Variant report

Variant	esv1794382
Chromosome Location	chr12:106679812-106699151
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1096)
CpG islands
(count:793)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:106682060-106682792	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:106694575-106694803	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:106689852-106690379	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:106696316-106696541	K562	blood:	n/a	n/a
5	ARID3A	chr12:106682208-106682655	K562	blood:	n/a	n/a
6	ARID3A	chr12:106696326-106697314	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:106695587-106695892	K562	blood:	n/a	n/a
8	ATF1	chr12:106694461-106694822	K562	blood:	n/a	n/a
9	ATF1	chr12:106682059-106682556	K562	blood:	n/a	n/a
10	ATF1	chr12:106695456-106695952	K562	blood:	n/a	n/a
11	ATF3	chr12:106682144-106682974	HCT-116	colon:	n/a	n/a
12	ATF3	chr12:106682214-106682545	K562	blood:	n/a	n/a
13	ATF3	chr12:106695512-106695916	K562	blood:	n/a	n/a
14	ATF3	chr12:106682163-106682731	A549	lung:	n/a	n/a
15	BACH1	chr12:106696326-106697437	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr12:106695656-106696052	K562	blood:	n/a	n/a
17	BACH1	chr12:106695484-106696089	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr12:106695373-106695811	K562	blood:	n/a	n/a
19	BCL3	chr12:106696167-106696916	A549	lung:	n/a	n/a
20	BCLAF1	chr12:106695503-106695990	K562	blood:	n/a	chr12:106695847-106695856
21	BHLHE40	chr12:106690019-106690329	A549	lung:	n/a	n/a
22	BHLHE40	chr12:106695590-106695939	A549	lung:	n/a	n/a
23	BHLHE40	chr12:106682303-106682954	K562	blood:	n/a	n/a
24	BHLHE40	chr12:106694564-106694869	HepG2	liver:	n/a	n/a
25	BHLHE40	chr12:106695562-106697456	HepG2	liver:	n/a	chr12:106696295-106696311 chr12:106695968-106695984
26	BHLHE40	chr12:106697945-106698257	HepG2	liver:	n/a	n/a
27	BHLHE40	chr12:106682252-106683058	HepG2	liver:	n/a	n/a
28	BHLHE40	chr12:106690042-106690272	K562	blood:	n/a	n/a
29	BHLHE40	chr12:106695200-106697453	GM12878	blood:	n/a	chr12:106696295-106696311 chr12:106695968-106695984
30	BHLHE40	chr12:106693161-106693361	K562	blood:	n/a	n/a
31	BHLHE40	chr12:106689842-106690380	HepG2	liver:	n/a	n/a
32	BHLHE40	chr12:106696230-106696604	A549	lung:	n/a	chr12:106696295-106696311
33	BHLHE40	chr12:106695347-106697430	K562	blood:	n/a	chr12:106696295-106696311 chr12:106695968-106695984
34	BHLHE40	chr12:106694534-106694864	K562	blood:	n/a	n/a
35	BRCA1	chr12:106696281-106696591	GM12878	blood:	n/a	n/a
36	BRCA1	chr12:106696320-106696870	HepG2	liver:	n/a	n/a
37	BRCA1	chr12:106695450-106695963	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr12:106697102-106697316	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr12:106696262-106696658	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr12:106696275-106696751	H1-hESC	embryonic stem cell:	n/a	n/a
41	CBX3	chr12:106689816-106690680	HCT-116	colon:	n/a	n/a
42	CBX3	chr12:106695314-106696047	K562	blood:	n/a	n/a
43	CBX3	chr12:106695509-106695957	K562	blood:	n/a	n/a
44	CCNT2	chr12:106694525-106694896	K562	blood:	n/a	n/a
45	CCNT2	chr12:106695379-106697332	K562	blood:	n/a	chr12:106696293-106696302 chr12:106696230-106696239 chr12:106696811-106696831 chr12:106695692-106695712 chr12:106697247-106697256 chr12:106696589-106696598 chr12:106697201-106697210
46	CEBPB	chr12:106682179-106682625	A549	lung:	n/a	chr12:106682428-106682439
47	CEBPB	chr12:106681954-106683336	HCT-116	colon:	n/a	chr12:106682428-106682439 chr12:106683094-106683105
48	CEBPB	chr12:106682139-106682619	HepG2	liver:	n/a	chr12:106682428-106682439
49	CEBPB	chr12:106685119-106685469	A549	lung:	n/a	n/a
50	CEBPB	chr12:106682038-106682846	HCT-116	colon:	n/a	chr12:106682428-106682439

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:106697165-106697215	A549	lung:	n/a
2	chr12:106696527-106696577	H1-hESC	embryonic stem cell:	embryo
3	chr12:106696673-106696723	HRPEpiC	eye:	n/a
4	chr12:106696255-106696305	A549	lung:	n/a
5	chr12:106696452-106696502	SKMC	muscle:	n/a
6	chr12:106696255-106696305	HCT-116	colon:	n/a
7	chr12:106696673-106696723	CMK	blood:	n/a
8	chr12:106696527-106696577	AG04450	lung:	fetal
9	chr12:106696384-106696434	GM06990	blood:	n/a
10	chr12:106697165-106697215	BJ	skin:	n/a
11	chr12:106696384-106696434	GM12878	blood:	n/a
12	chr12:106695932-106695982	GM12891	blood:	n/a
13	chr12:106695984-106696034	T-47D	breast:	n/a
14	chr12:106697165-106697215	AoSMC	blood vessel:	n/a
