Variant report

Variant	nsv1056263
Chromosome Location	chr17:44428669-44795260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2615)
CpG islands
(count:488)
Chromatin interactive
region (count:5)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2615 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:44791224-44791474	K562	blood:	n/a	chr17:44791227-44791242
2	ATF1	chr17:44439047-44439255	K562	blood:	n/a	n/a
3	BATF	chr17:44458389-44458723	GM12878	blood:	n/a	chr17:44458489-44458498 chr17:44458545-44458553
4	BATF	chr17:44585826-44586028	GM12878	blood:	n/a	n/a
5	BATF	chr17:44675819-44676288	GM12878	blood:	n/a	n/a
6	BATF	chr17:44462786-44463333	GM12878	blood:	n/a	chr17:44462802-44462811
7	BATF	chr17:44457898-44458200	GM12878	blood:	n/a	chr17:44458165-44458174
8	BATF	chr17:44457906-44458207	GM12878	blood:	n/a	chr17:44458165-44458174
9	BATF	chr17:44488796-44489164	GM12878	blood:	n/a	n/a
10	BATF	chr17:44643647-44644005	GM12878	blood:	n/a	n/a
11	BATF	chr17:44706376-44706744	GM12878	blood:	n/a	n/a
12	BATF	chr17:44680387-44680931	GM12878	blood:	n/a	chr17:44680402-44680411
13	BATF	chr17:44680386-44680933	GM12878	blood:	n/a	chr17:44680402-44680411
14	BATF	chr17:44512119-44512374	GM12878	blood:	n/a	n/a
15	BATF	chr17:44458415-44458691	GM12878	blood:	n/a	chr17:44458489-44458498 chr17:44458545-44458553
16	BATF	chr17:44628701-44628901	GM12878	blood:	n/a	n/a
17	BATF	chr17:44654451-44654736	GM12878	blood:	n/a	n/a
18	BATF	chr17:44627869-44628070	GM12878	blood:	n/a	n/a
19	BATF	chr17:44643605-44644005	GM12878	blood:	n/a	n/a
20	BATF	chr17:44626703-44627007	GM12878	blood:	n/a	n/a
21	BATF	chr17:44462787-44463331	GM12878	blood:	n/a	chr17:44462802-44462811
22	BATF	chr17:44644334-44644710	GM12878	blood:	n/a	chr17:44644547-44644558
23	BATF	chr17:44729691-44729946	GM12878	blood:	n/a	n/a
24	BATF	chr17:44644359-44644572	GM12878	blood:	n/a	chr17:44644547-44644558
25	BATF	chr17:44436526-44436811	GM12878	blood:	n/a	n/a
26	BATF	chr17:44675761-44676320	GM12878	blood:	n/a	n/a
27	BATF	chr17:44634730-44635083	GM12878	blood:	n/a	n/a
28	BATF	chr17:44626698-44626970	GM12878	blood:	n/a	n/a
29	BCL11A	chr17:44599190-44599377	GM12878	blood:	n/a	n/a
30	BCL11A	chr17:44680508-44680869	GM12878	blood:	n/a	chr17:44680542-44680551
31	BCL11A	chr17:44643631-44644020	GM12878	blood:	n/a	n/a
32	BCL11A	chr17:44675843-44676322	GM12878	blood:	n/a	n/a
33	BCL11A	chr17:44462908-44463254	GM12878	blood:	n/a	chr17:44462942-44462951
34	BCL11A	chr17:44706471-44706784	GM12878	blood:	n/a	n/a
35	BCL11A	chr17:44512094-44512335	GM12878	blood:	n/a	n/a
36	BCL11A	chr17:44512118-44512445	GM12878	blood:	n/a	n/a
37	BCL11A	chr17:44457922-44458218	GM12878	blood:	n/a	n/a
38	BCL11A	chr17:44729666-44729907	GM12878	blood:	n/a	n/a
39	BCL11A	chr17:44488891-44489204	GM12878	blood:	n/a	n/a
40	BCL11A	chr17:44643600-44643939	GM12878	blood:	n/a	n/a
41	BCL11A	chr17:44628685-44628870	GM12878	blood:	n/a	n/a
42	BCL11A	chr17:44706447-44706675	GM12878	blood:	n/a	n/a
43	BCL11A	chr17:44680433-44680905	GM12878	blood:	n/a	chr17:44680542-44680551 chr17:44680475-44680482
44	BCL11A	chr17:44626691-44627334	GM12878	blood:	n/a	n/a
45	BCL11A	chr17:44488867-44489095	GM12878	blood:	n/a	n/a
46	BCL11A	chr17:44729690-44730017	GM12878	blood:	n/a	n/a
47	BCL11A	chr17:44626773-44626954	GM12878	blood:	n/a	n/a
48	BCL11A	chr17:44458411-44458725	GM12878	blood:	n/a	n/a
49	BCL11A	chr17:44462833-44463305	GM12878	blood:	n/a	chr17:44462875-44462882 chr17:44462942-44462951
50	BHLHE40	chr17:44595964-44596207	HepG2	liver:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:44604660-44604710	LNCaP	prostate:	n/a
2	chr17:44790735-44790785	SK-N-MC	brain:	n/a
3	chr17:44785029-44785079	HCM	heart:	n/a
4	chr17:44702619-44702669	Caco-2	colon:	n/a
5	chr17:44604660-44604710	HRE	kidney:	n/a
6	chr17:44790735-44790785	T-47D	breast:	n/a
7	chr17:44785029-44785079	H1-hESC	embryonic stem cell:	embryo
8	chr17:44648385-44648435	HRE	kidney:	n/a
9	chr17:44604660-44604710	AG04449	skin:	fetal
10	chr17:44657394-44657444	AG04450	lung:	fetal
11	chr17:44790735-44790785	H1-hESC	embryonic stem cell:	embryo
12	chr17:44702619-44702669	Jurkat	blood:	n/a
