Variant report

Variant	nsv1054111
Chromosome Location	chr12:67556780-67865542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3872)
CpG islands
(count:1650)
Chromatin interactive
region (count:239)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:3872 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:67828699-67829280	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:67664013-67664397	HepG2	liver:	n/a	chr12:67664187-67664195
3	ARID3A	chr12:67662135-67663369	K562	blood:	n/a	n/a
4	ARID3A	chr12:67703123-67703203	K562	blood:	n/a	n/a
5	ARID3A	chr12:67835539-67836045	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:67809358-67809473	K562	blood:	n/a	n/a
7	ARID3A	chr12:67819021-67819107	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:67669321-67669824	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:67822223-67822716	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:67662278-67663327	HepG2	liver:	n/a	n/a
11	ATF1	chr12:67661998-67663385	K562	blood:	n/a	n/a
12	ATF2	chr12:67843161-67843990	GM12878	blood:	n/a	n/a
13	ATF2	chr12:67845722-67846370	GM12878	blood:	n/a	n/a
14	ATF2	chr12:67843164-67843893	GM12878	blood:	n/a	n/a
15	ATF2	chr12:67662116-67663451	GM12878	blood:	n/a	n/a
16	ATF2	chr12:67662424-67663281	GM12878	blood:	n/a	n/a
17	ATF2	chr12:67662376-67663106	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr12:67662394-67663276	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr12:67845726-67846595	GM12878	blood:	n/a	n/a
20	ATF3	chr12:67663238-67663417	K562	blood:	n/a	n/a
21	BACH1	chr12:67738241-67738268	K562	blood:	n/a	n/a
22	BACH1	chr12:67813589-67813997	K562	blood:	n/a	n/a
23	BACH1	chr12:67807509-67807919	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr12:67662117-67663453	K562	blood:	n/a	n/a
25	BACH1	chr12:67813286-67814163	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr12:67662357-67664197	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr12:67845795-67846529	GM12878	blood:	n/a	n/a
28	BATF	chr12:67775951-67776271	GM12878	blood:	n/a	n/a
29	BATF	chr12:67775991-67776267	GM12878	blood:	n/a	n/a
30	BATF	chr12:67845841-67846323	GM12878	blood:	n/a	n/a
31	BATF	chr12:67851609-67851978	GM12878	blood:	n/a	n/a
32	BATF	chr12:67843294-67843631	GM12878	blood:	n/a	chr12:67843595-67843603 chr12:67843432-67843443 chr12:67843433-67843443
33	BATF	chr12:67843260-67843650	GM12878	blood:	n/a	chr12:67843595-67843603 chr12:67843432-67843443 chr12:67843433-67843443
34	BCL11A	chr12:67845865-67846319	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:67843261-67843701	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:67845764-67846362	GM12878	blood:	n/a	n/a
37	BCL3	chr12:67845801-67846302	GM12878	blood:	n/a	n/a
38	BCL3	chr12:67662296-67663406	A549	lung:	n/a	chr12:67663103-67663112 chr12:67663389-67663402 chr12:67663097-67663110
39	BCL3	chr12:67662052-67663799	A549	lung:	n/a	chr12:67663103-67663112 chr12:67663389-67663402 chr12:67663097-67663110
40	BCL3	chr12:67845881-67846335	GM12878	blood:	n/a	n/a
41	BCL3	chr12:67843343-67843711	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:67663833-67664526	GM12878	blood:	n/a	chr12:67664184-67664193
43	BCLAF1	chr12:67843175-67843879	GM12878	blood:	n/a	n/a
44	BCLAF1	chr12:67845841-67846333	GM12878	blood:	n/a	n/a
45	BCLAF1	chr12:67662154-67663759	GM12878	blood:	n/a	chr12:67663103-67663112 chr12:67663389-67663402 chr12:67663097-67663110
46	BCLAF1	chr12:67845666-67846439	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:67835595-67835904	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:67819324-67819437	HepG2	liver:	n/a	n/a
49	BHLHE40	chr12:67662083-67663581	K562	blood:	n/a	n/a
50	BHLHE40	chr12:67851648-67851835	K562	blood:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67662725-67662775	AoSMC	blood vessel:	n/a
2	chr12:67662976-67663026	NB4	blood:	n/a
3	chr12:67813861-67813911	PFSK-1	brain:	n/a
4	chr12:67662725-67662775	AoSMC	blood vessel:	n/a
5	chr12:67662976-67663026	NB4	blood:	n/a
6	chr12:67813861-67813911	PFSK-1	brain:	n/a
7	chr12:67782441-67782491	BE2_C	brain:	n/a
