Variant report

Variant	nsv909344
Chromosome Location	chr18:7080135-7523336
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2379)
CpG islands
(count:1038)
Chromatin interactive
region (count:66)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2379 , 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	chr18:7177250-7177419	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7221435-7221630	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:7272482-7272549	HepG2	liver:	n/a	n/a
4	ATF1	chr18:7312250-7312257	K562	blood:	n/a	n/a
5	ATF1	chr18:7132553-7132560	K562	blood:	n/a	n/a
6	ATF3	chr18:7467741-7468000	K562	blood:	n/a	n/a
7	ATF3	chr18:7467727-7468106	HepG2	liver:	n/a	n/a
8	BACH1	chr18:7116400-7117142	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr18:7084153-7084355	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr18:7118078-7118189	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:7367519-7367591	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr18:7117579-7117851	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr18:7084298-7084351	K562	blood:	n/a	n/a
14	BATF	chr18:7084156-7084376	GM12878	blood:	n/a	chr18:7084240-7084250 chr18:7084239-7084250
15	BATF	chr18:7084118-7084383	GM12878	blood:	n/a	chr18:7084240-7084250 chr18:7084239-7084250
16	BHLHE40	chr18:7459819-7460275	HepG2	liver:	n/a	n/a
17	BHLHE40	chr18:7520517-7520690	HepG2	liver:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
18	BHLHE40	chr18:7177115-7177352	GM12878	blood:	n/a	n/a
19	BHLHE40	chr18:7520471-7520649	GM12878	blood:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
20	BHLHE40	chr18:7164647-7164942	K562	blood:	n/a	n/a
21	BHLHE40	chr18:7467767-7468063	K562	blood:	n/a	n/a
22	BHLHE40	chr18:7202966-7203132	K562	blood:	n/a	chr18:7203078-7203087 chr18:7203078-7203087 chr18:7203072-7203093 chr18:7203077-7203086 chr18:7203076-7203089
23	BHLHE40	chr18:7084175-7084353	GM12878	blood:	n/a	n/a
24	BHLHE40	chr18:7467750-7468067	HepG2	liver:	n/a	n/a
25	BHLHE40	chr18:7317788-7318028	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:7520520-7520629	K562	blood:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
27	BRCA1	chr18:7110400-7110419	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr18:7174539-7174936	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr18:7132805-7133551	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr18:7221518-7221712	HepG2	liver:	n/a	n/a
31	BRCA1	chr18:7166804-7166827	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr18:7151072-7151110	GM12878	blood:	n/a	n/a
33	BRCA1	chr18:7303527-7303574	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr18:7414190-7414195	GM12878	blood:	n/a	n/a
35	BRCA1	chr18:7452418-7452638	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr18:7458169-7458192	GM12878	blood:	n/a	n/a
37	CEBPB	chr18:7124342-7124593	A549	lung:	n/a	n/a
38	CEBPB	chr18:7397029-7397350	IMR90	lung:	n/a	chr18:7397192-7397203
39	CEBPB	chr18:7273655-7273939	A549	lung:	n/a	n/a
40	CEBPB	chr18:7139456-7139739	A549	lung:	n/a	n/a
41	CEBPB	chr18:7141612-7141742	HepG2	liver:	n/a	n/a
42	CEBPB	chr18:7200412-7200413	HepG2	liver:	n/a	n/a
43	CEBPB	chr18:7124301-7124624	IMR90	lung:	n/a	n/a
44	CEBPB	chr18:7492855-7493001	HepG2	liver:	n/a	chr18:7492946-7492957
45	CEBPB	chr18:7234816-7234956	K562	blood:	n/a	chr18:7234848-7234859 chr18:7234849-7234860
46	CEBPB	chr18:7161764-7162093	Hela-S3	cervix:	n/a	chr18:7161922-7161931 chr18:7161920-7161931 chr18:7161920-7161933
47	CEBPB	chr18:7184351-7184552	A549	lung:	n/a	n/a
48	CEBPB	chr18:7487811-7488113	IMR90	lung:	n/a	chr18:7487948-7487959 chr18:7487948-7487961 chr18:7487950-7487961
49	CEBPB	chr18:7487882-7488100	K562	blood:	n/a	chr18:7487948-7487959 chr18:7487948-7487961 chr18:7487950-7487961
50	CEBPB	chr18:7124290-7124563	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7122191-7122241	ovcar-3	ovarian:	n/a
2	chr18:7122191-7122241	ovcar-3	ovarian:	n/a
3	chr18:7118077-7118127	BJ	skin:	n/a
4	chr18:7231534-7231584	NHBE	bronchial:	n/a
5	chr18:7118077-7118127	U87	brain:	n/a
6	chr18:7117321-7117371	GM12878	blood:	n/a
7	chr18:7118122-7118172	GM12878	blood:	n/a
8	chr18:7118077-7118127	AG04450	lung:	fetal
9	chr18:7122191-7122241	ECC-1	luminal epithelium:	n/a
10	chr18:7117680-7117730	PrEC	prostate:	n/a
11	chr18:7116550-7116600	BE2_C	brain:	n/a
12	chr18:7117680-7117730	LNCaP	prostate:	n/a
13	chr18:7117680-7117730	CMK	blood:	n/a
14	chr18:7116550-7116600	K562	blood:	n/a
15	chr18:7118092-7118142	AG04450	lung:	fetal
16	chr18:7116700-7116750	ProgFib	skin:	n/a
17	chr18:7118077-7118127	GM12878	blood:	n/a
18	chr18:7118122-7118172	A549	lung:	n/a
