Variant report

Variant	nsv576813
Chromosome Location	chr18:44481641-44531283
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	chr18:44530288-44530439	K562	blood:	n/a	n/a
2	ARID3A	chr18:44497276-44497366	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:44497591-44498031	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:44497808-44498358	K562	blood:	n/a	n/a
5	ATF2	chr18:44497666-44498183	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr18:44497631-44498034	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr18:44497353-44497643	H1-hESC	embryonic stem cell:	n/a	chr18:44497464-44497473 chr18:44497464-44497484
8	ATF3	chr18:44497264-44497622	HepG2	liver:	n/a	chr18:44497464-44497473 chr18:44497464-44497484
9	ATF3	chr18:44497310-44497614	K562	blood:	n/a	chr18:44497464-44497473 chr18:44497464-44497484
10	BACH1	chr18:44497244-44498424	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:44498006-44498377	K562	blood:	n/a	n/a
12	BHLHE40	chr18:44496886-44497910	HepG2	liver:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497589-44497605 chr18:44497462-44497475 chr18:44497579-44497595 chr18:44497658-44497674 chr18:44497433-44497449
13	BHLHE40	chr18:44496660-44498028	GM12878	blood:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497589-44497605 chr18:44497462-44497475 chr18:44497579-44497595 chr18:44497658-44497674 chr18:44497433-44497449
14	BHLHE40	chr18:44497310-44497608	HepG2	liver:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497589-44497605 chr18:44497462-44497475 chr18:44497579-44497595 chr18:44497433-44497449
15	BHLHE40	chr18:44497301-44497544	A549	lung:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497462-44497475 chr18:44497433-44497449
16	BHLHE40	chr18:44496513-44498261	K562	blood:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497589-44497605 chr18:44497462-44497475 chr18:44497579-44497595 chr18:44497658-44497674 chr18:44497433-44497449
17	BHLHE40	chr18:44497289-44497537	HepG2	liver:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497462-44497475 chr18:44497433-44497449
18	BRCA1	chr18:44526800-44527412	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr18:44519517-44519902	HCT-116	colon:	n/a	n/a
20	CCNT2	chr18:44496873-44497870	K562	blood:	n/a	chr18:44497507-44497516 chr18:44497011-44497020
21	CCNT2	chr18:44498121-44498376	K562	blood:	n/a	n/a
22	CEBPB	chr18:44517542-44517844	HepG2	liver:	n/a	chr18:44517683-44517694
23	CEBPB	chr18:44519588-44519974	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr18:44496808-44497523	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr18:44519678-44519944	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr18:44519633-44519970	IMR90	lung:	n/a	n/a
27	CEBPB	chr18:44497762-44498282	H1-hESC	embryonic stem cell:	n/a	chr18:44497882-44497899
28	CEBPB	chr18:44497785-44498078	K562	blood:	n/a	chr18:44497882-44497899
29	CEBPB	chr18:44517540-44517817	IMR90	lung:	n/a	chr18:44517683-44517694
30	CEBPB	chr18:44517559-44517759	K562	blood:	n/a	chr18:44517683-44517694
31	CEBPD	chr18:44497959-44498409	K562	blood:	n/a	n/a
32	CEBPD	chr18:44497241-44497701	HepG2	liver:	n/a	n/a
33	CHD1	chr18:44498152-44498423	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr18:44497174-44497348	GM12878	blood:	n/a	n/a
35	CHD1	chr18:44497395-44497725	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr18:44497576-44497939	GM12878	blood:	n/a	n/a
37	CHD1	chr18:44496255-44496935	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr18:44526479-44527130	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr18:44496732-44498233	GM12878	blood:	n/a	chr18:44498043-44498053
40	CHD2	chr18:44497114-44497381	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr18:44497618-44497839	HepG2	liver:	n/a	n/a
42	CHD2	chr18:44526653-44526788	K562	blood:	n/a	n/a
43	CHD2	chr18:44497149-44497357	HepG2	liver:	n/a	n/a
44	CHD2	chr18:44496709-44497875	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr18:44497117-44497434	K562	blood:	n/a	n/a
46	CHD2	chr18:44497889-44498135	K562	blood:	n/a	chr18:44498043-44498053
47	CHD2	chr18:44497633-44498175	H1-hESC	embryonic stem cell:	n/a	chr18:44498043-44498053
48	CREB1	chr18:44497098-44497934	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr18:44497274-44497743	K562	blood:	n/a	n/a
