Variant report

Variant	rs60387072
Chromosome Location	chr17:17742617-17742618
allele	C/T
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	EP300	chr17:17742519-17744243	ECC-1	luminal epithelium:	n/a	chr17:17743601-17743610
2	POLR2A	chr17:17742584-17743932	SK-N-MC	brain:	n/a	n/a
3	POLR2A	chr17:17742600-17744794	MCF10A-Er-Src	breast:	n/a	n/a
4	POLR2A	chr17:17742483-17744566	K562	blood:	n/a	n/a
5	POLR2A	chr17:17742498-17744736	MCF10A-Er-Src	breast:	n/a	n/a
6	SIX5	chr17:17742448-17743929	A549	lung:	n/a	n/a
7	ARID3A	chr17:17742540-17743455	HepG2	liver:	n/a	n/a
8	POLR2A	chr17:17742263-17744054	K562	blood:	n/a	n/a
9	POLR2A	chr17:17742552-17744012	HepG2	liver:	n/a	n/a
10	POLR2A	chr17:17742583-17743995	K562	blood:	n/a	n/a
11	POLR2A	chr17:17742392-17745250	HepG2	liver:	n/a	n/a
12	FOXA1	chr17:17742581-17742959	HepG2	liver:	n/a	chr17:17742776-17742788
13	POLR2A	chr17:17742569-17743915	PANC-1	pancreas:	n/a	n/a
14	POLR2A	chr17:17742487-17744813	K562	blood:	n/a	n/a
15	SREBP2	chr17:17742514-17744556	GM12878	blood:	n/a	n/a
16	JUN	chr17:17742288-17745278	K562	blood:	n/a	chr17:17744936-17744947 chr17:17744409-17744420 chr17:17744410-17744419
17	POLR2A	chr17:17742437-17743973	K562	blood:	n/a	n/a
18	SP1	chr17:17742539-17744521	A549	lung:	n/a	chr17:17744207-17744216 chr17:17744209-17744222
19	POLR2A	chr17:17742389-17744775	Raji	blood:	n/a	n/a
20	POLR2A	chr17:17742539-17743857	K562	blood:	n/a	n/a
21	POLR2A	chr17:17742315-17744057	HCT-116	colon:	n/a	n/a
22	POLR2A	chr17:17742542-17744055	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr17:17742517-17743866	HepG2	liver:	n/a	n/a
24	HEY1	chr17:17742506-17744805	HepG2	liver:	n/a	chr17:17743428-17743443 chr17:17743788-17743803
25	POLR2A	chr17:17742308-17744905	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr17:17742525-17744846	PBDE	blood:	n/a	n/a
27	POLR2A	chr17:17742308-17742758	ECC-1	luminal epithelium:	n/a	n/a
28	POLR2A	chr17:17742443-17744686	HCT-116	colon:	n/a	n/a
29	POLR2A	chr17:17742525-17744722	GM12878	blood:	n/a	n/a
30	ZEB1	chr17:17742521-17744635	HepG2	liver:	n/a	chr17:17743689-17743698
31	MAX	chr17:17742527-17744530	A549	lung:	n/a	chr17:17744252-17744261 chr17:17742960-17742969 chr17:17744409-17744418
32	POLR2A	chr17:17742479-17744590	HCT-116	colon:	n/a	n/a
33	BCL3	chr17:17742543-17744025	A549	lung:	n/a	chr17:17743450-17743463 chr17:17743632-17743645 chr17:17743630-17743639
34	POLR2A	chr17:17742362-17744931	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr17:17742510-17744734	K562	blood:	n/a	n/a
36	POLR2A	chr17:17742538-17744065	ECC-1	luminal epithelium:	n/a	n/a
37	SREBP1	chr17:17742614-17744076	GM12878	blood:	n/a	chr17:17743544-17743555 chr17:17742955-17742969 chr17:17743543-17743553
38	POLR2A	chr17:17738728-17744957	HepG2	liver:	n/a	n/a
39	POLR2A	chr17:17742363-17745363	Hela-S3	cervix:	n/a	n/a
40	FOXA1	chr17:17742613-17742902	HepG2	liver:	n/a	chr17:17742776-17742788
41	MTA3	chr17:17742591-17744839	GM12878	blood:	n/a	n/a
42	POLR2A	chr17:17742521-17744048	PANC-1	pancreas:	n/a	n/a
43	IRF1	chr17:17742458-17743801	K562	blood:	n/a	chr17:17742809-17742823 chr17:17742813-17742823
44	RCOR1	chr17:17742585-17744342	K562	blood:	n/a	n/a
45	POLR2A	chr17:17742520-17744714	K562	blood:	n/a	n/a
46	HEY1	chr17:17742531-17743991	HepG2	liver:	n/a	chr17:17743428-17743443 chr17:17743788-17743803
47	POLR2A	chr17:17742497-17743949	K562	blood:	n/a	n/a
48	RCOR1	chr17:17742559-17743843	HepG2	liver:	n/a	n/a
49	GTF3C2	chr17:17741823-17742954	Hela-S3	cervix:	n/a	n/a
50	FOXA1	chr17:17742612-17743046	HepG2	liver:	n/a	chr17:17742776-17742788

No.	Distal block	Cell Line	Cell type
1	chr17:17630393..17635386-chr17:17740565..17747416,7	MCF-7	breast:
2	chr17:17742240..17744264-chr17:17791340..17793757,2	MCF-7	breast:
3	chr17:17580850..17587926-chr17:17737733..17744809,17	MCF-7	breast:
4	chr17:17742084..17742993-chr3:88107991..88108537,2	Hela-S3	cervix:
5	chr17:17594054..17595929-chr17:17740676..17742731,2	K562	blood:
6	chr17:17615835..17618255-chr17:17741726..17743796,2	K562	blood:
7	chr17:17741927..17743549-chr17:17824784..17826455,2	MCF-7	breast:
