Variant report

Variant	rs61764069
Chromosome Location	chr17:59489896-59489897
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:409)
CpG islands
(count:61)
Chromatin interactive
region (count:144)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr17:59489820-59489970	HCM	heart:	n/a	n/a
2	CTCF	chr17:59489840-59489990	GM06990	blood:	n/a	n/a
3	PAX5	chr17:59489711-59490060	GM12878	blood:	n/a	n/a
4	CTCF	chr17:59489753-59490043	ECC-1	luminal epithelium:	n/a	n/a
5	CTCF	chr17:59489755-59490057	GM10266	blood:	n/a	n/a
6	CTCF	chr17:59489820-59489970	AG10803	skin:	n/a	n/a
7	CTCF	chr17:59489820-59489970	HepG2	liver:	n/a	n/a
8	CTCF	chr17:59489726-59490106	Spleen_OC	spleen:	n/a	n/a
9	CTCF	chr17:59489820-59489970	GM12867	blood:	n/a	n/a
10	SIX5	chr17:59489498-59490193	A549	lung:	n/a	n/a
11	CTCF	chr17:59489860-59490010	WI-38	lung:	n/a	n/a
12	RXRA	chr17:59489732-59490028	GM12878	blood:	n/a	n/a
13	YY1	chr17:59489559-59490181	SK-N-SH_RA	brain:	n/a	n/a
14	JUND	chr17:59489857-59489970	H1-hESC	embryonic stem cell:	n/a	n/a
15	MBD4	chr17:59489670-59490180	HepG2	liver:	n/a	n/a
16	CTCF	chr17:59489768-59490010	MCF-7	breast:	n/a	n/a
17	RAD21	chr17:59489728-59490109	GM12878	blood:	n/a	n/a
18	MAX	chr17:59489358-59490419	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr17:59489694-59490065	SK-N-SH_RA	brain:	n/a	n/a
20	POLR2A	chr17:59489427-59490128	MCF10A-Er-Src	breast:	n/a	n/a
21	NFIC	chr17:59489653-59490526	HepG2	liver:	n/a	n/a
22	GTF2F1	chr17:59489851-59490042	H1-hESC	embryonic stem cell:	n/a	n/a
23	TCF12	chr17:59489128-59490537	A549	lung:	n/a	n/a
24	CEBPB	chr17:59489807-59490021	HepG2	liver:	n/a	n/a
25	POU2F2	chr17:59489765-59490101	GM12878	blood:	n/a	n/a
26	CTCF	chr17:59489820-59489970	HEEpiC	esophagus:	n/a	n/a
27	TFAP2C	chr17:59489352-59490198	Hela-S3	cervix:	n/a	n/a
28	TBP	chr17:59489870-59490804	HepG2	liver:	n/a	n/a
29	MAZ	chr17:59489750-59490439	HepG2	liver:	n/a	n/a
30	CTCF	chr17:59489800-59489950	HEEpiC	esophagus:	n/a	n/a
31	ZBTB7A	chr17:59489821-59490052	HepG2	liver:	n/a	n/a
32	MEF2A	chr17:59485767-59490640	SK-N-SH	brain:	n/a	chr17:59489068-59489076
33	JUND	chr17:59489446-59490185	A549	lung:	n/a	n/a
34	CTCF	chr17:59489640-59490088	T-47D	breast:	n/a	n/a
35	CTCF	chr17:59489820-59489970	HRE	kidney:	n/a	n/a
36	ZBTB7A	chr17:59489801-59490077	K562	blood:	n/a	n/a
37	CTCFL	chr17:59489813-59490016	K562	blood:	n/a	n/a
38	GATA3	chr17:59489693-59490109	T-47D	breast:	n/a	n/a
39	MAX	chr17:59489260-59491073	HepG2	liver:	n/a	n/a
40	GABPA	chr17:59489692-59490455	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr17:59489800-59489950	HCFaa	heart:	n/a	n/a
42	SP1	chr17:59489697-59490030	GM12878	blood:	n/a	n/a
43	MAX	chr17:59489737-59490526	H1-hESC	embryonic stem cell:	n/a	n/a
44	BHLHE40	chr17:59489500-59490043	GM12878	blood:	n/a	n/a
