Variant report

Variant	nsv1007237
Chromosome Location	chr1:186137724-186226502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1055)
CpG islands
(count:305)
Chromatin interactive
region (count:68)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:186164470-186165095	K562	blood:	n/a	n/a
2	ARID3A	chr1:186181744-186182021	HepG2	liver:	n/a	n/a
3	ATF1	chr1:186148236-186148436	K562	blood:	n/a	n/a
4	ATF1	chr1:186206098-186206346	K562	blood:	n/a	n/a
5	ATF1	chr1:186163269-186163597	K562	blood:	n/a	n/a
6	ATF1	chr1:186164466-186165060	K562	blood:	n/a	n/a
7	ATF2	chr1:186163525-186163835	GM12878	blood:	n/a	n/a
8	ATF2	chr1:186163575-186163895	GM12878	blood:	n/a	n/a
9	ATF3	chr1:186164451-186164924	K562	blood:	n/a	n/a
10	BACH1	chr1:186204569-186204783	K562	blood:	n/a	n/a
11	BATF	chr1:186147829-186148102	GM12878	blood:	n/a	chr1:186148011-186148021
12	BATF	chr1:186156692-186157077	GM12878	blood:	n/a	chr1:186156882-186156893
13	BATF	chr1:186163533-186163859	GM12878	blood:	n/a	chr1:186163701-186163712
14	BATF	chr1:186152289-186152642	GM12878	blood:	n/a	n/a
15	BATF	chr1:186147875-186148121	GM12878	blood:	n/a	chr1:186148011-186148021
16	BATF	chr1:186163566-186163845	GM12878	blood:	n/a	chr1:186163701-186163712
17	BATF	chr1:186152425-186152629	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:186163582-186163842	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:186163524-186163855	GM12878	blood:	n/a	n/a
20	BCL3	chr1:186201144-186201469	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:186153079-186153428	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:186163615-186163865	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:186139939-186139986	K562	blood:	n/a	n/a
24	BHLHE40	chr1:186148323-186148381	K562	blood:	n/a	n/a
25	BHLHE40	chr1:186214090-186214244	K562	blood:	n/a	n/a
26	BHLHE40	chr1:186164432-186165198	K562	blood:	n/a	n/a
27	BHLHE40	chr1:186156946-186157042	K562	blood:	n/a	n/a
28	CBX3	chr1:186149566-186149873	K562	blood:	n/a	n/a
29	CBX3	chr1:186205915-186206625	HCT-116	colon:	n/a	n/a
30	CBX3	chr1:186156598-186157974	HCT-116	colon:	n/a	n/a
31	CBX3	chr1:186164398-186165033	K562	blood:	n/a	n/a
32	CBX3	chr1:186163914-186164940	K562	blood:	n/a	n/a
33	CBX3	chr1:186163883-186164338	K562	blood:	n/a	n/a
34	CBX3	chr1:186163174-186163848	K562	blood:	n/a	n/a
35	CCNT2	chr1:186164491-186165138	K562	blood:	n/a	n/a
36	CEBPB	chr1:186179426-186179675	K562	blood:	n/a	chr1:186179554-186179565 chr1:186179553-186179566
37	CEBPB	chr1:186144807-186145109	HepG2	liver:	n/a	chr1:186144958-186144969
38	CEBPB	chr1:186206046-186206420	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:186153480-186153748	Hela-S3	cervix:	n/a	chr1:186153623-186153640
40	CEBPB	chr1:186156987-186157735	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:186179387-186179665	HepG2	liver:	n/a	chr1:186179554-186179565 chr1:186179553-186179566
42	CEBPB	chr1:186144922-186144992	Hela-S3	cervix:	n/a	chr1:186144958-186144969
43	CEBPB	chr1:186152356-186152821	HCT-116	colon:	n/a	n/a
44	CEBPB	chr1:186181706-186182095	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:186144833-186145062	A549	lung:	n/a	chr1:186144958-186144969
46	CEBPB	chr1:186152339-186152773	A549	lung:	n/a	n/a
47	CEBPB	chr1:186157386-186157754	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr1:186164362-186164947	K562	blood:	n/a	n/a
49	CEBPB	chr1:186148061-186148379	K562	blood:	n/a	n/a
50	CEBPB	chr1:186144805-186145117	K562	blood:	n/a	chr1:186144958-186144969

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:186175774-186175824	ECC-1	luminal epithelium:	n/a
2	chr1:186162050-186162100	HRCEpiC	kidney:	n/a
3	chr1:186159350-186159400	NHBE	bronchial:	n/a
4	chr1:186157555-186157605	HAEpiC	amniotic membrane:	n/a
5	chr1:186159350-186159400	HRCEpiC	kidney:	n/a
6	chr1:186162050-186162100	SK-N-MC	brain:	n/a
7	chr1:186159350-186159400	HepG2	liver:	n/a
8	chr1:186175774-186175824	U87	brain:	n/a
9	chr1:186159350-186159400	K562	blood:	n/a
10	chr1:186159350-186159400	MCF-7	breast:	n/a
11	chr1:186159350-186159400	SKMC	muscle:	n/a
12	chr1:186162050-186162100	GM19239	blood:	n/a
13	chr1:186177165-186177215	HEK293	kidney:	embryo
14	chr1:186157555-186157605	NH-A	brain:	n/a
15	chr1:186157555-186157605	Jurkat	blood:	n/a
16	chr1:186177165-186177215	MCF-7	breast:	n/a
17	chr1:186175774-186175824	NT2-D1	testis:	n/a
18	chr1:186159350-186159400	AG09309	skin:	n/a
19	chr1:186159350-186159400	NHDF-neo	bronchial:	n/a
20	chr1:186177165-186177215	HIPEpiC	eye:	n/a
21	chr1:186162050-186162100	Hepatocyte	liver:	n/a
22	chr1:186175774-186175824	HRE	kidney:	n/a
