Variant report

Variant	nsv520633
Chromosome Location	chr12:124548394-124683205
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1168)
CpG islands
(count:1284)
Chromatin interactive
region (count:55)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124615209-124615614	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:124673142-124673342	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:124633863-124633864	K562	blood:	n/a	n/a
4	ATF1	chr12:124675443-124675916	K562	blood:	n/a	n/a
5	ATF1	chr12:124594322-124594607	K562	blood:	n/a	n/a
6	ATF1	chr12:124646901-124647100	K562	blood:	n/a	n/a
7	ATF1	chr12:124674907-124675162	K562	blood:	n/a	n/a
8	ATF1	chr12:124663213-124663277	K562	blood:	n/a	n/a
9	ATF2	chr12:124632071-124632565	GM12878	blood:	n/a	n/a
10	ATF2	chr12:124675444-124675932	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:124609923-124610388	GM12878	blood:	n/a	n/a
12	ATF2	chr12:124625236-124626332	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr12:124611385-124611914	GM12878	blood:	n/a	n/a
14	ATF2	chr12:124625264-124625831	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr12:124609933-124610382	GM12878	blood:	n/a	n/a
16	ATF2	chr12:124675443-124675917	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr12:124604536-124604763	K562	blood:	n/a	n/a
18	ATF3	chr12:124594271-124594693	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr12:124594241-124594625	GM12878	blood:	n/a	n/a
20	ATF3	chr12:124675595-124675789	K562	blood:	n/a	n/a
21	ATF3	chr12:124555079-124555263	K562	blood:	n/a	n/a
22	ATF3	chr12:124594283-124594573	K562	blood:	n/a	n/a
23	ATF3	chr12:124594353-124594485	GM12878	blood:	n/a	n/a
24	ATF3	chr12:124594324-124594520	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr12:124594197-124594666	HepG2	liver:	n/a	n/a
26	ATF3	chr12:124594308-124594500	HepG2	liver:	n/a	n/a
27	BACH1	chr12:124582998-124583224	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr12:124625367-124625926	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr12:124680202-124680363	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr12:124611466-124611870	GM12878	blood:	n/a	chr12:124611701-124611712
31	BATF	chr12:124611396-124611955	GM12878	blood:	n/a	chr12:124611701-124611712
32	BATF	chr12:124610045-124610389	GM12878	blood:	n/a	n/a
33	BATF	chr12:124609954-124610413	GM12878	blood:	n/a	n/a
34	BATF	chr12:124573916-124574248	GM12878	blood:	n/a	n/a
35	BATF	chr12:124555279-124555468	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:124610023-124610397	GM12878	blood:	n/a	n/a
37	BCL11A	chr12:124610047-124610326	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:124611480-124611907	GM12878	blood:	n/a	n/a
39	BCL11A	chr12:124625465-124625715	H1-hESC	embryonic stem cell:	n/a	chr12:124625535-124625544 chr12:124625670-124625679
40	BCL3	chr12:124609965-124610331	GM12878	blood:	n/a	n/a
41	BCL3	chr12:124615151-124615562	A549	lung:	n/a	chr12:124615246-124615255
42	BCL3	chr12:124615186-124615669	A549	lung:	n/a	chr12:124615246-124615255
43	BCLAF1	chr12:124609938-124610440	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:124673057-124673342	HepG2	liver:	n/a	n/a
45	BHLHE40	chr12:124669051-124669266	K562	blood:	n/a	n/a
46	BHLHE40	chr12:124625770-124625909	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:124615696-124616067	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:124615211-124615604	HepG2	liver:	n/a	n/a
49	BHLHE40	chr12:124657027-124657097	K562	blood:	n/a	n/a
50	BHLHE40	chr12:124573203-124573420	K562	blood:	n/a	chr12:124573254-124573267

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124607875-124607925	Hepatocyte	liver:	n/a
2	chr12:124672621-124672671	PANC-1	pancreas:	n/a
3	chr12:124582865-124582915	AG10803	skin:	n/a
4	chr12:124607875-124607925	Hepatocyte	liver:	n/a
5	chr12:124672621-124672671	PANC-1	pancreas:	n/a
6	chr12:124582865-124582915	AG10803	skin:	n/a
7	chr12:124616497-124616547	NH-A	brain:	n/a
8	chr12:124585152-124585202	SKMC	muscle:	n/a
9	chr12:124616497-124616547	K562	blood:	n/a
10	chr12:124651970-124652020	MCF10A-Er-Src	breast:	n/a
11	chr12:124632549-124632599	HRCEpiC	kidney:	n/a
12	chr12:124616497-124616547	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:124556975-124557025	HNPCEpiC	eye:	n/a
14	chr12:124590434-124590484	H1-hESC	embryonic stem cell:	embryo
15	chr12:124607875-124607925	MCF-7	breast:	n/a
16	chr12:124600518-124600568	Jurkat	blood:	n/a
17	chr12:124600431-124600481	SK-N-SH	brain:	n/a
18	chr12:124590463-124590513	ProgFib	skin:	n/a
19	chr12:124556975-124557025	SKMC	muscle:	n/a
20	chr12:124586893-124586943	SK-N-SH_RA	brain:	n/a
21	chr12:124601493-124601543	T-47D	breast:	n/a
22	chr12:124626058-124626108	Jurkat	blood:	n/a
23	chr12:124672621-124672671	SK-N-SH_RA	brain:	n/a
24	chr12:124672621-124672671	GM19239	blood:	n/a
25	chr12:124661629-124661679	LNCaP	prostate:	n/a
26	chr12:124672621-124672671	HEEpiC	esophagus:	n/a
