Variant report

Variant	nsv898594
Chromosome Location	chr12:1916838-1952990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:1831)
Chromatin interactive
region (count:63)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:1920868-1921315	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:1934949-1935226	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:1947034-1947306	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:1925448-1925599	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:1922073-1922329	HepG2	liver:	n/a	n/a
6	ATF1	chr12:1921987-1922475	K562	blood:	n/a	n/a
7	ATF1	chr12:1950924-1951113	K562	blood:	n/a	n/a
8	ATF3	chr12:1922071-1922413	K562	blood:	n/a	n/a
9	ATF3	chr12:1922183-1922369	K562	blood:	n/a	n/a
10	BACH1	chr12:1929552-1929694	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr12:1925752-1926306	GM12878	blood:	n/a	n/a
12	BCL3	chr12:1925781-1926303	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:1919741-1919978	K562	blood:	n/a	n/a
14	BHLHE40	chr12:1925707-1926113	K562	blood:	n/a	n/a
15	BHLHE40	chr12:1940359-1940550	K562	blood:	n/a	n/a
16	BHLHE40	chr12:1931012-1931206	K562	blood:	n/a	n/a
17	BHLHE40	chr12:1940330-1940571	HepG2	liver:	n/a	n/a
18	BHLHE40	chr12:1920726-1921486	HepG2	liver:	n/a	chr12:1921279-1921288 chr12:1921277-1921290 chr12:1921273-1921294 chr12:1921280-1921289 chr12:1921279-1921288
19	BHLHE40	chr12:1934805-1934932	K562	blood:	n/a	chr12:1934844-1934853 chr12:1934844-1934853 chr12:1934838-1934859
20	BHLHE40	chr12:1931087-1931195	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:1921026-1921446	K562	blood:	n/a	chr12:1921279-1921288 chr12:1921277-1921290 chr12:1921273-1921294 chr12:1921280-1921289 chr12:1921279-1921288
22	BHLHE40	chr12:1921907-1922486	K562	blood:	n/a	n/a
23	BHLHE40	chr12:1922021-1922463	HepG2	liver:	n/a	n/a
24	BHLHE40	chr12:1934648-1935258	HepG2	liver:	n/a	chr12:1934844-1934853 chr12:1934844-1934853 chr12:1934838-1934859
25	BHLHE40	chr12:1919012-1919508	K562	blood:	n/a	n/a
26	CEBPB	chr12:1940191-1940633	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr12:1922087-1922482	MCF-7	breast:	n/a	n/a
28	CEBPB	chr12:1940264-1940533	K562	blood:	n/a	n/a
29	CEBPB	chr12:1922117-1922500	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:1949067-1949617	MCF-7	breast:	n/a	n/a
31	CEBPB	chr12:1922122-1922532	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:1940327-1940486	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:1947056-1947318	HepG2	liver:	n/a	n/a
34	CEBPB	chr12:1922125-1922504	HepG2	liver:	n/a	n/a
35	CEBPB	chr12:1922173-1922460	A549	lung:	n/a	n/a
36	CEBPB	chr12:1940161-1940619	MCF-7	breast:	n/a	n/a
37	CEBPB	chr12:1940068-1940655	MCF-7	breast:	n/a	n/a
38	CEBPB	chr12:1925008-1925361	HepG2	liver:	n/a	chr12:1925179-1925190
39	CEBPB	chr12:1944440-1944697	HepG2	liver:	n/a	chr12:1944546-1944557
40	CEBPB	chr12:1922143-1922487	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:1925068-1925245	K562	blood:	n/a	chr12:1925179-1925190
42	CEBPB	chr12:1944447-1944650	K562	blood:	n/a	chr12:1944546-1944557
43	CEBPB	chr12:1944453-1944613	H1-hESC	embryonic stem cell:	n/a	chr12:1944546-1944557
44	CEBPB	chr12:1922078-1922495	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:1934777-1935141	HepG2	liver:	n/a	n/a
46	CEBPB	chr12:1940057-1940681	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr12:1922099-1922524	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:1925053-1925265	IMR90	lung:	n/a	chr12:1925179-1925190
49	CEBPB	chr12:1922052-1922507	K562	blood:	n/a	n/a
50	CEBPB	chr12:1940230-1940589	IMR90	lung:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1945300-1945350	HepG2	liver:	n/a
2	chr12:1945300-1945350	HepG2	liver:	n/a
3	chr12:1947412-1947462	AG09319	gingival:	n/a
4	chr12:1947479-1947529	CMK	blood:	n/a
5	chr12:1948578-1948628	GM12878	blood:	n/a
6	chr12:1946957-1947007	HUVEC	blood vessel:	n/a
7	chr12:1938156-1938206	AG04450	lung:	fetal
8	chr12:1943889-1943939	HEEpiC	esophagus:	n/a
9	chr12:1949586-1949636	HCT-116	colon:	n/a
10	chr12:1928689-1928739	ECC-1	luminal epithelium:	n/a
11	chr12:1940618-1940668	BE2_C	brain:	n/a
12	chr12:1946957-1947007	ovcar-3	ovarian:	n/a
13	chr12:1947412-1947462	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:1949503-1949553	SKMC	muscle:	n/a
15	chr12:1949503-1949553	HMEC	breast:	n/a
16	chr12:1952798-1952848	HEEpiC	esophagus:	n/a
17	chr12:1948648-1948698	SAEC	small airway:	n/a
18	chr12:1929551-1929601	PrEC	prostate:	n/a
19	chr12:1949503-1949553	Caco-2	colon:	n/a
20	chr12:1943722-1943772	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:1940380-1940430	SKMC	muscle:	n/a