19	chr18:7230245-7230295	AoSMC	blood vessel:	n/a
20	chr18:7231086-7231136	MCF-7	breast:	n/a
21	chr18:7230489-7230539	Jurkat	blood:	n/a
22	chr18:7117790-7117840	ovcar-3	ovarian:	n/a
23	chr18:7229726-7229776	ProgFib	skin:	n/a
24	chr18:7117790-7117840	BE2_C	brain:	n/a
25	chr18:7231037-7231087	HEK293	kidney:	embryo
26	chr18:7118092-7118142	HIPEpiC	eye:	n/a
27	chr18:7117680-7117730	HL-60	blood:	n/a
28	chr18:7118122-7118172	GM12891	blood:	n/a
29	chr18:7230489-7230539	HCM	heart:	n/a
30	chr18:7122191-7122241	PANC-1	pancreas:	n/a
31	chr18:7230245-7230295	BJ	skin:	n/a
32	chr18:7117790-7117840	AG10803	skin:	n/a
33	chr18:7118122-7118172	HCT-116	colon:	n/a
34	chr18:7116550-7116600	CMK	blood:	n/a
35	chr18:7118092-7118142	NT2-D1	testis:	n/a
36	chr18:7231534-7231584	GM12878	blood:	n/a
37	chr18:7117680-7117730	HUVEC	blood vessel:	n/a
38	chr18:7231086-7231136	GM19239	blood:	n/a
39	chr18:7230245-7230295	HCF	heart:	n/a
40	chr18:7231534-7231584	SK-N-SH	brain:	n/a
41	chr18:7117680-7117730	HEK293	kidney:	embryo
42	chr18:7118092-7118142	Hepatocyte	liver:	n/a
43	chr18:7230245-7230295	AG10803	skin:	n/a
44	chr18:7231037-7231087	HRPEpiC	eye:	n/a
45	chr18:7116550-7116600	HEK293	kidney:	embryo
46	chr18:7116977-7117027	K562	blood:	n/a
47	chr18:7229726-7229776	SK-N-MC	brain:	n/a
48	chr18:7231534-7231584	SAEC	small airway:	n/a
49	chr18:7114654-7114704	U87	brain:	n/a
50	chr18:7117680-7117730	HRE	kidney:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:7122361..7123186-chr18:7164345..7164887,2	MCF-7	breast:
2	chr18:7509867..7511990-chr18:7516061..7517678,2	MCF-7	breast:
3	chr17:56708760..56709438-chr18:7282315..7283335,4	HCT-116	colon:
4	chr18:7168069..7170291-chr18:7171310..7174194,2	K562	blood:
5	chr18:7359797..7360512-chr20:46012695..46013367,2	MCF-7	breast:
6	chr18:7279579..7281833-chr18:7286057..7288878,2	K562	blood:
7	chr18:6919702..6920513-chr18:7174601..7175401,4	MCF-7	breast:
8	chr18:7219560..7222468-chr18:7224893..7227543,2	K562	blood:
9	chr18:7328260..7329783-chr18:7331392..7333431,2	K562	blood:
10	chr18:7121851..7123604-chr18:7131611..7134051,2	MCF-7	breast:
11	chr18:7022373..7023231-chr18:7176885..7177438,2	MCF-7	breast:
12	chr18:7277126..7280164-chr18:7281807..7285178,3	K562	blood:
13	chr18:7489323..7491482-chr18:7507564..7509092,2	K562	blood:
14	chr18:7336585..7339141-chr18:7354510..7356531,2	MCF-7	breast:
15	chr18:7037876..7039021-chr18:7176879..7177788,7	MCF-7	breast:
16	chr18:7089476..7091194-chr18:7109022..7111374,2	K562	blood:
17	chr18:7113301..7115369-chr18:7117851..7120461,2	K562	blood:
18	chr18:7514458..7516129-chr18:7523489..7525604,2	K562	blood:
19	chr18:7121851..7123604-chr18:7131611..7134051,2	MCF-7	breast:
20	chr18:7485561..7488328-chr18:7489989..7493519,3	K562	blood:
21	chr18:7037921..7038842-chr18:7174709..7175338,3	MCF-7	breast:
22	chr18:7037864..7039267-chr18:7176237..7177839,9	MCF-7	breast:
23	chr18:7271947..7272868-chr18:8480276..8481083,2	MCF-7	breast:
24	chr18:7328260..7329783-chr18:7331392..7333431,2	K562	blood:
25	chr18:7485561..7489531-chr18:7490547..7493519,3	K562	blood:
26	chr18:7305816..7308411-chr18:7309437..7311402,2	K562	blood:
27	chr10:8872309..8872938-chr18:7085701..7086284,2	MCF-7	breast:
28	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
29	chr18:7237095..7238838-chr18:7283799..7285892,2	K562	blood:
30	chr18:7272371..7272941-chr18:8480116..8480854,3	MCF-7	breast:
31	chr18:7305816..7308411-chr18:7309437..7311402,2	K562	blood:
32	chr18:7271986..7272913-chr18:7349191..7350194,3	MCF-7	breast:
33	chr18:7219560..7222468-chr18:7224893..7227543,2	K562	blood:
34	chr18:7209942..7211874-chr18:7214063..7215628,2	K562	blood:
35	chr17:56707566..56710325-chr18:7281315..7284315,3	K562	blood:
36	chr18:6920149..6920730-chr18:7177289..7177849,2	K562	blood:
37	chr18:7251040..7252681-chr18:7255832..7258659,2	K562	blood:
38	chr18:7088894..7091821-chr18:7101257..7103026,2	K562	blood:
39	chr18:7509867..7511990-chr18:7516061..7517678,2	MCF-7	breast:
40	chr18:7237095..7238838-chr18:7283799..7285892,2	K562	blood:
41	chr18:7271986..7272913-chr18:7349191..7350194,3	MCF-7	breast:
42	chr18:7209942..7211874-chr18:7214063..7215628,2	K562	blood:
43	chr18:7272328..7273061-chr18:7451989..7452918,2	MCF-7	breast:
44	chr18:7485561..7489531-chr18:7490547..7493519,3	K562	blood:
45	chr18:7465161..7467875-chr18:7484981..7486851,2	K562	blood:
46	chr1:117064094..117064942-chr18:7200217..7200777,2	MCF-7	breast:
47	chr18:7075127..7076974-chr18:7081757..7084393,2	K562	blood:
48	chr18:7038272..7039307-chr18:7176844..7177405,3	K562	blood:
49	chr18:7088894..7091821-chr18:7101257..7103026,2	K562	blood:
