Variant report

Variant	nsv468827
Chromosome Location	chr1:246226566-246313723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1106)
CpG islands
(count:611)
Chromatin interactive
region (count:97)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1106 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246306858-246307142	K562	blood:	n/a	n/a
2	ARID3A	chr1:246232168-246232911	K562	blood:	n/a	n/a
3	ARID3A	chr1:246254962-246255161	K562	blood:	n/a	n/a
4	ARID3A	chr1:246276744-246277369	K562	blood:	n/a	n/a
5	ARID3A	chr1:246303013-246303421	K562	blood:	n/a	n/a
6	ARID3A	chr1:246297019-246297023	K562	blood:	n/a	n/a
7	ARID3A	chr1:246303129-246303329	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:246274930-246275288	K562	blood:	n/a	n/a
9	ARID3A	chr1:246305649-246306059	K562	blood:	n/a	n/a
10	ARID3A	chr1:246269535-246270147	K562	blood:	n/a	n/a
11	ARID3A	chr1:246273822-246274255	K562	blood:	n/a	n/a
12	ARID3A	chr1:246268344-246268607	K562	blood:	n/a	n/a
13	ATF1	chr1:246274901-246275230	K562	blood:	n/a	n/a
14	ATF1	chr1:246241695-246242195	K562	blood:	n/a	n/a
15	ATF1	chr1:246269670-246270067	K562	blood:	n/a	n/a
16	ATF1	chr1:246271408-246271755	K562	blood:	n/a	n/a
17	ATF1	chr1:246304350-246304649	K562	blood:	n/a	n/a
18	ATF1	chr1:246254868-246255152	K562	blood:	n/a	n/a
19	ATF1	chr1:246280509-246280836	K562	blood:	n/a	n/a
20	ATF1	chr1:246273843-246274253	K562	blood:	n/a	n/a
21	ATF1	chr1:246303038-246303366	K562	blood:	n/a	n/a
22	ATF1	chr1:246305671-246306307	K562	blood:	n/a	n/a
23	ATF1	chr1:246284953-246285126	K562	blood:	n/a	n/a
24	ATF1	chr1:246276829-246277358	K562	blood:	n/a	n/a
25	ATF3	chr1:246302969-246303439	A549	lung:	n/a	n/a
26	ATF3	chr1:246305592-246306031	K562	blood:	n/a	n/a
27	ATF3	chr1:246302791-246303544	HCT-116	colon:	n/a	n/a
28	ATF3	chr1:246302787-246303663	HCT-116	colon:	n/a	n/a
29	ATF3	chr1:246268210-246268637	K562	blood:	n/a	n/a
30	BACH1	chr1:246274872-246275203	K562	blood:	n/a	n/a
31	BACH1	chr1:246273993-246274130	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr1:246273777-246274254	K562	blood:	n/a	n/a
33	BACH1	chr1:246280614-246280710	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr1:246291834-246292222	GM12878	blood:	n/a	n/a
35	BATF	chr1:246291897-246292170	GM12878	blood:	n/a	n/a
36	BCL3	chr1:246281606-246281983	GM12878	blood:	n/a	n/a
37	BCL3	chr1:246302964-246303540	A549	lung:	n/a	n/a
38	BCL3	chr1:246281648-246282014	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:246305718-246306283	K562	blood:	n/a	n/a
40	BHLHE40	chr1:246273673-246274211	K562	blood:	n/a	n/a
41	BHLHE40	chr1:246276749-246277594	K562	blood:	n/a	n/a
42	BHLHE40	chr1:246269858-246269979	K562	blood:	n/a	n/a
43	BHLHE40	chr1:246268352-246268551	K562	blood:	n/a	n/a
44	BHLHE40	chr1:246258872-246259140	K562	blood:	n/a	n/a
45	BHLHE40	chr1:246278823-246278895	K562	blood:	n/a	n/a
46	BHLHE40	chr1:246272061-246272063	K562	blood:	n/a	n/a
47	CBX3	chr1:246276690-246277651	K562	blood:	n/a	n/a
48	CBX3	chr1:246309059-246309568	K562	blood:	n/a	chr1:246309478-246309489
49	CBX3	chr1:246245179-246246286	K562	blood:	n/a	n/a
50	CBX3	chr1:246273628-246274320	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246231142-246231192	HepG2	liver:	n/a
2	chr1:246231142-246231192	HepG2	liver:	n/a
3	chr1:246310349-246310399	IMR90	lung:	fetal
4	chr1:246235275-246235325	HCT-116	colon:	n/a
5	chr1:246310349-246310399	Caco-2	colon:	n/a
6	chr1:246254283-246254333	HUVEC	blood vessel:	n/a
7	chr1:246310349-246310399	GM12891	blood:	n/a
8	chr1:246310349-246310399	U87	brain:	n/a
9	chr1:246305399-246305449	AG09309	skin:	n/a
10	chr1:246254283-246254333	AG04449	skin:	fetal
11	chr1:246310411-246310461	SK-N-SH_RA	brain:	n/a
12	chr1:246231142-246231192	HIPEpiC	eye:	n/a
13	chr1:246254338-246254388	HUVEC	blood vessel:	n/a
14	chr1:246254338-246254388	MCF10A-Er-Src	breast:	n/a
15	chr1:246231142-246231192	A549	lung:	n/a
16	chr1:246304208-246304258	HNPCEpiC	eye:	n/a
17	chr1:246254215-246254265	Jurkat	blood:	n/a
18	chr1:246231142-246231192	NH-A	brain:	n/a
19	chr1:246254338-246254388	SK-N-SH_RA	brain:	n/a
20	chr1:246305399-246305449	MCF10A-Er-Src	breast:	n/a
21	chr1:246254338-246254388	AG10803	skin:	n/a
22	chr1:246305399-246305449	NHDF-neo	bronchial:	n/a
23	chr1:246231142-246231192	GM12891	blood:	n/a
24	chr1:246310411-246310461	HCT-116	colon:	n/a
25	chr1:246235275-246235325	HRE	kidney:	n/a
26	chr1:246304208-246304258	NB4	blood:	n/a
27	chr1:246254338-246254388	Jurkat	blood:	n/a
28	chr1:246305399-246305449	HRCEpiC	kidney:	n/a
