00000236352	Chromatin interaction
ENSG00000181163	Chromatin interaction
ENSG00000132470	Chromatin interaction
ENSG00000034677	Chromatin interaction
ENSG00000103266	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000247828	Chromatin interaction
ENSG00000260021	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000112624	Chromatin interaction
ENSG00000141376	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000228288	Chromatin interaction
ENSG00000264853	Chromatin interaction
ENSG00000108479	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000242622	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000268603	Chromatin interaction
ENSG00000265595	Chromatin interaction
ENSG00000206573	Chromatin interaction
ENSG00000168137	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000066136	Chromatin interaction
ENSG00000206652	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000081019	Chromatin interaction
ENSG00000162129	Chromatin interaction
ENSG00000102225	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000231128	Chromatin interaction
ENSG00000164180	Chromatin interaction
ENSG00000240891	Chromatin interaction
ENSG00000155130	Chromatin interaction
ENSG00000108506	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000085433	Chromatin interaction
ENSG00000224738	Chromatin interaction
ENSG00000108395	Chromatin interaction
ENSG00000231437	Chromatin interaction
ENSG00000171385	Chromatin interaction
ENSG00000272145	Chromatin interaction
ENSG00000254402	Chromatin interaction
ENSG00000123066	Chromatin interaction
ENSG00000082701	Chromatin interaction
ENSG00000226471	Chromatin interaction
ENSG00000104522	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000101132	Chromatin interaction
ENSG00000132478	Chromatin interaction
ENSG00000244687	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs2286528	0.81[AFR][1000 genomes]
rs4459608	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57045595	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58832799	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59382073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59430864	1.00[ASN][1000 genomes]
rs60549606	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61068714	0.83[ASN][1000 genomes]
rs61764069	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs730562	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs734375	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73991913	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73991919	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs758600	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:127 , 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	chr17:59486600-59491000	Active TSS	Aorta	Aorta
5	chr17:59487000-59489800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
6	chr17:59487400-59490400	Bivalent Enhancer	Fetal Brain Male	brain
7	chr17:59487600-59490800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
8	chr17:59487800-59489800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
9	chr17:59487800-59489800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
10	chr17:59487800-59489800	Active TSS	Right Atrium	heart
11	chr17:59487800-59490400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr17:59487800-59490600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
13	chr17:59487800-59490600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
14	chr17:59487800-59490800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr17:59488000-59489800	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
16	chr17:59488000-59489800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr17:59488000-59489800	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
18	chr17:59488000-59490200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
19	chr17:59488000-59490200	Active TSS	Muscle Satellite Cultured Cells	--
20	chr17:59488000-59490400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
21	chr17:59488000-59490600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr17:59488000-59490600	Active TSS	Fetal Lung	lung
23	chr17:59488000-59490800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
24	chr17:59488000-59490800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr17:59488200-59489800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
26	chr17:59488200-59490200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr17:59488200-59490200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr17:59488200-59490200	Active TSS	Left Ventricle	heart
29	chr17:59488200-59490400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
30	chr17:59488200-59490400	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr17:59488200-59490400	Active TSS	NHLF	lung
32	chr17:59488200-59490600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr17:59488200-59490600	Active TSS	Brain Angular Gyrus	brain
34	chr17:59488200-59490600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
35	chr17:59488200-59490600	Active TSS	Esophagus	oesophagus
36	chr17:59488200-59490600	Active TSS	Gastric	stomach
37	chr17:59488200-59490800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
38	chr17:59488200-59490800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
39	chr17:59488200-59490800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr17:59488200-59490800	Active TSS	Brain Anterior Caudate	brain
41	chr17:59488200-59491000	Active TSS	Fetal Kidney	kidney
42	chr17:59488400-59489800	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
43	chr17:59488400-59489800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
44	chr17:59488400-59490200	Active TSS	Brain Substantia Nigra	brain
45	chr17:59488400-59490200	Weak transcription	Fetal Heart	heart
46	chr17:59488400-59490200	Active TSS	Small Intestine	intestine
47	chr17:59488400-59490400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr17:59488400-59490400	Flanking Active TSS	Liver	Liver
49	chr17:59488400-59491000	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr17:59488400-59491000	Flanking Active TSS	Placenta	Placenta

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