Variant report

Variant	nsv518642
Chromosome Location	chr18:196829-331506
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	chr18:323362-323666	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:268051-268209	K562	blood:	n/a	n/a
4	ARID3A	chr18:199881-200096	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:269422-269886	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:267953-268346	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:322588-322899	K562	blood:	n/a	n/a
8	ARID3A	chr18:322586-322907	HepG2	liver:	n/a	n/a
9	ATF1	chr18:267856-268252	K562	blood:	n/a	n/a
10	ATF1	chr18:322600-322859	K562	blood:	n/a	n/a
11	ATF2	chr18:267857-268299	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr18:267806-268299	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr18:267573-268458	GM12878	blood:	n/a	n/a
14	ATF2	chr18:267677-268450	GM12878	blood:	n/a	n/a
15	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
16	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
17	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
18	ATF3	chr18:322557-322878	K562	blood:	n/a	n/a
19	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
20	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
21	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
22	ATF3	chr18:323314-323635	K562	blood:	n/a	n/a
23	ATF3	chr18:322457-322909	K562	blood:	n/a	n/a
24	BACH1	chr18:267979-268355	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr18:322542-322828	GM12878	blood:	n/a	chr18:322737-322747
26	BATF	chr18:267919-268509	GM12878	blood:	n/a	n/a
27	BCL11A	chr18:267902-268405	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
28	BCL11A	chr18:219072-219489	GM12878	blood:	n/a	n/a
29	BCL3	chr18:267887-268393	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
30	BCL3	chr18:267839-268276	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
31	BCL3	chr18:217619-218231	K562	blood:	n/a	n/a
32	BCL3	chr18:267793-268331	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
33	BCLAF1	chr18:267773-268502	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
34	BCLAF1	chr18:267804-269077	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
35	BHLHE40	chr18:268183-268376	A549	lung:	n/a	n/a
36	BHLHE40	chr18:302234-302299	K562	blood:	n/a	n/a
37	BHLHE40	chr18:323381-323581	HepG2	liver:	n/a	n/a
38	BHLHE40	chr18:267862-268321	K562	blood:	n/a	chr18:268046-268062 chr18:268047-268063
39	BHLHE40	chr18:267842-268511	GM12878	blood:	n/a	chr18:268046-268062 chr18:268047-268063
40	BHLHE40	chr18:322531-322950	K562	blood:	n/a	n/a
41	BHLHE40	chr18:322602-322921	HepG2	liver:	n/a	n/a
42	BHLHE40	chr18:267852-268323	HepG2	liver:	n/a	chr18:268046-268062 chr18:268047-268063
43	BRCA1	chr18:267974-268246	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr18:267927-268244	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr18:267916-268222	HepG2	liver:	n/a	n/a
46	CBX3	chr18:271857-272187	K562	blood:	n/a	n/a
47	CBX3	chr18:267877-268270	K562	blood:	n/a	n/a
48	CBX3	chr18:268653-269146	K562	blood:	n/a	n/a
49	CBX3	chr18:322501-322885	K562	blood:	n/a	n/a
50	CBX3	chr18:322440-322947	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:319786-319836	AoSMC	blood vessel:	n/a
2	chr18:319786-319836	AoSMC	blood vessel:	n/a
3	chr18:213653-213703	HEEpiC	esophagus:	n/a
4	chr18:268256-268306	SK-N-MC	brain:	n/a
5	chr18:268135-268185	GM12878	blood:	n/a
6	chr18:268068-268118	NB4	blood:	n/a
7	chr18:268278-268328	MCF-7	breast:	n/a
8	chr18:319786-319836	SAEC	small airway:	n/a
9	chr18:264576-264626	GM12892	blood:	n/a
10	chr18:268131-268181	NB4	blood:	n/a
11	chr18:268381-268431	Caco-2	colon:	n/a
12	chr18:264576-264626	MCF-7	breast:	n/a
13	chr18:268256-268306	SK-N-SH	brain:	n/a
14	chr18:268166-268216	NHBE	bronchial:	n/a
15	chr18:264576-264626	LNCaP	prostate:	n/a
16	chr18:213653-213703	HNPCEpiC	eye:	n/a
17	chr18:264576-264626	IMR90	lung:	fetal
18	chr18:268135-268185	HPAEpiC	pulmonary alveolar:	n/a
19	chr18:268184-268234	MCF-7	breast:	n/a
20	chr18:264576-264626	AoSMC	blood vessel:	n/a
21	chr18:271673-271723	SK-N-SH_RA	brain:	n/a
22	chr18:268135-268185	AG09319	gingival:	n/a
23	chr18:319786-319836	ovcar-3	ovarian:	n/a
24	chr18:271673-271723	U87	brain:	n/a
25	chr18:268184-268234	NHBE	bronchial:	n/a
26	chr18:271673-271723	MCF10A-Er-Src	breast:	n/a
27	chr18:268601-268651	HCM	heart:	n/a
28	chr18:319786-319836	ECC-1	luminal epithelium:	n/a
29	chr18:267711-267761	GM06990	blood:	n/a
30	chr18:267637-267687	AG04450	lung:	fetal
