Variant report

Variant	esv1803659
Chromosome Location	chr5:36935129-37039857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:805)
CpG islands
(count:183)
Chromatin interactive
region (count:108)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37006632-37006811	K562	blood:	n/a	n/a
2	ARID3A	chr5:37002178-37002846	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:36944696-36945107	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37006056-37006376	K562	blood:	n/a	n/a
5	ARID3A	chr5:36962968-36963071	K562	blood:	n/a	n/a
6	ARID3A	chr5:36944203-36945211	K562	blood:	n/a	n/a
7	ATF1	chr5:36999925-37000005	K562	blood:	n/a	n/a
8	ATF2	chr5:36998676-36999169	GM12878	blood:	n/a	n/a
9	ATF2	chr5:36998719-36999066	GM12878	blood:	n/a	n/a
10	BATF	chr5:36998569-36998958	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:36955382-36955388	GM12878	blood:	n/a	n/a
12	BRCA1	chr5:36951118-36951430	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr5:36982251-36982514	K562	blood:	n/a	n/a
14	CCNT2	chr5:36954726-36954853	K562	blood:	n/a	n/a
15	CCNT2	chr5:36946283-36946471	K562	blood:	n/a	n/a
16	CCNT2	chr5:36998617-36998708	K562	blood:	n/a	n/a
17	CCNT2	chr5:36980063-36980115	K562	blood:	n/a	n/a
18	CEBPB	chr5:36982317-36982544	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr5:37038053-37038236	A549	lung:	n/a	n/a
20	CEBPB	chr5:37002663-37002913	A549	lung:	n/a	chr5:37002769-37002780
21	CEBPB	chr5:36993961-36994063	HepG2	liver:	n/a	chr5:36993984-36993997 chr5:36993985-36993996 chr5:36993984-36993995
22	CEBPB	chr5:37029056-37029373	HepG2	liver:	n/a	chr5:37029195-37029206
23	CEBPB	chr5:36934902-36935214	HepG2	liver:	n/a	chr5:36935065-36935076
24	CEBPB	chr5:37038046-37038223	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:37038037-37038237	K562	blood:	n/a	n/a
26	CEBPB	chr5:36936502-36936838	HepG2	liver:	n/a	chr5:36936639-36936650
27	CEBPB	chr5:37016444-37016893	IMR90	lung:	n/a	chr5:37016714-37016725 chr5:37016712-37016725
28	CEBPB	chr5:37029034-37029373	IMR90	lung:	n/a	chr5:37029195-37029206
29	CEBPB	chr5:36934936-36935214	A549	lung:	n/a	chr5:36935065-36935076
30	CEBPB	chr5:37029037-37029346	K562	blood:	n/a	chr5:37029195-37029206
31	CEBPB	chr5:37015819-37016038	HepG2	liver:	n/a	chr5:37015922-37015935 chr5:37015922-37015933
32	CEBPB	chr5:36934880-36935229	K562	blood:	n/a	chr5:36935065-36935076
33	CEBPB	chr5:37002298-37002962	Hela-S3	cervix:	n/a	chr5:37002769-37002780
34	CEBPB	chr5:36934973-36935215	Hela-S3	cervix:	n/a	chr5:36935065-36935076
35	CEBPB	chr5:36952917-36953126	Hela-S3	cervix:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
36	CEBPB	chr5:36934890-36935226	IMR90	lung:	n/a	chr5:36935065-36935076
37	CEBPB	chr5:37029035-37029370	A549	lung:	n/a	chr5:37029195-37029206
38	CEBPB	chr5:37002468-37002913	HepG2	liver:	n/a	chr5:37002769-37002780
39	CEBPB	chr5:36962325-36962389	A549	lung:	n/a	n/a
40	CEBPB	chr5:36952876-36953114	HepG2	liver:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
41	CREB1	chr5:36998600-36999215	GM12878	blood:	n/a	n/a
42	CREB1	chr5:36998699-36999144	GM12878	blood:	n/a	n/a
43	CTCF	chr5:36983700-36983850	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr5:36944820-36944970	HA-sp	spinal cord:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
45	CTCF	chr5:37006140-37006290	GM12864	blood:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
46	CTCF	chr5:36944860-36945010	HL-60	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
47	CTCF	chr5:36944781-36945066	Spleen_OC	spleen:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
48	CTCF	chr5:37006152-37006370	LNCaP	prostate:	n/a	chr5:37006234-37006242 chr5:37006229-37006247 chr5:37006224-37006245 chr5:37006230-37006246
49	CTCF	chr5:36945260-36945410	AG10803	skin:	n/a	n/a
50	CTCF	chr5:36944620-36944770	BE2_C	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37014180-37014230	AG04450	lung:	fetal
2	chr5:37014180-37014230	Caco-2	colon:	n/a
3	chr5:36986137-36986187	GM12892	blood:	n/a
4	chr5:36986137-36986187	HRPEpiC	eye:	n/a
5	chr5:36985656-36985706	GM19239	blood:	n/a
6	chr5:36985656-36985706	Jurkat	blood:	n/a
7	chr5:36986137-36986187	PFSK-1	brain:	n/a
8	chr5:37014180-37014230	HUVEC	blood vessel:	n/a
9	chr5:36985656-36985706	MCF-7	breast:	n/a
10	chr5:36986137-36986187	ECC-1	luminal epithelium:	n/a
11	chr5:37014180-37014230	SK-N-MC	brain:	n/a
12	chr5:36985656-36985706	PrEC	prostate:	n/a
13	chr5:37014180-37014230	AoSMC	blood vessel:	n/a
