Variant report

Variant	nsv883374
Chromosome Location	chr6:1454334-1558449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1983)
CpG islands
(count:2081)
Chromatin interactive
region (count:46)
LncRNA
region (count:78)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1983 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:1552675-1553036	K562	blood:	n/a	n/a
2	ARID3A	chr6:1515675-1515880	K562	blood:	n/a	n/a
3	ARID3A	chr6:1552717-1553056	HepG2	liver:	n/a	n/a
4	ATF1	chr6:1488764-1488968	K562	blood:	n/a	n/a
5	ATF1	chr6:1483041-1483184	K562	blood:	n/a	n/a
6	ATF2	chr6:1461408-1461899	GM12878	blood:	n/a	n/a
7	ATF2	chr6:1470181-1470958	GM12878	blood:	n/a	n/a
8	ATF2	chr6:1470217-1470770	GM12878	blood:	n/a	n/a
9	ATF2	chr6:1486557-1487042	GM12878	blood:	n/a	n/a
10	ATF2	chr6:1461388-1461929	GM12878	blood:	n/a	n/a
11	ATF2	chr6:1482597-1483006	GM12878	blood:	n/a	n/a
12	ATF2	chr6:1482358-1483118	GM12878	blood:	n/a	n/a
13	ATF3	chr6:1524299-1524568	K562	blood:	n/a	n/a
14	ATF3	chr6:1527479-1527744	GM12878	blood:	n/a	n/a
15	BACH1	chr6:1548614-1548659	K562	blood:	n/a	n/a
16	BACH1	chr6:1524226-1524623	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:1468509-1468687	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:1482543-1483339	GM12878	blood:	n/a	n/a
19	BATF	chr6:1483029-1483362	GM12878	blood:	n/a	n/a
20	BATF	chr6:1470262-1470580	GM12878	blood:	n/a	n/a
21	BATF	chr6:1461429-1461974	GM12878	blood:	n/a	chr6:1461681-1461692
22	BATF	chr6:1461413-1461965	GM12878	blood:	n/a	chr6:1461681-1461692
23	BATF	chr6:1485942-1486244	GM12878	blood:	n/a	chr6:1486067-1486077 chr6:1486109-1486120 chr6:1486066-1486077
24	BATF	chr6:1485974-1486188	GM12878	blood:	n/a	chr6:1486067-1486077 chr6:1486109-1486120 chr6:1486066-1486077
25	BCL11A	chr6:1470170-1470683	GM12878	blood:	n/a	chr6:1470566-1470574
26	BCL11A	chr6:1554809-1555163	GM12878	blood:	n/a	chr6:1554998-1555007
27	BCL11A	chr6:1461457-1461859	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:1461388-1461860	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:1554811-1555161	GM12878	blood:	n/a	chr6:1554998-1555007
30	BCL11A	chr6:1470256-1470642	GM12878	blood:	n/a	chr6:1470566-1470574
31	BCL3	chr6:1470299-1470707	GM12878	blood:	n/a	chr6:1470566-1470574
32	BCL3	chr6:1481474-1482054	A549	lung:	n/a	n/a
33	BCL3	chr6:1477692-1478220	A549	lung:	n/a	n/a
34	BCLAF1	chr6:1470202-1470830	GM12878	blood:	n/a	chr6:1470566-1470574
35	BCLAF1	chr6:1482506-1483066	GM12878	blood:	n/a	chr6:1482763-1482772
36	BCLAF1	chr6:1554879-1555195	GM12878	blood:	n/a	chr6:1554998-1555007
37	BCLAF1	chr6:1470091-1470598	GM12878	blood:	n/a	chr6:1470566-1470574
38	BCLAF1	chr6:1482502-1483149	GM12878	blood:	n/a	chr6:1482763-1482772
39	BHLHE40	chr6:1524272-1524644	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:1468275-1468837	GM12878	blood:	n/a	n/a
41	BHLHE40	chr6:1524202-1524663	K562	blood:	n/a	n/a
42	BHLHE40	chr6:1524267-1524582	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:1515488-1515832	K562	blood:	n/a	n/a
44	BHLHE40	chr6:1470226-1470875	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:1461481-1462029	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:1488829-1488956	K562	blood:	n/a	n/a
47	BHLHE40	chr6:1554441-1555547	GM12878	blood:	n/a	chr6:1555486-1555502
48	BRCA1	chr6:1512830-1512834	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr6:1478969-1479825	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr6:1481407-1482420	Hela-S3	cervix:	n/a	n/a

(count:2081 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:1527072-1527122	AG09319	gingival:	n/a
2	chr6:1555389-1555439	NHBE	bronchial:	n/a
3	chr6:1515580-1515630	HCPEpiC	choroid plexus:	n/a
4	chr6:1495082-1495132	NT2-D1	testis:	n/a
5	chr6:1552904-1552954	K562	blood:	n/a
6	chr6:1523080-1523130	ProgFib	skin:	n/a
7	chr6:1524190-1524240	HNPCEpiC	eye:	n/a
8	chr6:1527072-1527122	AG09319	gingival:	n/a