50	chr18:7336585..7339141-chr18:7354510..7356531,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC30-1	chr18:7276659-7277412	XLOC_012621
2	lnc-LAMA1-4	chr18:7508970-7509053	XLOC_012749
3	lnc-LAMA1-4	chr18:7509140-7509419	XLOC_012749
4	lnc-LRRC30-1	chr18:7272467-7272498	XLOC_012621
5	lnc-LAMA1-6	chr18:7130952-7131151	NONHSAT057154
6	lnc-LAMA1-7	chr18:7222430-7222682	l_1518_chr18:7222289-7223722_skeltalMuscle
7	lnc-LAMA1-7	chr18:7222290-7222419	l_1518_chr18:7222289-7223722_skeltalMuscle
8	lnc-LAMA1-7	chr18:7223429-7223722	l_1518_chr18:7222289-7223722_skeltalMuscle
9	lnc-LAMA1-6	chr18:7133440-7133733	NONHSAT057154
10	lnc-LAMA1-4	chr18:7508432-7508885	XLOC_012749

No data

Variant related genes	Relation type
LRRC30	TF binding region
ENSG00000212626	TF binding region
SLC25A51P2	TF binding region
LAMA1	TF binding region
LRRC30	CpG island
ENSG00000212626	CpG island
SLC25A51P2	CpG island
LAMA1	CpG island
ENSG00000264475	chromatin interactions
ENSG00000212195	chromatin interactions
TP53INP1	miRNA target sites

Extended variants
information (count: 16662 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:16662 , 50 per page) page: 1 2 3 4 5 6 7 ... 334

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16951199	chr18:7080135-7080136	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376446325	chr18:7080137-7080138	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs116800068	chr18:7080161-7080162	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs554550786	chr18:7080167-7080168	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs371015144	chr18:7080241-7080242	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs374395073	chr18:7080247-7080248	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs376290888	chr18:7080249-7080250	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs192526789	chr18:7080253-7080254	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs202206565	chr18:7080268-7080269	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs375402124	chr18:7080274-7080275	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs201415974	chr18:7080277-7080278	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs555597971	chr18:7080293-7080294	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs367866675	chr18:7080298-7080299	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs576482352	chr18:7080299-7080300	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs201607431	chr18:7080306-7080307	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs376345144	chr18:7080333-7080334	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs147676957	chr18:7080337-7080338	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs375547281	chr18:7080342-7080343	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs184206783	chr18:7080368-7080369	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs571937115	chr18:7080391-7080392	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs540825771	chr18:7080392-7080393	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs188147882	chr18:7080398-7080399	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs533018732	chr18:7080426-7080427	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs368875203	chr18:7080463-7080464	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs372394105	chr18:7080475-7080476	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs543055263	chr18:7080490-7080491	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs563269085	chr18:7080507-7080508	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs546615946	chr18:7080584-7080585	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs528998684	chr18:7080591-7080592	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs201815440	chr18:7080598-7080599	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs549098438	chr18:7080606-7080607	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs557749605	chr18:7080650-7080651	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs7242435	chr18:7080664-7080665	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs374737230	chr18:7080667-7080668	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs141933944	chr18:7080676-7080677	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs368567019	chr18:7080681-7080682	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs571161946	chr18:7080693-7080694	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs116882099	chr18:7080736-7080737	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs549921990	chr18:7080739-7080740	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs566837181	chr18:7080804-7080805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559776403	