Variant report

Variant	nsv576819
Chromosome Location	chr18:44602249-44677627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1161)
CpG islands
(count:1100)
Chromatin interactive
region (count:43)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44626756-44626914	K562	blood:	n/a	n/a
2	ARID3A	chr18:44622174-44622535	HepG2	liver:	n/a	n/a
3	ATF2	chr18:44646731-44647251	GM12878	blood:	n/a	n/a
4	ATF2	chr18:44646738-44647341	GM12878	blood:	n/a	n/a
5	ATF2	chr18:44676480-44677442	GM12878	blood:	n/a	n/a
6	BACH1	chr18:44676328-44676759	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr18:44646695-44647275	GM12878	blood:	n/a	n/a
8	BATF	chr18:44646658-44647355	GM12878	blood:	n/a	n/a
9	BCL11A	chr18:44640579-44640762	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr18:44646651-44647227	GM12878	blood:	n/a	n/a
11	BCL3	chr18:44676726-44677098	GM12878	blood:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
12	BCL3	chr18:44676555-44677346	A549	lung:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
13	BCL3	chr18:44676634-44677320	A549	lung:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
14	BCL3	chr18:44646767-44647250	GM12878	blood:	n/a	n/a
15	BCLAF1	chr18:44676300-44677253	GM12878	blood:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
16	BCLAF1	chr18:44646802-44647168	GM12878	blood:	n/a	n/a
17	BCLAF1	chr18:44676520-44677425	GM12878	blood:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
18	BHLHE40	chr18:44646804-44647255	GM12878	blood:	n/a	n/a
19	BHLHE40	chr18:44622279-44622498	HepG2	liver:	n/a	n/a
20	BHLHE40	chr18:44626653-44626985	K562	blood:	n/a	n/a
21	BHLHE40	chr18:44676328-44677091	GM12878	blood:	n/a	chr18:44676843-44676859
22	BHLHE40	chr18:44675924-44677495	K562	blood:	n/a	chr18:44676843-44676859
23	BHLHE40	chr18:44670436-44670781	K562	blood:	n/a	n/a
24	BHLHE40	chr18:44626733-44626933	GM12878	blood:	n/a	n/a
25	BRCA1	chr18:44676951-44677167	HepG2	liver:	n/a	n/a
26	BRCA1	chr18:44676397-44677399	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr18:44676668-44677056	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr18:44635171-44635246	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr18:44676371-44676502	HepG2	liver:	n/a	n/a
30	CCNT2	chr18:44675920-44677117	K562	blood:	n/a	chr18:44676913-44676922
31	CCNT2	chr18:44626661-44626940	K562	blood:	n/a	n/a
32	CEBPB	chr18:44669571-44669955	A549	lung:	n/a	n/a
33	CEBPB	chr18:44610752-44611050	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr18:44673273-44673569	K562	blood:	n/a	n/a
35	CEBPB	chr18:44606715-44606946	K562	blood:	n/a	n/a
36	CEBPB	chr18:44676340-44677114	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr18:44622196-44622467	HepG2	liver:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
38	CEBPB	chr18:44677595-44677615	K562	blood:	n/a	n/a
39	CEBPB	chr18:44605149-44605473	IMR90	lung:	n/a	chr18:44605310-44605323 chr18:44605310-44605321
40	CEBPB	chr18:44669597-44669853	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr18:44622151-44622507	H1-hESC	embryonic stem cell:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
42	CEBPB	chr18:44662175-44662365	A549	lung:	n/a	chr18:44662297-44662308 chr18:44662299-44662308
43	CEBPB	chr18:44669615-44669871	MCF-7	breast:	n/a	n/a
44	CEBPB	chr18:44622140-44622530	HepG2	liver:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
45	CEBPB	chr18:44669549-44669919	K562	blood:	n/a	n/a
46	CEBPB	chr18:44605165-44605373	K562	blood:	n/a	chr18:44605310-44605323 chr18:44605310-44605321
47	CEBPB	chr18:44605158-44605491	HepG2	liver:	n/a	chr18:44605310-44605323 chr18:44605310-44605321
48	CEBPB	chr18:44662148-44662455	HepG2	liver:	n/a	chr18:44662297-44662308 chr18:44662299-44662308
49	CEBPB	chr18:44669544-44669917	IMR90	lung:	n/a	n/a
50	CEBPB	chr18:44621924-44622527	HepG2	liver:	n/a	chr18:44622330-44622341 chr18:44622329-44622340

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44676672-44676722	Hepatocyte	liver:	n/a
2	chr18:44677236-44677286	HEEpiC	esophagus:	n/a
3	chr18:44676672-44676722	Hepatocyte	liver:	n/a
4	chr18:44677236-44677286	HEEpiC	esophagus:	n/a
5	chr18:44676764-44676814	Jurkat	blood:	n/a
6	chr18:44677553-44677603	SAEC	small airway:	n/a
7	chr18:44676672-44676722	AG04449	skin:	fetal
8	chr18:44676764-44676814	GM06990	blood:	n/a
9	chr18:44676421-44676471	HUVEC	blood vessel:	n/a
10	chr18:44676764-44676814	NB4	blood:	n/a
11	chr18:44644942-44644992	HCM	heart:	n/a
12	chr18:44674172-44674222	A549	lung:	n/a
13	chr18:44634946-44634996	MCF10A-Er-Src	breast:	n/a
14	chr18:44676959-44677009	AG04450	lung:	fetal
