Variant report

Variant	nsv1032350
Chromosome Location	chr9:6328167-6630686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3294)
CpG islands
(count:918)
Chromatin interactive
region (count:102)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:3294 , 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	chr9:6592072-6592556	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6585226-6585461	K562	blood:	n/a	n/a
3	ARID3A	chr9:6590416-6591246	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6552110-6552393	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6568252-6568419	K562	blood:	n/a	n/a
6	ARID3A	chr9:6542871-6542968	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6585150-6585539	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:6530270-6530987	HepG2	liver:	n/a	n/a
9	ATF1	chr9:6594559-6594926	K562	blood:	n/a	n/a
10	ATF1	chr9:6408431-6408699	K562	blood:	n/a	n/a
11	ATF2	chr9:6566455-6566850	GM12878	blood:	n/a	n/a
12	ATF2	chr9:6605130-6605645	GM12878	blood:	n/a	n/a
13	ATF2	chr9:6412410-6413365	GM12878	blood:	n/a	n/a
14	ATF2	chr9:6575185-6575710	GM12878	blood:	n/a	n/a
15	ATF2	chr9:6429200-6429720	GM12878	blood:	n/a	n/a
16	ATF2	chr9:6412216-6412546	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr9:6412411-6413372	GM12878	blood:	n/a	n/a
18	ATF2	chr9:6433329-6433785	GM12878	blood:	n/a	n/a
19	ATF2	chr9:6598244-6598868	GM12878	blood:	n/a	n/a
20	ATF2	chr9:6412893-6413353	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr9:6597976-6598892	GM12878	blood:	n/a	n/a
22	ATF2	chr9:6620437-6621001	GM12878	blood:	n/a	n/a
23	ATF3	chr9:6408408-6408659	K562	blood:	n/a	n/a
24	BACH1	chr9:6413473-6413555	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr9:6412549-6413272	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr9:6598357-6598887	GM12878	blood:	n/a	chr9:6598659-6598670
27	BATF	chr9:6592868-6593086	GM12878	blood:	n/a	n/a
28	BATF	chr9:6355807-6355988	GM12878	blood:	n/a	chr9:6355904-6355915
29	BATF	chr9:6433477-6433726	GM12878	blood:	n/a	n/a
30	BATF	chr9:6566437-6566727	GM12878	blood:	n/a	n/a
31	BATF	chr9:6620458-6620655	GM12878	blood:	n/a	n/a
32	BATF	chr9:6598389-6598834	GM12878	blood:	n/a	chr9:6598659-6598670
33	BCL11A	chr9:6594611-6594793	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:6598313-6598874	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:6605220-6605551	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:6429260-6429615	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:6412600-6413034	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:6412796-6413030	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:6575318-6575518	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:6605232-6605584	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:6598377-6598720	GM12878	blood:	n/a	n/a
42	BCL3	chr9:6566337-6566811	GM12878	blood:	n/a	n/a
43	BCL3	chr9:6412429-6413349	GM12878	blood:	n/a	chr9:6412547-6412560 chr9:6412552-6412565
44	BCL3	chr9:6558003-6558364	GM12878	blood:	n/a	n/a
45	BCL3	chr9:6598339-6598796	GM12878	blood:	n/a	n/a
46	BCL3	chr9:6575300-6575684	GM12878	blood:	n/a	n/a
47	BCLAF1	chr9:6412420-6413716	GM12878	blood:	n/a	chr9:6413655-6413664 chr9:6413653-6413666 chr9:6412547-6412560 chr9:6412552-6412565
48	BCLAF1	chr9:6575167-6575735	GM12878	blood:	n/a	n/a
49	BCLAF1	chr9:6598022-6598904	GM12878	blood:	n/a	n/a
50	BCLAF1	chr9:6598356-6598906	GM12878	blood:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6411086-6411136	HepG2	liver:	n/a
2	chr9:6412836-6412886	A549	lung:	n/a
3	chr9:6412836-6412886	GM12891	blood:	n/a
4	chr9:6411086-6411136	HepG2	liver:	n/a
5	chr9:6412836-6412886	A549	lung:	n/a
6	chr9:6412836-6412886	GM12891	blood:	n/a
7	chr9:6413852-6413902	PrEC	prostate:	n/a
8	chr9:6414194-6414244	GM12878	blood:	n/a
9	chr9:6532828-6532878	A549	lung:	n/a
10	chr9:6416274-6416324	AG09309	skin:	n/a
11	chr9:6413544-6413594	PANC-1	pancreas:	n/a
12	chr9:6328386-6328436	SK-N-SH	brain:	n/a
13	chr9:6328493-6328543	HL-60	blood:	n/a
14	chr9:6413167-6413217	HUVEC	blood vessel:	n/a
15	chr9:6412836-6412886	NHDF-neo	bronchial:	n/a
16	chr9:6412886-6412936	BE2_C	brain:	n/a
17	chr9:6328493-6328543	HAEpiC	amniotic membrane:	n/a
18	chr9:6413167-6413217	PANC-1	pancreas:	n/a
19	chr9:6328493-6328543	MCF10A-Er-Src	breast:	n/a
20	chr9:6328386-6328436	ovcar-3	ovarian:	n/a
21	chr9:6411086-6411136	HL-60	blood:	n/a
22	chr9:6414096-6414146	ProgFib	skin:	n/a
23	chr9:6412886-6412936	GM12892	blood:	n/a
24	chr9:6328493-6328543	MCF-7	breast:	n/a
25	chr9:6413045-6413095	GM19239	blood:	n/a
26	chr9:6411086-6411136	ECC-1	luminal epithelium:	n/a
27	chr9:6413544-6413594	HEEpiC	esophagus:	n/a
28	chr9:6411086-6411136	H1-hESC	embryonic stem cell:	embryo
