Variant report

Variant	rs2350976
Chromosome Location	chr17:17708529-17708530
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr17:17708452-17708559	HepG2	liver:	n/a	n/a
2	POLR2A	chr17:17708494-17711625	A549	lung:	n/a	n/a
3	POLR2A	chr17:17708518-17710432	HepG2	liver:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17699415..17703726-chr17:17706608..17710254,4	K562	blood:
2	chr17:17702735..17704555-chr17:17706937..17709032,2	MCF-7	breast:
3	chr17:17693130..17695676-chr17:17706574..17708717,2	K562	blood:
4	chr17:17706399..17710687-chr17:17711145..17715909,7	K562	blood:
5	chr17:17707124..17708984-chr17:17739423..17741026,2	K562	blood:
6	chr17:17586455..17590031-chr17:17707371..17710346,3	MCF-7	breast:
7	chr17:17693638..17695676-chr17:17707217..17709070,2	K562	blood:

No data

Variant related genes	Relation type
RAI1	TF binding region
ENSG00000108557	Chromatin interaction
ENSG00000072310	Chromatin interaction

Extended variants
information (count: 111 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10048206	0.80[MEX][hapmap]
rs1052299	0.82[CEU][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.84[TSI][hapmap]
rs11078406	0.80[MEX][hapmap]
rs1108648	1.00[JPT][hapmap]
rs11650649	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs11652144	0.83[AMR][1000 genomes]
rs11652881	0.95[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11654081	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11656665	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11657130	0.84[AMR][1000 genomes]
rs11657423	0.86[CEU][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.80[TSI][hapmap];0.82[AMR][1000 genomes]
rs11868035	0.82[CEU][hapmap]
rs12453837	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12941039	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs12941356	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12943500	0.82[JPT][hapmap]
rs12946746	0.82[AMR][1000 genomes]
rs12946913	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16960744	0.82[CEU][hapmap];0.80[MEX][hapmap]
rs1889018	0.86[CEU][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap];0.84[AMR][1000 genomes]
rs2236513	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs2297508	0.95[CEU][hapmap];0.92[EUR][1000 genomes]
rs2350977	0.80[MEX][hapmap]
rs3183702	0.82[CEU][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap]
rs3744115	1.00[JPT][hapmap];0.84[MEX][hapmap];0.84[TSI][hapmap]
rs3818717	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.87[TSI][hapmap];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4244602	0.82[JPT][hapmap]
rs4257260	0.80[MEX][hapmap]
rs4341796	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs4470201	0.80[MEX][hapmap]
rs4924822	1.00[JPT][hapmap];0.80[TSI][hapmap]
rs4924823	0.80[MEX][hapmap]
rs4925114	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]
rs4925115	0.91[CEU][hapmap];0.93[TSI][hapmap];0.88[EUR][1000 genomes]
rs4925119	0.91[CEU][hapmap];0.84[MEX][hapmap]
rs4925120	0.82[CEU][hapmap];0.80[MEX][hapmap]
rs4925123	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs4925125	0.80[MEX][hapmap]
rs4925126	0.80[MEX][hapmap]
rs4925129	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs4925130	0.82[JPT][hapmap];0.84[MEX][hapmap]
rs5002487	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs6502619	0.82[JPT][hapmap]
rs6502622	0.80[MEX][hapmap]
rs6502624	0.80[MEX][hapmap]
rs6502625	0.82[JPT][hapmap]
rs6502629	0.82[JPT][hapmap]
rs7207395	0.82[JPT][hapmap]
rs7213225	0.80[MEX][hapmap]
rs7222480	0.88[MEX][hapmap]
rs7224815	0.82[JPT][hapmap]
rs7359509	0.86[CEU][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap];0.82[AMR][1000 genomes]
rs7501812	1.00[JPT][hapmap];0.91[MEX][hapmap];0.80[TSI][hapmap]
rs7503334	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs7503747	0.85[AMR][1000 genomes]
rs8065416	0.80[MEX][hapmap]
rs8065563	0.82[JPT][hapmap];0.91[MEX][hapmap]
rs8066560	0.86[CEU][hapmap];0.80[MEX][hapmap]
rs8066982	0.80[MEX][hapmap]
rs8067439	0.95[CEU][hapmap];0.80[MEX][hapmap];0.95[TSI][hapmap];0.93[EUR][1000 genomes]
rs8070128	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs8070748	0.80[MEX][hapmap]
rs8073001	0.80[MEX][hapmap]
rs8078138	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs8078583	0.82[JPT][hapmap]
rs8079321	0.80[MEX][hapmap]
rs8080061	0.80[MEX][hapmap]
rs8080823	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs950966	0.82[JPT][hapmap];0.88[MEX][hapmap]
rs9891957	0.86[CEU][hapmap];1.00[JPT][hapmap]
rs9899634	0.86[CEU][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap]
rs9902941	0.86[CEU][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap]
rs9907246	1.00[JPT][hapmap];0.88[MEX][hapmap]
rs9907287	0.80[MEX][hapmap]
rs9912895	0.80[MEX][hapmap]
rs9915248	0.82[CEU][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.84[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:35 , 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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2350976	TOM1L2	cis	cerebellum	SCAN
rs2350976	TOM1L2	cis	parietal	SCAN