29	chr1:246310411-246310461	HepG2	liver:	n/a
30	chr1:246235275-246235325	HUVEC	blood vessel:	n/a
31	chr1:246231142-246231192	PFSK-1	brain:	n/a
32	chr1:246310411-246310461	NH-A	brain:	n/a
33	chr1:246254215-246254265	Hela-S3	cervix:	n/a
34	chr1:246254215-246254265	RPTEC	kidney:	n/a
35	chr1:246310485-246310535	HUVEC	blood vessel:	n/a
36	chr1:246231142-246231192	HRE	kidney:	n/a
37	chr1:246254283-246254333	HepG2	liver:	n/a
38	chr1:246305399-246305449	CMK	blood:	n/a
39	chr1:246304208-246304258	CMK	blood:	n/a
40	chr1:246254338-246254388	HL-60	blood:	n/a
41	chr1:246310349-246310399	SKMC	muscle:	n/a
42	chr1:246235275-246235325	A549	lung:	n/a
43	chr1:246254338-246254388	NHBE	bronchial:	n/a
44	chr1:246254338-246254388	AG04449	skin:	fetal
45	chr1:246254215-246254265	HRE	kidney:	n/a
46	chr1:246254215-246254265	SAEC	small airway:	n/a
47	chr1:246310411-246310461	T-47D	breast:	n/a
48	chr1:246310485-246310535	Hepatocyte	liver:	n/a
49	chr1:246254338-246254388	AG09319	gingival:	n/a
50	chr1:246231142-246231192	Hepatocyte	liver:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:246240012..246241655-chr1:246242133..246245121,2	K562	blood:
2	chr1:246280440..246281134-chr1:246613800..246614445,2	MCF-7	breast:
3	chr1:246242761..246244330-chr1:246271984..246274792,2	K562	blood:
4	chr1:246262654..246264469-chr1:246272321..246273994,2	K562	blood:
5	chr1:246260025..246262798-chr1:246267872..246269623,2	K562	blood:
6	chr1:246231832..246234229-chr1:246235006..246238019,3	K562	blood:
7	chr1:246285178..246287872-chr1:246288956..246290649,2	K562	blood:
8	chr1:246244386..246246974-chr1:246250751..246252687,2	K562	blood:
9	chr1:246287445..246289501-chr1:246320750..246323566,2	MCF-7	breast:
10	chr1:246273236..246275581-chr1:246292847..246295788,2	K562	blood:
11	chr1:246228312..246231050-chr1:246233097..246234864,3	K562	blood:
12	chr1:246279918..246282314-chr1:246283327..246286278,3	K562	blood:
13	chr1:246260025..246262798-chr1:246267872..246269623,2	K562	blood:
14	chr1:246254942..246257764-chr1:246259415..246261815,3	K562	blood:
15	chr1:246262654..246264469-chr1:246272321..246273994,2	K562	blood:
16	chr1:246177132..246177761-chr1:246280226..246281140,2	K562	blood:
17	chr1:246216293..246219228-chr1:246230787..246232706,2	K562	blood:
18	chr1:246304825..246308561-chr1:246370108..246374332,3	K562	blood:
19	chr1:246284694..246286450-chr1:246289366..246291707,2	MCF-7	breast:
20	chr1:246228312..246231050-chr1:246233097..246234864,3	K562	blood:
21	chr1:246280572..246283583-chr1:246290379..246294751,4	K562	blood:
22	chr1:246292574..246294808-chr1:246305134..246306846,2	K562	blood:
23	chr1:246273236..246275581-chr1:246292847..246295788,2	K562	blood:
24	chr1:246267010..246267515-chr5:115973253..115974226,2	MCF-7	breast:
25	chr1:246232489..246234482-chr1:246354523..246357372,2	K562	blood:
26	chr1:246280977..246283583-chr1:246293075..246294751,2	K562	blood:
27	chr1:246303201..246305225-chr1:246319673..246321317,2	MCF-7	breast:
28	chr1:246235580..246237637-chr1:246239913..246241714,2	K562	blood:
29	chr1:246290308..246292260-chr1:246292808..246295373,2	K562	blood:
30	chr1:246240012..246241655-chr1:246242133..246245121,2	K562	blood:
31	chr1:246278852..246281294-chr1:246310121..246311911,2	K562	blood:
32	chr1:246140863..246143596-chr1:246281335..246283913,2	K562	blood:
33	chr1:246231832..246234229-chr1:246235006..246238019,3	K562	blood:
34	chr1:246312948..246315744-chr1:246316397..246318467,2	MCF-7	breast:
35	chr1:246237075..246239017-chr1:246241942..246243808,2	K562	blood:
36	chr1:246259009..246261177-chr1:246350968..246353474,2	K562	blood:
37	chr1:246261803..246263776-chr1:246265418..246268035,2	K562	blood:
38	chr1:246279918..246282776-chr1:246284778..246286908,2	K562	blood:
39	chr1:246297778..246300991-chr1:246304218..246307827,5	K562	blood:
40	chr1:246244386..246246974-chr1:246250751..246252687,2	K562	blood:
41	chr1:246297174..246299753-chr1:246320284..246323072,2	K562	blood:
42	chr1:246283420..246285442-chr1:246309239..246311230,2	K562	blood:
43	chr1:246303495..246306229-chr1:246309475..246311302,2	MCF-7	breast:
44	chr1:246280572..246283583-chr1:246290379..246294751,4	K562	blood:
45	chr1:246278852..246281294-chr1:246310121..246311911,2	K562	blood:
46	chr1:246265696..246267807-chr1:246269289..246271146,2	MCF-7	breast:
47	chr1:246297778..246300991-chr1:246304218..246307827,5	K562	blood:
48	chr1:246222964..246225304-chr1:246227328..246228872,2	K562	blood:
49	chr1:246280620..246283372-chr1:246351784..246353873,2	K562	blood:
50	chr1:246283420..246285442-chr1:246309239..246311230,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF26B-2	chr1:246271928-246272019	ENSG00000226876.1
2	lnc-KIF26B-2	chr1:246274633-246274883	NONHSAT010700
3	lnc-KIF26B-2	chr1:246273081-246273195	NONHSAT010700
4	lnc-KIF26B-2	chr1:246276991-246277168	ENSG00000226876.1
5	lnc-KIF26B-2	chr1:246274633-246274831	ENSG00000226876.1
6	lnc-KIF26B-2	chr1:246276989-246277108	ENSG00000226876.1
7	lnc-KIF26B-2	chr1:246274628-246274831	ENSG00000226876.1
8	lnc-KIF26B-2	chr1:246273084-246273195	ENSG00000226876.1

No data

Variant related genes	Relation type
ENSG00000226876	TF binding region
SMYD3	TF binding region
ENSG00000226876	CpG island
SMYD3	CpG island
ENSG00000202184	chromatin interactions
ENSG00000185420	chromatin interactions
ENSG00000226876	chromatin interactions

Extended variants
information (count: 3869 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3869 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4445429	chr1:246226566-246226567	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372340277	chr1:246226580-246226581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563268911	chr1:246226619-246226620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573586303	chr1:246226620-246226621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373712343	chr1:246226637-246226638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562418205	chr1:246226648-246226649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559531944	chr1:246226685-246226686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527885898	chr1:246226715-246226716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376337619	chr1:246226732-246226733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547966062	chr1:246226737-246226738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4559466	chr1:246226769-246226770	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs4336819	chr1:246226810-246226811	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs185974902	chr1:246226822-246226823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567093013	chr1:246226825-246226826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145685635	chr1:246226841-246226842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370902397	chr1:246226860-246226861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557671691	chr1:246226863-246226864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535521657	chr1:246226894-246226895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112996385	chr1:246226944-246226945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559302426	chr1:246226948-246226949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575930988	chr1:246226960-246226961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75320021	chr1:246226995-246226996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534800275	chr1:246226996-246226997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140886946	chr1:246227049-246227050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577785179	chr1:246227070-246227071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144617256	chr1:246227084-246227085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557011004	chr1:246227086-246227087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374774646	chr1:246227088-246227089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573576253	chr1:246227095-246227096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6666355	chr1:246227102-246227103	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs140398391	chr1:246227134-246227135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6666367	chr1:246227141-246227142	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376067044	chr1:246227153-246227154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574895147	chr1:246227162-246227163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545145059	chr1:246227186-246227187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564646939	chr1:246227188-246227189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536409852	chr1:246227189-246227190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs66739676	chr1:246227234-246227235	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs563870911	chr1:246227273-246227274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74428296	