29	chr9:6414096-6414146	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:6414096-6414146	RPTEC	kidney:	n/a
31	chr9:6328386-6328436	H1-hESC	embryonic stem cell:	embryo
32	chr9:6416274-6416324	HUVEC	blood vessel:	n/a
33	chr9:6411086-6411136	GM19239	blood:	n/a
34	chr9:6416274-6416324	NT2-D1	testis:	n/a
35	chr9:6411086-6411136	PANC-1	pancreas:	n/a
36	chr9:6413045-6413095	HCPEpiC	choroid plexus:	n/a
37	chr9:6412991-6413041	SK-N-SH_RA	brain:	n/a
38	chr9:6413544-6413594	AG09309	skin:	n/a
39	chr9:6411086-6411136	NHDF-neo	bronchial:	n/a
40	chr9:6414096-6414146	AG09309	skin:	n/a
41	chr9:6413852-6413902	BE2_C	brain:	n/a
42	chr9:6413544-6413594	AoSMC	blood vessel:	n/a
43	chr9:6412991-6413041	AG04450	lung:	fetal
44	chr9:6416274-6416324	HAEpiC	amniotic membrane:	n/a
45	chr9:6414096-6414146	CMK	blood:	n/a
46	chr9:6413544-6413594	GM12891	blood:	n/a
47	chr9:6552115-6552165	PrEC	prostate:	n/a
48	chr9:6414096-6414146	MCF-7	breast:	n/a
49	chr9:6414194-6414244	NHBE	bronchial:	n/a
50	chr9:6413852-6413902	HepG2	liver:	n/a

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:6413061..6414947-chr9:6424688..6427649,3	MCF-7	breast:
2	chr9:6329167..6331675-chr9:6333759..6336639,2	K562	blood:
3	chr9:6389667..6391498-chr9:6396973..6399114,2	MCF-7	breast:
4	chr9:6588736..6590830-chr9:6680231..6682699,2	MCF-7	breast:
5	chr9:6417292..6420636-chr9:6422611..6425827,4	K562	blood:
6	chr1:8021266..8021839-chr9:6413033..6413897,2	Hela-S3	cervix:
7	chr11:64546386..64547209-chr9:6411955..6412774,2	NB4	blood:
8	chr9:6417024..6418829-chr9:6426585..6429333,3	K562	blood:
9	chr9:6415820..6417559-chr9:6421929..6423594,2	MCF-7	breast:
10	chr9:6412168..6415418-chr9:6418500..6425043,7	MCF-7	breast:
11	chr9:6412902..6414944-chr9:6415944..6418989,4	MCF-7	breast:
12	chr9:6448459..6451463-chr9:6451697..6454641,3	K562	blood:
13	chr1:11968667..11972683-chr9:6399248..6402268,5	K562	blood:
14	chr9:6411987..6416661-chr9:6426661..6431000,5	K562	blood:
15	chr9:6329167..6331675-chr9:6333759..6336639,2	K562	blood:
16	chr9:6354258..6354771-chr9:6567896..6568668,2	MCF-7	breast:
17	chr9:6411739..6415458-chr9:6420668..6426596,8	K562	blood:
18	chr9:6413056..6413599-chrX:150565656..150566334,2	Hela-S3	cervix:
19	chr9:6412621..6414719-chr9:6496485..6499094,2	K562	blood:
20	chr9:6523722..6524445-chr9:6667595..6668159,2	K562	blood:
21	chr9:6478983..6480805-chr9:6480868..6482878,2	K562	blood:
22	chr9:6412168..6415418-chr9:6418500..6425043,7	MCF-7	breast:
23	chr9:6411889..6413422-chr9:6565833..6568598,2	K562	blood:
24	chr9:6533272..6535800-chr9:6681069..6683891,2	K562	blood:
25	chr9:6412634..6415362-chr9:6415861..6419998,11	K562	blood:
26	chr9:6579960..6582259-chr9:6679731..6681701,2	MCF-7	breast:
27	chr9:6415820..6417559-chr9:6421929..6423594,2	MCF-7	breast:
28	chr9:6417024..6418829-chr9:6426585..6429333,3	K562	blood:
29	chr2:85132788..85133313-chr9:6412396..6412970,2	NB4	blood:
30	chr9:6410972..6413613-chr9:6564070..6565701,2	MCF-7	breast:
31	chr15:44718353..44719694-chr9:6411917..6413110,3	NB4	blood:
32	chr9:6593764..6596429-chr9:6597405..6599828,2	MCF-7	breast:
33	chr9:6411739..6416254-chr9:6422493..6426368,7	K562	blood:
34	chr9:6570923..6573857-chr9:6574160..6576030,2	K562	blood:
35	chr9:6443738..6445353-chr9:6446588..6448853,2	K562	blood:
36	chr9:6627812..6629680-chr9:6632614..6635740,3	MCF-7	breast:
37	chr9:6624229..6626158-chr9:6679853..6681433,2	MCF-7	breast:
38	chr9:6408551..6411662-chr9:6412630..6415165,4	MCF-7	breast:
39	chr9:6473054..6475074-chr9:6478186..6480540,2	K562	blood:
40	chr9:6354241..6354767-chr9:6667295..6668097,2	K562	blood:
41	chr9:6413244..6414955-chr9:6415894..6417896,3	MCF-7	breast:
42	chr6:26305236..26306818-chr9:6510894..6512414,2	K562	blood:
43	chr9:6411739..6415458-chr9:6420668..6426596,8	K562	blood:
44	chr9:6417900..6420636-chr9:6424327..6426106,2	K562	blood:
45	chr9:6352849..6355311-chr9:6679612..6682199,2	MCF-7	breast:
46	chr16:89882606..89883507-chr9:6490815..6491315,2	Hela-S3	cervix:
47	chr9:6550978..6552657-chr9:6561789..6563568,2	K562	blood:
48	chr9:6398344..6401128-chr9:6407574..6409551,2	K562	blood:
49	chr19:47616230..47616761-chr9:6413307..6414303,2	NB4	blood:
50	chr9:6488881..6491634-chr9:6498188..6500750,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPD52L3-2	chr9:6460573-6460581	NONHSAT130130
2	lnc-UHRF2-3	chr9:6529539-6529917	NONHSAT130138
3	lnc-C9orf38-2	chr9:6408524-6408756	NONHSAT130128
4	lnc-TPD52L3-2	chr9:6413777-6413911	NONHSAT130130
5	lnc-C9orf38-2	chr9:6408525-6408756	XLOC_007638
6	lnc-UHRF2-4	chr9:6542094-6542350	NONHSAT130139
7	lnc-TPD52L3-2	chr9:6433914-6434173	NONHSAT130130
8	lnc-TPD52L3-2	chr9:6420912-6421142	NONHSAT130130
9	lnc-C9orf38-1	chr9:6449340-6449558	ENSG00000233367.1
