Variant report

Variant	esv1797427
Chromosome Location	chr18:44774077-44788908
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	ATF2	chr18:44777730-44778344	H1-hESC	embryonic stem cell:	n/a	chr18:44778070-44778084 chr18:44778072-44778083
2	ATF2	chr18:44777843-44778295	H1-hESC	embryonic stem cell:	n/a	chr18:44778070-44778084 chr18:44778072-44778083
3	BACH1	chr18:44775313-44775375	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:44780932-44781270	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr18:44774919-44775077	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:44779792-44779941	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr18:44777974-44778152	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr18:44786740-44786945	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr18:44780830-44781199	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr18:44786507-44786999	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr18:44777890-44778108	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr18:44782989-44783003	GM12878	blood:	n/a	n/a
13	CHD2	chr18:44775170-44775530	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr18:44777788-44778315	H1-hESC	embryonic stem cell:	n/a	chr18:44778071-44778084
15	CREB1	chr18:44777727-44778339	H1-hESC	embryonic stem cell:	n/a	chr18:44778071-44778084
16	CREB1	chr18:44786718-44787104	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr18:44786680-44787148	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr18:44781037-44781363	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr18:44780860-44781331	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr18:44773776-44774256	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr18:44787697-44790840	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr18:44786631-44786998	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr18:44774693-44775689	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr18:44777625-44778343	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr18:44788380-44788530	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr18:44787700-44787850	AG09319	gingival:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
27	CTCF	chr18:44778004-44778140	Gliobla	brain:	n/a	n/a
28	CTCF	chr18:44778002-44778125	A549	lung:	n/a	n/a
29	CTCF	chr18:44786882-44786900	K562	blood:	n/a	n/a
30	CTCF	chr18:44787760-44787851	GM19238	blood:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
31	CTCF	chr18:44787732-44787855	Fibrobl	skin:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
32	CTCF	chr18:44787700-44787850	GM12872	blood:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
33	CTCF	chr18:44786440-44786590	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr18:44787737-44787863	Hela-S3	cervix:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
35	CTCF	chr18:44787670-44787964	H1-hESC	embryonic stem cell:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
36	CTCF	chr18:44787820-44787970	GM12869	blood:	n/a	n/a
37	CTCF	chr18:44787720-44787870	HepG2	liver:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
38	CTCF	chr18:44787700-44787850	HCT-116	colon:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
39	CTCF	chr18:44787624-44787952	H1-hESC	embryonic stem cell:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
40	CTCF	chr18:44786040-44786190	GM12866	blood:	n/a	n/a
41	CTCF	chr18:44787720-44787870	GM12875	blood:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
42	CTCF	chr18:44787575-44788010	H1-hESC	embryonic stem cell:	n/a	chr18:44787795-44787811 chr18:44787794-44787812
43	CTCF	chr18:44775000-44775150	GM12866	blood:	n/a	n/a
44	CTCF	chr18:44787780-44787930	A549	lung:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
45	CTCF	chr18:44787680-44787830	HCFaa	heart:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
46	CTCF	chr18:44787760-44787910	HUVEC	blood vessel:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
47	CTCF	chr18:44787720-44787870	GM12866	blood:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
48	CTCF	chr18:44787720-44787870	K562	blood:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
49	CTCF	chr18:44787780-44787930	GM12874	blood:	n/a	chr18:44787794-44787812 chr18:44787795-44787811
50	CTCF	chr18:44787740-44787890	HMF	breast:	n/a	chr18:44787794-44787812 chr18:44787795-44787811

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44787492-44787542	AG09309	skin:	n/a
2	chr18:44774923-44774973	HMEC	breast:	n/a
3	chr18:44787492-44787542	AG09309	skin:	n/a
4	chr18:44774923-44774973	HMEC	breast:	n/a
5	chr18:44774846-44774896	ProgFib	skin:	n/a
6	chr18:44784846-44784896	Jurkat	blood:	n/a
7	chr18:44786091-44786141	SAEC	small airway:	n/a
8	chr18:44788898-44788948	MCF10A-Er-Src	breast:	n/a
9	chr18:44785758-44785808	NT2-D1	testis:	n/a
10	chr18:44786091-44786141	ovcar-3	ovarian:	n/a
11	chr18:44774846-44774896	NT2-D1	testis:	n/a
12	chr18:44787585-44787635	BE2_C	brain:	n/a
13	chr18:44776850-44776900	NH-A	brain:	n/a
14	chr18:44781237-44781287	ProgFib	skin:	n/a
15	chr18:44777736-44777786	GM12892	blood:	n/a
16	chr18:44774923-44774973	SAEC	small airway:	n/a
17	chr18:44778021-44778071	BJ	skin:	n/a
18	chr18:44788898-44788948	H1-hESC	embryonic stem cell:	embryo
19	chr18:44775576-44775626	GM12892	blood:	n/a