14	chr5:36985656-36985706	BJ	skin:	n/a
15	chr5:36986137-36986187	HMEC	breast:	n/a
16	chr5:37014180-37014230	NHDF-neo	bronchial:	n/a
17	chr5:36985656-36985706	T-47D	breast:	n/a
18	chr5:37014180-37014230	HMEC	breast:	n/a
19	chr5:36985656-36985706	U87	brain:	n/a
20	chr5:36985656-36985706	GM12892	blood:	n/a
21	chr5:36985656-36985706	HAEpiC	amniotic membrane:	n/a
22	chr5:36985656-36985706	NHDF-neo	bronchial:	n/a
23	chr5:36986137-36986187	BJ	skin:	n/a
24	chr5:37014180-37014230	HAEpiC	amniotic membrane:	n/a
25	chr5:37014180-37014230	SKMC	muscle:	n/a
26	chr5:36986137-36986187	SK-N-SH	brain:	n/a
27	chr5:37014180-37014230	K562	blood:	n/a
28	chr5:36985656-36985706	AG09309	skin:	n/a
29	chr5:37014180-37014230	PFSK-1	brain:	n/a
30	chr5:36986137-36986187	AG10803	skin:	n/a
31	chr5:37014180-37014230	CMK	blood:	n/a
32	chr5:37014180-37014230	NH-A	brain:	n/a
33	chr5:36986137-36986187	PANC-1	pancreas:	n/a
34	chr5:36985656-36985706	SKMC	muscle:	n/a
35	chr5:36985656-36985706	BE2_C	brain:	n/a
36	chr5:36985656-36985706	RPTEC	kidney:	n/a
37	chr5:36986137-36986187	NH-A	brain:	n/a
38	chr5:36985656-36985706	HIPEpiC	eye:	n/a
39	chr5:37014180-37014230	HepG2	liver:	n/a
40	chr5:36985656-36985706	NH-A	brain:	n/a
41	chr5:36986137-36986187	CMK	blood:	n/a
42	chr5:37014180-37014230	GM06990	blood:	n/a
43	chr5:37014180-37014230	GM12878	blood:	n/a
44	chr5:37014180-37014230	Jurkat	blood:	n/a
45	chr5:36985656-36985706	AG10803	skin:	n/a
46	chr5:36986137-36986187	SAEC	small airway:	n/a
47	chr5:36985656-36985706	HPAEpiC	pulmonary alveolar:	n/a
48	chr5:37014180-37014230	H1-hESC	embryonic stem cell:	embryo
49	chr5:37014180-37014230	AG04449	skin:	fetal
50	chr5:37014180-37014230	PrEC	prostate:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:36876833..36878343-chr5:36989470..36991445,2	K562	blood:
2	chr5:36876324..36878732-chr5:36943861..36946469,3	K562	blood:
3	chr5:36875672..36878039-chr5:36951739..36953901,2	MCF-7	breast:
4	chr5:36744657..36745458-chr5:37006187..37006735,2	MCF-7	breast:
5	chr5:36874203..36876610-chr5:36934732..36937213,2	MCF-7	breast:
6	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
7	chr5:36876258..36877822-chr5:37004568..37007487,2	MCF-7	breast:
8	chr5:36743938..36745907-chr5:36986468..36988860,2	MCF-7	breast:
9	chr5:36932364..36935161-chr5:36941200..36944542,3	K562	blood:
10	chr5:36945026..36947869-chr5:36950785..36953502,2	K562	blood:
11	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
12	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
13	chr5:36875949..36878043-chr5:36936778..36939206,2	MCF-7	breast:
14	chr5:36738583..36742028-chr5:37005460..37008682,3	K562	blood:
15	chr5:36874857..36877485-chr5:36989379..36990958,2	MCF-7	breast:
16	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
17	chr5:36870958..36873840-chr5:36982182..36984989,2	MCF-7	breast:
18	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
19	chr5:37024346..37029453-chr5:37031923..37035955,4	K562	blood:
20	chr5:36728670..36729725-chr5:37005785..37006901,3	MCF-7	breast:
21	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
22	chr5:36991420..36994438-chr5:36995617..36998219,3	K562	blood:
23	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
24	chr5:36943349..36945887-chr5:36955686..36957216,2	K562	blood:
25	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
26	chr5:36987049..36989193-chr5:36992034..36994434,2	MCF-7	breast:
27	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
28	chr5:36943731..36946422-chr5:36953381..36955918,2	MCF-7	breast:
29	chr5:36989118..36992920-chr5:36994202..36998219,3	K562	blood:
30	chr5:36874711..36878038-chr5:36947695..36950933,3	K562	blood:
31	chr5:36876108..36878603-chr5:36945963..36949960,5	MCF-7	breast:
32	chr5:36924372..36926540-chr5:36962158..36964859,2	K562	blood:
33	chr5:37009245..37010939-chr5:37023761..37025926,2	K562	blood:
34	chr5:36744805..36746401-chr5:36997708..36999991,2	MCF-7	breast:
35	chr5:36956975..36959000-chr5:36961923..36964696,3	K562	blood:
36	chr5:36935171..36938055-chr5:36942349..36945199,2	MCF-7	breast:
37	chr5:36740003..36742433-chr5:37003090..37005628,2	MCF-7	breast:
38	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
39	chr5:36875559..36878395-chr5:36942609..36944650,2	MCF-7	breast:
40	chr5:36876484..36879168-chr5:36940218..36943816,3	MCF-7	breast:
41	chr5:36937263..36939579-chr5:36939659..36941382,2	MCF-7	breast:
42	chr5:37024346..37029453-chr5:37031923..37035955,4	K562	blood:
43	chr5:36875852..36878173-chr5:36948175..36949997,2	MCF-7	breast:
44	chr5:37014667..37016465-chr5:37026836..37029191,2	K562	blood:
45	chr3:109682867..109683387-chr5:36941291..36942072,2	MCF-7	breast:
46	chr5:36931581..36933729-chr5:36940700..36943226,2	MCF-7	breast:
47	chr5:36943349..36945887-chr5:36955686..36957216,2	K562	blood:
48	chr5:36870534..36872265-chr5:36955998..36958154,2	K562	blood:
49	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
50	chr5:37015380..37017502-chr5:37021890..37025377,3	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NIPBL	hsa-let-7a-5p	chr5:36996581-36996603
2	NIPBL	hsa-let-7b-5p	chr5:36996581-36996603
3	NIPBL	hsa-miR-183-5p	chr5:36996864-36996887

Variant related genes	Relation type
NIPBL	TF binding region
NIPBL	CpG island
ENSG00000164190	chromatin interactions

Extended variants
information (count: 3717 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3717 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192669	chr5:36935129-36935130	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563448308	chr5:36935158-36935159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573667369	chr5:36935175-36935176	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141586728	chr5:36935291-36935292	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs561280345	chr5:36935361-36935362	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs528451071	chr5:36935426-36935427	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs547005325	chr5:36935444-36935445	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs28420676	chr5:36935537-36935538	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs184359067	chr5:36935542-36935543	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs550663122	chr5:36935670-36935671	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569069266	chr5:36935674-36935675	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs116319376	chr5:36935764-36935765	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77956050	chr5:36935793-36935794	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544437400	chr5:36935964-36935965	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77561539	chr5:36935979-36935980	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs147004275	chr5:36936004-36936005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186913658	chr5:36936095-36936096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541425332	chr5:36936130-36936131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138225646	chr5:36936148-36936149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191756483	chr5:36936155-36936156	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577737555	chr5:36936157-36936158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs369862197	chr5:36936178-36936179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538691753	chr5:36936266-36936267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557104130	chr5:36936302-36936303	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575338946	chr5:36936365-36936366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546904751	chr5:36936553-36936554	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77455203	chr5:36936578-36936579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542832384	chr5:36936579-36936580	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs561006742	chr5:36936612-36936613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573056770	chr5:36936635-36936636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185027246	chr5:36936643-36936644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs189090686	chr5:36936668-36936669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181080254	chr5:36936697-36936698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566509578	chr5:36936749-36936750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185520347	chr5:36936768-36936769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376464204	chr5:36936797-36936798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563045913	chr5:36936855-36936856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557655221	chr5:36936919-36936920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530211791	chr5:36936924-36936925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548799667	chr5:36936935-36936936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566967941	