Variant report

Variant	nsv1056521
Chromosome Location	chr18:7010334-7169550
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1270)
CpG islands
(count:1222)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1270 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7022188-7022644	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7022230-7022646	K562	blood:	n/a	n/a
3	ATF1	chr18:7132553-7132560	K562	blood:	n/a	n/a
4	ATF3	chr18:7038175-7038573	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr18:7038250-7038543	K562	blood:	n/a	n/a
6	ATF3	chr18:7038209-7038542	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr18:7084298-7084351	K562	blood:	n/a	n/a
8	BACH1	chr18:7118078-7118189	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr18:7116400-7117142	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr18:7117579-7117851	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:7084153-7084355	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr18:7084118-7084383	GM12878	blood:	n/a	chr18:7084240-7084250 chr18:7084239-7084250
13	BATF	chr18:7084156-7084376	GM12878	blood:	n/a	chr18:7084240-7084250 chr18:7084239-7084250
14	BHLHE40	chr18:7023138-7023151	K562	blood:	n/a	n/a
15	BHLHE40	chr18:7038240-7038812	GM12878	blood:	n/a	n/a
16	BHLHE40	chr18:7021164-7021328	K562	blood:	n/a	n/a
17	BHLHE40	chr18:7070540-7070551	GM12878	blood:	n/a	n/a
18	BHLHE40	chr18:7022091-7022633	K562	blood:	n/a	n/a
19	BHLHE40	chr18:7038205-7038897	K562	blood:	n/a	n/a
20	BHLHE40	chr18:7038248-7038575	HepG2	liver:	n/a	n/a
21	BHLHE40	chr18:7164647-7164942	K562	blood:	n/a	n/a
22	BHLHE40	chr18:7017290-7017446	K562	blood:	n/a	n/a
23	BHLHE40	chr18:7035553-7035583	HepG2	liver:	n/a	n/a
24	BHLHE40	chr18:7084175-7084353	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:7071580-7071581	GM12878	blood:	n/a	n/a
26	BRCA1	chr18:7166804-7166827	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr18:7048113-7048439	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr18:7151072-7151110	GM12878	blood:	n/a	n/a
29	BRCA1	chr18:7132805-7133551	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr18:7110400-7110419	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr18:7038299-7039286	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr18:7124290-7124563	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr18:7161764-7162093	Hela-S3	cervix:	n/a	chr18:7161922-7161931 chr18:7161920-7161931 chr18:7161920-7161933
34	CEBPB	chr18:7139456-7139739	A549	lung:	n/a	n/a
35	CEBPB	chr18:7014648-7014905	K562	blood:	n/a	chr18:7014795-7014806 chr18:7014797-7014806 chr18:7014792-7014809 chr18:7014797-7014806 chr18:7014795-7014808 chr18:7014797-7014806 chr18:7014797-7014808 chr18:7014797-7014806 chr18:7014795-7014808
36	CEBPB	chr18:7124369-7124634	K562	blood:	n/a	n/a
37	CEBPB	chr18:7014650-7014904	IMR90	lung:	n/a	chr18:7014795-7014806 chr18:7014797-7014806 chr18:7014792-7014809 chr18:7014797-7014806 chr18:7014795-7014808 chr18:7014797-7014806 chr18:7014797-7014808 chr18:7014797-7014806 chr18:7014795-7014808
38	CEBPB	chr18:7079339-7079525	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr18:7073184-7073499	IMR90	lung:	n/a	chr18:7073333-7073344
40	CEBPB	chr18:7068335-7068635	HepG2	liver:	n/a	chr18:7068494-7068505 chr18:7068493-7068506
41	CEBPB	chr18:7134268-7134369	HepG2	liver:	n/a	n/a
42	CEBPB	chr18:7066664-7066830	HepG2	liver:	n/a	chr18:7066756-7066767 chr18:7066795-7066806
43	CEBPB	chr18:7069863-7070108	IMR90	lung:	n/a	n/a
44	CEBPB	chr18:7032383-7032487	A549	lung:	n/a	chr18:7032428-7032437 chr18:7032427-7032438 chr18:7032426-7032437
45	CEBPB	chr18:7068435-7068492	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr18:7124342-7124593	A549	lung:	n/a	n/a
47	CEBPB	chr18:7038162-7038975	Hela-S3	cervix:	n/a	chr18:7038753-7038764
48	CEBPB	chr18:7073215-7073431	HepG2	liver:	n/a	chr18:7073333-7073344
49	CEBPB	chr18:7043765-7043928	HepG2	liver:	n/a	chr18:7043834-7043845
50	CEBPB	chr18:7063827-7064119	A549	lung:	n/a	chr18:7063937-7063948

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7116977-7117027	AG09319	gingival:	n/a
2	chr18:7118092-7118142	HIPEpiC	eye:	n/a
3	chr18:7116977-7117027	AG09319	gingival:	n/a
4	chr18:7118092-7118142	HIPEpiC	eye:	n/a
5	chr18:7038943-7038993	HUVEC	blood vessel:	n/a
6	chr18:7114654-7114704	MCF10A-Er-Src	breast:	n/a
7	chr18:7011217-7011267	Hela-S3	cervix:	n/a
8	chr18:7011268-7011318	Hela-S3	cervix:	n/a
9	chr18:7011217-7011267	AG09319	gingival:	n/a