50	CREB1	chr18:44497190-44497746	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44494277-44494327	GM12878	blood:	n/a
2	chr18:44497499-44497549	HRE	kidney:	n/a
3	chr18:44497371-44497421	GM12878	blood:	n/a
4	chr18:44495064-44495114	PrEC	prostate:	n/a
5	chr18:44494277-44494327	GM12878	blood:	n/a
6	chr18:44497499-44497549	HRE	kidney:	n/a
7	chr18:44497371-44497421	GM12878	blood:	n/a
8	chr18:44495064-44495114	PrEC	prostate:	n/a
9	chr18:44497831-44497881	AG04449	skin:	fetal
10	chr18:44526605-44526655	HUVEC	blood vessel:	n/a
11	chr18:44498341-44498391	HEK293	kidney:	embryo
12	chr18:44523070-44523120	RPTEC	kidney:	n/a
13	chr18:44497371-44497421	LNCaP	prostate:	n/a
14	chr18:44526430-44526480	T-47D	breast:	n/a
15	chr18:44526743-44526793	HNPCEpiC	eye:	n/a
16	chr18:44526707-44526757	NT2-D1	testis:	n/a
17	chr18:44525710-44525760	ECC-1	luminal epithelium:	n/a
18	chr18:44526743-44526793	SAEC	small airway:	n/a
19	chr18:44496911-44496961	HCM	heart:	n/a
20	chr18:44494277-44494327	A549	lung:	n/a
21	chr18:44500261-44500311	PANC-1	pancreas:	n/a
22	chr18:44500261-44500311	AG10803	skin:	n/a
23	chr18:44497499-44497549	AoSMC	blood vessel:	n/a
24	chr18:44498341-44498391	GM12878	blood:	n/a
25	chr18:44526743-44526793	IMR90	lung:	fetal
26	chr18:44495671-44495721	GM12891	blood:	n/a
27	chr18:44495064-44495114	Caco-2	colon:	n/a
28	chr18:44497604-44497654	HUVEC	blood vessel:	n/a
29	chr18:44497499-44497549	ProgFib	skin:	n/a
30	chr18:44526707-44526757	HEEpiC	esophagus:	n/a
31	chr18:44498047-44498097	U87	brain:	n/a
32	chr18:44496911-44496961	HPAEpiC	pulmonary alveolar:	n/a
33	chr18:44500261-44500311	PrEC	prostate:	n/a
34	chr18:44495064-44495114	Hepatocyte	liver:	n/a
35	chr18:44495671-44495721	HCF	heart:	n/a
36	chr18:44494277-44494327	GM12891	blood:	n/a
37	chr18:44523070-44523120	SK-N-MC	brain:	n/a
38	chr18:44495876-44495926	AoSMC	blood vessel:	n/a
39	chr18:44526707-44526757	Hepatocyte	liver:	n/a
40	chr18:44526605-44526655	Hela-S3	cervix:	n/a
41	chr18:44527971-44528021	Hela-S3	cervix:	n/a
42	chr18:44525710-44525760	AoSMC	blood vessel:	n/a
43	chr18:44498341-44498391	IMR90	lung:	fetal
44	chr18:44527971-44528021	HRCEpiC	kidney:	n/a
45	chr18:44526867-44526917	ovcar-3	ovarian:	n/a
46	chr18:44496911-44496961	Hepatocyte	liver:	n/a
47	chr18:44523070-44523120	HIPEpiC	eye:	n/a
48	chr18:44497831-44497881	PANC-1	pancreas:	n/a
49	chr18:44496911-44496961	HMEC	breast:	n/a
50	chr18:44500261-44500311	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44494535..44496872-chr18:44526864..44529810,3	MCF-7	breast:
2	chr18:44494535..44496872-chr18:44526864..44529810,3	MCF-7	breast:
3	chr18:44491476..44494532-chr18:44496207..44498289,3	MCF-7	breast:
4	chr18:44497069..44499203-chr18:44524229..44526403,2	MCF-7	breast:
5	chr18:44496509..44498962-chr18:44499238..44501525,3	MCF-7	breast:
6	chr18:44492204..44495512-chr18:44495791..44498945,4	MCF-7	breast:
7	chr18:44422888..44425442-chr18:44495658..44497517,2	K562	blood:
8	chr11:65028772..65029575-chr18:44497156..44497741,2	NB4	blood:
9	chr18:44496509..44498962-chr18:44499238..44501525,3	MCF-7	breast:
10	chr18:44480442..44483446-chr18:44494668..44497985,3	K562	blood:
11	chr14:51900262..51903156-chr18:44496356..44498175,2	MCF-7	breast:
12	chr18:44488075..44490249-chr18:44496813..44499050,3	MCF-7	breast:
13	chr18:44526928..44528966-chr18:44543505..44545090,2	MCF-7	breast:
14	chr18:44497079..44497631-chr6:26123993..26124759,2	Hela-S3	cervix:
15	chr18:44488852..44491719-chr18:44494617..44499861,5	MCF-7	breast:
16	chr18:44486293..44487895-chr18:44496717..44498620,2	K562	blood:
17	chr18:44529742..44530665-chr18:44562546..44563169,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCEB3CL-2	chr18:44497285-44497383	NONHSAT059148
2	lnc-TCEB3CL-2	chr18:44485723-44486278	NONHSAT059149
3	lnc-TCEB3CL-2	chr18:44497285-44497313	NONHSAT059149
4	lnc-TCEB3CL-1	chr18:44487461-44487522	NONHSAT059150
5	lnc-TCEB3CL-1	chr18:44487621-44487962	NONHSAT059150
6	lnc-TCEB3CL-2	chr18:44483490-44483598	NONHSAT059148

Variant related genes	Relation type
PIAS2	TF binding region
KATNAL2	TF binding region
PIAS2	CpG island
KATNAL2	CpG island
ENSG00000258893	chromatin interactions