31	chr18:268031-268081	NB4	blood:	n/a
32	chr18:268131-268181	HCM	heart:	n/a
33	chr18:268031-268081	SKMC	muscle:	n/a
34	chr18:267637-267687	H1-hESC	embryonic stem cell:	embryo
35	chr18:267637-267687	LNCaP	prostate:	n/a
36	chr18:268135-268185	BE2_C	brain:	n/a
37	chr18:268031-268081	MCF-7	breast:	n/a
38	chr18:267637-267687	Hela-S3	cervix:	n/a
39	chr18:268031-268081	PFSK-1	brain:	n/a
40	chr18:268131-268181	Caco-2	colon:	n/a
41	chr18:268031-268081	AG10803	skin:	n/a
42	chr18:268031-268081	NHBE	bronchial:	n/a
43	chr18:268131-268181	IMR90	lung:	fetal
44	chr18:264576-264626	ProgFib	skin:	n/a
45	chr18:213653-213703	NH-A	brain:	n/a
46	chr18:267637-267687	MCF-7	breast:	n/a
47	chr18:268135-268185	SK-N-SH	brain:	n/a
48	chr18:268601-268651	ECC-1	luminal epithelium:	n/a
49	chr18:264576-264626	HL-60	blood:	n/a
50	chr18:268278-268328	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:267782..268602-chr2:228189553..228190377,2	Hela-S3	cervix:
2	chr18:273244..275466-chr18:289138..290909,2	K562	blood:
3	chr18:240829..243989-chr18:256150..258223,3	K562	blood:
4	chr18:272315..274100-chr18:321177..323834,2	K562	blood:
5	chr18:293551..294215-chr18:616120..617138,3	MCF-7	breast:
6	chr18:269653..272578-chr18:297355..299675,2	K562	blood:
7	chr18:286089..286649-chr18:19535847..19536611,2	K562	blood:
8	chr18:226421..229879-chr18:235133..238634,3	K562	blood:
9	chr18:269547..271961-chr18:280130..281760,2	K562	blood:
10	chr18:210157..212965-chr18:215977..218080,3	MCF-7	breast:
11	chr18:226491..228129-chr18:229681..231598,2	K562	blood:
12	chr18:192669..194380-chr18:209391..211565,2	K562	blood:
13	chr18:231648..233697-chr18:238465..240469,2	K562	blood:
14	chr18:200142..202919-chr18:214376..217072,2	K562	blood:
15	chr18:253259..255595-chr18:265697..268644,2	K562	blood:
16	chr18:212321..215040-chr18:215387..220438,4	K562	blood:
17	chr18:267460..269280-chr18:657302..659143,2	MCF-7	breast:
18	chr18:208647..210877-chr18:212851..214807,2	MCF-7	breast:
19	chr18:204844..208399-chr18:208509..211522,4	K562	blood:
20	chr18:258780..260589-chr18:262458..263959,2	MCF-7	breast:
21	chr18:196681..199674-chr18:200190..202098,2	K562	blood:
22	chr18:248314..250346-chr18:271820..273799,2	K562	blood:
23	chr18:222084..224693-chr18:231367..235268,3	K562	blood:
24	chr18:250566..253483-chr18:259670..262820,3	K562	blood:
25	chr18:249334..252987-chr18:265974..268103,4	MCF-7	breast:
26	chr18:233992..236480-chr18:246342..248551,2	K562	blood:
27	chr18:267932..269522-chr18:657904..660311,2	K562	blood:
28	chr18:224129..226932-chr18:263404..265975,2	K562	blood:
29	chr18:302419..306527-chr18:308522..311824,4	K562	blood:
30	chr18:218670..220555-chr18:223382..226341,3	K562	blood:
31	chr18:233093..235805-chr18:238186..240596,2	MCF-7	breast:
32	chr18:331361..333834-chr18:339514..341220,2	K562	blood:
33	chr18:266762..268550-chr18:321925..324261,2	K562	blood:
34	chr18:159584..161282-chr18:196677..199436,2	K562	blood:
35	chr18:248314..250346-chr18:271820..273799,2	K562	blood:
36	chr18:245161..246691-chr18:267290..268798,2	MCF-7	breast:
37	chr18:220949..222826-chr18:225843..227616,3	K562	blood:
38	chr18:248531..251029-chr18:267645..269804,2	K562	blood:
39	chr17:58235617..58237608-chr18:268202..269943,2	MCF-7	breast:
40	chr18:226011..228697-chr18:258254..260700,2	K562	blood:
41	chr18:251595..253868-chr18:269090..271217,2	K562	blood:
42	chr18:250537..252163-chr18:257039..259067,2	MCF-7	breast:
43	chr18:322375..323142-chr18:477353..477904,2	MCF-7	breast:
44	chr18:215700..218023-chr18:223770..226749,2	K562	blood:
45	chr18:226421..229879-chr18:235133..238634,3	K562	blood:
46	chr18:269454..272332-chr18:624341..626546,2	K562	blood:
47	chr18:248724..251192-chr18:298155..299664,2	K562	blood:
48	chr18:158218..160075-chr18:212830..215432,2	MCF-7	breast:
49	chr18:208647..210877-chr18:212851..214807,2	MCF-7	breast:
50	chr18:199995..202051-chr18:204177..206910,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COLEC12-6	chr18:253324-253897	expReg_chr18_62_-
2	lnc-USP14-4	chr18:316737-316986	ENSG00000264514.1
3	lnc-USP14-4	chr18:318868-319165	ENSG00000264514.1
4	lnc-COLEC12-1	chr18:317099-317366	ENSG00000264433.1
5	lnc-COLEC12-1	chr18:316740-316963	ENSG00000264433.1
6	lnc-USP14-4	chr18:314887-317129	XLOC_012601
7	lnc-USP14-4	chr18:317866-318033	XLOC_012601
8	lnc-USP14-6	chr18:270815-271054	NONHSAT056835
9	lnc-USP14-3	chr18:268148-270278	ENSG00000263884.1

No.	miRNA target gene	miRNA name	Chromosome Location
