Variant report

Variant	nsv541348
Chromosome Location	chr12:1432740-1584649
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1047)
CpG islands
(count:672)
Chromatin interactive
region (count:58)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1047 , 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	chr12:1548870-1549271	K562	blood:	n/a	n/a
2	ARID3A	chr12:1513918-1514099	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:1573073-1573605	K562	blood:	n/a	n/a
4	ARID3A	chr12:1439453-1440075	K562	blood:	n/a	n/a
5	ATF1	chr12:1573138-1573542	K562	blood:	n/a	n/a
6	ATF1	chr12:1548886-1549239	K562	blood:	n/a	n/a
7	ATF1	chr12:1478673-1479061	K562	blood:	n/a	n/a
8	ATF2	chr12:1554977-1555407	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr12:1554914-1555407	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr12:1579314-1579512	K562	blood:	n/a	n/a
11	BACH1	chr12:1578414-1578550	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:1468522-1468818	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr12:1434024-1434443	K562	blood:	n/a	chr12:1434243-1434257
14	BACH1	chr12:1464814-1464955	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr12:1434120-1434378	H1-hESC	embryonic stem cell:	n/a	chr12:1434243-1434257
16	BATF	chr12:1492872-1493055	GM12878	blood:	n/a	chr12:1492968-1492979
17	BATF	chr12:1434831-1435242	GM12878	blood:	n/a	chr12:1435047-1435057 chr12:1435046-1435057 chr12:1434932-1434942
18	BATF	chr12:1434858-1435166	GM12878	blood:	n/a	chr12:1435047-1435057 chr12:1435046-1435057 chr12:1434932-1434942
19	BCL11A	chr12:1498062-1498335	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:1555006-1555390	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr12:1553878-1554120	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:1545122-1545985	K562	blood:	n/a	chr12:1545828-1545841
23	BHLHE40	chr12:1532366-1532460	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:1579235-1579624	K562	blood:	n/a	chr12:1579424-1579433 chr12:1579424-1579433
25	BHLHE40	chr12:1479409-1479609	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:1437610-1437992	K562	blood:	n/a	n/a
27	BHLHE40	chr12:1544710-1545039	HepG2	liver:	n/a	n/a
28	BRCA1	chr12:1564047-1564155	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr12:1530240-1530689	HCT-116	colon:	n/a	n/a
30	CBX3	chr12:1530310-1530628	K562	blood:	n/a	n/a
31	CBX3	chr12:1530189-1530748	K562	blood:	n/a	n/a
32	CBX3	chr12:1572303-1572650	K562	blood:	n/a	n/a
33	CBX3	chr12:1530225-1530719	HCT-116	colon:	n/a	n/a
34	CCNT2	chr12:1573232-1573550	K562	blood:	n/a	n/a
35	CCNT2	chr12:1548856-1549207	K562	blood:	n/a	n/a
36	CEBPB	chr12:1539306-1539519	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:1503414-1503582	K562	blood:	n/a	n/a
38	CEBPB	chr12:1494201-1494391	MCF-7	breast:	n/a	chr12:1494322-1494333 chr12:1494357-1494370
39	CEBPB	chr12:1451492-1451637	IMR90	lung:	n/a	chr12:1451583-1451594
40	CEBPB	chr12:1554835-1555401	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr12:1494320-1494381	H1-hESC	embryonic stem cell:	n/a	chr12:1494322-1494333 chr12:1494357-1494370
42	CEBPB	chr12:1539393-1539453	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:1579165-1579311	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:1481573-1481833	HepG2	liver:	n/a	chr12:1481666-1481677
45	CEBPB	chr12:1548012-1548124	HepG2	liver:	n/a	chr12:1548058-1548069
46	CEBPB	chr12:1494183-1494472	K562	blood:	n/a	chr12:1494322-1494333 chr12:1494357-1494370
47	CEBPB	chr12:1447913-1448105	HepG2	liver:	n/a	chr12:1448033-1448044
48	CEBPB	chr12:1528717-1529028	HepG2	liver:	n/a	chr12:1528888-1528899
49	CEBPB	chr12:1451510-1451667	K562	blood:	n/a	chr12:1451583-1451594