10	chr18:7118077-7118127	HepG2	liver:	n/a
11	chr18:7116977-7117027	HCPEpiC	choroid plexus:	n/a
12	chr18:7026502-7026552	SK-N-MC	brain:	n/a
13	chr18:7011388-7011438	CMK	blood:	n/a
14	chr18:7038943-7038993	SKMC	muscle:	n/a
15	chr18:7117680-7117730	AoSMC	blood vessel:	n/a
16	chr18:7013954-7014004	SK-N-MC	brain:	n/a
17	chr18:7116700-7116750	NT2-D1	testis:	n/a
18	chr18:7116700-7116750	NHDF-neo	bronchial:	n/a
19	chr18:7118092-7118142	A549	lung:	n/a
20	chr18:7114654-7114704	GM12878	blood:	n/a
21	chr18:7118122-7118172	AG04449	skin:	fetal
22	chr18:7118122-7118172	HL-60	blood:	n/a
23	chr18:7117680-7117730	Caco-2	colon:	n/a
24	chr18:7011217-7011267	AG04449	skin:	fetal
25	chr18:7011388-7011438	Hepatocyte	liver:	n/a
26	chr18:7118122-7118172	T-47D	breast:	n/a
27	chr18:7114654-7114704	Jurkat	blood:	n/a
28	chr18:7012277-7012327	NHDF-neo	bronchial:	n/a
29	chr18:7117321-7117371	MCF10A-Er-Src	breast:	n/a
30	chr18:7038746-7038796	ovcar-3	ovarian:	n/a
31	chr18:7026502-7026552	AG09319	gingival:	n/a
32	chr18:7012277-7012327	U87	brain:	n/a
33	chr18:7118077-7118127	HRE	kidney:	n/a
34	chr18:7118092-7118142	SK-N-SH	brain:	n/a
35	chr18:7118092-7118142	HMEC	breast:	n/a
36	chr18:7038746-7038796	NH-A	brain:	n/a
37	chr18:7116700-7116750	T-47D	breast:	n/a
38	chr18:7118092-7118142	GM12892	blood:	n/a
39	chr18:7118122-7118172	HAEpiC	amniotic membrane:	n/a
40	chr18:7118092-7118142	HCPEpiC	choroid plexus:	n/a
41	chr18:7118092-7118142	PrEC	prostate:	n/a
42	chr18:7118077-7118127	PFSK-1	brain:	n/a
43	chr18:7011388-7011438	Jurkat	blood:	n/a
44	chr18:7026502-7026552	HRCEpiC	kidney:	n/a
45	chr18:7038943-7038993	IMR90	lung:	fetal
46	chr18:7117790-7117840	AG04449	skin:	fetal
47	chr18:7114654-7114704	U87	brain:	n/a
48	chr18:7118077-7118127	MCF-7	breast:	n/a
49	chr18:7038943-7038993	HEK293	kidney:	embryo
50	chr18:7118092-7118142	GM06990	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:7037864..7039267-chr18:7176237..7177839,9	MCF-7	breast:
2	chr18:7000202..7001073-chr18:7022068..7022574,2	MCF-7	breast:
3	chr18:7021223..7023717-chr18:7024236..7026839,2	K562	blood:
4	chr18:7065125..7067558-chr18:7070044..7072257,2	K562	blood:
5	chr18:7168069..7170291-chr18:7171310..7174194,2	K562	blood:
6	chr18:7027159..7030692-chr18:7032107..7035808,3	K562	blood:
7	chr18:7122361..7123186-chr18:7164345..7164887,2	MCF-7	breast:
8	chr18:7089476..7091194-chr18:7109022..7111374,2	K562	blood:
9	chr18:7075127..7076974-chr18:7081757..7084393,2	K562	blood:
10	chr18:7036570..7038224-chr18:7040056..7042597,2	K562	blood:
11	chr18:7065125..7067558-chr18:7070044..7072257,2	K562	blood:
12	chr18:6543387..6543995-chr18:7022410..7022919,2	MCF-7	breast:
13	chr18:7088894..7091821-chr18:7101257..7103026,2	K562	blood:
14	chr18:7037921..7038842-chr18:7174709..7175338,3	MCF-7	breast:
15	chr18:7121851..7123604-chr18:7131611..7134051,2	MCF-7	breast:
16	chr18:7089476..7091194-chr18:7109022..7111374,2	K562	blood:
17	chr18:7113301..7115369-chr18:7117851..7120461,2	K562	blood:
18	chr18:7088894..7091821-chr18:7101257..7103026,2	K562	blood:
19	chr10:8872309..8872938-chr18:7085701..7086284,2	MCF-7	breast:
20	chr18:7122361..7123186-chr18:7164345..7164887,2	MCF-7	breast:
21	chr18:7037876..7039021-chr18:7176879..7177788,7	MCF-7	breast:
22	chr18:7121851..7123604-chr18:7131611..7134051,2	MCF-7	breast:
23	chr18:7048858..7051211-chr18:7053600..7055903,2	K562	blood:
24	chr18:7038272..7039307-chr18:7176844..7177405,3	K562	blood:
25	chr18:7113301..7115369-chr18:7117851..7120461,2	K562	blood:
26	chr18:7021223..7023717-chr18:7024236..7026839,2	K562	blood:
27	chr18:7020746..7024249-chr18:7030338..7034002,3	K562	blood:
28	chr18:7027159..7030692-chr18:7032107..7035808,3	K562	blood:
29	chr18:6919577..6920920-chr18:7021120..7022839,20	MCF-7	breast:
30	chr18:7040001..7041926-chr18:7042263..7044974,2	K562	blood:
31	chr18:6919703..6920702-chr18:7022006..7023092,6	K562	blood:
32	chr18:7020746..7024249-chr18:7030338..7034002,3	K562	blood:
33	chr18:7022749..7024464-chr18:7031730..7034002,2	K562	blood:
34	chr18:6919688..6921091-chr18:7021888..7022978,20	MCF-7	breast:
35	chr18:7022373..7023231-chr18:7176885..7177438,2	MCF-7	breast:
36	chr18:7048858..7051211-chr18:7053600..7055903,2	K562	blood:
37	chr18:7022749..7024464-chr18:7031730..7034002,2	K562	blood:
38	chr18:5879195..5880069-chr18:7022387..7023035,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-6	chr18:7133440-7133733	NONHSAT057154
2	lnc-LAMA1-6	chr18:7130952-7131151	NONHSAT057154

