Variant report

Variant	nsv899214
Chromosome Location	chr12:66516692-66556960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1034)
CpG islands
(count:856)
Chromatin interactive
region (count:70)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1034 , 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	chr12:66538911-66539322	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:66524411-66525159	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:66534580-66534723	K562	blood:	n/a	n/a
4	ATF1	chr12:66525260-66525464	K562	blood:	n/a	n/a
5	ATF1	chr12:66543644-66544126	K562	blood:	n/a	n/a
6	ATF2	chr12:66524208-66524815	GM12878	blood:	n/a	n/a
7	BACH1	chr12:66534242-66534255	K562	blood:	n/a	n/a
8	BACH1	chr12:66524441-66524615	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr12:66524183-66524934	A549	lung:	n/a	chr12:66524535-66524544
10	BCL3	chr12:66524266-66524907	A549	lung:	n/a	chr12:66524535-66524544
11	BCLAF1	chr12:66524232-66524984	GM12878	blood:	n/a	chr12:66524535-66524544
12	BHLHE40	chr12:66524275-66524877	K562	blood:	n/a	n/a
13	BHLHE40	chr12:66524168-66524802	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:66535240-66535242	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:66524247-66524721	HepG2	liver:	n/a	n/a
16	BHLHE40	chr12:66525404-66525499	GM12878	blood:	n/a	n/a
17	BRCA1	chr12:66538857-66538892	HepG2	liver:	n/a	n/a
18	BRCA1	chr12:66524354-66524805	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr12:66524260-66524822	GM12878	blood:	n/a	n/a
20	BRCA1	chr12:66524624-66524790	HepG2	liver:	n/a	n/a
21	CBX3	chr12:66534415-66534895	K562	blood:	n/a	n/a
22	CBX3	chr12:66534445-66534936	K562	blood:	n/a	n/a
23	CBX3	chr12:66538887-66539389	HCT-116	colon:	n/a	n/a
24	CBX3	chr12:66534534-66534972	HCT-116	colon:	n/a	n/a
25	CBX3	chr12:66535113-66535435	K562	blood:	n/a	n/a
26	CBX3	chr12:66535073-66535425	K562	blood:	n/a	n/a
27	CBX3	chr12:66524292-66524948	K562	blood:	n/a	n/a
28	CBX3	chr12:66534421-66535011	HCT-116	colon:	n/a	n/a
29	CCNT2	chr12:66524430-66524898	K562	blood:	n/a	n/a
30	CCNT2	chr12:66543704-66543949	K562	blood:	n/a	chr12:66543714-66543734
31	CEBPB	chr12:66538830-66539192	MCF-7	breast:	n/a	n/a
32	CEBPB	chr12:66524576-66524614	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:66524386-66525093	A549	lung:	n/a	n/a
34	CEBPB	chr12:66524356-66524809	K562	blood:	n/a	n/a
35	CEBPB	chr12:66538861-66539210	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr12:66538818-66539205	A549	lung:	n/a	n/a
37	CEBPB	chr12:66524328-66525064	GM12878	blood:	n/a	n/a
38	CEBPB	chr12:66524340-66524801	A549	lung:	n/a	n/a
39	CEBPB	chr12:66524455-66524688	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:66524122-66525147	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:66555060-66555434	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:66538848-66539219	A549	lung:	n/a	n/a
43	CEBPB	chr12:66524406-66524882	K562	blood:	n/a	n/a
44	CEBPB	chr12:66524398-66524765	IMR90	lung:	n/a	n/a
45	CEBPB	chr12:66538924-66539137	HepG2	liver:	n/a	n/a
46	CEBPB	chr12:66555076-66555348	K562	blood:	n/a	n/a
47	CEBPB	chr12:66538735-66539293	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:66555160-66555476	A549	lung:	n/a	n/a
49	CEBPB	chr12:66543965-66544120	K562	blood:	n/a	n/a
50	CEBPB	chr12:66538901-66539235	H1-hESC	embryonic stem cell:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:66524651-66524701	GM12878	blood:	n/a
2	chr12:66524493-66524543	NT2-D1	testis:	n/a
3	chr12:66524651-66524701	GM12878	blood:	n/a
4	chr12:66524493-66524543	NT2-D1	testis:	n/a
5	chr12:66524770-66524820	AoSMC	blood vessel:	n/a
6	chr12:66517357-66517407	HCF	heart:	n/a
7	chr12:66524943-66524993	HNPCEpiC	eye:	n/a
8	chr12:66524493-66524543	GM12878	blood:	n/a
9	chr12:66524311-66524361	BJ	skin:	n/a
10	chr12:66524493-66524543	SK-N-SH	brain:	n/a
11	chr12:66524770-66524820	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:66524411-66524461	NHBE	bronchial:	n/a
13	chr12:66554863-66554913	U87	brain:	n/a
14	chr12:66517357-66517407	HMEC	breast:	n/a
15	chr12:66524584-66524634	ovcar-3	ovarian:	n/a
16	chr12:66554863-66554913	BJ	skin:	n/a
17	chr12:66524618-66524668	SK-N-SH_RA	brain:	n/a
18	chr12:66524618-66524668	AG09319	gingival:	n/a
19	chr12:66554863-66554913	CMK	blood:	n/a
20	chr12:66524581-66524631	SAEC	small airway:	n/a
21	chr12:66524311-66524361	NHBE	bronchial:	n/a
22	chr12:66554863-66554913	BE2_C	brain:	n/a
23	chr12:66521713-66521763	HAEpiC	amniotic membrane:	n/a
24	chr12:66524943-66524993	HIPEpiC	eye:	n/a