15	chr18:44676672-44676722	K562	blood:	n/a
16	chr18:44676764-44676814	AG09309	skin:	n/a
17	chr18:44676959-44677009	ovcar-3	ovarian:	n/a
18	chr18:44677139-44677189	GM12878	blood:	n/a
19	chr18:44677236-44677286	PrEC	prostate:	n/a
20	chr18:44674172-44674222	CMK	blood:	n/a
21	chr18:44676764-44676814	IMR90	lung:	fetal
22	chr18:44676962-44677012	MCF10A-Er-Src	breast:	n/a
23	chr18:44676656-44676706	PANC-1	pancreas:	n/a
24	chr18:44677236-44677286	HMEC	breast:	n/a
25	chr18:44626898-44626948	MCF-7	breast:	n/a
26	chr18:44676992-44677042	RPTEC	kidney:	n/a
27	chr18:44676757-44676807	GM12891	blood:	n/a
28	chr18:44676959-44677009	HPAEpiC	pulmonary alveolar:	n/a
29	chr18:44676992-44677042	GM12878	blood:	n/a
30	chr18:44634946-44634996	SK-N-MC	brain:	n/a
31	chr18:44618587-44618637	HRPEpiC	eye:	n/a
32	chr18:44676764-44676814	HPAEpiC	pulmonary alveolar:	n/a
33	chr18:44676959-44677009	HAEpiC	amniotic membrane:	n/a
34	chr18:44676764-44676814	HNPCEpiC	eye:	n/a
35	chr18:44677139-44677189	AG09319	gingival:	n/a
36	chr18:44676959-44677009	GM12892	blood:	n/a
37	chr18:44676757-44676807	HNPCEpiC	eye:	n/a
38	chr18:44676992-44677042	SK-N-MC	brain:	n/a
39	chr18:44676757-44676807	PFSK-1	brain:	n/a
40	chr18:44644942-44644992	HL-60	blood:	n/a
41	chr18:44677236-44677286	HIPEpiC	eye:	n/a
42	chr18:44676421-44676471	HCM	heart:	n/a
43	chr18:44676959-44677009	Hela-S3	cervix:	n/a
44	chr18:44676656-44676706	AoSMC	blood vessel:	n/a
45	chr18:44677236-44677286	H1-hESC	embryonic stem cell:	embryo
46	chr18:44634946-44634996	SK-N-SH	brain:	n/a
47	chr18:44626898-44626948	HL-60	blood:	n/a
48	chr18:44674172-44674222	MCF-7	breast:	n/a
49	chr18:44634946-44634996	AG09309	skin:	n/a
50	chr18:44644942-44644992	Hepatocyte	liver:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:44626392..44627213-chr18:44718440..44718955,2	MCF-7	breast:
2	chr18:44618074..44620983-chr18:44621410..44624299,2	K562	blood:
3	chr18:44667945..44673232-chr18:44673754..44678571,7	MCF-7	breast:
4	chr18:44623688..44626651-chr18:44786266..44788433,2	K562	blood:
5	chr18:44660900..44663835-chr18:44675479..44677959,3	MCF-7	breast:
6	chr18:44625997..44627852-chr18:44731582..44733974,3	K562	blood:
7	chr18:44669254..44671555-chr18:44682680..44684488,2	K562	blood:
8	chr1:205310411..205312346-chr18:44615284..44616803,2	MCF-7	breast:
9	chr18:44675372..44679287-chr18:44700113..44704114,10	MCF-7	breast:
10	chr18:44612247..44614708-chr18:44617059..44619635,2	K562	blood:
11	chr18:44626316..44626888-chr18:44718053..44718688,2	K562	blood:
12	chr18:44625943..44627276-chr18:44731016..44731992,4	MCF-7	breast:
13	chr18:44626654..44628817-chr18:44712742..44715143,2	MCF-7	breast:
14	chr18:44642698..44644448-chr18:44647501..44649189,2	K562	blood:
15	chr18:44668894..44671361-chr18:44675205..44677875,3	MCF-7	breast:
16	chr18:44667492..44671272-chr18:44701185..44704416,3	MCF-7	breast:
17	chr18:44599383..44602020-chr18:44603317..44605439,2	K562	blood:
18	chr18:44626319..44627308-chr18:44730999..44731988,9	MCF-7	breast:
19	chr18:44673432..44675834-chr18:44691617..44693277,2	MCF-7	breast:
20	chr18:44656520..44659372-chr18:44673623..44675752,2	K562	blood:
21	chr18:44631824..44634440-chr18:44636514..44640477,3	MCF-7	breast:
22	chr18:44621381..44624013-chr18:44625607..44627534,2	K562	blood:
23	chr17:79479596..79480269-chr18:44676737..44677238,2	HCT-116	colon:
24	chr18:44626381..44627618-chr18:44730985..44732225,13	K562	blood:
25	chr18:44663118..44666144-chr18:44673724..44676472,4	K562	blood:
26	chr18:44664428..44666267-chr18:44672303..44675573,3	K562	blood:
27	chr18:44676438..44677089-chr4:99849867..99850574,2	HCT-116	colon:
28	chr18:44626315..44627260-chr18:44809604..44810507,2	K562	blood:
29	chr18:44676561..44677117-chr21:38445057..38446026,2	Hela-S3	cervix:
30	chr18:44664428..44666267-chr18:44672303..44675573,3	K562	blood:
31	chr18:44666006..44667715-chr18:44675140..44677503,2	MCF-7	breast:
32	chr18:44675848..44678361-chr18:44699497..44704011,6	MCF-7	breast:
33	chr18:44618074..44620983-chr18:44621410..44624299,2	K562	blood:
34	chr18:44660900..44663835-chr18:44675479..44677959,3	MCF-7	breast:
35	chr18:44626566..44628357-chr18:44631236..44632776,2	MCF-7	breast:
36	chr18:44660861..44662516-chr18:44674947..44676839,2	K562	blood:
37	chr18:44631824..44634440-chr18:44636514..44640477,3	MCF-7	breast:
38	chr18:44642698..44644448-chr18:44647501..44649189,2	K562	blood:
39	chr18:44656520..44659372-chr18:44673623..44675752,2	K562	blood:
40	chr18:44676902..44678518-chr18:44699803..44701757,2	K562	blood:
41	chr18:44621381..44624013-chr18:44625607..44627534,2	K562	blood:
42	chr18:44648921..44650562-chr18:44675973..44678048,2	MCF-7	breast:
43	chr18:44624367..44626651-chr18:44785801..44788433,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-6	chr18:44663389-44663661	NONHSAT059155
2	lnc-KATNAL2-5	chr18:44632317-44634433	ENSG00000267724.1

No data

Variant related genes	Relation type
HDHD2	TF binding region
ENSG00000267800	TF binding region
ENSG00000267724	TF binding region
ENSG00000266957	TF binding region
HDHD2	CpG island
ENSG00000267800	CpG island
ENSG00000267724	CpG island
ENSG00000266957	CpG island
ENSG00000266957	chromatin interactions
ENSG00000263923	chromatin interactions
ENSG00000267800	chromatin interactions
ENSG00000167220	chromatin interactions
ENSG00000134049	chromatin interactions
ENSG00000151247	chromatin interactions
ENSG00000182670	chromatin interactions
ENSG00000185808	chromatin interactions
ENSG00000229947	chromatin interactions
ENSG00000267228	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000267724	chromatin interactions

Extended variants
information (count: 2749 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2749 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2289133	chr18:44602249-44602250	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72903273	chr18:44602265-44602266	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs2289132	chr18:44602292-44602293	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs370731738	chr18:44602306-44602307	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs569354226	chr18:44602326-44602327	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs72903277	chr18:44602334-44602335	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373261940	chr18:44602446-44602447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571111694	chr18:44602454-44602455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530576075	chr18:44602465-44602466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551801912	chr18:44602507-44602508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188761460	chr18:44602533-44602534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72903278	chr18:44602552-44602553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181272564	chr18:44602560-44602561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553101592	chr18:44602575-44602576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35446976	chr18:44602622-44602623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35279407	chr18:44602646-44602647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371980650	chr18:44602654-44602655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573016767	chr18:44602669-44602670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554146403	chr18:44602765-44602766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150282054	chr18:44602809-44602810	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575372659	chr18:44602814-44602815	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs3214657	chr18:44602817-44602818	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375348432	chr18:44602837-44602838	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111983018	chr18:44602857-44602858	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2289131	chr18:44602864-44602865	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs577609898	chr18:44602917-44602918	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553109600	chr18:44602943-44602944	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138943284	chr18:44602966-44602967	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371373288	chr18:44603080-44603081	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560121376	chr18:44603086-44603087	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369081668	chr18:44603100-44603101	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185335822	chr18:44603107-44603108	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149412241	chr18:44603129-44603130	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549230819	chr18:44603130-44603131	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563062423	chr18:44603134-44603135	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531845337	chr18:44603155-44603156	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35925389	chr18:44603169-44603170	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397858370	chr18:44603170-44603171	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201947500	chr18:44603183-44603184	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189854939	chr18:44603185-44603186	