10	lnc-C9orf38-2	chr9:6411815-6411865	NONHSAT130128
11	lnc-UHRF2-5	chr9:6568844-6569360	NONHSAT130143
12	lnc-C9orf38-1	chr9:6415145-6415563	ENSG00000233367.1
13	lnc-C9orf38-2	chr9:6411816-6411865	XLOC_007638

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	UHRF2	hsa-let-7a-5p	chr9:6495947-6495968
2	UHRF2	hsa-let-7a-5p	chr9:6506445-6506465
3	UHRF2	hsa-let-7a-5p	chr9:6506458-6506465

Variant related genes	Relation type
TPD52L3	TF binding region
ENSG00000252110	TF binding region
C9orf38	TF binding region
UHRF2	TF binding region
ENSG00000237158	TF binding region
RN7SL25P	TF binding region
ENSG00000233367	TF binding region
GLDC	TF binding region
TPD52L3	CpG island
ENSG00000252110	CpG island
C9orf38	CpG island
UHRF2	CpG island
ENSG00000237158	CpG island
RN7SL25P	CpG island
ENSG00000233367	CpG island
GLDC	CpG island
ENSG00000237158	chromatin interactions
ENSG00000128590	chromatin interactions
ENSG00000137936	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000116288	chromatin interactions
ENSG00000107077	chromatin interactions
ENSG00000187741	chromatin interactions
ENSG00000178445	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000215066	chromatin interactions
ENSG00000177683	chromatin interactions
ENSG00000233367	chromatin interactions
ENSG00000260464	chromatin interactions
ENSG00000259595	chromatin interactions
ENSG00000269038	chromatin interactions
ENSG00000211575	chromatin interactions
ENSG00000252110	chromatin interactions
ENSG00000147854	chromatin interactions
ENSG00000160131	chromatin interactions
ENSG00000137770	chromatin interactions

Extended variants
information (count: 13526 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:13526 , 50 per page) page: 1 2 3 4 5 6 7 ... 271

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142261307	chr9:6328171-6328172	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs186996748	chr9:6328203-6328204	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs543015868	chr9:6328244-6328245	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs116398118	chr9:6328292-6328293	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs546748538	chr9:6328299-6328300	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs528972296	chr9:6328301-6328302	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs190981957	chr9:6328307-6328308	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs559875779	chr9:6328311-6328312	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs35303419	chr9:6328342-6328343	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs151257191	chr9:6328355-6328356	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs111908711	chr9:6328357-6328358	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539490870	chr9:6328408-6328409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374420240	chr9:6328421-6328422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571668408	chr9:6328433-6328434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11553814	chr9:6328440-6328441	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs537397783	chr9:6328441-6328442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549412300	chr9:6328493-6328494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117475693	chr9:6328504-6328505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141637710	chr9:6328507-6328508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147074821	chr9:6328511-6328512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370187738	chr9:6328523-6328524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369317872	chr9:6328548-6328549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373611509	chr9:6328556-6328557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377508099	chr9:6328562-6328563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10975545	chr9:6328563-6328564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376747813	chr9:6328592-6328593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143960234	chr9:6328596-6328597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374167147	chr9:6328611-6328612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369621175	chr9:6328624-6328625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373494234	chr9:6328630-6328631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138795326	chr9:6328643-6328644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142792619	chr9:6328649-6328650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554477691	chr9:6328673-6328674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371715772	chr9:6328676-6328677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377070373	chr9:6328678-6328679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200354889	