22	chr12:1929265-1929315	AoSMC	blood vessel:	n/a
23	chr12:1947412-1947462	BJ	skin:	n/a
24	chr12:1949586-1949636	PFSK-1	brain:	n/a
25	chr12:1948578-1948628	SK-N-SH	brain:	n/a
26	chr12:1949586-1949636	AG09319	gingival:	n/a
27	chr12:1949586-1949636	ovcar-3	ovarian:	n/a
28	chr12:1928689-1928739	HRCEpiC	kidney:	n/a
29	chr12:1928689-1928739	ovcar-3	ovarian:	n/a
30	chr12:1928689-1928739	IMR90	lung:	fetal
31	chr12:1930326-1930376	SK-N-SH	brain:	n/a
32	chr12:1928481-1928531	NHDF-neo	bronchial:	n/a
33	chr12:1947479-1947529	AG04450	lung:	fetal
34	chr12:1948648-1948698	AG04449	skin:	fetal
35	chr12:1940380-1940430	HCT-116	colon:	n/a
36	chr12:1946957-1947007	HAEpiC	amniotic membrane:	n/a
37	chr12:1928481-1928531	SAEC	small airway:	n/a
38	chr12:1948578-1948628	MCF-7	breast:	n/a
39	chr12:1922067-1922117	AG04449	skin:	fetal
40	chr12:1940452-1940502	HRCEpiC	kidney:	n/a
41	chr12:1945300-1945350	AoSMC	blood vessel:	n/a
42	chr12:1928689-1928739	A549	lung:	n/a
43	chr12:1928481-1928531	GM12891	blood:	n/a
44	chr12:1937968-1938018	HL-60	blood:	n/a
45	chr12:1937877-1937927	SK-N-MC	brain:	n/a
46	chr12:1949503-1949553	NHBE	bronchial:	n/a
47	chr12:1928481-1928531	AoSMC	blood vessel:	n/a
48	chr12:1937877-1937927	HL-60	blood:	n/a
49	chr12:1930326-1930376	NHBE	bronchial:	n/a
50	chr12:1949503-1949553	HEK293	kidney:	embryo

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:1915615..1917986-chr12:1924786..1926838,2	K562	blood:
2	chr12:1741511..1744510-chr12:1943871..1945697,2	K562	blood:
3	chr12:1933541..1935951-chr12:1940567..1942424,2	K562	blood:
4	chr12:1918012..1920353-chr12:1939627..1941633,2	MCF-7	breast:
5	chr12:1923072..1925795-chr12:1938699..1940589,2	MCF-7	breast:
6	chr12:1950335..1952773-chr12:1969860..1971374,2	MCF-7	breast:
7	chr12:1920587..1924096-chr12:1946145..1949569,4	MCF-7	breast:
8	chr12:1932447..1935067-chr12:1939828..1942115,3	MCF-7	breast:
9	chr12:1945477..1946181-chr12:2041443..2042003,2	MCF-7	breast:
10	chr12:1947774..1950374-chr12:1986873..1988503,2	MCF-7	breast:
11	chr12:1947284..1949728-chr12:2036486..2038838,2	MCF-7	breast:
12	chr12:1905374..1907142-chr12:1951674..1953593,2	MCF-7	breast:
13	chr12:1905343..1907993-chr12:1944504..1948626,5	MCF-7	breast:
14	chr12:1905054..1907716-chr12:1943766..1946105,3	MCF-7	breast:
15	chr12:1930362..1931932-chr12:1934662..1936789,2	MCF-7	breast:
16	chr12:1799987..1802012-chr12:1946925..1950411,3	MCF-7	breast:
17	chr12:1909603..1910441-chr12:1945244..1945817,2	MCF-7	breast:
18	chr12:1910081..1912246-chr12:1949040..1950547,2	K562	blood:
19	chr12:1944160..1952960-chr12:2039965..2049915,22	MCF-7	breast:
20	chr12:1923163..1923961-chr12:1939620..1940160,2	MCF-7	breast:
21	chr12:1945750..1946705-chr12:2048995..2049750,2	MCF-7	breast:
22	chr12:1915615..1917986-chr12:1924786..1926838,2	K562	blood:
23	chr12:1737994..1740960-chr12:1947307..1949303,2	MCF-7	breast:
24	chr12:1947643..1951345-chr12:1957413..1959557,3	MCF-7	breast:
25	chr12:1912567..1917043-chr12:1917472..1921043,5	K562	blood:
26	chr12:1923072..1925795-chr12:1938699..1940589,2	MCF-7	breast:
27	chr12:1950359..1950994-chr12:2041053..2041904,2	MCF-7	breast:
28	chr12:1904001..1906826-chr12:1919472..1921344,2	K562	blood:
29	chr12:1905406..1906059-chr12:1939762..1940329,2	MCF-7	breast:
30	chr12:1923163..1923961-chr12:1939620..1940160,2	MCF-7	breast:
31	chr12:1905042..1905969-chr12:1944742..1945885,3	MCF-7	breast:
32	chr12:1876884..1877711-chr12:1950746..1951257,2	MCF-7	breast:
33	chr12:1930362..1931932-chr12:1934662..1936789,2	MCF-7	breast:
34	chr12:1945038..1946828-chr12:1971867..1974133,2	K562	blood:
35	chr12:1901985..1907754-chr12:1946580..1951659,8	MCF-7	breast:
36	chr12:1933541..1935951-chr12:1940567..1942424,2	K562	blood:
37	chr12:1950359..1950994-chr12:2041053..2041904,3	MCF-7	breast:
38	chr12:1797292..1800039-chr12:1940442..1943362,2	MCF-7	breast:
39	chr12:1925102..1928805-chr12:1946979..1949915,3	MCF-7	breast:
40	chr12:1951607..1953524-chr12:2057455..2059714,2	MCF-7	breast:
41	chr12:1910843..1912522-chr12:1945003..1947651,2	MCF-7	breast:
42	chr12:1947445..1949197-chr12:2016726..2018832,2	MCF-7	breast:
43	chr12:1921269..1923557-chr12:2112437..2115050,2	MCF-7	breast:
44	chr12:1940153..1940669-chr12:2041125..2041895,2	MCF-7	breast:
45	chr12:1946363..1947932-chr12:2045137..2046691,2	MCF-7	breast:
46	chr12:1923170..1924049-chr12:2041180..2042060,3	MCF-7	breast:
47	chr12:1949517..1951136-chr12:2022065..2024789,2	MCF-7	breast:
48	chr11:62647795..62648738-chr12:1919373..1920206,2	NB4	blood:
49	chr12:1949995..1951546-chr12:1955088..1956789,2	MCF-7	breast:
50	chr12:1939207..1940397-chr12:1950388..1951271,5	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADIPOR2-2	chr12:1940101-1940134	NONHSAT025429
2	lnc-ADIPOR2-2	chr12:1936576-1936760	NONHSAT025428
3	lnc-ADIPOR2-2	chr12:1929649-1929980	NONHSAT025427
4	lnc-ADIPOR2-2	chr12:1936576-1936796	NONHSAT025431
5	lnc-ADIPOR2-2	chr12:1936895-1936963	NONHSAT025428
6	lnc-ADIPOR2-2	chr12:1929750-1929980	NONHSAT025431
7	lnc-ADIPOR2-2	chr12:1929676-1929980	NONHSAT025428
8	lnc-ADIPOR2-2	chr12:1937242-1937381	NONHSAT025429
9	lnc-ADIPOR2-2	chr12:1936895-1936982	NONHSAT025431
10	lnc-ADIPOR2-2	chr12:1936576-1936796	NONHSAT025429
11	lnc-ADIPOR2-2	chr12:1936573-1936894	NONHSAT025427
12	lnc-ADIPOR2-2	chr12:1929738-1929980	NONHSAT025429
13	lnc-LRTM2-5	chr12:1917593-1917645	NONHSAT025423

No data

Variant related genes	Relation type
CACNA2D4	TF binding region
LRTM2	TF binding region
CACNA2D4	CpG island
LRTM2	CpG island
ENSG00000203593	chromatin interactions
ENSG00000166159	chromatin interactions
ENSG00000151065	chromatin interactions
ENSG00000006831	chromatin interactions
ENSG00000235049	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000111186	chromatin interactions
ENSG00000151062	chromatin interactions

Extended variants
information (count: 1845 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1845 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11611260	chr12:1916838-1916839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546377960	chr12:1916839-1916840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs561828446	chr12:1916851-1916852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78552495	chr12:1916904-1916905	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550572583	chr12:1916905-1916906	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568725343	chr12:1916906-1916907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539424602	chr12:1916910-1916911	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186393052	chr12:1916922-1916923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs571152113	chr12:1916935-1916936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535240870	chr12:1916966-1916967	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553560963	chr12:1916970-1916971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550646496	chr12:1916977-1916978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147297642	chr12:1916988-1916989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191657141	chr12:1917003-1917004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs557413485	chr12:1917034-1917035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140960416	chr12:1917043-1917044	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183056456	chr12:1917083-1917084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117611152	chr12:1917099-1917100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535857870	chr12:1917133-1917134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369396079	chr12:1917152-1917153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572757109	chr12:1917176-1917177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540041086	chr12:1917178-1917179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79845762	chr12:1917188-1917189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146379874	chr12:1917220-1917221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35467437	chr12:1917221-1917222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386759492	chr12:1917222-1917223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199979604	chr12:1917224-1917225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200006269	chr12:1917225-1917226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374338444	chr12:1917247-1917248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560878896	chr12:1917248-1917249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144908361	chr12:1917262-1917263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs80062255	chr12:1917392-1917393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551355389	chr12:1917393-1917394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571164258	chr12:1917405-1917406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553261982	chr12:1917418-1917419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549760114	chr12:1917450-1917451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568597386	chr12:1917455-1917456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536027137	chr12:1917493-1917494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557218852	