Variant report

Variant	nsv899045
Chromosome Location	chr12:42118062-42174431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:150)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:150 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:42124696-42124730	K562	blood:	n/a	n/a
2	BATF	chr12:42163639-42163958	GM12878	blood:	n/a	chr12:42163817-42163828
3	BHLHE40	chr12:42163876-42163902	GM12878	blood:	n/a	n/a
4	BRCA1	chr12:42120460-42120497	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr12:42168438-42168448	GM12878	blood:	n/a	n/a
6	CEBPB	chr12:42137707-42138068	A549	lung:	n/a	chr12:42137885-42137896
7	CEBPB	chr12:42137718-42138172	A549	lung:	n/a	chr12:42137885-42137896
8	CEBPB	chr12:42137695-42138075	Hela-S3	cervix:	n/a	chr12:42137885-42137896
9	CEBPB	chr12:42137753-42137991	IMR90	lung:	n/a	chr12:42137885-42137896
10	CEBPB	chr12:42137663-42138046	A549	lung:	n/a	chr12:42137885-42137896
11	CEBPB	chr12:42137716-42138058	HepG2	liver:	n/a	chr12:42137885-42137896
12	CHD2	chr12:42154920-42154928	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr12:42137691-42137951	A549	lung:	n/a	n/a
14	CTCF	chr12:42139700-42139850	GM12871	blood:	n/a	n/a
15	CTCF	chr12:42139480-42139630	HepG2	liver:	n/a	n/a
16	CTCF	chr12:42122955-42123114	GM12878	blood:	n/a	n/a
17	CTCF	chr12:42155515-42155541	GM20000	blood:	n/a	n/a
18	CTCF	chr12:42139503-42139695	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:42122960-42123110	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:42139574-42139616	GM19239	blood:	n/a	n/a
21	CTCF	chr12:42155707-42155754	LNCaP	prostate:	n/a	n/a
22	CTCF	chr12:42139337-42139739	MCF-7	breast:	n/a	n/a
23	CTCF	chr12:42136894-42136930	K562	blood:	n/a	n/a
24	CTCF	chr12:42139549-42139609	LNCaP	prostate:	n/a	n/a
25	CTCF	chr12:42136780-42136930	GM12865	blood:	n/a	n/a
26	CTCF	chr12:42136820-42136970	RPTEC	kidney:	n/a	n/a
27	CTCF	chr12:42139500-42139650	HCT-116	colon:	n/a	n/a
28	CTCF	chr12:42139480-42139630	HCT-116	colon:	n/a	n/a
29	CTCF	chr12:42139515-42139642	HepG2	liver:	n/a	n/a
30	CTCF	chr12:42123000-42123150	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:42139480-42139630	GM12871	blood:	n/a	n/a
32	CTCF	chr12:42139560-42139710	GM12873	blood:	n/a	n/a
33	CTCF	chr12:42139537-42139628	GM12892	blood:	n/a	n/a
34	CTCF	chr12:42139520-42139670	GM06990	blood:	n/a	n/a
35	CTCF	chr12:42139480-42139630	GM12865	blood:	n/a	n/a
36	CTCF	chr12:42139569-42139625	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr12:42139480-42139630	GM12872	blood:	n/a	n/a
38	CTCF	chr12:42139487-42139675	HepG2	liver:	n/a	n/a
39	CTCF	chr12:42139520-42139670	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr12:42139531-42139639	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:42136839-42136983	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr12:42139520-42139655	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:42136860-42137010	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:42123017-42123076	HepG2	liver:	n/a	n/a
45	CTCF	chr12:42136860-42137010	HCT-116	colon:	n/a	n/a
46	CTCF	chr12:42136889-42136940	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr12:42123010-42123043	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:42136780-42136930	HEK293	kidney:	n/a	n/a
49	CTCF	chr12:42136877-42136920	GM12878	blood:	n/a	n/a
50	CTCF	chr12:42136820-42136970	GM12875	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:42124611-42124661	NH-A	brain:	n/a
2	chr12:42124611-42124661	GM12891	blood:	n/a
3	chr12:42124611-42124661	A549	lung:	n/a
4	chr12:42124611-42124661	HL-60	blood:	n/a
5	chr12:42124611-42124661	HCM	heart:	n/a
6	chr12:42124611-42124661	T-47D	breast:	n/a
7	chr12:42124611-42124661	AG10803	skin:	n/a
8	chr12:42124611-42124661	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:42124611-42124661	NHDF-neo	bronchial:	n/a