chr5:36936953-36936954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189504879	chr5:36937037-36937038	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181445951	chr5:36937057-36937058	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571225397	chr5:36937078-36937079	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538681198	chr5:36937098-36937099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs186176995	chr5:36937101-36937102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76434229	chr5:36937120-36937121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs73093844	chr5:36937172-36937173	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188537793	chr5:36937173-36937174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554719907	chr5:36937192-36937193	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2691 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36907400-36938200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:36919600-36938200	Weak transcription	Pancreas	Pancrea
3	chr5:36919800-36953000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr5:36919800-36961600	Weak transcription	K562	blood
5	chr5:36920400-36951400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr5:36923600-36943600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr5:36924600-36943600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr5:36924800-36939000	Weak transcription	Fetal Thymus	thymus
9	chr5:36924800-36955200	Weak transcription	Dnd41	blood
10	chr5:36925600-36935200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr5:36926000-36936800	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr5:36926600-36939400	Weak transcription	Fetal Intestine Small	intestine
13	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr5:36928200-36935200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr5:36928200-36935400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr5:36929000-36938000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:36929600-36947400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr5:36929800-36937400	Weak transcription	HSMM	muscle
19	chr5:36929800-36939400	Weak transcription	Osteobl	bone
20	chr5:36930000-36937000	Weak transcription	A549	lung
21	chr5:36930000-36938000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr5:36930000-36945000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:36930800-36940000	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr5:36931200-36936600	Weak transcription	Fetal Heart	heart
25	chr5:36931200-36939400	Weak transcription	Hela-S3	cervix
26	chr5:36931800-36938000	Weak transcription	Left Ventricle	heart
27	chr5:36931800-36938200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr5:36931800-36938400	Weak transcription	Ovary	ovary
29	chr5:36932200-36940000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr5:36932200-36940000	Weak transcription	Brain Angular Gyrus	brain
31	chr5:36932400-36943200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:36933200-36935200	Weak transcription	Psoas Muscle	Psoas
33	chr5:36933200-36936600	Weak transcription	Liver	Liver
34	chr5:36933200-36940200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:36933200-36944000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr5:36933200-36962000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:36933400-36949600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:36934000-36935400	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr5:36934000-36935600	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr5:36934000-36936800	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr5:36934000-36936800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr5:36934400-36935200	Enhancers	Primary T cells from cord blood	blood
43	chr5:36934400-36935200	Enhancers	HUVEC	blood vessel
44	chr5:36934600-36935400	Weak transcription	Small Intestine	intestine
45	chr5:36934600-36936800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr5:36934600-36941000	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr5:36934800-36935200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr5:36934800-36936200	Enhancers	Colon Smooth Muscle	Colon
49	chr5:36934800-36937000	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr5:36935000-36936000	Strong transcription	Primary B cells from cord blood	blood

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