Variant report

Variant	nsv515510
Chromosome Location	chr1:246319482-246386134
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1029)
CpG islands
(count:488)
Chromatin interactive
region (count:87)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr1:246332132-246332717	K562	blood:	n/a	n/a
3	ARID3A	chr1:246378134-246379212	K562	blood:	n/a	n/a
4	ARID3A	chr1:246340416-246340426	K562	blood:	n/a	n/a
5	ARID3A	chr1:246329377-246329956	K562	blood:	n/a	n/a
6	ARID3A	chr1:246378433-246378571	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:246333485-246334689	K562	blood:	n/a	n/a
8	ARID3A	chr1:246364034-246364381	K562	blood:	n/a	n/a
9	ARID3A	chr1:246351102-246351709	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:246351173-246351659	K562	blood:	n/a	n/a
11	ARID3A	chr1:246339570-246339954	K562	blood:	n/a	n/a
12	ARID3A	chr1:246345414-246346141	K562	blood:	n/a	n/a
13	ARID3A	chr1:246339492-246340117	HepG2	liver:	n/a	n/a
14	ATF1	chr1:246378205-246378667	K562	blood:	n/a	n/a
15	ATF1	chr1:246376288-246376805	K562	blood:	n/a	n/a
16	ATF1	chr1:246333942-246334272	K562	blood:	n/a	n/a
17	ATF1	chr1:246329490-246330061	K562	blood:	n/a	n/a
18	ATF1	chr1:246370614-246370654	K562	blood:	n/a	n/a
19	ATF1	chr1:246332388-246332644	K562	blood:	n/a	n/a
20	ATF1	chr1:246345391-246346206	K562	blood:	n/a	n/a
21	ATF1	chr1:246363474-246363487	K562	blood:	n/a	n/a
22	ATF2	chr1:246378108-246378612	GM12878	blood:	n/a	n/a
23	ATF2	chr1:246378137-246378580	GM12878	blood:	n/a	n/a
24	ATF3	chr1:246378129-246378678	K562	blood:	n/a	n/a
25	BACH1	chr1:246329773-246329841	K562	blood:	n/a	n/a
26	BACH1	chr1:246383042-246383141	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr1:246319997-246320403	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr1:246351235-246351409	K562	blood:	n/a	n/a
29	BACH1	chr1:246378344-246378673	K562	blood:	n/a	n/a
30	BACH1	chr1:246330166-246330170	K562	blood:	n/a	n/a
31	BACH1	chr1:246364134-246364441	K562	blood:	n/a	n/a
32	BACH1	chr1:246320102-246320303	K562	blood:	n/a	n/a
33	BACH1	chr1:246345481-246345569	K562	blood:	n/a	n/a
34	BATF	chr1:246378240-246378549	GM12878	blood:	n/a	n/a
35	BATF	chr1:246378267-246378548	GM12878	blood:	n/a	n/a
36	BATF	chr1:246335864-246336205	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:246378236-246378598	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:246378302-246378519	GM12878	blood:	n/a	n/a
39	BCL3	chr1:246363416-246363803	GM12878	blood:	n/a	n/a
40	BCL3	chr1:246363403-246363824	GM12878	blood:	n/a	n/a
41	BCLAF1	chr1:246378155-246378681	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:246329378-246329918	K562	blood:	n/a	n/a
43	BHLHE40	chr1:246350195-246350531	K562	blood:	n/a	n/a
44	BHLHE40	chr1:246345487-246345852	K562	blood:	n/a	n/a
45	BHLHE40	chr1:246344600-246344773	K562	blood:	n/a	n/a
46	BHLHE40	chr1:246383064-246383373	HepG2	liver:	n/a	n/a
47	BHLHE40	chr1:246377992-246378738	K562	blood:	n/a	n/a
48	BHLHE40	chr1:246339707-246340060	HepG2	liver:	n/a	n/a
49	BHLHE40	chr1:246338246-246338277	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:246378250-246378658	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246370933-246370983	Caco-2	colon:	n/a
2	chr1:246363574-246363624	HNPCEpiC	eye:	n/a
3	chr1:246324811-246324861	H1-hESC	embryonic stem cell:	embryo
4	chr1:246324811-246324861	BJ	skin:	n/a
5	chr1:246363660-246363710	AG09309	skin:	n/a
6	chr1:246363574-246363624	HRCEpiC	kidney:	n/a
7	chr1:246324811-246324861	PANC-1	pancreas:	n/a
8	chr1:246320475-246320525	Hepatocyte	liver:	n/a
9	chr1:246378510-246378560	IMR90	lung:	fetal
10	chr1:246320475-246320525	HRE	kidney:	n/a
11	chr1:246363697-246363747	MCF10A-Er-Src	breast:	n/a
12	chr1:246383021-246383071	Caco-2	colon:	n/a
13	chr1:246363697-246363747	NH-A	brain:	n/a
14	chr1:246383021-246383071	HRPEpiC	eye:	n/a
15	chr1:246320475-246320525	H1-hESC	embryonic stem cell:	embryo
16	chr1:246320475-246320525	NB4	blood:	n/a
17	chr1:246378510-246378560	HEEpiC	esophagus:	n/a
18	chr1:246363697-246363747	HCPEpiC	choroid plexus:	n/a
19	chr1:246370933-246370983	HCT-116	colon:	n/a
20	chr1:246378510-246378560	NT2-D1	testis:	n/a
21	chr1:246363660-246363710	MCF10A-Er-Src	breast:	n/a
22	chr1:246383021-246383071	SK-N-SH	brain:	n/a
23	chr1:246363660-246363710	GM12892	blood:	n/a
24	chr1:246324811-246324861	AG04450	lung:	fetal