1	THOC1	hsa-miR-186-5p	chr18:214607-214625
2	USP14	hsa-miR-204-5p	chr18:212024-212043
3	THOC1	hsa-miR-186-5p	chr18:225149-225174
4	COLEC12	hsa-miR-26b-5p	chr18:319583-319605
5	COLEC12	hsa-miR-7-5p	chr18:319760-319781
6	USP14	hsa-miR-204-5p	chr18:213710-213731
7	COLEC12	hsa-miR-9-5p	chr18:319479-319497
8	COLEC12	hsa-miR-9-5p	chr18:319484-319478

Variant related genes	Relation type
THOC1	TF binding region
ENSG00000263884	TF binding region
ENSG00000264433	TF binding region
ENSG00000264514	TF binding region
THOC1	CpG island
ENSG00000263884	CpG island
ENSG00000264433	CpG island
ENSG00000264514	CpG island
ENSG00000132199	chromatin interactions
ENSG00000130723	chromatin interactions
ENSG00000263006	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000263884	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000168958	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000176912	chromatin interactions
ENSG00000236432	chromatin interactions
ENSG00000176890	chromatin interactions
ENSG00000101557	chromatin interactions

Extended variants
information (count: 4965 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4965 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs655781	chr18:196829-196830	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140103581	chr18:196849-196850	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2846335	chr18:196902-196903	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187310161	chr18:196906-196907	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35399373	chr18:196926-196927	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs33932265	chr18:196927-196928	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143697685	chr18:196945-196946	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544036493	chr18:196957-196958	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546773402	chr18:196972-196973	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146804768	chr18:196983-196984	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34496489	chr18:196993-196994	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs549412337	chr18:197044-197045	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191791660	chr18:197059-197060	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184862776	chr18:197065-197066	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569179733	chr18:197104-197105	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571791614	chr18:197148-197149	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532753073	chr18:197156-197157	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560224883	chr18:197178-197179	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187727329	chr18:197210-197211	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368355459	chr18:197264-197265	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568634428	chr18:197281-197282	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12965796	chr18:197292-197293	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371312622	chr18:197325-197326	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140349579	chr18:197340-197341	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566126625	chr18:197440-197441	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142601914	chr18:197450-197451	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558822142	chr18:197453-197454	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76588552	chr18:197469-197470	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577014216	chr18:197483-197484	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544413942	chr18:197493-197494	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192723185	chr18:197498-197499	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111903285	chr18:197512-197513	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543124762	chr18:197563-197564	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374232333	chr18:197586-197587	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368715697	chr18:197595-197596	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372129870	chr18:197607-197608	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561315326	chr18:197608-197609	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374976489	chr18:197613-197614	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200800220	chr18:197645-197646	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369296322	