Variant report

Variant	nsv1002238
Chromosome Location	chr3:85357855-85719373
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	chr3:85552489-85553162	K562	blood:	n/a	chr3:85552542-85552558
2	ARID3A	chr3:85554724-85556040	K562	blood:	n/a	chr3:85555983-85555999 chr3:85555685-85555701
3	ARID3A	chr3:85616263-85616538	K562	blood:	n/a	n/a
4	ARID3A	chr3:85625316-85625516	K562	blood:	n/a	n/a
5	ARID3A	chr3:85553514-85553826	K562	blood:	n/a	n/a
6	ARID3A	chr3:85609707-85609851	HepG2	liver:	n/a	n/a
7	BACH1	chr3:85501073-85501146	K562	blood:	n/a	n/a
8	BACH1	chr3:85531095-85531395	K562	blood:	n/a	n/a
9	BACH1	chr3:85556142-85556514	K562	blood:	n/a	n/a
10	BATF	chr3:85701555-85701806	GM12878	blood:	n/a	n/a
11	BCLAF1	chr3:85552292-85553331	K562	blood:	n/a	n/a
12	BHLHE40	chr3:85616320-85616579	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:85553505-85553787	K562	blood:	n/a	n/a
14	CBX3	chr3:85553411-85553733	K562	blood:	n/a	n/a
15	CCNT2	chr3:85553578-85553965	K562	blood:	n/a	n/a
16	CEBPB	chr3:85415054-85415293	HepG2	liver:	n/a	chr3:85415166-85415177
17	CEBPB	chr3:85543996-85544393	HepG2	liver:	n/a	chr3:85544227-85544236 chr3:85544226-85544237 chr3:85544227-85544236 chr3:85544225-85544238 chr3:85544227-85544236
18	CEBPB	chr3:85511875-85512135	A549	lung:	n/a	chr3:85511970-85511983 chr3:85511970-85511981 chr3:85511970-85511983 chr3:85511972-85511983
19	CEBPB	chr3:85712972-85713211	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:85716928-85717195	Hela-S3	cervix:	n/a	chr3:85717078-85717089
21	CEBPB	chr3:85511812-85512152	HepG2	liver:	n/a	chr3:85511970-85511983 chr3:85511970-85511981 chr3:85511970-85511983 chr3:85511972-85511983
22	CEBPB	chr3:85716915-85717247	HepG2	liver:	n/a	chr3:85717078-85717089
23	CEBPB	chr3:85547505-85548196	K562	blood:	n/a	chr3:85547688-85547701 chr3:85547688-85547699
24	CEBPB	chr3:85547552-85547836	A549	lung:	n/a	chr3:85547688-85547701 chr3:85547688-85547699
25	CEBPB	chr3:85478280-85478610	A549	lung:	n/a	chr3:85478503-85478516 chr3:85478503-85478514 chr3:85478426-85478437
26	CEBPB	chr3:85496609-85496958	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:85512310-85512572	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:85478290-85478609	HepG2	liver:	n/a	chr3:85478503-85478516 chr3:85478503-85478514 chr3:85478426-85478437
29	CEBPB	chr3:85509318-85509320	A549	lung:	n/a	n/a
30	CEBPB	chr3:85478317-85478581	K562	blood:	n/a	chr3:85478503-85478516 chr3:85478503-85478514 chr3:85478426-85478437
31	CEBPB	chr3:85609588-85609927	HepG2	liver:	n/a	chr3:85609764-85609775 chr3:85609765-85609776 chr3:85609764-85609777
32	CEBPB	chr3:85533186-85533637	K562	blood:	n/a	n/a
33	CEBPB	chr3:85468128-85468436	K562	blood:	n/a	chr3:85468277-85468290 chr3:85468279-85468290 chr3:85468279-85468288
34	CEBPB	chr3:85712947-85713259	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:85547542-85547873	IMR90	lung:	n/a	chr3:85547688-85547701 chr3:85547688-85547699
36	CEBPB	chr3:85544051-85544392	A549	lung:	n/a	chr3:85544227-85544236 chr3:85544226-85544237 chr3:85544227-85544236 chr3:85544225-85544238 chr3:85544227-85544236
37	CEBPB	chr3:85440604-85440910	HepG2	liver:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
38	CEBPB	chr3:85440573-85440896	A549	lung:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
39	CEBPB	chr3:85547527-85547844	HepG2	liver:	n/a	chr3:85547688-85547701 chr3:85547688-85547699
40	CEBPB	chr3:85440575-85440914	IMR90	lung:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
41	CEBPB	chr3:85478291-85478605	IMR90	lung:	n/a	chr3:85478503-85478516 chr3:85478503-85478514 chr3:85478426-85478437