8	chr12:67662897-67662947	SAEC	small airway:	n/a
9	chr12:67835705-67835755	HCF	heart:	n/a
10	chr12:67665055-67665105	GM19239	blood:	n/a
11	chr12:67660403-67660453	T-47D	breast:	n/a
12	chr12:67663092-67663142	BJ	skin:	n/a
13	chr12:67666891-67666941	Jurkat	blood:	n/a
14	chr12:67813861-67813911	GM19239	blood:	n/a
15	chr12:67662897-67662947	HCT-116	colon:	n/a
16	chr12:67670688-67670738	HEK293	kidney:	embryo
17	chr12:67752236-67752286	H1-hESC	embryonic stem cell:	embryo
18	chr12:67662516-67662566	HUVEC	blood vessel:	n/a
19	chr12:67662589-67662639	AG09319	gingival:	n/a
20	chr12:67807625-67807675	HUVEC	blood vessel:	n/a
21	chr12:67813861-67813911	H1-hESC	embryonic stem cell:	embryo
22	chr12:67835705-67835755	HRCEpiC	kidney:	n/a
23	chr12:67662589-67662639	AG04449	skin:	fetal
24	chr12:67663226-67663276	BE2_C	brain:	n/a
25	chr12:67663226-67663276	HEK293	kidney:	embryo
26	chr12:67670688-67670738	HEEpiC	esophagus:	n/a
27	chr12:67665055-67665105	SAEC	small airway:	n/a
28	chr12:67813861-67813911	HIPEpiC	eye:	n/a
29	chr12:67670688-67670738	HUVEC	blood vessel:	n/a
30	chr12:67782441-67782491	AG04449	skin:	fetal
31	chr12:67663479-67663529	SK-N-SH_RA	brain:	n/a
32	chr12:67663012-67663062	AG10803	skin:	n/a
33	chr12:67663083-67663133	NT2-D1	testis:	n/a
34	chr12:67663012-67663062	NHBE	bronchial:	n/a
35	chr12:67663042-67663092	HCF	heart:	n/a
36	chr12:67813861-67813911	NB4	blood:	n/a
37	chr12:67830705-67830755	H1-hESC	embryonic stem cell:	embryo
38	chr12:67665055-67665105	HRPEpiC	eye:	n/a
39	chr12:67663479-67663529	HNPCEpiC	eye:	n/a
40	chr12:67670688-67670738	HAEpiC	amniotic membrane:	n/a
41	chr12:67662516-67662566	SK-N-SH_RA	brain:	n/a
42	chr12:67835705-67835755	GM06990	blood:	n/a
43	chr12:67664046-67664096	SK-N-SH	brain:	n/a
44	chr12:67670688-67670738	PrEC	prostate:	n/a
45	chr12:67662976-67663026	PFSK-1	brain:	n/a
46	chr12:67663479-67663529	ProgFib	skin:	n/a
47	chr12:67663479-67663529	K562	blood:	n/a
48	chr12:67663042-67663092	NT2-D1	testis:	n/a
49	chr12:67662516-67662566	SKMC	muscle:	n/a
50	chr12:67662516-67662566	ECC-1	luminal epithelium:	n/a

(count:239 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:67701166..67703768-chr12:67717126..67719527,2	MCF-7	breast:
2	chr12:67685431..67687281-chr12:67692983..67694546,2	MCF-7	breast:
3	chr12:67673864..67678122-chr12:67685372..67688266,4	K562	blood:
4	chr12:67749556..67750279-chr12:67835286..67835947,2	MCF-7	breast:
5	chr12:67834794..67836374-chr12:67858992..67861448,2	K562	blood:
6	chr12:67859635..67861520-chr12:67936585..67938194,2	MCF-7	breast:
7	chr12:67853049..67855700-chr12:68045078..68047637,2	MCF-7	breast:
8	chr12:67807149..67807779-chr12:68336675..68337459,2	MCF-7	breast:
9	chr12:67708442..67711026-chr12:67711731..67713764,2	MCF-7	breast:
10	chr12:67655079..67657081-chr12:67663033..67665904,3	K562	blood:
11	chr12:67839783..67841299-chr12:68041016..68043134,2	MCF-7	breast:
12	chr12:67708442..67711026-chr12:67711731..67713764,2	MCF-7	breast:
13	chr12:67714913..67718592-chr12:67718971..67722103,3	K562	blood:
14	chr12:67554880..67555774-chr12:67809025..67809838,2	MCF-7	breast:
15	chr12:67662594..67666429-chr12:67679888..67683393,4	K562	blood:
16	chr12:67593545..67595294-chr12:67601266..67602833,2	K562	blood:
17	chr12:67678774..67680822-chr12:67683989..67686617,2	MCF-7	breast:
18	chr12:67655772..67657475-chr12:67658776..67661766,2	K562	blood:
19	chr12:67697667..67699390-chr12:67705731..67708067,2	K562	blood:
20	chr12:67713525..67718128-chr12:67719850..67722693,5	MCF-7	breast:
21	chr12:67849296..67851766-chr12:68042448..68044741,2	MCF-7	breast:
22	chr12:67663258..67665425-chr12:67739869..67742001,2	K562	blood:
23	chr12:67699472..67703250-chr12:67704428..67707950,5	K562	blood:
24	chr12:67852217..67854302-chr12:68040942..68043272,2	MCF-7	breast:
25	chr12:67820987..67823729-chr12:67825470..67827435,2	K562	blood:
26	chr12:67674261..67676215-chr12:67685675..67687691,2	MCF-7	breast:
27	chr12:67674561..67677422-chr12:67679504..67681796,2	MCF-7	breast:
28	chr12:67662842..67663417-chr16:89882588..89883442,2	Hela-S3	cervix:
29	chr12:67661368..67664788-chr12:67696254..67698548,3	MCF-7	breast:
30	chr12:67708053..67712275-chr12:67717926..67720355,3	K562	blood:
31	chr12:67835015..67836626-chr12:68041629..68043874,2	MCF-7	breast:
32	chr12:67822398..67825852-chr12:67826641..67830656,5	MCF-7	breast:
33	chr12:67662879..67663570-chr22:19973947..19974893,2	HCT-116	colon:
34	chr12:67479380..67480285-chr12:67669243..67670001,2	MCF-7	breast:
35	chr12:67708479..67710797-chr12:67718354..67720777,2	MCF-7	breast:
36	chr12:67748303..67751189-chr12:68042035..68043967,2	MCF-7	breast:
37	chr12:67712989..67715089-chr12:67716509..67719238,2	K562	blood:
38	chr12:67635019..67637081-chr12:67662707..67665597,2	K562	blood:
39	chr12:67803949..67805716-chr12:67809296..67811931,2	MCF-7	breast:
40	chr12:67646762..67649274-chr12:67652316..67653916,2	MCF-7	breast:
41	chr12:67652317..67654299-chr12:67658127..67660959,2	K562	blood:
42	chr12:67757297..67760146-chr12:67769461..67771948,2	MCF-7	breast:
43	chr12:67599661..67601633-chr12:67605002..67607357,2	K562	blood:
44	chr12:67749483..67750180-chr12:67770492..67771031,2	MCF-7	breast:
45	chr12:67662963..67663736-chr5:43018653..43019184,2	Hela-S3	cervix:
46	chr12:67462768..67464522-chr12:67660868..67664362,4	MCF-7	breast:
47	chr12:67709812..67710332-chr4:99531489..99532009,2	MCF-7	breast:
48	chr12:67707079..67709730-chr12:67721053..67723374,2	K562	blood:
49	chr12:67661017..67663110-chr12:67715146..67717539,2	K562	blood:
50	chr12:67762520..67764368-chr12:67764796..67766674,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAND1-1	chr12:67814937-67815084	XLOC_009790
2	lnc-GRIP1-4	chr12:67836568-67836838	XLOC_010112
3	lnc-DYRK2-3	chr12:67711527-67713732	NONHSAT029248
4	lnc-GRIP1-4	chr12:67836074-67836339	ENSG00000256172
5	lnc-CAND1-2	chr12:67745216-67745819	NONHSAT029249
6	lnc-CAND1-1	chr12:67788395-67788662	XLOC_009790
7	lnc-DYRK2-3	chr12:67708478-67708952	ENSG00000247008
8	lnc-GRIP1-8	chr12:67659622-67660746	NONHSAT140080
9	lnc-GRIP1-8	chr12:67656109-67663060	NONHSAT029243
10	lnc-GRIP1-3	chr12:67829112-67829296	XLOC_010111
11	lnc-DYRK2-3	chr12:67711527-67713730	ENSG00000247008
12	lnc-GRIP1-4	chr12:67834936-67835252	XLOC_010112
13	lnc-GRIP1-3	chr12:67829415-67829455	XLOC_010111
14	lnc-GRIP1-4	chr12:67834935-67835252	NONHSAT029254
15	lnc-GRIP1-9	chr12:67818052-67818766	NONHSAT029251
16	lnc-GRIP1-4	chr12:67834778-67835252	ENSG00000256172
17	lnc-GRIP1-4	chr12:67836567-67836838	NONHSAT029254

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CAND1	hsa-miR-186-5p	chr12:67706949-67706970
2	CAND1	hsa-miR-186-5p	chr12:67707508-67707528
3	CAND1	hsa-miR-1	chr12:67707549-67707570
4	CAND1	hsa-miR-1	chr12:67707805-67707827

Variant related genes	Relation type
CAND1	TF binding region
MRPL40P1	TF binding region
NTAN1P3	TF binding region
ENSG00000256172	TF binding region
GGTA2P	TF binding region
CAND1	CpG island
MRPL40P1	CpG island
NTAN1P3	CpG island
ENSG00000256172	CpG island
GGTA2P	CpG island
ENSG00000006712	chromatin interactions
ENSG00000256172	chromatin interactions
ENSG00000127334	chromatin interactions
ENSG00000256248	chromatin interactions
ENSG00000053501	chromatin interactions
ENSG00000124092	chromatin interactions
ENSG00000188186	chromatin interactions
ENSG00000091039	chromatin interactions
ENSG00000063322	chromatin interactions
ENSG00000187741	chromatin interactions
ENSG00000099889	chromatin interactions
ENSG00000108107	chromatin interactions
ENSG00000177738	chromatin interactions
ENSG00000061936	chromatin interactions
ENSG00000237766	chromatin interactions
ENSG00000111530	chromatin interactions
YWHAH	miRNA target sites
SIPA1L2	miRNA target sites

Extended variants
information (count: 9182 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:9182 , 50 per page) page: 1 2 3 4 5 6 7 ... 184

