Variant report

Variant	nsv899048
Chromosome Location	chr12:44209423-44307888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:884)
CpG islands
(count:733)
Chromatin interactive
region (count:83)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:884 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:44241268-44241339	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:44276374-44276788	K562	blood:	n/a	n/a
3	ARID3A	chr12:44215642-44215646	K562	blood:	n/a	n/a
4	ARID3A	chr12:44234193-44234206	K562	blood:	n/a	n/a
5	ARID3A	chr12:44276355-44276754	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:44229830-44229899	HepG2	liver:	n/a	n/a
7	ATF1	chr12:44273177-44273350	K562	blood:	n/a	n/a
8	ATF1	chr12:44255098-44255324	K562	blood:	n/a	n/a
9	ATF1	chr12:44223434-44223638	K562	blood:	n/a	n/a
10	ATF1	chr12:44241252-44241331	K562	blood:	n/a	n/a
11	BACH1	chr12:44229428-44230312	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr12:44209960-44210403	GM12878	blood:	n/a	n/a
13	BATF	chr12:44210000-44210383	GM12878	blood:	n/a	n/a
14	BCL3	chr12:44229661-44230047	GM12878	blood:	n/a	chr12:44229828-44229837 chr12:44229874-44229887 chr12:44229757-44229770 chr12:44229805-44229814 chr12:44229782-44229795
15	BCL3	chr12:44209961-44210448	GM12878	blood:	n/a	n/a
16	BCL3	chr12:44209996-44210411	GM12878	blood:	n/a	n/a
17	BCL3	chr12:44219519-44219812	GM12878	blood:	n/a	n/a
18	BCL3	chr12:44229008-44229466	GM12878	blood:	n/a	n/a
19	BCL3	chr12:44229114-44229461	GM12878	blood:	n/a	n/a
20	BCLAF1	chr12:44276289-44276746	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:44229104-44230011	GM12878	blood:	n/a	chr12:44229828-44229837 chr12:44229874-44229887 chr12:44229757-44229770 chr12:44229805-44229814 chr12:44229782-44229795
22	BCLAF1	chr12:44229343-44230176	GM12878	blood:	n/a	chr12:44229828-44229837 chr12:44229874-44229887 chr12:44229757-44229770 chr12:44229805-44229814 chr12:44229782-44229795
23	BHLHE40	chr12:44246543-44246807	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:44229215-44230776	HepG2	liver:	n/a	chr12:44229871-44229887 chr12:44229754-44229770 chr12:44229553-44229569
25	BHLHE40	chr12:44229418-44230932	GM12878	blood:	n/a	chr12:44229871-44229887 chr12:44229754-44229770 chr12:44229553-44229569
26	BHLHE40	chr12:44229328-44230758	K562	blood:	n/a	chr12:44229871-44229887 chr12:44229754-44229770 chr12:44229553-44229569
27	BRCA1	chr12:44229394-44229644	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr12:44241087-44241601	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr12:44250939-44250955	GM12878	blood:	n/a	n/a
30	CBX3	chr12:44241774-44242309	K562	blood:	n/a	n/a
31	CCNT2	chr12:44229395-44230377	K562	blood:	n/a	chr12:44229655-44229664 chr12:44229516-44229525
32	CEBPB	chr12:44235161-44235405	K562	blood:	n/a	chr12:44235273-44235284
33	CEBPB	chr12:44241101-44241441	A549	lung:	n/a	chr12:44241269-44241280
34	CEBPB	chr12:44288808-44288983	A549	lung:	n/a	n/a
35	CEBPB	chr12:44231536-44231779	Hela-S3	cervix:	n/a	chr12:44231643-44231654 chr12:44231642-44231655
36	CEBPB	chr12:44255421-44255932	IMR90	lung:	n/a	n/a
37	CEBPB	chr12:44241046-44241615	ECC-1	luminal epithelium:	n/a	chr12:44241269-44241280
38	CEBPB	chr12:44235161-44235368	A549	lung:	n/a	chr12:44235273-44235284
39	CEBPB	chr12:44288254-44288320	A549	lung:	n/a	n/a
40	CEBPB	chr12:44234872-44235414	HepG2	liver:	n/a	chr12:44235273-44235284
41	CEBPB	chr12:44240980-44241686	HCT-116	colon:	n/a	chr12:44241269-44241280
42	CEBPB	chr12:44229431-44229858	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr12:44260823-44260903	K562	blood:	n/a	n/a
44	CEBPB	chr12:44260219-44260462	HepG2	liver:	n/a	chr12:44260328-44260339
45	CEBPB	chr12:44235105-44235423	IMR90	lung:	n/a	chr12:44235273-44235284
46	CEBPB	chr12:44213468-44213485	K562	blood:	n/a	n/a
47	CEBPB	chr12:44241054-44241502	ECC-1	luminal epithelium:	n/a	chr12:44241269-44241280
48	CEBPB	chr12:44235245-44235321	H1-hESC	embryonic stem cell:	n/a	chr12:44235273-44235284
49	CEBPB	chr12:44223747-44223983	K562	blood:	n/a	n/a
50	CEBPB	chr12:44241099-44241500	A549	lung:	n/a	chr12:44241269-44241280

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:44255515-44255565	HEEpiC	esophagus:	n/a
2	chr12:44255515-44255565	HEEpiC	esophagus:	n/a
3	chr12:44229880-44229930	GM06990	blood:	n/a
4	chr12:44229886-44229936	HCPEpiC	choroid plexus:	n/a
5	chr12:44223041-44223091	HEK293	kidney:	embryo
6	chr12:44229711-44229761	PANC-1	pancreas:	n/a
7	chr12:44229886-44229936	GM06990	blood:	n/a
8	chr12:44226393-44226443	NB4	blood:	n/a
9	chr12:44229711-44229761	BJ	skin:	n/a
10	chr12:44255515-44255565	ECC-1	luminal epithelium:	n/a
11	chr12:44229886-44229936	ProgFib	skin:	n/a