20	chr18:44786426-44786476	Hepatocyte	liver:	n/a
21	chr18:44785758-44785808	SK-N-SH	brain:	n/a
22	chr18:44775413-44775463	HEEpiC	esophagus:	n/a
23	chr18:44787728-44787778	SK-N-SH_RA	brain:	n/a
24	chr18:44775576-44775626	AG10803	skin:	n/a
25	chr18:44774846-44774896	U87	brain:	n/a
26	chr18:44775009-44775059	GM12891	blood:	n/a
27	chr18:44778236-44778286	HPAEpiC	pulmonary alveolar:	n/a
28	chr18:44776850-44776900	HAEpiC	amniotic membrane:	n/a
29	chr18:44784846-44784896	BJ	skin:	n/a
30	chr18:44775009-44775059	AG09319	gingival:	n/a
31	chr18:44774846-44774896	PrEC	prostate:	n/a
32	chr18:44774054-44774104	HL-60	blood:	n/a
33	chr18:44774054-44774104	GM06990	blood:	n/a
34	chr18:44786886-44786936	AG09309	skin:	n/a
35	chr18:44784846-44784896	A549	lung:	n/a
36	chr18:44787585-44787635	GM12891	blood:	n/a
37	chr18:44786426-44786476	HAEpiC	amniotic membrane:	n/a
38	chr18:44778021-44778071	HCT-116	colon:	n/a
39	chr18:44785758-44785808	SAEC	small airway:	n/a
40	chr18:44778021-44778071	HepG2	liver:	n/a
41	chr18:44774054-44774104	HUVEC	blood vessel:	n/a
42	chr18:44787492-44787542	HL-60	blood:	n/a
43	chr18:44777736-44777786	CMK	blood:	n/a
44	chr18:44777799-44777849	NT2-D1	testis:	n/a
45	chr18:44776850-44776900	HIPEpiC	eye:	n/a
46	chr18:44787492-44787542	RPTEC	kidney:	n/a
47	chr18:44778083-44778133	HEK293	kidney:	embryo
48	chr18:44787585-44787635	NHBE	bronchial:	n/a
49	chr18:44778236-44778286	HCM	heart:	n/a
50	chr18:44787585-44787635	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44778191..44780835-chr18:44785176..44787814,2	K562	blood:
2	chr18:44779645..44782742-chr18:44785627..44788634,4	MCF-7	breast:
3	chr18:44778191..44780835-chr18:44785176..44787814,2	K562	blood:
4	chr18:44779645..44782742-chr18:44785627..44788634,4	MCF-7	breast:
5	chr18:44778191..44780835-chr18:44785049..44787814,3	K562	blood:
6	chr18:44624367..44626651-chr18:44785801..44788433,2	K562	blood:
7	chr18:44778191..44780835-chr18:44785049..44787814,3	K562	blood:
8	chr18:44623688..44626651-chr18:44786266..44788433,2	K562	blood:
9	chr18:44774382..44776213-chr18:44776745..44778357,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SKOR2-1	chr18:44775960-44776161	l_1576_chr18:44775959-44801844_lung

Variant related genes	Relation type
SKOR2	TF binding region
SKOR2	CpG island
ENSG00000215474	chromatin interactions

Extended variants
information (count: 518 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527709393	chr18:44774205-44774206	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112028746	chr18:44774243-44774244	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547771874	chr18:44774248-44774249	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567654123	chr18:44774280-44774281	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536799808	chr18:44774351-44774352	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556360473	chr18:44774437-44774438	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570262618	chr18:44774466-44774467	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs57216407	chr18:44774515-44774516	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184619951	chr18:44774555-44774556	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111300606	chr18:44774674-44774675	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538819920	chr18:44774688-44774689	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558842471	chr18:44774715-44774716	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572355272	chr18:44774813-44774814	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188936589	chr18:44774842-44774843	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373929593	chr18:44774853-44774854	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539853928	chr18:44774971-44774972	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561108578	chr18:44775019-44775020	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs202063106	chr18:44775028-44775029	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553394854	chr18:44775093-44775094	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573556023	chr18:44775112-44775113	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542738210	chr18:44775117-44775118	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376365161	chr18:44775124-44775125	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562428417	chr18:44775173-44775174	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531550684	chr18:44775183-44775184	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371202595	chr18:44775210-44775211	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549741504	chr18:44775219-44775220	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574685057	chr18:44775244-44775245	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545196247	chr18:44775361-44775362	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565183201	chr18:44775390-44775391	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527623475	chr18:44775421-44775422	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs542732248	chr18:44775422-44775423	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs547709375	chr18:44775423-44775424	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs567677759	chr18:44775466-44775467	