25	chr12:66528416-66528466	HL-60	blood:	n/a
26	chr12:66524943-66524993	Caco-2	colon:	n/a
27	chr12:66554863-66554913	Caco-2	colon:	n/a
28	chr12:66528416-66528466	HepG2	liver:	n/a
29	chr12:66524584-66524634	GM06990	blood:	n/a
30	chr12:66524651-66524701	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:66524791-66524841	HUVEC	blood vessel:	n/a
32	chr12:66524311-66524361	ProgFib	skin:	n/a
33	chr12:66524618-66524668	AoSMC	blood vessel:	n/a
34	chr12:66524584-66524634	CMK	blood:	n/a
35	chr12:66524651-66524701	Hela-S3	cervix:	n/a
36	chr12:66517357-66517407	HEEpiC	esophagus:	n/a
37	chr12:66554863-66554913	ECC-1	luminal epithelium:	n/a
38	chr12:66521713-66521763	AG09309	skin:	n/a
39	chr12:66524791-66524841	HEK293	kidney:	embryo
40	chr12:66524618-66524668	HEK293	kidney:	embryo
41	chr12:66528416-66528466	NT2-D1	testis:	n/a
42	chr12:66524770-66524820	HCPEpiC	choroid plexus:	n/a
43	chr12:66524943-66524993	RPTEC	kidney:	n/a
44	chr12:66528416-66528466	HCM	heart:	n/a
45	chr12:66524651-66524701	BJ	skin:	n/a
46	chr12:66528416-66528466	ovcar-3	ovarian:	n/a
47	chr12:66524770-66524820	HRPEpiC	eye:	n/a
48	chr12:66524791-66524841	ProgFib	skin:	n/a
49	chr12:66524651-66524701	SAEC	small airway:	n/a
50	chr12:66554863-66554913	HPAEpiC	pulmonary alveolar:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:66512241..66514451-chr12:66541871..66543985,2	K562	blood:
2	chr12:66536884..66539272-chr12:66539698..66542601,2	MCF-7	breast:
3	chr12:66535914..66538687-chr12:66565341..66566985,2	K562	blood:
4	chr12:66547017..66548905-chr12:66563527..66565099,2	MCF-7	breast:
5	chr12:66524578..66525111-chr17:39939745..39940370,2	MCF-7	breast:
6	chr12:66523523..66525670-chr12:66539584..66541563,2	MCF-7	breast:
7	chr1:145096186..145098889-chr12:66522673..66525529,2	MCF-7	breast:
8	chr12:66539081..66541895-chr12:66541952..66543781,2	K562	blood:
9	chr12:66523095..66527368-chr12:66532414..66535159,4	MCF-7	breast:
10	chr12:66538732..66539320-chr12:66627446..66628005,2	MCF-7	breast:
11	chr12:66529650..66532056-chr12:66539532..66541211,2	MCF-7	breast:
12	chr12:66524156..66526872-chr12:66529144..66534313,4	K562	blood:
13	chr12:66550852..66561080-chr12:66561565..66565303,15	MCF-7	breast:
14	chr12:66537517..66539175-chr12:66547161..66549206,2	MCF-7	breast:
15	chr12:66532321..66535206-chr12:66536994..66538662,2	K562	blood:
16	chr12:66523311..66525203-chr12:66696051..66697589,2	MCF-7	breast:
17	chr12:66512970..66515802-chr12:66525883..66527400,2	MCF-7	breast:
18	chr12:66504685..66506522-chr12:66524649..66526191,2	K562	blood:
19	chr12:66543718..66546794-chr12:66562322..66564805,3	MCF-7	breast:
20	chr12:66523095..66527368-chr12:66532414..66535159,4	MCF-7	breast:
21	chr12:66538882..66543480-chr12:66561851..66566115,6	MCF-7	breast:
22	chr12:66523098..66524616-chr12:66537392..66539632,2	MCF-7	breast:
23	chr12:66539081..66541895-chr12:66541952..66543781,2	K562	blood:
24	chr12:66523453..66525027-chr12:66562451..66564555,2	K562	blood:
25	chr12:66532840..66534600-chr12:66537441..66539657,2	MCF-7	breast:
26	chr12:66541034..66542734-chr12:66544918..66547664,2	K562	blood:
27	chr12:66538639..66542023-chr12:66544775..66548196,3	MCF-7	breast:
28	chr12:66536884..66539272-chr12:66539698..66542601,2	MCF-7	breast:
29	chr12:66548703..66551216-chr12:66555058..66558052,2	MCF-7	breast:
30	chr12:66533040..66534906-chr12:66624306..66626654,2	MCF-7	breast:
31	chr12:66524156..66526872-chr12:66529144..66534313,4	K562	blood:
32	chr12:66530596..66534894-chr12:66562580..66565717,4	K562	blood:
33	chr12:66537517..66539175-chr12:66547161..66549206,2	MCF-7	breast:
34	chr12:66538639..66542023-chr12:66544775..66548196,3	MCF-7	breast:
35	chr12:66520160..66522337-chr12:66557451..66559274,2	MCF-7	breast:
36	chr12:66556389..66558004-chr12:66572118..66574414,2	MCF-7	breast:
37	chr12:66524573..66525113-chrX:16737374..16737993,2	Hela-S3	cervix:
38	chr12:66523792..66527078-chr12:66561013..66565049,6	MCF-7	breast:
39	chr12:66524156..66526085-chr12:66529096..66530644,2	K562	blood:
40	chr12:66506596..66509423-chr12:66515723..66518011,2	K562	blood:
41	chr12:66554922..66556425-chr12:66697932..66699503,2	K562	blood:
42	chr12:66523081..66526604-chr12:66560988..66564576,8	MCF-7	breast:
43	chr12:66517857..66521080-chr12:66522803..66525691,6	MCF-7	breast:
44	chr12:66514117..66516247-chr12:66517268..66518852,2	MCF-7	breast:
45	chr12:66541034..66542734-chr12:66544918..66547664,2	K562	blood:
46	chr12:66524217..66527472-chr12:66531631..66536698,7	K562	blood:
47	chr12:66524431..66524938-chr17:36981117..36982103,2	Hela-S3	cervix:
48	chr12:66521057..66526734-chr12:66560807..66565257,7	K562	blood:
49	chr12:66539518..66541895-chr12:66542239..66543781,2	K562	blood:
50	chr12:66517556..66521125-chr12:66522874..66526131,5	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LLPH-3	chr12:66532504-66532717	NONHSAT029221
2	lnc-IRAK3-1	chr12:66524578-66525829	NONHSAT029220
3	lnc-LLPH-3	chr12:66531609-66531946	NONHSAT029221

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LLPH	hsa-miR-34a-5p	chr12:66517537-66517558

Variant related genes	Relation type
TMBIM4	TF binding region
LLPH	TF binding region
ENSG00000239335	TF binding region
TMBIM4	CpG island
LLPH	CpG island
ENSG00000239335	CpG island
ENSG00000169895	chromatin interactions
ENSG00000263791	chromatin interactions
ENSG00000239335	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000139233	chromatin interactions
ENSG00000127311	chromatin interactions
ENSG00000108296	chromatin interactions
ENSG00000155957	chromatin interactions

Extended variants
information (count: 1397 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7974649	chr12:66516692-66516693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546642126	chr12:66516720-66516721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527302702	chr12:66516732-66516733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2576188	chr12:66516760-66516761	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs535082048	chr12:66516785-66516786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555289474	chr12:66516835-66516836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537657469	chr12:66516851-66516852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557083072	chr12:66516876-66516877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143234456	chr12:66516910-66516911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs67387970	chr12:66516911-66516912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201078272	chr12:66516912-66516913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201204558	chr12:66516913-66516914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs56711130	chr12:66516914-66516915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201588599	chr12:66516915-66516916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199763168	chr12:66516917-66516918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200562149	chr12:66516920-66516921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545856784	chr12:66516923-66516924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113866309	chr12:66516948-66516949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140807993	chr12:66517004-66517005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573219746	chr12:66517006-66517007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541856902	chr12:66517029-66517030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149716740	chr12:66517035-66517036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560341762	chr12:66517047-66517048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185051445	chr12:66517056-66517057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11834285	chr12:66517057-66517058	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs564247494	chr12:66517059-66517060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533144212	chr12:66517072-66517073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546745721	chr12:66517129-66517130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370029931	chr12:66517135-66517136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566440108	chr12:66517140-66517141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528924084	chr12:66517154-66517155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529109417	chr12:66517157-66517158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145589839	chr12:66517283-66517284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568736935	chr12:66517300-66517301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537316350	chr12:66517339-66517340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141287101	chr12:66517346-66517347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570746723	chr12:66517348-66517349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539623850	chr12:66517352-66517353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553100633	chr12:66517357-66517358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573250062	