50	CEBPB	chr12:1483204-1483533	IMR90	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1459744-1459794	T-47D	breast:	n/a
2	chr12:1459744-1459794	T-47D	breast:	n/a
3	chr12:1499803-1499853	BJ	skin:	n/a
4	chr12:1459744-1459794	HIPEpiC	eye:	n/a
5	chr12:1478761-1478811	ECC-1	luminal epithelium:	n/a
6	chr12:1489532-1489582	HepG2	liver:	n/a
7	chr12:1485704-1485754	MCF10A-Er-Src	breast:	n/a
8	chr12:1489532-1489582	HCF	heart:	n/a
9	chr12:1489532-1489582	T-47D	breast:	n/a
10	chr12:1485599-1485649	K562	blood:	n/a
11	chr12:1499803-1499853	HEK293	kidney:	embryo
12	chr12:1566674-1566724	U87	brain:	n/a
13	chr12:1566674-1566724	SK-N-SH	brain:	n/a
14	chr12:1499803-1499853	PFSK-1	brain:	n/a
15	chr12:1482931-1482981	SKMC	muscle:	n/a
16	chr12:1566674-1566724	Caco-2	colon:	n/a
17	chr12:1499803-1499853	GM06990	blood:	n/a
18	chr12:1466280-1466330	PFSK-1	brain:	n/a
19	chr12:1459744-1459794	GM19239	blood:	n/a
20	chr12:1485599-1485649	AG09319	gingival:	n/a
21	chr12:1489532-1489582	MCF10A-Er-Src	breast:	n/a
22	chr12:1553525-1553575	PANC-1	pancreas:	n/a
23	chr12:1485704-1485754	BE2_C	brain:	n/a
24	chr12:1466280-1466330	K562	blood:	n/a
25	chr12:1489532-1489582	MCF-7	breast:	n/a
26	chr12:1485599-1485649	Jurkat	blood:	n/a
27	chr12:1478761-1478811	HIPEpiC	eye:	n/a
28	chr12:1485704-1485754	HMEC	breast:	n/a
29	chr12:1553525-1553575	LNCaP	prostate:	n/a
30	chr12:1466280-1466330	IMR90	lung:	fetal
31	chr12:1499803-1499853	Hela-S3	cervix:	n/a
32	chr12:1459744-1459794	MCF10A-Er-Src	breast:	n/a
33	chr12:1459744-1459794	SK-N-MC	brain:	n/a
34	chr12:1566674-1566724	SK-N-SH_RA	brain:	n/a
35	chr12:1489532-1489582	GM12892	blood:	n/a
36	chr12:1489532-1489582	SK-N-MC	brain:	n/a
37	chr12:1499803-1499853	HUVEC	blood vessel:	n/a
38	chr12:1555160-1555210	LNCaP	prostate:	n/a
39	chr12:1489532-1489582	HUVEC	blood vessel:	n/a
40	chr12:1489532-1489582	LNCaP	prostate:	n/a
41	chr12:1485704-1485754	GM19239	blood:	n/a
42	chr12:1566674-1566724	HAEpiC	amniotic membrane:	n/a
43	chr12:1478761-1478811	GM06990	blood:	n/a
44	chr12:1499803-1499853	GM19239	blood:	n/a
45	chr12:1459744-1459794	PFSK-1	brain:	n/a
46	chr12:1485704-1485754	HNPCEpiC	eye:	n/a
47	chr12:1553525-1553575	ECC-1	luminal epithelium:	n/a
48	chr12:1485704-1485754	HUVEC	blood vessel:	n/a
49	chr12:1459744-1459794	NT2-D1	testis:	n/a
50	chr12:1553525-1553575	CMK	blood:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:1474380..1476005-chr12:1477724..1479472,2	MCF-7	breast:
2	chr12:1484070..1486223-chr12:1652088..1653588,2	K562	blood:
3	chr12:1483885..1486721-chr12:1488016..1490382,2	K562	blood:
4	chr12:1446375..1449359-chr12:1461325..1463031,2	K562	blood:
5	chr12:1424048..1426819-chr12:1445516..1448128,2	MCF-7	breast:
6	chr12:1477160..1479008-chr12:1480395..1483486,3	K562	blood:
7	chr12:1570379..1574393-chr12:1574873..1580232,6	K562	blood:
8	chr12:1576576..1578608-chr12:1579584..1581182,2	MCF-7	breast:
9	chr12:1478838..1481812-chr12:1484445..1488758,4	K562	blood:
10	chr12:1570379..1574393-chr12:1574873..1580232,6	K562	blood:
11	chr12:1446527..1449359-chr12:1461325..1463038,2	K562	blood:
12	chr12:1435926..1439325-chr12:1439627..1443045,4	K562	blood:
13	chr12:1474380..1476005-chr12:1477724..1479472,2	MCF-7	breast:
14	chr12:1555691..1558581-chr12:1571205..1573342,2	K562	blood:
15	chr12:1555691..1558581-chr12:1571205..1573342,2	K562	blood:
16	chr12:1446375..1449359-chr12:1461325..1463031,2	K562	blood:
17	chr12:1468373..1470006-chr12:1472386..1474129,2	K562	blood:
18	chr12:1572175..1574157-chr12:1679717..1682384,2	K562	blood:
19	chr12:1571396..1573540-chr12:1576737..1578978,2	K562	blood:
20	chr12:1565787..1568238-chr12:1569679..1572728,3	K562	blood:
21	chr12:1434502..1436559-chr12:1440756..1442388,2	K562	blood:
22	chr12:1478838..1481812-chr12:1484445..1488758,4	K562	blood:
23	chr12:1574896..1578788-chr12:1580467..1583397,5	K562	blood:
24	chr12:1434502..1436559-chr12:1440756..1442388,2	K562	blood:
25	chr12:1577937..1578888-chr12:1653877..1654562,2	MCF-7	breast:
26	chr12:1495608..1498215-chr12:1504232..1506102,2	MCF-7	breast:
27	chr12:1540247..1543011-chr12:1543041..1545032,3	MCF-7	breast:
28	chr12:1428172..1430846-chr12:1431367..1432976,2	K562	blood:
29	chr12:1571396..1573540-chr12:1576737..1578978,2	K562	blood:
30	chr12:1495608..1498215-chr12:1504232..1506102,2	MCF-7	breast:
31	chr12:1511281..1513414-chr12:1522113..1524386,2	K562	blood:
32	chr12:1437851..1440138-chr12:1641572..1643434,2	K562	blood:
33	chr12:1509342..1510930-chr12:1517317..1520243,2	K562	blood:
34	chr12:1576576..1578608-chr12:1579584..1581182,2	MCF-7	breast:
35	chr12:1477160..1479008-chr12:1480395..1483486,3	K562	blood:
36	chr12:1565787..1568238-chr12:1569679..1572728,3	K562	blood:
37	chr12:1569039..1571648-chr12:1571859..1575051,3	K562	blood:
38	chr12:1574896..1578788-chr12:1580467..1583397,5	K562	blood:
39	chr12:1484589..1487489-chr12:1514413..1516038,2	K562	blood:
40	chr12:1483885..1486721-chr12:1488016..1490382,2	K562	blood:
41	chr12:1545095..1547287-chr12:1641789..1644190,2	K562	blood:
42	chr12:1484589..1487489-chr12:1514413..1516038,2	K562	blood:
43	chr12:1446335..1449950-chr12:1451320..1454152,3	K562	blood:
44	chr12:1446335..1449950-chr12:1451320..1454152,3	K562	blood:
45	chr12:1574896..1578285-chr12:1580467..1583397,5	K562	blood:
46	chr12:1509342..1511317-chr12:1517042..1518817,2	K562	blood:
47	chr12:1446527..1449359-chr12:1461325..1463038,2	K562	blood:
48	chr12:1540247..1543011-chr12:1543041..1545032,3	MCF-7	breast:
49	chr12:1435926..1439325-chr12:1439627..1443045,4	K562	blood:
50	chr12:1322894..1325087-chr12:1546213..1548025,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WNT5B-4	chr12:1494999-1495168	ENSG00000267285.1
2	lnc-WNK1-3	chr12:1539443-1539964	NONHSAT025391
3	lnc-FBXL14-3	chr12:1499755-1500668	ENSG00000249028.2
4	lnc-WNT5B-3	chr12:1527811-1527832	NONHSAT025390
5	lnc-WNT5B-2	chr12:1537296-1537353	l_579_chr12:1534935-1538482_brain
6	lnc-WNT5B-3	chr12:1527841-1529046	NONHSAT025390
7	lnc-WNT5B-5	chr12:1481894-1483851	l_578_NR_028415
8	lnc-FBXL14-3	chr12:1489226-1490399	ENSG00000249028.2
9	lnc-WNT5B-3	chr12:1526670-1527796	NONHSAT025390
10	lnc-WNT5B-5	chr12:1479918-1480203	l_578_NR_028415
11	lnc-FBXL14-3	chr12:1489226-1490399	ENSG00000249028
12	lnc-FBXL14-3	chr12:1499759-1500668	ENSG00000249028
13	lnc-WNK1-3	chr12:1553728-1553796	NONHSAT025391
14	lnc-WNT5B-4	chr12:1495750-1496153	ENSG00000267285.1
15	lnc-WNT5B-2	chr12:1537658-1538482	l_579_chr12:1534935-1538482_brain
16	lnc-WNT5B-2	chr12:1534936-1535759	l_579_chr12:1534935-1538482_brain

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ERC1	hsa-miR-26b-5p	chr12:1553734-1553754

Variant related genes	Relation type
ERC1	TF binding region
ENSG00000267285	TF binding region
ENSG00000249028	TF binding region
ERC1	CpG island
ENSG00000267285	CpG island
ENSG00000249028	CpG island
ENSG00000082805	chromatin interactions
TMEM14A	miRNA target sites
NFYB	miRNA target sites

Extended variants
information (count: 6513 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:6513 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73034952	chr12:1432741-1432742	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546130765	chr12:1432758-1432759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374627760	chr12:1432764-1432765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113551007	chr12:1432774-1432775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73034954	chr12:1432799-1432800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs114541517	