13	chr17:44439469-44439519	LNCaP	prostate:	n/a
14	chr17:44657154-44657204	A549	lung:	n/a
15	chr17:44785029-44785079	NHDF-neo	bronchial:	n/a
16	chr17:44657154-44657204	NB4	blood:	n/a
17	chr17:44648385-44648435	HRCEpiC	kidney:	n/a
18	chr17:44785029-44785079	AG09319	gingival:	n/a
19	chr17:44790735-44790785	HRCEpiC	kidney:	n/a
20	chr17:44785029-44785079	NH-A	brain:	n/a
21	chr17:44604660-44604710	PFSK-1	brain:	n/a
22	chr17:44604660-44604710	HUVEC	blood vessel:	n/a
23	chr17:44657394-44657444	HNPCEpiC	eye:	n/a
24	chr17:44657394-44657444	MCF-7	breast:	n/a
25	chr17:44702619-44702669	AG04450	lung:	fetal
26	chr17:44657394-44657444	HRCEpiC	kidney:	n/a
27	chr17:44702619-44702669	Hela-S3	cervix:	n/a
28	chr17:44604660-44604710	HEEpiC	esophagus:	n/a
29	chr17:44785029-44785079	IMR90	lung:	fetal
30	chr17:44785029-44785079	ProgFib	skin:	n/a
31	chr17:44657394-44657444	Hela-S3	cervix:	n/a
32	chr17:44439469-44439519	GM19239	blood:	n/a
33	chr17:44785029-44785079	HAEpiC	amniotic membrane:	n/a
34	chr17:44702619-44702669	PrEC	prostate:	n/a
35	chr17:44657154-44657204	HCT-116	colon:	n/a
36	chr17:44439469-44439519	HAEpiC	amniotic membrane:	n/a
37	chr17:44785029-44785079	HRCEpiC	kidney:	n/a
38	chr17:44604660-44604710	BJ	skin:	n/a
39	chr17:44702619-44702669	NHBE	bronchial:	n/a
40	chr17:44657154-44657204	AG04449	skin:	fetal
41	chr17:44785029-44785079	U87	brain:	n/a
42	chr17:44648385-44648435	LNCaP	prostate:	n/a
43	chr17:44657154-44657204	SK-N-MC	brain:	n/a
44	chr17:44604660-44604710	NT2-D1	testis:	n/a
45	chr17:44657394-44657444	AG10803	skin:	n/a
46	chr17:44790735-44790785	GM06990	blood:	n/a
47	chr17:44439469-44439519	HRPEpiC	eye:	n/a
48	chr17:44439469-44439519	ECC-1	luminal epithelium:	n/a
49	chr17:44790735-44790785	Jurkat	blood:	n/a
50	chr17:44657154-44657204	HCPEpiC	choroid plexus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:44793480..44795717-chr17:44798517..44800537,2	MCF-7	breast:
2	chr17:44791299..44793121-chr17:44854894..44857732,2	MCF-7	breast:
3	chr17:44789439..44791140-chr17:44792595..44794517,2	MCF-7	breast:
4	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
5	chr17:44567076..44568576-chr17:59642520..59644055,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NSF-3	chr17:44614900-44615180	NONHSAT054211
2	lnc-NSF-1	chr17:44663233-44663284	l_1459_chr17:44663232-44671620_testes
3	lnc-WNT3-2	chr17:44793730-44793944	expReg_chr17_8951_-
4	lnc-LRRC37A2-1	chr17:44680600-44680663	ucscGeneNc_uc002iot_1
5	lnc-NSF-2	chr17:44620700-44622821	NONHSAT054212
6	lnc-ARL17B-1	chr17:44639835-44640161	ENSG00000232300.1
7	lnc-WNT3-3	chr17:44793046-44793367	expReg_chr17_8945_-
8	lnc-LRRC37A2-1	chr17:44687052-44688810	ucscGeneNc_uc002iot_1
9	lnc-ARL17B-1	chr17:44636196-44638051	ENSG00000232300.1
10	lnc-LRRC37A2-1	chr17:44685215-44685279	ucscGeneNc_uc002iot_1
11	lnc-NSF-1	chr17:44671411-44671620	l_1459_chr17:44663232-44671620_testes
12	lnc-LRRC37A2-1	chr17:44684607-44685035	ucscGeneNc_uc002iot_1
13	lnc-NSF-1	chr17:44670559-44670675	l_1459_chr17:44663232-44671620_testes
14	lnc-NSF-1	chr17:44668501-44668700	l_1459_chr17:44663232-44671620_testes

No data

Variant related genes	Relation type
NSF	TF binding region
NSFP1	TF binding region
ARL17B	TF binding region
ENSG00000266497	TF binding region
RN7SL199P	TF binding region
FAM215B	TF binding region
ARL17A	TF binding region
LRRC37A2	TF binding region
NSF	CpG island
NSFP1	CpG island
ARL17B	CpG island
ENSG00000266497	CpG island
RN7SL199P	CpG island
FAM215B	CpG island
ARL17A	CpG island
LRRC37A2	CpG island
ENSG00000213326	chromatin interactions
ENSG00000073969	chromatin interactions

Extended variants
