Variant report

Variant	nsv522397
Chromosome Location	chr18:44451644-44516088
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	chr18:44477101-44477471	K562	blood:	n/a	n/a
2	ARID3A	chr18:44497276-44497366	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:44473328-44473647	K562	blood:	n/a	n/a
4	ARID3A	chr18:44497591-44498031	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:44497808-44498358	K562	blood:	n/a	n/a
6	ATF2	chr18:44471501-44472211	GM12878	blood:	n/a	n/a
7	ATF2	chr18:44472744-44473161	GM12878	blood:	n/a	n/a
8	ATF2	chr18:44471610-44472123	GM12878	blood:	n/a	n/a
9	ATF2	chr18:44472744-44473213	GM12878	blood:	n/a	n/a
10	ATF2	chr18:44497666-44498183	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr18:44497631-44498034	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr18:44497310-44497614	K562	blood:	n/a	chr18:44497464-44497473 chr18:44497464-44497484
13	ATF3	chr18:44497264-44497622	HepG2	liver:	n/a	chr18:44497464-44497473 chr18:44497464-44497484
14	ATF3	chr18:44497353-44497643	H1-hESC	embryonic stem cell:	n/a	chr18:44497464-44497473 chr18:44497464-44497484
15	BACH1	chr18:44497244-44498424	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr18:44498006-44498377	K562	blood:	n/a	n/a
17	BATF	chr18:44471618-44472136	GM12878	blood:	n/a	n/a
18	BATF	chr18:44473522-44473945	GM12878	blood:	n/a	n/a
19	BATF	chr18:44472874-44473243	GM12878	blood:	n/a	n/a
20	BATF	chr18:44471586-44472149	GM12878	blood:	n/a	n/a
21	BATF	chr18:44479284-44479611	GM12878	blood:	n/a	n/a
22	BCL11A	chr18:44472893-44473129	GM12878	blood:	n/a	n/a
23	BCL11A	chr18:44473554-44473920	GM12878	blood:	n/a	n/a
24	BCL11A	chr18:44471573-44472194	GM12878	blood:	n/a	n/a
25	BCL11A	chr18:44472834-44473198	GM12878	blood:	n/a	n/a
26	BCL11A	chr18:44471673-44472126	GM12878	blood:	n/a	n/a
27	BCL3	chr18:44471673-44472090	GM12878	blood:	n/a	n/a
28	BCLAF1	chr18:44471569-44472170	GM12878	blood:	n/a	n/a
29	BCLAF1	chr18:44471682-44472127	GM12878	blood:	n/a	n/a
30	BCLAF1	chr18:44479274-44479625	GM12878	blood:	n/a	n/a
31	BCLAF1	chr18:44472705-44473247	GM12878	blood:	n/a	n/a
32	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
33	BHLHE40	chr18:44477182-44477209	K562	blood:	n/a	n/a
34	BHLHE40	chr18:44497301-44497544	A549	lung:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497462-44497475 chr18:44497433-44497449
35	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
36	BHLHE40	chr18:44497289-44497537	HepG2	liver:	n/a	chr18:44497463-44497472 chr18:44497464-44497473 chr18:44497462-44497475 chr18:44497433-44497449
37	BHLHE40	chr18:44472810-44473155	GM12878	blood:	n/a	n/a
38	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
39	BHLHE40	chr18:44471627-44472267	GM12878	blood:	n/a	n/a
40	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
41	CBX3	chr18:44457530-44457901	K562	blood:	n/a	n/a
42	CBX3	chr18:44468967-44469242	K562	blood:	n/a	n/a
43	CBX3	chr18:44457629-44457896	K562	blood:	n/a	n/a
44	CCNT2	chr18:44498121-44498376	K562	blood:	n/a	n/a
45	CCNT2	chr18:44496873-44497870	K562	blood:	n/a	chr18:44497507-44497516 chr18:44497011-44497020
46	CCNT2	chr18:44473385-44473579	K562	blood:	n/a	chr18:44473427-44473447
47	CEBPB	chr18:44463929-44464129	HepG2	liver:	n/a	chr18:44464038-44464049
48	CEBPB	chr18:44472810-44473307	GM12878	blood:	n/a	n/a
49	CEBPB	chr18:44471581-44472177	GM12878	blood:	n/a	n/a
50	CEBPB	chr18:44453364-44453629	K562	blood:	n/a	chr18:44453467-44453478

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44498047-44498097	SK-N-SH	brain:	n/a
2	chr18:44496911-44496961	NB4	blood:	n/a
3	chr18:44500261-44500311	ProgFib	skin:	n/a
4	chr18:44497499-44497549	GM12892	blood:	n/a
5	chr18:44497371-44497421	HCPEpiC	choroid plexus:	n/a
6	chr18:44497499-44497549	ProgFib	skin:	n/a
7	chr18:44494277-44494327	SAEC	small airway:	n/a
8	chr18:44497831-44497881	HCPEpiC	choroid plexus:	n/a
9	chr18:44500261-44500311	AG04449	skin:	fetal
10	chr18:44498047-44498097	HRPEpiC	eye:	n/a
11	chr18:44495064-44495114	HCT-116	colon:	n/a
12	chr18:44497371-44497421	ProgFib	skin:	n/a
13	chr18:44498341-44498391	HCPEpiC	choroid plexus:	n/a
14	chr18:44498341-44498391	T-47D	breast:	n/a
15	chr18:44495876-44495926	HCF	heart:	n/a
16	chr18:44497831-44497881	NHBE	bronchial:	n/a
17	chr18:44497831-44497881	PANC-1	pancreas:	n/a
18	chr18:44500261-44500311	AG10803	skin:	n/a
19	chr18:44497831-44497881	HNPCEpiC	eye:	n/a
20	chr18:44498047-44498097	CMK	blood:	n/a
21	chr18:44496911-44496961	GM12878	blood:	n/a
22	chr18:44495876-44495926	GM12892	blood:	n/a
23	chr18:44497604-44497654	GM12878	blood:	n/a
24	chr18:44498341-44498391	GM06990	blood:	n/a
25	chr18:44494277-44494327	Jurkat	blood:	n/a
26	chr18:44496911-44496961	PFSK-1	brain:	n/a
27	chr18:44495671-44495721	H1-hESC	embryonic stem cell:	embryo
28	chr18:44494277-44494327	T-47D	breast:	n/a
29	chr18:44498341-44498391	HRCEpiC	kidney:	n/a
30	chr18:44497831-44497881	GM12892	blood:	n/a
31	chr18:44498341-44498391	SK-N-MC	brain:	n/a
32	chr18:44495876-44495926	H1-hESC	embryonic stem cell:	embryo
33	chr18:44498047-44498097	HEK293	kidney:	embryo
34	chr18:44495671-44495721	GM12892	blood:	n/a
35	chr18:44498341-44498391	MCF-7	breast:	n/a
36	chr18:44495671-44495721	MCF-7	breast:	n/a
37	chr18:44498341-44498391	SK-N-SH	brain:	n/a
38	chr18:44495671-44495721	CMK	blood:	n/a
39	chr18:44500261-44500311	HIPEpiC	eye:	n/a
