Variant report

Variant	nsv898921
Chromosome Location	chr12:25106961-25184896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1091)
CpG islands
(count:672)
Chromatin interactive
region (count:26)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1091 , 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	chr12:25144476-25144780	K562	blood:	n/a	n/a
2	ARID3A	chr12:25107210-25107505	K562	blood:	n/a	n/a
3	ARID3A	chr12:25113270-25113490	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:25144426-25144777	HepG2	liver:	n/a	n/a
5	ATF1	chr12:25131266-25131285	K562	blood:	n/a	n/a
6	ATF1	chr12:25107171-25107439	K562	blood:	n/a	n/a
7	ATF2	chr12:25108188-25108699	GM12878	blood:	n/a	n/a
8	ATF2	chr12:25148919-25149548	GM12878	blood:	n/a	n/a
9	ATF2	chr12:25150745-25151673	GM12878	blood:	n/a	n/a
10	ATF2	chr12:25158175-25158872	GM12878	blood:	n/a	n/a
11	ATF2	chr12:25150550-25151595	GM12878	blood:	n/a	n/a
12	ATF2	chr12:25108201-25108724	GM12878	blood:	n/a	n/a
13	ATF2	chr12:25158241-25158794	GM12878	blood:	n/a	n/a
14	ATF2	chr12:25173237-25174329	GM12878	blood:	n/a	n/a
15	ATF2	chr12:25173389-25174067	GM12878	blood:	n/a	n/a
16	ATF3	chr12:25113154-25113554	K562	blood:	n/a	n/a
17	BACH1	chr12:25132351-25132797	K562	blood:	n/a	n/a
18	BATF	chr12:25108192-25108691	GM12878	blood:	n/a	n/a
19	BATF	chr12:25149027-25149355	GM12878	blood:	n/a	n/a
20	BATF	chr12:25113285-25113545	GM12878	blood:	n/a	n/a
21	BATF	chr12:25150978-25151378	GM12878	blood:	n/a	n/a
22	BATF	chr12:25112916-25113279	GM12878	blood:	n/a	n/a
23	BATF	chr12:25149044-25149365	GM12878	blood:	n/a	n/a
24	BATF	chr12:25173453-25173900	GM12878	blood:	n/a	chr12:25173776-25173784
25	BATF	chr12:25108262-25108690	GM12878	blood:	n/a	n/a
26	BATF	chr12:25150981-25151458	GM12878	blood:	n/a	n/a
27	BATF	chr12:25112988-25113554	GM12878	blood:	n/a	n/a
28	BATF	chr12:25173538-25173926	GM12878	blood:	n/a	chr12:25173776-25173784
29	BCL11A	chr12:25150900-25151425	GM12878	blood:	n/a	chr12:25151070-25151079
30	BCL11A	chr12:25108234-25108543	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:25173405-25173992	GM12878	blood:	n/a	chr12:25173772-25173781
32	BCL11A	chr12:25108163-25108623	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:25173474-25173871	GM12878	blood:	n/a	chr12:25173772-25173781
34	BCL11A	chr12:25150977-25151346	GM12878	blood:	n/a	chr12:25151070-25151079
35	BCL3	chr12:25150928-25151439	GM12878	blood:	n/a	chr12:25151070-25151079
36	BCL3	chr12:25173450-25173989	GM12878	blood:	n/a	chr12:25173772-25173781
37	BCL3	chr12:25158206-25158707	GM12878	blood:	n/a	chr12:25158532-25158539 chr12:25158655-25158664
38	BCL3	chr12:25108158-25108691	GM12878	blood:	n/a	n/a
39	BCL3	chr12:25173514-25173949	GM12878	blood:	n/a	chr12:25173772-25173781
40	BCLAF1	chr12:25150815-25151670	GM12878	blood:	n/a	chr12:25151070-25151079
41	BCLAF1	chr12:25173285-25174012	GM12878	blood:	n/a	chr12:25173772-25173781
42	BCLAF1	chr12:25173365-25173958	GM12878	blood:	n/a	chr12:25173772-25173781
43	BCLAF1	chr12:25150819-25151469	GM12878	blood:	n/a	chr12:25151070-25151079
44	BHLHE40	chr12:25158133-25158912	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:25150898-25151630	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:25113235-25113435	K562	blood:	n/a	n/a
47	BHLHE40	chr12:25173504-25173981	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:25153532-25153534	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:25108275-25108547	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:25157455-25157695	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:25151263-25151313	NH-A	brain:	n/a
2	chr12:25151263-25151313	NH-A	brain:	n/a
3	chr12:25147218-25147268	MCF-7	breast:	n/a
4	chr12:25150402-25150452	NB4	blood:	n/a
5	chr12:25177892-25177942	SK-N-SH	brain:	n/a
6	chr12:25148943-25148993	NHDF-neo	bronchial:	n/a
7	chr12:25150608-25150658	CMK	blood:	n/a
8	chr12:25150608-25150658	SK-N-SH_RA	brain:	n/a
9	chr12:25150530-25150580	NHBE	bronchial:	n/a
10	chr12:25148943-25148993	HEK293	kidney:	embryo