27	chr12:124586893-124586943	ECC-1	luminal epithelium:	n/a
28	chr12:124616497-124616547	ECC-1	luminal epithelium:	n/a
29	chr12:124586893-124586943	RPTEC	kidney:	n/a
30	chr12:124642214-124642264	RPTEC	kidney:	n/a
31	chr12:124582865-124582915	GM12892	blood:	n/a
32	chr12:124586893-124586943	GM19239	blood:	n/a
33	chr12:124616497-124616547	HEK293	kidney:	embryo
34	chr12:124661629-124661679	NHDF-neo	bronchial:	n/a
35	chr12:124585152-124585202	Jurkat	blood:	n/a
36	chr12:124585444-124585494	HCPEpiC	choroid plexus:	n/a
37	chr12:124585152-124585202	HEK293	kidney:	embryo
38	chr12:124632549-124632599	AG10803	skin:	n/a
39	chr12:124626058-124626108	U87	brain:	n/a
40	chr12:124585152-124585202	Hela-S3	cervix:	n/a
41	chr12:124661629-124661679	Jurkat	blood:	n/a
42	chr12:124600518-124600568	SK-N-SH	brain:	n/a
43	chr12:124600431-124600481	HAEpiC	amniotic membrane:	n/a
44	chr12:124590434-124590484	SK-N-SH_RA	brain:	n/a
45	chr12:124556975-124557025	HL-60	blood:	n/a
46	chr12:124585152-124585202	CMK	blood:	n/a
47	chr12:124601493-124601543	NH-A	brain:	n/a
48	chr12:124590434-124590484	SKMC	muscle:	n/a
49	chr12:124582865-124582915	PFSK-1	brain:	n/a
50	chr12:124586893-124586943	NB4	blood:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:124655778..124658443-chr12:124671523..124673328,2	MCF-7	breast:
2	chr12:124547553..124549096-chr12:124550673..124553525,2	K562	blood:
3	chr12:124547212..124549096-chr12:124550673..124553525,3	K562	blood:
4	chr12:124563279..124565745-chr12:124567751..124569613,2	K562	blood:
5	chr12:124668358..124672315-chr12:124673653..124677298,4	K562	blood:
6	chr12:124583853..124585676-chr12:124587897..124589981,2	MCF-7	breast:
7	chr12:124674017..124675949-chr12:124744781..124746712,2	MCF-7	breast:
8	chr12:124638145..124640068-chr12:124640920..124643094,2	K562	blood:
9	chr12:124657896..124659881-chr12:124667349..124669461,2	K562	blood:
10	chr12:124673738..124676426-chr12:124681447..124683597,2	MCF-7	breast:
11	chr12:124628921..124630461-chr12:124632753..124634421,2	K562	blood:
12	chr12:124547212..124549096-chr12:124550673..124553525,3	K562	blood:
13	chr12:124677047..124679151-chr12:124697605..124700364,2	MCF-7	breast:
14	chr12:124547553..124549096-chr12:124550673..124553525,2	K562	blood:
15	chr12:124676315..124677962-chr12:124678657..124681009,2	MCF-7	breast:
16	chr12:124628921..124630461-chr12:124632753..124634421,2	K562	blood:
17	chr12:124581557..124584588-chr12:124587697..124590714,3	K562	blood:
18	chr12:124601171..124602980-chr12:124607988..124610923,3	K562	blood:
19	chr12:124583853..124585676-chr12:124587897..124589981,2	MCF-7	breast:
20	chr12:124581557..124584588-chr12:124587697..124590714,3	K562	blood:
21	chr12:124673692..124676490-chr12:124681372..124684204,2	K562	blood:
22	chr12:124679432..124681822-chr12:124687516..124690464,2	K562	blood:
23	chr12:124671342..124675404-chr12:124675749..124680438,5	MCF-7	breast:
24	chr12:124651829..124653697-chr12:125395051..125397207,2	K562	blood:
25	chr12:124646500..124647369-chr12:124805388..124806131,3	MCF-7	breast:
26	chr12:124675809..124678194-chr12:124692945..124695855,2	K562	blood:
27	chr12:124654056..124655953-chr12:124657708..124659430,2	K562	blood:
28	chr12:124601171..124602980-chr12:124607988..124610923,3	K562	blood:
29	chr12:124650437..124653353-chr12:124656676..124658500,2	MCF-7	breast:
30	chr12:124569269..124571295-chr12:124672073..124674047,2	MCF-7	breast:
31	chr12:124676315..124677962-chr12:124678657..124681009,2	MCF-7	breast:
32	chr12:124674009..124675617-chr12:124796765..124798920,2	MCF-7	breast:
33	chr12:124668358..124672315-chr12:124673653..124677298,4	K562	blood:
34	chr12:124654056..124655953-chr12:124657708..124659430,2	K562	blood:
35	chr12:124650437..124653353-chr12:124656676..124658500,2	MCF-7	breast:
36	chr12:124667796..124669612-chr12:124670954..124672712,2	K562	blood:
37	chr12:124673340..124677254-chr12:124691442..124694738,3	MCF-7	breast:
38	chr12:124673738..124676426-chr12:124681447..124683597,2	MCF-7	breast:
39	chr12:124587267..124589633-chr12:124591820..124594336,2	K562	blood:
40	chr12:124644644..124645497-chr18:42602277..42602805,2	MCF-7	breast:
41	chr12:124563279..124565745-chr12:124567751..124569613,2	K562	blood:
42	chr12:124522354..124525198-chr12:124549022..124551115,2	MCF-7	breast:
43	chr12:124667740..124669717-chr12:124675023..124677753,2	MCF-7	breast:
44	chr12:124638145..124640068-chr12:124640920..124643094,2	K562	blood:
45	chr12:124671342..124675404-chr12:124675749..124680438,5	MCF-7	breast:
46	chr12:124655778..124658443-chr12:124671523..124673328,2	MCF-7	breast:
47	chr12:124604134..124606540-chr12:124636044..124638114,2	K562	blood:
48	chr12:124667740..124669717-chr12:124675023..124677753,2	MCF-7	breast:
49	chr12:124604134..124606540-chr12:124636044..124638114,2	K562	blood:
50	chr12:124667796..124669612-chr12:124670954..124672712,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF664-1	chr12:124559470-124559839	XLOC_009925
