Variant report

Variant	esv1793478
Chromosome Location	chr17:45518444-45671051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1829)
CpG islands
(count:732)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1829 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45570956-45571035	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:45569946-45569952	K562	blood:	n/a	n/a
3	ARID3A	chr17:45569945-45570183	HepG2	liver:	n/a	n/a
4	ATF1	chr17:45569891-45570104	K562	blood:	n/a	n/a
5	ATF2	chr17:45569649-45570147	GM12878	blood:	n/a	n/a
6	ATF3	chr17:45569872-45570174	K562	blood:	n/a	n/a
7	ATF3	chr17:45569636-45570283	A549	lung:	n/a	n/a
8	ATF3	chr17:45569734-45570294	A549	lung:	n/a	n/a
9	ATF3	chr17:45569908-45570164	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:45569861-45570142	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr17:45579678-45580209	GM12878	blood:	n/a	chr17:45580000-45580010
12	BATF	chr17:45578032-45578241	GM12878	blood:	n/a	n/a
13	BATF	chr17:45569645-45570111	GM12878	blood:	n/a	n/a
14	BATF	chr17:45579872-45580148	GM12878	blood:	n/a	chr17:45580000-45580010
15	BCL11A	chr17:45579757-45579928	GM12878	blood:	n/a	n/a
16	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
17	BCL11A	chr17:45579668-45580125	GM12878	blood:	n/a	chr17:45579999-45580008
18	BCLAF1	chr17:45569636-45570116	GM12878	blood:	n/a	chr17:45569672-45569681
19	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
20	BHLHE40	chr17:45569774-45570248	HepG2	liver:	n/a	n/a
21	BHLHE40	chr17:45569762-45570255	K562	blood:	n/a	n/a
22	BHLHE40	chr17:45605793-45605974	HepG2	liver:	n/a	n/a
23	BHLHE40	chr17:45569785-45570156	A549	lung:	n/a	n/a
24	BHLHE40	chr17:45569767-45570239	GM12878	blood:	n/a	n/a
25	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
26	BHLHE40	chr17:45569770-45570296	HepG2	liver:	n/a	n/a
27	BRCA1	chr17:45569743-45570065	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr17:45579916-45580110	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr17:45569445-45570802	K562	blood:	n/a	n/a
30	CBX3	chr17:45569612-45570280	K562	blood:	n/a	n/a
31	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
32	CBX3	chr17:45577979-45578350	K562	blood:	n/a	n/a
33	CCNT2	chr17:45569865-45570079	K562	blood:	n/a	n/a
34	CCNT2	chr17:45608329-45608370	K562	blood:	n/a	n/a
35	CEBPB	chr17:45644646-45644894	Hela-S3	cervix:	n/a	chr17:45644788-45644801
36	CEBPB	chr17:45593807-45594016	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr17:45570637-45571182	HepG2	liver:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571024-45571037 chr17:45571025-45571036
38	CEBPB	chr17:45569945-45570228	A549	lung:	n/a	n/a
39	CEBPB	chr17:45589395-45589618	K562	blood:	n/a	n/a
40	CEBPB	chr17:45609557-45609591	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr17:45569950-45569994	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr17:45569950-45570239	IMR90	lung:	n/a	n/a
43	CEBPB	chr17:45580366-45580376	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr17:45616205-45616431	K562	blood:	n/a	chr17:45616275-45616286
45	CEBPB	chr17:45569930-45570084	HepG2	liver:	n/a	n/a