10	chr12:42124611-42124661	H1-hESC	embryonic stem cell:	embryo
11	chr12:42124611-42124661	Hela-S3	cervix:	n/a
12	chr12:42124611-42124661	HepG2	liver:	n/a
13	chr12:42124611-42124661	SAEC	small airway:	n/a
14	chr12:42124611-42124661	GM12878	blood:	n/a
15	chr12:42124611-42124661	PrEC	prostate:	n/a
16	chr12:42124611-42124661	HRE	kidney:	n/a
17	chr12:42124611-42124661	K562	blood:	n/a
18	chr12:42124611-42124661	NHBE	bronchial:	n/a
19	chr12:42124611-42124661	ovcar-3	ovarian:	n/a
20	chr12:42124611-42124661	HEK293	kidney:	embryo
21	chr12:42124611-42124661	NT2-D1	testis:	n/a
22	chr12:42124611-42124661	AG09319	gingival:	n/a
23	chr12:42124611-42124661	Jurkat	blood:	n/a
24	chr12:42124611-42124661	HAEpiC	amniotic membrane:	n/a
25	chr12:42124611-42124661	GM06990	blood:	n/a
26	chr12:42124611-42124661	HEEpiC	esophagus:	n/a
27	chr12:42124611-42124661	Caco-2	colon:	n/a
28	chr12:42124611-42124661	BJ	skin:	n/a
29	chr12:42124611-42124661	HRPEpiC	eye:	n/a
30	chr12:42124611-42124661	GM12892	blood:	n/a
31	chr12:42124611-42124661	HIPEpiC	eye:	n/a
32	chr12:42124611-42124661	MCF-7	breast:	n/a
33	chr12:42124611-42124661	PANC-1	pancreas:	n/a
34	chr12:42124611-42124661	HUVEC	blood vessel:	n/a
35	chr12:42124611-42124661	RPTEC	kidney:	n/a
36	chr12:42124611-42124661	PFSK-1	brain:	n/a
37	chr12:42124611-42124661	AG04449	skin:	fetal
38	chr12:42124611-42124661	ProgFib	skin:	n/a
39	chr12:42124611-42124661	SK-N-SH	brain:	n/a
40	chr12:42124611-42124661	HCPEpiC	choroid plexus:	n/a
41	chr12:42124611-42124661	LNCaP	prostate:	n/a
42	chr12:42124611-42124661	SKMC	muscle:	n/a
43	chr12:42124611-42124661	IMR90	lung:	fetal
44	chr12:42124611-42124661	AG09309	skin:	n/a
45	chr12:42124611-42124661	MCF10A-Er-Src	breast:	n/a
46	chr12:42124611-42124661	Hepatocyte	liver:	n/a
47	chr12:42124611-42124661	HCT-116	colon:	n/a
48	chr12:42124611-42124661	SK-N-SH_RA	brain:	n/a
49	chr12:42124611-42124661	NB4	blood:	n/a
50	chr12:42124611-42124661	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:42129312..42132862-chr12:42133070..42135450,3	K562	blood:
2	chr12:42116428..42118645-chr12:42119416..42120993,2	MCF-7	breast:
3	chr12:41658168..41658718-chr12:42139304..42140019,2	MCF-7	breast:
4	chr12:42129312..42132862-chr12:42133070..42135450,3	K562	blood:
5	chr12:42116428..42118645-chr12:42119416..42120993,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDZRN4-1	chr12:42157991-42158067	ENSG00000257784.1
2	lnc-PDZRN4-1	chr12:42159122-42159375	XLOC_009714
3	lnc-PDZRN4-1	chr12:42158025-42158067	ENSG00000257784.1
4	lnc-PDZRN4-1	chr12:42157956-42158067	XLOC_009714
5	lnc-PDZRN4-1	chr12:42159122-42159375	XLOC_009714
6	lnc-PDZRN4-1	chr12:42159122-42159368	XLOC_009714
7	lnc-PDZRN4-1	chr12:42159122-42159368	XLOC_009714
8	lnc-PDZRN4-1	chr12:42159122-42159368	XLOC_009714
9	lnc-PDZRN4-1	chr12:42157980-42158061	XLOC_009714
10	lnc-PDZRN4-1	chr12:42157980-42158047	XLOC_009714
11	lnc-PDZRN4-1	chr12:42157955-42158083	NONHSAT027752
12	lnc-PDZRN4-1	chr12:42157956-42158067	XLOC_009714
13	lnc-PDZRN4-1	chr12:42158540-42158608	ENSG00000257784.1
14	lnc-PDZRN4-1	chr12:42158539-42158654	NONHSAT027752
15	lnc-PDZRN4-1	chr12:42158540-42158608	XLOC_009714
16	lnc-PDZRN4-1	chr12:42159122-42159383	ENSG00000257784.1
17	lnc-PDZRN4-1	chr12:42159121-42159375	NONHSAT027752
18	lnc-PDZRN4-1	chr12:42158546-42158608	XLOC_009714
19	lnc-PDZRN4-1	chr12:42159122-42159375	XLOC_009714
20	lnc-PDZRN4-1	chr12:42159122-42159368	XLOC_009714
21	lnc-PDZRN4-1	chr12:42159122-42159378	NONHSAT027756
22	lnc-PDZRN4-1	chr12:42159122-42159360	ENSG00000257784.1
23	lnc-PDZRN4-1	chr12:42157980-42158059	XLOC_009714
24	lnc-PDZRN4-1	chr12:42157956-42158067	XLOC_009714
25	lnc-PDZRN4-1	chr12:42158540-42158654	XLOC_009714
26	lnc-PDZRN4-1	chr12:42157963-42158061	NONHSAT027756