9	chr6:1555389-1555439	NHBE	bronchial:	n/a
10	chr6:1515580-1515630	HCPEpiC	choroid plexus:	n/a
11	chr6:1495082-1495132	NT2-D1	testis:	n/a
12	chr6:1552904-1552954	K562	blood:	n/a
13	chr6:1523080-1523130	ProgFib	skin:	n/a
14	chr6:1524190-1524240	HNPCEpiC	eye:	n/a
15	chr6:1555080-1555130	GM19239	blood:	n/a
16	chr6:1514372-1514422	HRPEpiC	eye:	n/a
17	chr6:1464363-1464413	ECC-1	luminal epithelium:	n/a
18	chr6:1464075-1464125	BE2_C	brain:	n/a
19	chr6:1527072-1527122	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:1524190-1524240	AoSMC	blood vessel:	n/a
21	chr6:1524618-1524668	PFSK-1	brain:	n/a
22	chr6:1552904-1552954	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:1516613-1516663	CMK	blood:	n/a
24	chr6:1511822-1511872	BJ	skin:	n/a
25	chr6:1524618-1524668	GM12878	blood:	n/a
26	chr6:1556357-1556407	HRE	kidney:	n/a
27	chr6:1464363-1464413	PFSK-1	brain:	n/a
28	chr6:1495099-1495149	SK-N-SH_RA	brain:	n/a
29	chr6:1523080-1523130	NB4	blood:	n/a
30	chr6:1552904-1552954	HEK293	kidney:	embryo
31	chr6:1515524-1515574	ovcar-3	ovarian:	n/a
32	chr6:1523751-1523801	PANC-1	pancreas:	n/a
33	chr6:1555389-1555439	HIPEpiC	eye:	n/a
34	chr6:1555080-1555130	K562	blood:	n/a
35	chr6:1497870-1497920	AG09319	gingival:	n/a
36	chr6:1496338-1496388	HEEpiC	esophagus:	n/a
37	chr6:1496338-1496388	PANC-1	pancreas:	n/a
38	chr6:1515797-1515847	SK-N-SH_RA	brain:	n/a
39	chr6:1464075-1464125	BJ	skin:	n/a
40	chr6:1511822-1511872	HEK293	kidney:	embryo
41	chr6:1523751-1523801	MCF10A-Er-Src	breast:	n/a
42	chr6:1516613-1516663	HCF	heart:	n/a
43	chr6:1481524-1481574	GM12891	blood:	n/a
44	chr6:1496324-1496374	MCF-7	breast:	n/a
45	chr6:1555311-1555361	HCF	heart:	n/a
46	chr6:1527072-1527122	PrEC	prostate:	n/a
47	chr6:1515524-1515574	SK-N-SH_RA	brain:	n/a
48	chr6:1524618-1524668	MCF10A-Er-Src	breast:	n/a
49	chr6:1464075-1464125	GM12892	blood:	n/a
50	chr6:1524494-1524544	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:1522639..1525978-chr6:1527169..1529799,4	K562	blood:
2	chr6:1536939..1538440-chr6:1580470..1582016,2	K562	blood:
3	chr6:1486362..1489306-chr6:1493339..1496950,3	MCF-7	breast:
4	chr6:1538946..1541527-chr6:1548502..1550339,2	K562	blood:
5	chr6:1525690..1526651-chr6:1641283..1642196,5	MCF-7	breast:
6	chr6:1540042..1541785-chr6:1551983..1554224,2	MCF-7	breast:
7	chr6:1519265..1521988-chr6:1525887..1527460,2	MCF-7	breast:
8	chr5:5481094..5482017-chr6:1551963..1552934,2	MCF-7	breast:
9	chr6:1481665..1482260-chr6:1525723..1526611,2	MCF-7	breast:
10	chr6:1542695..1544862-chr6:1553978..1556042,2	MCF-7	breast:
11	chr6:1525690..1526651-chr6:1641283..1642196,7	MCF-7	breast:
12	chr6:1500795..1502944-chr6:1503456..1505946,2	K562	blood:
13	chr6:1519265..1521988-chr6:1525887..1527460,2	MCF-7	breast:
14	chr6:1539970..1541513-chr6:1545338..1547191,2	MCF-7	breast:
15	chr6:1538946..1541527-chr6:1548502..1550339,2	K562	blood:
16	chr6:1522925..1524634-chr6:1528835..1530960,2	MCF-7	breast:
17	chr6:1499127..1499629-chr6:1552167..1552877,2	MCF-7	breast:
18	chr6:1479047..1481857-chr6:1490107..1492242,2	K562	blood:
19	chr6:1554542..1557319-chr6:2236589..2238217,2	MCF-7	breast:
20	chr6:1470658..1472658-chr6:1477304..1479311,2	K562	blood:
21	chr6:1525299..1527850-chr6:1532850..1536880,3	K562	blood:
22	chr6:1500696..1503622-chr6:1553281..1556067,2	MCF-7	breast:
23	chr6:1509944..1512299-chr6:1514047..1516903,3	K562	blood:
24	chr6:1544489..1546894-chr6:1554034..1556093,2	MCF-7	breast:
25	chr6:1557340..1559925-chr6:1576437..1579057,2	MCF-7	breast:
26	chr6:1499127..1499629-chr6:1552167..1552877,2	MCF-7	breast:
27	chr6:1498802..1499697-chr6:1552475..1552977,2	MCF-7	breast:
28	chr6:1500795..1502944-chr6:1503456..1505946,2	K562	blood:
29	chr6:1546489..1548541-chr6:1551535..1553787,2	K562	blood:
30	chr6:1544489..1546894-chr6:1554034..1556093,2	MCF-7	breast:
31	chr6:1500696..1503622-chr6:1553281..1556067,2	MCF-7	breast:
32	chr6:1503806..1505893-chr6:1514309..1516547,2	K562	blood:
33	chr6:1486362..1489306-chr6:1493339..1496950,3	MCF-7	breast:
34	chr6:1481665..1482260-chr6:1525723..1526611,2	MCF-7	breast:
35	chr6:1491682..1493226-chr6:1495770..1497573,2	K562	blood:
36	chr6:1476822..1479650-chr6:1479865..1482359,2	K562	blood:
37	chr6:1476822..1479650-chr6:1479865..1482359,2	K562	blood:
38	chr6:1546489..1548541-chr6:1551535..1553787,2	K562	blood:
39	chr6:1470658..1472658-chr6:1477304..1479311,2	K562	blood:
40	chr6:1498802..1499697-chr6:1552475..1552977,2	MCF-7	breast:
41	chr6:1491682..1493226-chr6:1495770..1497573,2	K562	blood:
42	chr6:1542695..1544862-chr6:1553978..1556042,2	MCF-7	breast:
43	chr6:1540042..1541785-chr6:1551983..1554224,2	MCF-7	breast:
44	chr6:1479047..1481857-chr6:1490107..1492242,2	K562	blood:
45	chr6:1525299..1527850-chr6:1532850..1536880,3	K562	blood:
46	chr6:1539970..1541513-chr6:1545338..1547191,2	MCF-7	breast:

(count:78 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXF2-7	chr6:1485931-1486160	NONHSAT106500
2	lnc-FOXC1-6	chr6:1523749-1523796	NONHSAT106510
3	lnc-GMDS-9	chr6:1474837-1477102	NONHSAT106495
4	lnc-GMDS-6	chr6:1548086-1553288	NONHSAT106514
5	lnc-FOXC1-2	chr6:1509048-1509149	NONHSAT106502
6	lnc-FOXF2-7	chr6:1489026-1489445	NONHSAT106500
7	lnc-FOXC1-2	chr6:1498564-1498777	NONHSAT106502
8	lnc-FOXF2-7	chr6:1488529-1488668	NONHSAT106498
9	lnc-FOXC1-6	chr6:1521895-1522170	NONHSAT106509
10	lnc-FOXC1-2	chr6:1515206-1515556	NONHSAT106502
11	lnc-GMDS-8	chr6:1528599-1529146	ENSG00000272279.1
12	lnc-FOXF2-7	chr6:1485931-1486160	NONHSAT106498
13	lnc-FOXF2-7	chr6:1489026-1489445	NONHSAT106498
14	lnc-GMDS-6	chr6:1548086-1553288	NONHSAT106513
15	lnc-FOXF2-7	chr6:1485462-1485630	NONHSAT106498
16	lnc-GMDS-10	chr6:1459088-1459336	NONHSAT106492
17	lnc-FOXC1-6	chr6:1524730-1528405	NONHSAT106510
18	lnc-FOXC1-2	chr6:1509048-1509219	NONHSAT106505
19	lnc-GMDS-6	chr6:1557578-1557683	NONHSAT106515
20	lnc-FOXC1-2	chr6:1490481-1490878	NONHSAT106502
21	lnc-FOXF2-7	chr6:1488811-1488858	NONHSAT106498
22	lnc-FOXC1-2	chr6:1518995-1519016	NONHSAT106502
23	lnc-FOXC1-6	chr6:1522278-1522394	NONHSAT106509
24	lnc-FOXC1-2	chr6:1496350-1496458	ENSG00000251522
25	lnc-FOXC1-2	chr6:1546211-1546716	NONHSAT106502
26	lnc-GMDS-6	chr6:1555917-1556410	NONHSAT106515
27	lnc-FOXC1-6	chr6:1522658-1522933	NONHSAT106510
28	lnc-FOXF2-7	chr6:1488811-1488858	NONHSAT106499
29	lnc-FOXC1-2	chr6:1518931-1518984	NONHSAT106502
30	lnc-FOXC1-6	chr6:1522986-1523033	NONHSAT106509
31	lnc-FOXF2-1	chr6:1490003-1490173	XLOC_005123
32	lnc-GMDS-6	chr6:1555160-1555653	NONHSAT106514
33	lnc-GMDS-6	chr6:1556821-1556926	NONHSAT106513
34	lnc-FOXC1-6	chr6:1521381-1521538	NONHSAT106510
35	lnc-GMDS-10	chr6:1489649-1489842	NONHSAT106492
36	lnc-FOXC1-5	chr6:1557340-1557475	NONHSAT106518
37	lnc-GMDS-6	chr6:1555160-1555653	NONHSAT106513
38	lnc-GMDS-10	chr6:1464374-1464548	NONHSAT106492
39	lnc-FOXC1-2	chr6:1498564-1498777	NONHSAT106505
40	lnc-GMDS-6	chr6:1548843-1554045	NONHSAT106515
41	lnc-FOXF2-7	chr6:1486291-1486560	NONHSAT106500
42	lnc-FOXF2-7	chr6:1486291-1486560	NONHSAT106498
43	lnc-FOXF2-7	chr6:1487680-1487953	NONHSAT106500
44	lnc-FOXC1-6	chr6:1523967-1527642	NONHSAT106509
45	lnc-GMDS-10	chr6:1454395-1454467	NONHSAT106490
46	lnc-FOXF2-7	chr6:1487680-1487953	NONHSAT106499
47	lnc-FOXF2-7	chr6:1485931-1486160	NONHSAT106499
48	lnc-FOXF2-7	chr6:1488529-1488668	NONHSAT106499
49	lnc-FOXC1-5	chr6:1557705-1557862	NONHSAT106518
50	lnc-FOXC1-2	chr6:1496359-1496458	NONHSAT106506

No data

Variant related genes	Relation type
ENSG00000218027	TF binding region
ENSG00000272279	TF binding region
RN7SL352P	TF binding region
ENSG00000218027	CpG island
ENSG00000272279	CpG island
RN7SL352P	CpG island
ENSG00000272279	chromatin interactions
ENSG00000218027	chromatin interactions
HS2ST1	miRNA target sites
SLC7A11	miRNA target sites
