Variant report

Variant	nsv533962
Chromosome Location	chr1:246321447-246501692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1996)
CpG islands
(count:1224)
Chromatin interactive
region (count:132)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246383173-246383457	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:246476713-246476913	K562	blood:	n/a	n/a
3	ARID3A	chr1:246329377-246329956	K562	blood:	n/a	n/a
4	ARID3A	chr1:246351102-246351709	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:246469874-246470465	K562	blood:	n/a	n/a
6	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
7	ARID3A	chr1:246333485-246334689	K562	blood:	n/a	n/a
8	ARID3A	chr1:246332132-246332717	K562	blood:	n/a	n/a
9	ARID3A	chr1:246351173-246351659	K562	blood:	n/a	n/a
10	ARID3A	chr1:246340416-246340426	K562	blood:	n/a	n/a
11	ARID3A	chr1:246444896-246445377	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:246378134-246379212	K562	blood:	n/a	n/a
13	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
14	ARID3A	chr1:246378433-246378571	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:246339570-246339954	K562	blood:	n/a	n/a
16	ARID3A	chr1:246364034-246364381	K562	blood:	n/a	n/a
17	ARID3A	chr1:246443886-246444158	K562	blood:	n/a	n/a
18	ARID3A	chr1:246345414-246346141	K562	blood:	n/a	n/a
19	ARID3A	chr1:246409804-246409947	K562	blood:	n/a	n/a
20	ARID3A	chr1:246339492-246340117	HepG2	liver:	n/a	n/a
21	ARID3A	chr1:246468839-246469426	K562	blood:	n/a	n/a
22	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
23	ATF1	chr1:246333942-246334272	K562	blood:	n/a	n/a
24	ATF1	chr1:246445017-246445192	K562	blood:	n/a	n/a
25	ATF1	chr1:246363474-246363487	K562	blood:	n/a	n/a
26	ATF1	chr1:246501515-246501774	K562	blood:	n/a	n/a
27	ATF1	chr1:246370614-246370654	K562	blood:	n/a	n/a
28	ATF1	chr1:246332388-246332644	K562	blood:	n/a	n/a
29	ATF1	chr1:246345391-246346206	K562	blood:	n/a	n/a
30	ATF1	chr1:246376288-246376805	K562	blood:	n/a	n/a
31	ATF1	chr1:246469981-246470295	K562	blood:	n/a	n/a
32	ATF1	chr1:246378205-246378667	K562	blood:	n/a	n/a
33	ATF1	chr1:246329490-246330061	K562	blood:	n/a	n/a
34	ATF2	chr1:246378108-246378612	GM12878	blood:	n/a	n/a
35	ATF2	chr1:246378137-246378580	GM12878	blood:	n/a	n/a
36	ATF2	chr1:246492949-246493723	GM12878	blood:	n/a	n/a
37	ATF2	chr1:246493100-246493631	GM12878	blood:	n/a	n/a
38	ATF3	chr1:246378129-246378678	K562	blood:	n/a	n/a
39	BACH1	chr1:246345481-246345569	K562	blood:	n/a	n/a
40	BACH1	chr1:246469053-246469366	K562	blood:	n/a	n/a
41	BACH1	chr1:246364134-246364441	K562	blood:	n/a	n/a
42	BACH1	chr1:246330166-246330170	K562	blood:	n/a	n/a
43	BACH1	chr1:246469627-246470581	K562	blood:	n/a	n/a
44	BACH1	chr1:246329773-246329841	K562	blood:	n/a	n/a
45	BACH1	chr1:246378344-246378673	K562	blood:	n/a	n/a
46	BACH1	chr1:246383042-246383141	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr1:246426231-246426459	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr1:246351235-246351409	K562	blood:	n/a	n/a
49	BACH1	chr1:246469042-246469374	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr1:246469926-246470676	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246416688-246416738	HCT-116	colon:	n/a
2	chr1:246446300-246446350	PFSK-1	brain:	n/a
3	chr1:246414665-246414715	RPTEC	kidney:	n/a
4	chr1:246370933-246370983	U87	brain:	n/a
5	chr1:246416688-246416738	HCT-116	colon:	n/a
6	chr1:246446300-246446350	PFSK-1	brain:	n/a
7	chr1:246414665-246414715	RPTEC	kidney:	n/a
8	chr1:246370933-246370983	U87	brain:	n/a
9	chr1:246363660-246363710	PANC-1	pancreas:	n/a
10	chr1:246363660-246363710	A549	lung:	n/a
11	chr1:246415568-246415618	GM19239	blood:	n/a
12	chr1:246466280-246466330	GM19239	blood:	n/a
13	chr1:246415568-246415618	GM12891	blood:	n/a
14	chr1:246370933-246370983	BE2_C	brain:	n/a
15	chr1:246415555-246415605	HCT-116	colon:	n/a
16	chr1:246414665-246414715	HCT-116	colon:	n/a
17	chr1:246415568-246415618	HIPEpiC	eye:	n/a
18	chr1:246415176-246415226	HCPEpiC	choroid plexus:	n/a
19	chr1:246363660-246363710	U87	brain:	n/a
20	chr1:246363697-246363747	ECC-1	luminal epithelium:	n/a
21	chr1:246363574-246363624	Hela-S3	cervix:	n/a
22	chr1:246370933-246370983	HAEpiC	amniotic membrane:	n/a
23	chr1:246415176-246415226	K562	blood:	n/a
24	chr1:246415176-246415226	HUVEC	blood vessel:	n/a
25	chr1:246363574-246363624	A549	lung:	n/a
26	chr1:246415165-246415215	GM19239	blood:	n/a
27	chr1:246363574-246363624	HCPEpiC	choroid plexus:	n/a