chr18:7080805-7080806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62083498	chr18:7080809-7080810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535458853	chr18:7080818-7080819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555487853	chr18:7080894-7080895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146316554	chr18:7080895-7080896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376597767	chr18:7080976-7080977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534517832	chr18:7080978-7080979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138152648	chr18:7081073-7081074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34105215	chr18:7081097-7081098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577884581	chr18:7081098-7081099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Breast cancer	22522925	CNVD
Burkitt''s lymphoma	20823134	CNVD
Acute myeloid leukemia	17377590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2808 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7065000-7083800	Weak transcription	HMEC	breast
2	chr18:7067400-7082400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr18:7069800-7089400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr18:7069800-7090800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr18:7070000-7084400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr18:7070000-7087400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr18:7073000-7082800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr18:7073400-7083000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr18:7073800-7084400	Weak transcription	Fetal Brain Female	brain
10	chr18:7075600-7080400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr18:7076000-7080600	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr18:7076200-7080200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr18:7077800-7081400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr18:7078000-7081400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr18:7078600-7080200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:7078600-7080400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr18:7079000-7080600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr18:7079200-7080400	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr18:7079200-7080600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr18:7079200-7080800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr18:7079600-7080400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr18:7079600-7080800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr18:7079800-7090800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr18:7080000-7089800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr18:7080000-7090800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr18:7080200-7084200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr18:7080200-7089200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr18:7080400-7082600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr18:7080400-7083800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr18:7080400-7088000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr18:7080400-7096800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr18:7080600-7084200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr18:7080600-7084600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr18:7080600-7087800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr18:7080800-7084000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr18:7080800-7090400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr18:7081400-7082000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr18:7081400-7089000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr18:7081600-7082800	Enhancers	Osteobl	bone
40	chr18:7082000-7082400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr18:7082400-7082800	Enhancers	Fetal Kidney	kidney
42	chr18:7082400-7083000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr18:7082400-7084400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr18:7082600-7082800	Enhancers	NH-A	brain
45	chr18:7082600-7083000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr18:7082800-7083000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr18:7082800-7083000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr18:7082800-7083000	Enhancers	Fetal Brain Male	brain
49	chr18:7082800-7083000	Enhancers	Fetal Intestine Small	intestine
50	chr18:7082800-7083000	Enhancers	Hela-S3	cervix

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