Variant report

Variant	esv3389115
Chromosome Location	chr12:39221256-39448458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2196)
CpG islands
(count:976)
Chromatin interactive
region (count:52)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2196 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:39285777-39286637	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:39300558-39300682	K562	blood:	n/a	n/a
3	ARID3A	chr12:39300494-39300860	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:39377087-39377287	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:39397543-39397858	HepG2	liver:	n/a	n/a
6	ATF1	chr12:39284008-39284252	K562	blood:	n/a	n/a
7	ATF1	chr12:39436838-39437126	K562	blood:	n/a	n/a
8	ATF1	chr12:39279955-39280086	K562	blood:	n/a	n/a
9	ATF2	chr12:39298537-39299243	GM12878	blood:	n/a	n/a
10	ATF2	chr12:39300121-39301011	GM12878	blood:	n/a	n/a
11	ATF2	chr12:39298529-39299822	GM12878	blood:	n/a	n/a
12	ATF2	chr12:39300305-39300945	GM12878	blood:	n/a	n/a
13	ATF3	chr12:39300228-39300807	A549	lung:	n/a	chr12:39300324-39300337
14	ATF3	chr12:39300365-39300843	A549	lung:	n/a	n/a
15	ATF3	chr12:39285710-39286359	A549	lung:	n/a	n/a
16	ATF3	chr12:39299347-39299915	A549	lung:	n/a	n/a
17	ATF3	chr12:39285802-39286224	A549	lung:	n/a	n/a
18	ATF3	chr12:39298460-39299097	A549	lung:	n/a	chr12:39299077-39299086
19	BACH1	chr12:39406696-39407064	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:39300395-39300863	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr12:39266655-39266656	K562	blood:	n/a	n/a
22	BACH1	chr12:39298839-39300096	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr12:39300359-39300867	GM12878	blood:	n/a	n/a
24	BATF	chr12:39286146-39286543	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:39300494-39300852	GM12878	blood:	n/a	chr12:39300564-39300577
26	BCL3	chr12:39298956-39299761	A549	lung:	n/a	chr12:39298957-39298970
27	BCL3	chr12:39300378-39300735	GM12878	blood:	n/a	chr12:39300564-39300577
28	BCL3	chr12:39285844-39286500	A549	lung:	n/a	chr12:39286325-39286332
29	BCL3	chr12:39298658-39299050	GM12878	blood:	n/a	chr12:39298957-39298970
30	BCL3	chr12:39285771-39286377	A549	lung:	n/a	chr12:39286325-39286332
31	BCLAF1	chr12:39298496-39299659	GM12878	blood:	n/a	chr12:39298957-39298970
32	BCLAF1	chr12:39300289-39300959	GM12878	blood:	n/a	chr12:39300564-39300577
33	BCLAF1	chr12:39300278-39300864	GM12878	blood:	n/a	chr12:39300564-39300577
34	BCLAF1	chr12:39298576-39299858	GM12878	blood:	n/a	chr12:39298957-39298970
35	BHLHE40	chr12:39284315-39284633	GM12878	blood:	n/a	chr12:39284487-39284496 chr12:39284487-39284496
36	BHLHE40	chr12:39285799-39286240	A549	lung:	n/a	n/a
37	BHLHE40	chr12:39298710-39299023	A549	lung:	n/a	n/a
38	BHLHE40	chr12:39288323-39288627	GM12878	blood:	n/a	chr12:39288427-39288448 chr12:39288431-39288444
39	BHLHE40	chr12:39285801-39286415	HepG2	liver:	n/a	n/a
40	BHLHE40	chr12:39300420-39300708	K562	blood:	n/a	n/a
41	BHLHE40	chr12:39296363-39296497	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:39298120-39298226	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:39300370-39301239	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:39274182-39274265	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:39298621-39299502	K562	blood:	n/a	n/a
46	BHLHE40	chr12:39313132-39313245	K562	blood:	n/a	n/a
47	BHLHE40	chr12:39285981-39286182	K562	blood:	n/a	n/a
48	BHLHE40	chr12:39292224-39292367	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:39298606-39300030	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:39300332-39300812	HepG2	liver:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39299844-39299894	PrEC	prostate:	n/a
2	chr12:39300744-39300794	NH-A	brain:	n/a
3	chr12:39298639-39298689	Caco-2	colon:	n/a
4	chr12:39300142-39300192	HRE	kidney:	n/a
5	chr12:39299326-39299376	HL-60	blood:	n/a
6	chr12:39299716-39299766	NH-A	brain:	n/a
7	chr12:39299844-39299894	GM12892	blood:	n/a
8	chr12:39300142-39300192	NH-A	brain:	n/a
9	chr12:39300744-39300794	MCF-7	breast:	n/a
10	chr12:39299716-39299766	RPTEC	kidney:	n/a
11	chr12:39298824-39298874	NHBE	bronchial:	n/a
12	chr12:39298824-39298874	MCF10A-Er-Src	breast:	n/a
13	chr12:39299132-39299182	BJ	skin:	n/a
14	chr12:39300744-39300794	HCT-116	colon:	n/a
15	chr12:39298639-39298689	HNPCEpiC	eye:	n/a
16	chr12:39299501-39299551	K562	blood:	n/a
17	chr12:39299511-39299561	H1-hESC	embryonic stem cell:	embryo
18	chr12:39300142-39300192	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:39299844-39299894	HL-60	blood:	n/a
20	chr12:39300744-39300794	PFSK-1	brain:	n/a
21	chr12:39300142-39300192	K562	blood:	n/a
22	chr12:39302027-39302077	GM12892	blood:	n/a
23	chr12:39299716-39299766	Hepatocyte	liver:	n/a
24	chr12:39300142-39300192	HCM	heart:	n/a
25	chr12:39300744-39300794	SKMC	muscle:	n/a
