Variant report

Variant	nsv557795
Chromosome Location	chr12:25129015-25157129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:25144426-25144777	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:25144476-25144780	K562	blood:	n/a	n/a
3	ATF1	chr12:25131266-25131285	K562	blood:	n/a	n/a
4	ATF2	chr12:25148919-25149548	GM12878	blood:	n/a	n/a
5	ATF2	chr12:25150745-25151673	GM12878	blood:	n/a	n/a
6	ATF2	chr12:25150550-25151595	GM12878	blood:	n/a	n/a
7	BACH1	chr12:25132351-25132797	K562	blood:	n/a	n/a
8	BATF	chr12:25150981-25151458	GM12878	blood:	n/a	n/a
9	BATF	chr12:25149044-25149365	GM12878	blood:	n/a	n/a
10	BATF	chr12:25149027-25149355	GM12878	blood:	n/a	n/a
11	BATF	chr12:25150978-25151378	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:25150977-25151346	GM12878	blood:	n/a	chr12:25151070-25151079
13	BCL11A	chr12:25150900-25151425	GM12878	blood:	n/a	chr12:25151070-25151079
14	BCL3	chr12:25150928-25151439	GM12878	blood:	n/a	chr12:25151070-25151079
15	BCLAF1	chr12:25150819-25151469	GM12878	blood:	n/a	chr12:25151070-25151079
16	BCLAF1	chr12:25150815-25151670	GM12878	blood:	n/a	chr12:25151070-25151079
17	BHLHE40	chr12:25153532-25153534	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:25150898-25151630	GM12878	blood:	n/a	n/a
19	BRCA1	chr12:25150343-25150564	GM12878	blood:	n/a	n/a
20	CEBPB	chr12:25150942-25151407	GM12878	blood:	n/a	n/a
21	CEBPB	chr12:25150284-25151671	GM12878	blood:	n/a	n/a
22	CHD1	chr12:25148474-25149571	GM12878	blood:	n/a	n/a
23	CHD1	chr12:25150266-25151684	GM12878	blood:	n/a	n/a
24	CHD2	chr12:25149106-25149482	GM12878	blood:	n/a	n/a
25	CHD2	chr12:25150269-25151618	GM12878	blood:	n/a	n/a
26	CHD2	chr12:25139566-25139585	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr12:25150211-25151690	GM12878	blood:	n/a	n/a
28	CREB1	chr12:25150870-25151556	GM12878	blood:	n/a	n/a
29	CTCF	chr12:25144480-25144630	HBMEC	blood vessel:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
30	CTCF	chr12:25144500-25144650	AoAF	blood vessel:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
31	CTCF	chr12:25144620-25144770	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr12:25144300-25144450	GM12867	blood:	n/a	n/a
33	CTCF	chr12:25144504-25144675	GM10266	blood:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
34	CTCF	chr12:25144540-25144690	HEK293	kidney:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
35	CTCF	chr12:25144360-25144826	GM12878	blood:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
36	CTCF	chr12:25144200-25144350	GM06990	blood:	n/a	n/a
37	CTCF	chr12:25144500-25144650	HRE	kidney:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
38	CTCF	chr12:25144500-25144650	BJ	skin:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
39	CTCF	chr12:25144540-25144690	BE2_C	brain:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
40	CTCF	chr12:25144223-25144335	GM12891	blood:	n/a	n/a
41	CTCF	chr12:25144500-25144650	HEEpiC	esophagus:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
42	CTCF	chr12:25137960-25138110	HepG2	liver:	n/a	n/a
43	CTCF	chr12:25144500-25144650	GM12872	blood:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
44	CTCF	chr12:25144477-25144719	Kidney_OC	kidney:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
45	CTCF	chr12:25144498-25144706	GM13977	blood:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
46	CTCF	chr12:25144520-25144670	GM12873	blood:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
47	CTCF	chr12:25144500-25144650	HPF	lung:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
48	CTCF	chr12:25144306-25144933	HCT-116	colon:	n/a	chr12:25144861-25144869 chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
49	CTCF	chr12:25144478-25144730	Hela-S3	cervix:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609
50	CTCF	chr12:25144427-25144744	K562	blood:	n/a	chr12:25144592-25144608 chr12:25144594-25144607 chr12:25144593-25144614 chr12:25144591-25144609

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:25151263-25151313	GM12892	blood:	n/a
2	chr12:25150608-25150658	Caco-2	colon:	n/a
3	chr12:25148943-25148993	T-47D	breast:	n/a
4	chr12:25150608-25150658	AG09319	gingival:	n/a
5	chr12:25150626-25150676	BE2_C	brain:	n/a
6	chr12:25150626-25150676	AG09319	gingival:	n/a
7	chr12:25148943-25148993	BE2_C	brain:	n/a
8	chr12:25156888-25156938	MCF10A-Er-Src	breast:	n/a
9	chr12:25147218-25147268	GM06990	blood:	n/a
10	chr12:25150530-25150580	PANC-1	pancreas:	n/a
11	chr12:25151263-25151313	BJ	skin:	n/a
12	chr12:25151353-25151403	HNPCEpiC	eye:	n/a
13	chr12:25150402-25150452	CMK	blood:	n/a
14	chr12:25148943-25148993	ProgFib	skin:	n/a
15	chr12:25150626-25150676	NB4	blood:	n/a
16	chr12:25148943-25148993	HepG2	liver:	n/a
17	chr12:25150608-25150658	PrEC	prostate:	n/a
18	chr12:25151263-25151313	K562	blood:	n/a
19	chr12:25151263-25151313	HNPCEpiC	eye:	n/a
20	chr12:25150530-25150580	RPTEC	kidney:	n/a
21	chr12:25156888-25156938	HRE	kidney:	n/a
22	chr12:25147218-25147268	HL-60	blood:	n/a
23	chr12:25150608-25150658	PANC-1	pancreas:	n/a
24	chr12:25150626-25150676	PANC-1	pancreas:	n/a
25	chr12:25150608-25150658	HIPEpiC	eye:	n/a
26	chr12:25150402-25150452	GM12892	blood:	n/a
27	chr12:25150608-25150658	U87	brain:	n/a
28	chr12:25148943-25148993	NT2-D1	testis:	n/a
29	chr12:25151263-25151313	NHDF-neo	bronchial:	n/a
30	chr12:25150608-25150658	GM12891	blood:	n/a
