Variant report

Variant	nsv892171
Chromosome Location	chr9:6648607-6703997
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1946)
CpG islands
(count:610)
Chromatin interactive
region (count:115)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1946 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6683465-6683727	K562	blood:	n/a	n/a
2	ARID3A	chr9:6664541-6665413	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6680666-6681844	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6667619-6667991	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6673778-6673994	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6702813-6703015	K562	blood:	n/a	n/a
7	ARID3A	chr9:6667709-6667966	K562	blood:	n/a	n/a
8	ATF1	chr9:6681148-6681907	K562	blood:	n/a	n/a
9	ATF1	chr9:6683332-6683728	K562	blood:	n/a	n/a
10	ATF2	chr9:6703375-6704596	GM12878	blood:	n/a	n/a
11	ATF2	chr9:6703839-6704309	GM12878	blood:	n/a	n/a
12	ATF2	chr9:6680902-6681966	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr9:6654912-6655463	GM12878	blood:	n/a	n/a
14	ATF2	chr9:6703987-6704605	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr9:6654995-6655416	GM12878	blood:	n/a	n/a
16	ATF2	chr9:6680648-6682329	GM12878	blood:	n/a	n/a
17	ATF2	chr9:6689798-6690646	GM12878	blood:	n/a	n/a
18	ATF2	chr9:6703874-6704656	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr9:6680771-6682208	GM12878	blood:	n/a	n/a
20	ATF2	chr9:6683034-6683764	GM12878	blood:	n/a	n/a
21	ATF2	chr9:6681171-6681904	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr9:6673244-6673922	GM12878	blood:	n/a	n/a
23	ATF2	chr9:6683093-6683781	GM12878	blood:	n/a	n/a
24	ATF3	chr9:6681128-6681460	HepG2	liver:	n/a	chr9:6681281-6681290 chr9:6681270-6681290
25	ATF3	chr9:6664294-6664873	A549	lung:	n/a	n/a
26	ATF3	chr9:6681111-6681416	H1-hESC	embryonic stem cell:	n/a	chr9:6681281-6681290 chr9:6681270-6681290
27	ATF3	chr9:6703937-6704598	GM12878	blood:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
28	ATF3	chr9:6681117-6681516	K562	blood:	n/a	chr9:6681281-6681290 chr9:6681270-6681290
29	ATF3	chr9:6680937-6681651	GM12878	blood:	n/a	chr9:6681281-6681290 chr9:6681270-6681290
30	ATF3	chr9:6703900-6704493	H1-hESC	embryonic stem cell:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
31	ATF3	chr9:6681561-6681854	K562	blood:	n/a	chr9:6681721-6681741
32	ATF3	chr9:6703940-6704551	HepG2	liver:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
33	ATF3	chr9:6681099-6681405	GM12878	blood:	n/a	chr9:6681281-6681290 chr9:6681270-6681290
34	ATF3	chr9:6664488-6664934	A549	lung:	n/a	n/a
35	ATF3	chr9:6703946-6704478	A549	lung:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
36	ATF3	chr9:6703972-6704567	H1-hESC	embryonic stem cell:	n/a	chr9:6704101-6704111
37	ATF3	chr9:6681031-6681807	A549	lung:	n/a	chr9:6681281-6681290 chr9:6681270-6681290 chr9:6681721-6681741
38	ATF3	chr9:6681132-6681923	A549	lung:	n/a	chr9:6681281-6681290 chr9:6681270-6681290 chr9:6681721-6681741
39	BACH1	chr9:6680705-6681903	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr9:6703514-6704556	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr9:6667638-6667964	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr9:6684511-6684834	H1-hESC	embryonic stem cell:	n/a	n/a
43	BATF	chr9:6655058-6655371	GM12878	blood:	n/a	n/a
44	BATF	chr9:6683124-6683704	GM12878	blood:	n/a	n/a
45	BATF	chr9:6681559-6681850	GM12878	blood:	n/a	n/a
46	BATF	chr9:6683125-6683562	GM12878	blood:	n/a	n/a
47	BATF	chr9:6656332-6656632	GM12878	blood:	n/a	n/a
48	BCL11A	chr9:6689923-6690208	GM12878	blood:	n/a	n/a
49	BCL11A	chr9:6673395-6673768	GM12878	blood:	n/a	n/a
50	BCL11A	chr9:6655034-6655412	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6680800-6680850	T-47D	breast:	n/a
2	chr9:6681415-6681465	HL-60	blood:	n/a
3	chr9:6700000-6700050	GM06990	blood:	n/a
4	chr9:6703605-6703655	CMK	blood:	n/a
5	chr9:6681608-6681658	HCPEpiC	choroid plexus:	n/a
6	chr9:6680923-6680973	HRE	kidney:	n/a