ENSG00000078043	chromatin interactions
ENSG00000167216	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000266996	chromatin interactions
ENSG00000014138	chromatin interactions
ENSG00000180596	chromatin interactions

Extended variants
information (count: 1362 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539855022	chr18:44481645-44481646	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs191417304	chr18:44481660-44481661	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs573703565	chr18:44481661-44481662	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs542406059	chr18:44481667-44481668	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376234005	chr18:44481722-44481723	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs149371199	chr18:44481729-44481730	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531484313	chr18:44481796-44481797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs114351839	chr18:44481822-44481823	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528309580	chr18:44481848-44481849	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs71364570	chr18:44481932-44481933	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368057835	chr18:44481972-44481973	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs539971783	chr18:44482150-44482151	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs182297240	chr18:44482170-44482171	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547478400	chr18:44482182-44482183	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs34702120	chr18:44482206-44482207	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs58675073	chr18:44482223-44482224	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs186700833	chr18:44482255-44482256	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371914466	chr18:44482318-44482319	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144690299	chr18:44482356-44482357	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs115271233	chr18:44482363-44482364	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539248158	chr18:44482423-44482424	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148498708	chr18:44482436-44482437	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs191159275	chr18:44482456-44482457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs533781782	chr18:44482478-44482479	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs375298379	chr18:44482519-44482520	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs553529204	chr18:44482549-44482550	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs145301176	chr18:44482561-44482562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs34371288	chr18:44482589-44482590	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs72915071	chr18:44482654-44482655	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs151004543	chr18:44482657-44482658	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555862549	chr18:44482667-44482668	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs138207310	chr18:44482714-44482715	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184710142	chr18:44482796-44482797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs368610293	chr18:44482799-44482800	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147206849	chr18:44482832-44482833	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs565141910	chr18:44482838-44482839	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs527627578	chr18:44482869-44482870	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs541398994	chr18:44482873-44482874	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188892062	chr18:44483017-44483018	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527454990	chr18:44483075-44483076	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs77026283	chr18:44483179-44483180	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576524589	chr18:44483198-44483199	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs185268676	chr18:44483199-44483200	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs138585966	chr18:44483201-44483202	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs200371441	chr18:44483284-44483285	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs189697578	chr18:44483289-44483290	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532704517	chr18:44483291-44483292	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7240843	chr18:44483293-44483294	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs572650013	chr18:44483348-44483349	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs566355208	chr18:44483385-44483386	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Breast cancer	21509527	CNVD