23	chr1:186159350-186159400	AoSMC	blood vessel:	n/a
24	chr1:186162050-186162100	NH-A	brain:	n/a
25	chr1:186159350-186159400	RPTEC	kidney:	n/a
26	chr1:186177165-186177215	HUVEC	blood vessel:	n/a
27	chr1:186159350-186159400	Hepatocyte	liver:	n/a
28	chr1:186177165-186177215	A549	lung:	n/a
29	chr1:186175774-186175824	K562	blood:	n/a
30	chr1:186159350-186159400	H1-hESC	embryonic stem cell:	embryo
31	chr1:186157555-186157605	H1-hESC	embryonic stem cell:	embryo
32	chr1:186157555-186157605	SK-N-SH_RA	brain:	n/a
33	chr1:186162050-186162100	MCF-7	breast:	n/a
34	chr1:186157555-186157605	HMEC	breast:	n/a
35	chr1:186175774-186175824	H1-hESC	embryonic stem cell:	embryo
36	chr1:186159350-186159400	HAEpiC	amniotic membrane:	n/a
37	chr1:186177165-186177215	CMK	blood:	n/a
38	chr1:186175774-186175824	BJ	skin:	n/a
39	chr1:186157555-186157605	HRPEpiC	eye:	n/a
40	chr1:186157555-186157605	NHDF-neo	bronchial:	n/a
41	chr1:186175774-186175824	AG09319	gingival:	n/a
42	chr1:186162050-186162100	AG10803	skin:	n/a
43	chr1:186177165-186177215	SK-N-SH	brain:	n/a
44	chr1:186162050-186162100	GM06990	blood:	n/a
45	chr1:186157555-186157605	GM19239	blood:	n/a
46	chr1:186177165-186177215	H1-hESC	embryonic stem cell:	embryo
47	chr1:186175774-186175824	ovcar-3	ovarian:	n/a
48	chr1:186175774-186175824	GM12878	blood:	n/a
49	chr1:186162050-186162100	PANC-1	pancreas:	n/a
50	chr1:186162050-186162100	HEEpiC	esophagus:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:186156618..186158956-chr1:186211856..186214828,2	MCF-7	breast:
2	chr1:186148276..186150071-chr1:186151136..186154406,3	MCF-7	breast:
3	chr1:186148276..186150071-chr1:186151136..186154406,3	MCF-7	breast:
4	chr1:186187914..186190760-chr1:186196544..186198970,2	MCF-7	breast:
5	chr1:186096850..186099197-chr1:186175663..186177778,2	MCF-7	breast:
6	chr1:186152958..186154907-chr1:186156624..186160486,3	K562	blood:
7	chr1:186146345..186149254-chr1:186156186..186157868,2	MCF-7	breast:
8	chr1:186163396..186166003-chr1:186180456..186181975,2	K562	blood:
9	chr1:185649957..185650829-chr1:186181415..186182551,4	MCF-7	breast:
10	chr1:186177265..186179469-chr1:186180273..186181904,2	MCF-7	breast:
11	chr1:186124564..186125385-chr1:186181815..186182420,2	K562	blood:
12	chr1:185782674..185783372-chr1:186181707..186182270,2	MCF-7	breast:
13	chr1:186138357..186140135-chr1:186140794..186142310,2	MCF-7	breast:
14	chr1:186123615..186126375-chr1:186164064..186165601,2	MCF-7	breast:
15	chr1:186193990..186196724-chr1:186199808..186201349,2	K562	blood:
16	chr1:186149621..186151252-chr1:186152993..186154563,2	K562	blood:
17	chr1:186196248..186199242-chr1:186200494..186202096,2	K562	blood:
18	chr1:186120755..186125088-chr1:186200720..186204325,6	MCF-7	breast:
19	chr1:185689564..185690516-chr1:186181513..186182292,3	MCF-7	breast:
20	chr1:186048997..186051706-chr1:186197290..186199226,2	K562	blood:
21	chr1:186121917..186122845-chr1:186201039..186202141,3	MCF-7	breast:
22	chr1:185782207..185784224-chr1:186141376..186143598,2	MCF-7	breast:
23	chr1:185284673..185286716-chr1:186197993..186200205,2	MCF-7	breast:
24	chr1:186163396..186166003-chr1:186180456..186181975,2	K562	blood:
25	chr1:186196478..186198082-chr1:186200897..186203093,2	MCF-7	breast:
26	chr1:185782229..185782806-chr1:186181471..186182170,3	K562	blood:
27	chr1:186215823..186217650-chr1:186219942..186222008,2	K562	blood:
28	chr1:185975804..185978755-chr1:186156792..186158359,2	MCF-7	breast:
29	chr1:185782255..185783272-chr1:186181370..186182154,4	MCF-7	breast:
30	chr1:186193196..186195433-chr12:120730117..120732240,2	MCF-7	breast:
31	chr1:186162031..186163745-chr1:186166331..186169038,2	MCF-7	breast:
32	chr1:186209219..186212126-chr1:186214924..186216938,2	MCF-7	breast:
33	chr1:186195416..186198253-chr1:186344477..186346582,2	K562	blood:
34	chr1:186177265..186179469-chr1:186180273..186181904,2	MCF-7	breast:
35	chr1:185689319..185692155-chr1:186180753..186183476,2	MCF-7	breast:
36	chr1:186156618..186158956-chr1:186211856..186214828,2	MCF-7	breast:
37	chr1:186138817..186141455-chr1:186147158..186149563,2	MCF-7	breast:
38	chr1:186124541..186125379-chr1:186181423..186182257,5	MCF-7	breast:
39	chr1:186144068..186146572-chr1:186148557..186150337,3	K562	blood:
40	chr1:186139865..186142101-chr1:186144863..186146945,2	K562	blood:
41	chr1:186196248..186199242-chr1:186200494..186202096,2	K562	blood:
42	chr1:186138357..186140135-chr1:186140794..186142310,2	MCF-7	breast:
43	chr1:186196478..186198082-chr1:186200897..186203093,2	MCF-7	breast:
44	chr1:186162031..186163745-chr1:186166331..186169038,2	MCF-7	breast:
45	chr1:186197416..186201292-chr1:186202438..186207046,5	K562	blood:
46	chr1:186139865..186142101-chr1:186144863..186146945,2	K562	blood:
47	chr1:186157994..186159538-chr1:186169856..186171398,2	MCF-7	breast:
48	chr1:186152958..186154907-chr1:186156624..186160486,3	K562	blood:
49	chr1:185689629..185690434-chr1:186181457..186182167,3	K562	blood:
50	chr1:186197416..186201292-chr1:186202438..186207046,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPR-1	chr1:186146177-186146434	ENSG00000224691.1
2	lnc-TPR-1	chr1:186145946-186146040	ENSG00000224691.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HMCN1	hsa-miR-335-5p	chr1:186159069-186159092

Variant related genes	Relation type
HMCN1	TF binding region
ENSG00000224691	TF binding region
HMCN1	CpG island
ENSG00000224691	CpG island
ENSG00000047410	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000157181	chromatin interactions
ENSG00000224691	chromatin interactions
ENSG00000143341	chromatin interactions
ENSG00000116679	chromatin interactions

Extended variants
information (count: 2842 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2842 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6672327	chr1:186137724-186137725	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200173458	chr1:186137743-186137744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538718628	chr1:186137759-186137760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554959610	chr1:186137777-186137778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573444669	chr1:186137792-186137793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375660951	chr1:186137797-186137798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368958873	chr1:186137808-186137809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540542425	chr1:186137828-186137829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147192615	chr1:186137856-186137857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs180854373	chr1:186137892-186137893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531554305	chr1:186137899-186137900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76229657	chr1:186137908-186137909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544287084	chr1:186137928-186137929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377175195	chr1:186137945-186137946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563041824	chr1:186137947-186137948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536505084	chr1:186137959-186137960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529848145	chr1:186138003-186138004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140548319	chr1:186138011-186138012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567689334	chr1:186138051-186138052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144473865	chr1:186138101-186138102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147851347	chr1:186138110-186138111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34758823	chr1:186138122-186138123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552518827	chr1:186138173-186138174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556898283	chr1:186138176-186138177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184198924	chr1:186138177-186138178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139007687	chr1:186138217-186138218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556402025	chr1:186138257-186138258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61831352	chr1:186138263-186138264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568193980	chr1:186138302-186138303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539356536	chr1:186138361-186138362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190697550	chr1:186138372-186138373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201913865	chr1:186138460-186138461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182251258	chr1:186138462-186138463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566745621	chr1:186138533-186138534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7552106	chr1:186138555-186138556	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs113090437	chr1:186138558-186138559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576820784	chr1:186138607-186138608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544247905	chr1:186138621-186138622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs56174211	chr1:186138655-186138656	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs574836373	