12	chr12:44229880-44229930	BE2_C	brain:	n/a
13	chr12:44233924-44233974	HRPEpiC	eye:	n/a
14	chr12:44233924-44233974	U87	brain:	n/a
15	chr12:44226393-44226443	SKMC	muscle:	n/a
16	chr12:44216812-44216862	HCT-116	colon:	n/a
17	chr12:44229711-44229761	NHDF-neo	bronchial:	n/a
18	chr12:44229711-44229761	LNCaP	prostate:	n/a
19	chr12:44292779-44292829	Caco-2	colon:	n/a
20	chr12:44233924-44233974	PFSK-1	brain:	n/a
21	chr12:44223041-44223091	HRCEpiC	kidney:	n/a
22	chr12:44229711-44229761	SAEC	small airway:	n/a
23	chr12:44230058-44230108	Jurkat	blood:	n/a
24	chr12:44216812-44216862	HEEpiC	esophagus:	n/a
25	chr12:44229880-44229930	AG09309	skin:	n/a
26	chr12:44229713-44229763	CMK	blood:	n/a
27	chr12:44223041-44223091	GM19239	blood:	n/a
28	chr12:44292779-44292829	HL-60	blood:	n/a
29	chr12:44226393-44226443	AG10803	skin:	n/a
30	chr12:44255515-44255565	HepG2	liver:	n/a
31	chr12:44229711-44229761	ProgFib	skin:	n/a
32	chr12:44292779-44292829	HCF	heart:	n/a
33	chr12:44229886-44229936	A549	lung:	n/a
34	chr12:44229886-44229936	HL-60	blood:	n/a
35	chr12:44230058-44230108	HIPEpiC	eye:	n/a
36	chr12:44255515-44255565	HCF	heart:	n/a
37	chr12:44230058-44230108	SKMC	muscle:	n/a
38	chr12:44229512-44229562	A549	lung:	n/a
39	chr12:44223041-44223091	HCPEpiC	choroid plexus:	n/a
40	chr12:44230058-44230108	GM12878	blood:	n/a
41	chr12:44292779-44292829	MCF10A-Er-Src	breast:	n/a
42	chr12:44229711-44229761	PFSK-1	brain:	n/a
43	chr12:44229713-44229763	NT2-D1	testis:	n/a
44	chr12:44292779-44292829	SAEC	small airway:	n/a
45	chr12:44229713-44229763	MCF-7	breast:	n/a
46	chr12:44229512-44229562	HCF	heart:	n/a
47	chr12:44216812-44216862	GM19239	blood:	n/a
48	chr12:44229713-44229763	GM12878	blood:	n/a
49	chr12:44230058-44230108	AG04450	lung:	fetal
50	chr12:44229880-44229930	Jurkat	blood:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:44195094..44197185-chr12:44236657..44238234,2	MCF-7	breast:
2	chr12:44207357..44209830-chr12:44214435..44216907,3	K562	blood:
3	chr12:44199765..44202625-chr12:44253112..44255967,2	MCF-7	breast:
4	chr12:44199160..44201447-chr12:44218209..44220923,3	K562	blood:
5	chr12:44228275..44231774-chr12:44233118..44235282,4	K562	blood:
6	chr12:44266572..44268712-chr12:44270596..44273370,2	K562	blood:
7	chr12:44232840..44235795-chr12:44270241..44273607,3	MCF-7	breast:
8	chr12:44228652..44231485-chr12:44241299..44244187,4	MCF-7	breast:
9	chr12:44233044..44234573-chr12:44243919..44245645,2	MCF-7	breast:
10	chr12:44170161..44170978-chr12:44276181..44276998,6	MCF-7	breast:
11	chr12:44233044..44234573-chr12:44243919..44245645,2	MCF-7	breast:
12	chr12:44224786..44227179-chr12:44228814..44231665,3	MCF-7	breast:
13	chr12:44214277..44216042-chr12:44228504..44230810,2	MCF-7	breast:
14	chr12:44228573..44230259-chr12:44245451..44247090,2	MCF-7	breast:
15	chr12:44211292..44214632-chr12:44215797..44219471,3	K562	blood:
16	chr12:44151301..44154228-chr12:44227613..44229712,2	K562	blood:
17	chr12:44203831..44205856-chr12:44214140..44216950,2	MCF-7	breast:
18	chr12:44197755..44201002-chr12:44273238..44276377,3	MCF-7	breast:
19	chr12:43895288..43896089-chr12:44276115..44276753,2	MCF-7	breast:
20	chr12:44211292..44214632-chr12:44215797..44219471,3	K562	blood:
21	chr12:43838710..43839367-chr12:44275853..44276638,2	MCF-7	breast:
22	chr12:44266260..44268712-chr12:44270370..44272096,2	K562	blood:
23	chr12:44195581..44201373-chr12:44212394..44217979,6	K562	blood:
24	chr12:44232705..44235583-chr12:44238617..44240545,3	K562	blood:
25	chr12:44232840..44235795-chr12:44270241..44273607,3	MCF-7	breast:
26	chr12:44215623..44218391-chr12:44230316..44232380,2	K562	blood:
27	chr12:44199742..44201462-chr12:44209107..44211356,2	K562	blood:
28	chr12:44236123..44237958-chr12:44238199..44240039,2	MCF-7	breast:
29	chr12:44218902..44220494-chr12:44234363..44236818,2	K562	blood:
30	chr12:44236889..44239645-chr12:44240734..44243980,3	MCF-7	breast:
31	chr12:44216999..44219539-chr12:44220290..44222155,2	MCF-7	breast:
32	chr12:44170101..44170969-chr12:44276130..44276954,2	K562	blood:
33	chr12:44226167..44226990-chr6:154619063..154619990,2	MCF-7	breast:
34	chr12:44207357..44209830-chr12:44214435..44216907,3	K562	blood:
35	chr12:44219284..44222535-chr12:44223504..44226954,3	MCF-7	breast:
36	chr12:44266572..44268712-chr12:44270596..44273370,2	K562	blood:
37	chr12:44219284..44222535-chr12:44223504..44226954,3	MCF-7	breast:
38	chr12:44291890..44294959-chr12:44297148..44301402,3	MCF-7	breast:
39	chr12:44197555..44202082-chr12:44219321..44224097,7	MCF-7	breast:
40	chr12:44283945..44286115-chr12:44291023..44293431,2	MCF-7	breast:
41	chr12:44283945..44286115-chr12:44291023..44293431,2	MCF-7	breast:
42	chr12:44169860..44172008-chr12:44220305..44222660,2	MCF-7	breast:
43	chr12:44197746..44199436-chr12:44249235..44251144,2	K562	blood:
44	chr12:44199252..44200247-chr12:44229479..44230019,2	MCF-7	breast:
45	chr12:44218902..44220494-chr12:44234363..44236818,2	K562	blood:
46	chr12:44266260..44268712-chr12:44270370..44272096,2	K562	blood:
47	chr12:44127316..44130313-chr12:44278484..44280502,2	K562	blood:
48	chr12:44229793..44232258-chr12:44238778..44241759,3	K562	blood:
49	chr12:44203878..44205579-chr12:44209943..44211835,2	K562	blood:
50	chr12:44198221..44201924-chr12:44226822..44231143,11	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM117	TF binding region
TMEM117	CpG island
ENSG00000139174	chromatin interactions
ENSG00000139173	chromatin interactions
ENSG00000124243	chromatin interactions
ENSG00000151239	chromatin interactions
ENSG00000198001	chromatin interactions
ENSG00000129317	chromatin interactions

Extended variants
information (count: 3812 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3812 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17093754	chr12:44209423-44209424	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555717129	chr12:44209453-44209454	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554663005	chr12:44209508-44209509	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs139241645	chr12:44209553-44209554	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185300282	chr12:44209567-44209568	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs11182280	chr12:44209584-44209585	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs576009130	chr12:44209616-44209617	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543612627	chr12:44209714-44209715	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145333605	chr12:44209725-44209726	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs577722498	chr12:44209729-44209730	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544974457	chr12:44209730-44209731	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553924687	chr12:44209748-44209749	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs61567111	chr12:44209763-44209764	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542895358	chr12:44209778-44209779	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147696842	chr12:44209785-44209786	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs370070526	chr12:44209908-44209909	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs528245599	chr12:44209958-44209959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs191085172	chr12:44209981-44209982	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs547493096	chr12:44210007-44210008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs73280469	chr12:44210052-44210053	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs117445305	chr12:44210093-44210094	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs142386909	chr12:44210108-44210109	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570017400	chr12:44210129-44210130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs540956951	chr12:44210172-44210173	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537372083	chr12:44210229-44210230	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs559207836	chr12:44210233-44210234	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs144823695	chr12:44210244-44210245	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs535190463	chr12:44210261-44210262	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs182454181	chr12:44210264-44210265	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs147928191	chr12:44210266-44210267	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs187777929	chr12:44210310-44210311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375827182	chr12:44210362-44210363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs556718793	chr12:44210394-44210395	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575157185	chr12:44210453-44210454	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs192072259	chr12:44210489-44210490	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183359149	chr12:44210550-44210551	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528271423	chr12:44210556-44210557	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540081201	chr12:44210599-44210600	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs187526975	chr12:44210637-44210638	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533282462	chr12:44210681-44210682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373282170	