26	chr12:39296476-39296526	SKMC	muscle:	n/a
27	chr12:39299844-39299894	ovcar-3	ovarian:	n/a
28	chr12:39299132-39299182	BE2_C	brain:	n/a
29	chr12:39299844-39299894	GM12878	blood:	n/a
30	chr12:39302027-39302077	PrEC	prostate:	n/a
31	chr12:39298639-39298689	A549	lung:	n/a
32	chr12:39299844-39299894	SK-N-SH	brain:	n/a
33	chr12:39299364-39299414	ECC-1	luminal epithelium:	n/a
34	chr12:39300142-39300192	AG04449	skin:	fetal
35	chr12:39299501-39299551	Caco-2	colon:	n/a
36	chr12:39299546-39299596	GM12892	blood:	n/a
37	chr12:39298639-39298689	GM12892	blood:	n/a
38	chr12:39299364-39299414	Caco-2	colon:	n/a
39	chr12:39296476-39296526	SK-N-SH_RA	brain:	n/a
40	chr12:39299716-39299766	MCF10A-Er-Src	breast:	n/a
41	chr12:39299364-39299414	IMR90	lung:	fetal
42	chr12:39298824-39298874	GM12891	blood:	n/a
43	chr12:39299364-39299414	AG04450	lung:	fetal
44	chr12:39299132-39299182	PrEC	prostate:	n/a
45	chr12:39299326-39299376	SAEC	small airway:	n/a
46	chr12:39299546-39299596	SAEC	small airway:	n/a
47	chr12:39299726-39299776	Caco-2	colon:	n/a
48	chr12:39299546-39299596	MCF-7	breast:	n/a
49	chr12:39300744-39300794	BE2_C	brain:	n/a
50	chr12:39299326-39299376	HRE	kidney:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:39290114..39292966-chr12:39295688..39297919,2	K562	blood:
2	chr12:39256596..39258957-chr12:39260248..39262001,2	K562	blood:
3	chr12:39300444..39301044-chr12:39497356..39498030,2	K562	blood:
4	chr12:39378140..39380661-chr12:39381373..39384205,2	MCF-7	breast:
5	chr12:39343718..39345753-chr12:39348375..39350244,2	K562	blood:
6	chr12:39298720..39299544-chr8:95565528..95566062,2	Hela-S3	cervix:
7	chr12:39298360..39299282-chr5:99870676..99871194,2	Hela-S3	cervix:
8	chr12:39406167..39408502-chr12:39412272..39414594,2	K562	blood:
9	chr12:39298324..39299381-chr7:141251113..141251796,3	Hela-S3	cervix:
10	chr12:39290114..39292966-chr12:39295688..39297919,2	K562	blood:
11	chr12:39285246..39287445-chr12:39289748..39291988,2	K562	blood:
12	chr12:39396332..39398967-chr12:39400620..39403550,2	K562	blood:
13	chr12:39245335..39247195-chr12:39261964..39264062,2	K562	blood:
14	chr12:39268478..39271402-chr12:39288578..39290820,2	K562	blood:
15	chr12:39244997..39247195-chr12:39261092..39264062,2	K562	blood:
16	chr12:38721798..38722714-chr12:39305427..39306254,2	MCF-7	breast:
17	chr12:39429919..39432388-chr12:39432739..39435549,2	K562	blood:
18	chr12:39229849..39232031-chr12:39233828..39236430,2	K562	blood:
19	chr12:39320556..39323665-chr12:39326717..39328717,3	K562	blood:
20	chr12:39299074..39299955-chr9:26892301..26892993,2	Hela-S3	cervix:
21	chr1:45196572..45197199-chr12:39300046..39300549,2	Hela-S3	cervix:
22	chr12:39256596..39258957-chr12:39260248..39262001,2	K562	blood:
23	chr12:39245335..39247195-chr12:39261964..39264062,2	K562	blood:
24	chr12:39342874..39345523-chr12:39354497..39356508,3	K562	blood:
25	chr12:39268478..39271402-chr12:39288578..39290820,2	K562	blood:
26	chr12:39294074..39295589-chr12:39295957..39298877,2	K562	blood:
27	chr12:39314389..39315587-chr12:39497082..39498251,11	MCF-7	breast:
28	chr12:39295565..39299427-chr12:39307532..39310185,3	K562	blood:
29	chr12:39223144..39224945-chr12:39229587..39231926,2	K562	blood:
30	chr12:39314380..39315501-chr12:39497292..39498019,4	MCF-7	breast:
31	chr12:39319182..39321686-chr4:39639319..39641692,2	MCF-7	breast:
32	chr12:39300010..39300760-chr3:119814285..119814942,2	Hela-S3	cervix:
33	chr12:39285246..39287445-chr12:39289748..39291988,2	K562	blood:
34	chr12:39433107..39434027-chr17:57914832..57915487,2	MCF-7	breast:
35	chr12:39244997..39247195-chr12:39261092..39264062,2	K562	blood:
36	chr12:39299427..39300247-chr6:17706649..17707521,2	Hela-S3	cervix:
37	chr12:39229849..39232031-chr12:39233828..39236430,2	K562	blood:
38	chr12:39299154..39299960-chr4:40632090..40632777,2	Hela-S3	cervix:
39	chr12:39295565..39299427-chr12:39307532..39310185,3	K562	blood:
40	chr12:39396332..39398967-chr12:39400620..39403550,2	K562	blood:
41	chr12:39447659..39449539-chr12:39460077..39462876,2	K562	blood:
42	chr12:39342874..39345523-chr12:39354497..39356508,3	K562	blood:
43	chr12:39315885..39316656-chr16:75018113..75018792,2	MCF-7	breast:
44	chr12:39406167..39408502-chr12:39412272..39414594,2	K562	blood:
45	chr12:39378140..39380661-chr12:39381373..39384205,2	MCF-7	breast:
46	chr12:39294074..39295589-chr12:39295957..39298877,2	K562	blood:
47	chr12:39314606..39315315-chr12:39497081..39498041,2	K562	blood:
48	chr12:39298727..39299416-chr20:30328091..30329027,2	Hela-S3	cervix:
49	chr12:39320556..39323665-chr12:39326717..39328717,3	K562	blood:
50	chr12:39429919..39432388-chr12:39432739..39435549,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10B-1	chr12:39303112-39303322	NONHSAT027691
2	lnc-ALG10B-9	chr12:39246195-39246232	ucscGeneNc_uc001rml_1
3	lnc-ALG10B-1	chr12:39300253-39300495	ENSG00000257718.1