40	chr18:44500261-44500311	GM06990	blood:	n/a
41	chr18:44497604-44497654	CMK	blood:	n/a
42	chr18:44498341-44498391	HUVEC	blood vessel:	n/a
43	chr18:44497499-44497549	HCM	heart:	n/a
44	chr18:44497371-44497421	PrEC	prostate:	n/a
45	chr18:44498047-44498097	HL-60	blood:	n/a
46	chr18:44498341-44498391	ovcar-3	ovarian:	n/a
47	chr18:44494277-44494327	GM12891	blood:	n/a
48	chr18:44494277-44494327	Hela-S3	cervix:	n/a
49	chr18:44494277-44494327	U87	brain:	n/a
50	chr18:44498341-44498391	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44497079..44497631-chr6:26123993..26124759,2	Hela-S3	cervix:
2	chr18:44407516..44409436-chr18:44454245..44456431,2	K562	blood:
3	chr18:44488075..44490249-chr18:44496813..44499050,3	MCF-7	breast:
4	chr18:44480442..44483446-chr18:44494668..44497985,3	K562	blood:
5	chr18:44494535..44496872-chr18:44526864..44529810,3	MCF-7	breast:
6	chr18:44475450..44476987-chr18:44497045..44499673,2	K562	blood:
7	chr18:44491476..44494532-chr18:44496207..44498289,3	MCF-7	breast:
8	chr11:65028772..65029575-chr18:44497156..44497741,2	NB4	blood:
9	chr18:44422888..44425442-chr18:44495658..44497517,2	K562	blood:
10	chr14:51900262..51903156-chr18:44496356..44498175,2	MCF-7	breast:
11	chr18:44486293..44487895-chr18:44496717..44498620,2	K562	blood:
12	chr18:44468278..44470904-chr18:44471891..44475725,3	MCF-7	breast:
13	chr18:44492204..44495512-chr18:44495791..44498945,4	MCF-7	breast:
14	chr18:44496509..44498962-chr18:44499238..44501525,3	MCF-7	breast:
15	chr18:44488852..44491719-chr18:44494617..44499861,5	MCF-7	breast:
16	chr18:44496509..44498962-chr18:44499238..44501525,3	MCF-7	breast:
17	chr18:44468278..44470904-chr18:44471891..44475725,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCEB3CL-2	chr18:44497285-44497383	NONHSAT059148
2	lnc-TCEB3CL-2	chr18:44470995-44471017	NONHSAT059148
3	lnc-TCEB3CL-2	chr18:44497285-44497313	NONHSAT059149
4	lnc-TCEB3CL-2	chr18:44473394-44473494	NONHSAT059148
5	lnc-TCEB3CL-1	chr18:44487621-44487962	NONHSAT059150
6	lnc-TCEB3CL-1	chr18:44487461-44487522	NONHSAT059150
7	lnc-TCEB3CL-2	chr18:44485723-44486278	NONHSAT059149
8	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
ENSG00000180596	chromatin interactions
ENSG00000014138	chromatin interactions
ENSG00000167216	chromatin interactions
ENSG00000180573	chromatin interactions

Extended variants
information (count: 1926 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1926 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12454431	chr18:44451644-44451645	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531721739	chr18:44451662-44451663	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs555941850	chr18:44451665-44451666	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs202223268	chr18:44451676-44451677	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs72911116	chr18:44451719-44451720	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs554534718	chr18:44451739-44451740	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs556533927	chr18:44451752-44451753	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs115929032	chr18:44451762-44451763	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs545475164	chr18:44451788-44451789	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs560788155	chr18:44451830-44451831	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs528206993	chr18:44451840-44451841	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs541621989	chr18:44451850-44451851	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs561925363	chr18:44451854-44451855	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs148078925	chr18:44451919-44451920	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs141794270	chr18:44452049-44452050	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192251050	chr18:44452070-44452071	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72911118	chr18:44452128-44452129	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs74741090	chr18:44452132-44452133	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566817001	chr18:44452148-44452149	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181898712	chr18:44452162-44452163	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555633673	chr18:44452230-44452231	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117774215	chr18:44452237-44452238	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56009869	chr18:44452251-44452252	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs186870653	chr18:44452262-44452263	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73437151	chr18:44452313-44452314	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs376516880	chr18:44452322-44452323	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149309831	chr18:44452328-44452329	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190228881	chr18:44452368-44452369	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370997885	chr18:44452485-44452486	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182574994	chr18:44452493-44452494	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572807046	chr18:44452562-44452563	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77528543	chr18:44452587-44452588	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186895122	