Variant report

Variant	nsv604775
Chromosome Location	chr6:140948427-141219060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1276)
CpG islands
(count:122)
Chromatin interactive
region (count:46)
LncRNA
region (count:14)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1276 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:141178980-141179277	K562	blood:	n/a	n/a
2	ATF1	chr6:141057542-141057722	K562	blood:	n/a	n/a
3	ATF1	chr6:141218607-141218807	K562	blood:	n/a	n/a
4	ATF1	chr6:141095400-141095672	K562	blood:	n/a	n/a
5	ATF1	chr6:141032327-141032490	K562	blood:	n/a	n/a
6	ATF2	chr6:141095241-141095760	GM12878	blood:	n/a	n/a
7	ATF2	chr6:141130657-141131259	GM12878	blood:	n/a	n/a
8	ATF2	chr6:140962459-140962964	GM12878	blood:	n/a	n/a
9	ATF2	chr6:141130615-141131385	GM12878	blood:	n/a	n/a
10	ATF2	chr6:141095239-141095755	GM12878	blood:	n/a	n/a
11	BACH1	chr6:141066206-141066385	K562	blood:	n/a	n/a
12	BACH1	chr6:141066249-141066420	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr6:141095289-141095760	GM12878	blood:	n/a	chr6:141095560-141095570 chr6:141095559-141095570
14	BATF	chr6:140962532-140962960	GM12878	blood:	n/a	n/a
15	BATF	chr6:141095303-141095730	GM12878	blood:	n/a	chr6:141095560-141095570 chr6:141095559-141095570
16	BATF	chr6:141130673-141131290	GM12878	blood:	n/a	n/a
17	BATF	chr6:140962571-140962917	GM12878	blood:	n/a	n/a
18	BATF	chr6:141065980-141066438	GM12878	blood:	n/a	chr6:141066245-141066256
19	BATF	chr6:141066029-141066341	GM12878	blood:	n/a	chr6:141066245-141066256
20	BATF	chr6:141179510-141179919	GM12878	blood:	n/a	n/a
21	BATF	chr6:140999274-140999525	GM12878	blood:	n/a	n/a
22	BATF	chr6:140957343-140957787	GM12878	blood:	n/a	n/a
23	BATF	chr6:141130703-141131094	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:141130716-141131254	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:141130675-141131273	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:140962597-140962976	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:141095314-141095662	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
28	BCL11A	chr6:141095345-141095639	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
29	BCL11A	chr6:140962665-140962965	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:140957373-140957725	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:141079725-141079897	GM12878	blood:	n/a	n/a
32	BCL3	chr6:141130776-141131187	GM12878	blood:	n/a	n/a
33	BCL3	chr6:141095338-141095693	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
34	BCLAF1	chr6:140957284-140957740	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:141130632-141131257	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:141095199-141095818	GM12878	blood:	n/a	chr6:141095559-141095568 chr6:141095558-141095567
37	BHLHE40	chr6:140962545-140962966	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:141178965-141179291	K562	blood:	n/a	n/a
39	BHLHE40	chr6:141179621-141179991	K562	blood:	n/a	n/a
40	BHLHE40	chr6:141032530-141032747	GM12878	blood:	n/a	n/a
41	BHLHE40	chr6:141218694-141218754	K562	blood:	n/a	n/a
42	CBX3	chr6:140948115-140948497	K562	blood:	n/a	n/a
43	CBX3	chr6:141095286-141095712	HCT-116	colon:	n/a	n/a
44	CBX3	chr6:141068268-141068538	K562	blood:	n/a	n/a
45	CBX3	chr6:141089349-141089584	K562	blood:	n/a	n/a
46	CCNT2	chr6:141006502-141006618	K562	blood:	n/a	n/a
47	CEBPB	chr6:141178787-141179735	IMR90	lung:	n/a	chr6:141179299-141179310 chr6:141178917-141178930 chr6:141179300-141179311 chr6:141179299-141179312 chr6:141179299-141179312 chr6:141179299-141179310 chr6:141179357-141179368
48	CEBPB	chr6:141179179-141179486	A549	lung:	n/a	chr6:141179299-141179310 chr6:141179300-141179311 chr6:141179299-141179312 chr6:141179299-141179312 chr6:141179299-141179310 chr6:141179357-141179368
49	CEBPB	chr6:141218598-141218858	K562	blood:	n/a	n/a
50	CEBPB	chr6:140992588-140992943	HepG2	liver:	n/a	chr6:140992865-140992876