8	chr17:17589077..17591460-chr17:17741926..17746377,4	MCF-7	breast:
9	chr17:17740765..17742638-chr18:3245655..3247781,2	MCF-7	breast:
10	chr12:57038481..57041021-chr17:17741070..17743316,2	K562	blood:
11	chr17:17583946..17588364-chr17:17740477..17744360,6	MCF-7	breast:
12	chr17:17741798..17744569-chr17:17877349..17878945,2	K562	blood:
13	chr17:17741535..17743958-chr17:17764231..17767571,3	K562	blood:
14	chr17:17741084..17743223-chr17:17876153..17877806,2	MCF-7	breast:
15	chr17:17596357..17599284-chr17:17741696..17744327,3	MCF-7	breast:
16	chr17:17742275..17745067-chr17:17764534..17767182,3	MCF-7	breast:
17	chr17:17672192..17674299-chr17:17741443..17743483,2	K562	blood:
18	chr15:101459148..101459862-chr17:17742416..17743107,2	Hela-S3	cervix:
19	chr17:17622624..17624957-chr17:17740328..17743276,2	K562	blood:

Variant related genes	Relation type
SREBF1	TF binding region
ENSG00000259583	Chromatin interaction
ENSG00000163320	Chromatin interaction
ENSG00000175662	Chromatin interaction
ENSG00000223979	Chromatin interaction
ENSG00000110955	Chromatin interaction
ENSG00000108557	Chromatin interaction
ENSG00000207031	Chromatin interaction
ENSG00000171962	Chromatin interaction
ENSG00000101608	Chromatin interaction
ENSG00000229729	Chromatin interaction
ENSG00000272688	Chromatin interaction
ENSG00000237328	Chromatin interaction
ENSG00000154237	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs59948477	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299834	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299839	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299846	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299887	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73301842	1.00[AMR][1000 genomes]
rs73301851	1.00[AMR][1000 genomes]
rs73301854	1.00[AMR][1000 genomes]
rs73301865	1.00[AMR][1000 genomes]
rs73301873	1.00[AMR][1000 genomes]
rs73301880	1.00[AMR][1000 genomes]
rs8066353	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8077514	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8080949	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv907752	chr17:17569012-17750907	Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
5	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
6	nsv907753	chr17:17573539-17747289	Genic enhancers Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv907754	chr17:17573539-17782404	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
8	nsv1061126	chr17:17578826-17803194	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
9	nsv543238	chr17:17578826-17803194	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv833385	chr17:17594037-17765578	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
11	nsv1058884	chr17:17594370-17803194	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv543240	chr17:17594370-17803194	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv1064176	chr17:17596222-17803194	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
14	nsv543242	chr17:17596222-17803194	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv1062361	chr17:17598407-17746899	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
16	nsv543243	chr17:17598407-17746899	Genic enhancers Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
17	nsv907756	chr17:17619859-17747289	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
18	nsv522668	chr17:17619859-17752809	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
19	nsv907757	chr17:17619859-17752809	Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
20	nsv907758	chr17:17619859-17782404	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
21	nsv907759	chr17:17619859-17802478	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
22	nsv1059949	chr17:17632590-17803194	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
23	nsv543244	chr17:17632590-17803194	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
24	nsv907760	chr17:17649423-17782404	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
25	nsv907761	chr17:17649423-17802478	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