25	chr1:246378510-246378560	NB4	blood:	n/a
26	chr1:246363697-246363747	PFSK-1	brain:	n/a
27	chr1:246363660-246363710	BJ	skin:	n/a
28	chr1:246363574-246363624	HepG2	liver:	n/a
29	chr1:246363660-246363710	BE2_C	brain:	n/a
30	chr1:246324811-246324861	U87	brain:	n/a
31	chr1:246324811-246324861	SKMC	muscle:	n/a
32	chr1:246383021-246383071	GM12892	blood:	n/a
33	chr1:246370933-246370983	NB4	blood:	n/a
34	chr1:246383021-246383071	K562	blood:	n/a
35	chr1:246320475-246320525	LNCaP	prostate:	n/a
36	chr1:246378510-246378560	PrEC	prostate:	n/a
37	chr1:246363697-246363747	HNPCEpiC	eye:	n/a
38	chr1:246370933-246370983	A549	lung:	n/a
39	chr1:246324811-246324861	RPTEC	kidney:	n/a
40	chr1:246370933-246370983	HEEpiC	esophagus:	n/a
41	chr1:246383021-246383071	HRCEpiC	kidney:	n/a
42	chr1:246383021-246383071	HCF	heart:	n/a
43	chr1:246320475-246320525	CMK	blood:	n/a
44	chr1:246363697-246363747	HIPEpiC	eye:	n/a
45	chr1:246324811-246324861	K562	blood:	n/a
46	chr1:246378510-246378560	BE2_C	brain:	n/a
47	chr1:246324811-246324861	HRCEpiC	kidney:	n/a
48	chr1:246363574-246363624	GM06990	blood:	n/a
49	chr1:246363697-246363747	ECC-1	luminal epithelium:	n/a
50	chr1:246378510-246378560	A549	lung:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:246259009..246261177-chr1:246350968..246353474,2	K562	blood:
2	chr1:246339928..246341615-chr1:246379189..246380773,2	K562	blood:
3	chr1:246371493..246375018-chr1:246378492..246381970,3	MCF-7	breast:
4	chr1:246377070..246379889-chr1:246380725..246383126,2	MCF-7	breast:
5	chr1:246350132..246352497-chr1:246355470..246357930,3	K562	blood:
6	chr1:246337373..246339084-chr1:246350131..246351894,2	K562	blood:
7	chr1:246358405..246360090-chr1:246368790..246371523,2	K562	blood:
8	chr1:246359779..246363741-chr1:246364321..246369637,8	K562	blood:
9	chr1:246357127..246361362-chr1:246362304..246364273,3	K562	blood:
10	chr1:246327940..246330525-chr1:246331503..246335844,5	K562	blood:
11	chr1:246353361..246355066-chr1:246367112..246369364,2	K562	blood:
12	chr1:246313570..246315182-chr1:246317792..246320324,2	K562	blood:
13	chr1:246383754..246387049-chr1:246387673..246391431,4	K562	blood:
14	chr1:246331480..246334124-chr1:246374874..246378179,3	K562	blood:
15	chr1:246349919..246351757-chr1:246469177..246472168,2	K562	blood:
16	chr1:246303120..246308295-chr1:246314639..246320743,10	K562	blood:
17	chr1:246339516..246341539-chr1:246347667..246350231,2	K562	blood:
18	chr1:246363848..246365407-chr1:246365927..246368390,2	K562	blood:
19	chr1:246377128..246379304-chr1:246383039..246386771,4	K562	blood:
20	chr1:246343018..246344728-chr1:246345131..246347522,2	K562	blood:
21	chr1:246353361..246355066-chr1:246367112..246369364,2	K562	blood:
22	chr1:246331255..246333673-chr1:246367321..246369174,2	K562	blood:
23	chr1:246385164..246386821-chr1:246393908..246395594,2	K562	blood:
24	chr1:246314921..246318931-chr1:246320889..246326868,8	K562	blood:
25	chr1:246318198..246320733-chr1:246329438..246331827,2	K562	blood:
26	chr1:246363710..246365911-chr1:246369956..246372011,2	MCF-7	breast:
27	chr1:246346688..246348274-chr1:246353285..246354827,2	K562	blood:
28	chr1:246361048..246363741-chr1:246366833..246369637,3	K562	blood:
29	chr1:246175301..246176197-chr1:246366037..246366781,3	MCF-7	breast:
30	chr1:246330748..246332762-chr1:246362456..246364545,2	K562	blood:
31	chr1:246331480..246335528-chr1:246374874..246378179,5	K562	blood:
32	chr1:246356282..246358197-chr1:246359640..246362588,2	K562	blood:
33	chr1:246357089..246359442-chr1:246368577..246370809,2	MCF-7	breast:
34	chr1:246289069..246291889-chr1:246319993..246322054,2	K562	blood:
35	chr1:246358405..246360090-chr1:246368790..246371523,2	K562	blood:
36	chr1:246377128..246379304-chr1:246383039..246386771,4	K562	blood:
37	chr1:246303201..246305225-chr1:246319673..246321317,2	MCF-7	breast:
38	chr1:246339516..246341539-chr1:246347667..246350231,2	K562	blood:
39	chr1:246333304..246334819-chr1:246336998..246339159,2	K562	blood:
40	chr1:246345857..246348884-chr1:246378191..246381575,3	K562	blood:
41	chr1:246325662..246328463-chr1:246355771..246358059,2	K562	blood:
42	chr1:246346688..246348274-chr1:246353285..246354827,2	K562	blood:
43	chr1:246349442..246351799-chr1:246370064..246372967,2	K562	blood:
44	chr1:246318198..246320733-chr1:246329438..246331827,2	K562	blood:
45	chr1:246356574..246358892-chr1:246371653..246374292,2	K562	blood:
46	chr1:246344344..246347615-chr1:246349712..246352735,4	K562	blood:
47	chr1:246316166..246317895-chr1:246320248..246322834,2	MCF-7	breast:
48	chr1:246331255..246333673-chr1:246367321..246369174,2	K562	blood:
49	chr1:246342636..246345247-chr1:246351643..246353293,2	K562	blood:
50	chr1:246377070..246379889-chr1:246380725..246383126,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNST-4	chr1:246342080-246342506	NONHSAT010702

No data

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

Extended variants
information (count: 2891 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2891 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4654092	chr1:246319482-246319483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552587693	chr1:246319489-246319490	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs555420659	chr1:246319562-246319563	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs188622637	chr1:246319657-246319658	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs112368894	chr1:246319660-246319661	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554806951	chr1:246319684-246319685	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs574644533	chr1:246319758-246319759	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs533737021	chr1:246319766-246319767	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs554082155	chr1:246319784-246319785	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs76521091	chr1:246319785-246319786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs192573136	chr1:246319789-246319790	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs144919931	chr1:246319794-246319795	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs376444709	chr1:246319836-246319837	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs138634966	chr1:246319870-246319871	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs534921330	chr1:246319873-246319874	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs113428444	chr1:246319886-246319887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs10924523	chr1:246319900-246319901	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs540446573	chr1:246319949-246319950	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs560873469	chr1:246319977-246319978	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs184421386	chr1:246319986-246319987	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs552623380	chr1:246320006-246320007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371180119	chr1:246320033-246320034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531851841	chr1:246320036-246320037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111280794	chr1:246320037-246320038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568457412	chr1:246320062-246320063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77300093	chr1:246320076-246320077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553671044	chr1:246320126-246320127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577802890	chr1:246320151-246320152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75023968	chr1:246320163-246320164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539321450	chr1:246320172-246320173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555746072	chr1:246320181-246320182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374592234	chr1:246320259-246320260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535573468	chr1:246320292-246320293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34996644	chr1:246320304-246320305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143536686	chr1:246320323-246320324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148329461	chr1:246320331-246320332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572028284	chr1:246320347-246320348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375256539	chr1:246320348-246320349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188975725	chr1:246320389-246320390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143069598	chr1:246320416-246320417	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs532841158	