No data

Variant related genes	Relation type
ENSG00000264475	TF binding region
SLC25A51P2	TF binding region
LAMA1	TF binding region
ENSG00000265869	TF binding region
ENSG00000264475	CpG island
SLC25A51P2	CpG island
LAMA1	CpG island
ENSG00000265869	CpG island
ENSG00000101680	chromatin interactions
ENSG00000264475	chromatin interactions

Extended variants
information (count: 7084 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:7084 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372314380	chr18:7010347-7010348	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115127419	chr18:7010348-7010349	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141036112	chr18:7010372-7010373	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146912301	chr18:7010374-7010375	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139372717	chr18:7010382-7010383	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369973467	chr18:7010391-7010392	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535197995	chr18:7010401-7010402	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372620545	chr18:7010405-7010406	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74825364	chr18:7010428-7010429	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551135923	chr18:7010488-7010489	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185973342	chr18:7010494-7010495	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190043184	chr18:7010498-7010499	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34670191	chr18:7010539-7010540	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546463099	chr18:7010560-7010561	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566773885	chr18:7010580-7010581	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538526192	chr18:7010587-7010588	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558755539	chr18:7010624-7010625	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182662457	chr18:7010626-7010627	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186633592	chr18:7010638-7010639	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112516825	chr18:7010654-7010655	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115823055	chr18:7010672-7010673	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554290382	chr18:7010687-7010688	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565533223	chr18:7010697-7010698	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530906544	chr18:7010748-7010749	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568040262	chr18:7010749-7010750	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs59231474	chr18:7010757-7010758	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553264690	chr18:7010775-7010776	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73938539	chr18:7010807-7010808	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs73938540	chr18:7010808-7010809	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs71360057	chr18:7010857-7010858	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575758378	chr18:7010908-7010909	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544597768	chr18:7010930-7010931	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192323992	chr18:7010946-7010947	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530105710	chr18:7010948-7010949	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554998693	chr18:7010963-7010964	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369589916	chr18:7010966-7010967	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111262460	chr18:7010976-7010977	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560041075	chr18:7010977-7010978	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532280201	chr18:7010978-7010979	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552093977	chr18:7010996-7010997	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568807069	chr18:7011006-7011007	Strong transcription Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531233561	chr18:7011031-7011032	Strong transcription Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534628529	chr18:7011036-7011037	Strong transcription Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547766895	chr18:7011047-7011048	Strong transcription Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142705347	chr18:7011070-7011071	Strong