Variant report

Variant	nsv1067432
Chromosome Location	chr18:219990-290812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:286488-286736	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:268051-268209	K562	blood:	n/a	n/a
3	ARID3A	chr18:267953-268346	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:269422-269886	HepG2	liver:	n/a	n/a
5	ATF1	chr18:267856-268252	K562	blood:	n/a	n/a
6	ATF2	chr18:267806-268299	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr18:267857-268299	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr18:267573-268458	GM12878	blood:	n/a	n/a
9	ATF2	chr18:267677-268450	GM12878	blood:	n/a	n/a
10	ATF3	chr18:267842-268358	GM12878	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
11	ATF3	chr18:267904-268183	GM12878	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
12	ATF3	chr18:267819-268244	K562	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
13	ATF3	chr18:267636-268296	H1-hESC	embryonic stem cell:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
14	ATF3	chr18:267854-268179	HepG2	liver:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
15	ATF3	chr18:267910-268154	H1-hESC	embryonic stem cell:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
16	BACH1	chr18:267979-268355	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr18:267919-268509	GM12878	blood:	n/a	n/a
18	BCL11A	chr18:267902-268405	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
19	BCL3	chr18:267839-268276	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
20	BCL3	chr18:267793-268331	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
21	BCL3	chr18:267887-268393	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
22	BCLAF1	chr18:267773-268502	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
23	BCLAF1	chr18:267804-269077	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
24	BHLHE40	chr18:267852-268323	HepG2	liver:	n/a	chr18:268046-268062 chr18:268047-268063
25	BHLHE40	chr18:267862-268321	K562	blood:	n/a	chr18:268046-268062 chr18:268047-268063
26	BHLHE40	chr18:268183-268376	A549	lung:	n/a	n/a
27	BHLHE40	chr18:267842-268511	GM12878	blood:	n/a	chr18:268046-268062 chr18:268047-268063
28	BRCA1	chr18:267974-268246	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr18:267916-268222	HepG2	liver:	n/a	n/a
30	BRCA1	chr18:267927-268244	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr18:268653-269146	K562	blood:	n/a	n/a
32	CBX3	chr18:271857-272187	K562	blood:	n/a	n/a
33	CBX3	chr18:267701-268641	K562	blood:	n/a	n/a
34	CBX3	chr18:267877-268270	K562	blood:	n/a	n/a
35	CCNT2	chr18:267628-268513	K562	blood:	n/a	n/a
36	CEBPB	chr18:269538-269869	K562	blood:	n/a	n/a
37	CEBPB	chr18:269678-269795	K562	blood:	n/a	n/a
38	CEBPB	chr18:227537-227565	HepG2	liver:	n/a	chr18:227540-227551 chr18:227540-227553
39	CEBPB	chr18:267818-268289	K562	blood:	n/a	n/a
40	CEBPB	chr18:267829-268561	GM12878	blood:	n/a	n/a
41	CEBPB	chr18:268092-268184	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr18:227512-227598	K562	blood:	n/a	chr18:227540-227551 chr18:227540-227553
43	CEBPD	chr18:267595-268288	HepG2	liver:	n/a	n/a
44	CEBPD	chr18:267772-268726	K562	blood:	n/a	n/a
45	CHD1	chr18:268180-268771	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr18:267960-268495	GM12878	blood:	n/a	chr18:268135-268145
47	CHD2	chr18:267938-268278	Hela-S3	cervix:	n/a	chr18:268135-268145
48	CHD2	chr18:267987-268408	K562	blood:	n/a	chr18:268135-268145
49	CHD2	chr18:267821-268371	H1-hESC	embryonic stem cell:	n/a	chr18:268135-268145
50	CHD2	chr18:267876-268311	HepG2	liver:	n/a	chr18:268135-268145

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:268031-268081	CMK	blood:	n/a
2	chr18:268031-268081	CMK	blood:	n/a
3	chr18:268184-268234	AG10803	skin:	n/a
4	chr18:268601-268651	HCT-116	colon:	n/a
5	chr18:268256-268306	T-47D	breast:	n/a
6	chr18:267711-267761	GM12892	blood:	n/a
7	chr18:268381-268431	K562	blood:	n/a
8	chr18:268601-268651	HL-60	blood:	n/a
9	chr18:267711-267761	HRCEpiC	kidney:	n/a
10	chr18:268068-268118	AG04450	lung:	fetal
11	chr18:268278-268328	ECC-1	luminal epithelium:	n/a
12	chr18:268256-268306	HAEpiC	amniotic membrane:	n/a
13	chr18:268031-268081	NH-A	brain:	n/a
14	chr18:268184-268234	NB4	blood:	n/a
15	chr18:268601-268651	AG10803	skin:	n/a
16	chr18:268256-268306	AG04449	skin:	fetal
17	chr18:268184-268234	Caco-2	colon:	n/a
18	chr18:268135-268185	NT2-D1	testis:	n/a
19	chr18:268068-268118	MCF10A-Er-Src	breast:	n/a
