Variant report

Variant	esv1792649
Chromosome Location	chr17:44627136-44849634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2362)
CpG islands
(count:1586)
Chromatin interactive
region (count:94)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:2362 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

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	chr17:44835995-44836332	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:44842431-44842556	K562	blood:	n/a	n/a
4	ARID3A	chr17:44848353-44848382	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:44842060-44842168	K562	blood:	n/a	n/a
6	ARID3A	chr17:44791224-44791474	K562	blood:	n/a	chr17:44791227-44791242
7	ATF2	chr17:44849532-44850202	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr17:44820302-44820522	K562	blood:	n/a	n/a
9	ATF3	chr17:44820329-44820506	K562	blood:	n/a	n/a
10	BATF	chr17:44643605-44644005	GM12878	blood:	n/a	n/a
11	BATF	chr17:44675819-44676288	GM12878	blood:	n/a	n/a
12	BATF	chr17:44634730-44635083	GM12878	blood:	n/a	n/a
13	BATF	chr17:44627869-44628070	GM12878	blood:	n/a	n/a
14	BATF	chr17:44729691-44729946	GM12878	blood:	n/a	n/a
15	BATF	chr17:44628701-44628901	GM12878	blood:	n/a	n/a
16	BATF	chr17:44643647-44644005	GM12878	blood:	n/a	n/a
17	BATF	chr17:44680386-44680933	GM12878	blood:	n/a	chr17:44680402-44680411
18	BATF	chr17:44644334-44644710	GM12878	blood:	n/a	chr17:44644547-44644558
19	BATF	chr17:44680387-44680931	GM12878	blood:	n/a	chr17:44680402-44680411
20	BATF	chr17:44675761-44676320	GM12878	blood:	n/a	n/a
21	BATF	chr17:44644359-44644572	GM12878	blood:	n/a	chr17:44644547-44644558
22	BATF	chr17:44706376-44706744	GM12878	blood:	n/a	n/a
23	BATF	chr17:44654451-44654736	GM12878	blood:	n/a	n/a
24	BCL11A	chr17:44643600-44643939	GM12878	blood:	n/a	n/a
25	BCL11A	chr17:44706471-44706784	GM12878	blood:	n/a	n/a
26	BCL11A	chr17:44680433-44680905	GM12878	blood:	n/a	chr17:44680542-44680551 chr17:44680475-44680482
27	BCL11A	chr17:44628685-44628870	GM12878	blood:	n/a	n/a
28	BCL11A	chr17:44675843-44676322	GM12878	blood:	n/a	n/a
29	BCL11A	chr17:44729666-44729907	GM12878	blood:	n/a	n/a
30	BCL11A	chr17:44706447-44706675	GM12878	blood:	n/a	n/a
31	BCL11A	chr17:44729690-44730017	GM12878	blood:	n/a	n/a
32	BCL11A	chr17:44626691-44627334	GM12878	blood:	n/a	n/a
33	BCL11A	chr17:44643631-44644020	GM12878	blood:	n/a	n/a
34	BCL11A	chr17:44680508-44680869	GM12878	blood:	n/a	chr17:44680542-44680551
35	BCL3	chr17:44847603-44848555	A549	lung:	n/a	chr17:44847975-44847984 chr17:44848483-44848496
36	BCL3	chr17:44835849-44836359	A549	lung:	n/a	chr17:44836231-44836240
37	BHLHE40	chr17:44842085-44842706	K562	blood:	n/a	n/a
38	BHLHE40	chr17:44813601-44813729	GM12878	blood:	n/a	n/a
39	BHLHE40	chr17:44820255-44820536	K562	blood:	n/a	n/a
40	BHLHE40	chr17:44848024-44848264	K562	blood:	n/a	n/a
41	BHLHE40	chr17:44826849-44826861	K562	blood:	n/a	n/a
42	BHLHE40	chr17:44658897-44659167	HepG2	liver:	n/a	n/a
43	BHLHE40	chr17:44849507-44849791	K562	blood:	n/a	n/a
44	BRCA1	chr17:44847779-44847904	HepG2	liver:	n/a	n/a
45	BRCA1	chr17:44849472-44850007	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr17:44656873-44657506	K562	blood:	n/a	n/a
47	CBX3	chr17:44848081-44848699	K562	blood:	n/a	n/a
48	CBX3	chr17:44847453-44847958	K562	blood:	n/a	n/a
49	CBX3	chr17:44842003-44842772	K562	blood:	n/a	n/a
50	CBX3	chr17:44656415-44656822	K562	blood:	n/a	n/a