chr1:246227284-246227285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs398054016	chr1:246227286-246227287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369614558	chr1:246227300-246227301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78065703	chr1:246227302-246227303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190846480	chr1:246227328-246227329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180970872	chr1:246227334-246227335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534768911	chr1:246227387-246227388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551490083	chr1:246227458-246227459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571407300	chr1:246227465-246227466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536892015	chr1:246227475-246227476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557219221	chr1:246227476-246227477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246203800-246257600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:246211200-246229400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:246224600-246230800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:246226200-246226600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:246226200-246226600	Enhancers	Psoas Muscle	Psoas
6	chr1:246226200-246226600	Enhancers	Right Atrium	heart
7	chr1:246226200-246226600	Enhancers	K562	blood
8	chr1:246226200-246226800	Enhancers	Adipose Nuclei	Adipose
9	chr1:246226200-246226800	Enhancers	Left Ventricle	heart
10	chr1:246226200-246226800	Enhancers	Lung	lung
11	chr1:246226200-246230600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:246226400-246226600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:246226400-246226600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:246226400-246227800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr1:246226400-246228000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:246226400-246230000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr1:246226600-246226800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr1:246226600-246227000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:246226600-246231000	Weak transcription	K562	blood
20	chr1:246226800-246227800	Weak transcription	Lung	lung
21	chr1:246226800-246228000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:246227000-246227200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:246227200-246227600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr1:246227400-246229400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:246227400-246229800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:246227400-246230800	Weak transcription	Ovary	ovary
27	chr1:246227600-246228400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:246227600-246229000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:246227600-246229600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr1:246227800-246228000	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr1:246227800-246228200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr1:246227800-246228200	Enhancers	Lung	lung
33	chr1:246227800-246229200	Enhancers	HepG2	liver
34	chr1:246227800-246230600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr1:246227800-246231400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:246227800-246232200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:246228000-246228200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:246228000-246228400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:246228000-246231200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr1:246228000-246232000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:246228200-246228400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr1:246228200-246228600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr1:246228200-246228600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:246228200-246229200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr1:246228200-246229400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr1:246228400-246228800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:246228400-246229800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:246228400-246230400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:246228400-246231800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:246228400-246232000	Enhancers	HUES64 Cell Line	embryonic stem cell

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