chr12:1432802-1432803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189720787	chr12:1432838-1432839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61913082	chr12:1432843-1432844	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs550594318	chr12:1432844-1432845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73034957	chr12:1432951-1432952	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs368126286	chr12:1432990-1432991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557697222	chr12:1433058-1433059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566591375	chr12:1433060-1433061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180695466	chr12:1433061-1433062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6489279	chr12:1433069-1433070	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs186318252	chr12:1433075-1433076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7966310	chr12:1433077-1433078	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs368378475	chr12:1433094-1433095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6489280	chr12:1433147-1433148	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs6489281	chr12:1433182-1433183	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs969360	chr12:1433194-1433195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150849616	chr12:1433199-1433200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576530765	chr12:1433239-1433240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564112884	chr12:1433259-1433260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs36203689	chr12:1433283-1433284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376953172	chr12:1433289-1433290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562028027	chr12:1433307-1433308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570817194	chr12:1433341-1433342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528592748	chr12:1433342-1433343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75966437	chr12:1433348-1433349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190771134	chr12:1433386-1433387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183769749	chr12:1433438-1433439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73036621	chr12:1433441-1433442	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534587940	chr12:1433443-1433444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111856414	chr12:1433485-1433486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149565766	chr12:1433487-1433488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551116302	chr12:1433516-1433517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566458633	chr12:1433537-1433538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533913470	chr12:1433570-1433571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555498363	chr12:1433590-1433591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61913083	chr12:1433598-1433599	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs535679307	chr12:1433651-1433652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74057131	chr12:1433695-1433696	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73036623	chr12:1433706-1433707	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs188350835	chr12:1433707-1433708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73036624	chr12:1433783-1433784	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572893665	chr12:1433802-1433803	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs139984037	chr12:1433805-1433806	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs557026589	chr12:1433806-1433807	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs562929494	chr12:1433855-1433856	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Autism	22495311	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Melanoma	20877625	CNVD