2	lnc-ZNF664-2	chr12:124572821-124573024	XLOC_009926
3	lnc-FAM101A-2	chr12:124634145-124634337	XLOC_009927
4	lnc-ZNF664-2	chr12:124599655-124599680	XLOC_009926
5	lnc-FAM101A-2	chr12:124634216-124634337	XLOC_009927
6	lnc-FAM101A-2	chr12:124680004-124680015	XLOC_009927
7	lnc-ZNF664-2	chr12:124574282-124574327	XLOC_009926
8	lnc-ZNF664-2	chr12:124570308-124573142	ENSG00000269923.1
9	lnc-ZNF664-2	chr12:124574591-124574717	XLOC_009926
10	lnc-ZNF664-2	chr12:124575119-124575483	XLOC_009926
11	lnc-ZNF664-2	chr12:124575119-124575483	XLOC_009926
12	lnc-ZNF664-2	chr12:124574282-124574327	XLOC_009926
13	lnc-ZNF664-1	chr12:124558542-124558567	XLOC_009925
14	lnc-ZNF664-2	chr12:124631771-124631821	XLOC_009926
15	lnc-ZNF664-2	chr12:124575119-124576008	XLOC_009926
16	lnc-ZNF664-2	chr12:124575119-124575483	XLOC_009926
17	lnc-ZNF664-2	chr12:124599655-124599680	XLOC_009926
18	lnc-ZNF664-2	chr12:124574282-124574327	XLOC_009926
19	lnc-ZNF664-2	chr12:124574594-124574626	XLOC_009926

No data

Variant related genes	Relation type
ENSG00000269923	TF binding region
ENSG00000269923	CpG island
ENSG00000269923	chromatin interactions
GMNN	miRNA target sites
CNOT6	miRNA target sites
NUDT12	miRNA target sites
TLN2	miRNA target sites
RELA	miRNA target sites
IP6K1	miRNA target sites
CD46	miRNA target sites
NUFIP2	miRNA target sites

Extended variants
information (count: 5262 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:5262 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10846592	chr12:124548394-124548395	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569476703	chr12:124548416-124548417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536933747	chr12:124548538-124548539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554877904	chr12:124548541-124548542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141186136	chr12:124548558-124548559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534038174	chr12:124548576-124548577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10846593	chr12:124548581-124548582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs375052815	chr12:124548589-124548590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577405623	chr12:124548605-124548606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569908405	chr12:124548625-124548626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550548269	chr12:124548664-124548665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575483785	chr12:124548665-124548666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112370518	chr12:124548706-124548707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560950330	chr12:124548716-124548717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528244902	chr12:124548717-124548718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535469914	chr12:124548721-124548722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367650861	chr12:124548722-124548723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370843070	chr12:124548745-124548746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150329715	chr12:124548787-124548788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555434505	chr12:124548788-124548789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559506671	chr12:124548795-124548796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56127918	chr12:124548798-124548799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566964214	chr12:124548823-124548824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1716386	chr12:124548900-124548901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568799459	chr12:124548921-124548922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536562468	chr12:124548941-124548942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548817795	chr12:124548967-124548968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368031465	chr12:124548987-124548988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566961490	chr12:124549137-124549138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534433639	chr12:124549167-124549168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10846594	chr12:124549174-124549175	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs138009668	chr12:124549264-124549265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374994318	chr12:124549332-124549333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149512784	chr12:124549338-124549339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574749002	chr12:124549347-124549348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377405348	chr12:124549406-124549407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542564700	chr12:124549428-124549429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74691570	