(count:1586 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:44657394-44657444	ovcar-3	ovarian:	n/a
2	chr17:44648385-44648435	IMR90	lung:	fetal
3	chr17:44845861-44845911	AG04449	skin:	fetal
4	chr17:44702619-44702669	AG04450	lung:	fetal
5	chr17:44834262-44834312	AoSMC	blood vessel:	n/a
6	chr17:44824478-44824528	SK-N-SH	brain:	n/a
7	chr17:44803928-44803978	AG09319	gingival:	n/a
8	chr17:44847268-44847318	CMK	blood:	n/a
9	chr17:44835681-44835731	MCF-7	breast:	n/a
10	chr17:44821280-44821330	HUVEC	blood vessel:	n/a
11	chr17:44648385-44648435	AG04449	skin:	fetal
12	chr17:44648385-44648435	PrEC	prostate:	n/a
13	chr17:44843875-44843925	HAEpiC	amniotic membrane:	n/a
14	chr17:44824478-44824528	HNPCEpiC	eye:	n/a
15	chr17:44849214-44849264	K562	blood:	n/a
16	chr17:44810162-44810212	SK-N-MC	brain:	n/a
17	chr17:44799470-44799520	AG09309	skin:	n/a
18	chr17:44820573-44820623	MCF10A-Er-Src	breast:	n/a
19	chr17:44657394-44657444	Hepatocyte	liver:	n/a
20	chr17:44820573-44820623	PANC-1	pancreas:	n/a
21	chr17:44802702-44802752	SK-N-SH	brain:	n/a
22	chr17:44820573-44820623	NH-A	brain:	n/a
23	chr17:44845861-44845911	SKMC	muscle:	n/a
24	chr17:44845777-44845827	U87	brain:	n/a
25	chr17:44657154-44657204	NT2-D1	testis:	n/a
26	chr17:44845861-44845911	AG04450	lung:	fetal
27	chr17:44657154-44657204	H1-hESC	embryonic stem cell:	embryo
28	chr17:44834262-44834312	SK-N-MC	brain:	n/a
29	chr17:44810162-44810212	BJ	skin:	n/a
30	chr17:44812378-44812428	GM12878	blood:	n/a
31	chr17:44799588-44799638	H1-hESC	embryonic stem cell:	embryo
32	chr17:44799470-44799520	PFSK-1	brain:	n/a
33	chr17:44824478-44824528	HL-60	blood:	n/a
34	chr17:44845777-44845827	AG04449	skin:	fetal
35	chr17:44849214-44849264	IMR90	lung:	fetal
36	chr17:44845777-44845827	ovcar-3	ovarian:	n/a
37	chr17:44847427-44847477	BJ	skin:	n/a
38	chr17:44657154-44657204	NB4	blood:	n/a
39	chr17:44847268-44847318	ProgFib	skin:	n/a
40	chr17:44802702-44802752	AoSMC	blood vessel:	n/a
41	chr17:44810162-44810212	HNPCEpiC	eye:	n/a
42	chr17:44843875-44843925	SK-N-SH_RA	brain:	n/a
43	chr17:44849214-44849264	BJ	skin:	n/a
44	chr17:44845861-44845911	SAEC	small airway:	n/a
45	chr17:44835681-44835731	RPTEC	kidney:	n/a
46	chr17:44820573-44820623	HRPEpiC	eye:	n/a
47	chr17:44821280-44821330	A549	lung:	n/a
48	chr17:44843875-44843925	NHBE	bronchial:	n/a
49	chr17:44820573-44820623	AG04450	lung:	fetal
50	chr17:44702619-44702669	HAEpiC	amniotic membrane:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:44823632..44825811-chr17:44831938..44833806,2	K562	blood:
2	chr17:44812780..44815644-chr17:44839923..44842823,2	K562	blood:
3	chr17:44820992..44822869-chr17:44847358..44849527,2	K562	blood:
4	chr17:44808673..44811660-chr17:44847775..44850081,2	K562	blood:
5	chr17:44818942..44822528-chr17:44824445..44826575,4	K562	blood:
6	chr17:44823632..44825811-chr17:44831938..44833806,2	K562	blood:
7	chr17:44801354..44803469-chr17:44805636..44807734,2	K562	blood:
8	chr17:44846645..44849185-chr17:44896689..44899109,2	MCF-7	breast:
9	chr17:44809047..44811071-chr17:44813381..44815876,2	K562	blood:
10	chr17:44813669..44815710-chr17:44826122..44828858,2	K562	blood:
11	chr17:44797929..44800251-chr17:44801008..44803313,2	K562	blood:
12	chr17:44834549..44837328-chr17:44842622..44845050,2	K562	blood:
13	chr17:44806392..44808378-chr17:44817039..44819825,2	K562	blood:
14	chr17:44836082..44838287-chr17:44847835..44850037,2	MCF-7	breast:
15	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
16	chr17:44843310..44845974-chr17:44848991..44851957,3	MCF-7	breast:
17	chr17:44801247..44804412-chr17:44846741..44850099,3	K562	blood:
18	chr17:44845867..44847496-chr17:44895029..44897224,2	K562	blood:
19	chr17:44821369..44826185-chr17:44846753..44849990,6	K562	blood:
20	chr17:44820992..44822869-chr17:44847358..44849527,2	K562	blood:
21	chr17:44837102..44839238-chr17:44845941..44848841,2	K562	blood:
22	chr17:44848118..44848659-chr5:65439946..65440535,2	Hela-S3	cervix:
23	chr17:44267872..44270663-chr17:44839838..44842513,2	K562	blood:
24	chr17:44806392..44808378-chr17:44817039..44819825,2	K562	blood:
25	chr17:44809047..44811071-chr17:44813381..44815876,2	K562	blood:
26	chr17:44834549..44837328-chr17:44842622..44845050,2	K562	blood:
27	chr17:44833407..44835634-chr17:44872755..44874510,2	K562	blood:
28	chr17:44813669..44815710-chr17:44826122..44828858,2	K562	blood:
29	chr17:44825152..44828455-chr17:44829776..44834617,4	MCF-7	breast:
30	chr17:44840704..44842981-chr17:44847991..44849653,2	MCF-7	breast:
31	chr17:44808203..44811071-chr17:44813381..44816398,3	K562	blood:
32	chr17:44848353..44849074-chr6:26158086..26158790,2	Hela-S3	cervix:
33	chr17:44841367..44842987-chr17:44894656..44897026,2	K562	blood:
34	chr17:44830114..44832534-chr17:44845890..44849410,4	K562	blood:
35	chr17:44848371..44851556-chr17:44854343..44857073,3	MCF-7	breast:
36	chr17:44801336..44803073-chr17:44904905..44907821,2	K562	blood:
37	chr17:44848117..44849092-chr4:25235386..25236084,2	Hela-S3	cervix:
38	chr17:44845310..44847853-chr17:44872083..44874051,2	K562	blood:
39	chr17:44054020..44055535-chr17:44843944..44845683,2	K562	blood:
40	chr17:44839344..44841120-chr17:44841937..44843876,2	K562	blood:
41	chr17:44848344..44850894-chr17:44852175..44854837,4	MCF-7	breast:
42	chr17:44799962..44803131-chr17:44820339..44824064,3	K562	blood:
43	chr17:44836082..44838287-chr17:44847835..44850037,2	MCF-7	breast:
44	chr17:44801354..44803469-chr17:44805636..44807734,2	K562	blood:
45	chr17:44848363..44849947-chr17:45003750..45005877,2	K562	blood:
46	chr17:44789439..44791140-chr17:44792595..44794517,2	MCF-7	breast:
47	chr17:44848565..44850557-chr17:44896605..44898581,4	K562	blood:
48	chr17:44832715..44835385-chr17:44845501..44848268,3	K562	blood:
49	chr17:44833273..44837088-chr17:44837902..44840947,3	K562	blood:
50	chr11:61559555..61560161-chr17:44848660..44849342,2	Hela-S3	cervix:

(count:12 , 50 per page) page: 1

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

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NSF	hsa-miR-16-5p	chr17:44834358-44834378
2	NSF	hsa-miR-215-5p	chr17:44834306-44834328
3	NSF	hsa-miR-192-5p	chr17:44834306-44834328
4	NSF	hsa-miR-26b-5p	chr17:44834076-44834097
5	NSF	hsa-miR-193b-3p	chr17:44834631-44834653
6	NSF	hsa-miR-26b-5p	chr17:44834807-44834828
7	NSF	hsa-miR-103a-3p	chr17:44833388-44833410

Variant related genes	Relation type
NSF	TF binding region
ARL17A	TF binding region
FAM215B	TF binding region
RPS7P11	TF binding region
NSF	CpG island
ARL17A	CpG island
FAM215B	CpG island
RPS7P11	CpG island
ENSG00000261886	chromatin interactions
ENSG00000120071	chromatin interactions
ENSG00000168496	chromatin interactions
ENSG00000207601	chromatin interactions
ENSG00000262633	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000213326	chromatin interactions
ENSG00000134825	chromatin interactions
ENSG00000038210	chromatin interactions
ENSG00000073969	chromatin interactions
ENSG00000153914	chromatin interactions
ENSG00000108379	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000108433	chromatin interactions

