Variant report

Variant	nsv537169
Chromosome Location	chr4:88046263-88235018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2555)
CpG islands
(count:1221)
Chromatin interactive
region (count:158)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:2)

(count:2555 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:88087091-88087374	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:88199339-88199978	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:88093214-88093353	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:88196507-88196704	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:88156680-88157295	K562	blood:	n/a	n/a
6	ARID3A	chr4:88191313-88191649	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:88108251-88108254	K562	blood:	n/a	n/a
8	ARID3A	chr4:88195615-88195678	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:88156979-88157295	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:88141770-88142252	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:88134617-88135271	K562	blood:	n/a	n/a
12	ATF1	chr4:88175943-88176099	K562	blood:	n/a	n/a
13	ATF1	chr4:88072080-88072363	K562	blood:	n/a	n/a
14	ATF1	chr4:88153471-88153674	K562	blood:	n/a	n/a
15	ATF2	chr4:88227219-88227557	GM12878	blood:	n/a	n/a
16	ATF2	chr4:88071926-88072383	GM12878	blood:	n/a	n/a
17	ATF2	chr4:88227105-88227643	GM12878	blood:	n/a	n/a
18	ATF2	chr4:88141262-88141907	GM12878	blood:	n/a	n/a
19	ATF2	chr4:88141210-88141610	GM12878	blood:	n/a	n/a
20	ATF3	chr4:88106587-88106939	K562	blood:	n/a	n/a
21	ATF3	chr4:88199549-88199769	HepG2	liver:	n/a	n/a
22	ATF3	chr4:88199339-88199930	HepG2	liver:	n/a	n/a
23	ATF3	chr4:88223744-88223892	K562	blood:	n/a	n/a
24	ATF3	chr4:88153354-88153755	K562	blood:	n/a	n/a
25	BACH1	chr4:88156772-88157149	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:88191402-88191656	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:88141460-88142122	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr4:88140841-88141044	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr4:88072006-88072261	GM12878	blood:	n/a	n/a
30	BATF	chr4:88227243-88227499	GM12878	blood:	n/a	chr4:88227386-88227397
31	BATF	chr4:88228029-88228308	GM12878	blood:	n/a	n/a
32	BCL11A	chr4:88141401-88141728	GM12878	blood:	n/a	n/a
33	BCL3	chr4:88227213-88227544	GM12878	blood:	n/a	n/a
34	BCL3	chr4:88225796-88226325	A549	lung:	n/a	n/a
35	BCL3	chr4:88141436-88141999	GM12878	blood:	n/a	n/a
36	BCLAF1	chr4:88140613-88141755	GM12878	blood:	n/a	n/a
37	BCLAF1	chr4:88140719-88141844	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:88140584-88142060	GM12878	blood:	n/a	n/a
39	BHLHE40	chr4:88156888-88157301	K562	blood:	n/a	n/a
40	BHLHE40	chr4:88078550-88078561	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:88140497-88142000	K562	blood:	n/a	n/a
42	BHLHE40	chr4:88199328-88199876	HepG2	liver:	n/a	n/a
