Variant report

Variant	nsv908569
Chromosome Location	chr17:45537395-45603094
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1144)
CpG islands
(count:366)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1144 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45569945-45570183	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:45570956-45571035	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:45569946-45569952	K562	blood:	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	chr17:45569636-45570283	A549	lung:	n/a	n/a
7	ATF3	chr17:45569908-45570164	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr17:45569734-45570294	A549	lung:	n/a	n/a
9	ATF3	chr17:45569872-45570174	K562	blood:	n/a	n/a
10	BACH1	chr17:45569861-45570142	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr17:45579872-45580148	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	chr17:45579678-45580209	GM12878	blood:	n/a	chr17:45580000-45580010
15	BCL11A	chr17:45579668-45580125	GM12878	blood:	n/a	chr17:45579999-45580008
16	BCL11A	chr17:45579757-45579928	GM12878	blood:	n/a	n/a
17	BCLAF1	chr17:45569636-45570116	GM12878	blood:	n/a	chr17:45569672-45569681
18	BHLHE40	chr17:45569762-45570255	K562	blood:	n/a	n/a
19	BHLHE40	chr17:45569785-45570156	A549	lung:	n/a	n/a
20	BHLHE40	chr17:45569770-45570296	HepG2	liver:	n/a	n/a
21	BHLHE40	chr17:45569774-45570248	HepG2	liver:	n/a	n/a
22	BHLHE40	chr17:45569767-45570239	GM12878	blood:	n/a	n/a
23	BRCA1	chr17:45579916-45580110	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr17:45569743-45570065	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr17:45569612-45570280	K562	blood:	n/a	n/a
26	CBX3	chr17:45577979-45578350	K562	blood:	n/a	n/a
27	CBX3	chr17:45569445-45570802	K562	blood:	n/a	n/a
28	CCNT2	chr17:45569865-45570079	K562	blood:	n/a	n/a
29	CEBPB	chr17:45569930-45570084	HepG2	liver:	n/a	n/a
30	CEBPB	chr17:45569950-45570239	IMR90	lung:	n/a	n/a
31	CEBPB	chr17:45569940-45570140	HepG2	liver:	n/a	n/a
32	CEBPB	chr17:45569419-45570032	GM12878	blood:	n/a	n/a
33	CEBPB	chr17:45570649-45571036	A549	lung:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571025-45571036
34	CEBPB	chr17:45570637-45571182	HepG2	liver:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571024-45571037 chr17:45571025-45571036
35	CEBPB	chr17:45589310-45589646	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr17:45589395-45589618	K562	blood:	n/a	n/a
37	CEBPB	chr17:45569746-45570250	K562	blood:	n/a	n/a
38	CEBPB	chr17:45593807-45594016	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr17:45570633-45571101	K562	blood:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571024-45571037 chr17:45571025-45571036
40	CEBPB	chr17:45596411-45596603	IMR90	lung:	n/a	n/a
41	CEBPB	chr17:45569945-45570228	A549	lung:	n/a	n/a
42	CEBPB	chr17:45579500-45579717	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr17:45579926-45580036	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr17:45549562-45549781	HepG2	liver:	n/a	n/a
