Variant report

Variant	nsv1020653
Chromosome Location	chr6:24557870-24638244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:861)
CpG islands
(count:368)
Chromatin interactive
region (count:80)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:24566749-24566949	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:24581382-24581649	HepG2	liver:	n/a	n/a
3	ATF1	chr6:24583673-24583987	K562	blood:	n/a	n/a
4	ATF2	chr6:24583571-24583950	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:24601156-24601442	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr6:24583778-24583996	GM12878	blood:	n/a	n/a
7	BRCA1	chr6:24589724-24589913	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr6:24636098-24636185	HepG2	liver:	n/a	chr6:24636153-24636164 chr6:24636152-24636165
9	CEBPB	chr6:24559888-24560155	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:24610103-24610351	K562	blood:	n/a	chr6:24610248-24610259
11	CEBPB	chr6:24559891-24560160	K562	blood:	n/a	n/a
12	CEBPB	chr6:24581446-24581685	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:24581421-24581705	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:24603584-24603822	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:24610120-24610341	HepG2	liver:	n/a	chr6:24610248-24610259
16	CEBPB	chr6:24583538-24584701	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr6:24610095-24610286	A549	lung:	n/a	chr6:24610248-24610259
18	CHD2	chr6:24589694-24589917	HepG2	liver:	n/a	n/a
19	CHD2	chr6:24581382-24581644	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr6:24583775-24583888	GM12878	blood:	n/a	n/a
21	CHD2	chr6:24589669-24589926	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr6:24589561-24589940	K562	blood:	n/a	n/a
23	CREB1	chr6:24614831-24615248	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr6:24583519-24583949	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr6:24614879-24615237	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr6:24583780-24583930	HCFaa	heart:	n/a	n/a
27	CTCF	chr6:24581420-24581570	Hela-S3	cervix:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
28	CTCF	chr6:24583620-24583770	HAc	cerebellar:	n/a	n/a
29	CTCF	chr6:24601260-24601410	HCM	heart:	n/a	n/a
30	CTCF	chr6:24601227-24601409	GM19238	blood:	n/a	n/a
31	CTCF	chr6:24575182-24575243	GM12891	blood:	n/a	n/a
32	CTCF	chr6:24581400-24581550	NB4	blood:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
33	CTCF	chr6:24581420-24581570	HUVEC	blood vessel:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
34	CTCF	chr6:24629000-24629150	WI-38	lung:	n/a	n/a
35	CTCF	chr6:24583780-24583930	Caco-2	colon:	n/a	n/a
36	CTCF	chr6:24583760-24583910	GM12866	blood:	n/a	n/a
37	CTCF	chr6:24601220-24601370	GM12867	blood:	n/a	n/a
38	CTCF	chr6:24583760-24583910	GM06990	blood:	n/a	n/a
39	CTCF	chr6:24581440-24581590	HPF	lung:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
40	CTCF	chr6:24581400-24581550	HRE	kidney:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
41	CTCF	chr6:24583460-24583562	GM19239	blood:	n/a	n/a
42	CTCF	chr6:24601292-24601316	ProgFib	skin:	n/a	n/a
43	CTCF	chr6:24581400-24581550	HVMF	connective:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
44	CTCF	chr6:24601280-24601430	AG09319	gingival:	n/a	n/a
45	CTCF	chr6:24581400-24581550	GM12875	blood:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
46	CTCF	chr6:24583620-24583770	HCM	heart:	n/a	n/a
47	CTCF	chr6:24583709-24583952	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr6:24581365-24581630	HepG2	liver:	n/a	chr6:24581490-24581508 chr6:24581493-24581506 chr6:24581492-24581513
49	CTCF	chr6:24583610-24584077	GM12878	blood:	n/a	n/a
50	CTCF	chr6:24601220-24601370	GM12875	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:24588956-24589006	GM19239	blood:	n/a
2	chr6:24588956-24589006	IMR90	lung:	fetal
3	chr6:24588956-24589006	GM19239	blood:	n/a
4	chr6:24588956-24589006	IMR90	lung:	fetal
5	chr6:24588956-24589006	HIPEpiC	eye:	n/a
6	chr6:24583723-24583773	RPTEC	kidney:	n/a
7	chr6:24583614-24583664	HL-60	blood:	n/a
8	chr6:24583723-24583773	NHDF-neo	bronchial:	n/a
9	chr6:24583848-24583898	T-47D	breast:	n/a
10	chr6:24588956-24589006	HRCEpiC	kidney:	n/a
11	chr6:24583614-24583664	GM12892	blood:	n/a
12	chr6:24583848-24583898	H1-hESC	embryonic stem cell:	embryo
13	chr6:24583723-24583773	AG10803	skin:	n/a
14	chr6:24588956-24589006	GM12891	blood:	n/a
15	chr6:24583723-24583773	NT2-D1	testis:	n/a
16	chr6:24583614-24583664	PANC-1	pancreas:	n/a