11	chr12:25177892-25177942	GM12892	blood:	n/a
12	chr12:25157146-25157196	NHBE	bronchial:	n/a
13	chr12:25150626-25150676	PFSK-1	brain:	n/a
14	chr12:25177892-25177942	NH-A	brain:	n/a
15	chr12:25147218-25147268	HRCEpiC	kidney:	n/a
16	chr12:25150402-25150452	HAEpiC	amniotic membrane:	n/a
17	chr12:25150530-25150580	AG09309	skin:	n/a
18	chr12:25151353-25151403	Hepatocyte	liver:	n/a
19	chr12:25150608-25150658	HPAEpiC	pulmonary alveolar:	n/a
20	chr12:25150608-25150658	AoSMC	blood vessel:	n/a
21	chr12:25151353-25151403	NHDF-neo	bronchial:	n/a
22	chr12:25177892-25177942	HRPEpiC	eye:	n/a
23	chr12:25147218-25147268	AG09309	skin:	n/a
24	chr12:25150626-25150676	H1-hESC	embryonic stem cell:	embryo
25	chr12:25148943-25148993	HAEpiC	amniotic membrane:	n/a
26	chr12:25156888-25156938	GM12891	blood:	n/a
27	chr12:25157146-25157196	PrEC	prostate:	n/a
28	chr12:25150530-25150580	GM19239	blood:	n/a
29	chr12:25150608-25150658	HUVEC	blood vessel:	n/a
30	chr12:25148943-25148993	NHBE	bronchial:	n/a
31	chr12:25150608-25150658	HRPEpiC	eye:	n/a
32	chr12:25151353-25151403	LNCaP	prostate:	n/a
33	chr12:25150608-25150658	HCM	heart:	n/a
34	chr12:25150402-25150452	Jurkat	blood:	n/a
35	chr12:25150402-25150452	HCPEpiC	choroid plexus:	n/a
36	chr12:25147218-25147268	AG04449	skin:	fetal
37	chr12:25148943-25148993	HUVEC	blood vessel:	n/a
38	chr12:25147218-25147268	HRPEpiC	eye:	n/a
39	chr12:25150530-25150580	CMK	blood:	n/a
40	chr12:25151263-25151313	GM12891	blood:	n/a
41	chr12:25150608-25150658	HL-60	blood:	n/a
42	chr12:25150402-25150452	AG04449	skin:	fetal
43	chr12:25177892-25177942	HRCEpiC	kidney:	n/a
44	chr12:25150626-25150676	SK-N-SH_RA	brain:	n/a
45	chr12:25150402-25150452	LNCaP	prostate:	n/a
46	chr12:25150626-25150676	T-47D	breast:	n/a
47	chr12:25151263-25151313	PFSK-1	brain:	n/a
48	chr12:25150530-25150580	NT2-D1	testis:	n/a
49	chr12:25151263-25151313	MCF10A-Er-Src	breast:	n/a
50	chr12:25177892-25177942	HUVEC	blood vessel:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:25159267..25162918-chr12:25164061..25168654,4	K562	blood:
2	chr12:25153768..25156029-chr12:25157028..25159477,2	K562	blood:
3	chr12:25157102..25158926-chr12:25161698..25164141,3	K562	blood:
4	chr12:25144639..25145222-chr12:25283398..25284249,2	MCF-7	breast:
5	chr12:25096555..25099417-chr12:25125856..25128677,2	K562	blood:
6	chr12:25130633..25132240-chr12:25154864..25156882,2	K562	blood:
7	chr12:25143896..25146815-chr12:25280565..25283315,2	MCF-7	breast:
8	chr12:25122036..25125234-chr12:25131347..25134064,3	K562	blood:
9	chr12:25148159..25150582-chr12:25154112..25156525,2	K562	blood:
10	chr12:25151498..25156029-chr12:25156662..25159477,4	K562	blood:
11	chr12:25103176..25105758-chr12:25114864..25117821,2	K562	blood:
12	chr12:25112900..25113752-chr12:25283318..25284098,2	K562	blood:
13	chr12:25171864..25173987-chr12:25176023..25178205,2	K562	blood:
14	chr12:25153768..25156029-chr12:25157028..25159477,2	K562	blood:
15	chr12:25142483..25144894-chr12:25145567..25148386,2	K562	blood:
16	chr12:25142482..25144723-chr12:25148559..25150612,2	K562	blood:
17	chr12:25100091..25101732-chr12:25123501..25126492,2	K562	blood:
18	chr12:25130633..25132240-chr12:25154864..25156882,2	K562	blood:
19	chr12:25098421..25101147-chr12:25131341..25133426,2	K562	blood:
20	chr12:25144337..25145003-chr12:25283318..25284116,2	K562	blood:
21	chr12:25142483..25144894-chr12:25145567..25148386,2	K562	blood:
22	chr12:25157102..25158926-chr12:25161698..25164141,3	K562	blood:
23	chr12:25144178..25145423-chr12:25271630..25272711,4	MCF-7	breast:
24	chr12:25144165..25145116-chr12:25540096..25541033,2	K562	blood:
25	chr12:25122036..25125234-chr12:25131347..25134064,3	K562	blood:
26	chr12:25151498..25156029-chr12:25156662..25159477,4	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRMP-2	chr12:25112988-25113092	ENSG00000255921.1
2	lnc-LRMP-2	chr12:25110868-25111208	ENSG00000255921.1
3	lnc-BCAT1-4	chr12:25146370-25147261	NONHSAT027337
4	lnc-LRMP-2	chr12:25110061-25110174	ENSG00000255921.1
5	lnc-BCAT1-4	chr12:25150166-25150373	NONHSAT027337