Chromatin state (count:113 , 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	chr17:17690000-17711200	Weak transcription	Hela-S3	cervix
4	chr17:17695400-17723800	Strong transcription	Dnd41	blood
5	chr17:17696600-17711600	Strong transcription	Fetal Lung	lung
6	chr17:17696800-17708600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr17:17696800-17708800	Weak transcription	Psoas Muscle	Psoas
8	chr17:17696800-17709600	Weak transcription	HSMM	muscle
9	chr17:17696800-17712200	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr17:17697000-17708600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr17:17697000-17708800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr17:17697000-17711400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr17:17697000-17711600	Strong transcription	Gastric	stomach
14	chr17:17697000-17711800	Strong transcription	Fetal Brain Female	brain
15	chr17:17697000-17712400	Strong transcription	Fetal Intestine Large	intestine
16	chr17:17697000-17712600	Strong transcription	Fetal Intestine Small	intestine
17	chr17:17697200-17714800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr17:17697200-17715200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr17:17697200-17715200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr17:17697200-17715800	Strong transcription	Thymus	Thymus
21	chr17:17697400-17712000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr17:17697400-17712200	Strong transcription	Lung	lung
23	chr17:17697400-17713800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr17:17697400-17715400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr17:17697600-17715000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr17:17698000-17713600	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr17:17698000-17715000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr17:17698200-17713400	Weak transcription	HUVEC	blood vessel
29	chr17:17699200-17709200	Weak transcription	HepG2	liver
30	chr17:17699600-17709800	Strong transcription	A549	lung
31	chr17:17700200-17711200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr17:17700200-17712400	Weak transcription	Primary B cells from peripheral blood	blood
33	chr17:17701200-17709200	Weak transcription	Stomach Mucosa	stomach
34	chr17:17703000-17708800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr17:17703000-17710200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr17:17703000-17710600	Strong transcription	Spleen	Spleen
37	chr17:17703000-17712000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr17:17703200-17713400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr17:17703400-17708600	Strong transcription	Fetal Muscle Leg	muscle
40	chr17:17704000-17712600	Strong transcription	Fetal Stomach	stomach
41	chr17:17704200-17708800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr17:17704200-17712600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr17:17704400-17709400	Strong transcription	Stomach Smooth Muscle	stomach
44	chr17:17704600-17708600	Strong transcription	Fetal Muscle Trunk	muscle
45	chr17:17704800-17708600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr17:17704800-17709200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr17:17704800-17711000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr17:17705200-17708800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr17:17705200-17709000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr17:17705200-17709400	Strong transcription	Ovary	ovary

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