42	CEBPB	chr3:85691919-85692024	A549	lung:	n/a	chr3:85691926-85691939 chr3:85691926-85691939
43	CEBPB	chr3:85423130-85423398	A549	lung:	n/a	chr3:85423236-85423247
44	CEBPB	chr3:85423114-85423389	IMR90	lung:	n/a	chr3:85423236-85423247
45	CEBPB	chr3:85716957-85717186	H1-hESC	embryonic stem cell:	n/a	chr3:85717078-85717089
46	CEBPB	chr3:85716904-85717234	A549	lung:	n/a	chr3:85717078-85717089
47	CEBPB	chr3:85496661-85496884	A549	lung:	n/a	n/a
48	CEBPB	chr3:85712982-85713235	A549	lung:	n/a	n/a
49	CEBPB	chr3:85716924-85717225	K562	blood:	n/a	chr3:85717078-85717089
50	CEBPB	chr3:85509356-85509533	HepG2	liver:	n/a	chr3:85509405-85509418 chr3:85509406-85509417

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:85544609-85544659	Hepatocyte	liver:	n/a
2	chr3:85544609-85544659	Hepatocyte	liver:	n/a
3	chr3:85512134-85512184	MCF-7	breast:	n/a
4	chr3:85544609-85544659	ECC-1	luminal epithelium:	n/a
5	chr3:85544609-85544659	HCPEpiC	choroid plexus:	n/a
6	chr3:85553266-85553316	SAEC	small airway:	n/a
7	chr3:85544609-85544659	SK-N-SH_RA	brain:	n/a
8	chr3:85544609-85544659	HEEpiC	esophagus:	n/a
9	chr3:85512134-85512184	ECC-1	luminal epithelium:	n/a
10	chr3:85553266-85553316	HAEpiC	amniotic membrane:	n/a
11	chr3:85544609-85544659	HCM	heart:	n/a
12	chr3:85544609-85544659	GM06990	blood:	n/a
13	chr3:85553266-85553316	GM12891	blood:	n/a
14	chr3:85553266-85553316	HEEpiC	esophagus:	n/a
15	chr3:85544609-85544659	HMEC	breast:	n/a
16	chr3:85512134-85512184	ovcar-3	ovarian:	n/a
17	chr3:85512134-85512184	NHBE	bronchial:	n/a
18	chr3:85553266-85553316	GM06990	blood:	n/a
19	chr3:85553266-85553316	HEK293	kidney:	embryo
20	chr3:85512134-85512184	Caco-2	colon:	n/a
21	chr3:85553266-85553316	HCPEpiC	choroid plexus:	n/a
22	chr3:85512134-85512184	GM12891	blood:	n/a
23	chr3:85544609-85544659	Hela-S3	cervix:	n/a
24	chr3:85544609-85544659	PANC-1	pancreas:	n/a
25	chr3:85512134-85512184	HL-60	blood:	n/a
26	chr3:85553266-85553316	BE2_C	brain:	n/a
27	chr3:85553266-85553316	PANC-1	pancreas:	n/a
28	chr3:85544609-85544659	AG04449	skin:	fetal
29	chr3:85512134-85512184	NB4	blood:	n/a
30	chr3:85512134-85512184	HNPCEpiC	eye:	n/a
31	chr3:85544609-85544659	HRPEpiC	eye:	n/a
32	chr3:85544609-85544659	NHBE	bronchial:	n/a
33	chr3:85544609-85544659	AG09319	gingival:	n/a
34	chr3:85544609-85544659	MCF10A-Er-Src	breast:	n/a
35	chr3:85553266-85553316	LNCaP	prostate:	n/a
36	chr3:85512134-85512184	ProgFib	skin:	n/a
37	chr3:85553266-85553316	HCM	heart:	n/a
38	chr3:85544609-85544659	NT2-D1	testis:	n/a
39	chr3:85544609-85544659	HAEpiC	amniotic membrane:	n/a
40	chr3:85553266-85553316	SK-N-SH	brain:	n/a
41	chr3:85553266-85553316	SK-N-MC	brain:	n/a
42	chr3:85512134-85512184	SK-N-SH	brain:	n/a
43	chr3:85553266-85553316	AG10803	skin:	n/a
44	chr3:85553266-85553316	SK-N-SH_RA	brain:	n/a
45	chr3:85553266-85553316	NT2-D1	testis:	n/a
46	chr3:85553266-85553316	Caco-2	colon:	n/a
47	chr3:85553266-85553316	PrEC	prostate:	n/a
48	chr3:85544609-85544659	HEK293	kidney:	embryo
49	chr3:85512134-85512184	PFSK-1	brain:	n/a
50	chr3:85553266-85553316	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:85510863..85513429-chr3:85513950..85516943,2	MCF-7	breast:
2	chr3:85495270..85496821-chr3:85554377..85556655,2	K562	blood:
3	chr3:85534090..85536047-chr3:85539153..85540993,2	K562	blood:
4	chr3:84291765..84296920-chr3:85550637..85554814,6	K562	blood:
5	chr3:85353354..85354461-chr3:85391496..85392792,4	MCF-7	breast:
6	chr3:85457628..85458566-chr3:130193477..130193997,2	MCF-7	breast:
7	chr3:84994697..84996927-chr3:85551100..85552839,2	K562	blood:
8	chr3:85512744..85515419-chr3:85552866..85554640,2	K562	blood:
9	chr3:85522112..85524399-chr3:85525908..85528436,3	K562	blood:
10	chr3:85500332..85501905-chr3:85547491..85549616,2	K562	blood:
11	chr3:85476815..85480076-chr3:85489792..85493283,3	K562	blood:
12	chr3:85550792..85552939-chr3:85620775..85622757,2	K562	blood:
13	chr3:85500332..85501905-chr3:85547491..85549616,2	K562	blood:
14	chr3:85425596..85428443-chr3:85428590..85430282,2	K562	blood:
15	chr3:85486960..85489003-chr3:85551718..85553697,2	K562	blood:
16	chr3:85522328..85524379-chr3:85551882..85554402,2	K562	blood:
17	chr3:85512744..85515419-chr3:85552866..85554640,2	K562	blood:
18	chr3:85510863..85513429-chr3:85513950..85516943,2	MCF-7	breast:
19	chr3:85550694..85553715-chr3:85562655..85565189,4	K562	blood:
20	chr3:85364029..85366181-chr3:85371658..85373734,2	K562	blood:
21	chr3:85616525..85619382-chr3:85621735..85623491,2	K562	blood:
22	chr3:85476815..85480076-chr3:85489792..85493283,3	K562	blood:
23	chr3:85401815..85404016-chr3:85405205..85407101,2	K562	blood:
24	chr3:85353254..85353869-chr3:85625261..85626043,2	MCF-7	breast:
25	chr3:85401815..85404016-chr3:85405205..85407101,2	K562	blood:
26	chr3:85582405..85584379-chr3:85589105..85591498,2	K562	blood:
27	chr3:85364029..85366181-chr3:85371658..85373734,2	K562	blood:
28	chr3:85518552..85520271-chr3:85525173..85526982,2	K562	blood:
29	chr3:85520722..85524381-chr3:85549502..85554850,5	K562	blood:
30	chr3:85353629..85354290-chr3:85624959..85625479,2	K562	blood:
31	chr3:85528291..85540418-chr3:85548148..85554862,16	K562	blood:
32	chr3:85023240..85023756-chr3:85409642..85410352,2	MCF-7	breast:
33	chr3:85550694..85553715-chr3:85562655..85565189,4	K562	blood:
34	chr3:85487121..85488806-chr3:85536380..85538383,2	K562	blood:
35	chr3:85425596..85428443-chr3:85428590..85430282,2	K562	blood:
36	chr3:85520722..85524381-chr3:85549502..85554850,5	K562	blood:
37	chr3:85353497..85354172-chr3:85624891..85625399,2	MCF-7	breast:
38	chr3:85528291..85540418-chr3:85548148..85554862,16	K562	blood:
39	chr3:85455981..85458898-chr3:85554544..85556051,2	K562	blood:
40	chr3:85509846..85512397-chr3:85550866..85553089,2	K562	blood:
41	chr3:85409636..85410536-chr3:85624933..85625875,2	MCF-7	breast:
42	chr3:85508686..85510616-chr3:85515146..85516824,2	K562	blood:
43	chr3:85493785..85495457-chr3:85500033..85502991,2	K562	blood:
44	chr3:85551480..85554348-chr3:85623401..85624978,2	K562	blood:
45	chr3:85691376..85694166-chr3:85695879..85697418,2	K562	blood:
46	chr3:85569919..85571559-chr3:85571800..85574471,2	K562	blood:
47	chr3:85513919..85516830-chr3:85552866..85555627,2	K562	blood:
48	chr3:85550792..85552939-chr3:85620775..85622757,2	K562	blood:
49	chr3:85512384..85516287-chr3:85548853..85551591,3	K562	blood:
50	chr22:22050906..22053807-chr3:85561046..85562647,2	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5688	chr3:85434911-85434932	MIMAT0022479

Variant related genes	Relation type
MIR5688	TF binding region
MIR5688	CpG island

Extended variants
information (count: 9443 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:9443 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559914353	chr3:85357857-85357858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190650566	chr3:85357858-85357859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551898293	chr3:85357859-85357860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181951520	chr3:85357882-85357883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543104920	chr3:85357902-85357903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79070801	chr3:85357965-85357966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371572584	chr3:85357967-85357968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183673531	