4	lnc-ALG10B-9	chr12:39249765-39249873	ucscGeneNc_uc001rml_1
5	lnc-ALG10B-2	chr12:39317620-39317740	XLOC_009709
6	lnc-ALG10B-2	chr12:39313439-39313539	XLOC_009709
7	lnc-ALG10B-1	chr12:39300141-39300495	NONHSAT027691
8	lnc-ALG10B-9	chr12:39245581-39245613	ucscGeneNc_uc001rml_1
9	lnc-ALG10B-1	chr12:39303112-39303394	ENSG00000257718.1
10	lnc-CPNE8-3	chr12:39390514-39390684	NONHSAT027694
11	lnc-ALG10B-9	chr12:39245702-39245864	ucscGeneNc_uc001rml_1
12	lnc-ALG10B-9	chr12:39247667-39247781	ucscGeneNc_uc001rml_1
13	lnc-CPNE8-3	chr12:39388605-39388738	NONHSAT027694
14	lnc-ALG10B-9	chr12:39249076-39249111	ucscGeneNc_uc001rml_1
15	lnc-ALG10B-9	chr12:39250532-39250827	ucscGeneNc_uc001rml_1

No data

Variant related genes	Relation type
ENSG00000257718	TF binding region
CPNE8	TF binding region
ENSG00000252801	TF binding region
ENSG00000257586	TF binding region
ENSG00000257718	CpG island
CPNE8	CpG island
ENSG00000252801	CpG island
ENSG00000257586	CpG island
ENSG00000247877	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000103091	chromatin interactions
ENSG00000006530	chromatin interactions
ENSG00000124789	chromatin interactions
ENSG00000174132	chromatin interactions
ENSG00000164944	chromatin interactions
ENSG00000163683	chromatin interactions
ENSG00000120159	chromatin interactions
ENSG00000255458	chromatin interactions
ENSG00000163694	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000253704	chromatin interactions

Extended variants
information (count: 4880 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4880 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150945061	chr12:39221270-39221271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549584534	chr12:39221314-39221315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563000368	chr12:39221384-39221385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531812406	chr12:39221393-39221394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551814796	chr12:39221398-39221399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372121317	chr12:39221424-39221425	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377046952	chr12:39221463-39221464	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190672153	chr12:39221558-39221559	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73089574	chr12:39221559-39221560	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs113334088	chr12:39221617-39221618	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372817137	chr12:39221630-39221631	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373154748	chr12:39221652-39221653	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12307978	chr12:39221685-39221686	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536075019	chr12:39221708-39221709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537043894	chr12:39221769-39221770	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555915709	chr12:39221855-39221856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575751413	chr12:39221909-39221910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538308426	chr12:39221917-39221918	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558530409	chr12:39221969-39221970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144598950	chr12:39222013-39222014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73089577	chr12:39222015-39222016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146644910	chr12:39222104-39222105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182583499	chr12:39222112-39222113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113039305	chr12:39222122-39222123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368819517	chr12:39222167-39222168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141402486	chr12:39222179-39222180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76374391	chr12:39222185-39222186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78744832	chr12:39222277-39222278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558958034	chr12:39222405-39222406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145146381	chr12:39222410-39222411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374744197	chr12:39222441-39222442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527724039	chr12:39222443-39222444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571431987	chr12:39222474-39222475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538585094	chr12:39222485-39222486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547752925	chr12:39222492-39222493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138899478	chr12:39222496-39222497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536110219	