information (count: 2250 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2250 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2667877	chr17:44428826-44428827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567480717	chr17:44429009-44429010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536042269	chr17:44429078-44429079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200627290	chr17:44429082-44429083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550140262	chr17:44429323-44429324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569919246	chr17:44429324-44429325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539045460	chr17:44429378-44429379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558958467	chr17:44429555-44429556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201886329	chr17:44429649-44429650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138163080	chr17:44429659-44429660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35595570	chr17:44430254-44430255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199741679	chr17:44430319-44430320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572594564	chr17:44430400-44430401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535149175	chr17:44430432-44430433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554753087	chr17:44430433-44430434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575019266	chr17:44430495-44430496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543655238	chr17:44430503-44430504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148963648	chr17:44430663-44430664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35413275	chr17:44431058-44431059	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs36069309	chr17:44431144-44431145	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs62073908	chr17:44431346-44431347	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs374416748	chr17:44431613-44431614	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs143844730	chr17:44431614-44431615	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs34033114	chr17:44431713-44431714	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs151055464	chr17:44432036-44432037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563640376	chr17:44432190-44432191	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs577079093	chr17:44432205-44432206	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544618479	chr17:44432230-44432231	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs371122498	chr17:44432307-44432308	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs62073910	chr17:44432418-44432419	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs189814532	chr17:44432422-44432423	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs62073911	chr17:44432458-44432459	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs62073912	chr17:44432462-44432463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146306618	chr17:44432891-44432892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62073914	chr17:44433027-44433028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111865921	chr17:44433173-44433174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564509489	chr17:44433288-44433289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527270546	chr17:44433322-44433323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs62073915	chr17:44433370-44433371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62073916	chr17:44433386-44433387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560811594	chr17:44433414-44433415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529902051	chr17:44433432-44433433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28575782	chr17:44433437-44433438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62073917	chr17:44433510-44433511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141435810	chr17:44433861-44433862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62073919	chr17:44434309-44434310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150304852	chr17:44434425-44434426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549961780	chr17:44434527-44434528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138829502	chr17:44434541-44434542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569983147	chr17:44434638-44434639	Weak transcription	TF binding region	1 gene(s)	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
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	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