chr12:66517358-66517359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181303252	chr12:66517376-66517377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555429265	chr12:66517377-66517378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11544759	chr12:66517416-66517417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544485368	chr12:66517434-66517435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564349919	chr12:66517473-66517474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549086999	chr12:66517536-66517537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540418864	chr12:66517564-66517565	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556770296	chr12:66517567-66517568	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs375032855	chr12:66517571-66517572	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs370487416	chr12:66517578-66517579	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:2190 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66501600-66517600	Weak transcription	Right Ventricle	heart
2	chr12:66501800-66516800	Weak transcription	NHEK	skin
3	chr12:66502000-66518000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:66502400-66518400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:66509000-66518200	Weak transcription	Esophagus	oesophagus
6	chr12:66509000-66519800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:66509000-66523800	Weak transcription	Pancreas	Pancrea
8	chr12:66509200-66523600	Weak transcription	Gastric	stomach
9	chr12:66509600-66518000	Weak transcription	Ovary	ovary
10	chr12:66511400-66518200	Weak transcription	Fetal Kidney	kidney
11	chr12:66512000-66522200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:66512600-66518000	Weak transcription	Psoas Muscle	Psoas
13	chr12:66512800-66517800	Weak transcription	K562	blood
14	chr12:66513200-66516800	Weak transcription	Fetal Stomach	stomach
15	chr12:66513200-66517400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr12:66513400-66517200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr12:66513400-66517600	Weak transcription	Colon Smooth Muscle	Colon
18	chr12:66513400-66518200	Weak transcription	Aorta	Aorta
19	chr12:66513600-66517000	Weak transcription	HepG2	liver
20	chr12:66513600-66518000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr12:66513600-66518200	Weak transcription	Fetal Brain Male	brain
22	chr12:66513600-66522400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr12:66513600-66522600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:66513600-66522600	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr12:66513600-66523400	Weak transcription	Small Intestine	intestine
26	chr12:66513600-66523800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:66513800-66518600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr12:66513800-66521000	Strong transcription	Dnd41	blood
29	chr12:66513800-66522400	Strong transcription	Fetal Thymus	thymus
30	chr12:66513800-66522600	Strong transcription	Adipose Nuclei	Adipose
31	chr12:66514000-66517000	Weak transcription	Fetal Intestine Small	intestine
32	chr12:66514000-66518000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr12:66514000-66518000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:66514000-66518200	Weak transcription	Colonic Mucosa	Colon
35	chr12:66514000-66522400	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr12:66514000-66522600	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr12:66514000-66522600	Strong transcription	Fetal Muscle Leg	muscle
38	chr12:66514200-66519400	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr12:66514200-66519800	Strong transcription	HSMM	muscle
40	chr12:66514200-66521200	Strong transcription	Primary T cells from cord blood	blood
41	chr12:66514200-66521400	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr12:66514200-66522600	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr12:66514200-66522600	Strong transcription	NHDF-Ad	bronchial
44	chr12:66514200-66523200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:66514400-66518200	Strong transcription	Left Ventricle	heart
46	chr12:66514400-66520600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr12:66514400-66523800	Weak transcription	Spleen	Spleen
48	chr12:66514600-66519200	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr12:66514600-66519800	Strong transcription	Fetal Muscle Trunk	muscle
50	chr12:66514600-66521600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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