No data

Variant related genes	Relation type
ENSG00000257784	TF binding region
ENSG00000257784	CpG island

Extended variants
information (count: 1676 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1676 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12809229	chr12:42118062-42118063	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543845473	chr12:42118135-42118136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533385876	chr12:42118147-42118148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142216092	chr12:42118169-42118170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574676177	chr12:42118177-42118178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551639446	chr12:42118200-42118201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79133382	chr12:42118210-42118211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560281770	chr12:42118234-42118235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567180147	chr12:42118245-42118246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533525155	chr12:42118269-42118270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11181125	chr12:42118273-42118274	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs34295041	chr12:42118337-42118338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563856062	chr12:42118339-42118340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73124230	chr12:42118344-42118345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79812136	chr12:42118358-42118359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549752899	chr12:42118364-42118365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183005986	chr12:42118368-42118369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2645837	chr12:42118424-42118425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529574523	chr12:42118457-42118458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547801383	chr12:42118476-42118477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375874131	chr12:42118485-42118486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111651763	chr12:42118522-42118523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369489468	chr12:42118532-42118533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570378473	chr12:42118590-42118591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375628885	chr12:42118595-42118596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17129721	chr12:42118611-42118612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188440342	chr12:42118616-42118617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11181126	chr12:42118642-42118643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs570163886	chr12:42118644-42118645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200930892	chr12:42118678-42118679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144492109	chr12:42118729-42118730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573986463	chr12:42118733-42118734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535720385	chr12:42118808-42118809	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs183008897	chr12:42118857-42118858	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs187712458	chr12:42118952-42118953	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs369498047	chr12:42118984-42118985	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs545602978	chr12:42118988-42118989	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs563792696	chr12:42118997-42118998	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs11181128	chr12:42119127-42119128	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs571785834	chr12:42119203-42119204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543186456	chr12:42119236-42119237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191585312	chr12:42119239-42119240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577902767	chr12:42119252-42119253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34752499	chr12:42119269-42119270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72516189	chr12:42119278-42119279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561701921	chr12:42119281-42119282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370583905	chr12:42119287-42119288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528902678	chr12:42119312-42119313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114497700	chr12:42119329-42119330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75541990	chr12:42119330-42119331	Weak transcription Enhancers	n/a	n/a	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
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
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42103000-42118800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:42117600-42118400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:42117800-42118400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:42118000-42118800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:42118800-42119000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr12:42118800-42119200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:42119000-42119400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:42119200-42121800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:42119400-42119800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr12:42120000-42120600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:42120600-42121000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:42120600-42123800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr12:42120600-42124800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:42121000-42125000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:42121800-42124200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr12:42123800-42126200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr12:42124200-42125200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:42124200-42125600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:42124400-42125400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr12:42124800-42125400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr12:42125000-42125600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr12:42125000-42125600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:42125000-42125800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:42125200-42125600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:42125200-42125600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr12:42125200-42126200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:42125400-42125600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr12:42125400-42126200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr12:42126200-42126400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:42126200-42126400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:42126200-42130800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr12:42130800-42132200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr12:42131200-42132000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr12:42132000-42132200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:42132800-42133000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:42141200-42142800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:42141200-42142800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:42141400-42142800	Enhancers	Primary hematopoietic stem cells	blood
39	chr12:42142000-42142600	Enhancers	HUVEC	blood vessel
40	chr12:42149200-42149400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:42149400-42150400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:42150400-42151000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr12:42151000-42158000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:42155600-42156400	Enhancers	Fetal Brain Male	brain
45	chr12:42158000-42158600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr12:42158600-42165600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:42161000-42161600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr12:42161000-42161600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr12:42161000-42162000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr12:42161200-42161600	Enhancers	H1 Cell Line	embryonic stem cell

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