chr12:1917528-1917529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191006683	chr12:1917551-1917552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139602506	chr12:1917553-1917554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147542855	chr12:1917563-1917564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114110272	chr12:1917564-1917565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375038286	chr12:1917572-1917573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572822336	chr12:1917617-1917618	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs540101605	chr12:1917618-1917619	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs555618114	chr12:1917655-1917656	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369071947	chr12:1917685-1917686	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544386702	chr12:1917733-1917734	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139447553	chr12:1917769-1917770	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	22488967	CNVD

Chromatin state (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1905600-1928600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:1910800-1920000	Weak transcription	Primary B cells from cord blood	blood
3	chr12:1911600-1919200	Weak transcription	Osteobl	bone
4	chr12:1912800-1917000	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr12:1913400-1917000	Enhancers	Duodenum Mucosa	Duodenum
6	chr12:1913800-1917000	Enhancers	Fetal Intestine Large	intestine
7	chr12:1913800-1917600	Enhancers	Placenta	Placenta
8	chr12:1913800-1918800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr12:1913800-1920000	Enhancers	Fetal Thymus	thymus
10	chr12:1913800-1920400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr12:1914000-1917600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:1914000-1917600	Enhancers	Fetal Intestine Small	intestine
13	chr12:1914000-1920400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:1914200-1918400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr12:1914200-1918600	Weak transcription	K562	blood
16	chr12:1914200-1919600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:1914200-1919800	Weak transcription	Primary T cells from cord blood	blood
18	chr12:1914200-1920000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr12:1914200-1920600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr12:1914400-1917400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr12:1914400-1918800	Weak transcription	Brain Germinal Matrix	brain
22	chr12:1914400-1919800	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr12:1914400-1919800	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr12:1914400-1920400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:1914600-1917800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:1915200-1917800	Weak transcription	Spleen	Spleen
27	chr12:1915200-1919600	Weak transcription	Lung	lung
28	chr12:1915600-1917600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr12:1915600-1917800	Enhancers	Fetal Brain Male	brain
30	chr12:1915600-1920600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr12:1916000-1919200	Weak transcription	Adipose Nuclei	Adipose
32	chr12:1916000-1919800	Weak transcription	NHDF-Ad	bronchial
33	chr12:1916000-1921200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr12:1916000-1921600	Weak transcription	HSMM	muscle
35	chr12:1916200-1918000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr12:1916200-1918200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr12:1916200-1918400	Weak transcription	Left Ventricle	heart
38	chr12:1916400-1917000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr12:1916600-1917000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr12:1916600-1917600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr12:1916600-1918800	Enhancers	HepG2	liver
42	chr12:1916800-1917000	Enhancers	Right Ventricle	heart
43	chr12:1916800-1919000	Weak transcription	Fetal Muscle Leg	muscle
44	chr12:1917000-1917800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr12:1917000-1919600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr12:1917000-1919600	Weak transcription	Right Ventricle	heart
47	chr12:1917000-1919800	Weak transcription	Duodenum Mucosa	Duodenum
48	chr12:1917000-1920600	Weak transcription	Fetal Intestine Large	intestine
49	chr12:1917000-1923000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr12:1917400-1918000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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