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182452736	chr12:67567206-67567207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs117280052	chr12:67567286-67567287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549765440	chr12:67567310-67567311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187085189	chr12:67567317-67567318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149464431	chr12:67567320-67567321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144124042	chr12:67567322-67567323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535441730	chr12:67567326-67567327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530902068	chr12:67567371-67567372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190344874	chr12:67567400-67567401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565825706	chr12:67567403-67567404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539507459	chr12:67567427-67567428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558332040	chr12:67567457-67567458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576531699	chr12:67567468-67567469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544108307	chr12:67567475-67567476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148263494	chr12:67567497-67567498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368549312	chr12:67567519-67567520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75490455	chr12:67567525-67567526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541840041	chr12:67567573-67567574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560333181	chr12:67567590-67567591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527394844	chr12:67567599-67567600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532436325	chr12:67567620-67567621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545534994	chr12:67567635-67567636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564330320	chr12:67567687-67567688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531371146	chr12:67567697-67567698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181674248	chr12:67567705-67567706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185856457	chr12:67567746-67567747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529295429	chr12:67567757-67567758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141872517	chr12:67567845-67567846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565690675	chr12:67567847-67567848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146231740	chr12:67567857-67567858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551549338	chr12:67567883-67567884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570262809	chr12:67567895-67567896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537225262	chr12:67567902-67567903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556069126	chr12:67567910-67567911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574374939	chr12:67567950-67567951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535297222	chr12:67567957-67567958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74098648	chr12:67567986-67567987	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572045001	chr12:67567998-67567999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369142318	chr12:67568006-67568007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139350140	chr12:67568053-67568054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564011577	chr12:67568056-67568057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143695272	chr12:67568098-67568099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575115797	chr12:67568116-67568117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114007823	chr12:67568132-67568133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561504163	chr12:67568170-67568171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372227429	chr12:67568177-67568178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146341667	chr12:67568236-67568237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190231836	chr12:67568255-67568256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528912998	chr12:67568283-67568284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559336518	chr12:67568294-67568295	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	19115005	CNVD
