Variant report

Variant	esv1804597
Chromosome Location	chr17:44380009-44792469
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3299)
CpG islands
(count:611)
Chromatin interactive
region (count:3)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3299 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

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	chr17:44462786-44463333	GM12878	blood:	n/a	chr17:44462802-44462811
4	BATF	chr17:44654451-44654736	GM12878	blood:	n/a	n/a
5	BATF	chr17:44675819-44676288	GM12878	blood:	n/a	n/a
6	BATF	chr17:44626703-44627007	GM12878	blood:	n/a	n/a
7	BATF	chr17:44426424-44426637	GM12878	blood:	n/a	chr17:44426612-44426623
8	BATF	chr17:44626698-44626970	GM12878	blood:	n/a	n/a
9	BATF	chr17:44416874-44417227	GM12878	blood:	n/a	n/a
10	BATF	chr17:44458389-44458723	GM12878	blood:	n/a	chr17:44458489-44458498 chr17:44458545-44458553
11	BATF	chr17:44512119-44512374	GM12878	blood:	n/a	n/a
12	BATF	chr17:44425712-44426070	GM12878	blood:	n/a	n/a
13	BATF	chr17:44644359-44644572	GM12878	blood:	n/a	chr17:44644547-44644558
14	BATF	chr17:44436526-44436811	GM12878	blood:	n/a	n/a
15	BATF	chr17:44680387-44680931	GM12878	blood:	n/a	chr17:44680402-44680411
16	BATF	chr17:44585826-44586028	GM12878	blood:	n/a	n/a
17	BATF	chr17:44426399-44426775	GM12878	blood:	n/a	chr17:44426612-44426623
18	BATF	chr17:44425670-44426070	GM12878	blood:	n/a	n/a
19	BATF	chr17:44462787-44463331	GM12878	blood:	n/a	chr17:44462802-44462811
20	BATF	chr17:44488796-44489164	GM12878	blood:	n/a	n/a
21	BATF	chr17:44458415-44458691	GM12878	blood:	n/a	chr17:44458489-44458498 chr17:44458545-44458553
22	BATF	chr17:44627869-44628070	GM12878	blood:	n/a	n/a
23	BATF	chr17:44680386-44680933	GM12878	blood:	n/a	chr17:44680402-44680411
24	BATF	chr17:44706376-44706744	GM12878	blood:	n/a	n/a
25	BATF	chr17:44643647-44644005	GM12878	blood:	n/a	n/a
26	BATF	chr17:44644334-44644710	GM12878	blood:	n/a	chr17:44644547-44644558
27	BATF	chr17:44729691-44729946	GM12878	blood:	n/a	n/a
28	BATF	chr17:44457898-44458200	GM12878	blood:	n/a	chr17:44458165-44458174
29	BATF	chr17:44643605-44644005	GM12878	blood:	n/a	n/a
30	BATF	chr17:44408832-44409108	GM12878	blood:	n/a	n/a
31	BATF	chr17:44408815-44409145	GM12878	blood:	n/a	n/a
32	BATF	chr17:44457906-44458207	GM12878	blood:	n/a	chr17:44458165-44458174
33	BATF	chr17:44675761-44676320	GM12878	blood:	n/a	n/a
34	BATF	chr17:44628701-44628901	GM12878	blood:	n/a	n/a
35	BATF	chr17:44634730-44635083	GM12878	blood:	n/a	n/a
36	BCL11A	chr17:44675843-44676322	GM12878	blood:	n/a	n/a
37	BCL11A	chr17:44512118-44512445	GM12878	blood:	n/a	n/a
38	BCL11A	chr17:44626773-44626954	GM12878	blood:	n/a	n/a
39	BCL11A	chr17:44512094-44512335	GM12878	blood:	n/a	n/a
40	BCL11A	chr17:44488891-44489204	GM12878	blood:	n/a	n/a
41	BCL11A	chr17:44425696-44426085	GM12878	blood:	n/a	n/a
42	BCL11A	chr17:44408911-44409092	GM12878	blood:	n/a	n/a
43	BCL11A	chr17:44488867-44489095	GM12878	blood:	n/a	n/a
44	BCL11A	chr17:44462833-44463305	GM12878	blood:	n/a	chr17:44462875-44462882 chr17:44462942-44462951
45	BCL11A	chr17:44729666-44729907	GM12878	blood:	n/a	n/a
46	BCL11A	chr17:44425665-44426004	GM12878	blood:	n/a	n/a
47	BCL11A	chr17:44680433-44680905	GM12878	blood:	n/a	chr17:44680542-44680551 chr17:44680475-44680482
48	BCL11A	chr17:44680508-44680869	GM12878	blood:	n/a	chr17:44680542-44680551
49	BCL11A	chr17:44729690-44730017	GM12878	blood:	n/a	n/a
50	BCL11A	chr17:44410832-44411017	GM12878	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:44648385-44648435	GM06990	blood:	n/a
2	chr17:44648385-44648435	GM06990	blood:	n/a
3	chr17:44648385-44648435	HPAEpiC	pulmonary alveolar:	n/a