chr1:186138703-186138704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541972951	chr1:186138835-186138836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560263577	chr1:186138851-186138852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190816842	chr1:186138860-186138861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376907765	chr1:186138866-186138867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56267286	chr1:186138904-186138905	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs541035641	chr1:186138964-186138965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564413664	chr1:186139010-186139011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373191436	chr1:186139012-186139013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531329134	chr1:186139016-186139017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549701752	chr1:186139035-186139036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	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
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186114600-186160800	Weak transcription	Fetal Kidney	kidney
2	chr1:186133600-186160800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:186133800-186147800	Weak transcription	Left Ventricle	heart
4	chr1:186134600-186139600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:186134600-186152200	Weak transcription	NH-A	brain
6	chr1:186134800-186139800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:186134800-186147000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:186135000-186146400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:186135000-186147800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:186136200-186138000	Weak transcription	Lung	lung
11	chr1:186136200-186152400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:186136200-186153200	Weak transcription	Fetal Lung	lung
13	chr1:186136200-186157600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:186136800-186157000	Weak transcription	Aorta	Aorta
15	chr1:186137000-186152800	Weak transcription	Liver	Liver
16	chr1:186137200-186152000	Weak transcription	Adipose Nuclei	Adipose
17	chr1:186137400-186138200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:186138200-186144400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:186138800-186144600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:186139200-186147600	Weak transcription	NHDF-Ad	bronchial
21	chr1:186139600-186140400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:186139800-186140200	Enhancers	Right Atrium	heart
23	chr1:186139800-186140600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:186140200-186148000	Weak transcription	Right Atrium	heart
25	chr1:186140400-186144400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:186140600-186144200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:186141400-186145800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr1:186144200-186144400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:186144400-186145000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:186144400-186145000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr1:186144400-186145400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:186144400-186145400	Enhancers	HMEC	breast
33	chr1:186144400-186145600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:186144400-186145800	Enhancers	NHEK	skin
35	chr1:186144600-186145000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:186145000-186145600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:186145000-186147800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:186145000-186158400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr1:186145400-186147000	Weak transcription	HMEC	breast
40	chr1:186145400-186151200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:186145600-186146000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:186145600-186147000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:186145800-186147200	Weak transcription	NHEK	skin
44	chr1:186146000-186147400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:186146400-186146600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:186146600-186147000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:186147000-186148400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:186147000-186148600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:186147000-186148800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:186147000-186148800	Enhancers	HMEC	breast

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