20	chr18:268256-268306	NH-A	brain:	n/a
21	chr18:268256-268306	HRPEpiC	eye:	n/a
22	chr18:268184-268234	HCF	heart:	n/a
23	chr18:268135-268185	AG04450	lung:	fetal
24	chr18:268135-268185	Hela-S3	cervix:	n/a
25	chr18:267711-267761	PANC-1	pancreas:	n/a
26	chr18:268278-268328	NT2-D1	testis:	n/a
27	chr18:268166-268216	MCF-7	breast:	n/a
28	chr18:267711-267761	CMK	blood:	n/a
29	chr18:268166-268216	GM12878	blood:	n/a
30	chr18:268278-268328	NB4	blood:	n/a
31	chr18:268256-268306	HPAEpiC	pulmonary alveolar:	n/a
32	chr18:267637-267687	BE2_C	brain:	n/a
33	chr18:268135-268185	A549	lung:	n/a
34	chr18:268256-268306	HCM	heart:	n/a
35	chr18:267711-267761	SK-N-SH	brain:	n/a
36	chr18:268601-268651	NT2-D1	testis:	n/a
37	chr18:271673-271723	MCF-7	breast:	n/a
38	chr18:268135-268185	AG09309	skin:	n/a
39	chr18:271673-271723	BJ	skin:	n/a
40	chr18:267711-267761	SAEC	small airway:	n/a
41	chr18:268166-268216	GM06990	blood:	n/a
42	chr18:271673-271723	GM12892	blood:	n/a
43	chr18:267637-267687	AG04450	lung:	fetal
44	chr18:271673-271723	HAEpiC	amniotic membrane:	n/a
45	chr18:268031-268081	HCM	heart:	n/a
46	chr18:267637-267687	AG04449	skin:	fetal
47	chr18:268068-268118	A549	lung:	n/a
48	chr18:268381-268431	T-47D	breast:	n/a
49	chr18:268184-268234	Hepatocyte	liver:	n/a
50	chr18:268135-268185	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:225339..228063-chr18:231717..233482,2	K562	blood:
2	chr18:269547..271961-chr18:280130..281760,2	K562	blood:
3	chr18:110119..112537-chr18:266561..268595,2	MCF-7	breast:
4	chr18:286251..287151-chr18:616097..616992,3	MCF-7	breast:
5	chr18:251747..253552-chr18:262672..265291,2	K562	blood:
6	chr18:274502..277151-chr18:285374..288213,2	K562	blood:
7	chr18:229127..231742-chr18:269257..272237,2	K562	blood:
8	chr18:240829..243989-chr18:256150..258223,3	K562	blood:
9	chr18:222084..224693-chr18:231367..235268,3	K562	blood:
10	chr18:233093..235805-chr18:238186..240596,2	MCF-7	breast:
11	chr18:250843..253350-chr18:266351..269442,3	MCF-7	breast:
12	chr18:226491..228129-chr18:229681..231598,2	K562	blood:
13	chr18:253259..255595-chr18:265697..268644,2	K562	blood:
14	chr18:157295..159730-chr18:266988..268701,2	MCF-7	breast:
15	chr18:272315..274100-chr18:321177..323834,2	K562	blood:
16	chr18:263619..266135-chr18:272357..275080,2	MCF-7	breast:
17	chr18:273244..275466-chr18:289138..290909,2	K562	blood:
18	chr18:226011..228697-chr18:258254..260700,2	K562	blood:
19	chr18:240829..243989-chr18:256150..258223,3	K562	blood:
20	chr18:286140..286815-chr18:616539..617291,2	MCF-7	breast:
21	chr18:215700..218023-chr18:223770..226749,2	K562	blood:
22	chr18:217625..220298-chr18:220450..222344,2	K562	blood:
23	chr18:267460..269280-chr18:657302..659143,2	MCF-7	breast:
24	chr18:233093..235805-chr18:238186..240596,2	MCF-7	breast:
25	chr18:258780..260589-chr18:262458..263959,2	MCF-7	breast:
26	chr18:257542..263185-chr18:266000..270349,8	MCF-7	breast:
27	chr1:147806762..147807332-chr18:268331..269254,2	Hela-S3	cervix:
28	chr18:225092..228063-chr18:231717..233531,3	K562	blood:
29	chr18:231648..233697-chr18:238465..240469,2	K562	blood:
30	chr18:266657..270720-chr18:273015..278448,7	MCF-7	breast:
31	chr18:226421..229879-chr18:235133..238634,3	K562	blood:
32	chr18:262066..265680-chr18:266517..269152,4	MCF-7	breast:
33	chr18:231648..233697-chr18:238465..240469,2	K562	blood:
34	chr18:250566..253483-chr18:259670..262820,3	K562	blood:
35	chr18:250537..252163-chr18:257039..259067,2	MCF-7	breast:
36	chr18:219579..224693-chr18:231367..234811,5	K562	blood:
37	chr18:245161..246691-chr18:267290..268798,2	MCF-7	breast:
38	chr18:286089..286649-chr18:19535847..19536611,2	K562	blood:
39	chr18:273825..276341-chr18:276906..279543,2	K562	blood:
40	chr18:229127..231742-chr18:269257..272237,2	K562	blood:
41	chr18:266563..269513-chr18:596555..599263,2	K562	blood:
42	chr18:228215..230385-chr18:232509..234575,2	K562	blood:
43	chr18:267932..269522-chr18:657904..660311,2	K562	blood:
44	chr18:226421..229879-chr18:235133..238634,3	K562	blood:
45	chr18:254095..260758-chr18:263922..270842,11	K562	blood:
46	chr18:277729..280050-chr18:615244..618128,2	MCF-7	breast:
47	chr18:158012..160007-chr18:265808..268303,2	MCF-7	breast:
48	chr18:218670..220555-chr18:223382..226341,3	K562	blood:
49	chr18:224129..226932-chr18:263404..265975,2	K562	blood:
50	chr18:251595..253868-chr18:269090..271217,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP14-3	chr18:268148-270278	ENSG00000263884.1