4	chr17:44657394-44657444	BJ	skin:	n/a
5	chr17:44657394-44657444	HMEC	breast:	n/a
6	chr17:44790735-44790785	HCT-116	colon:	n/a
7	chr17:44394546-44394596	PrEC	prostate:	n/a
8	chr17:44648385-44648435	AG09319	gingival:	n/a
9	chr17:44790735-44790785	AG04450	lung:	fetal
10	chr17:44394546-44394596	GM19239	blood:	n/a
11	chr17:44394546-44394596	Hepatocyte	liver:	n/a
12	chr17:44648385-44648435	IMR90	lung:	fetal
13	chr17:44439469-44439519	AG04450	lung:	fetal
14	chr17:44394546-44394596	HCF	heart:	n/a
15	chr17:44657154-44657204	HAEpiC	amniotic membrane:	n/a
16	chr17:44604660-44604710	HRE	kidney:	n/a
17	chr17:44657154-44657204	Hela-S3	cervix:	n/a
18	chr17:44702619-44702669	HCPEpiC	choroid plexus:	n/a
19	chr17:44394546-44394596	BJ	skin:	n/a
20	chr17:44604660-44604710	PFSK-1	brain:	n/a
21	chr17:44418204-44418254	SKMC	muscle:	n/a
22	chr17:44790735-44790785	ovcar-3	ovarian:	n/a
23	chr17:44418204-44418254	HAEpiC	amniotic membrane:	n/a
24	chr17:44648385-44648435	CMK	blood:	n/a
25	chr17:44790735-44790785	U87	brain:	n/a
26	chr17:44702619-44702669	HNPCEpiC	eye:	n/a
27	chr17:44648385-44648435	HCF	heart:	n/a
28	chr17:44657394-44657444	SAEC	small airway:	n/a
29	chr17:44394546-44394596	HAEpiC	amniotic membrane:	n/a
30	chr17:44439469-44439519	K562	blood:	n/a
31	chr17:44418204-44418254	HNPCEpiC	eye:	n/a
32	chr17:44702619-44702669	NHDF-neo	bronchial:	n/a
33	chr17:44439469-44439519	T-47D	breast:	n/a
34	chr17:44394546-44394596	GM12892	blood:	n/a
35	chr17:44790735-44790785	K562	blood:	n/a
36	chr17:44418204-44418254	AoSMC	blood vessel:	n/a
37	chr17:44657154-44657204	GM12892	blood:	n/a
38	chr17:44785029-44785079	NT2-D1	testis:	n/a
39	chr17:44394546-44394596	K562	blood:	n/a
40	chr17:44702619-44702669	LNCaP	prostate:	n/a
41	chr17:44394546-44394596	RPTEC	kidney:	n/a
42	chr17:44439469-44439519	MCF10A-Er-Src	breast:	n/a
43	chr17:44439469-44439519	BJ	skin:	n/a
44	chr17:44790735-44790785	SK-N-SH	brain:	n/a
45	chr17:44657394-44657444	HCF	heart:	n/a
46	chr17:44657154-44657204	Caco-2	colon:	n/a
47	chr17:44790735-44790785	AG09309	skin:	n/a
48	chr17:44657394-44657444	SKMC	muscle:	n/a
49	chr17:44439469-44439519	HUVEC	blood vessel:	n/a
50	chr17:44604660-44604710	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:44567076..44568576-chr17:59642520..59644055,2	MCF-7	breast:
2	chr17:44791299..44793121-chr17:44854894..44857732,2	MCF-7	breast:
3	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC37A2-1	chr17:44685215-44685279	ucscGeneNc_uc002iot_1
2	lnc-NSF-3	chr17:44614900-44615180	NONHSAT054211
3	lnc-ARL17B-1	chr17:44636196-44638051	ENSG00000232300.1
4	lnc-NSF-1	chr17:44663233-44663284	l_1459_chr17:44663232-44671620_testes
5	lnc-ARL17B-1	chr17:44639835-44640161	ENSG00000232300.1
6	lnc-NSF-2	chr17:44620700-44622821	NONHSAT054212
7	lnc-AC217773.1-3	chr17:44397045-44397325	NONHSAT054210
8	lnc-NSF-1	chr17:44671411-44671620	l_1459_chr17:44663232-44671620_testes
9	lnc-LRRC37A2-1	chr17:44680600-44680663	ucscGeneNc_uc002iot_1
10	lnc-NSF-1	chr17:44670559-44670675	l_1459_chr17:44663232-44671620_testes
11	lnc-LRRC37A2-1	chr17:44684607-44685035	ucscGeneNc_uc002iot_1
12	lnc-LRRC37A2-1	chr17:44687052-44688810	ucscGeneNc_uc002iot_1
13	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
RN7SL199P	TF binding region
ARL17A	TF binding region
ARL17B	TF binding region
RN7SL656P	TF binding region
ENSG00000266497	TF binding region
FAM215B	TF binding region
LRRC37A2	TF binding region
NSF	CpG island
NSFP1	CpG island
RN7SL199P	CpG island
ARL17A	CpG island
ARL17B	CpG island
RN7SL656P	CpG island
ENSG00000266497	CpG island
FAM215B	CpG island
LRRC37A2	CpG island