chr9:6328684-6328685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201977309	chr9:6328686-6328687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368800447	chr9:6328695-6328696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370065176	chr9:6328696-6328697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78770668	chr9:6328698-6328699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147413366	chr9:6328710-6328711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75202744	chr9:6328739-6328740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17853209	chr9:6328745-6328746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542980966	chr9:6328748-6328749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561333352	chr9:6328762-6328763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573329913	chr9:6328774-6328775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142696829	chr9:6328796-6328797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77788073	chr9:6328797-6328798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548511287	chr9:6328811-6328812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372625824	chr9:6328813-6328814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Dyslexia	22102821	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:5400 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6328200-6328400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:6328400-6335800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:6329000-6329400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:6329000-6329600	Enhancers	GM12878-XiMat	blood
5	chr9:6329800-6332400	Enhancers	HUVEC	blood vessel
6	chr9:6330600-6332000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr9:6335800-6336400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:6336200-6336400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:6342200-6342400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:6342400-6352000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr9:6342600-6342800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr9:6342800-6343000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr9:6348000-6348400	Enhancers	HepG2	liver
14	chr9:6348600-6348800	Enhancers	GM12878-XiMat	blood
15	chr9:6351000-6355800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr9:6351400-6352800	Enhancers	Hela-S3	cervix
17	chr9:6351800-6352200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:6352000-6352200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:6352000-6352200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:6352000-6352200	Enhancers	HMEC	breast
21	chr9:6352000-6352400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr9:6352200-6352600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:6352200-6353800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:6352200-6354000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:6352400-6354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:6352400-6354400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:6352600-6353000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:6352800-6353800	Weak transcription	Hela-S3	cervix
29	chr9:6353000-6353200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr9:6353200-6354000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:6353800-6354800	Enhancers	Hela-S3	cervix
32	chr9:6354000-6354200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:6354000-6354800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr9:6354000-6354800	Enhancers	Primary B cells from peripheral blood	blood
35	chr9:6354000-6357200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr9:6354000-6357200	Enhancers	Muscle Satellite Cultured Cells	--
37	chr9:6354000-6357400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:6354000-6357400	Enhancers	HMEC	breast
39	chr9:6354000-6357400	Enhancers	Osteobl	bone
40	chr9:6354000-6358200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:6354200-6354800	Enhancers	Primary B cells from cord blood	blood
42	chr9:6354200-6354800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr9:6354200-6354800	Enhancers	HUVEC	blood vessel
44	chr9:6354200-6355000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr9:6354400-6354600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:6354400-6356800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr9:6354400-6357200	Enhancers	NHDF-Ad	bronchial
48	chr9:6354400-6357400	Enhancers	GM12878-XiMat	blood
49	chr9:6354400-6357400	Enhancers	NHLF	lung
50	chr9:6354600-6355200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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