28	chr1:246451744-246451794	GM19239	blood:	n/a
29	chr1:246383021-246383071	BJ	skin:	n/a
30	chr1:246415214-246415264	GM12891	blood:	n/a
31	chr1:246414665-246414715	ProgFib	skin:	n/a
32	chr1:246378510-246378560	PFSK-1	brain:	n/a
33	chr1:246466280-246466330	NB4	blood:	n/a
34	chr1:246324811-246324861	SK-N-SH	brain:	n/a
35	chr1:246383021-246383071	HEK293	kidney:	embryo
36	chr1:246414840-246414890	NB4	blood:	n/a
37	chr1:246414840-246414890	SK-N-SH_RA	brain:	n/a
38	chr1:246363574-246363624	K562	blood:	n/a
39	chr1:246415165-246415215	AoSMC	blood vessel:	n/a
40	chr1:246378510-246378560	SK-N-SH_RA	brain:	n/a
41	chr1:246414665-246414715	LNCaP	prostate:	n/a
42	chr1:246415568-246415618	NB4	blood:	n/a
43	chr1:246363574-246363624	Hepatocyte	liver:	n/a
44	chr1:246378510-246378560	Jurkat	blood:	n/a
45	chr1:246414840-246414890	H1-hESC	embryonic stem cell:	embryo
46	chr1:246451744-246451794	LNCaP	prostate:	n/a
47	chr1:246324811-246324861	U87	brain:	n/a
48	chr1:246415165-246415215	HEEpiC	esophagus:	n/a
49	chr1:246415214-246415264	LNCaP	prostate:	n/a
50	chr1:246429789-246429839	HRCEpiC	kidney:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:246345662..246347517-chr1:246349747..246352735,2	K562	blood:
2	chr1:246175475..246176180-chr1:246409421..246410353,2	MCF-7	breast:
3	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
4	chr1:246345857..246348884-chr1:246378191..246381575,3	K562	blood:
5	chr1:246323812..246327417-chr1:246344916..246347036,3	K562	blood:
6	chr1:246333304..246334819-chr1:246336998..246339159,2	K562	blood:
7	chr1:246331853..246336135-chr1:246348494..246351528,4	K562	blood:
8	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
9	chr1:246446720..246449077-chr1:246451672..246454637,2	K562	blood:
10	chr1:246151420..246154131-chr1:246468233..246469966,2	K562	blood:
11	chr1:246343018..246344728-chr1:246345131..246347522,2	K562	blood:
12	chr1:246304825..246308561-chr1:246370108..246374332,3	K562	blood:
13	chr1:246363710..246365911-chr1:246369956..246372011,2	MCF-7	breast:
14	chr1:246477291..246479573-chr1:246484385..246486637,2	K562	blood:
15	chr1:246331853..246336135-chr1:246348494..246351528,4	K562	blood:
16	chr1:246356282..246358197-chr1:246359640..246362588,2	K562	blood:
17	chr1:246323883..246327083-chr1:246329402..246331782,5	K562	blood:
18	chr1:246371493..246375018-chr1:246378492..246381970,3	MCF-7	breast:
19	chr1:246185726..246188370-chr1:246444618..246447428,2	K562	blood:
20	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
21	chr1:246389393..246391368-chr1:246392967..246394891,2	K562	blood:
22	chr1:246363848..246365407-chr1:246365927..246368390,2	K562	blood:
23	chr1:246451778..246454398-chr1:246470226..246471898,2	K562	blood:
24	chr1:246357089..246359442-chr1:246368577..246370809,2	MCF-7	breast:
25	chr1:246350132..246352497-chr1:246355470..246357930,3	K562	blood:
26	chr1:246357127..246361362-chr1:246362304..246364273,3	K562	blood:
27	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
28	chr1:246356773..246358540-chr1:246441873..246443730,2	K562	blood:
29	chr1:246346688..246348274-chr1:246353285..246354827,2	K562	blood:
30	chr1:246349359..246351191-chr1:246361403..246363953,2	K562	blood:
31	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
32	chr1:246337373..246339084-chr1:246350131..246351894,2	K562	blood:
33	chr1:246353223..246355045-chr1:246376088..246378374,2	K562	blood:
34	chr1:246385164..246386821-chr1:246393908..246395594,2	K562	blood:
35	chr1:246339928..246341615-chr1:246379189..246380773,2	K562	blood:
36	chr1:246175573..246176199-chr1:246409475..246409997,2	K562	blood:
37	chr1:246343018..246344728-chr1:246345131..246347522,2	K562	blood:
38	chr1:246327940..246330525-chr1:246331503..246335844,5	K562	blood:
39	chr1:246353361..246355066-chr1:246367112..246369364,2	K562	blood:
40	chr1:246389393..246391368-chr1:246392967..246395959,3	K562	blood:
41	chr1:246358405..246360090-chr1:246368790..246371523,2	K562	blood:
42	chr1:246359779..246363741-chr1:246364321..246369637,8	K562	blood:
43	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
44	chr1:246358405..246360090-chr1:246368790..246371523,2	K562	blood:
45	chr1:246363710..246365911-chr1:246369956..246372011,2	MCF-7	breast:
46	chr1:246314921..246318931-chr1:246320889..246326868,8	K562	blood:
47	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
48	chr1:246353223..246355045-chr1:246376088..246378374,2	K562	blood:
49	chr1:246392871..246395828-chr1:246399439..246401491,2	K562	blood:
50	chr1:246359779..246363741-chr1:246364321..246369637,8	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFB2M-2	chr1:246485586-246485740	ENSG00000230184.1
2	lnc-CNST-4	chr1:246342080-246342506	NONHSAT010702
3	lnc-TFB2M-2	chr1:246484965-246485170	ENSG00000230184.1

No data

Variant related genes	Relation type
CHCHD4P5	TF binding region
SMYD3	TF binding region
SMYD3-IT1	TF binding region
RNU6-1283P	TF binding region
CHCHD4P5	CpG island
SMYD3	CpG island
SMYD3-IT1	CpG island
RNU6-1283P	CpG island
ENSG00000230184	chromatin interactions
ENSG00000185420	chromatin interactions
ENSG00000202184	chromatin interactions

Extended variants
information (count: 7622 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:7622 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181814045	chr1:246321456-246321457	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs548965145	chr1:246321483-246321484	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs565497103	chr1:246321486-246321487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs143825146	chr1:246321558-246321559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs113906350	chr1:246321563-246321564	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs111636273	chr1:246321568-246321569	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs577790322	chr1:246321592-246321593	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs540071914	chr1:246321604-246321605	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs367651779	chr1:246321671-246321672	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs556761054	chr1:246321689-246321690	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs576830560	chr1:246321765-246321766	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs148139404	chr1:246321767-246321768	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs147335449	chr1:246321814-246321815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562123606	chr1:246321825-246321826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139964236	chr1:246321837-246321838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572705297	chr1:246321867-246321868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149829020	chr1:246321887-246321888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564453773	chr1:246321890-246321891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186409796	chr1:246321909-246321910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190463543	chr1:246321936-246321937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563095160	chr1:246321951-246321952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12038071	chr1:246321952-246321953	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549047544	chr1:246322024-246322025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57816539	chr1:246322034-246322035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183061029	chr1:246322067-246322068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551340064	chr1:246322101-246322102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186174781	chr1:246322191-246322192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369591111	chr1:246322217-246322218	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs191465794	chr1:246322222-246322223	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570223459	chr1:246322284-246322285	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs76053391	chr1:246322295-246322296	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs75943811	chr1:246322296-246322297	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs114792659	chr1:246322314-246322315	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs115495379	chr1:246322324-246322325	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs541103558	chr1:246322332-246322333	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557700137	chr1:246322340-246322341	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs182439776	chr1:246322419-246322420	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs543469025	chr1:246322421-246322422	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs563430663	chr1:246322454-246322455	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs529122974	chr1:246322472-246322473	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs148429896	chr1:246322476-246322477	