45	BRCA1	chr17:59489846-59489931	GM12878	blood:	n/a	n/a
46	CTCF	chr17:59489775-59490040	LNCaP	prostate:	n/a	n/a
47	ZNF143	chr17:59488142-59490296	H1-hESC	embryonic stem cell:	n/a	n/a
48	RAD21	chr17:59489382-59490427	H1-hESC	embryonic stem cell:	n/a	n/a
49	TAF1	chr17:59489397-59490026	A549	lung:	n/a	n/a
50	CTCF	chr17:59489820-59489970	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:59489852-59489902	HepG2	liver:	n/a
2	chr17:59489852-59489902	SKMC	muscle:	n/a
3	chr17:59489852-59489902	HEK293	kidney:	embryo
4	chr17:59489852-59489902	HCF	heart:	n/a
5	chr17:59489852-59489902	HL-60	blood:	n/a
6	chr17:59489852-59489902	NT2-D1	testis:	n/a
7	chr17:59489852-59489902	Hepatocyte	liver:	n/a
8	chr17:59489852-59489902	HRPEpiC	eye:	n/a
9	chr17:59489852-59489902	A549	lung:	n/a
10	chr17:59489852-59489902	MCF-7	breast:	n/a
11	chr17:59489852-59489902	HCPEpiC	choroid plexus:	n/a
12	chr17:59489852-59489902	T-47D	breast:	n/a
13	chr17:59489852-59489902	U87	brain:	n/a
14	chr17:59489852-59489902	ECC-1	luminal epithelium:	n/a
15	chr17:59489852-59489902	NB4	blood:	n/a
16	chr17:59489852-59489902	HAEpiC	amniotic membrane:	n/a
17	chr17:59489852-59489902	K562	blood:	n/a
18	chr17:59489852-59489902	GM12878	blood:	n/a
19	chr17:59489852-59489902	BJ	skin:	n/a
20	chr17:59489852-59489902	AG09319	gingival:	n/a
21	chr17:59489852-59489902	AG09309	skin:	n/a
22	chr17:59489852-59489902	ProgFib	skin:	n/a
23	chr17:59489852-59489902	ovcar-3	ovarian:	n/a
24	chr17:59489852-59489902	PANC-1	pancreas:	n/a
25	chr17:59489852-59489902	GM06990	blood:	n/a
26	chr17:59489852-59489902	PFSK-1	brain:	n/a
27	chr17:59489852-59489902	Jurkat	blood:	n/a
28	chr17:59489852-59489902	MCF10A-Er-Src	breast:	n/a
29	chr17:59489852-59489902	AG04450	lung:	fetal
30	chr17:59489852-59489902	SAEC	small airway:	n/a
31	chr17:59489852-59489902	IMR90	lung:	fetal
32	chr17:59489852-59489902	CMK	blood:	n/a
33	chr17:59489852-59489902	NHDF-neo	bronchial:	n/a
34	chr17:59489852-59489902	HNPCEpiC	eye:	n/a
35	chr17:59489852-59489902	HRE	kidney:	n/a
36	chr17:59489852-59489902	Hela-S3	cervix:	n/a
37	chr17:59489852-59489902	HPAEpiC	pulmonary alveolar:	n/a
38	chr17:59489852-59489902	HUVEC	blood vessel:	n/a
39	chr17:59489852-59489902	RPTEC	kidney:	n/a
40	chr17:59489852-59489902	HCM	heart:	n/a
41	chr17:59489852-59489902	HRCEpiC	kidney:	n/a
42	chr17:59489852-59489902	SK-N-MC	brain:	n/a
43	chr17:59489852-59489902	PrEC	prostate:	n/a
44	chr17:59489852-59489902	LNCaP	prostate:	n/a
45	chr17:59489852-59489902	NH-A	brain:	n/a
46	chr17:59489852-59489902	AoSMC	blood vessel:	n/a
47	chr17:59489852-59489902	NHBE	bronchial:	n/a
48	chr17:59489852-59489902	SK-N-SH	brain:	n/a
49	chr17:59489852-59489902	GM12892	blood:	n/a
50	chr17:59489852-59489902	AG04449	skin:	fetal