Extended variants
information (count: 2522 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:2522 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549980674	chr17:44627518-44627519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146980124	chr17:44627649-44627650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532845432	chr17:44627656-44627657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552594860	chr17:44627687-44627688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571262878	chr17:44627689-44627690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533541468	chr17:44627752-44627753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553995612	chr17:44627753-44627754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375704825	chr17:44627761-44627762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567392033	chr17:44627763-44627764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561374205	chr17:44627768-44627769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377287461	chr17:44627769-44627770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556403676	chr17:44627773-44627774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371029882	chr17:44627782-44627783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374452768	chr17:44627853-44627854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200371089	chr17:44627879-44627880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373316671	chr17:44628042-44628043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576109821	chr17:44628078-44628079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570576616	chr17:44628088-44628089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147180978	chr17:44628094-44628095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547121655	chr17:44628106-44628107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568666334	chr17:44628120-44628121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138841665	chr17:44628125-44628126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572436046	chr17:44628134-44628135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554852949	chr17:44628137-44628138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541043973	chr17:44628167-44628168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554512890	chr17:44628205-44628206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs28398293	chr17:44628221-44628222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543466957	chr17:44628282-44628283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563589156	chr17:44628302-44628303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532589283	chr17:44628322-44628323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546512466	chr17:44628344-44628345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559774132	chr17:44628349-44628350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528756529	chr17:44628448-44628449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547431336	chr17:44628450-44628451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567230972	chr17:44628454-44628455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529817314	chr17:44628456-44628457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549898458	chr17:44628466-44628467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569871808	chr17:44628485-44628486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577762162	chr17:44628491-44628492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538439897	chr17:44628531-44628532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558839681	chr17:44628668-44628669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565856159	chr17:44628704-44628705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534567911	chr17:44628728-44628729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554550138	chr17:44628797-44628798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574492558	chr17:44628826-44628827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147393839	chr17:44628864-44628865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201121186	chr17:44629230-44629231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557021593	chr17:44630044-44630045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561639754	chr17:44630070-44630071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577397672	chr17:44630071-44630072	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	16397240	CNVD
Prostate cancer	17217626	CNVD
Autism	22817714	CNVD

Chromatin state (count:2490 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44567600-44633600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr17:44580400-44628600	Weak transcription	Fetal Stomach	stomach
3	chr17:44605600-44628000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr17:44606000-44632400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr17:44610400-44628000	Weak transcription	Spleen	Spleen
6	chr17:44610600-44627800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr17:44611000-44633200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr17:44611400-44628000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr17:44611600-44633800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr17:44612200-44634200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr17:44612400-44627800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr17:44612400-44637600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr17:44614600-44632400	Weak transcription	Fetal Intestine Small	intestine
14	chr17:44617400-44632400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr17:44617800-44627800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr17:44617800-44634200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr17:44618600-44632200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr17:44618600-44632200	Weak transcription	Osteobl	bone
19	chr17:44619000-44632400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr17:44619000-44632400	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr17:44619000-44634200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr17:44619200-44634200	Weak transcription	HSMMtube	muscle
23	chr17:44619400-44627800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr17:44619400-44632200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr17:44619600-44627800	Weak transcription	Adipose Nuclei	Adipose
26	chr17:44619600-44627800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr17:44619600-44629400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr17:44619600-44632200	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr17:44619600-44632200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr17:44619600-44632200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr17:44619600-44632400	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr17:44619600-44634000	Weak transcription	Brain Hippocampus Middle	brain
33	chr17:44619600-44634200	Weak transcription	Duodenum Mucosa	Duodenum
34	chr17:44619600-44634200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr17:44619800-44631800	Weak transcription	A549	lung
36	chr17:44619800-44632000	Weak transcription	Placenta	Placenta
37	chr17:44620400-44631400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr17:44620400-44632200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr17:44620800-44634200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr17:44621000-44629800	Weak transcription	Primary B cells from peripheral blood	blood
41	chr17:44621200-44629600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr17:44621200-44632200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr17:44621200-44657400	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr17:44624000-44627600	Weak transcription	Gastric	stomach
45	chr17:44624000-44634400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr17:44624800-44632200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr17:44625000-44627400	Weak transcription	Brain Angular Gyrus	brain
48	chr17:44625800-44628600	Weak transcription	Fetal Intestine Large	intestine
49	chr17:44625800-44628600	Weak transcription	Left Ventricle	heart
50	chr17:44626000-44627200	Strong transcription	Primary monocytes fromperipheralblood	blood

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