17	chr6:24588956-24589006	NH-A	brain:	n/a
18	chr6:24588956-24589006	HCPEpiC	choroid plexus:	n/a
19	chr6:24583848-24583898	HRPEpiC	eye:	n/a
20	chr6:24588956-24589006	HCT-116	colon:	n/a
21	chr6:24583614-24583664	GM06990	blood:	n/a
22	chr6:24583614-24583664	K562	blood:	n/a
23	chr6:24583848-24583898	HCM	heart:	n/a
24	chr6:24583848-24583898	HEEpiC	esophagus:	n/a
25	chr6:24583848-24583898	GM06990	blood:	n/a
26	chr6:24588956-24589006	ovcar-3	ovarian:	n/a
27	chr6:24583477-24583527	LNCaP	prostate:	n/a
28	chr6:24588956-24589006	SK-N-SH_RA	brain:	n/a
29	chr6:24583614-24583664	NHDF-neo	bronchial:	n/a
30	chr6:24583496-24583546	HMEC	breast:	n/a
31	chr6:24583723-24583773	SAEC	small airway:	n/a
32	chr6:24583614-24583664	A549	lung:	n/a
33	chr6:24583723-24583773	NH-A	brain:	n/a
34	chr6:24583477-24583527	HNPCEpiC	eye:	n/a
35	chr6:24583496-24583546	NHDF-neo	bronchial:	n/a
36	chr6:24583614-24583664	HIPEpiC	eye:	n/a
37	chr6:24583496-24583546	GM19239	blood:	n/a
38	chr6:24588956-24589006	Hepatocyte	liver:	n/a
39	chr6:24583848-24583898	HCT-116	colon:	n/a
40	chr6:24583723-24583773	AG09319	gingival:	n/a
41	chr6:24583848-24583898	IMR90	lung:	fetal
42	chr6:24583496-24583546	PFSK-1	brain:	n/a
43	chr6:24583848-24583898	SKMC	muscle:	n/a
44	chr6:24583848-24583898	ECC-1	luminal epithelium:	n/a
45	chr6:24588956-24589006	NT2-D1	testis:	n/a
46	chr6:24583723-24583773	BE2_C	brain:	n/a
47	chr6:24583723-24583773	A549	lung:	n/a
48	chr6:24583496-24583546	NT2-D1	testis:	n/a
49	chr6:24583848-24583898	ProgFib	skin:	n/a
50	chr6:24583723-24583773	NB4	blood:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:24627003..24628828-chr6:24631433..24632977,2	MCF-7	breast:
2	chr6:24521872..24523462-chr6:24559517..24561128,2	K562	blood:
3	chr6:24573525..24576686-chr6:24578975..24580891,3	K562	blood:
4	chr6:24605172..24607164-chr6:24613229..24614959,2	MCF-7	breast:
5	chr6:24583561..24585775-chr6:24695731..24698506,2	MCF-7	breast:
6	chr6:24617593..24620390-chr6:24645811..24647952,2	MCF-7	breast:
7	chr6:24590802..24593221-chr6:24599918..24601431,2	K562	blood:
8	chr6:24586729..24589298-chr6:24716794..24718796,2	K562	blood:
9	chr6:24578480..24581116-chr6:24582256..24584782,2	MCF-7	breast:
10	chr6:24608901..24611617-chr6:24616065..24618620,2	K562	blood:
11	chr6:24578930..24581415-chr6:24684398..24686867,2	K562	blood:
12	chr6:24580984..24581965-chr6:24667233..24667814,2	K562	blood:
13	chr6:24493986..24495664-chr6:24558273..24561120,2	MCF-7	breast:
14	chr6:24493837..24495499-chr6:24561911..24564321,2	MCF-7	breast:
15	chr6:24617631..24619264-chr6:24620165..24621847,2	MCF-7	breast:
16	chr6:24604712..24607440-chr6:24620282..24623625,3	K562	blood:
17	chr6:24614182..24617626-chr6:24618812..24622750,3	MCF-7	breast:
18	chr6:24495596..24498223-chr6:24565020..24567302,2	MCF-7	breast:
19	chr6:24563668..24565517-chr6:24568197..24570013,2	MCF-7	breast:
20	chr6:24631674..24633873-chr6:24634528..24637854,3	K562	blood:
21	chr6:24593795..24596889-chr6:24599933..24601863,3	K562	blood:
22	chr6:24544075..24545945-chr6:24559657..24561591,2	MCF-7	breast:
23	chr6:24567288..24570936-chr6:24575661..24578652,4	K562	blood:
24	chr6:24624408..24625994-chr6:24628936..24631566,2	K562	blood:
25	chr6:24583756..24584313-chr6:24695395..24696001,2	MCF-7	breast:
26	chr6:24581022..24581594-chr6:24695757..24696453,3	K562	blood:
27	chr6:24581200..24583513-chr6:24694242..24695890,2	MCF-7	breast:
28	chr6:24583415..24585210-chr6:24588851..24590739,2	K562	blood:
29	chr6:24583515..24584121-chr6:24612514..24613415,2	K562	blood:
30	chr6:24580547..24584375-chr6:24665231..24668702,6	MCF-7	breast:
31	chr6:24570050..24571845-chr6:24573649..24576621,2	K562	blood:
32	chr6:24617631..24619264-chr6:24620165..24621847,2	MCF-7	breast:
33	chr6:24596221..24598717-chr6:24684990..24687804,2	MCF-7	breast:
34	chr6:24570050..24571845-chr6:24573649..24576621,2	K562	blood:
35	chr6:24580668..24582664-chr6:24719148..24720850,2	K562	blood:
36	chr6:24555919..24558537-chr6:24563270..24565102,2	MCF-7	breast:
37	chr6:24560740..24563562-chr6:24720108..24721849,2	MCF-7	breast:
38	chr6:24590802..24593221-chr6:24599918..24601431,2	K562	blood:
39	chr6:24627114..24630074-chr6:24633308..24635849,2	K562	blood:
40	chr6:24605172..24607164-chr6:24613229..24614959,2	MCF-7	breast:
41	chr6:24574766..24576618-chr6:24701897..24704252,2	K562	blood:
42	chr6:24563668..24565517-chr6:24568197..24570013,2	MCF-7	breast:
43	chr6:24593795..24596889-chr6:24599933..24601863,3	K562	blood:
44	chr6:24601929..24604741-chr6:24605284..24606848,2	K562	blood:
45	chr6:24627003..24628828-chr6:24631433..24632977,2	MCF-7	breast:
46	chr6:24570345..24573148-chr6:24573437..24575149,2	K562	blood:
47	chr6:24580785..24582089-chr6:24695048..24696580,9	MCF-7	breast:
48	chr6:24583421..24584285-chr6:24695932..24696466,3	K562	blood:
49	chr6:24631674..24633873-chr6:24634528..24637854,3	K562	blood:
50	chr6:24601929..24604741-chr6:24605284..24606848,2	K562	blood:

No data

Variant related genes	Relation type
KRT8P43	TF binding region
KRT8P43	CpG island
ENSG00000112294	chromatin interactions
ENSG00000112312	chromatin interactions
ENSG00000272345	chromatin interactions
ENSG00000112293	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000137261	chromatin interactions
ENSG00000111802	chromatin interactions
ENSG00000112304	chromatin interactions

Extended variants
information (count: 3141 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3141 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147062927	chr6:24557903-24557904	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs568427885	chr6:24557912-24557913	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560646365	chr6:24557992-24557993	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs527668416	chr6:24558024-24558025	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs113557096	chr6:24558029-24558030	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs111390244	chr6:24558034-24558035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188658152	chr6:24558057-24558058	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371402773	chr6:24558085-24558086	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs191983069	chr6:24558099-24558100	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539684392	chr6:24558137-24558138	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs807539	chr6:24558192-24558193	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570257071	chr6:24558233-24558234	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113940774	chr6:24558345-24558346	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs531759915	chr6:24558361-24558362	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs369387069	chr6:24558369-24558370	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs375755587	chr6:24558378-24558379	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs9467228	chr6:24558392-24558393	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs554161397	chr6:24558432-24558433	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs2760168	chr6:24558433-24558434	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs35237166	chr6:24558444-24558445	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs539823314	chr6:24558475-24558476	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs571343543	chr6:24558501-24558502	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs112514454	chr6:24558502-24558503	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs2760167	chr6:24558519-24558520	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138291389	chr6:24558571-24558572	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs372256630	chr6:24558593-24558594	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs142251978	chr6:24558594-24558595	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs2817258	chr6:24558596-24558597	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs199820109	chr6:24558600-24558601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200809216	chr6:24558601-24558602	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201482317	chr6:24558604-24558605	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs59328032	chr6:24558620-24558621	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs199626048	chr6:24558628-24558629	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200408961	chr6:24558629-24558630	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs59650679	chr6:24558632-24558633	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs70974919	chr6:24558635-24558636	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs531520262	chr6:24558643-24558644	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs2744542	chr6:24558675-24558676	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs561940372	chr6:24558687-24558688	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs2760166	chr6:24558756-24558757	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs555272706	chr6:24558765-24558766	