chr12:124549506-124549507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555851261	chr12:124549508-124549509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75442607	chr12:124549515-124549516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544441723	chr12:124550874-124550875	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs533403068	chr12:124550895-124550896	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs556062073	chr12:124550961-124550962	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs200984229	chr12:124551033-124551034	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs373091408	chr12:124551034-124551035	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs113257051	chr12:124551042-124551043	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs58449918	chr12:124551080-124551081	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541528017	chr12:124551082-124551083	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs560116482	chr12:124551086-124551087	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs528384730	chr12:124551158-124551159	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1303 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124539400-124549600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:124550800-124551600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:124551000-124551600	ZNF genes & repeats	Brain Hippocampus Middle	brain
4	chr12:124551600-124552000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:124552000-124555800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:124553000-124557600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:124553600-124553800	Enhancers	Stomach Mucosa	stomach
8	chr12:124553800-124563200	Weak transcription	Stomach Mucosa	stomach
9	chr12:124554600-124555000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:124554600-124555400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:124554600-124555400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:124554800-124555000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr12:124554800-124555600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:124554800-124560400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:124555000-124555600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr12:124555000-124556400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:124555200-124555400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr12:124555200-124555600	Enhancers	NHEK	skin
19	chr12:124555200-124558000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr12:124555400-124557400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr12:124555400-124557400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr12:124555400-124558200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:124555400-124558800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr12:124555400-124558800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:124555400-124558800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:124555600-124556200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr12:124555600-124557000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:124555600-124557200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr12:124555600-124558800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:124555800-124556200	Enhancers	Fetal Lung	lung
31	chr12:124555800-124557000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr12:124555800-124558600	Enhancers	Fetal Stomach	stomach
33	chr12:124555800-124558800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr12:124555800-124558800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:124556000-124557200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:124556000-124558800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr12:124556000-124558800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:124556200-124557200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr12:124556200-124557600	Weak transcription	Fetal Lung	lung
40	chr12:124556400-124556600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:124556400-124556800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:124556400-124557400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:124556400-124558600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr12:124556600-124557200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:124556600-124557600	Enhancers	HUVEC	blood vessel
46	chr12:124556800-124559400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr12:124556800-124559600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:124556800-124560800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr12:124557000-124557400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:124557000-124557600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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