31	chr12:25150626-25150676	PFSK-1	brain:	n/a
32	chr12:25151353-25151403	Jurkat	blood:	n/a
33	chr12:25156888-25156938	AG04449	skin:	fetal
34	chr12:25150626-25150676	NHDF-neo	bronchial:	n/a
35	chr12:25151353-25151403	Hela-S3	cervix:	n/a
36	chr12:25151263-25151313	Jurkat	blood:	n/a
37	chr12:25150608-25150658	HMEC	breast:	n/a
38	chr12:25147218-25147268	HCF	heart:	n/a
39	chr12:25151263-25151313	AoSMC	blood vessel:	n/a
40	chr12:25147218-25147268	AG10803	skin:	n/a
41	chr12:25151353-25151403	SK-N-SH_RA	brain:	n/a
42	chr12:25147218-25147268	GM19239	blood:	n/a
43	chr12:25151353-25151403	ovcar-3	ovarian:	n/a
44	chr12:25150608-25150658	HRE	kidney:	n/a
45	chr12:25156888-25156938	HepG2	liver:	n/a
46	chr12:25150626-25150676	ProgFib	skin:	n/a
47	chr12:25148943-25148993	AG10803	skin:	n/a
48	chr12:25150608-25150658	NB4	blood:	n/a
49	chr12:25147218-25147268	PANC-1	pancreas:	n/a
50	chr12:25150402-25150452	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:25122036..25125234-chr12:25131347..25134064,3	K562	blood:
2	chr12:25153768..25156029-chr12:25157028..25159477,2	K562	blood:
3	chr12:25142483..25144894-chr12:25145567..25148386,2	K562	blood:
4	chr12:25130633..25132240-chr12:25154864..25156882,2	K562	blood:
5	chr12:25098421..25101147-chr12:25131341..25133426,2	K562	blood:
6	chr12:25142482..25144723-chr12:25148559..25150612,2	K562	blood:
7	chr12:25144178..25145423-chr12:25271630..25272711,4	MCF-7	breast:
8	chr12:25144165..25145116-chr12:25540096..25541033,2	K562	blood:
9	chr12:25157102..25158926-chr12:25161698..25164141,3	K562	blood:
10	chr12:25153768..25156029-chr12:25157028..25159477,2	K562	blood:
11	chr12:25151498..25156029-chr12:25156662..25159477,4	K562	blood:
12	chr12:25148159..25150582-chr12:25154112..25156525,2	K562	blood:
13	chr12:25144337..25145003-chr12:25283318..25284116,2	K562	blood:
14	chr12:25130633..25132240-chr12:25154864..25156882,2	K562	blood:
15	chr12:25151498..25156029-chr12:25156662..25159477,4	K562	blood:
16	chr12:25142483..25144894-chr12:25145567..25148386,2	K562	blood:
17	chr12:25144639..25145222-chr12:25283398..25284249,2	MCF-7	breast:
18	chr12:25143896..25146815-chr12:25280565..25283315,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCAT1-4	chr12:25146370-25147261	NONHSAT027337
2	lnc-BCAT1-4	chr12:25150166-25150373	NONHSAT027337

Variant related genes	Relation type
C12orf77	TF binding region
C12orf77	CpG island
ENSG00000226397	chromatin interactions

Extended variants
information (count: 876 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10842443	chr12:25129015-25129016	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144431910	chr12:25129023-25129024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181178142	chr12:25129035-25129036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547140742	chr12:25129041-25129042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559002339	chr12:25129093-25129094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576355561	chr12:25129096-25129097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529874508	chr12:25129101-25129102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548047184	chr12:25129102-25129103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569957084	chr12:25129104-25129105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536905799	chr12:25129152-25129153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187028243	chr12:25129192-25129193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552446791	chr12:25129201-25129202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535365928	chr12:25129205-25129206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570904162	chr12:25129206-25129207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139252634	chr12:25129236-25129237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553536436	chr12:25129249-25129250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191408202	chr12:25129290-25129291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2649771	chr12:25129291-25129292	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs182397632	chr12:25129294-25129295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531284251	chr12:25129299-25129300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111347316	chr12:25129302-25129303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546221760	chr12:25129310-25129311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564439814	chr12:25129312-25129313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112085979	chr12:25129313-25129314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186581786	chr12:25129322-25129323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559038206	chr12:25129335-25129336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142147057	chr12:25129360-25129361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548373239	chr12:25129382-25129383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150806506	chr12:25129396-25129397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530729473	chr12:25129421-25129422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139186547	chr12:25129425-25129426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116767901	chr12:25129435-25129436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572681188	