43	BHLHE40	chr4:88199507-88199750	HepG2	liver:	n/a	n/a
44	BHLHE40	chr4:88052580-88052767	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:88071988-88072326	GM12878	blood:	n/a	n/a
46	BHLHE40	chr4:88053174-88053577	GM12878	blood:	n/a	chr4:88053382-88053403 chr4:88053387-88053396
47	BHLHE40	chr4:88199420-88199720	HepG2	liver:	n/a	n/a
48	BHLHE40	chr4:88157050-88157244	HepG2	liver:	n/a	n/a
49	BRCA1	chr4:88225715-88226363	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr4:88141602-88141983	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88141939-88141989	HCM	heart:	n/a
2	chr4:88141939-88141989	HCM	heart:	n/a
3	chr4:88157084-88157134	NH-A	brain:	n/a
4	chr4:88157096-88157146	NT2-D1	testis:	n/a
5	chr4:88141915-88141965	Hepatocyte	liver:	n/a
6	chr4:88140994-88141044	HUVEC	blood vessel:	n/a
7	chr4:88233933-88233983	HCF	heart:	n/a
8	chr4:88233933-88233983	HAEpiC	amniotic membrane:	n/a
9	chr4:88142275-88142325	T-47D	breast:	n/a
10	chr4:88141802-88141852	PrEC	prostate:	n/a
11	chr4:88233933-88233983	HCPEpiC	choroid plexus:	n/a
12	chr4:88140436-88140486	Caco-2	colon:	n/a
13	chr4:88141939-88141989	GM12891	blood:	n/a
14	chr4:88140436-88140486	AG10803	skin:	n/a
15	chr4:88084297-88084347	AG04449	skin:	fetal
16	chr4:88110161-88110211	T-47D	breast:	n/a
17	chr4:88140436-88140486	HCPEpiC	choroid plexus:	n/a
18	chr4:88141275-88141325	HUVEC	blood vessel:	n/a
19	chr4:88233933-88233983	Jurkat	blood:	n/a
20	chr4:88233933-88233983	HUVEC	blood vessel:	n/a
21	chr4:88142275-88142325	Hela-S3	cervix:	n/a
22	chr4:88141826-88141876	GM12891	blood:	n/a
23	chr4:88049275-88049325	PrEC	prostate:	n/a
24	chr4:88141275-88141325	HRPEpiC	eye:	n/a
25	chr4:88225834-88225884	HEEpiC	esophagus:	n/a
26	chr4:88233933-88233983	HRE	kidney:	n/a
27	chr4:88110161-88110211	HAEpiC	amniotic membrane:	n/a
28	chr4:88141915-88141965	SK-N-MC	brain:	n/a
29	chr4:88140994-88141044	BJ	skin:	n/a
30	chr4:88049275-88049325	IMR90	lung:	fetal
31	chr4:88059376-88059426	T-47D	breast:	n/a
32	chr4:88049275-88049325	T-47D	breast:	n/a
33	chr4:88140994-88141044	Hela-S3	cervix:	n/a
34	chr4:88059376-88059426	AG09309	skin:	n/a
35	chr4:88140261-88140311	MCF10A-Er-Src	breast:	n/a
36	chr4:88142275-88142325	PANC-1	pancreas:	n/a
37	chr4:88141826-88141876	ProgFib	skin:	n/a
38	chr4:88084297-88084347	Hela-S3	cervix:	n/a
39	chr4:88157084-88157134	HEEpiC	esophagus:	n/a
40	chr4:88141317-88141367	HepG2	liver:	n/a
41	chr4:88141826-88141876	Jurkat	blood:	n/a
42	chr4:88157096-88157146	HEEpiC	esophagus:	n/a
43	chr4:88141802-88141852	Caco-2	colon:	n/a
44	chr4:88110161-88110211	HCF	heart:	n/a
45	chr4:88059376-88059426	HCPEpiC	choroid plexus:	n/a
46	chr4:88157096-88157146	Caco-2	colon:	n/a
47	chr4:88084297-88084347	U87	brain:	n/a
48	chr4:88084297-88084347	NT2-D1	testis:	n/a
49	chr4:88157096-88157146	HUVEC	blood vessel:	n/a
50	chr4:88157096-88157146	Hepatocyte	liver:	n/a