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs144067562	chr1:246322477-246322478	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs564630039	chr1:246322540-246322541	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs113597276	chr1:246322554-246322555	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs551112563	chr1:246322565-246322566	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs75802944	chr1:246322578-246322579	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs530633174	chr1:246322588-246322589	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs538528083	chr1:246322624-246322625	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs562547752	chr1:246322629-246322630	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs550737646	chr1:246322732-246322733	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246277800-246327800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:246304800-246324200	Weak transcription	Primary T cells from cord blood	blood
3	chr1:246311800-246323000	Weak transcription	Lung	lung
4	chr1:246312200-246322400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:246312200-246325400	Weak transcription	Gastric	stomach
6	chr1:246312400-246322400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:246314200-246369000	Weak transcription	Aorta	Aorta
8	chr1:246315800-246324400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:246317400-246322400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:246317600-246329200	Weak transcription	Esophagus	oesophagus
11	chr1:246319400-246321600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr1:246319800-246321600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr1:246319800-246324000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:246320000-246321600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr1:246320000-246321600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:246320000-246321600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:246320000-246325000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:246320000-246325000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:246320200-246325000	Weak transcription	NH-A	brain
20	chr1:246320400-246321600	Enhancers	Primary hematopoietic stem cells	blood
21	chr1:246320400-246321600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:246320400-246321600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:246320400-246321800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr1:246320400-246321800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr1:246320400-246322200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:246320400-246324800	Weak transcription	Osteobl	bone
27	chr1:246320400-246325200	Weak transcription	NHLF	lung
28	chr1:246320600-246321600	Weak transcription	Ovary	ovary
29	chr1:246320600-246322400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr1:246320600-246324000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:246320800-246324800	Weak transcription	Spleen	Spleen
32	chr1:246321200-246322400	Weak transcription	Placenta	Placenta
33	chr1:246321200-246322600	Weak transcription	HMEC	breast
34	chr1:246321200-246324800	Weak transcription	NHDF-Ad	bronchial
35	chr1:246321400-246321600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:246321400-246321600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr1:246321400-246322600	Weak transcription	K562	blood
38	chr1:246321400-246324600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:246321400-246324600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:246321400-246324800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:246321400-246325200	Weak transcription	Adipose Nuclei	Adipose
42	chr1:246321600-246323800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:246321600-246324400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:246321600-246326400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:246321600-246327000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr1:246321600-246327000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:246321600-246344000	Weak transcription	Primary hematopoietic stem cells	blood
48	chr1:246321800-246322200	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr1:246322200-246323000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr1:246322200-246324600	Enhancers	NHEK	skin

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