CD36	miRNA target sites
SLC6A4	miRNA target sites
USP6	miRNA target sites

Extended variants
information (count: 4645 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4645 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2816251	chr6:1454334-1454335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565060637	chr6:1454369-1454370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548771633	chr6:1454390-1454391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75508437	chr6:1454397-1454398	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs528204284	chr6:1454428-1454429	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs80229529	chr6:1454487-1454488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560826978	chr6:1454595-1454596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183423557	chr6:1454616-1454617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557693681	chr6:1454625-1454626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369335417	chr6:1454659-1454660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567825314	chr6:1454676-1454677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536872752	chr6:1454677-1454678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552052089	chr6:1454728-1454729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151304002	chr6:1454731-1454732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79473890	chr6:1454737-1454738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186990730	chr6:1454750-1454751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75519099	chr6:1454759-1454760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565344448	chr6:1454782-1454783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140588730	chr6:1454822-1454823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575670116	chr6:1454841-1454842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114500737	chr6:1454842-1454843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150485746	chr6:1454863-1454864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542787372	chr6:1454865-1454866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191832540	chr6:1454884-1454885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528183436	chr6:1454914-1454915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551188141	chr6:1454918-1454919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530083379	chr6:1454924-1454925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2816252	chr6:1454972-1454973	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs111390948	chr6:1455051-1455052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530535565	chr6:1455062-1455063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541781742	chr6:1455091-1455092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77681096	chr6:1455144-1455145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183451647	chr6:1455149-1455150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186683261	chr6:1455181-1455182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528256991	chr6:1455220-1455221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572654221	chr6:1455230-1455231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142377609	chr6:1455270-1455271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146507145	chr6:1455289-1455290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575203100	chr6:1455300-1455301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139179743	chr6:1455335-1455336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370507330	chr6:1455344-1455345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554574294	chr6:1455380-1455381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113612423	chr6:1455447-1455448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35820121	