Extended variants
information (count: 2448 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2448 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558958452	chr17:44392140-44392141	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs2667827	chr17:44392145-44392146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs144143290	chr17:44392154-44392155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541567328	chr17:44392217-44392218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs1895687	chr17:44392539-44392540	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561354598	chr17:44392658-44392659	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs530274753	chr17:44392659-44392660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs113547483	chr17:44392732-44392733	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs62073235	chr17:44393080-44393081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200290934	chr17:44393289-44393290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs543994265	chr17:44393290-44393291	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563832352	chr17:44393292-44393293	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs532797396	chr17:44393293-44393294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs375958280	chr17:44393296-44393297	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs549273578	chr17:44393298-44393299	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs550976043	chr17:44393323-44393324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs570879838	chr17:44393669-44393670	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527269202	chr17:44393953-44393954	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs547124469	chr17:44393956-44393957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs537462963	chr17:44393979-44393980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567346144	chr17:44393987-44393988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536102437	chr17:44393988-44393989	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs556276115	chr17:44393994-44393995	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs569868203	chr17:44393998-44393999	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs563869643	chr17:44394501-44394502	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532713747	chr17:44394508-44394509	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs550053872	chr17:44394528-44394529	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs3096456	chr17:44394562-44394563	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs3096457	chr17:44394566-44394567	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs546114665	chr17:44394579-44394580	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs374208115	chr17:44394633-44394634	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs368890608	chr17:44394715-44394716	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs527328230	chr17:44394809-44394810	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs386797388	chr17:44394818-44394819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs62073236	chr17:44395689-44395690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111881224	chr17:44395830-44395831	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs62073237	chr17:44396253-44396254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs147325373	chr17:44396400-44396401	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs113766101	chr17:44396525-44396526	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs368430259	chr17:44396539-44396540	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs367559358	chr17:44396877-44396878	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs62073239	chr17:44396906-44396907	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs2552461	chr17:44396946-44396947	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs28445920	chr17:44396960-44396961	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs546984645	chr17:44397283-44397284	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs532397561	chr17:44401406-44401407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552357999	chr17:44401463-44401464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565992012	chr17:44401466-44401467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534879403	chr17:44401482-44401483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548313086	chr17:44401652-44401653	Weak 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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD

Chromatin state (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44401400-44409600	Weak transcription	Liver	Liver
2	chr17:44401600-44430200	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr17:44407200-44439000	Weak transcription	Fetal Stomach	stomach
4	chr17:44408000-44410800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr17:44413200-44426000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr17:44414800-44431200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:44426000-44426400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr17:44426000-44426400	Enhancers	Primary B cells from peripheral blood	blood
9	chr17:44426400-44431200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr17:44426400-44439000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr17:44428400-44431200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr17:44439000-44439400	Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr17:44439000-44439400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr17:44439000-44439400	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr17:44439000-44439600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr17:44439000-44439600	Active TSS	Fetal Intestine Large	intestine
17	chr17:44439000-44439600	Active TSS	Fetal Intestine Small	intestine
18	chr17:44439000-44439600	Active TSS	Fetal Stomach	stomach
19	chr17:44439000-44439600	Active TSS	Pancreas	Pancrea
20	chr17:44439000-44439600	Active TSS	Right Atrium	heart
21	chr17:44439000-44439600	Active TSS	Dnd41	blood
22	chr17:44439000-44439600	Active TSS	Osteobl	bone
23	chr17:44439000-44439800	Active TSS	Fetal Thymus	thymus
24	chr17:44439200-44439600	Active TSS	Brain Germinal Matrix	brain
25	chr17:44439200-44439600	Active TSS	Fetal Kidney	kidney
26	chr17:44455200-44463400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr17:44461600-44461800	Enhancers	Primary T cells fromperipheralblood	blood
28	chr17:44461800-44465200	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr17:44463400-44463800	Enhancers	Primary B cells from peripheral blood	blood
30	chr17:44470600-44470800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr17:44471000-44495200	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr17:44477600-44477800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr17:44477800-44478600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr17:44478600-44478800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr17:44478800-44492600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr17:44482600-44488800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr17:44485200-44497800	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr17:44485600-44499800	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr17:44486600-44487000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr17:44486600-44487600	Enhancers	Osteobl	bone
41	chr17:44487000-44489600	Weak transcription	Primary B cells from peripheral blood	blood
42	chr17:44489600-44490000	Enhancers	Primary B cells from peripheral blood	blood
43	chr17:44489600-44490000	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr17:44490400-44490600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr17:44495200-44495600	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr17:44495600-44497600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr17:44526600-44552800	Weak transcription	Primary B cells from peripheral blood	blood
48	chr17:44533200-44534800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr17:44533800-44555400	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr17:44534400-44537400	Weak transcription	Primary monocytes fromperipheralblood	blood

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