Neuroticism	17667963	CNVD
Prostate cancer	19156837	CNVD
Williams-beuren syndrome	18553513	CNVD
Mental retardation	17847001	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
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22817714	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD

Chromatin state (count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44401600-44430200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr17:44407200-44439000	Weak transcription	Fetal Stomach	stomach
3	chr17:44414800-44431200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr17:44426400-44431200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr17:44426400-44439000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr17:44428400-44431200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr17:44439000-44439400	Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr17:44439000-44439400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr17:44439000-44439400	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr17:44439000-44439600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr17:44439000-44439600	Active TSS	Fetal Intestine Large	intestine
12	chr17:44439000-44439600	Active TSS	Fetal Intestine Small	intestine
13	chr17:44439000-44439600	Active TSS	Fetal Stomach	stomach
14	chr17:44439000-44439600	Active TSS	Pancreas	Pancrea
15	chr17:44439000-44439600	Active TSS	Right Atrium	heart
16	chr17:44439000-44439600	Active TSS	Dnd41	blood
17	chr17:44439000-44439600	Active TSS	Osteobl	bone
18	chr17:44439000-44439800	Active TSS	Fetal Thymus	thymus
19	chr17:44439200-44439600	Active TSS	Brain Germinal Matrix	brain
20	chr17:44439200-44439600	Active TSS	Fetal Kidney	kidney
21	chr17:44455200-44463400	Weak transcription	Primary B cells from peripheral blood	blood
22	chr17:44461600-44461800	Enhancers	Primary T cells fromperipheralblood	blood
23	chr17:44461800-44465200	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr17:44463400-44463800	Enhancers	Primary B cells from peripheral blood	blood
25	chr17:44470600-44470800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr17:44471000-44495200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr17:44477600-44477800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr17:44477800-44478600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr17:44478600-44478800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr17:44478800-44492600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr17:44482600-44488800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr17:44485200-44497800	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr17:44485600-44499800	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr17:44486600-44487000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr17:44486600-44487600	Enhancers	Osteobl	bone
36	chr17:44487000-44489600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr17:44489600-44490000	Enhancers	Primary B cells from peripheral blood	blood
38	chr17:44489600-44490000	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr17:44490400-44490600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr17:44495200-44495600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr17:44495600-44497600	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr17:44526600-44552800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr17:44533200-44534800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr17:44533800-44555400	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr17:44534400-44537400	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr17:44534800-44535200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr17:44535200-44567200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr17:44537200-44539800	Weak transcription	Primary T cells from cord blood	blood
49	chr17:44537400-44537600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
50	chr17:44537600-44555400	Weak transcription	Primary monocytes fromperipheralblood	blood

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