Cancer	20164920	CNVD
Lung adenocarcinoma	17982442	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bone cancer	16732325	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	17850661	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3987 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67567200-67568400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:67568800-67569000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:67578400-67578600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
4	chr12:67578400-67578800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:67578600-67578800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
6	chr12:67585800-67586800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr12:67586200-67586600	Enhancers	Brain Germinal Matrix	brain
8	chr12:67591400-67591600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:67591800-67592800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr12:67591800-67593600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr12:67592800-67593200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:67593000-67593200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:67593600-67594000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:67593800-67595000	Enhancers	Fetal Intestine Small	intestine
15	chr12:67594000-67594200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr12:67594200-67595600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:67594400-67594600	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr12:67594600-67613800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr12:67594800-67596400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:67595000-67595400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:67595400-67596200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr12:67595600-67596600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:67595800-67596200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:67595800-67596400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:67596000-67596200	Enhancers	GM12878-XiMat	blood
26	chr12:67596200-67596800	Flanking Active TSS	GM12878-XiMat	blood
27	chr12:67596200-67597000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr12:67596800-67597000	Enhancers	GM12878-XiMat	blood
29	chr12:67598200-67601800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:67600200-67602000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:67601800-67602200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:67602000-67602800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:67602000-67602800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr12:67602400-67603200	Active TSS	Right Atrium	heart
35	chr12:67602800-67603000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:67603000-67603200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:67604600-67605400	Enhancers	HepG2	liver
38	chr12:67613800-67614000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr12:67616000-67616200	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr12:67616200-67616600	Enhancers	Stomach Smooth Muscle	stomach
41	chr12:67616200-67617200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr12:67616600-67617400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr12:67616800-67617400	Enhancers	Primary B cells from peripheral blood	blood
44	chr12:67617000-67617200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:67617000-67617400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr12:67617000-67617800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:67625200-67625400	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr12:67625200-67626800	Enhancers	Rectal Smooth Muscle	rectum
49	chr12:67625200-67627000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:67625600-67626000	Active TSS	Stomach Smooth Muscle	stomach

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