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201168653	chr18:44603187-44603188	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201577616	chr18:44603189-44603190	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199935966	chr18:44603191-44603192	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572018265	chr18:44603193-44603194	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs36095873	chr18:44603199-44603200	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs559255871	chr18:44603201-44603202	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566480815	chr18:44603205-44603206	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535507630	chr18:44603206-44603207	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555188553	chr18:44603210-44603211	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569009376	chr18:44603211-44603212	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1751 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44579800-44630200	Weak transcription	Right Ventricle	heart
2	chr18:44586800-44629600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr18:44587200-44630600	Weak transcription	Brain Anterior Caudate	brain
4	chr18:44587600-44629400	Weak transcription	Liver	Liver
5	chr18:44587800-44603400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr18:44588200-44621600	Weak transcription	Left Ventricle	heart
7	chr18:44591800-44602800	Weak transcription	Brain Angular Gyrus	brain
8	chr18:44594200-44603800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr18:44594400-44603200	Weak transcription	Brain Substantia Nigra	brain
10	chr18:44594600-44602800	Weak transcription	Adipose Nuclei	Adipose
11	chr18:44598200-44630000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr18:44600000-44602600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr18:44601000-44602800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr18:44601400-44602400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr18:44601400-44602400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr18:44601400-44602400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr18:44601400-44602400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr18:44601400-44602400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr18:44601400-44602400	Enhancers	HSMMtube	muscle
20	chr18:44601400-44608000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr18:44601600-44602400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr18:44601600-44602400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr18:44601600-44602400	Flanking Active TSS	Hela-S3	cervix
24	chr18:44601600-44602600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr18:44601600-44602800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr18:44601600-44603000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr18:44601600-44603200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr18:44601800-44602400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr18:44602000-44602400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr18:44602000-44603600	Enhancers	Brain Hippocampus Middle	brain
31	chr18:44602000-44603800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr18:44602000-44604800	Weak transcription	HSMM	muscle
33	chr18:44602200-44602400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr18:44602200-44602400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr18:44602200-44610800	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr18:44602200-44630000	Weak transcription	Fetal Muscle Leg	muscle
37	chr18:44602400-44603000	Enhancers	Hela-S3	cervix
38	chr18:44602400-44604000	Weak transcription	Spleen	Spleen
39	chr18:44602400-44611600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr18:44602600-44603600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr18:44602800-44603200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr18:44602800-44603400	Enhancers	Brain Angular Gyrus	brain
43	chr18:44602800-44604000	Strong transcription	Adipose Nuclei	Adipose
44	chr18:44603200-44603400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr18:44603200-44603400	Enhancers	Brain Substantia Nigra	brain
46	chr18:44603200-44603600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr18:44603400-44603600	Active TSS	Brain Cingulate Gyrus	brain
48	chr18:44603400-44603800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr18:44603400-44603800	Flanking Active TSS	Brain Angular Gyrus	brain
50	chr18:44603400-44607200	Weak transcription	Ovary	ovary

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