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:141167819-141167869	SAEC	small airway:	n/a
2	chr6:141167819-141167869	HRE	kidney:	n/a
3	chr6:141167819-141167869	AG04450	lung:	fetal
4	chr6:140957775-140957825	HCF	heart:	n/a
5	chr6:140957775-140957825	AG09319	gingival:	n/a
6	chr6:141167819-141167869	BE2_C	brain:	n/a
7	chr6:140957775-140957825	GM19239	blood:	n/a
8	chr6:140957775-140957825	SAEC	small airway:	n/a
9	chr6:141167819-141167869	PrEC	prostate:	n/a
10	chr6:141167819-141167869	NT2-D1	testis:	n/a
11	chr6:141167819-141167869	GM12878	blood:	n/a
12	chr6:140957775-140957825	Hepatocyte	liver:	n/a
13	chr6:140957775-140957825	GM12892	blood:	n/a
14	chr6:140957775-140957825	HEEpiC	esophagus:	n/a
15	chr6:141167819-141167869	HL-60	blood:	n/a
16	chr6:141167819-141167869	HRCEpiC	kidney:	n/a
17	chr6:140957775-140957825	AG09309	skin:	n/a
18	chr6:141167819-141167869	K562	blood:	n/a
19	chr6:141167819-141167869	GM06990	blood:	n/a
20	chr6:140957775-140957825	H1-hESC	embryonic stem cell:	embryo
21	chr6:141167819-141167869	ECC-1	luminal epithelium:	n/a
22	chr6:140957775-140957825	PrEC	prostate:	n/a
23	chr6:141167819-141167869	PANC-1	pancreas:	n/a
24	chr6:140957775-140957825	CMK	blood:	n/a
25	chr6:141167819-141167869	HUVEC	blood vessel:	n/a
26	chr6:140957775-140957825	HCPEpiC	choroid plexus:	n/a
27	chr6:140957775-140957825	HMEC	breast:	n/a
28	chr6:141167819-141167869	SKMC	muscle:	n/a
29	chr6:140957775-140957825	NB4	blood:	n/a
30	chr6:141167819-141167869	HepG2	liver:	n/a
31	chr6:141167819-141167869	AG09309	skin:	n/a
32	chr6:141167819-141167869	HRPEpiC	eye:	n/a
33	chr6:141167819-141167869	RPTEC	kidney:	n/a
34	chr6:140957775-140957825	AG04450	lung:	fetal
35	chr6:140957775-140957825	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:140957775-140957825	NH-A	brain:	n/a
37	chr6:140957775-140957825	SKMC	muscle:	n/a
38	chr6:141167819-141167869	HNPCEpiC	eye:	n/a
39	chr6:141167819-141167869	SK-N-MC	brain:	n/a
40	chr6:140957775-140957825	HUVEC	blood vessel:	n/a
41	chr6:141167819-141167869	Jurkat	blood:	n/a
42	chr6:141167819-141167869	HCPEpiC	choroid plexus:	n/a
43	chr6:140957775-140957825	AG04449	skin:	fetal
44	chr6:140957775-140957825	LNCaP	prostate:	n/a
45	chr6:140957775-140957825	HNPCEpiC	eye:	n/a
46	chr6:141167819-141167869	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:140957775-140957825	Jurkat	blood:	n/a
48	chr6:141167819-141167869	T-47D	breast:	n/a
49	chr6:141167819-141167869	Hepatocyte	liver:	n/a
50	chr6:140957775-140957825	GM12878	blood:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:141147468..141149344-chr6:141153230..141155525,2	K562	blood:
2	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
3	chr6:141186030..141188645-chr6:141209021..141211970,2	K562	blood:
4	chr6:140128805..140131673-chr6:141152750..141154839,2	K562	blood:
5	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
6	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
7	chr6:141142470..141143996-chr6:141149245..141150819,2	K562	blood:
8	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
9	chr6:141218727..141221164-chr6:141224854..141227033,2	K562	blood:
10	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
11	chr6:141212782..141215020-chr6:141216248..141219853,3	K562	blood:
12	chr6:141069422..141072199-chr6:141082873..141085142,2	K562	blood:
13	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
14	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
15	chr6:141142470..141143996-chr6:141149245..141150819,2	K562	blood:
16	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
17	chr6:141147468..141149344-chr6:141153230..141155525,2	K562	blood:
18	chr6:141212782..141215020-chr6:141216248..141219853,3	K562	blood:
19	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
20	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
21	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
22	chr6:141203363..141207943-chr6:141209189..141214513,5	K562	blood:
23	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
24	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
25	chr2:225923916..225924696-chr6:141138966..141139702,2	MCF-7	breast:
26	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
27	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
28	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
29	chr6:141203363..141207943-chr6:141209189..141214513,5	K562	blood:
30	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
31	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
32	chr6:141069422..141072199-chr6:141082873..141085142,2	K562	blood:
33	chr6:141186030..141188645-chr6:141209021..141211970,2	K562	blood:
34	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
35	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
36	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
37	chr6:139691177..139693399-chr6:140971784..140974474,2	MCF-7	breast:
38	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
39	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
40	chr6:141210884..141213823-chr6:141384643..141387034,2	K562	blood:
41	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
42	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
43	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
44	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
45	chr6:141212244..141214629-chr6:141219189..141220964,2	MCF-7	breast:
46	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMBR-2	chr6:141167095-141167471	NONHSAT115288
2	lnc-GJE1-8	chr6:141082666-141083399	NONHSAT115287
3	lnc-NMBR-2	chr6:141185039-141185580	NONHSAT115288
4	lnc-NMBR-2	chr6:141173956-141174061	ENSG00000234147
5	lnc-NMBR-2	chr6:141137269-141138214	NONHSAT115288
6	lnc-HECA-10	chr6:140972927-140973185	l_3279_chr6:140928454-140973185_placenta
7	lnc-NMBR-8	chr6:141215649-141215754	NONHSAT115290
8	lnc-NMBR-2	chr6:141184986-141185033	NONHSAT115288
9	lnc-NMBR-2	chr6:141184950-141184976	NONHSAT115288
10	lnc-NMBR-2	chr6:141216940-141217067	NONHSAT115288
11	lnc-NMBR-8	chr6:141208788-141209134	NONHSAT115290
12	lnc-NMBR-2	chr6:141173956-141174059	NONHSAT115288
13	lnc-NMBR-2	chr6:141128740-141128958	NONHSAT115288
14	lnc-NMBR-2	chr6:141167095-141167441	ENSG00000234147