Chromatin state (count:1111 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44469000-44489200	Weak transcription	Fetal Stomach	stomach
2	chr18:44469800-44481800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr18:44469800-44493600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr18:44469800-44493800	Weak transcription	Lung	lung
5	chr18:44469800-44494600	Weak transcription	Fetal Brain Male	brain
6	chr18:44469800-44495200	Weak transcription	Hela-S3	cervix
7	chr18:44469800-44495400	Weak transcription	Brain Anterior Caudate	brain
8	chr18:44469800-44496000	Weak transcription	HSMMtube	muscle
9	chr18:44469800-44496400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr18:44470200-44482800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr18:44470200-44484000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr18:44470400-44486200	Weak transcription	Fetal Muscle Trunk	muscle
13	chr18:44470600-44493000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr18:44470600-44495600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr18:44470800-44482200	Weak transcription	Aorta	Aorta
16	chr18:44470800-44482800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr18:44470800-44483400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr18:44470800-44483400	Weak transcription	Fetal Brain Female	brain
19	chr18:44470800-44484400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr18:44470800-44486800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr18:44470800-44493200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr18:44470800-44495200	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr18:44470800-44495600	Weak transcription	Thymus	Thymus
24	chr18:44470800-44495800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr18:44470800-44495800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr18:44470800-44495800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr18:44471000-44483200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr18:44471000-44484400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr18:44471000-44484600	Weak transcription	Ovary	ovary
30	chr18:44471000-44485400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr18:44471000-44487000	Weak transcription	Dnd41	blood
32	chr18:44471000-44488200	Weak transcription	HMEC	breast
33	chr18:44471000-44489000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr18:44471000-44495400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr18:44471000-44495400	Weak transcription	Fetal Thymus	thymus
36	chr18:44471000-44495600	Weak transcription	HUVEC	blood vessel
37	chr18:44471000-44495800	Weak transcription	HSMM	muscle
38	chr18:44471200-44493200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr18:44471200-44495400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr18:44471200-44495400	Weak transcription	Primary B cells from cord blood	blood
41	chr18:44472200-44493800	Weak transcription	Left Ventricle	heart
42	chr18:44473600-44486200	Weak transcription	Fetal Lung	lung
43	chr18:44473800-44493400	Weak transcription	Fetal Heart	heart
44	chr18:44474400-44483000	Weak transcription	Primary B cells from peripheral blood	blood
45	chr18:44474400-44490800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr18:44474400-44493000	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr18:44474400-44493600	Weak transcription	HepG2	liver
48	chr18:44474600-44481800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr18:44474600-44481800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr18:44474800-44493000	Weak transcription	Primary T helper cells fromperipheralblood	blood

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