2	lnc-USP14-6	chr18:270815-271054	NONHSAT056835
3	lnc-COLEC12-6	chr18:253324-253897	expReg_chr18_62_-

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	THOC1	hsa-miR-186-5p	chr18:225149-225174

Variant related genes	Relation type
THOC1	TF binding region
ENSG00000263884	TF binding region
THOC1	CpG island
ENSG00000263884	CpG island
ENSG00000132199	chromatin interactions
ENSG00000168958	chromatin interactions
ENSG00000101557	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000176912	chromatin interactions
ENSG00000263884	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000236432	chromatin interactions
ENSG00000176890	chromatin interactions
ENSG00000263006	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000130723	chromatin interactions

Extended variants
information (count: 2394 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2394 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557309003	chr18:220042-220043	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs8087639	chr18:220071-220072	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147965190	chr18:220084-220085	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs554795161	chr18:220113-220114	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs140175829	chr18:220226-220227	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540392487	chr18:220233-220234	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs145389731	chr18:220281-220282	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576847892	chr18:220296-220297	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs543899157	chr18:220300-220301	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs534889445	chr18:220312-220313	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530060357	chr18:220335-220336	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs8094221	chr18:220341-220342	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs548625847	chr18:220388-220389	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560456097	chr18:220397-220398	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs147667118	chr18:220416-220417	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs35020790	chr18:220442-220443	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs376886079	chr18:220443-220444	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186375498	chr18:220458-220459	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs371225773	chr18:220515-220516	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs368905354	chr18:220527-220528	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140909951	chr18:220564-220565	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs672856	chr18:220658-220659	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs149800377	chr18:220706-220707	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554856741	chr18:220730-220731	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs551085100	chr18:220733-220734	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs573171745	chr18:220735-220736	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554584027	chr18:220747-220748	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376549125	chr18:220757-220758	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189660043	chr18:220808-220809	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs544290018	chr18:220836-220837	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568520527	chr18:220903-220904	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs180944215	chr18:220921-220922	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34104816	chr18:220926-220927	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113991656	chr18:220942-220943	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541819533	chr18:221015-221016	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs145742284	chr18:221071-221072	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs674727	chr18:221102-221103	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs663186	chr18:221131-221132	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs185938138	chr18:221145-221146	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573482816	chr18:221159-221160	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs114579562	chr18:221175-221176	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551062752	