15	chr12:106696891-106696941	LNCaP	prostate:	n/a
16	chr12:106696452-106696502	GM12878	blood:	n/a
17	chr12:106695998-106696048	ECC-1	luminal epithelium:	n/a
18	chr12:106695932-106695982	AG10803	skin:	n/a
19	chr12:106696255-106696305	NH-A	brain:	n/a
20	chr12:106695932-106695982	HepG2	liver:	n/a
21	chr12:106695984-106696034	MCF-7	breast:	n/a
22	chr12:106695998-106696048	HEEpiC	esophagus:	n/a
23	chr12:106696527-106696577	SAEC	small airway:	n/a
24	chr12:106696525-106696575	Hepatocyte	liver:	n/a
25	chr12:106696673-106696723	Hela-S3	cervix:	n/a
26	chr12:106696891-106696941	NHBE	bronchial:	n/a
27	chr12:106695998-106696048	Caco-2	colon:	n/a
28	chr12:106697165-106697215	CMK	blood:	n/a
29	chr12:106696255-106696305	GM06990	blood:	n/a
30	chr12:106696384-106696434	HMEC	breast:	n/a
31	chr12:106696452-106696502	HCT-116	colon:	n/a
32	chr12:106696255-106696305	AG04449	skin:	fetal
33	chr12:106696452-106696502	Caco-2	colon:	n/a
34	chr12:106697165-106697215	GM06990	blood:	n/a
35	chr12:106696673-106696723	AoSMC	blood vessel:	n/a
36	chr12:106696384-106696434	NT2-D1	testis:	n/a
37	chr12:106695984-106696034	HCT-116	colon:	n/a
38	chr12:106681933-106681983	GM12878	blood:	n/a
39	chr12:106696527-106696577	K562	blood:	n/a
40	chr12:106697165-106697215	Jurkat	blood:	n/a
41	chr12:106696891-106696941	CMK	blood:	n/a
42	chr12:106697297-106697347	Hepatocyte	liver:	n/a
43	chr12:106695932-106695982	HEK293	kidney:	embryo
44	chr12:106695932-106695982	ovcar-3	ovarian:	n/a
45	chr12:106696673-106696723	HUVEC	blood vessel:	n/a
46	chr12:106696452-106696502	HRPEpiC	eye:	n/a
47	chr12:106696525-106696575	NHDF-neo	bronchial:	n/a
48	chr12:106696525-106696575	PANC-1	pancreas:	n/a
49	chr12:106696384-106696434	HEEpiC	esophagus:	n/a
50	chr12:106681933-106681983	NB4	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:106641570..106642137-chr12:106697112..106697741,2	MCF-7	breast:
2	chr12:106679091..106681654-chr12:106715669..106717926,2	MCF-7	breast:
3	chr12:106679605..106682241-chr12:106684127..106685839,2	K562	blood:
4	chr12:106640063..106644049-chr12:106694395..106698756,11	MCF-7	breast:
5	chr12:106681884..106684629-chr12:106690142..106692721,2	MCF-7	breast:
6	chr12:106641882..106643930-chr12:106685440..106687264,2	MCF-7	breast:
7	chr12:106693946..106698218-chr12:106750404..106754111,7	MCF-7	breast:
8	chr12:106693434..106696954-chr12:106697519..106701215,4	MCF-7	breast:
9	chr12:106683028..106684657-chr12:106684829..106686398,2	MCF-7	breast:
10	chr12:106679605..106682241-chr12:106684127..106685839,2	K562	blood:
11	chr12:106691206..106693706-chr12:106694212..106695819,2	K562	blood:
12	chr12:106638556..106642995-chr12:106679966..106686733,8	MCF-7	breast:
13	chr12:106693434..106696954-chr12:106697519..106701215,4	MCF-7	breast:
14	chr12:106682888..106685086-chr12:106695950..106698366,2	MCF-7	breast:
15	chr12:106640373..106642748-chr12:106682387..106685392,3	MCF-7	breast:
16	chr12:106532442..106534765-chr12:106681065..106683519,2	MCF-7	breast:
17	chr12:106637683..106639757-chr12:106691523..106693781,3	MCF-7	breast:
18	chr12:106680960..106683354-chr12:106688699..106690520,2	K562	blood:
19	chr12:106639341..106642339-chr12:106691161..106693366,2	MCF-7	breast:
20	chr12:106698636..106700298-chr12:106705423..106707807,2	K562	blood:
21	chr12:106676469..106679734-chr12:106680347..106683277,4	MCF-7	breast:
22	chr12:106680059..106682241-chr12:106684339..106687312,2	K562	blood:
23	chr12:106673784..106675625-chr12:106681211..106683347,2	MCF-7	breast:
24	chr12:106695562..106697778-chr12:106698885..106700984,2	K562	blood:
25	chr12:106683028..106684657-chr12:106684829..106686398,2	MCF-7	breast:
26	chr12:106675049..106678623-chr12:106679950..106682858,3	K562	blood:
27	chr12:106647187..106649805-chr12:106683824..106686258,2	MCF-7	breast:
28	chr12:106680059..106682241-chr12:106684339..106687312,2	K562	blood:
29	chr12:106695715..106698780-chr12:106751795..106753760,4	K562	blood:
30	chr12:106672236..106673860-chr12:106685895..106688017,2	MCF-7	breast:
31	chr12:106686272..106688271-chr12:106702208..106703818,2	MCF-7	breast:
32	chr12:106681884..106684629-chr12:106690142..106692721,2	MCF-7	breast:
33	chr12:106532573..106534349-chr12:106680398..106683180,2	MCF-7	breast:
34	chr12:106639346..106644112-chr12:106694122..106698214,13	MCF-7	breast:
35	chr12:106694726..106698780-chr12:106749876..106753760,9	K562	blood:
36	chr12:106680960..106683354-chr12:106688699..106690520,2	K562	blood:
37	chr12:106688729..106691851-chr12:106693637..106696966,3	MCF-7	breast:
38	chr12:106620350..106621264-chr12:106684714..106685651,2	MCF-7	breast:

No data

Variant related genes	Relation type
TCP11L2	TF binding region
RNU7-94P	TF binding region
CKAP4	TF binding region
TCP11L2	CpG island
RNU7-94P	CpG island
CKAP4	CpG island
ENSG00000258355	chromatin interactions
ENSG00000238609	chromatin interactions
ENSG00000136026	chromatin interactions
ENSG00000166046	chromatin interactions
ENSG00000074590	chromatin interactions
ENSG00000013503	chromatin interactions

Extended variants
information (count: 719 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17038336	chr12:106679812-106679813	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138721485	chr12:106679820-106679821	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529504895	chr12:106679821-106679822	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565617386	chr12:106679826-106679827	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75607870	chr12:106679846-106679847	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531030926	chr12:106679849-106679850	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs181575381	chr12:106679865-106679866	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs567956431	chr12:106679874-106679875	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs185268354	chr12:106679909-106679910	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs374427613	chr12:106679930-106679931	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs117263813	chr12:106679937-106679938	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs532994047	chr12:106679969-106679970	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs566908196	chr12:106680007-106680008	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs551178679	chr12:106680066-106680067	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs116205604	chr12:106680077-106680078	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs555629974	chr12:106680096-106680097	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs191359420	chr12:106680158-106680159	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs182787205	chr12:106680179-106680180	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs565883265	chr12:106680212-106680213	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs574571628	chr12:106680236-106680237	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs540185883	chr12:106680266-106680267	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs141654905	chr12:106680301-106680302	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs35077858	chr12:106680310-106680311	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs560379456	chr12:106680315-106680316	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs199749908	chr12:106680333-106680334	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs531994986	chr12:106680348-106680349	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs187706784	chr12:106680361-106680362	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs534767413	chr12:106680364-106680365	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs148963071	chr12:106680373-106680374	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs191122535	chr12:106680387-106680388	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs548256854	chr12:106680420-106680421	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs567806538	chr12:106680421-106680422	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs530290319	chr12:106680471-106680472	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs546996324	chr12:106680472-106680473	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs183269766	chr12:106680477-106680478	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs181647366	chr12:106680516-106680517	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs539039652	chr12:106680524-106680525	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs555127381	chr12:106680601-106680602	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs143702380	chr12:106680615-106680616	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs73388527	chr12:106680621-106680622	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187943191	chr12:106680644-106680645	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs555025294	chr12:106680704-106680705	