Variant report

Variant	nsv1014637
Chromosome Location	chr1:174265631-174826765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3204)
CpG islands
(count:793)
Chromatin interactive
region (count:221)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3204 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174716815-174717112	K562	blood:	n/a	chr1:174716831-174716847
2	ARID3A	chr1:174810183-174810205	K562	blood:	n/a	n/a
3	ARID3A	chr1:174716791-174717117	HepG2	liver:	n/a	chr1:174716831-174716847
4	ARID3A	chr1:174651647-174652006	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:174658514-174659032	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:174396120-174396181	K562	blood:	n/a	n/a
7	ARID3A	chr1:174739150-174739460	K562	blood:	n/a	n/a
8	ARID3A	chr1:174635164-174635969	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:174661452-174661781	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:174818480-174818752	K562	blood:	n/a	n/a
11	ARID3A	chr1:174695329-174695619	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:174781657-174782212	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:174739151-174739446	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:174617608-174617676	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:174713138-174713467	K562	blood:	n/a	n/a
16	ARID3A	chr1:174382888-174383024	K562	blood:	n/a	n/a
17	ARID3A	chr1:174683012-174683217	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:174695783-174695969	K562	blood:	n/a	n/a
19	ARID3A	chr1:174688382-174688690	HepG2	liver:	n/a	n/a
20	ATF1	chr1:174768688-174769078	K562	blood:	n/a	n/a
21	ATF1	chr1:174493199-174493227	K562	blood:	n/a	n/a
22	ATF1	chr1:174769981-174770160	K562	blood:	n/a	n/a
23	ATF1	chr1:174277912-174277913	K562	blood:	n/a	n/a
24	ATF1	chr1:174823141-174823326	K562	blood:	n/a	n/a
25	ATF1	chr1:174448222-174448255	K562	blood:	n/a	n/a
26	ATF1	chr1:174618881-174619077	K562	blood:	n/a	n/a
27	ATF1	chr1:174784312-174784545	K562	blood:	n/a	n/a
28	ATF1	chr1:174715256-174715682	K562	blood:	n/a	n/a
29	ATF1	chr1:174735929-174736142	K562	blood:	n/a	n/a
30	ATF1	chr1:174428850-174428929	K562	blood:	n/a	n/a
31	ATF1	chr1:174484804-174484808	K562	blood:	n/a	n/a
32	ATF1	chr1:174397299-174397520	K562	blood:	n/a	n/a
33	ATF1	chr1:174577440-174577441	K562	blood:	n/a	n/a
34	ATF2	chr1:174768580-174769355	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr1:174758499-174758970	GM12878	blood:	n/a	n/a
36	ATF2	chr1:174367341-174367790	GM12878	blood:	n/a	n/a
37	ATF2	chr1:174758538-174758981	GM12878	blood:	n/a	n/a
38	ATF2	chr1:174768485-174769398	GM12878	blood:	n/a	n/a
39	ATF2	chr1:174768663-174769294	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr1:174784116-174785183	GM12878	blood:	n/a	n/a
41	ATF2	chr1:174787293-174787853	GM12878	blood:	n/a	n/a
42	ATF2	chr1:174784425-174785216	GM12878	blood:	n/a	n/a
43	ATF2	chr1:174768311-174769484	GM12878	blood:	n/a	n/a
44	ATF2	chr1:174755854-174756363	GM12878	blood:	n/a	n/a
45	ATF2	chr1:174367318-174367778	GM12878	blood:	n/a	n/a
46	ATF2	chr1:174810826-174811243	GM12878	blood:	n/a	n/a
47	ATF2	chr1:174810860-174811256	GM12878	blood:	n/a	n/a
48	ATF3	chr1:174649329-174649527	K562	blood:	n/a	n/a
49	ATF3	chr1:174661436-174661792	K562	blood:	n/a	n/a
50	ATF3	chr1:174784258-174784445	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174526483-174526533	ECC-1	luminal epithelium:	n/a
2	chr1:174417967-174418017	AG04449	skin:	fetal
3	chr1:174319673-174319723	IMR90	lung:	fetal
4	chr1:174680586-174680636	H1-hESC	embryonic stem cell:	embryo
5	chr1:174779911-174779961	T-47D	breast:	n/a
6	chr1:174565337-174565387	AG10803	skin:	n/a
7	chr1:174352684-174352734	GM12878	blood:	n/a
8	chr1:174769548-174769598	AG09309	skin:	n/a
9	chr1:174526483-174526533	RPTEC	kidney:	n/a
10	chr1:174526483-174526533	HIPEpiC	eye:	n/a
11	chr1:174417175-174417225	NHDF-neo	bronchial:	n/a
12	chr1:174417967-174418017	HRCEpiC	kidney:	n/a
13	chr1:174417375-174417425	GM12891	blood:	n/a
14	chr1:174417375-174417425	AoSMC	blood vessel:	n/a
15	chr1:174565337-174565387	ECC-1	luminal epithelium:	n/a
16	chr1:174417967-174418017	Jurkat	blood:	n/a
17	chr1:174680586-174680636	BJ	skin:	n/a
18	chr1:174352684-174352734	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:174417175-174417225	Hepatocyte	liver:	n/a
20	chr1:174787829-174787879	BE2_C	brain:	n/a
21	chr1:174769548-174769598	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:174787829-174787879	NT2-D1	testis:	n/a
23	chr1:174417967-174418017	HRE	kidney:	n/a
24	chr1:174680847-174680897	CMK	blood:	n/a
25	chr1:174769548-174769598	NHDF-neo	bronchial:	n/a
26	chr1:174319673-174319723	NH-A	brain:	n/a