chr3:85357979-85357980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567935072	chr3:85358001-85358002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535756743	chr3:85358024-85358025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6780644	chr3:85358043-85358044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs188037353	chr3:85358075-85358076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs180760032	chr3:85358084-85358085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550743644	chr3:85358114-85358115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558325536	chr3:85358162-85358163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116406578	chr3:85358193-85358194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35989208	chr3:85358197-85358198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543893427	chr3:85358210-85358211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185607475	chr3:85358217-85358218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551741981	chr3:85358271-85358272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191141917	chr3:85358316-85358317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541745502	chr3:85358320-85358321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571585702	chr3:85358385-85358386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369532611	chr3:85358409-85358410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559791564	chr3:85358424-85358425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533613500	chr3:85358431-85358432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551565592	chr3:85358432-85358433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563493127	chr3:85358449-85358450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558207390	chr3:85358465-85358466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182167774	chr3:85358468-85358469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549430208	chr3:85358496-85358497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76013930	chr3:85358504-85358505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34344683	chr3:85358527-85358528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528862165	chr3:85358542-85358543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149564535	chr3:85358570-85358571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs13085678	chr3:85358591-85358592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539703534	chr3:85358602-85358603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186537574	chr3:85358614-85358615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144371351	chr3:85358622-85358623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570704612	chr3:85358681-85358682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113475736	chr3:85358799-85358800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374951706	chr3:85358804-85358805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1005690	chr3:85358806-85358807	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs192322881	chr3:85358824-85358825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183696335	chr3:85358835-85358836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553288458	chr3:85358846-85358847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573801487	chr3:85358889-85358890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567087199	chr3:85358945-85358946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs578187849	chr3:85358978-85358979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141040886	chr3:85358995-85358996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Autism	22102821	CNVD
