Variant report

Variant	rs8078820
Chromosome Location	chr17:59478591-59478592
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:19)
CpG islands
(count:61)
Chromatin interactive
region (count:85)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:19 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr17:59468390-59479830	ProgFib	skin:	n/a	n/a
2	SUZ12	chr17:59473583-59483306	NT2-D1	testis:	n/a	n/a
3	GATA2	chr17:59478170-59479037	SH-SY5Y	brain:	n/a	n/a
4	ZNF263	chr17:59477651-59478767	HEK293-T-REx	kidney:	n/a	chr17:59477827-59477848
5	MXI1	chr17:59473914-59480739	SK-N-SH	brain:	n/a	n/a
6	POLR2A	chr17:59477995-59479760	SK-N-SH	brain:	n/a	n/a
7	HDAC2	chr17:59474717-59482617	MCF-7	breast:	n/a	chr17:59476354-59476363 chr17:59480823-59480832
8	CTBP2	chr17:59478138-59479685	H1-hESC	embryonic stem cell:	n/a	n/a
9	TEAD4	chr17:59474770-59479769	A549	lung:	n/a	n/a
10	POLR2A	chr17:59473262-59482475	IMR90	lung:	n/a	n/a
11	SUZ12	chr17:59477100-59483936	H1-hESC	embryonic stem cell:	n/a	n/a
12	TAF1	chr17:59478214-59478599	SK-N-SH	brain:	n/a	n/a
13	POLR2A	chr17:59477719-59478926	H1-neurons	neurons:	n/a	n/a
14	POLR2A	chr17:59477854-59479425	H1-neurons	neurons:	n/a	n/a
15	RAD21	chr17:59478159-59479499	IMR90	lung:	n/a	chr17:59479445-59479457
16	GATA3	chr17:59477741-59479657	MCF-7	breast:	n/a	n/a
17	MAX	chr17:59474705-59482813	MCF-7	breast:	n/a	chr17:59480404-59480414 chr17:59475824-59475831 chr17:59479783-59479793 chr17:59480615-59480622
18	SIN3AK20	chr17:59477976-59479736	SK-N-SH	brain:	n/a	n/a
19	TAF1	chr17:59478421-59478792	SK-N-SH	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:59478579-59478629	T-47D	breast:	n/a
2	chr17:59478579-59478629	H1-hESC	embryonic stem cell:	embryo
3	chr17:59478579-59478629	HAEpiC	amniotic membrane:	n/a
4	chr17:59478579-59478629	Jurkat	blood:	n/a
5	chr17:59478579-59478629	NB4	blood:	n/a
6	chr17:59478579-59478629	HepG2	liver:	n/a
7	chr17:59478579-59478629	ECC-1	luminal epithelium:	n/a
8	chr17:59478579-59478629	SK-N-SH	brain:	n/a
9	chr17:59478579-59478629	HPAEpiC	pulmonary alveolar:	n/a
10	chr17:59478579-59478629	HCT-116	colon:	n/a
11	chr17:59478579-59478629	ProgFib	skin:	n/a
12	chr17:59478579-59478629	HIPEpiC	eye:	n/a
13	chr17:59478579-59478629	AG09319	gingival:	n/a
14	chr17:59478579-59478629	AG04450	lung:	fetal
15	chr17:59478579-59478629	ovcar-3	ovarian:	n/a
16	chr17:59478579-59478629	AG04449	skin:	fetal
17	chr17:59478579-59478629	BJ	skin:	n/a
18	chr17:59478579-59478629	A549	lung:	n/a
19	chr17:59478579-59478629	GM12878	blood:	n/a
20	chr17:59478579-59478629	NHDF-neo	bronchial:	n/a
21	chr17:59478579-59478629	AG09309	skin:	n/a
22	chr17:59478579-59478629	SK-N-SH_RA	brain:	n/a
23	chr17:59478579-59478629	HCF	heart:	n/a
24	chr17:59478579-59478629	HRPEpiC	eye:	n/a
25	chr17:59478579-59478629	RPTEC	kidney:	n/a
26	chr17:59478579-59478629	NHBE	bronchial:	n/a
27	chr17:59478579-59478629	AG10803	skin:	n/a
28	chr17:59478579-59478629	PFSK-1	brain:	n/a
29	chr17:59478579-59478629	HL-60	blood:	n/a
30	chr17:59478579-59478629	Hela-S3	cervix:	n/a
31	chr17:59478579-59478629	IMR90	lung:	fetal
32	chr17:59478579-59478629	SK-N-MC	brain:	n/a
33	chr17:59478579-59478629	HRCEpiC	kidney:	n/a
34	chr17:59478579-59478629	GM12892	blood:	n/a
35	chr17:59478579-59478629	NT2-D1	testis:	n/a
36	chr17:59478579-59478629	PrEC	prostate:	n/a
37	chr17:59478579-59478629	HRE	kidney:	n/a
38	chr17:59478579-59478629	PANC-1	pancreas:	n/a
39	chr17:59478579-59478629	CMK	blood:	n/a
40	chr17:59478579-59478629	GM06990	blood:	n/a
41	chr17:59478579-59478629	MCF-7	breast:	n/a
42	chr17:59478579-59478629	BE2_C	brain:	n/a
43	chr17:59478579-59478629	HMEC	breast:	n/a
44	chr17:59478579-59478629	Hepatocyte	liver:	n/a
45	chr17:59478579-59478629	GM19239	blood:	n/a
46	chr17:59478579-59478629	HUVEC	blood vessel:	n/a
47	chr17:59478579-59478629	HEK293	kidney:	embryo
48	chr17:59478579-59478629	LNCaP	prostate:	n/a