Ewing''s sarcoma	19144156	CNVD

Chromatin state (count:2828 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1387400-1453400	Weak transcription	Thymus	Thymus
2	chr12:1387600-1441400	Weak transcription	HepG2	liver
3	chr12:1391200-1434000	Weak transcription	A549	lung
4	chr12:1404800-1442600	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr12:1413800-1447600	Weak transcription	Gastric	stomach
6	chr12:1416200-1434400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr12:1416400-1434000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr12:1420200-1440600	Weak transcription	Primary T cells from cord blood	blood
9	chr12:1423000-1435400	Weak transcription	Fetal Thymus	thymus
10	chr12:1424400-1433400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:1424800-1442200	Weak transcription	Fetal Stomach	stomach
12	chr12:1428000-1442200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr12:1428000-1447600	Weak transcription	Ovary	ovary
14	chr12:1428200-1433200	Weak transcription	K562	blood
15	chr12:1428200-1434000	Weak transcription	Small Intestine	intestine
16	chr12:1428200-1441600	Weak transcription	Pancreas	Pancrea
17	chr12:1428200-1442800	Weak transcription	Fetal Muscle Leg	muscle
18	chr12:1428200-1443200	Weak transcription	Fetal Brain Female	brain
19	chr12:1428200-1447600	Weak transcription	Left Ventricle	heart
20	chr12:1428200-1448800	Weak transcription	Psoas Muscle	Psoas
21	chr12:1428200-1449000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr12:1428200-1449000	Weak transcription	Aorta	Aorta
23	chr12:1428200-1455000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:1428200-1500400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr12:1428400-1432800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr12:1428400-1433000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr12:1428400-1433000	Weak transcription	Fetal Brain Male	brain
28	chr12:1428400-1436400	Weak transcription	Fetal Heart	heart
29	chr12:1428400-1438800	Weak transcription	Fetal Intestine Small	intestine
30	chr12:1428400-1438800	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr12:1428400-1440600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:1428400-1440800	Weak transcription	Brain Angular Gyrus	brain
33	chr12:1428600-1434000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr12:1428600-1434200	Weak transcription	Brain Anterior Caudate	brain
35	chr12:1428600-1440400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:1428600-1440400	Weak transcription	NHEK	skin
37	chr12:1428600-1441200	Weak transcription	Brain Germinal Matrix	brain
38	chr12:1428800-1433800	Weak transcription	Colon Smooth Muscle	Colon
39	chr12:1428800-1434200	Weak transcription	Adipose Nuclei	Adipose
40	chr12:1429000-1433000	Weak transcription	Fetal Lung	lung
41	chr12:1429200-1434000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:1429200-1434400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr12:1429600-1434000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr12:1431000-1435600	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr12:1432200-1433600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:1432400-1433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:1432600-1433000	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr12:1432600-1433800	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr12:1432600-1433800	Weak transcription	Primary B cells from cord blood	blood
50	chr12:1432600-1433800	Enhancers	Monocytes-CD14+_RO01746	blood

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