46	CEBPB	chr17:45570649-45571036	A549	lung:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571025-45571036
47	CEBPB	chr17:45569746-45570250	K562	blood:	n/a	n/a
48	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
49	CEBPB	chr17:45665732-45665756	K562	blood:	n/a	n/a
50	CEBPB	chr17:45665580-45665831	IMR90	lung:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45609121-45609171	A549	lung:	n/a
2	chr17:45604514-45604564	Hela-S3	cervix:	n/a
3	chr17:45609121-45609171	NH-A	brain:	n/a
4	chr17:45573695-45573745	SK-N-MC	brain:	n/a
5	chr17:45570048-45570098	SK-N-SH	brain:	n/a
6	chr17:45573695-45573745	HCPEpiC	choroid plexus:	n/a
7	chr17:45609121-45609171	SAEC	small airway:	n/a
8	chr17:45573695-45573745	NH-A	brain:	n/a
9	chr17:45570048-45570098	A549	lung:	n/a
10	chr17:45608114-45608164	HNPCEpiC	eye:	n/a
11	chr17:45570168-45570218	IMR90	lung:	fetal
12	chr17:45612338-45612388	NB4	blood:	n/a
13	chr17:45608315-45608365	H1-hESC	embryonic stem cell:	embryo
14	chr17:45570048-45570098	NB4	blood:	n/a
15	chr17:45569959-45570009	BJ	skin:	n/a
16	chr17:45566670-45566720	Caco-2	colon:	n/a
17	chr17:45604514-45604564	AG09309	skin:	n/a
18	chr17:45612338-45612388	HAEpiC	amniotic membrane:	n/a
19	chr17:45608823-45608873	SK-N-MC	brain:	n/a
20	chr17:45569959-45570009	HAEpiC	amniotic membrane:	n/a
21	chr17:45608114-45608164	HCM	heart:	n/a
22	chr17:45604514-45604564	NB4	blood:	n/a
23	chr17:45569959-45570009	HUVEC	blood vessel:	n/a
24	chr17:45566670-45566720	ProgFib	skin:	n/a
25	chr17:45608315-45608365	SK-N-SH_RA	brain:	n/a
26	chr17:45566670-45566720	HEEpiC	esophagus:	n/a
27	chr17:45608823-45608873	HEK293	kidney:	embryo
28	chr17:45566670-45566720	NT2-D1	testis:	n/a
29	chr17:45608315-45608365	BE2_C	brain:	n/a
30	chr17:45608823-45608873	NHBE	bronchial:	n/a
31	chr17:45570048-45570098	H1-hESC	embryonic stem cell:	embryo
32	chr17:45570168-45570218	HepG2	liver:	n/a
33	chr17:45608114-45608164	Jurkat	blood:	n/a
34	chr17:45608114-45608164	IMR90	lung:	fetal
35	chr17:45608315-45608365	IMR90	lung:	fetal
36	chr17:45609121-45609171	Caco-2	colon:	n/a
37	chr17:45608114-45608164	U87	brain:	n/a
38	chr17:45604514-45604564	T-47D	breast:	n/a
39	chr17:45569959-45570009	NB4	blood:	n/a
40	chr17:45569959-45570009	HCT-116	colon:	n/a
41	chr17:45608114-45608164	A549	lung:	n/a
42	chr17:45608114-45608164	HepG2	liver:	n/a
43	chr17:45609121-45609171	RPTEC	kidney:	n/a
44	chr17:45573695-45573745	Hela-S3	cervix:	n/a
45	chr17:45570168-45570218	HCF	heart:	n/a
46	chr17:45604514-45604564	HRE	kidney:	n/a
47	chr17:45604514-45604564	AG10803	skin:	n/a
48	chr17:45608823-45608873	HNPCEpiC	eye:	n/a
49	chr17:45608823-45608873	HEEpiC	esophagus:	n/a
50	chr17:45604514-45604564	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
2	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
3	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
4	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
5	chr17:45567844..45569771-chr17:45694216..45696585,2	K562	blood:
6	chr17:45568465..45570063-chr17:45725230..45727294,2	K562	blood:
7	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C17orf57-1	chr17:45522601-45522883	NONHSAT054305

