Variant report

Variant	nsv877170
Chromosome Location	chr3:94790666-95564838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1635)
CpG islands
(count:305)
Chromatin interactive
region (count:59)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1635 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:95530415-95530417	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:95020945-95021158	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:95060166-95060565	HepG2	liver:	n/a	n/a
4	ATF1	chr3:95373822-95374011	K562	blood:	n/a	n/a
5	ATF1	chr3:95389684-95389856	K562	blood:	n/a	n/a
6	ATF2	chr3:95440827-95441176	GM12878	blood:	n/a	chr3:95440985-95440992
7	ATF2	chr3:95106325-95106837	GM12878	blood:	n/a	n/a
8	ATF2	chr3:95106361-95106757	GM12878	blood:	n/a	n/a
9	BACH1	chr3:95062110-95062463	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:95259001-95259010	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:95106405-95106603	GM12878	blood:	n/a	n/a
12	BATF	chr3:94867079-94867278	GM12878	blood:	n/a	chr3:94867158-94867169
13	BATF	chr3:95450656-95450962	GM12878	blood:	n/a	chr3:95450813-95450824
14	BATF	chr3:95424738-95425007	GM12878	blood:	n/a	chr3:95424828-95424839 chr3:95424833-95424843
15	BATF	chr3:95424667-95425007	GM12878	blood:	n/a	chr3:95424828-95424839 chr3:95424833-95424843
16	BATF	chr3:95227008-95227313	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:95106290-95106831	GM12878	blood:	n/a	n/a
18	BCL11A	chr3:95424711-95425000	GM12878	blood:	n/a	chr3:95424831-95424840 chr3:95424812-95424821 chr3:95424832-95424841
19	BCL11A	chr3:95226985-95227360	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:95424746-95424977	GM12878	blood:	n/a	chr3:95424831-95424840 chr3:95424812-95424821 chr3:95424832-95424841
21	BCL11A	chr3:95106312-95106826	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:95258863-95259155	GM12878	blood:	n/a	chr3:95259123-95259132
23	BCLAF1	chr3:95106402-95106792	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:94839934-94840050	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:95440920-95441120	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:95111736-95111867	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:95106231-95106911	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:95075531-95076132	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:95076429-95076540	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:95286194-95286482	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:95077334-95077335	GM12878	blood:	n/a	n/a
32	BRCA1	chr3:95531931-95531996	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr3:95035182-95035246	GM12878	blood:	n/a	n/a
34	BRCA1	chr3:94916763-94916781	GM12878	blood:	n/a	n/a
35	BRCA1	chr3:95348822-95348968	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:94849900-94850155	HepG2	liver:	n/a	n/a
37	CEBPB	chr3:95275852-95276014	HepG2	liver:	n/a	chr3:95275907-95275918
38	CEBPB	chr3:95016776-95017129	A549	lung:	n/a	chr3:95016932-95016943
39	CEBPB	chr3:95440805-95441175	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:95148473-95148611	H1-hESC	embryonic stem cell:	n/a	chr3:95148564-95148577 chr3:95148564-95148577 chr3:95148566-95148575 chr3:95148564-95148575 chr3:95148566-95148577 chr3:95148566-95148575 chr3:95148564-95148577 chr3:95148566-95148575 chr3:95148566-95148577 chr3:95148566-95148575
41	CEBPB	chr3:95440783-95441165	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr3:95016809-95017118	HepG2	liver:	n/a	chr3:95016932-95016943
43	CEBPB	chr3:95389689-95389953	A549	lung:	n/a	chr3:95389809-95389822 chr3:95389809-95389822 chr3:95389810-95389821
44	CEBPB	chr3:95121140-95121202	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr3:95012213-95012510	IMR90	lung:	n/a	chr3:95012363-95012376 chr3:95012363-95012376
46	CEBPB	chr3:95276601-95276888	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:95025563-95026102	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:94852969-94853285	Hela-S3	cervix:	n/a	chr3:94853151-94853162
49	CEBPB	chr3:94827289-94827503	A549	lung:	n/a	chr3:94827386-94827397
50	CEBPB	chr3:95408171-95408180	H1-hESC	embryonic stem cell:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:95456922-95456972	Hepatocyte	liver:	n/a
2	chr3:95402607-95402657	GM12878	blood:	n/a
3	chr3:95402607-95402657	U87	brain:	n/a
4	chr3:95402607-95402657	HIPEpiC	eye:	n/a
5	chr3:95464101-95464151	H1-hESC	embryonic stem cell:	embryo
6	chr3:95402607-95402657	SAEC	small airway:	n/a
7	chr3:95038960-95039010	HCPEpiC	choroid plexus:	n/a
8	chr3:95402225-95402275	AG04450	lung:	fetal
9	chr3:95464101-95464151	HCM	heart:	n/a
10	chr3:95402225-95402275	HEK293	kidney:	embryo
11	chr3:95456922-95456972	HRE	kidney:	n/a
12	chr3:95456922-95456972	NT2-D1	testis:	n/a
13	chr3:95464101-95464151	SK-N-MC	brain:	n/a
14	chr3:95456922-95456972	NB4	blood:	n/a