chr12:25129450-25129451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558443465	chr12:25129481-25129482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs61242160	chr12:25129504-25129505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147994742	chr12:25129511-25129512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78341227	chr12:25129513-25129514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs202037081	chr12:25129514-25129515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565292936	chr12:25129521-25129522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564829595	chr12:25129531-25129532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568569243	chr12:25129557-25129558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11047735	chr12:25129588-25129589	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs375951526	chr12:25129698-25129699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368981130	chr12:25129726-25129727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575797718	chr12:25129737-25129738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190987655	chr12:25129738-25129739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35809911	chr12:25129746-25129747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558066852	chr12:25129767-25129768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2645900	chr12:25129782-25129783	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs77548437	chr12:25129854-25129855	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
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
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17133270	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung adenocarcinoma	17982442	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:25128400-25129200	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr12:25128400-25133600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:25128600-25129200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:25128600-25129800	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr12:25128800-25132200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:25128800-25132200	Weak transcription	K562	blood
7	chr12:25129000-25132200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:25129200-25130200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:25129200-25132400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:25129600-25130000	Enhancers	GM12878-XiMat	blood
11	chr12:25129800-25131000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr12:25130000-25130400	Enhancers	Dnd41	blood
13	chr12:25130000-25130400	Flanking Active TSS	GM12878-XiMat	blood
14	chr12:25130200-25130600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr12:25130400-25130800	Enhancers	GM12878-XiMat	blood
16	chr12:25130600-25132000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr12:25130800-25132400	Weak transcription	GM12878-XiMat	blood
18	chr12:25131000-25132200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr12:25132000-25132600	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr12:25132000-25132800	Enhancers	Primary B cells from peripheral blood	blood
21	chr12:25132200-25132600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:25132200-25132600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr12:25132200-25132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:25132200-25133200	Enhancers	K562	blood
25	chr12:25132400-25132600	Enhancers	GM12878-XiMat	blood
26	chr12:25132400-25132800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:25132400-25133400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:25132600-25133200	Weak transcription	GM12878-XiMat	blood
29	chr12:25132600-25133200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr12:25132800-25133400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:25133200-25133400	Enhancers	GM12878-XiMat	blood
32	chr12:25133400-25133600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr12:25133400-25133600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:25136000-25136400	Enhancers	Placenta	Placenta
35	chr12:25141000-25152000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:25141600-25141800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:25143400-25144400	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr12:25144400-25144600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr12:25144400-25144600	Enhancers	Fetal Thymus	thymus
40	chr12:25144400-25145000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr12:25144400-25145600	Enhancers	Primary B cells from cord blood	blood
42	chr12:25144600-25146000	Weak transcription	Fetal Thymus	thymus
43	chr12:25144800-25148400	Enhancers	GM12878-XiMat	blood
44	chr12:25145000-25150600	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr12:25145600-25146200	Weak transcription	Primary B cells from cord blood	blood
46	chr12:25145600-25150400	Enhancers	Primary B cells from peripheral blood	blood
47	chr12:25146000-25146800	Enhancers	Fetal Thymus	thymus
48	chr12:25146200-25149000	Enhancers	Primary B cells from cord blood	blood
49	chr12:25146200-25149800	Weak transcription	Aorta	Aorta
50	chr12:25146400-25146600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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