chr12:39222507-39222508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79460764	chr12:39222623-39222624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186864044	chr12:39222648-39222649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115929599	chr12:39222665-39222666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376622012	chr12:39222668-39222669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149393818	chr12:39222679-39222680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114237010	chr12:39222712-39222713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534351914	chr12:39222733-39222734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368067952	chr12:39222739-39222740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202195649	chr12:39222766-39222767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17523988	chr12:39222785-39222786	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370608802	chr12:39222836-39222837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543304176	chr12:39222866-39222867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117074655	chr12:39222882-39222883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Colorectal cancer	16272173	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39203200-39276000	Weak transcription	Aorta	Aorta
2	chr12:39204000-39284800	Weak transcription	Lung	lung
3	chr12:39204800-39228800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:39204800-39231800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr12:39205600-39223200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:39205600-39229400	Weak transcription	HMEC	breast
7	chr12:39206400-39225800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:39206600-39243800	Weak transcription	Left Ventricle	heart
9	chr12:39206600-39249200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr12:39206800-39221400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr12:39206800-39226200	Weak transcription	GM12878-XiMat	blood
12	chr12:39206800-39241400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr12:39206800-39241400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:39216000-39237400	Weak transcription	Hela-S3	cervix
15	chr12:39217600-39232800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr12:39217800-39221400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr12:39218200-39223200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:39219200-39242600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr12:39219400-39221600	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr12:39219400-39229000	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr12:39221000-39223000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:39221200-39221800	Strong transcription	Liver	Liver
23	chr12:39221400-39221800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr12:39221400-39222000	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr12:39221600-39223800	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr12:39221800-39227800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr12:39221800-39251800	Weak transcription	Liver	Liver
28	chr12:39222000-39223200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr12:39223000-39227800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:39223200-39223600	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr12:39223200-39224000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:39223600-39238400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr12:39223800-39225800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr12:39224000-39241800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr12:39225600-39226400	Enhancers	Adipose Nuclei	Adipose
36	chr12:39225800-39226000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:39225800-39226200	Weak transcription	Esophagus	oesophagus
38	chr12:39225800-39230400	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr12:39226000-39226400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:39226000-39229000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:39226200-39226400	Enhancers	Esophagus	oesophagus
42	chr12:39226200-39226400	ZNF genes & repeats	GM12878-XiMat	blood
43	chr12:39226200-39226600	Enhancers	Right Atrium	heart
44	chr12:39226400-39227600	Weak transcription	GM12878-XiMat	blood
45	chr12:39227600-39227800	ZNF genes & repeats	GM12878-XiMat	blood
46	chr12:39227800-39228000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr12:39227800-39228600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr12:39227800-39237200	Weak transcription	GM12878-XiMat	blood
49	chr12:39228000-39231400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:39228600-39232000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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