Variant report

Variant	nsv471701
Chromosome Location	chr17:45511583-45698942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2405)
CpG islands
(count:858)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2405 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45569946-45569952	K562	blood:	n/a	n/a
2	ARID3A	chr17:45697829-45698241	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:45569945-45570183	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:45570956-45571035	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:45693174-45693540	K562	blood:	n/a	n/a
6	ATF1	chr17:45569891-45570104	K562	blood:	n/a	n/a
7	ATF2	chr17:45569649-45570147	GM12878	blood:	n/a	n/a
8	ATF3	chr17:45569734-45570294	A549	lung:	n/a	n/a
9	ATF3	chr17:45569636-45570283	A549	lung:	n/a	n/a
10	ATF3	chr17:45569908-45570164	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr17:45569872-45570174	K562	blood:	n/a	n/a
12	BACH1	chr17:45688008-45688377	K562	blood:	n/a	n/a
13	BACH1	chr17:45569861-45570142	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr17:45688020-45688343	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr17:45569645-45570111	GM12878	blood:	n/a	n/a
16	BATF	chr17:45688022-45688356	GM12878	blood:	n/a	chr17:45688193-45688204
17	BATF	chr17:45688037-45688336	GM12878	blood:	n/a	chr17:45688193-45688204
18	BATF	chr17:45578032-45578241	GM12878	blood:	n/a	n/a
19	BATF	chr17:45579678-45580209	GM12878	blood:	n/a	chr17:45580000-45580010
20	BATF	chr17:45579872-45580148	GM12878	blood:	n/a	chr17:45580000-45580010
21	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
22	BCL11A	chr17:45579757-45579928	GM12878	blood:	n/a	n/a
23	BCL11A	chr17:45579668-45580125	GM12878	blood:	n/a	chr17:45579999-45580008
24	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
25	BCLAF1	chr17:45569636-45570116	GM12878	blood:	n/a	chr17:45569672-45569681
26	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
27	BHLHE40	chr17:45569767-45570239	GM12878	blood:	n/a	n/a
28	BHLHE40	chr17:45569785-45570156	A549	lung:	n/a	n/a
29	BHLHE40	chr17:45569774-45570248	HepG2	liver:	n/a	n/a
30	BHLHE40	chr17:45569770-45570296	HepG2	liver:	n/a	n/a
31	BHLHE40	chr17:45605793-45605974	HepG2	liver:	n/a	n/a
32	BHLHE40	chr17:45569762-45570255	K562	blood:	n/a	n/a
33	BRCA1	chr17:45569743-45570065	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr17:45682094-45682251	HepG2	liver:	n/a	n/a
35	BRCA1	chr17:45579916-45580110	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr17:45569612-45570280	K562	blood:	n/a	n/a
37	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
38	CBX3	chr17:45569445-45570802	K562	blood:	n/a	n/a
39	CBX3	chr17:45697551-45698344	HCT-116	colon:	n/a	n/a
40	CBX3	chr17:45577979-45578350	K562	blood:	n/a	n/a
41	CCNT2	chr17:45608329-45608370	K562	blood:	n/a	n/a
42	CCNT2	chr17:45569865-45570079	K562	blood:	n/a	n/a
43	CEBPB	chr17:45616172-45616360	K562	blood:	n/a	chr17:45616275-45616286
44	CEBPB	chr17:45579926-45580036	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
46	CEBPB	chr17:45687180-45687630	A549	lung:	n/a	chr17:45687274-45687285
47	CEBPB	chr17:45665732-45665756	K562	blood:	n/a	n/a
48	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
49	CEBPB	chr17:45687378-45687406	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr17:45569940-45570140	HepG2	liver:	n/a	n/a

(count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45566670-45566720	HRE	kidney:	n/a
2	chr17:45608114-45608164	IMR90	lung:	fetal
3	chr17:45608114-45608164	HNPCEpiC	eye:	n/a
4	chr17:45604514-45604564	HIPEpiC	eye:	n/a
5	chr17:45566670-45566720	HRE	kidney:	n/a
6	chr17:45608114-45608164	IMR90	lung:	fetal
7	chr17:45608114-45608164	HNPCEpiC	eye:	n/a
8	chr17:45604514-45604564	HIPEpiC	eye:	n/a
9	chr17:45608114-45608164	HCPEpiC	choroid plexus:	n/a
10	chr17:45608315-45608365	ProgFib	skin:	n/a
11	chr17:45608114-45608164	Hela-S3	cervix:	n/a
12	chr17:45681383-45681433	SK-N-SH	brain:	n/a
13	chr17:45570133-45570183	NB4	blood:	n/a
14	chr17:45566670-45566720	AG09309	skin:	n/a
15	chr17:45608114-45608164	AoSMC	blood vessel:	n/a
16	chr17:45681383-45681433	HRCEpiC	kidney:	n/a
17	chr17:45570168-45570218	Jurkat	blood:	n/a
18	chr17:45608315-45608365	HEEpiC	esophagus:	n/a
19	chr17:45608315-45608365	A549	lung:	n/a
20	chr17:45570133-45570183	IMR90	lung:	fetal
21	chr17:45608114-45608164	AG04450	lung:	fetal
22	chr17:45573695-45573745	HEK293	kidney:	embryo
23	chr17:45570133-45570183	SKMC	muscle:	n/a
24	chr17:45612338-45612388	SK-N-SH	brain:	n/a
25	chr17:45573695-45573745	AG04449	skin:	fetal
26	chr17:45573695-45573745	AG10803	skin:	n/a
27	chr17:45566670-45566720	SKMC	muscle:	n/a
28	chr17:45609121-45609171	Caco-2	colon:	n/a
29	chr17:45570133-45570183	MCF10A-Er-Src	breast:	n/a
30	chr17:45569959-45570009	HPAEpiC	pulmonary alveolar:	n/a
31	chr17:45566670-45566720	HIPEpiC	eye:	n/a
32	chr17:45570168-45570218	ovcar-3	ovarian:	n/a
33	chr17:45612338-45612388	CMK	blood:	n/a
34	chr17:45612338-45612388	MCF-7	breast:	n/a
35	chr17:45570168-45570218	HepG2	liver:	n/a
36	chr17:45608823-45608873	NT2-D1	testis:	n/a
37	chr17:45608315-45608365	ECC-1	luminal epithelium:	n/a
38	chr17:45608114-45608164	HRCEpiC	kidney:	n/a
39	chr17:45569959-45570009	BE2_C	brain:	n/a