26	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
27	nsv907762	chr17:17668071-17802478	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
28	nsv907763	chr17:17673824-17749822	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
29	nsv907764	chr17:17673824-17754633	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
30	nsv907765	chr17:17682484-17802478	Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
31	nsv907766	chr17:17682484-17957348	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
32	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
33	nsv907768	chr17:17709136-17747289	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17740400-17742800	Enhancers	GM12878-XiMat	blood
2	chr17:17740400-17743000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:17740400-17743000	Enhancers	NHDF-Ad	bronchial
4	chr17:17740400-17743200	Weak transcription	Aorta	Aorta
5	chr17:17740600-17743000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr17:17740600-17743000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr17:17740600-17743000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr17:17740600-17743000	Enhancers	Brain Anterior Caudate	brain
9	chr17:17740600-17743000	Enhancers	Esophagus	oesophagus
10	chr17:17740600-17743000	Enhancers	Fetal Muscle Trunk	muscle
11	chr17:17740600-17743000	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr17:17740600-17743000	Enhancers	HUVEC	blood vessel
13	chr17:17740600-17743000	Enhancers	NHLF	lung
14	chr17:17740600-17743200	Enhancers	Lung	lung
15	chr17:17740600-17743200	Weak transcription	Ovary	ovary
16	chr17:17740600-17743400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr17:17740800-17742800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr17:17740800-17742800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr17:17740800-17742800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr17:17740800-17742800	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr17:17740800-17742800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr17:17740800-17742800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr17:17740800-17742800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr17:17740800-17742800	Enhancers	Liver	Liver
25	chr17:17740800-17742800	Enhancers	Duodenum Mucosa	Duodenum
26	chr17:17740800-17742800	Enhancers	Fetal Intestine Large	intestine
27	chr17:17740800-17742800	Enhancers	Fetal Intestine Small	intestine
28	chr17:17740800-17742800	Enhancers	Fetal Thymus	thymus
29	chr17:17740800-17742800	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr17:17740800-17743000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr17:17740800-17743000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr17:17740800-17743000	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr17:17740800-17743000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr17:17740800-17743000	Enhancers	Primary B cells from peripheral blood	blood
35	chr17:17740800-17743000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr17:17740800-17743000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr17:17740800-17743000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr17:17740800-17743000	Enhancers	Brain Hippocampus Middle	brain
39	chr17:17740800-17743000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr17:17740800-17743000	Enhancers	Colon Smooth Muscle	Colon
41	chr17:17740800-17743000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr17:17740800-17743000	Enhancers	Fetal Muscle Leg	muscle
43	chr17:17740800-17743000	Enhancers	Placenta	Placenta
44	chr17:17740800-17743000	Enhancers	Stomach Mucosa	stomach
45	chr17:17740800-17743000	Enhancers	Thymus	Thymus
46	chr17:17740800-17743200	Enhancers	Primary B cells from cord blood	blood
47	chr17:17740800-17743200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr17:17741000-17742800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr17:17741000-17742800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr17:17741000-17742800	Weak transcription	Fetal Brain Male	brain

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