15	chr3:95464101-95464151	AoSMC	blood vessel:	n/a
16	chr3:95402225-95402275	GM12892	blood:	n/a
17	chr3:95456922-95456972	HRPEpiC	eye:	n/a
18	chr3:95038960-95039010	LNCaP	prostate:	n/a
19	chr3:95402225-95402275	AG10803	skin:	n/a
20	chr3:95464101-95464151	AG04450	lung:	fetal
21	chr3:95402607-95402657	NH-A	brain:	n/a
22	chr3:95464101-95464151	HCF	heart:	n/a
23	chr3:95038960-95039010	HCF	heart:	n/a
24	chr3:95402225-95402275	HCT-116	colon:	n/a
25	chr3:95038960-95039010	T-47D	breast:	n/a
26	chr3:95464101-95464151	SKMC	muscle:	n/a
27	chr3:95456922-95456972	SK-N-SH	brain:	n/a
28	chr3:95402607-95402657	GM06990	blood:	n/a
29	chr3:95402225-95402275	PFSK-1	brain:	n/a
30	chr3:95464101-95464151	NH-A	brain:	n/a
31	chr3:95464101-95464151	GM19239	blood:	n/a
32	chr3:95038960-95039010	H1-hESC	embryonic stem cell:	embryo
33	chr3:95038960-95039010	GM12878	blood:	n/a
34	chr3:95402225-95402275	PANC-1	pancreas:	n/a
35	chr3:95464101-95464151	GM12892	blood:	n/a
36	chr3:95456922-95456972	ProgFib	skin:	n/a
37	chr3:95456922-95456972	SAEC	small airway:	n/a
38	chr3:95456922-95456972	HEEpiC	esophagus:	n/a
39	chr3:95464101-95464151	NT2-D1	testis:	n/a
40	chr3:95402607-95402657	K562	blood:	n/a
41	chr3:95456922-95456972	K562	blood:	n/a
42	chr3:95456922-95456972	GM06990	blood:	n/a
43	chr3:95402607-95402657	Hepatocyte	liver:	n/a
44	chr3:95456922-95456972	HCF	heart:	n/a
45	chr3:95402225-95402275	GM06990	blood:	n/a
46	chr3:95456922-95456972	Caco-2	colon:	n/a
47	chr3:95464101-95464151	NHDF-neo	bronchial:	n/a
48	chr3:95402607-95402657	HPAEpiC	pulmonary alveolar:	n/a
49	chr3:95402225-95402275	Hela-S3	cervix:	n/a
50	chr3:95038960-95039010	HIPEpiC	eye:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:62608866..62609588-chr3:94930688..94931197,2	Hela-S3	cervix:
2	chr3:95199079..95200769-chr3:95213742..95216359,2	MCF-7	breast:
3	chr3:95526423..95529164-chr3:95534021..95536837,2	MCF-7	breast:
4	chr3:95227832..95230728-chr3:95231863..95234539,2	MCF-7	breast:
5	chr3:94817887..94820811-chr3:94823727..94825470,2	MCF-7	breast:
6	chr3:94840742..94842445-chr3:94846541..94849507,2	K562	blood:
7	chr3:94790247..94791777-chr3:94793265..94795089,2	MCF-7	breast:
8	chr3:95405066..95405997-chr3:95445545..95446305,2	MCF-7	breast:
9	chr3:95048765..95050742-chr3:95059845..95061354,2	MCF-7	breast:
10	chr3:95227832..95230728-chr3:95231863..95234539,2	MCF-7	breast:
11	chr3:94912857..94914770-chr3:94921596..94924370,2	MCF-7	breast:
12	chr3:94709818..94710517-chr3:95057153..95057747,2	MCF-7	breast:
13	chr3:94969252..94971265-chr3:94976399..94979300,2	MCF-7	breast:
14	chr10:8094404..8097320-chr3:95095070..95097036,2	MCF-7	breast:
15	chr3:95183591..95185575-chr3:95191564..95193527,2	MCF-7	breast:
16	chr3:94709479..94710037-chr3:95470756..95471273,2	MCF-7	breast:
17	chr3:94852529..94855191-chr3:94858249..94861078,2	MCF-7	breast:
18	chr3:95142063..95144000-chr3:95146430..95148215,2	K562	blood:
19	chr3:95114773..95115375-chr4:14681490..14682465,2	MCF-7	breast:
20	chr3:94817887..94820811-chr3:94823727..94825470,2	MCF-7	breast:
21	chr3:94817300..94819086-chr3:94851388..94853327,2	K562	blood:
22	chr3:94881976..94883745-chr3:94887711..94889312,2	K562	blood:
23	chr3:94979836..94981879-chr3:94985858..94987938,2	MCF-7	breast:
24	chr3:94776805..94778652-chr3:94799142..94801105,2	K562	blood:
25	chr3:95195068..95197467-chr3:95198859..95200862,2	MCF-7	breast:
26	chr3:94817300..94819086-chr3:94851388..94853327,2	K562	blood:
27	chr3:95195068..95197467-chr3:95198859..95200862,2	MCF-7	breast:
28	chr3:94806462..94808177-chr3:94814453..94816989,2	K562	blood:
29	chr3:94912857..94914770-chr3:94921596..94924370,2	MCF-7	breast:
30	chr3:95048765..95050742-chr3:95059845..95061354,2	MCF-7	breast:
31	chr16:88876297..88877909-chr3:95289984..95292587,2	MCF-7	breast:
32	chr3:94709509..94710453-chr3:95235578..95236144,3	MCF-7	breast:
33	chr3:94790247..94791777-chr3:94793265..94795089,2	MCF-7	breast:
34	chr3:94877501..94880060-chr3:94881740..94883902,2	MCF-7	breast:
35	chr3:95240322..95240859-chr3:95470769..95471546,2	MCF-7	breast:
36	chr3:95018524..95019390-chr9:5887461..5888104,2	MCF-7	breast:
37	chr11:73286935..73287612-chr3:95303237..95304152,2	MCF-7	breast:
38	chr3:94979836..94981879-chr3:94985858..94987938,2	MCF-7	breast:
39	chr3:95090441..95093398-chr3:95112736..95115593,2	MCF-7	breast:
40	chr3:94881976..94883745-chr3:94887711..94889312,2	K562	blood:
41	chr3:95142063..95144000-chr3:95146430..95148215,2	K562	blood:
42	chr3:95090441..95093398-chr3:95112736..95115593,2	MCF-7	breast:
43	chr3:95240322..95240859-chr3:95470769..95471546,2	MCF-7	breast:
44	chr3:94840742..94842445-chr3:94846541..94849507,2	K562	blood:
45	chr3:94852529..94855191-chr3:94858249..94861078,2	MCF-7	breast:
46	chr3:95199079..95200769-chr3:95213742..95216359,2	MCF-7	breast:
47	chr3:95412505..95414167-chr3:95415119..95417100,2	MCF-7	breast:
48	chr3:94934431..94935951-chr3:94936179..94938719,2	K562	blood:
49	chr3:94877501..94880060-chr3:94881740..94883902,2	MCF-7	breast:
50	chr3:95412505..95414167-chr3:95415119..95417100,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NSUN3-1	chr3:94807002-94807138	NONHSAT090743
2	lnc-NSUN3-1	chr3:94807002-94807138	ENSG00000239589
3	lnc-NSUN3-3	chr3:95131564-95131698	NONHSAT090745
4	lnc-DHFRL1-3	chr3:95387254-95387609	NONHSAT090746
5	lnc-DHFRL1-3	chr3:95382088-95382184	NONHSAT090746
6	lnc-EPHA6-6	chr3:95328585-95328971	expReg_chr3_6592_+
7	lnc-DHFRL1-3	chr3:95399846-95399969	NONHSAT090746
8	lnc-NSUN3-3	chr3:95112646-95112775	NONHSAT090745
9	lnc-NSUN3-1	chr3:94857030-94857161	NONHSAT090743
10	lnc-DHFRL1-3	chr3:95387164-95387609	NONHSAT090748
11	lnc-DHFRL1-3	chr3:95373267-95374691	NONHSAT090746
12	lnc-DHFRL1-3	chr3:95373812-95374682	NONHSAT090747
13	lnc-DHFRL1-3	chr3:95400302-95400325	NONHSAT090748
14	lnc-DHFRL1-3	chr3:95401445-95402037	NONHSAT090746
15	lnc-NSUN3-1	chr3:94870874-94871353	ENSG00000239589
16	lnc-NSUN3-1	chr3:94890764-94891221	NONHSAT090744
17	lnc-DHFRL1-3	chr3:95401445-95401565	NONHSAT090748
18	lnc-NSUN3-1	chr3:94857070-94857159	ENSG00000239589

No data

Variant related genes	Relation type
MTHFD2P1	TF binding region
RPS18P6	TF binding region
MTHFD2P1	CpG island
RPS18P6	CpG island
ENSG00000243350	chromatin interactions
ENSG00000198931	chromatin interactions
ENSG00000197308	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000107485	chromatin interactions

Extended variants
information (count: 10774 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:10774 , 50 per page) page: 1 2 3 4 5 6 7 ... 216

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111377413	chr3:94807020-94807021	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs570810494	chr3:94807026-94807027	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs539848477	chr3:94807103-94807104	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs551862407	chr3:94831228-94831229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533440085	chr3:94831257-94831258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568852581	chr3:94831263-94831264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138413879	chr3:94831275-94831276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376328661	chr3:94831279-94831280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537528529	chr3:94831284-94831285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9882838	chr3:94831290-94831291	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369193902	chr3:94831295-94831296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183936767	chr3:94831303-94831304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534433547	chr3:94831339-94831340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188782940	chr3:94831357-94831358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546431468	chr3:94831358-94831359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150584225	chr3:94831362-94831363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368449975	chr3:94831366-94831367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs71326849	chr3:94831376-94831377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139602856	chr3:94831389-94831390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149249974	chr3:94831431-94831432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536943472	chr3:94831435-94831436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558654647	chr3:94831459-94831460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77108736	chr3:94831520-94831521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561889431	chr3:94831554-94831555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527791416	chr3:94831574-94831575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539994726	chr3:94831580-94831581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559939631	chr3:94831587-94831588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532241067	chr3:94831631-94831632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552479359	chr3:94831633-94831634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568740716	chr3:94831728-94831729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73850311	chr3:94831755-94831756	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs547967189	chr3:94831769-94831770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9864255	chr3:94831817-94831818	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533876098	chr3:94831836-94831837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139209186	chr3:94831842-94831843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116944055	chr3:94831846-94831847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571068709	chr3:94831847-94831848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540794712	