Variant report

Variant	nsv529596
Chromosome Location	chr17:44485771-44820329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2346)
CpG islands
(count:854)
Chromatin interactive
region (count:27)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2346 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:44803563-44803581	K562	blood:	n/a	n/a
2	ARID3A	chr17:44791224-44791474	K562	blood:	n/a	chr17:44791227-44791242
3	ATF3	chr17:44820329-44820506	K562	blood:	n/a	n/a
4	ATF3	chr17:44820302-44820522	K562	blood:	n/a	n/a
5	BATF	chr17:44644359-44644572	GM12878	blood:	n/a	chr17:44644547-44644558
6	BATF	chr17:44706376-44706744	GM12878	blood:	n/a	n/a
7	BATF	chr17:44627869-44628070	GM12878	blood:	n/a	n/a
8	BATF	chr17:44643605-44644005	GM12878	blood:	n/a	n/a
9	BATF	chr17:44680386-44680933	GM12878	blood:	n/a	chr17:44680402-44680411
10	BATF	chr17:44675819-44676288	GM12878	blood:	n/a	n/a
11	BATF	chr17:44680387-44680931	GM12878	blood:	n/a	chr17:44680402-44680411
12	BATF	chr17:44643647-44644005	GM12878	blood:	n/a	n/a
13	BATF	chr17:44512119-44512374	GM12878	blood:	n/a	n/a
14	BATF	chr17:44488796-44489164	GM12878	blood:	n/a	n/a
15	BATF	chr17:44654451-44654736	GM12878	blood:	n/a	n/a
16	BATF	chr17:44585826-44586028	GM12878	blood:	n/a	n/a
17	BATF	chr17:44626698-44626970	GM12878	blood:	n/a	n/a
18	BATF	chr17:44628701-44628901	GM12878	blood:	n/a	n/a
19	BATF	chr17:44675761-44676320	GM12878	blood:	n/a	n/a
20	BATF	chr17:44634730-44635083	GM12878	blood:	n/a	n/a
21	BATF	chr17:44729691-44729946	GM12878	blood:	n/a	n/a
22	BATF	chr17:44626703-44627007	GM12878	blood:	n/a	n/a
23	BATF	chr17:44644334-44644710	GM12878	blood:	n/a	chr17:44644547-44644558
24	BCL11A	chr17:44643600-44643939	GM12878	blood:	n/a	n/a
25	BCL11A	chr17:44626691-44627334	GM12878	blood:	n/a	n/a
26	BCL11A	chr17:44488867-44489095	GM12878	blood:	n/a	n/a
27	BCL11A	chr17:44706447-44706675	GM12878	blood:	n/a	n/a
28	BCL11A	chr17:44675843-44676322	GM12878	blood:	n/a	n/a
29	BCL11A	chr17:44643631-44644020	GM12878	blood:	n/a	n/a
30	BCL11A	chr17:44512094-44512335	GM12878	blood:	n/a	n/a
31	BCL11A	chr17:44628685-44628870	GM12878	blood:	n/a	n/a
32	BCL11A	chr17:44599190-44599377	GM12878	blood:	n/a	n/a
33	BCL11A	chr17:44512118-44512445	GM12878	blood:	n/a	n/a
34	BCL11A	chr17:44706471-44706784	GM12878	blood:	n/a	n/a
35	BCL11A	chr17:44680433-44680905	GM12878	blood:	n/a	chr17:44680542-44680551 chr17:44680475-44680482
36	BCL11A	chr17:44729690-44730017	GM12878	blood:	n/a	n/a
37	BCL11A	chr17:44626773-44626954	GM12878	blood:	n/a	n/a