chr12:44210687-44210688	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs551830094	chr12:44210701-44210702	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569971906	chr12:44210706-44210707	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs12819903	chr12:44210711-44210712	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs12827138	chr12:44210719-44210720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530899746	chr12:44210735-44210736	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs549420806	chr12:44210810-44210811	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs567912641	chr12:44210868-44210869	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs535333621	chr12:44210880-44210881	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs116244321	chr12:44210884-44210885	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Neurodevelopmental disorder	22521361	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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44202000-44217800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:44207600-44210200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:44208400-44210000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:44208400-44223600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:44208800-44210000	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr12:44209200-44209800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr12:44209200-44209800	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr12:44209400-44209800	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr12:44209400-44209800	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr12:44209400-44210200	Enhancers	Fetal Intestine Small	intestine
11	chr12:44209600-44209800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr12:44210000-44210200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:44210200-44210400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr12:44213400-44214200	Active TSS	Placenta	Placenta
15	chr12:44217000-44218200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:44217800-44218200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr12:44218000-44218400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr12:44218000-44218600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:44218000-44218600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr12:44218200-44218400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr12:44218200-44218400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr12:44218200-44220200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr12:44218600-44220000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:44219800-44220400	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr12:44220000-44220200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:44220000-44221800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:44220400-44220600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr12:44220400-44223000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr12:44221800-44225000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:44222000-44224200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:44222200-44224200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr12:44222800-44224000	Enhancers	NHEK	skin
33	chr12:44223000-44223200	Enhancers	Hela-S3	cervix
34	chr12:44223000-44223400	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr12:44223000-44223800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr12:44223000-44223800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr12:44223000-44223800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:44223000-44223800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:44223000-44224200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:44223200-44223400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr12:44223200-44223400	Enhancers	Osteobl	bone
42	chr12:44223200-44223600	Flanking Active TSS	Hela-S3	cervix
43	chr12:44223200-44223800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr12:44223200-44223800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:44223200-44223800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr12:44223200-44224200	Enhancers	Placenta	Placenta
47	chr12:44223400-44227600	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr12:44223400-44229000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr12:44223400-44229000	Weak transcription	Osteobl	bone
50	chr12:44223600-44224000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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