27	chr1:174779911-174779961	SKMC	muscle:	n/a
28	chr1:174417175-174417225	SK-N-SH_RA	brain:	n/a
29	chr1:174417967-174418017	PANC-1	pancreas:	n/a
30	chr1:174565337-174565387	BE2_C	brain:	n/a
31	chr1:174417175-174417225	A549	lung:	n/a
32	chr1:174680847-174680897	Hela-S3	cervix:	n/a
33	chr1:174319673-174319723	H1-hESC	embryonic stem cell:	embryo
34	chr1:174662459-174662509	AoSMC	blood vessel:	n/a
35	chr1:174526483-174526533	NH-A	brain:	n/a
36	chr1:174526483-174526533	GM12891	blood:	n/a
37	chr1:174417375-174417425	Hela-S3	cervix:	n/a
38	chr1:174417175-174417225	NT2-D1	testis:	n/a
39	chr1:174565337-174565387	H1-hESC	embryonic stem cell:	embryo
40	chr1:174769548-174769598	PrEC	prostate:	n/a
41	chr1:174680586-174680636	HCM	heart:	n/a
42	chr1:174680847-174680897	NHDF-neo	bronchial:	n/a
43	chr1:174526483-174526533	IMR90	lung:	fetal
44	chr1:174417375-174417425	A549	lung:	n/a
45	chr1:174417967-174418017	SAEC	small airway:	n/a
46	chr1:174417375-174417425	HRPEpiC	eye:	n/a
47	chr1:174526483-174526533	GM12892	blood:	n/a
48	chr1:174662459-174662509	HIPEpiC	eye:	n/a
49	chr1:174787829-174787879	HRCEpiC	kidney:	n/a
50	chr1:174352684-174352734	NB4	blood:	n/a

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:174382438..174383401-chr1:174695381..174696315,3	MCF-7	breast:
2	chr1:174367483..174370019-chr1:174372739..174376540,3	K562	blood:
3	chr1:174766907..174768674-chr1:174967181..174969614,2	K562	blood:
4	chr1:174382494..174383374-chr1:174713222..174713791,2	MCF-7	breast:
5	chr1:174532659..174534724-chr1:174536541..174539409,2	K562	blood:
6	chr1:174743787..174746424-chr1:174752563..174755000,2	K562	blood:
7	chr1:174738634..174740164-chr1:175067816..175070617,2	K562	blood:
8	chr1:174294663..174296200-chr1:174300746..174303006,2	MCF-7	breast:
9	chr1:174821981..174824251-chr1:174829499..174831997,2	K562	blood:
10	chr1:174738859..174740087-chr1:175094536..175095080,4	K562	blood:
11	chr1:174226894..174227818-chr1:174695415..174695933,2	MCF-7	breast:
12	chr1:174775809..174777668-chr1:174781118..174782806,2	K562	blood:
13	chr1:174790254..174793205-chr1:174795715..174797901,2	K562	blood:
14	chr1:174420628..174423006-chr1:174424339..174426436,2	K562	blood:
15	chr1:174736386..174740944-chr1:174964309..174969947,11	K562	blood:
16	chr1:174527785..174529980-chr1:174530540..174532967,2	MCF-7	breast:
17	chr1:174787124..174790078-chr1:174796659..174798420,2	K562	blood:
18	chr1:174367483..174370019-chr1:174373894..174376540,2	K562	blood:
19	chr1:174743159..174744986-chr1:174753040..174755320,2	MCF-7	breast:
20	chr1:174231956..174232498-chr1:174695300..174696266,2	MCF-7	breast:
21	chr1:174740970..174743035-chr1:174745224..174747898,3	K562	blood:
22	chr1:173991563..173993480-chr1:174352055..174354802,2	K562	blood:
23	chr1:174566765..174568988-chr1:174739021..174740535,2	K562	blood:
24	chr1:174790148..174791754-chr1:174795715..174797239,2	K562	blood:
25	chr1:174328732..174330689-chr1:174332303..174334086,2	K562	blood:
26	chr1:174758880..174761152-chr1:174967654..174970317,2	MCF-7	breast:
27	chr1:174817467..174820158-chr1:174824485..174827835,3	K562	blood:
28	chr1:174737447..174741477-chr1:174966880..174970168,5	MCF-7	breast:
29	chr1:174537054..174539369-chr1:174541231..174544062,3	K562	blood:
30	chr1:174409528..174411154-chr1:174416998..174418836,2	MCF-7	breast:
31	chr1:174737035..174739319-chr1:174960271..174963005,2	K562	blood:
32	chr1:174524894..174527021-chr1:174528165..174529898,2	K562	blood:
33	chr1:174544631..174547612-chr1:174552869..174554719,2	MCF-7	breast:
34	chr1:174756924..174758922-chr1:174761115..174763759,2	K562	blood:
35	chr1:174420516..174421195-chr1:174712811..174713329,2	MCF-7	breast:
36	chr1:174447279..174449920-chr1:174453391..174456617,3	K562	blood:
37	chr1:174420323..174421165-chr1:174695373..174696419,3	MCF-7	breast:
38	chr1:174721746..174724723-chr1:174724742..174726249,2	K562	blood:
39	chr1:174382438..174383401-chr1:174695381..174696315,3	MCF-7	breast:
40	chr1:174739153..174739796-chr1:174967269..174968128,2	MCF-7	breast:
41	chr1:174692833..174695289-chr1:174700778..174702469,2	MCF-7	breast:
42	chr1:174761076..174764017-chr1:174764212..174765845,2	MCF-7	breast:
43	chr1:174292133..174293963-chr1:174301470..174303626,2	MCF-7	breast:
44	chr1:174420516..174421195-chr1:174712811..174713329,2	MCF-7	breast:
45	chr1:174412862..174415441-chr1:174418910..174422017,3	K562	blood:
46	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:
47	chr1:174420323..174421165-chr1:174695373..174696419,3	MCF-7	breast:
48	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
49	chr1:174694751..174696916-chr1:174698462..174700573,2	K562	blood:
50	chr1:174532659..174534724-chr1:174536541..174539409,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RC3H1-4	chr1:174336243-174337177	NONHSAT007733

No data

Variant related genes	Relation type
BANF1P4	TF binding region
ENSG00000237317	TF binding region
GPR52	TF binding region
NDUFAF4P4	TF binding region
RABGAP1L	TF binding region
ENSG00000266125	TF binding region
BANF1P4	CpG island
ENSG00000237317	CpG island
GPR52	CpG island
NDUFAF4P4	CpG island
RABGAP1L	CpG island
ENSG00000266125	CpG island
ENSG00000259942	chromatin interactions
ENSG00000227373	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000120333	chromatin interactions
ENSG00000203737	chromatin interactions
ENSG00000152061	chromatin interactions
ENSG00000224977	chromatin interactions
ENSG00000252552	chromatin interactions
ENSG00000231378	chromatin interactions

Extended variants
information (count: 19885 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:19885 , 50 per page) page: 1 2 3 4 5 6 7 ... 398

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548083968	chr1:174265635-174265636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567653298	chr1:174265656-174265657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536545728	chr1:174265657-174265658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554986117	chr1:174265686-174265687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113036117	chr1:174265713-174265714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537950298	chr1:174265725-174265726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557541467	chr1:174265789-174265790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577785688	chr1:174265800-174265801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575553997	chr1:174265912-174265913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115903246	chr1:174265931-174265932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553991245	chr1:174265952-174265953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544255067	chr1:174265970-174265971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574028602	chr1:174266082-174266083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542931348	chr1:174266088-174266089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562878155	chr1:174266150-174266151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112396024	chr1:174266171-174266172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs137923387	chr1:174266174-174266175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142387562	chr1:174266206-174266207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145936089	chr1:174266239-174266240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183159128	chr1:174266290-174266291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139433356	chr1:174266303-174266304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187352952	chr1:174266334-174266335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567512233	chr1:174266359-174266360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530127656	chr1:174266378-174266379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550016683	chr1:174266401-174266402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372699742	chr1:174266432-174266433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192349385	chr1:174266496-174266497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537410655	chr1:174266539-174266540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183313329	chr1:174266541-174266542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568284602	chr1:174266591-174266592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535421553	chr1:174266595-174266596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7555067	chr1:174266642-174266643	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs554046825	chr1:174266656-174266657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573837299	chr1:174266660-174266661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115264542	chr1:174266671-174266672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532304380	chr1:174266672-174266673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188660302	chr1:174266688-174266689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191635407	chr1:174266730-174266731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149643505	chr1:174266733-174266734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182824607	chr1:174266736-174266737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565260986	