Prostate cancer	21307934	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85352000-85365800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr3:85352600-85366000	Weak transcription	Fetal Brain Male	brain
3	chr3:85353000-85366600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:85353600-85358200	Weak transcription	Brain Angular Gyrus	brain
5	chr3:85355400-85358200	Weak transcription	Brain Hippocampus Middle	brain
6	chr3:85355600-85368600	Weak transcription	Brain Anterior Caudate	brain
7	chr3:85357800-85358200	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr3:85357800-85360000	Enhancers	Brain Substantia Nigra	brain
9	chr3:85358200-85358600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr3:85358200-85359000	Enhancers	Brain Angular Gyrus	brain
11	chr3:85358200-85359000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr3:85358200-85359200	Enhancers	Brain Hippocampus Middle	brain
13	chr3:85358800-85359600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:85359000-85359600	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr3:85359200-85359600	Weak transcription	Brain Hippocampus Middle	brain
16	chr3:85359600-85359800	Enhancers	Brain Hippocampus Middle	brain
17	chr3:85359600-85366000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr3:85359800-85366000	Weak transcription	Brain Hippocampus Middle	brain
19	chr3:85360000-85365400	Weak transcription	Brain Substantia Nigra	brain
20	chr3:85362200-85362800	Enhancers	A549	lung
21	chr3:85365400-85366200	Enhancers	Brain Substantia Nigra	brain
22	chr3:85365800-85366200	Enhancers	Brain Cingulate Gyrus	brain
23	chr3:85366000-85366200	Enhancers	Brain Hippocampus Middle	brain
24	chr3:85366000-85366400	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr3:85366600-85366800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:85368400-85368600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:85368400-85373800	Weak transcription	Brain Angular Gyrus	brain
28	chr3:85368600-85369000	ZNF genes & repeats	Brain Anterior Caudate	brain
29	chr3:85369000-85377000	Weak transcription	Brain Anterior Caudate	brain
30	chr3:85369200-85370800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr3:85370800-85371600	Enhancers	Liver	Liver
32	chr3:85373800-85374400	Enhancers	Brain Angular Gyrus	brain
33	chr3:85374000-85374400	Enhancers	Brain Substantia Nigra	brain
34	chr3:85377000-85377600	Enhancers	Brain Anterior Caudate	brain
35	chr3:85383600-85383800	Enhancers	Brain Hippocampus Middle	brain
36	chr3:85383800-85384400	Weak transcription	Brain Hippocampus Middle	brain
37	chr3:85384400-85384800	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr3:85384400-85385000	Active TSS	Brain Hippocampus Middle	brain
39	chr3:85384600-85385400	Active TSS	Brain Anterior Caudate	brain
40	chr3:85384800-85385000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
41	chr3:85384800-85385000	Enhancers	Brain Substantia Nigra	brain
42	chr3:85384800-85385200	Active TSS	A549	lung
43	chr3:85384800-85385400	Active TSS	Brain Angular Gyrus	brain
44	chr3:85385000-85385200	Enhancers	Liver	Liver
45	chr3:85385000-85385200	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr3:85385000-85385400	Active TSS	Brain Cingulate Gyrus	brain
47	chr3:85385000-85385400	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr3:85385000-85385400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr3:85385000-85385400	Active TSS	Brain Substantia Nigra	brain
50	chr3:85385200-85386600	Weak transcription	Brain Hippocampus Middle	brain

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