(count:144 , 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	chr17:59489834..59490453-chr17:59652319..59652838,2	MCF-7	breast:
19	chr17:59489585..59490693-chr20:49409810..49410733,3	MCF-7	breast:
20	chr17:57936511..57937414-chr17:59489781..59490328,2	MCF-7	breast:
21	chr17:59488387..59491331-chr17:73367342..73369969,2	MCF-7	breast:
22	chr1:202779094..202781986-chr17:59489238..59490887,2	MCF-7	breast:
23	chr17:59312551..59313435-chr17:59489579..59490104,2	MCF-7	breast:
24	chr17:59489293..59491949-chr8:125051873..125054864,2	MCF-7	breast:
25	chr17:59489613..59491206-chr17:59800419..59803266,2	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	chr17:59489874..59490819-chr17:59629776..59630756,2	MCF-7	breast:
47	chr17:59487584..59490320-chr17:60003961..60006356,2	MCF-7	breast:
48	chr17:59489819..59490342-chr17:59764278..59764797,2	MCF-7	breast:
49	chr17:59489572..59490208-chr17:59646822..59647354,2	MCF-7	breast:
50	chr17:59488570..59491510-chr6:31618990..31620979,2	MCF-7	breast:

No data

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

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

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

rs_ID	r²[population]
rs4459608	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57045595	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58036240	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58832799	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59382073	0.90[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]
rs730562	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs734375	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73991913	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:14 , 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	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
10	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
11	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
12	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
13	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
14	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	chr17:59486400-59490600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
2	chr17:59486400-59490800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr17:59486600-59491000	Active TSS	Aorta	Aorta
4	chr17:59487400-59490400	Bivalent Enhancer	Fetal Brain Male	brain
5	chr17:59487600-59490800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
6	chr17:59487800-59490400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr17:59487800-59490600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
8	chr17:59487800-59490600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
9	chr17:59487800-59490800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr17:59488000-59490200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
11	chr17:59488000-59490200	Active TSS	Muscle Satellite Cultured Cells	--
12	chr17:59488000-59490400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
13	chr17:59488000-59490600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
14	chr17:59488000-59490600	Active TSS	Fetal Lung	lung
15	chr17:59488000-59490800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
16	chr17:59488000-59490800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr17:59488200-59490200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr17:59488200-59490200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr17:59488200-59490200	Active TSS	Left Ventricle	heart
20	chr17:59488200-59490400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
21	chr17:59488200-59490400	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr17:59488200-59490400	Active TSS	NHLF	lung
23	chr17:59488200-59490600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr17:59488200-59490600	Active TSS	Brain Angular Gyrus	brain
25	chr17:59488200-59490600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
26	chr17:59488200-59490600	Active TSS	Esophagus	oesophagus
27	chr17:59488200-59490600	Active TSS	Gastric	stomach
28	chr17:59488200-59490800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
29	chr17:59488200-59490800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr17:59488200-59490800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr17:59488200-59490800	Active TSS	Brain Anterior Caudate	brain
32	chr17:59488200-59491000	Active TSS	Fetal Kidney	kidney
33	chr17:59488400-59490200	Active TSS	Brain Substantia Nigra	brain
34	chr17:59488400-59490200	Weak transcription	Fetal Heart	heart
35	chr17:59488400-59490200	Active TSS	Small Intestine	intestine
36	chr17:59488400-59490400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr17:59488400-59490400	Flanking Active TSS	Liver	Liver
38	chr17:59488400-59491000	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr17:59488400-59491000	Flanking Active TSS	Placenta	Placenta
40	chr17:59488600-59490000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr17:59488600-59490200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr17:59488600-59490600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr17:59488600-59490600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
44	chr17:59488600-59490600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
45	chr17:59488600-59490800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr17:59488600-59490800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
47	chr17:59488600-59491000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr17:59488800-59490000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
49	chr17:59488800-59490400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
50	chr17:59488800-59490400	Active TSS	A549	lung

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