45	CEBPB	chr17:45569950-45569994	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr17:45580366-45580376	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr17:45569865-45570260	Hela-S3	cervix:	n/a	n/a
48	CEBPD	chr17:45569673-45569842	HepG2	liver:	n/a	n/a
49	CEBPD	chr17:45569936-45570114	HepG2	liver:	n/a	n/a
50	CEBPD	chr17:45569615-45569858	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45570168-45570218	NHDF-neo	bronchial:	n/a
2	chr17:45570168-45570218	HEK293	kidney:	embryo
3	chr17:45569959-45570009	NH-A	brain:	n/a
4	chr17:45570168-45570218	RPTEC	kidney:	n/a
5	chr17:45570133-45570183	GM12891	blood:	n/a
6	chr17:45573695-45573745	AG04450	lung:	fetal
7	chr17:45570168-45570218	HMEC	breast:	n/a
8	chr17:45570133-45570183	NHBE	bronchial:	n/a
9	chr17:45570168-45570218	A549	lung:	n/a
10	chr17:45573695-45573745	HEK293	kidney:	embryo
11	chr17:45570133-45570183	HCPEpiC	choroid plexus:	n/a
12	chr17:45570133-45570183	H1-hESC	embryonic stem cell:	embryo
13	chr17:45570168-45570218	Caco-2	colon:	n/a
14	chr17:45570168-45570218	PFSK-1	brain:	n/a
15	chr17:45569959-45570009	SAEC	small airway:	n/a
16	chr17:45570048-45570098	NB4	blood:	n/a
17	chr17:45570048-45570098	GM12878	blood:	n/a
18	chr17:45569959-45570009	LNCaP	prostate:	n/a
19	chr17:45573695-45573745	Caco-2	colon:	n/a
20	chr17:45569959-45570009	HNPCEpiC	eye:	n/a
21	chr17:45569959-45570009	HepG2	liver:	n/a
22	chr17:45566670-45566720	ECC-1	luminal epithelium:	n/a
23	chr17:45566670-45566720	BE2_C	brain:	n/a
24	chr17:45570168-45570218	GM12891	blood:	n/a
25	chr17:45570133-45570183	PrEC	prostate:	n/a
26	chr17:45570168-45570218	ovcar-3	ovarian:	n/a
27	chr17:45569959-45570009	HRCEpiC	kidney:	n/a
28	chr17:45573695-45573745	T-47D	breast:	n/a
29	chr17:45570048-45570098	RPTEC	kidney:	n/a
30	chr17:45569959-45570009	T-47D	breast:	n/a
31	chr17:45570133-45570183	HRPEpiC	eye:	n/a
32	chr17:45570168-45570218	AG04450	lung:	fetal
33	chr17:45570133-45570183	Hepatocyte	liver:	n/a
34	chr17:45573695-45573745	GM06990	blood:	n/a
35	chr17:45570133-45570183	HEK293	kidney:	embryo
36	chr17:45569959-45570009	Caco-2	colon:	n/a
37	chr17:45573695-45573745	SK-N-SH	brain:	n/a
38	chr17:45570048-45570098	GM12891	blood:	n/a
39	chr17:45573695-45573745	BJ	skin:	n/a
40	chr17:45569959-45570009	HPAEpiC	pulmonary alveolar:	n/a
41	chr17:45569959-45570009	PrEC	prostate:	n/a
42	chr17:45569959-45570009	H1-hESC	embryonic stem cell:	embryo
43	chr17:45566670-45566720	Caco-2	colon:	n/a
44	chr17:45570168-45570218	Hela-S3	cervix:	n/a
45	chr17:45569959-45570009	SK-N-SH	brain:	n/a
46	chr17:45570048-45570098	ECC-1	luminal epithelium:	n/a
47	chr17:45566670-45566720	U87	brain:	n/a
48	chr17:45570133-45570183	GM19239	blood:	n/a
49	chr17:45570168-45570218	HCPEpiC	choroid plexus:	n/a
50	chr17:45570133-45570183	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:45567844..45569771-chr17:45694216..45696585,2	K562	blood:
2	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
3	chr17:45568465..45570063-chr17:45725230..45727294,2	K562	blood:

No data

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

Extended variants
information (count: 2142 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:2142 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9914653	chr17:45537395-45537396	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543522813	chr17:45537415-45537416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148446373	chr17:45537441-45537442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532505086	chr17:45537445-45537446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552593584	chr17:45537485-45537486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185198859	chr17:45537488-45537489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528775705	chr17:45537534-45537535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189658188	chr17:45537537-45537538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568528334	chr17:45537588-45537589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551824407	chr17:45537603-45537604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9908393	chr17:45537607-45537608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs372330542	chr17:45537628-45537629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62076533	chr17:45537642-45537643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538287920	chr17:45537695-45537696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139540561	chr17:45537711-45537712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565672151	chr17:45537712-45537713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567417001	chr17:45537733-45537734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546600080	chr17:45537758-45537759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568026654	chr17:45537760-45537761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113648076	chr17:45537829-45537830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369058082	chr17:45537863-45537864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543904417	chr17:45537906-45537907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557212634	chr17:45537984-45537985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181343235	chr17:45538141-45538142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2446763	chr17:45538161-45538162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546251553	chr17:45538245-45538246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185174946	chr17:45538246-45538247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146651517	chr17:45538251-45538252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542132420	chr17:45538292-45538293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373236036	chr17:45538297-45538298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55883342	chr17:45538310-45538311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs2446764	chr17:45538323-45538324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12952902	chr17:45538383-45538384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12952905	chr17:45538389-45538390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200818591	chr17:45538440-45538441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370140293	chr17:45538441-45538442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56286432	chr17:45538442-45538443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397833429	chr17:45538494-45538495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188415680	chr17:45538518-45538519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551146426	chr17:45538567-45538568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569459025	chr17:45538602-45538603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532062744	chr17:45538658-45538659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551770255	chr17:45538812-45538813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556094438	chr17:45538817-45538818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565307067	chr17:45538892-45538893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7219598	chr17:45538906-45538907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7219599	chr17:45538907-45538908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7219605	chr17:45538914-45538915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7207841	chr17:45538917-45538918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139116941	chr17:45538922-45538923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

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

Chromatin state (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	chr17:45501600-45555400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr17:45501600-45556400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr17:45501800-45547400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr17:45501800-45550200	Weak transcription	Ovary	ovary
7	chr17:45502200-45548000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr17:45502800-45548600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr17:45503200-45545400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr17:45505200-45550200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr17:45507200-45555000	Weak transcription	Fetal Thymus	thymus
12	chr17:45507600-45554200	Weak transcription	Left Ventricle	heart
13	chr17:45512200-45550200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr17:45513000-45544000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr17:45513400-45545400	Weak transcription	Liver	Liver
16	chr17:45515400-45551600	Weak transcription	Fetal Intestine Large	intestine
17	chr17:45515600-45554200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr17:45516000-45556400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr17:45516800-45553200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr17:45517000-45550600	Weak transcription	Adipose Nuclei	Adipose
21	chr17:45517200-45547600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr17:45517400-45547400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr17:45517600-45550200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr17:45518000-45568800	Weak transcription	K562	blood
25	chr17:45518200-45554200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr17:45518400-45545800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr17:45518400-45550200	Weak transcription	Lung	lung
28	chr17:45518600-45569200	Weak transcription	Brain Anterior Caudate	brain
29	chr17:45519000-45545400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr17:45519000-45551600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr17:45519400-45569400	Weak transcription	Primary B cells from peripheral blood	blood
32	chr17:45519600-45550200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr17:45519800-45555000	Weak transcription	Thymus	Thymus
34	chr17:45520000-45542400	Weak transcription	Fetal Lung	lung
35	chr17:45520000-45550600	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr17:45520200-45549200	Weak transcription	HepG2	liver
37	chr17:45521000-45547200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr17:45521000-45550800	Weak transcription	Osteobl	bone
39	chr17:45521400-45543800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr17:45521400-45545400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr17:45523200-45556400	Weak transcription	GM12878-XiMat	blood
42	chr17:45526200-45556000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr17:45526400-45568800	Weak transcription	Brain Angular Gyrus	brain
44	chr17:45526600-45568800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr17:45527000-45568800	Weak transcription	Colon Smooth Muscle	Colon
46	chr17:45527800-45568800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr17:45528200-45544800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr17:45528200-45550200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr17:45528800-45550400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr17:45529000-45549400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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