38	BCL11A	chr17:44488891-44489204	GM12878	blood:	n/a	n/a
39	BCL11A	chr17:44680508-44680869	GM12878	blood:	n/a	chr17:44680542-44680551
40	BCL11A	chr17:44729666-44729907	GM12878	blood:	n/a	n/a
41	BHLHE40	chr17:44820255-44820536	K562	blood:	n/a	n/a
42	BHLHE40	chr17:44595964-44596207	HepG2	liver:	n/a	n/a
43	BHLHE40	chr17:44600671-44600894	HepG2	liver:	n/a	n/a
44	BHLHE40	chr17:44658897-44659167	HepG2	liver:	n/a	n/a
45	BHLHE40	chr17:44813601-44813729	GM12878	blood:	n/a	n/a
46	CBX3	chr17:44656873-44657506	K562	blood:	n/a	n/a
47	CBX3	chr17:44656415-44656822	K562	blood:	n/a	n/a
48	CBX3	chr17:44820213-44820584	K562	blood:	n/a	n/a
49	CEBPB	chr17:44803716-44804004	K562	blood:	n/a	n/a
50	CEBPB	chr17:44712957-44713150	IMR90	lung:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:44702619-44702669	ovcar-3	ovarian:	n/a
2	chr17:44648385-44648435	K562	blood:	n/a
3	chr17:44802702-44802752	HRE	kidney:	n/a
4	chr17:44785029-44785079	MCF10A-Er-Src	breast:	n/a
5	chr17:44799518-44799568	GM19239	blood:	n/a
6	chr17:44648385-44648435	ProgFib	skin:	n/a
7	chr17:44799470-44799520	HRE	kidney:	n/a
8	chr17:44803928-44803978	HRCEpiC	kidney:	n/a
9	chr17:44657154-44657204	HPAEpiC	pulmonary alveolar:	n/a
10	chr17:44785029-44785079	CMK	blood:	n/a
11	chr17:44604660-44604710	CMK	blood:	n/a
12	chr17:44799518-44799568	Hepatocyte	liver:	n/a
13	chr17:44812378-44812428	AG10803	skin:	n/a
14	chr17:44802702-44802752	HCM	heart:	n/a
15	chr17:44799470-44799520	T-47D	breast:	n/a
16	chr17:44799470-44799520	ECC-1	luminal epithelium:	n/a
17	chr17:44648385-44648435	HRE	kidney:	n/a
18	chr17:44810162-44810212	K562	blood:	n/a
19	chr17:44802702-44802752	GM12891	blood:	n/a
20	chr17:44799588-44799638	NHBE	bronchial:	n/a
21	chr17:44790735-44790785	AG04449	skin:	fetal
22	chr17:44799588-44799638	AG04449	skin:	fetal
23	chr17:44604660-44604710	A549	lung:	n/a
24	chr17:44812378-44812428	HEK293	kidney:	embryo
25	chr17:44802702-44802752	GM19239	blood:	n/a
26	chr17:44785029-44785079	SK-N-SH	brain:	n/a
27	chr17:44657154-44657204	T-47D	breast:	n/a
28	chr17:44812378-44812428	T-47D	breast:	n/a
29	chr17:44799588-44799638	BE2_C	brain:	n/a
30	chr17:44785029-44785079	Caco-2	colon:	n/a
31	chr17:44702619-44702669	NT2-D1	testis:	n/a
32	chr17:44799518-44799568	HRCEpiC	kidney:	n/a
33	chr17:44604660-44604710	HCPEpiC	choroid plexus:	n/a
34	chr17:44648385-44648435	HUVEC	blood vessel:	n/a
35	chr17:44799518-44799568	GM12892	blood:	n/a
36	chr17:44657154-44657204	HCT-116	colon:	n/a
37	chr17:44657154-44657204	SK-N-SH	brain:	n/a