49	chr17:59478579-59478629	AoSMC	blood vessel:	n/a
50	chr17:59478579-59478629	SAEC	small airway:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:59474707..59482954-chr20:45984179..45991970,21	MCF-7	breast:
2	chr17:59475645..59478788-chr7:5462326..5465715,3	MCF-7	breast:
3	chr10:74036416..74038370-chr17:59477900..59480470,2	MCF-7	breast:
4	chr17:57915289..57917492-chr17:59475690..59478863,6	MCF-7	breast:
5	chr17:59470038..59471787-chr17:59478375..59480606,2	K562	blood:
6	chr17:59477279..59479183-chr17:59870460..59872520,2	MCF-7	breast:
7	chr17:58601262..58603520-chr17:59476586..59479561,3	MCF-7	breast:
8	chr17:59415713..59496229-chr20:49401322..49431802,760	MCF-7	breast:
9	chr17:57914760..57924876-chr17:59472133..59480361,28	MCF-7	breast:
10	chr17:57918266..57925909-chr17:59474699..59479743,11	MCF-7	breast:
11	chr17:59477552..59479078-chr6:32935128..32937807,2	MCF-7	breast:
12	chr17:59477933..59479445-chr9:92259435..92261128,2	MCF-7	breast:
13	chr17:59468937..59480240-chr20:49340039..49356868,49	MCF-7	breast:
14	chr10:6245319..6247600-chr17:59477846..59479369,2	MCF-7	breast:
15	chr17:59236660..59239548-chr17:59477347..59479433,2	MCF-7	breast:
16	chr12:1799825..1801584-chr17:59476233..59479039,2	MCF-7	breast:
17	chr1:112546090..112547991-chr17:59478108..59480526,2	MCF-7	breast:
18	chr17:59468469..59482635-chr20:45977748..45992950,51	MCF-7	breast:
19	chr17:59476334..59478740-chr7:100183272..100185013,2	MCF-7	breast:
20	chr17:57929360..57930969-chr17:59478398..59481379,3	MCF-7	breast:
21	chr17:59477876..59478765-chr20:49406499..49407614,3	MCF-7	breast:
22	chr17:59476401..59478732-chr17:59488339..59490282,10	MCF-7	breast:
23	chr17:59475983..59478702-chr20:60717939..60720042,2	MCF-7	breast:
24	chr17:59476586..59479504-chr20:45944218..45947716,4	MCF-7	breast:
25	chr17:56706858..56710627-chr17:59472052..59479583,11	MCF-7	breast:
26	chr17:59476268..59478751-chr17:73774327..73777038,2	MCF-7	breast:
27	chr17:59477761..59480587-chr18:812483..814918,2	MCF-7	breast:
28	chr1:149858261..149860142-chr17:59476311..59478808,2	MCF-7	breast:
29	chr17:59093635..59095394-chr17:59477039..59478884,2	MCF-7	breast:
30	chr17:59478047..59480711-chr7:42997001..42999058,2	MCF-7	breast:
31	chr17:59476370..59478594-chr2:24298301..24300623,2	MCF-7	breast:
32	chr17:58963859..58966065-chr17:59476840..59479002,2	MCF-7	breast:
33	chr17:59476717..59479924-chr6:6757897..6761293,3	MCF-7	breast:
34	chr17:57183794..57185492-chr17:59476524..59479346,2	MCF-7	breast:
35	chr15:78831864..78834406-chr17:59476584..59478636,2	MCF-7	breast:
36	chr17:59478017..59478808-chr20:49411353..49411946,2	MCF-7	breast:
37	chr17:59475037..59478844-chr20:46130288..46133221,4	MCF-7	breast:
38	chr17:59476916..59479068-chr4:16227271..16228837,2	MCF-7	breast:
39	chr11:62607389..62609946-chr17:59474359..59478741,7	MCF-7	breast:
40	chr17:59476007..59480817-chr20:55837817..55844035,9	MCF-7	breast:
41	chr17:59474584..59479937-chr20:48725175..48731303,15	MCF-7	breast:
42	chr17:59477079..59481029-chr20:46128798..46132223,4	MCF-7	breast:
43	chr17:59478204..59480463-chr7:1892056..1894919,2	MCF-7	breast:
44	chr17:59477135..59479003-chr5:177630296..177633273,2	MCF-7	breast:
45	chr17:59477651..59479888-chr6:89671941..89673981,2	MCF-7	breast:
46	chr11:65190161..65193929-chr17:59476956..59480011,3	MCF-7	breast:
47	chr17:59478442..59480320-chr2:227663816..227665961,2	MCF-7	breast:
48	chr17:59476095..59478850-chr2:208488248..208491247,2	MCF-7	breast:
49	chr17:59476579..59478920-chr20:49410968..49412298,14	MCF-7	breast:
50	chr17:59477621..59480570-chr6:27113149..27115368,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267131	TF binding region
ENSG00000267280	TF binding region
ENSG00000267280	CpG island
ENSG00000267131	CpG island
ENSG00000135269	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000196420	Chromatin interaction