7	chr9:6700000-6700050	AG04450	lung:	fetal
8	chr9:6681608-6681658	K562	blood:	n/a
9	chr9:6681415-6681465	GM06990	blood:	n/a
10	chr9:6700000-6700050	HCPEpiC	choroid plexus:	n/a
11	chr9:6680932-6680982	HCM	heart:	n/a
12	chr9:6703949-6703999	H1-hESC	embryonic stem cell:	embryo
13	chr9:6681608-6681658	AG09319	gingival:	n/a
14	chr9:6681608-6681658	NHDF-neo	bronchial:	n/a
15	chr9:6681608-6681658	MCF10A-Er-Src	breast:	n/a
16	chr9:6680923-6680973	MCF-7	breast:	n/a
17	chr9:6681559-6681609	AG09309	skin:	n/a
18	chr9:6680932-6680982	Hela-S3	cervix:	n/a
19	chr9:6683274-6683324	HEEpiC	esophagus:	n/a
20	chr9:6680923-6680973	GM12878	blood:	n/a
21	chr9:6680800-6680850	NH-A	brain:	n/a
22	chr9:6680932-6680982	SAEC	small airway:	n/a
23	chr9:6680800-6680850	HCPEpiC	choroid plexus:	n/a
24	chr9:6680932-6680982	HCT-116	colon:	n/a
25	chr9:6683274-6683324	HNPCEpiC	eye:	n/a
26	chr9:6683274-6683324	MCF10A-Er-Src	breast:	n/a
27	chr9:6681415-6681465	HMEC	breast:	n/a
28	chr9:6680923-6680973	RPTEC	kidney:	n/a
29	chr9:6703949-6703999	PANC-1	pancreas:	n/a
30	chr9:6681415-6681465	HCF	heart:	n/a
31	chr9:6681559-6681609	HIPEpiC	eye:	n/a
32	chr9:6700000-6700050	HCM	heart:	n/a
33	chr9:6700000-6700050	NHDF-neo	bronchial:	n/a
34	chr9:6703949-6703999	NHDF-neo	bronchial:	n/a
35	chr9:6681415-6681465	NHBE	bronchial:	n/a
36	chr9:6703605-6703655	HCF	heart:	n/a
37	chr9:6681415-6681465	SK-N-MC	brain:	n/a
38	chr9:6703605-6703655	AG10803	skin:	n/a
39	chr9:6681415-6681465	RPTEC	kidney:	n/a
40	chr9:6680800-6680850	HepG2	liver:	n/a
41	chr9:6703949-6703999	BJ	skin:	n/a
42	chr9:6680923-6680973	SKMC	muscle:	n/a
43	chr9:6680800-6680850	HNPCEpiC	eye:	n/a
44	chr9:6703949-6703999	Jurkat	blood:	n/a
45	chr9:6681559-6681609	MCF10A-Er-Src	breast:	n/a
46	chr9:6681559-6681609	HCT-116	colon:	n/a
47	chr9:6680923-6680973	Hela-S3	cervix:	n/a
48	chr9:6680932-6680982	IMR90	lung:	fetal
49	chr9:6681559-6681609	HEEpiC	esophagus:	n/a
50	chr9:6703605-6703655	PFSK-1	brain:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:52026416..52027352-chr9:6680809..6681352,2	NB4	blood:
2	chr9:6644301..6646741-chr9:6667847..6669482,2	MCF-7	breast:
3	chr9:6669357..6672334-chr9:6679173..6682127,3	MCF-7	breast:
4	chr17:7834821..7835603-chr9:6681148..6681758,2	NB4	blood:
5	chr9:6680669..6682912-chr9:6702581..6705387,2	MCF-7	breast:
6	chr9:6665749..6668244-chr9:6673822..6675444,2	MCF-7	breast:
7	chr9:6681100..6681879-chrX:153626091..153627039,2	NB4	blood:
8	chr9:6680768..6683764-chr9:6756005..6759658,4	MCF-7	breast:
9	chr9:6680639..6682955-chr9:6686831..6689135,2	MCF-7	breast:
10	chr9:6698340..6700152-chr9:6701946..6704339,2	MCF-7	breast:
11	chr9:6667615..6669315-chr9:6679006..6681464,2	K562	blood:
12	chr9:6690617..6692723-chr9:6701607..6704265,2	MCF-7	breast:
13	chr1:109632782..109633775-chr9:6680831..6681750,2	NB4	blood:
14	chr9:6585232..6587306-chr9:6664888..6666750,2	MCF-7	breast:
15	chr9:6681423..6683704-chr9:6710640..6713020,2	MCF-7	breast:
16	chr9:6682207..6684667-chr9:6707689..6709841,2	K562	blood:
17	chr1:224575474..224576206-chr9:6680757..6681693,2	NB4	blood:
18	chr5:166256227..166256733-chr9:6703705..6704305,2	MCF-7	breast:
19	chr2:192542408..192543057-chr9:6680954..6681934,2	NB4	blood:
20	chr20:3747959..3748789-chr9:6681040..6681979,2	NB4	blood:
21	chr9:6671740..6675372-chr9:6679558..6683814,6	MCF-7	breast:
22	chr17:19551151..19551842-chr9:6681285..6682068,2	Hela-S3	cervix:
23	chr9:6683289..6684884-chr9:6702645..6704262,2	MCF-7	breast:
24	chr12:56320720..56321452-chr9:6681130..6681988,2	NB4	blood:
25	chr15:65596841..65597490-chr9:6680775..6681724,2	NB4	blood:
26	chr9:6656639..6659482-chr9:6662780..6664665,3	MCF-7	breast:
27	chr9:6661026..6667542-chr9:6678514..6683695,9	MCF-7	breast:
28	chr9:6685128..6687481-chr9:6715768..6718010,2	MCF-7	breast:
29	chr12:91346285..91346785-chr9:6680944..6681459,2	NB4	blood:
30	chr5:166255725..166256712-chr9:6703618..6704233,2	MCF-7	breast:
31	chr9:6654607..6656764-chr9:6663214..6664911,2	K562	blood:
32	chr9:6679611..6682734-chr9:6683304..6686457,4	MCF-7	breast:
33	chr11:118991755..118992281-chr9:6681143..6681754,2	NB4	blood:
34	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
35	chr9:6672368..6674682-chr9:6676645..6678823,3	MCF-7	breast:
36	chr9:6680506..6681363-chrX:40943980..40944586,2	NB4	blood:
37	chr9:6684635..6686737-chr9:6757059..6759167,2	MCF-7	breast:
38	chr9:6681451..6683371-chr9:6705864..6707945,2	MCF-7	breast:
39	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
40	chr9:6693828..6696318-chr9:6715075..6717694,2	MCF-7	breast:
41	chr19:42363580..42364427-chr9:6681324..6682242,2	NB4	blood:
42	chr9:6680103..6682666-chr9:6784102..6786978,2	K562	blood:
43	chr9:6683289..6684884-chr9:6702645..6704262,2	MCF-7	breast:
44	chr9:6412059..6414733-chr9:6680071..6683116,4	K562	blood:
45	chr7:148892469..148893164-chr9:6680524..6681026,2	NB4	blood:
46	chr9:6645871..6648933-chr9:6680309..6682972,3	MCF-7	breast:
47	chr9:6680896..6681724-chr9:86535475..86536351,2	HCT-116	colon:
48	chr9:6680639..6682955-chr9:6686831..6689135,2	MCF-7	breast:
49	chr9:6667615..6669315-chr9:6679006..6681464,2	K562	blood:
50	chr9:6699861..6702298-chr9:6702749..6705225,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-13	chr9:6663657-6663792	NONHSAT130148
2	lnc-KDM4C-14	chr9:6660407-6661044	NONHSAT130146
3	lnc-KDM4C-13	chr9:6662424-6662810	NONHSAT130148
4	lnc-KDM4C-12	chr9:6675284-6675614	NONHSAT130149
5	lnc-KDM4C-14	chr9:6661783-6661845	NONHSAT130146
6	lnc-KDM4C-5	chr9:6670425-6670690	NONHSAT130145
7	lnc-KDM4C-14	chr9:6661651-6661936	NONHSAT130147
8	lnc-KDM4C-11	chr9:6697542-6697780	NONHSAT130150
9	lnc-KDM4C-5	chr9:6669544-6669728	NONHSAT130145
10	lnc-KDM4C-13	chr9:6663156-6663366	NONHSAT130148
11	lnc-KDM4C-14	chr9:6661291-6661345	NONHSAT130146
12	lnc-KDM4C-5	chr9:6669544-6669728	ENSG00000236924.1
13	lnc-KDM4C-11	chr9:6694471-6694653	NONHSAT130150
14	lnc-KDM4C-5	chr9:6670425-6670635	ENSG00000236924.1

No data

Variant related genes	Relation type
RNF2P1	TF binding region
RN7SL123P	TF binding region
ENSG00000229611	TF binding region
ENSG00000232946	TF binding region
ENSG00000229057	TF binding region
GLDC	TF binding region
RNF2P1	CpG island
RN7SL123P	CpG island
ENSG00000229611	CpG island
ENSG00000232946	CpG island
ENSG00000229057	CpG island
GLDC	CpG island
ENSG00000168944	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000232946	chromatin interactions
ENSG00000105327	chromatin interactions
ENSG00000065357	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000170037	chromatin interactions
ENSG00000236924	chromatin interactions
ENSG00000229611	chromatin interactions
ENSG00000229057	chromatin interactions
ENSG00000107036	chromatin interactions
ENSG00000225489	chromatin interactions
ENSG00000206147	chromatin interactions
ENSG00000170043	chromatin interactions
ENSG00000147854	chromatin interactions
ENSG00000173559	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000107077	chromatin interactions
ENSG00000273382	chromatin interactions
ENSG00000197323	chromatin interactions
ENSG00000170265	chromatin interactions
ENSG00000117308	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000266863	chromatin interactions
ENSG00000134602	chromatin interactions
ENSG00000215717	chromatin interactions
ENSG00000160271	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000165115	chromatin interactions
ENSG00000105372	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000101220	chromatin interactions
ENSG00000079999	chromatin interactions
ENSG00000178445	chromatin interactions
ENSG00000162065	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000170473	chromatin interactions
ENSG00000177426	chromatin interactions
ENSG00000051009	chromatin interactions
ENSG00000132259	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000273355	chromatin interactions
ENSG00000231381	chromatin interactions
ENSG00000150768	chromatin interactions
ENSG00000102786	chromatin interactions

Extended variants