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs78662974	chr12:106680743-106680744	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs533952770	chr12:106680747-106680748	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs553803739	chr12:106680755-106680756	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs576679176	chr12:106680766-106680767	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs567292959	chr12:106680776-106680777	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs562182871	chr12:106680783-106680784	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs73197506	chr12:106680789-106680790	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148104909	chr12:106680812-106680813	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Autism	22495311	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
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106666200-106680800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:106676600-106681000	Weak transcription	Stomach Mucosa	stomach
3	chr12:106677000-106681400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr12:106677200-106682200	Weak transcription	Fetal Intestine Large	intestine
5	chr12:106677200-106683600	Enhancers	HepG2	liver
6	chr12:106678400-106680000	Enhancers	Left Ventricle	heart
7	chr12:106678400-106680000	Enhancers	Right Atrium	heart
8	chr12:106678600-106682800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr12:106678600-106688800	Weak transcription	Lung	lung
10	chr12:106678800-106681000	Weak transcription	NHEK	skin
11	chr12:106678800-106681400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:106678800-106682600	Weak transcription	Brain Angular Gyrus	brain
13	chr12:106678800-106682600	Weak transcription	HSMMtube	muscle
14	chr12:106679000-106682400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr12:106679000-106682400	Weak transcription	HUVEC	blood vessel
16	chr12:106679000-106682600	Weak transcription	Esophagus	oesophagus
17	chr12:106679200-106680400	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr12:106679400-106680000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
19	chr12:106679600-106680000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:106679600-106680000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:106679600-106680000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr12:106679600-106680000	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr12:106679600-106680000	Bivalent Enhancer	GM12878-XiMat	blood
24	chr12:106679600-106680200	Enhancers	Primary B cells from peripheral blood	blood
25	chr12:106679800-106680800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:106680000-106680200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr12:106680000-106680800	Weak transcription	Left Ventricle	heart
28	chr12:106680000-106681800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr12:106680000-106682600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:106680000-106695200	Weak transcription	Right Atrium	heart
31	chr12:106680200-106681400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr12:106680400-106684600	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr12:106680800-106681000	Enhancers	Left Ventricle	heart
34	chr12:106680800-106683400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:106680800-106683400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:106680800-106683400	Enhancers	HMEC	breast
37	chr12:106681000-106681200	Weak transcription	Left Ventricle	heart
38	chr12:106681000-106681400	Enhancers	Stomach Mucosa	stomach
39	chr12:106681000-106682400	Enhancers	Hela-S3	cervix
40	chr12:106681000-106682600	Enhancers	NHEK	skin
41	chr12:106681000-106683400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr12:106681200-106681400	Enhancers	Osteobl	bone
43	chr12:106681200-106682400	Enhancers	A549	lung
44	chr12:106681200-106683400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:106681400-106682000	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr12:106681400-106682400	Weak transcription	Stomach Mucosa	stomach
47	chr12:106681400-106683200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:106681400-106683200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr12:106681400-106683400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr12:106681400-106683600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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