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs376817644	chr18:44775498-44775499	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs530026226	chr18:44775523-44775524	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs550260759	chr18:44775570-44775571	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs75440550	chr18:44775571-44775572	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs181508916	chr18:44775572-44775573	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs141813697	chr18:44775650-44775651	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs186333451	chr18:44775690-44775691	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs535034255	chr18:44775691-44775692	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs554823760	chr18:44775714-44775715	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573616673	chr18:44775763-44775764	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs372176880	chr18:44775764-44775765	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs573388364	chr18:44775829-44775830	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs189614084	chr18:44775893-44775894	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs2668771	chr18:44775897-44775898	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs576009305	chr18:44775925-44775926	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545114277	chr18:44775936-44775937	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs150480380	chr18:44775988-44775989	Bivalent Enhancer Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44772600-44774200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr18:44772800-44774400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
3	chr18:44772800-44774400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
4	chr18:44772800-44775400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
5	chr18:44773000-44774400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
6	chr18:44773200-44774200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr18:44773200-44774200	Bivalent Enhancer	Ovary	ovary
8	chr18:44773200-44774400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr18:44773200-44774400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
10	chr18:44773200-44774400	Bivalent Enhancer	Spleen	Spleen
11	chr18:44773200-44774800	Bivalent Enhancer	Lung	lung
12	chr18:44773400-44774200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr18:44773400-44774200	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr18:44773400-44774200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr18:44773400-44774800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
16	chr18:44773600-44774200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
17	chr18:44773600-44774200	Enhancers	Primary hematopoietic stem cells	blood
18	chr18:44773600-44774200	Enhancers	Pancreas	Pancrea
19	chr18:44773600-44774200	Flanking Bivalent TSS/Enh	Right Ventricle	heart
20	chr18:44773600-44774400	Enhancers	Gastric	stomach
21	chr18:44773600-44774400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
22	chr18:44773600-44775000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr18:44773800-44774200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr18:44773800-44774200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
25	chr18:44773800-44774800	Enhancers	Liver	Liver
26	chr18:44774000-44774200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr18:44774000-44774200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr18:44774000-44774200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr18:44774000-44774200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
30	chr18:44774000-44774200	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr18:44774000-44774200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr18:44774000-44774200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr18:44774000-44774200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr18:44774000-44774200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
35	chr18:44774000-44774200	Bivalent Enhancer	Brain Hippocampus Middle	brain
36	chr18:44774000-44774200	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
37	chr18:44774000-44774400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
38	chr18:44774000-44774400	Bivalent Enhancer	Brain Germinal Matrix	brain
39	chr18:44774000-44774400	Bivalent Enhancer	Fetal Brain Male	brain
40	chr18:44774200-44774400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:44774200-44774400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr18:44774200-44774400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr18:44774200-44774400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr18:44774200-44774400	Bivalent/Poised TSS	Psoas Muscle	Psoas
45	chr18:44774200-44774800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr18:44774200-44774800	Weak transcription	Pancreas	Pancrea
47	chr18:44774200-44775000	Bivalent Enhancer	Right Ventricle	heart
48	chr18:44774400-44774600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
49	chr18:44774400-44774600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr18:44774400-44774800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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