chr3:94831855-94831856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556842303	chr3:94831859-94831860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576354073	chr3:94831861-94831862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191115374	chr3:94831862-94831863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144036644	chr3:94831889-94831890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79720048	chr3:94831925-94831926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529695312	chr3:94831960-94831961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541145069	chr3:94831962-94831963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183584945	chr3:94831970-94831971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs9812403	chr3:94831984-94831985	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146861038	chr3:94832041-94832042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551968043	chr3:94832042-94832043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs3843865	chr3:94832102-94832103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD
Autism	20531469	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Hereditary coagulopathy	21993689	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:94831200-94831800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:94831400-94832400	Enhancers	Hela-S3	cervix
3	chr3:94839600-94840600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:94839800-94840200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:94839800-94840400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:94839800-94840600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr3:94839800-94840600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:94840200-94855200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:94840400-94842200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:94840600-94843400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:94840600-94844000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:94842200-94842400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:94842400-94843000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:94842800-94844000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr3:94843000-94844000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:94843400-94843600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:94844000-94844200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:94844000-94845800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr3:94844000-94845800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr3:94844200-94845800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:94845800-94846200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr3:94845800-94846400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:94845800-94846800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:94846200-94849600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:94846800-94847800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:94847800-94848000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:94849600-94850600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:94850600-94853600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:94851800-94852000	Enhancers	Colon Smooth Muscle	Colon
30	chr3:94853000-94854600	Enhancers	Fetal Heart	heart
31	chr3:94853600-94854600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:94853800-94854200	Enhancers	Colon Smooth Muscle	Colon
33	chr3:94853800-94854400	Enhancers	Rectal Smooth Muscle	rectum
34	chr3:94853800-94854600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:94854000-94854400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr3:94854000-94855000	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr3:94855200-94855400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:94863400-94863600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr3:94863600-94864600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:94864400-94865200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:94864400-94865400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:94864600-94865200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:94864600-94865200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:94864600-94865200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:94864600-94865400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr3:94865000-94865200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr3:94865200-94870400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr3:94865200-94870400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:94865200-94870400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:94865400-94870400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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