40	chr17:45608823-45608873	HAEpiC	amniotic membrane:	n/a
41	chr17:45573695-45573745	RPTEC	kidney:	n/a
42	chr17:45569959-45570009	AG04449	skin:	fetal
43	chr17:45608315-45608365	NHDF-neo	bronchial:	n/a
44	chr17:45690396-45690446	NH-A	brain:	n/a
45	chr17:45690396-45690446	HEK293	kidney:	embryo
46	chr17:45570168-45570218	HPAEpiC	pulmonary alveolar:	n/a
47	chr17:45609121-45609171	HEEpiC	esophagus:	n/a
48	chr17:45608315-45608365	SK-N-MC	brain:	n/a
49	chr17:45608823-45608873	NB4	blood:	n/a
50	chr17:45608315-45608365	HMEC	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45695726..45697562-chr17:45698247..45700833,3	K562	blood:
2	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
3	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:
4	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
5	chr17:45697869..45699408-chr17:45722972..45724595,2	K562	blood:
6	chr17:45695726..45697562-chr17:45698247..45700833,3	K562	blood:
7	chr17:45399473..45401724-chr17:45692079..45694320,2	K562	blood:
8	chr17:45698425..45699322-chr17:45867182..45867731,2	MCF-7	breast:
9	chr17:45694580..45697420-chr17:45726459..45728756,2	K562	blood:
10	chr17:45567844..45569771-chr17:45694216..45696585,2	K562	blood:
11	chr17:45679584..45682875-chr17:45684553..45688203,6	K562	blood:
12	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
13	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
14	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
15	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:
16	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
17	chr17:45568465..45570063-chr17:45725230..45727294,2	K562	blood:

(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
MRPL45P2	TF binding region
ENSG00000206734	TF binding region
NPEPPS	CpG island
MRPL45P2	CpG island
ENSG00000206734	CpG island
ENSG00000228782	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000141279	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000263766	chromatin interactions
ENSG00000263293	chromatin interactions

Extended variants
information (count: 6275 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:6275 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557650646	chr17:45511647-45511648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564073682	chr17:45511681-45511682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116071339	chr17:45511687-45511688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539989669	chr17:45511688-45511689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373739576	chr17:45511691-45511692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572095225	chr17:45511694-45511695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541101082	chr17:45511748-45511749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560757432	chr17:45511772-45511773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574341333	chr17:45511831-45511832	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs149821929	chr17:45511851-45511852	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs568262205	chr17:45511858-45511859	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs546824292	chr17:45511901-45511902	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs533270303	chr17:45511932-45511933	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs563197018	chr17:45511984-45511985	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs551424303	chr17:45511995-45511996	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs532183105	chr17:45512046-45512047	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs117958322	chr17:45512051-45512052	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs112757678	chr17:45512125-45512126	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs183455840	chr17:45512128-45512129	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs186721982	chr17:45512130-45512131	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs568374686	chr17:45512140-45512141	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs114912937	chr17:45512173-45512174	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs551297687	chr17:45512264-45512265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561878320	chr17:45512274-45512275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2125466	chr17:45512305-45512306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571204112	chr17:45512334-45512335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371625083	chr17:45512345-45512346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147918512	chr17:45512412-45512413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527837325	chr17:45512443-45512444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4338849	chr17:45512483-45512484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs111522771	chr17:45512487-45512488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567041789	chr17:45512492-45512493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534436277	chr17:45512555-45512556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529042198	chr17:45512559-45512560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554621838	