No data

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000206734	TF binding region
MRPL45P2	TF binding region
NPEPPS	CpG island
ENSG00000206734	CpG island
MRPL45P2	CpG island
ENSG00000129514	chromatin interactions
ENSG00000141279	chromatin interactions
ENSG00000263766	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000228782	chromatin interactions

Extended variants
information (count: 5144 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:5144 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537122558	chr17:45518507-45518508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs36044203	chr17:45518517-45518518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527400275	chr17:45518522-45518523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377382625	chr17:45518529-45518530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548761088	chr17:45518540-45518541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184272966	chr17:45518543-45518544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62076510	chr17:45518583-45518584	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs536108897	chr17:45518648-45518649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376328681	chr17:45518721-45518722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35426644	chr17:45518762-45518763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4060814	chr17:45518763-45518764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71141909	chr17:45518764-45518765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58910634	chr17:45518765-45518766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555213834	chr17:45518798-45518799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537645891	chr17:45518801-45518802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575087041	chr17:45518862-45518863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188271094	chr17:45518913-45518914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76604421	chr17:45518960-45518961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs80035840	chr17:45519005-45519006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116801497	chr17:45519100-45519101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181029184	chr17:45519168-45519169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558302064	chr17:45519315-45519316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201659806	chr17:45519364-45519365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368683693	chr17:45519365-45519366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571980709	chr17:45519374-45519375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540970866	chr17:45519404-45519405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185350082	chr17:45519501-45519502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560809246	chr17:45519567-45519568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529929720	chr17:45519594-45519595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73324468	chr17:45519623-45519624	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563123464	chr17:45519631-45519632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532534582	chr17:45519709-45519710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373991871	chr17:45519790-45519791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190189006	chr17:45519792-45519793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565960543	chr17:45519796-45519797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115324565	chr17:45519807-45519808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548906828	chr17:45519819-45519820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568807580	chr17:45520005-45520006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538674419	chr17:45520012-45520013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35740884	chr17:45520028-45520029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182464215	chr17:45520034-45520035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186594202	chr17:45520090-45520091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147531107	chr17:45520103-45520104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554158071	chr17:45520112-45520113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538369957	chr17:45520138-45520139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558577068	chr17:45520166-45520167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367872713	chr17:45520198-45520199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541062253	chr17:45520301-45520302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201403133	chr17:45520428-45520429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370297134	chr17:45520494-45520495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	21163964	CNVD
Epithelial cancer	20478067	CNVD

Chromatin state (count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45501400-45554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:45501400-45554400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr17:45501600-45520200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr17:45501600-45555400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr17:45501600-45556400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr17:45501800-45533400	Weak transcription	Gastric	stomach
7	chr17:45501800-45547400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr17:45501800-45550200	Weak transcription	Ovary	ovary
9	chr17:45502200-45548000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr17:45502800-45548600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr17:45503200-45545400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr17:45505200-45550200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr17:45506400-45523000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr17:45507200-45555000	Weak transcription	Fetal Thymus	thymus
15	chr17:45507600-45519800	Weak transcription	HepG2	liver
16	chr17:45507600-45554200	Weak transcription	Left Ventricle	heart
17	chr17:45508000-45521000	Weak transcription	Fetal Intestine Small	intestine
18	chr17:45509400-45527800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr17:45509600-45527800	Weak transcription	Fetal Stomach	stomach
20	chr17:45512200-45530400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr17:45512200-45530800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr17:45512200-45550200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr17:45513000-45544000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr17:45513400-45545400	Weak transcription	Liver	Liver
25	chr17:45514000-45530200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr17:45515000-45519400	Weak transcription	Primary T cells from cord blood	blood
27	chr17:45515400-45551600	Weak transcription	Fetal Intestine Large	intestine
28	chr17:45515600-45554200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr17:45515800-45531800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr17:45516000-45556400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr17:45516200-45531800	Weak transcription	Esophagus	oesophagus
32	chr17:45516800-45553200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr17:45517000-45550600	Weak transcription	Adipose Nuclei	Adipose
34	chr17:45517200-45547600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr17:45517400-45547400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr17:45517600-45520200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr17:45517600-45530200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr17:45517600-45550200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr17:45518000-45519000	Weak transcription	Primary hematopoietic stem cells	blood
40	chr17:45518000-45568800	Weak transcription	K562	blood
41	chr17:45518200-45554200	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr17:45518400-45520400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr17:45518400-45521400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr17:45518400-45545800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr17:45518400-45550200	Weak transcription	Lung	lung
46	chr17:45518600-45520400	Weak transcription	Hela-S3	cervix
47	chr17:45518600-45569200	Weak transcription	Brain Anterior Caudate	brain
48	chr17:45518800-45530200	Weak transcription	Fetal Muscle Leg	muscle
49	chr17:45519000-45519600	Strong transcription	Primary hematopoietic stem cells	blood
50	chr17:45519000-45545400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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