No data

Variant related genes	Relation type
LRMP	TF binding region
ENSG00000258879	TF binding region
C12orf77	TF binding region
ENSG00000213736	TF binding region
BCAT1	TF binding region
LRMP	CpG island
ENSG00000258879	CpG island
C12orf77	CpG island
ENSG00000213736	CpG island
BCAT1	CpG island
ENSG00000226397	chromatin interactions
ENSG00000258879	chromatin interactions
ENSG00000118308	chromatin interactions

Extended variants
information (count: 2814 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2814 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12819423	chr12:25106961-25106962	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369219693	chr12:25106970-25106971	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs539503116	chr12:25106978-25106979	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs186882109	chr12:25107017-25107018	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs550010336	chr12:25107055-25107056	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs574068318	chr12:25107084-25107085	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs192037784	chr12:25107105-25107106	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs562946072	chr12:25107117-25107118	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs10842439	chr12:25107130-25107131	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs183914755	chr12:25107225-25107226	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs377681469	chr12:25107240-25107241	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs186827255	chr12:25107249-25107250	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs371423737	chr12:25107258-25107259	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs117483419	chr12:25107264-25107265	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs191238380	chr12:25107266-25107267	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs117901929	chr12:25107288-25107289	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs143081136	chr12:25107293-25107294	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs568964939	chr12:25107303-25107304	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs115027848	chr12:25107317-25107318	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs142814062	chr12:25107318-25107319	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs146979923	chr12:25107325-25107326	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs75968033	chr12:25107352-25107353	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs182285534	chr12:25107357-25107358	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs187316738	chr12:25107376-25107377	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs192880275	chr12:25107386-25107387	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs185272704	chr12:25107493-25107494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs578030118	chr12:25107506-25107507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377192121	chr12:25107546-25107547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141781376	chr12:25107554-25107555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199951718	chr12:25107556-25107557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553928131	chr12:25107600-25107601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572420644	chr12:25107649-25107650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs17322922	chr12:25107660-25107661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
34	rs202221058	chr12:25107705-25107706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561529232	chr12:25107763-25107764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114805719	chr12:25107852-25107853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562756080	chr12:25107853-25107854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543861949	chr12:25107860-25107861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562631102	chr12:25107882-25107883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546128874	chr12:25107885-25107886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116606791	chr12:25107919-25107920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566646820	chr12:25107924-25107925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs56001114	chr12:25107929-25107930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527589609	chr12:25107940-25107941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549221339	chr12:25107975-25107976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567441750	chr12:25107980-25107981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7965671	chr12:25107985-25107986	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs34960650	chr12:25108014-25108015	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs571438636	chr12:25108016-25108017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538710791	chr12:25108042-25108043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:25105600-25107000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr12:25105800-25107400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:25105800-25114800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:25106000-25107200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:25106200-25109800	Enhancers	GM12878-XiMat	blood
6	chr12:25106600-25108600	Enhancers	K562	blood
7	chr12:25107000-25107600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr12:25107200-25107400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:25107400-25107600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:25107400-25107800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:25107800-25114600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr12:25108600-25109000	Flanking Active TSS	K562	blood
13	chr12:25109000-25109600	Enhancers	K562	blood
14	chr12:25109800-25112800	Weak transcription	GM12878-XiMat	blood
15	chr12:25112800-25113800	Enhancers	GM12878-XiMat	blood
16	chr12:25113200-25113400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:25113400-25113600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr12:25113400-25113800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr12:25113400-25113800	Enhancers	Pancreas	Pancrea
20	chr12:25113400-25115000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr12:25113600-25115200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr12:25113800-25116400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:25113800-25128400	Weak transcription	Pancreas	Pancrea
24	chr12:25114400-25114600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:25114600-25115000	ZNF genes & repeats	Right Atrium	heart
26	chr12:25114600-25115600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:25114600-25115600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:25114800-25115400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:25114800-25115400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:25115000-25115400	Enhancers	NHEK	skin
31	chr12:25115200-25116600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr12:25115200-25116600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr12:25115600-25116000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:25115600-25116600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr12:25115800-25116600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr12:25116000-25116400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr12:25116000-25117000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:25116600-25117000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr12:25116600-25119400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr12:25117000-25118200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:25118000-25120400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr12:25118600-25119600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr12:25119000-25121600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr12:25119600-25119800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr12:25119800-25120200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr12:25120200-25120400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:25120200-25120600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr12:25120400-25120600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:25120400-25128600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr12:25120600-25121000	Enhancers	Monocytes-CD14+_RO01746	blood

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