chr17:45512570-45512571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114005747	chr17:45512742-45512743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192354126	chr17:45512746-45512747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577329331	chr17:45512775-45512776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556528227	chr17:45512809-45512810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370348358	chr17:45512878-45512879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75054318	chr17:45512894-45512895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370737853	chr17:45512908-45512909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141752129	chr17:45512921-45512922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184826279	chr17:45512922-45512923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528252668	chr17:45512942-45512943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147054437	chr17:45512959-45512960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567938007	chr17:45513029-45513030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9899859	chr17:45513049-45513050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs550572442	chr17:45513056-45513057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs36124511	chr17:45513089-45513090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3027 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45501400-45514600	Weak transcription	Primary T cells from cord blood	blood
2	chr17:45501400-45554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr17:45501400-45554400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr17:45501600-45511800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr17:45501600-45511800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr17:45501600-45515600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr17:45501600-45520200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr17:45501600-45555400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr17:45501600-45556400	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr17:45501800-45511800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr17:45501800-45511800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr17:45501800-45512400	Weak transcription	Primary B cells from cord blood	blood
13	chr17:45501800-45533400	Weak transcription	Gastric	stomach
14	chr17:45501800-45547400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr17:45501800-45550200	Weak transcription	Ovary	ovary
16	chr17:45502200-45513600	Weak transcription	Fetal Brain Male	brain
17	chr17:45502200-45548000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr17:45502800-45548600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr17:45503000-45512000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr17:45503200-45511800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr17:45503200-45511800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr17:45503200-45512200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr17:45503200-45545400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr17:45505200-45550200	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr17:45506400-45523000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr17:45507200-45555000	Weak transcription	Fetal Thymus	thymus
27	chr17:45507600-45519800	Weak transcription	HepG2	liver
28	chr17:45507600-45554200	Weak transcription	Left Ventricle	heart
29	chr17:45507800-45511800	Weak transcription	Fetal Intestine Large	intestine
30	chr17:45508000-45521000	Weak transcription	Fetal Intestine Small	intestine
31	chr17:45509400-45527800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr17:45509600-45527800	Weak transcription	Fetal Stomach	stomach
33	chr17:45511800-45512000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr17:45511800-45512000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr17:45511800-45512200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr17:45511800-45512200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr17:45511800-45512200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr17:45511800-45512200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
39	chr17:45512200-45513200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr17:45512200-45514800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr17:45512200-45530400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr17:45512200-45530800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr17:45512200-45550200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr17:45513000-45544000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr17:45513400-45545400	Weak transcription	Liver	Liver
46	chr17:45514000-45530200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr17:45514600-45515000	ZNF genes & repeats	Primary T cells from cord blood	blood
48	chr17:45514800-45515600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr17:45514800-45516400	Weak transcription	K562	blood
50	chr17:45514800-45517600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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