transcription Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375033370	chr18:7011123-7011124	Strong transcription Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553541690	chr18:7011160-7011161	Strong transcription Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370970641	chr18:7011268-7011269	Strong transcription Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs188847580	chr18:7011269-7011270	Strong transcription Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs539235719	chr18:7011274-7011275	Strong transcription Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Breast cancer	17133270	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Burkitt''s lymphoma	20823134	CNVD
Acute myeloid leukemia	17377590	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1556 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:6957800-7020800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:6960600-7022800	Weak transcription	Fetal Brain Female	brain
3	chr18:6960600-7026400	Weak transcription	Brain Substantia Nigra	brain
4	chr18:6978400-7013600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr18:6982800-7011200	Weak transcription	Ovary	ovary
6	chr18:6993000-7011400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr18:6995400-7011200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr18:6995400-7017000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr18:6995400-7036800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr18:6998000-7011200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr18:6998400-7011400	Weak transcription	Fetal Kidney	kidney
12	chr18:7002000-7017800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr18:7002400-7013800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr18:7004200-7022600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr18:7004800-7011600	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr18:7004800-7017400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr18:7005000-7051800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr18:7005200-7012400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr18:7005200-7041400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr18:7005400-7017800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr18:7006000-7010400	Strong transcription	HUES48 Cell Line	embryonic stem cell
22	chr18:7006000-7017800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
23	chr18:7006200-7011000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr18:7007200-7018400	Weak transcription	Fetal Brain Male	brain
25	chr18:7007400-7013400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr18:7007600-7011400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr18:7008000-7017400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr18:7008200-7010400	Strong transcription	HMEC	breast
29	chr18:7008600-7011400	Weak transcription	Hela-S3	cervix
30	chr18:7008800-7014400	Strong transcription	H9 Cell Line	embryonic stem cell
31	chr18:7008800-7031800	Weak transcription	Osteobl	bone
32	chr18:7009600-7011400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr18:7009800-7010800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr18:7010000-7010400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr18:7010000-7010800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr18:7010000-7011800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr18:7010200-7010400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr18:7010200-7011400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr18:7010200-7013400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr18:7010400-7011200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr18:7010400-7011800	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr18:7010400-7013400	Weak transcription	HMEC	breast
43	chr18:7010400-7037400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr18:7010800-7011200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr18:7010800-7012000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr18:7011000-7011800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr18:7011000-7013200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr18:7011200-7011400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr18:7011200-7011800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr18:7011200-7011800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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