Variant report

Variant	rs12953299
Chromosome Location	chr17:17726648-17726649
allele	A/G
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	POLR2A	chr17:17726284-17726949	PANC-1	pancreas:	n/a	n/a
2	CREB1	chr17:17726635-17727656	A549	lung:	n/a	n/a
3	POLR2A	chr17:17726491-17727196	MCF-7	breast:	n/a	n/a
4	POLR2A	chr17:17726583-17726986	HL-60	blood:	n/a	n/a
5	SP1	chr17:17726536-17727859	A549	lung:	n/a	chr17:17727032-17727043 chr17:17727706-17727720 chr17:17727705-17727717 chr17:17727705-17727717 chr17:17727267-17727279 chr17:17727077-17727098 chr17:17727268-17727282 chr17:17727707-17727716 chr17:17727269-17727278 chr17:17727706-17727715 chr17:17727267-17727279 chr17:17727706-17727716
6	POLR2A	chr17:17726505-17727149	MCF-7	breast:	n/a	n/a
7	MXI1	chr17:17726590-17726901	GM12878	blood:	n/a	n/a
8	POLR2A	chr17:17726322-17727003	H1-neurons	neurons:	n/a	n/a
9	POLR2A	chr17:17723997-17728661	K562	blood:	n/a	n/a
10	POLR2A	chr17:17726507-17728636	HepG2	liver:	n/a	n/a
11	MAX	chr17:17726532-17728380	A549	lung:	n/a	n/a
12	POLR2A	chr17:17726646-17727013	ECC-1	luminal epithelium:	n/a	n/a
13	POLR2A	chr17:17726400-17727574	NB4	blood:	n/a	n/a
14	HA-E2F1	chr17:17726572-17726967	MCF-7	breast:	n/a	n/a
15	SREBP1	chr17:17726236-17727727	GM12878	blood:	n/a	chr17:17727063-17727074
16	POLR2A	chr17:17725575-17726837	A549	lung:	n/a	n/a
17	POLR2A	chr17:17725297-17728677	K562	blood:	n/a	n/a
18	POLR2A	chr17:17723703-17728433	PBDE	blood:	n/a	n/a
19	TFAP2C	chr17:17726508-17728084	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr17:17726590-17727800	GM12891	blood:	n/a	n/a
21	POLR2A	chr17:17726173-17727565	PFSK-1	brain:	n/a	n/a
22	SP1	chr17:17726581-17727758	A549	lung:	n/a	chr17:17727032-17727043 chr17:17727706-17727720 chr17:17727705-17727717 chr17:17727705-17727717 chr17:17727267-17727279 chr17:17727077-17727098 chr17:17727268-17727282 chr17:17727707-17727716 chr17:17727269-17727278 chr17:17727706-17727715 chr17:17727267-17727279 chr17:17727706-17727716
23	POLR2A	chr17:17726432-17726921	HCT-116	colon:	n/a	n/a
24	MAX	chr17:17726508-17727564	ECC-1	luminal epithelium:	n/a	n/a
25	ZEB1	chr17:17726548-17726961	GM12878	blood:	n/a	n/a
26	BCL3	chr17:17725850-17726985	A549	lung:	n/a	n/a
27	SIN3A	chr17:17726514-17727482	H1-hESC	embryonic stem cell:	n/a	chr17:17727092-17727103
28	POLR2A	chr17:17712185-17727861	K562	blood:	n/a	n/a
29	MAX	chr17:17726456-17728739	HepG2	liver:	n/a	n/a
30	POLR2A	chr17:17726609-17726981	ECC-1	luminal epithelium:	n/a	n/a
31	REST	chr17:17726398-17726954	A549	lung:	n/a	chr17:17726480-17726487 chr17:17726458-17726472
32	MAX	chr17:17726561-17727614	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr17:17726646-17726940	HCT-116	colon:	n/a	n/a
34	POLR2A	chr17:17726529-17726952	SK-N-MC	brain:	n/a	n/a
35	SIN3AK20	chr17:17726563-17726993	H1-hESC	embryonic stem cell:	n/a	n/a
36	STAT5A	chr17:17726449-17726868	GM12878	blood:	n/a	n/a
37	EP300	chr17:17726550-17727603	ECC-1	luminal epithelium:	n/a	n/a
38	POLR2A	chr17:17726555-17727019	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr17:17726503-17726750	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr17:17726014-17726930	HepG2	liver:	n/a	n/a
41	MAX	chr17:17726306-17728751	A549	lung:	n/a	n/a
42	POLR2A	chr17:17726470-17726717	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAZ	chr17:17726220-17727869	IMR90	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:17584408..17586554-chr17:17725797..17727625,2	K562	blood:
2	chr17:17583643..17586896-chr17:17724231..17729521,8	MCF-7	breast:
3	chr17:17724980..17727565-chr17:17764878..17766852,2	MCF-7	breast:
4	chr17:17584806..17586554-chr17:17724863..17727625,2	K562	blood:
5	chr17:17726446..17727206-chr17:17739539..17740685,3	Hela-S3	cervix:

Variant related genes	Relation type
SREBF1	TF binding region
ENSG00000108557	Chromatin interaction
ENSG00000175662	Chromatin interaction
ENSG00000072310	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10048206	0.80[CEU][hapmap]
rs1052299	1.00[CHB][hapmap]
rs11078406	0.80[CEU][hapmap]
rs1108648	1.00[CHB][hapmap]
rs11650649	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs11656840	0.83[CEU][hapmap]
rs11657423	1.00[CHB][hapmap];0.87[CHD][hapmap];0.91[ASN][1000 genomes]
rs12600546	0.80[CEU][hapmap]
rs12936927	0.88[ASN][1000 genomes]
rs12941039	1.00[CHB][hapmap]
rs12943500	1.00[CHB][hapmap]
rs1889018	1.00[CHB][hapmap]
rs2350977	0.80[CEU][hapmap]
rs3744115	1.00[CHB][hapmap]
rs4077828	0.80[CEU][hapmap]
rs4244602	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs4257260	0.80[CEU][hapmap]
rs4341796	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs4413022	0.83[CEU][hapmap]
rs4470201	0.80[CEU][hapmap]
rs4925123	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs4925126	0.80[CEU][hapmap]
rs4925129	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs4925130	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs5002487	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs6502619	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs6502622	0.80[CEU][hapmap]
rs6502624	0.80[CEU][hapmap]
rs6502625	1.00[CHB][hapmap]
rs6502627	0.80[CEU][hapmap]