chr18:197671-197672	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs503086	chr18:197672-197673	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376235145	chr18:197673-197674	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369122052	chr18:197708-197709	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558058697	chr18:197720-197721	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199730789	chr18:197728-197729	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74816514	chr18:197729-197730	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150098659	chr18:197730-197731	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541001257	chr18:197731-197732	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138654675	chr18:197740-197741	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546226392	chr18:197742-197743	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	21865298	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:2782 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:159600-199000	Weak transcription	Colonic Mucosa	Colon
2	chr18:159800-199200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:160000-203000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr18:160200-210800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr18:160200-218000	Weak transcription	Stomach Mucosa	stomach
6	chr18:160200-218400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr18:160600-203200	Weak transcription	Psoas Muscle	Psoas
8	chr18:168800-198200	Weak transcription	Spleen	Spleen
9	chr18:171400-199200	Weak transcription	Right Ventricle	heart
10	chr18:174000-198000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr18:178200-210800	Weak transcription	Pancreas	Pancrea
12	chr18:180800-197400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr18:180800-197600	Weak transcription	Fetal Brain Male	brain
14	chr18:180800-205000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr18:180800-205400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:181000-210800	Weak transcription	Small Intestine	intestine
17	chr18:181400-197000	Weak transcription	Brain Germinal Matrix	brain
18	chr18:181600-197000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr18:182200-199000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr18:182800-200200	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr18:184400-197000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr18:184600-197000	Weak transcription	Colon Smooth Muscle	Colon
23	chr18:184600-197000	Weak transcription	HSMM	muscle
24	chr18:186600-197000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr18:186600-198000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr18:190200-199000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr18:190400-197000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr18:192000-199400	Weak transcription	A549	lung
29	chr18:192200-199200	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr18:192800-205600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr18:193200-218800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr18:193400-227000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr18:193600-197600	Strong transcription	NHEK	skin
34	chr18:193800-197400	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr18:193800-219200	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr18:194200-206000	Weak transcription	Fetal Heart	heart
37	chr18:194600-199000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr18:194800-207400	Strong transcription	Placenta	Placenta
39	chr18:194800-207600	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr18:194800-207800	Strong transcription	Fetal Thymus	thymus
41	chr18:195000-204400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr18:195000-206400	Strong transcription	NH-A	brain
43	chr18:195000-206600	Strong transcription	NHDF-Ad	bronchial
44	chr18:195000-207200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr18:195000-213400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr18:195200-197800	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr18:195200-201600	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr18:195200-206600	Strong transcription	K562	blood
49	chr18:195200-207600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr18:195200-209400	Strong transcription	HUES64 Cell Line	embryonic stem cell

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