ENSG00000126790	Chromatin interaction
ENSG00000083307	Chromatin interaction
ENSG00000273355	Chromatin interaction
ENSG00000199032	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000006831	Chromatin interaction
ENSG00000163349	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000167964	Chromatin interaction
ENSG00000171385	Chromatin interaction
ENSG00000115128	Chromatin interaction
ENSG00000178057	Chromatin interaction
ENSG00000231437	Chromatin interaction
ENSG00000101182	Chromatin interaction
ENSG00000111880	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000153107	Chromatin interaction
ENSG00000182095	Chromatin interaction
ENSG00000267882	Chromatin interaction
ENSG00000254024	Chromatin interaction
ENSG00000244300	Chromatin interaction
ENSG00000179348	Chromatin interaction
ENSG00000235527	Chromatin interaction
ENSG00000130703	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000273451	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000105185	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000132478	Chromatin interaction
ENSG00000169047	Chromatin interaction
ENSG00000041357	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000103342	Chromatin interaction
ENSG00000266163	Chromatin interaction
ENSG00000231119	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000272622	Chromatin interaction
ENSG00000200156	Chromatin interaction
ENSG00000197846	Chromatin interaction
ENSG00000224738	Chromatin interaction
ENSG00000176105	Chromatin interaction
ENSG00000236352	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000198162	Chromatin interaction
ENSG00000108395	Chromatin interaction
ENSG00000170836	Chromatin interaction
ENSG00000197451	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000169762	Chromatin interaction
ENSG00000272953	Chromatin interaction
ENSG00000062725	Chromatin interaction
ENSG00000144401	Chromatin interaction
ENSG00000224532	Chromatin interaction
ENSG00000106009	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000110700	Chromatin interaction
ENSG00000124243	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000187013	Chromatin interaction
ENSG00000263327	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000207605	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000225362	Chromatin interaction
ENSG00000178149	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000184402	Chromatin interaction
ENSG00000219626	Chromatin interaction
ENSG00000204257	Chromatin interaction
ENSG00000141376	Chromatin interaction
ENSG00000175895	Chromatin interaction
ENSG00000050130	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000244687	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1076393	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1132179	0.88[EUR][1000 genomes]
rs12451524	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2286524	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3744449	1.00[EUR][1000 genomes]
rs3760369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4455026	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59051236	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7208889	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7214900	0.92[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs729782	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs740753	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs740754	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8066348	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8075606	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8080990	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 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	esv3429164	chr17:59475870-59479468	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	156 gene(s)	inside rSNPs	diseases