chr1:246320430-246320431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs192284498	chr1:246320461-246320462	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs184709271	chr1:246320553-246320554	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs531784873	chr1:246320646-246320647	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs548580723	chr1:246320677-246320678	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs149719399	chr1:246320696-246320697	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs568576330	chr1:246320720-246320721	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs561755472	chr1:246320763-246320764	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs529201715	chr1:246320832-246320833	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs77620137	chr1:246320852-246320853	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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

Chromatin state (count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr1:246306600-246320000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:246309200-246319800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr1:246311800-246323000	Weak transcription	Lung	lung
6	chr1:246312200-246319600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:246312200-246320200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:246312200-246322400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:246312200-246325400	Weak transcription	Gastric	stomach
10	chr1:246312400-246322400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:246312800-246321200	Weak transcription	Primary B cells from cord blood	blood
12	chr1:246314200-246369000	Weak transcription	Aorta	Aorta
13	chr1:246315600-246320200	Weak transcription	Spleen	Spleen
14	chr1:246315800-246319600	Weak transcription	NHLF	lung
15	chr1:246315800-246319800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:246315800-246320200	Weak transcription	Ovary	ovary
17	chr1:246315800-246324400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:246316600-246320400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr1:246317400-246322400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:246317600-246320000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:246317600-246329200	Weak transcription	Esophagus	oesophagus
22	chr1:246317800-246319800	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr1:246318000-246319600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:246318000-246320000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:246318000-246320400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr1:246318000-246320400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:246318000-246321400	Enhancers	K562	blood
28	chr1:246318400-246321400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:246318600-246321400	Enhancers	Adipose Nuclei	Adipose
30	chr1:246319000-246320800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr1:246319000-246321400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:246319200-246319600	Enhancers	GM12878-XiMat	blood
33	chr1:246319200-246319800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:246319200-246320000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:246319200-246320400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:246319200-246320400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr1:246319200-246320400	Enhancers	HUVEC	blood vessel
38	chr1:246319200-246320400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr1:246319200-246320600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:246319200-246321200	Enhancers	NHDF-Ad	bronchial
41	chr1:246319400-246320000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:246319400-246320200	Enhancers	NH-A	brain
43	chr1:246319400-246320400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:246319400-246320400	Enhancers	Osteobl	bone
45	chr1:246319400-246321600	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr1:246319600-246320000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:246319600-246320000	Enhancers	Hela-S3	cervix
48	chr1:246319600-246320000	Enhancers	HSMM	muscle
49	chr1:246319600-246320400	Enhancers	NHLF	lung
50	chr1:246319600-246320600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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