(count:158 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:88113855..88115991-chr4:88116279..88119127,2	K562	blood:
2	chr4:88066236..88067961-chr4:88070218..88071867,2	K562	blood:
3	chr4:88057518..88060731-chr4:88068893..88070799,3	MCF-7	breast:
4	chr4:88122650..88125039-chr4:88136374..88138823,2	K562	blood:
5	chr4:88078325..88080937-chr4:88140370..88142263,2	K562	blood:
6	chr4:88002713..88005662-chr4:88048003..88049629,2	K562	blood:
7	chr4:88038128..88040369-chr4:88146803..88148813,2	MCF-7	breast:
8	chr4:88056797..88059006-chr4:88063394..88065724,2	K562	blood:
9	chr4:88144868..88146807-chr4:88149730..88152275,2	K562	blood:
10	chr4:88062349..88065075-chr4:88140777..88142398,2	K562	blood:
11	chr4:88127634..88129911-chr4:88140164..88142825,2	MCF-7	breast:
12	chr4:87969741..87972043-chr4:88141021..88142542,2	MCF-7	breast:
13	chr4:88056797..88059006-chr4:88063394..88065724,2	K562	blood:
14	chr4:88132419..88135036-chr4:88191101..88193543,2	K562	blood:
15	chr4:88080730..88082898-chr4:88152157..88153805,2	K562	blood:
16	chr4:87836003..87837844-chr4:88123291..88126235,2	K562	blood:
17	chr4:88125915..88129051-chr4:88140439..88142912,3	MCF-7	breast:
18	chr4:88149928..88151591-chr4:88152274..88153901,2	K562	blood:
19	chr4:88091038..88092796-chr4:88094355..88096189,2	K562	blood:
20	chr4:88090797..88093455-chr4:88106518..88109486,2	K562	blood:
21	chr4:88124197..88126878-chr4:88132263..88134622,2	K562	blood:
22	chr4:88039768..88041712-chr4:88052225..88054445,2	K562	blood:
23	chr4:87855857..87857774-chr4:88064541..88066623,2	MCF-7	breast:
24	chr4:88055050..88057902-chr4:88066373..88068330,2	K562	blood:
25	chr4:88071641..88072544-chr4:88156633..88157658,5	MCF-7	breast:
26	chr4:87855268..87857472-chr4:88140405..88143113,3	MCF-7	breast:
27	chr4:87925170..87928506-chr4:88140421..88143207,4	MCF-7	breast:
28	chr4:88107394..88109938-chr4:88116999..88119590,2	MCF-7	breast:
29	chr4:88127634..88129911-chr4:88140164..88142825,2	MCF-7	breast:
30	chr4:88226132..88228278-chr4:88229243..88230944,2	MCF-7	breast:
31	chr4:88139583..88141697-chr4:88158453..88160526,2	MCF-7	breast:
32	chr4:88190901..88191577-chr4:88769909..88770797,2	MCF-7	breast:
33	chr4:88072049..88072620-chr4:88386607..88387532,2	K562	blood:
34	chr4:88090535..88092796-chr4:88094689..88097042,2	K562	blood:
35	chr4:87843608..87844207-chr4:88156694..88157622,2	K562	blood:
36	chr4:88122650..88125039-chr4:88136374..88138823,2	K562	blood:
37	chr4:88066236..88067961-chr4:88070218..88071867,2	K562	blood:
38	chr10:46970031..46970993-chr4:88194361..88194882,2	MCF-7	breast:
39	chr4:88048723..88050274-chr4:88159971..88161821,2	K562	blood:
40	chr4:88183411..88186658-chr4:88187924..88190841,3	K562	blood:
41	chr4:88139395..88142439-chr4:88311139..88313328,4	K562	blood:
42	chr4:88099435..88101886-chr4:88139410..88141295,2	K562	blood:
43	chr4:87854638..87857344-chr4:88139505..88141852,2	K562	blood:
44	chr4:88114740..88116540-chr4:88140553..88142711,2	K562	blood:
45	chr4:88140757..88143363-chr4:88155950..88159185,5	K562	blood:
46	chr4:88139374..88140911-chr4:88152150..88153664,2	K562	blood:
47	chr4:88127993..88130668-chr4:88131834..88134458,2	MCF-7	breast:
48	chr4:88112928..88115867-chr4:88140450..88142503,2	MCF-7	breast:
49	chr4:88148735..88151393-chr4:88155626..88158606,3	K562	blood:
50	chr4:88121861..88123898-chr4:88140212..88141957,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL8-2	chr4:88065070-88066502	ucscGeneNc_uc003hqf_1
2	lnc-AFF1-1	chr4:88198781-88198895	XLOC_003601
3	lnc-HSD17B13-1	chr4:88187887-88187974	XLOC_004009
4	lnc-KLHL8-1	chr4:88140676-88142542	ENSG00000250163.1
5	lnc-AFF1-1	chr4:88199776-88199855	XLOC_003601
6	lnc-HSD17B13-1	chr4:88183083-88183251	XLOC_004009
7	lnc-KLHL8-2	chr4:88073571-88073718	ucscGeneNc_uc003hqf_1
8	lnc-KLHL8-2	chr4:88074663-88075026	ucscGeneNc_uc003hqf_1
9	lnc-KLHL8-1	chr4:88161410-88161466	ENSG00000250163.1
10	lnc-AFF1-1	chr4:88192262-88192330	XLOC_003601