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4465	chr6:141004992-141005013	MIMAT0018992

No data

Variant related genes	Relation type
RPS3AP24	TF binding region
ENSG00000234147	TF binding region
ENSG00000221336	TF binding region
MIR4465	TF binding region
RPS3AP24	CpG island
ENSG00000234147	CpG island
ENSG00000221336	CpG island
MIR4465	CpG island

Extended variants
information (count: 8572 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:8572 , 50 per page) page: 1 2 3 4 5 6 7 ... 172

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1577654	chr6:140948427-140948428	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548669051	chr6:140948466-140948467	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570186753	chr6:140948529-140948530	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537994202	chr6:140948604-140948605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550014050	chr6:140948607-140948608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545405182	chr6:140948609-140948610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538554563	chr6:140948640-140948641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565406550	chr6:140948668-140948669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554063997	chr6:140948705-140948706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565525608	chr6:140948710-140948711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535865678	chr6:140948719-140948720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554196205	chr6:140948788-140948789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534603745	chr6:140948818-140948819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs207467474	chr6:140948839-140948840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543153959	chr6:140948852-140948853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558878554	chr6:140948875-140948876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577393388	chr6:140948894-140948895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375585844	chr6:140948912-140948913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192992444	chr6:140948921-140948922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541344366	chr6:140948989-140948990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139437048	chr6:140948993-140948994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560009326	chr6:140949029-140949030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530090724	chr6:140949048-140949049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542250016	chr6:140949085-140949086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7450177	chr6:140949106-140949107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7453124	chr6:140949114-140949115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149511707	chr6:140949129-140949130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7450255	chr6:140949132-140949133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184745957	chr6:140949159-140949160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146022720	chr6:140949186-140949187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571332433	chr6:140949197-140949198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7743591	chr6:140949230-140949231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs547342588	chr6:140949242-140949243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7743749	chr6:140949275-140949276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs80220825	chr6:140949309-140949310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190247161	chr6:140949392-140949393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527972181	chr6:140949397-140949398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536723343	chr6:140949462-140949463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558651558	chr6:140949566-140949567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181495204	chr6:140949683-140949684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548137562	chr6:140949710-140949711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139980137	chr6:140949833-140949834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7768627	chr6:140949869-140949870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375878096	chr6:140949987-140949988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575223265	chr6:140950097-140950098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542587964	chr6:140950142-140950143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184755736	chr6:140950200-140950201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530956638	chr6:140950204-140950205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557942346	chr6:140950267-140950268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9321779	chr6:140950269-140950270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140946600-140948600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:140948600-140991200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:140949000-140957400	Weak transcription	Right Atrium	heart
4	chr6:140954200-140954800	Enhancers	Fetal Heart	heart
5	chr6:140954800-140956800	Weak transcription	Fetal Heart	heart
6	chr6:140956600-140957200	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr6:140956800-140958000	Enhancers	Fetal Heart	heart
8	chr6:140956800-140958400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:140957200-140957400	Enhancers	Brain Germinal Matrix	brain
10	chr6:140957200-140957400	Enhancers	Fetal Brain Female	brain
11	chr6:140957200-140957400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr6:140957200-140958200	Active TSS	Brain Anterior Caudate	brain
13	chr6:140957400-140957600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:140957400-140957600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:140957400-140957600	Active TSS	GM12878-XiMat	blood
16	chr6:140957400-140957800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:140957400-140957800	Enhancers	Primary B cells from peripheral blood	blood
18	chr6:140957400-140957800	Enhancers	Fetal Kidney	kidney
19	chr6:140957400-140958000	Active TSS	Brain Angular Gyrus	brain
20	chr6:140957400-140958000	Flanking Active TSS	Brain Germinal Matrix	brain
21	chr6:140957400-140958000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:140957400-140958200	Active TSS	Brain Cingulate Gyrus	brain
23	chr6:140957400-140958200	Active TSS	Brain Hippocampus Middle	brain
24	chr6:140957400-140958200	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr6:140957400-140958200	Active TSS	Brain Substantia Nigra	brain
26	chr6:140957400-140958200	Active TSS	Right Atrium	heart
27	chr6:140957400-140958400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr6:140957400-140958400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:140957400-140958400	Flanking Active TSS	Fetal Brain Female	brain
30	chr6:140957400-140958400	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr6:140957400-140958400	Enhancers	Fetal Stomach	stomach
32	chr6:140957400-140958600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:140957400-140958600	Enhancers	Fetal Brain Male	brain
34	chr6:140957600-140957800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr6:140957600-140958000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:140957600-140958000	Flanking Active TSS	GM12878-XiMat	blood
37	chr6:140957600-140958200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr6:140957600-140958400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr6:140957600-140958400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr6:140957600-140958600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr6:140957600-140958600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:140957600-140958600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr6:140957800-140958000	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr6:140957800-140958200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:140957800-140958200	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr6:140957800-140958200	Active TSS	Fetal Kidney	kidney
47	chr6:140957800-140958200	Enhancers	Stomach Smooth Muscle	stomach
48	chr6:140957800-140958400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr6:140957800-140958400	Active TSS	Rectal Smooth Muscle	rectum
50	chr6:140957800-140958600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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