chr6:1455459-1455460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573866536	chr6:1455475-1455476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542601563	chr6:1455490-1455491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149381783	chr6:1455496-1455497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528280945	chr6:1455550-1455551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191331452	chr6:1455556-1455557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1474721	chr6:1455570-1455571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1432 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:1453600-1464200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:1456000-1456200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:1456000-1456200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:1456200-1462600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:1456200-1468000	Weak transcription	Right Atrium	heart
6	chr6:1457800-1461400	Weak transcription	Hela-S3	cervix
7	chr6:1461200-1462400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:1461200-1462600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:1461200-1463000	Enhancers	GM12878-XiMat	blood
10	chr6:1461200-1463000	Enhancers	HMEC	breast
11	chr6:1461400-1462200	Enhancers	NHEK	skin
12	chr6:1461400-1462400	Enhancers	Hela-S3	cervix
13	chr6:1461600-1462000	Enhancers	Osteobl	bone
14	chr6:1461600-1462600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:1461800-1462600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:1462000-1462600	Enhancers	HSMM	muscle
17	chr6:1462200-1465000	Weak transcription	NHEK	skin
18	chr6:1462400-1463400	Weak transcription	Hela-S3	cervix
19	chr6:1462400-1465200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:1462600-1463600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:1463000-1465000	Weak transcription	HMEC	breast
22	chr6:1463000-1467800	Weak transcription	GM12878-XiMat	blood
23	chr6:1463200-1464400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr6:1463200-1464600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr6:1463200-1464600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr6:1463200-1464600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:1463400-1463600	Enhancers	Hela-S3	cervix
28	chr6:1463400-1464000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr6:1463400-1464600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr6:1463400-1464800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr6:1463600-1464000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:1463600-1464400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr6:1463800-1464600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr6:1464000-1465000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:1464000-1468200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr6:1464200-1464600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:1464400-1464600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:1464400-1465600	Enhancers	NHDF-Ad	bronchial
39	chr6:1464400-1468000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr6:1464400-1468200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr6:1464600-1467800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr6:1464600-1468000	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr6:1464600-1468000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr6:1464600-1468000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr6:1464600-1473400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:1464800-1468200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:1465000-1465600	Enhancers	HMEC	breast
48	chr6:1465000-1465600	Enhancers	HSMMtube	muscle
49	chr6:1465000-1465600	Enhancers	NHEK	skin
50	chr6:1465200-1465400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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