rs6502629	1.00[CHB][hapmap]
rs7207395	1.00[CHB][hapmap]
rs7213225	0.80[CEU][hapmap]
rs7214002	0.83[CEU][hapmap]
rs7222480	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs7224815	1.00[CHB][hapmap]
rs7359509	1.00[CHB][hapmap]
rs7501812	1.00[CHB][hapmap]
rs7503334	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs8065416	0.80[CEU][hapmap]
rs8065563	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs8066982	0.80[CEU][hapmap]
rs8070128	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs8070748	0.80[CEU][hapmap]
rs8073001	0.80[CEU][hapmap]
rs8078138	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs8078583	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs8080823	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs950966	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs9890341	0.80[CEU][hapmap]
rs9891957	1.00[CHB][hapmap]
rs9899634	1.00[CHB][hapmap];0.87[CHD][hapmap];0.91[ASN][1000 genomes]
rs9907246	1.00[CHB][hapmap]
rs9912895	0.80[CEU][hapmap]
rs9915248	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:34 , 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	nsv907767	chr17:17709136-17733760	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
34	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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs12953299	TOM1L2	cis	cerebellum	SCAN
rs12953299	TOM1L2	cis	parietal	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17718200-17728600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr17:17722800-17726800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr17:17723200-17730000	Enhancers	Stomach Mucosa	stomach
4	chr17:17723600-17727600	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr17:17723800-17726800	Flanking Active TSS	Liver	Liver
6	chr17:17723800-17728800	Enhancers	Gastric	stomach
7	chr17:17724000-17726800	Transcr. at gene 5' and 3'	NHEK	skin
8	chr17:17724200-17726800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr17:17724200-17726800	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr17:17724200-17726800	Transcr. at gene 5' and 3'	K562	blood
11	chr17:17724400-17726800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
12	chr17:17724400-17726800	Flanking Active TSS	Adipose Nuclei	Adipose
13	chr17:17724400-17726800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
14	chr17:17724400-17727000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr17:17724600-17726800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr17:17724600-17726800	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr17:17724800-17726800	Flanking Active TSS	Colonic Mucosa	Colon
18	chr17:17724800-17726800	Flanking Active TSS	Right Atrium	heart
19	chr17:17724800-17726800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr17:17725000-17729600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr17:17725200-17726800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
22	chr17:17725200-17726800	Flanking Active TSS	Rectal Smooth Muscle	rectum
23	chr17:17725200-17726800	Enhancers	Spleen	Spleen
24	chr17:17725400-17726800	Flanking Active TSS	Fetal Thymus	thymus
25	chr17:17725400-17726800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
26	chr17:17725400-17726800	Transcr. at gene 5' and 3'	HepG2	liver
27	chr17:17725400-17727000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr17:17725400-17727000	Flanking Active TSS	HMEC	breast
29	chr17:17725600-17726800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr17:17725600-17726800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr17:17725600-17726800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr17:17725600-17727200	Active TSS	Brain Substantia Nigra	brain
33	chr17:17725600-17727200	Enhancers	HUVEC	blood vessel
34	chr17:17725600-17728600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr17:17725800-17726800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr17:17725800-17726800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr17:17725800-17726800	Flanking Active TSS	Fetal Intestine Large	intestine
38	chr17:17725800-17726800	Flanking Active TSS	Fetal Muscle Leg	muscle
39	chr17:17725800-17726800	Flanking Active TSS	Left Ventricle	heart
40	chr17:17725800-17726800	Flanking Active TSS	Right Ventricle	heart
41	chr17:17725800-17726800	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
42	chr17:17725800-17726800	Flanking Active TSS	Small Intestine	intestine
43	chr17:17725800-17727000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr17:17725800-17727000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr17:17725800-17727000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr17:17726000-17726800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr17:17726000-17726800	Flanking Active TSS	Primary hematopoietic stem cells	blood
48	chr17:17726000-17726800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr17:17726000-17726800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr17:17726000-17726800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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