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2744543	chr6:24558798-24558799	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs375051989	chr6:24558850-24558851	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs79052063	chr6:24558883-24558884	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs371653318	chr6:24558943-24558944	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533417174	chr6:24558997-24558998	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116198745	chr6:24559007-24559008	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2251350	chr6:24559023-24559024	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs807540	chr6:24559029-24559030	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs367826172	chr6:24559061-24559062	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
small cell lung cancer	20016488	CNVD
XY gonadal dysgenesis	20685758	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24496200-24583000	Weak transcription	Hela-S3	cervix
2	chr6:24535200-24566600	Weak transcription	Brain Germinal Matrix	brain
3	chr6:24535200-24591200	Weak transcription	Fetal Brain Male	brain
4	chr6:24535600-24560600	Weak transcription	Brain Anterior Caudate	brain
5	chr6:24535600-24560600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:24535600-24563200	Weak transcription	Brain Angular Gyrus	brain
7	chr6:24535600-24583400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr6:24539200-24583200	Weak transcription	Fetal Intestine Small	intestine
9	chr6:24548400-24583400	Weak transcription	A549	lung
10	chr6:24550200-24566400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:24552600-24568800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr6:24554600-24563600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr6:24556600-24559200	Weak transcription	Fetal Brain Female	brain
14	chr6:24559200-24559600	Enhancers	Pancreas	Pancrea
15	chr6:24559200-24559800	Strong transcription	Fetal Brain Female	brain
16	chr6:24559600-24577600	Weak transcription	Pancreas	Pancrea
17	chr6:24559800-24563200	Weak transcription	Fetal Brain Female	brain
18	chr6:24560600-24560800	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:24560600-24561000	Enhancers	Psoas Muscle	Psoas
20	chr6:24560600-24561600	Strong transcription	Brain Anterior Caudate	brain
21	chr6:24560600-24562000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:24560800-24561000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:24561600-24563200	Weak transcription	Brain Anterior Caudate	brain
24	chr6:24561800-24562200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:24562000-24563200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr6:24562400-24583400	Weak transcription	Right Atrium	heart
27	chr6:24563200-24564400	Strong transcription	Brain Angular Gyrus	brain
28	chr6:24563200-24564400	Strong transcription	Brain Anterior Caudate	brain
29	chr6:24563200-24564400	Bivalent Enhancer	HepG2	liver
30	chr6:24563200-24565200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:24563200-24565200	Strong transcription	Fetal Brain Female	brain
32	chr6:24563400-24565000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:24563600-24564800	Strong transcription	Brain Inferior Temporal Lobe	brain
34	chr6:24564000-24564800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:24564400-24564600	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr6:24564400-24583400	Weak transcription	Brain Angular Gyrus	brain
37	chr6:24564400-24583400	Weak transcription	Brain Anterior Caudate	brain
38	chr6:24564800-24566200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr6:24565200-24569600	Weak transcription	Fetal Brain Female	brain
40	chr6:24565200-24570000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr6:24566200-24567000	Strong transcription	Brain Inferior Temporal Lobe	brain
42	chr6:24566200-24567000	Enhancers	HepG2	liver
43	chr6:24566400-24566800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr6:24566600-24567000	Strong transcription	Brain Germinal Matrix	brain
45	chr6:24566600-24567000	Enhancers	Osteobl	bone
46	chr6:24566800-24567000	Enhancers	Fetal Muscle Leg	muscle
47	chr6:24566800-24568400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr6:24567000-24568800	Weak transcription	Brain Germinal Matrix	brain
49	chr6:24567000-24569800	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr6:24568000-24568800	Bivalent Enhancer	HepG2	liver

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