Variant report

Variant	rs4925114
Chromosome Location	chr17:17711270-17711271
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUND	chr17:17710910-17711369	A549	lung:	n/a	n/a
2	POLR2A	chr17:17708648-17711645	Hela-S3	cervix:	n/a	n/a
3	BCL3	chr17:17710579-17711697	A549	lung:	n/a	n/a
4	POLR2A	chr17:17711116-17711409	A549	lung:	n/a	n/a
5	POLR2A	chr17:17710610-17711564	Hela-S3	cervix:	n/a	n/a
6	MYC	chr17:17711258-17711315	MCF-7	breast:	n/a	n/a
7	POLR2A	chr17:17710649-17711683	H1-neurons	neurons:	n/a	n/a
8	POLR2A	chr17:17711042-17711436	HepG2	liver:	n/a	n/a
9	TFAP2C	chr17:17711006-17711485	Hela-S3	cervix:	n/a	chr17:17711276-17711291 chr17:17711307-17711322
10	POLR2A	chr17:17711102-17711393	A549	lung:	n/a	n/a
11	POLR2A	chr17:17710781-17711309	MCF10A-Er-Src	breast:	n/a	n/a
12	POLR2A	chr17:17711168-17711412	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr17:17708494-17711625	A549	lung:	n/a	n/a
14	POLR2A	chr17:17710694-17711710	U87	brain:	n/a	n/a
15	POLR2A	chr17:17710766-17711662	U87	brain:	n/a	n/a
16	MYC	chr17:17711269-17711354	MCF-7	breast:	n/a	n/a
17	POLR2A	chr17:17710973-17711347	GM12878	blood:	n/a	n/a
18	POLR2A	chr17:17710701-17711650	HepG2	liver:	n/a	n/a
19	POLR2A	chr17:17711144-17711613	K562	blood:	n/a	n/a
20	BCL3	chr17:17710771-17711643	A549	lung:	n/a	n/a
21	POLR2A	chr17:17710927-17711301	GM12878	blood:	n/a	n/a
22	POLR2A	chr17:17711248-17711310	K562	blood:	n/a	n/a
23	POLR2A	chr17:17711079-17711574	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr17:17710740-17711551	PANC-1	pancreas:	n/a	n/a
25	POLR2A	chr17:17710563-17711702	MCF-7	breast:	n/a	n/a
26	POLR2A	chr17:17710739-17711629	SK-N-MC	brain:	n/a	n/a
27	POLR2A	chr17:17710378-17711579	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr17:17711143-17711386	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr17:17710897-17711304	U87	brain:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17685362..17690405-chr17:17711256..17718354,8	MCF-7	breast:
2	chr17:17596211..17599216-chr17:17709321..17712358,3	MCF-7	breast:
3	chr17:17634554..17636650-chr17:17709495..17711657,2	MCF-7	breast:
4	chr17:17702786..17705545-chr17:17709001..17711709,2	K562	blood:

No data

Variant related genes	Relation type
RAI1	TF binding region
ENSG00000108557	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1052299	0.86[CEU][hapmap];0.84[TSI][hapmap]
rs1108648	0.84[CEU][hapmap]
rs11649804	0.81[CEU][hapmap];0.91[GIH][hapmap]
rs11652881	0.91[CEU][hapmap];1.00[CHB][hapmap];0.87[GIH][hapmap];0.84[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11654081	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11656665	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs11656775	0.87[GIH][hapmap]
rs11657423	0.91[CEU][hapmap];0.83[MEX][hapmap]
rs11868035	0.86[CEU][hapmap]
rs12453837	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12946913	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16960744	0.86[CEU][hapmap];0.82[TSI][hapmap]
rs1889018	0.91[CEU][hapmap]
rs2236513	0.85[CEU][hapmap]
rs2297508	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2350976	0.95[CEU][hapmap];1.00[CHB][hapmap];0.87[GIH][hapmap];0.84[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3183702	0.86[CEU][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap]
rs3744115	0.82[CEU][hapmap];0.84[TSI][hapmap]
rs3818717	0.91[CEU][hapmap];1.00[CHB][hapmap];0.83[TSI][hapmap];0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4584886	0.83[MEX][hapmap]
rs4924822	0.82[CEU][hapmap];0.84[TSI][hapmap]
rs4925109	0.90[GIH][hapmap]
rs4925115	0.95[CEU][hapmap];0.88[MEX][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes]
rs4925119	0.86[CEU][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap]
rs4925120	0.86[CEU][hapmap];0.82[TSI][hapmap]
rs7359509	0.91[CEU][hapmap]
rs7501812	0.82[CEU][hapmap]
rs8066560	0.90[CEU][hapmap];0.87[MEX][hapmap]
rs8067439	0.90[CEU][hapmap];0.90[GIH][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9891957	0.90[CEU][hapmap]
rs9899634	0.91[CEU][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap]
rs9900803	0.87[GIH][hapmap]
rs9902941	0.91[CEU][hapmap];0.82[TSI][hapmap]
rs9915248	0.86[CEU][hapmap];0.84[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:37 , 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	esv1804029	chr17:17669662-17714250	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
29	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
30	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
31	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
32	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
33	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
34	nsv526904	chr17:17696755-17715101	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
35	nsv817753	chr17:17696755-17715101	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
36	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
37	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
rs4925114	TOM1L2	cis	parietal	SCAN
rs4925114	TOM1L2	cis	cerebellum	SCAN

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17688000-17715000	Weak transcription	Small Intestine	intestine
2	chr17:17688600-17714200	Weak transcription	NHDF-Ad	bronchial
3	chr17:17695400-17723800	Strong transcription	Dnd41	blood
4	chr17:17696600-17711600	Strong transcription	Fetal Lung	lung
5	chr17:17696800-17712200	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr17:17697000-17711400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr17:17697000-17711600	Strong transcription	Gastric	stomach
8	chr17:17697000-17711800	Strong transcription	Fetal Brain Female	brain
9	chr17:17697000-17712400	Strong transcription	Fetal Intestine Large	intestine
10	chr17:17697000-17712600	Strong transcription	Fetal Intestine Small	intestine
11	chr17:17697200-17714800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr17:17697200-17715200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr17:17697200-17715200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr17:17697200-17715800	Strong transcription	Thymus	Thymus
15	chr17:17697400-17712000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr17:17697400-17712200	Strong transcription	Lung	lung
17	chr17:17697400-17713800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr17:17697400-17715400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr17:17697600-17715000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr17:17698000-17713600	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr17:17698000-17715000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr17:17698200-17713400	Weak transcription	HUVEC	blood vessel
23	chr17:17700200-17712400	Weak transcription	Primary B cells from peripheral blood	blood
24	chr17:17703000-17712000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr17:17703200-17713400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr17:17704000-17712600	Strong transcription	Fetal Stomach	stomach
27	chr17:17704200-17712600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr17:17706600-17711600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr17:17707000-17711600	Strong transcription	NHLF	lung
30	chr17:17707000-17723000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr17:17707200-17712400	Strong transcription	Brain Germinal Matrix	brain
32	chr17:17707400-17722400	Weak transcription	Primary B cells from cord blood	blood
33	chr17:17707600-17713400	Weak transcription	Aorta	Aorta
34	chr17:17707800-17713800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr17:17707800-17715000	Weak transcription	K562	blood
36	chr17:17708000-17713200	Weak transcription	Fetal Brain Male	brain
37	chr17:17708000-17713600	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr17:17708000-17715400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr17:17708000-17723600	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr17:17708400-17711400	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr17:17708400-17711800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr17:17708400-17716600	Enhancers	Fetal Heart	heart
43	chr17:17708600-17712400	Genic enhancers	Fetal Muscle Leg	muscle
44	chr17:17708600-17712600	Genic enhancers	Fetal Muscle Trunk	muscle
45	chr17:17708800-17711400	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr17:17708800-17711400	Enhancers	Right Atrium	heart
47	chr17:17708800-17712200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr17:17708800-17713200	Weak transcription	Rectal Smooth Muscle	rectum
49	chr17:17708800-17713400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr17:17709000-17713600	Weak transcription	Primary monocytes fromperipheralblood	blood

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