15	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
16	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
17	esv3356501	chr17:59476195-59479343	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	156 gene(s)	inside rSNPs	diseases
18	esv3406346	chr17:59476220-59479068	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59473400-59479800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
2	chr17:59474200-59479000	Active TSS	Aorta	Aorta
3	chr17:59474200-59481000	Active TSS	NHDF-Ad	bronchial
4	chr17:59474400-59479800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
5	chr17:59475000-59479200	Active TSS	HSMM	muscle
6	chr17:59475000-59480400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
7	chr17:59475400-59478800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr17:59475400-59479600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
9	chr17:59475800-59479400	Active TSS	Osteobl	bone
10	chr17:59476200-59478600	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr17:59476200-59478600	Active TSS	Muscle Satellite Cultured Cells	--
12	chr17:59476200-59478600	Active TSS	Fetal Kidney	kidney
13	chr17:59476200-59478800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr17:59476200-59479000	Active TSS	HSMMtube	muscle
15	chr17:59476200-59479600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr17:59476400-59478600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr17:59476400-59478600	Bivalent/Poised TSS	Thymus	Thymus
18	chr17:59476400-59479000	Active TSS	Ovary	ovary
19	chr17:59476400-59479400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr17:59476600-59480600	Active TSS	Right Atrium	heart
21	chr17:59476800-59478600	Active TSS	NH-A	brain
22	chr17:59476800-59479000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr17:59476800-59479000	Bivalent/Poised TSS	Colonic Mucosa	Colon
24	chr17:59476800-59479000	Active TSS	Lung	lung
25	chr17:59476800-59479200	Active TSS	Right Ventricle	heart
26	chr17:59476800-59479600	Active TSS	Pancreas	Pancrea
27	chr17:59477000-59479000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
28	chr17:59477200-59480400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
29	chr17:59477200-59482200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
30	chr17:59477400-59478600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr17:59477400-59478600	Active TSS	HepG2	liver
32	chr17:59477400-59478800	Bivalent/Poised TSS	NHEK	skin
33	chr17:59477400-59479800	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
34	chr17:59477800-59478600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr17:59477800-59480400	Active TSS	Gastric	stomach
36	chr17:59477800-59482000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
37	chr17:59478000-59478600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr17:59478000-59478600	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr17:59478000-59478600	Flanking Active TSS	A549	lung
40	chr17:59478000-59478800	Bivalent Enhancer	Primary B cells from cord blood	blood
41	chr17:59478000-59478800	Bivalent/Poised TSS	Brain Angular Gyrus	brain
42	chr17:59478000-59478800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
43	chr17:59478000-59479000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
44	chr17:59478000-59479000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
45	chr17:59478000-59479000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
46	chr17:59478000-59479200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr17:59478000-59479200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
48	chr17:59478000-59479200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr17:59478000-59479400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
50	chr17:59478000-59479600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

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