chr18:44452588-44452589	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575544794	chr18:44452605-44452606	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189733908	chr18:44452643-44452644	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558608603	chr18:44452659-44452660	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529806766	chr18:44452662-44452663	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564893045	chr18:44452733-44452734	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530523728	chr18:44452767-44452768	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146240156	chr18:44452829-44452830	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568545208	chr18:44452864-44452865	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537424337	chr18:44452898-44452899	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543841807	chr18:44452981-44452982	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554464077	chr18:44452987-44452988	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529365347	chr18:44453001-44453002	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544255141	chr18:44453057-44453058	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182651692	chr18:44453101-44453102	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6507709	chr18:44453138-44453139	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs538076163	chr18:44453169-44453170	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139234937	chr18:44453170-44453171	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	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:1547 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44399200-44457000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr18:44407600-44453200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr18:44435000-44457400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr18:44435400-44456000	Weak transcription	Fetal Kidney	kidney
5	chr18:44437200-44461600	Weak transcription	Ovary	ovary
6	chr18:44440400-44453400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr18:44440400-44468400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr18:44447600-44457400	Weak transcription	Fetal Heart	heart
9	chr18:44448000-44456400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
10	chr18:44448000-44460600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr18:44449000-44457400	Weak transcription	HSMMtube	muscle
12	chr18:44449000-44468600	Weak transcription	Pancreas	Pancrea
13	chr18:44449000-44468600	Weak transcription	NHLF	lung
14	chr18:44449200-44455200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr18:44449200-44455800	Weak transcription	Lung	lung
16	chr18:44449200-44456800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr18:44449200-44457200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr18:44449200-44457400	Weak transcription	Aorta	Aorta
19	chr18:44449200-44457400	Weak transcription	Brain Hippocampus Middle	brain
20	chr18:44449200-44457400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr18:44449200-44457400	Weak transcription	Left Ventricle	heart
22	chr18:44449200-44457400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr18:44449200-44457400	Weak transcription	Thymus	Thymus
24	chr18:44449200-44458800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr18:44449400-44453600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr18:44449400-44454200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr18:44449400-44455400	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr18:44449400-44455600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr18:44449400-44455600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr18:44449400-44455800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr18:44449400-44457200	Weak transcription	Spleen	Spleen
32	chr18:44449400-44457400	Weak transcription	Colon Smooth Muscle	Colon
33	chr18:44449600-44453000	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr18:44449600-44453400	Weak transcription	HMEC	breast
35	chr18:44449600-44454400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr18:44449600-44455600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr18:44449600-44455600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr18:44449600-44455800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr18:44449600-44457000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr18:44449600-44457200	Weak transcription	HepG2	liver
41	chr18:44449600-44457600	Weak transcription	Right Ventricle	heart
42	chr18:44449800-44456400	Weak transcription	Primary B cells from peripheral blood	blood
43	chr18:44449800-44468400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr18:44450000-44455000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr18:44450200-44453600	Weak transcription	Fetal Muscle Trunk	muscle
46	chr18:44450200-44455200	Weak transcription	Fetal Intestine Large	intestine
47	chr18:44450200-44455400	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr18:44450200-44455600	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr18:44450200-44455600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr18:44450200-44455600	Weak transcription	Duodenum Mucosa	Duodenum

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