information (count: 3111 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3111 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2578286	chr9:6648607-6648608	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543255730	chr9:6648609-6648610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191739890	chr9:6648617-6648618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183255167	chr9:6648622-6648623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188083892	chr9:6648633-6648634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556240820	chr9:6648637-6648638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567953562	chr9:6648659-6648660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189790772	chr9:6648672-6648673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530624275	chr9:6648707-6648708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553541216	chr9:6648708-6648709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2890723	chr9:6648728-6648729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs182149903	chr9:6648738-6648739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557917030	chr9:6648777-6648778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186887761	chr9:6648789-6648790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113498840	chr9:6648793-6648794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140720890	chr9:6648795-6648796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376889953	chr9:6648796-6648797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562155780	chr9:6648799-6648800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529223258	chr9:6648800-6648801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548698034	chr9:6648806-6648807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192370083	chr9:6648819-6648820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559552452	chr9:6648822-6648823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533448086	chr9:6648833-6648834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373092049	chr9:6648834-6648835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2918180	chr9:6648838-6648839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
26	rs550924668	chr9:6648841-6648842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568051586	chr9:6648842-6648843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7466251	chr9:6648845-6648846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553848002	chr9:6648849-6648850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140538562	chr9:6648850-6648851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539126127	chr9:6648852-6648853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557978732	chr9:6648853-6648854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184951324	chr9:6648857-6648858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557284487	chr9:6648861-6648862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188624879	chr9:6648863-6648864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541099326	chr9:6648864-6648865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375722774	chr9:6648867-6648868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567881277	chr9:6648869-6648870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150044661	chr9:6648871-6648872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192997420	chr9:6648874-6648875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145360732	chr9:6648878-6648879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184810785	chr9:6648879-6648880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs386732130	chr9:6648882-6648883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545430374	chr9:6648883-6648884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2918179	chr9:6648884-6648885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577874710	chr9:6648891-6648892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529173663	chr9:6648894-6648895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145167319	chr9:6648895-6648896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181261439	chr9:6648897-6648898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183455974	chr9:6648899-6648900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	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