chr18:221226-221227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191033878	chr18:221228-221229	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs536266995	chr18:221290-221291	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs62073495	chr18:221350-221351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs566856284	chr18:221357-221358	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534210589	chr18:221410-221411	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558929274	chr18:221526-221527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12959862	chr18:221535-221536	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79299806	chr18:221545-221546	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	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
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	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
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	21865298	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:193400-227000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr18:195200-231200	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr18:195400-220600	Strong transcription	Dnd41	blood
4	chr18:195400-228000	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr18:195400-233000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr18:199800-251000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr18:206000-220800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr18:206400-222200	Weak transcription	Fetal Brain Male	brain
9	chr18:208800-227200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr18:209000-220800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr18:209200-220400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr18:209200-220400	Strong transcription	Placenta	Placenta
13	chr18:209200-220600	Strong transcription	Adipose Nuclei	Adipose
14	chr18:209200-228200	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr18:209400-230000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr18:209400-230000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr18:209600-220400	Strong transcription	A549	lung
18	chr18:210200-228000	Strong transcription	Osteobl	bone
19	chr18:210400-224000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr18:210600-220200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr18:210800-225400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr18:212000-256400	Weak transcription	Gastric	stomach
23	chr18:214400-251600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr18:214400-252000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr18:215800-244000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr18:217000-223800	Weak transcription	Brain Substantia Nigra	brain
27	chr18:217200-247000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr18:217400-220000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr18:217800-221000	ZNF genes & repeats	GM12878-XiMat	blood
30	chr18:217800-221200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
31	chr18:218000-220200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
32	chr18:218000-220400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
33	chr18:218000-222600	Weak transcription	Right Ventricle	heart
34	chr18:218000-229400	Weak transcription	Fetal Intestine Small	intestine
35	chr18:218000-267400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr18:218200-221200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
37	chr18:218200-222400	Weak transcription	Hela-S3	cervix
38	chr18:218200-245400	Weak transcription	Aorta	Aorta
39	chr18:218400-223000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr18:218400-245600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr18:218600-222200	Weak transcription	NHDF-Ad	bronchial
42	chr18:218600-222400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr18:218600-222400	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr18:218600-222400	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr18:218600-222400	Weak transcription	HSMMtube	muscle
46	chr18:218600-222600	Weak transcription	Brain Cingulate Gyrus	brain
47	chr18:218600-222600	Weak transcription	Left Ventricle	heart
48	chr18:218600-222800	Weak transcription	NHLF	lung
49	chr18:218600-223400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr18:218600-223800	Weak transcription	Ovary	ovary

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