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5705	chr4:88221657-88221679	MIMAT0022499

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KLHL8	hsa-miR-215-5p	chr4:88084625-88084648
2	KLHL8	hsa-miR-192-5p	chr4:88084625-88084648

Variant related genes	Relation type
ENSG00000250572	TF binding region
GAPDHP60	TF binding region
MIR5705	TF binding region
ENSG00000248196	TF binding region
KLHL8	TF binding region
ENSG00000250572	CpG island
GAPDHP60	CpG island
MIR5705	CpG island
ENSG00000248196	CpG island
KLHL8	CpG island
ENSG00000177879	chromatin interactions
ENSG00000145782	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000141569	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000248196	chromatin interactions
ENSG00000140391	chromatin interactions
ENSG00000172493	chromatin interactions
ENSG00000250572	chromatin interactions
ENSG00000246526	chromatin interactions
ENSG00000163633	chromatin interactions
ENSG00000267342	chromatin interactions
ENSG00000198189	chromatin interactions
ENSG00000145332	chromatin interactions
ENSG00000204176	chromatin interactions
ENSG00000245146	chromatin interactions
ENSG00000248180	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000163636	chromatin interactions
CREBZF	miRNA target sites
CREG1	miRNA target sites

Extended variants
information (count: 6221 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6221 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138303532	chr4:88046274-88046275	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201481403	chr4:88046275-88046276	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554771868	chr4:88046308-88046309	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200864911	chr4:88046328-88046329	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187722791	chr4:88046351-88046352	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111965220	chr4:88046359-88046360	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556771939	chr4:88046412-88046413	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558721002	chr4:88046542-88046543	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534694401	chr4:88046547-88046548	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569229531	chr4:88046549-88046550	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577015060	chr4:88046581-88046582	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541375612	chr4:88046611-88046612	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553206942	chr4:88046619-88046620	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574104458	chr4:88046642-88046643	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537777512	chr4:88046668-88046669	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113175784	chr4:88046687-88046688	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574782629	chr4:88046694-88046695	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554832418	chr4:88046712-88046713	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575230782	chr4:88046736-88046737	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574307747	chr4:88046744-88046745	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541775786	chr4:88046798-88046799	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563262104	chr4:88046812-88046813	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77556057	chr4:88046851-88046852	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75061967	chr4:88046852-88046853	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74814949	chr4:88046867-88046868	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371119680	chr4:88046873-88046874	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192507799	chr4:88046889-88046890	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183538843	chr4:88046890-88046891	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374186904	chr4:88046900-88046901	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2926512	chr4:88046938-88046939	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs3775209	chr4:88046946-88046947	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs77972447	chr4:88046957-88046958	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374593222	chr4:88046969-88046970	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34301637	chr4:88046986-88046987	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114471446	chr4:88046997-88046998	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530053579	chr4:88047010-88047011	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560912203	chr4:88047051-88047052	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35866418	chr4:88047057-88047058	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548532883	chr4:88047081-88047082	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141556671	chr4:88047084-88047085	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116821033	chr4:88047097-88047098	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558626532	chr4:88047162-88047163	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114429017	chr4:88047192-88047193	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146177255	chr4:88047193-88047194	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201798342	chr4:88047194-88047195	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371560903	chr4:88047200-88047201	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374178859	chr4:88047201-88047202	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs200376457	chr4:88047233-88047234	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs574764828	chr4:88047244-88047245	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs201348911	chr4:88047254-88047255	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	20952505	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD

Chromatin state (count:2283 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88019000-88072200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:88026400-88063600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr4:88026600-88055600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr4:88030000-88048800	Weak transcription	A549	lung
5	chr4:88030600-88057600	Weak transcription	Brain Germinal Matrix	brain
6	chr4:88032800-88059000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr4:88033600-88047600	Weak transcription	HSMM	muscle
8	chr4:88035600-88056800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr4:88035600-88063800	Strong transcription	Primary T cells from cord blood	blood
10	chr4:88036400-88063600	Weak transcription	Fetal Brain Male	brain
11	chr4:88036800-88046600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:88036800-88046800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:88036800-88059200	Weak transcription	Fetal Brain Female	brain
14	chr4:88038400-88046600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr4:88038800-88046800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:88038800-88047000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr4:88039600-88046800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr4:88040000-88047200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:88040000-88052000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:88041200-88048800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr4:88041800-88046600	Weak transcription	Thymus	Thymus
22	chr4:88042200-88046600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr4:88042200-88046800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:88042400-88049000	Strong transcription	HepG2	liver
25	chr4:88042600-88046800	Weak transcription	Pancreas	Pancrea
26	chr4:88042800-88046600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:88042800-88046600	Weak transcription	Esophagus	oesophagus
28	chr4:88042800-88046600	Weak transcription	Gastric	stomach
29	chr4:88042800-88046600	Weak transcription	Small Intestine	intestine
30	chr4:88042800-88046800	Weak transcription	Colonic Mucosa	Colon
31	chr4:88042800-88069400	Strong transcription	Placenta	Placenta
32	chr4:88043000-88046600	Weak transcription	Lung	lung
33	chr4:88043000-88046600	Weak transcription	Spleen	Spleen
34	chr4:88043000-88061400	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr4:88043200-88047800	Weak transcription	NH-A	brain
36	chr4:88043400-88048600	Weak transcription	Stomach Mucosa	stomach
37	chr4:88043400-88064800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:88043600-88046400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr4:88043600-88046600	Weak transcription	Brain Anterior Caudate	brain
40	chr4:88043600-88046800	Weak transcription	Aorta	Aorta
41	chr4:88043600-88046800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr4:88043600-88047200	Weak transcription	Osteobl	bone
43	chr4:88043600-88049000	Weak transcription	Right Atrium	heart
44	chr4:88043600-88064600	Strong transcription	GM12878-XiMat	blood
45	chr4:88043800-88046400	Weak transcription	Brain Hippocampus Middle	brain
46	chr4:88043800-88046600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:88043800-88046600	Weak transcription	Fetal Muscle Leg	muscle
48	chr4:88043800-88046600	Weak transcription	NHLF	lung
49	chr4:88043800-88046800	Weak transcription	HSMMtube	muscle
50	chr4:88043800-88048600	Weak transcription	Brain Angular Gyrus	brain

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