chr1:174266744-174266745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527822756	chr1:174266777-174266778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552418096	chr1:174266814-174266815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144373537	chr1:174266817-174266818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116107992	chr1:174266821-174266822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368979355	chr1:174266843-174266844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148776788	chr1:174266844-174266845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557044470	chr1:174266938-174266939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570290170	chr1:174267072-174267073	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376909385	chr1:174267122-174267123	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	19404257	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:3341 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174214600-174270000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:174240000-174270600	Weak transcription	Colonic Mucosa	Colon
3	chr1:174242800-174277200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr1:174243800-174275800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:174244400-174274000	Weak transcription	Fetal Heart	heart
6	chr1:174246200-174284200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr1:174249800-174270000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:174250600-174270200	Weak transcription	Psoas Muscle	Psoas
9	chr1:174251200-174275800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr1:174251400-174270000	Weak transcription	Brain Substantia Nigra	brain
11	chr1:174251400-174270000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr1:174251400-174276000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:174259400-174266400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr1:174259400-174270000	Weak transcription	Thymus	Thymus
15	chr1:174259400-174270200	Weak transcription	Gastric	stomach
16	chr1:174259600-174266600	Weak transcription	Left Ventricle	heart
17	chr1:174259600-174267000	Weak transcription	Right Ventricle	heart
18	chr1:174259600-174270000	Weak transcription	Aorta	Aorta
19	chr1:174259600-174272200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:174259600-174276200	Weak transcription	Brain Anterior Caudate	brain
21	chr1:174259600-174277800	Weak transcription	K562	blood
22	chr1:174259800-174270200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:174259800-174273800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr1:174259800-174274000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr1:174260000-174270000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr1:174260200-174266400	Weak transcription	Fetal Intestine Small	intestine
27	chr1:174260200-174269800	Weak transcription	Lung	lung
28	chr1:174260200-174270000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr1:174260200-174270000	Weak transcription	Fetal Stomach	stomach
30	chr1:174260200-174270000	Weak transcription	Ovary	ovary
31	chr1:174260200-174270000	Weak transcription	Pancreas	Pancrea
32	chr1:174260200-174270200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:174260200-174270200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:174260200-174274000	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr1:174260200-174275800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr1:174260400-174266200	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr1:174260400-174266400	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr1:174260400-174269600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr1:174260400-174269600	Weak transcription	Fetal Intestine Large	intestine
40	chr1:174260400-174269800	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr1:174260400-174270000	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr1:174260400-174270000	Weak transcription	Liver	Liver
43	chr1:174260400-174270200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr1:174260400-174270400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:174260400-174276200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr1:174260400-174277200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:174260600-174267000	Weak transcription	Duodenum Mucosa	Duodenum
48	chr1:174260600-174269600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr1:174260600-174270400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr1:174260600-174275600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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