38	chr17:44799518-44799568	GM12891	blood:	n/a
39	chr17:44657394-44657444	PFSK-1	brain:	n/a
40	chr17:44702619-44702669	HL-60	blood:	n/a
41	chr17:44790735-44790785	AG09309	skin:	n/a
42	chr17:44790735-44790785	NHDF-neo	bronchial:	n/a
43	chr17:44803928-44803978	ProgFib	skin:	n/a
44	chr17:44657154-44657204	ECC-1	luminal epithelium:	n/a
45	chr17:44803928-44803978	HAEpiC	amniotic membrane:	n/a
46	chr17:44790735-44790785	HCM	heart:	n/a
47	chr17:44810162-44810212	BE2_C	brain:	n/a
48	chr17:44785029-44785079	HCPEpiC	choroid plexus:	n/a
49	chr17:44799518-44799568	NHDF-neo	bronchial:	n/a
50	chr17:44790735-44790785	GM12891	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:44804689..44809871-chr17:44845472..44850072,6	K562	blood:
2	chr17:44816270..44819088-chr17:44845691..44848257,2	MCF-7	breast:
3	chr17:44801354..44803469-chr17:44805636..44807734,2	K562	blood:
4	chr17:44567076..44568576-chr17:59642520..59644055,2	MCF-7	breast:
5	chr17:44809047..44811071-chr17:44813381..44815876,2	K562	blood:
6	chr17:44819607..44821857-chr17:44848285..44851793,3	MCF-7	breast:
7	chr17:44808203..44811071-chr17:44813381..44816398,3	K562	blood:
8	chr17:44793480..44795717-chr17:44798517..44800537,2	MCF-7	breast:
9	chr17:44818564..44820440-chr17:44888540..44890190,2	K562	blood:
10	chr17:44789439..44791140-chr17:44792595..44794517,2	MCF-7	breast:
11	chr17:44797929..44800251-chr17:44801008..44803313,2	K562	blood:
12	chr17:44791299..44793121-chr17:44854894..44857732,2	MCF-7	breast:
13	chr17:44806392..44808378-chr17:44817039..44819825,2	K562	blood:
14	chr17:44818942..44822528-chr17:44824445..44826575,4	K562	blood:
15	chr17:44813669..44815710-chr17:44826122..44828858,2	K562	blood:
16	chr17:44801354..44803469-chr17:44805636..44807734,2	K562	blood:
17	chr17:44812780..44815644-chr17:44839923..44842823,2	K562	blood:
18	chr17:44811116..44812890-chr17:44818858..44821196,2	MCF-7	breast:
19	chr17:44806392..44808378-chr17:44817039..44819825,2	K562	blood:
20	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
21	chr17:44811116..44812890-chr17:44818858..44821196,2	MCF-7	breast:
22	chr17:44799962..44803131-chr17:44820339..44824064,3	K562	blood:
23	chr17:44808673..44811660-chr17:44847775..44850081,2	K562	blood:
24	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
25	chr17:44801336..44803073-chr17:44904905..44907821,2	K562	blood:
26	chr17:44808203..44811071-chr17:44813381..44816398,3	K562	blood:
27	chr17:44809047..44811071-chr17:44813381..44815876,2	K562	blood:

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

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

No data

Variant related genes	Relation type
NSF	TF binding region
RN7SL199P	TF binding region
ARL17A	TF binding region
ENSG00000266497	TF binding region
FAM215B	TF binding region
LRRC37A2	TF binding region
RPS7P11	TF binding region
NSF	CpG island
RN7SL199P	CpG island
ARL17A	CpG island
ENSG00000266497	CpG island
FAM215B	CpG island
LRRC37A2	CpG island
RPS7P11	CpG island
ENSG00000073969	chromatin interactions
ENSG00000213326	chromatin interactions

Extended variants
information (count: 2724 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:2724 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182999002	chr17:44485795-44485796	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs150178284	chr17:44485796-44485797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143789424	chr17:44486215-44486216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571530874	chr17:44486643-44486644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199492352	chr17:44486668-44486669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527953249	chr17:44486804-44486805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546301188	chr17:44486849-44486850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560128343	chr17:44486872-44486873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528848147	chr17:44487010-44487011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148137458	chr17:44487271-44487272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548714200	chr17:44487316-44487317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568563670	chr17:44487440-44487441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375519911	chr17:44487482-44487483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537656455	chr17:44487519-44487520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551124966	chr17:44487793-44487794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571470536	chr17:44487794-44487795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141923080	chr17:44487955-44487956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534124902	chr17:44489725-44489726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146904804	chr17:44489742-44489743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553769250	chr17:44489751-44489752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574021612	chr17:44489827-44489828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536645737	chr17:44490166-44490167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556699617	chr17:44490230-44490231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576565864	chr17:44490289-44490290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139316775	chr17:44490467-44490468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554908577	chr17:44490703-44490704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370964719	chr17:44490763-44490764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545633932	chr17:44490824-44490825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143014641	chr17:44490939-44490940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147452371	chr17:44491736-44491737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565448276	chr17:44491880-44491881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369716634	chr17:44491887-44491888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572532003	chr17:44491893-44491894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541749533	chr17:44491965-44491966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561419764	chr17:44492192-44492193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139332514	chr17:44492251-44492252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528860348	chr17:44492714-44492715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373592313	chr17:44493314-44493315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548527826	chr17:44493339-44493340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149586816	chr17:44494110-44494111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531275839	chr17:44494121-44494122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551165530	chr17:44494261-44494262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144265871	chr17:44494308-44494309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571457686	chr17:44494326-44494327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374569899	chr17:44494339-44494340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547718442	chr17:44494352-44494353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146715079	chr17:44494386-44494387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536656188	chr17:44494394-44494395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556563463	chr17:44494400-44494401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370083802	chr17:44494455-44494456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
Breast cancer	16397240	CNVD
Prostate cancer	17217626	CNVD
Autism	22817714	CNVD

Chromatin state (count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44471000-44495200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr17:44478800-44492600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr17:44482600-44488800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr17:44485200-44497800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr17:44485600-44499800	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr17:44486600-44487000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr17:44486600-44487600	Enhancers	Osteobl	bone
8	chr17:44487000-44489600	Weak transcription	Primary B cells from peripheral blood	blood
9	chr17:44489600-44490000	Enhancers	Primary B cells from peripheral blood	blood
10	chr17:44489600-44490000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr17:44490400-44490600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:44495200-44495600	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr17:44495600-44497600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr17:44526600-44552800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr17:44533200-44534800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr17:44533800-44555400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr17:44534400-44537400	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr17:44534800-44535200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr17:44535200-44567200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr17:44537200-44539800	Weak transcription	Primary T cells from cord blood	blood
21	chr17:44537400-44537600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
22	chr17:44537600-44555400	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr17:44552800-44553400	Enhancers	Primary B cells from peripheral blood	blood
24	chr17:44553400-44553800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr17:44553800-44554000	Enhancers	Primary B cells from peripheral blood	blood
26	chr17:44554000-44566200	Weak transcription	Primary B cells from peripheral blood	blood
27	chr17:44554200-44577800	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr17:44554600-44567000	Weak transcription	Fetal Stomach	stomach
29	chr17:44555200-44577800	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr17:44555400-44556200	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr17:44555400-44556800	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr17:44556200-44566800	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr17:44556800-44564200	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr17:44563000-44571000	Weak transcription	Fetal Intestine Large	intestine
35	chr17:44563000-44580200	Weak transcription	Stomach Smooth Muscle	stomach
36	chr17:44563200-44583200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr17:44564200-44564600	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr17:44564200-44582000	Weak transcription	Fetal Intestine Small	intestine
39	chr17:44564600-44566600	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr17:44565400-44581800	Weak transcription	Left Ventricle	heart
41	chr17:44565600-44581800	Weak transcription	Gastric	stomach
42	chr17:44566000-44578800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr17:44566000-44580000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr17:44566000-44581600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr17:44566200-44567600	Strong transcription	Primary B cells from peripheral blood	blood
46	chr17:44566200-44570000	Weak transcription	Fetal Brain Female	brain
47	chr17:44566600-44567200	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr17:44566600-44571600	Weak transcription	Pancreas	Pancrea
49	chr17:44566800-44567600	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr17:44566800-44571200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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