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6646600-6649600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:6646600-6656800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:6646800-6657000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:6647000-6656600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr9:6647400-6648800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr9:6647600-6649000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:6647600-6654600	Weak transcription	GM12878-XiMat	blood
8	chr9:6648000-6656600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr9:6648200-6649400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:6648200-6653800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:6648200-6670400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr9:6648400-6649400	Weak transcription	HepG2	liver
13	chr9:6648400-6658200	Weak transcription	A549	lung
14	chr9:6648400-6669400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr9:6648400-6680400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr9:6648600-6649200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr9:6648600-6649200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:6648600-6649400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr9:6648600-6652800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr9:6648600-6653600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr9:6648600-6656600	Weak transcription	Liver	Liver
22	chr9:6648600-6677600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr9:6648600-6680400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr9:6648800-6680400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr9:6649000-6650000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr9:6649200-6649600	Genic enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:6649200-6649800	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr9:6649400-6649800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr9:6649400-6649800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:6649400-6650000	Enhancers	HepG2	liver
31	chr9:6649600-6651600	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr9:6649800-6652600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr9:6649800-6656600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:6649800-6664200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:6650000-6657000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:6650000-6658400	Weak transcription	HepG2	liver
37	chr9:6651600-6652800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr9:6652600-6654200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
39	chr9:6652800-6653200	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr9:6652800-6654000	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr9:6653200-6656800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr9:6653600-6654000	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr9:6654000-6656600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr9:6654000-6669400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr9:6654200-6656600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr9:6654600-6654800	Enhancers	GM12878-XiMat	blood
47	chr9:6654800-6655200	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr9:6654800-6655400	Enhancers	Primary B cells from peripheral blood	blood
49	chr9:6654800-6655600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:6654800-6655600	Enhancers	Fetal Thymus	thymus

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