Variant report

Variant	nsv559157
Chromosome Location	chr12:63142592-63163019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:253)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63154673-63154993	K562	blood:	n/a	n/a
2	ATF1	chr12:63154614-63155006	K562	blood:	n/a	n/a
3	ATF3	chr12:63144505-63145292	A549	lung:	n/a	n/a
4	ATF3	chr12:63144597-63145254	A549	lung:	n/a	n/a
5	ATF3	chr12:63154468-63154981	A549	lung:	n/a	n/a
6	ATF3	chr12:63154389-63155035	A549	lung:	n/a	n/a
7	BACH1	chr12:63155509-63155528	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:63154207-63154864	GM12878	blood:	n/a	chr12:63154556-63154567
9	BATF	chr12:63154555-63154733	GM12878	blood:	n/a	chr12:63154556-63154567
10	BCL3	chr12:63154339-63155345	A549	lung:	n/a	n/a
11	BCL3	chr12:63144433-63145380	A549	lung:	n/a	n/a
12	BCL3	chr12:63154417-63155077	A549	lung:	n/a	n/a
13	BCL3	chr12:63151709-63152448	A549	lung:	n/a	n/a
14	BHLHE40	chr12:63154686-63154938	K562	blood:	n/a	n/a
15	BHLHE40	chr12:63155579-63155615	K562	blood:	n/a	n/a
16	CCNT2	chr12:63154656-63154917	K562	blood:	n/a	n/a
17	CEBPB	chr12:63144662-63145184	A549	lung:	n/a	n/a
18	CEBPB	chr12:63144681-63145336	A549	lung:	n/a	n/a
19	CEBPB	chr12:63143910-63144106	K562	blood:	n/a	chr12:63143966-63143977
20	CEBPB	chr12:63154445-63155195	A549	lung:	n/a	n/a
21	CEBPB	chr12:63152037-63152505	IMR90	lung:	n/a	n/a
22	CEBPB	chr12:63143802-63144154	A549	lung:	n/a	chr12:63143966-63143977
23	CEBPB	chr12:63143801-63144082	HepG2	liver:	n/a	chr12:63143966-63143977
24	CEBPD	chr12:63154636-63154945	K562	blood:	n/a	n/a
25	CEBPD	chr12:63154564-63154943	K562	blood:	n/a	n/a
26	CREB1	chr12:63144858-63145210	A549	lung:	n/a	n/a
27	CTCF	chr12:63159001-63159024	GM13976	blood:	n/a	n/a
28	CTCF	chr12:63155540-63155690	HMF	breast:	n/a	n/a
29	CTCF	chr12:63155560-63155710	HMF	breast:	n/a	n/a
30	CTCF	chr12:63161180-63161330	AG10803	skin:	n/a	n/a
31	CTCF	chr12:63155740-63155890	HAc	cerebellar:	n/a	n/a
32	CUX1	chr12:63154671-63154866	K562	blood:	n/a	n/a
33	E2F4	chr12:63160196-63160292	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr12:63154623-63154726	GM12878	blood:	n/a	n/a
35	ELF1	chr12:63154449-63154889	A549	lung:	n/a	n/a
36	ELK1	chr12:63151416-63151507	GM12878	blood:	n/a	n/a
37	EP300	chr12:63154649-63155009	K562	blood:	n/a	n/a
38	EP300	chr12:63144462-63145923	A549	lung:	n/a	chr12:63144892-63144906
39	EP300	chr12:63151855-63152496	A549	lung:	n/a	n/a
40	EP300	chr12:63154074-63155214	A549	lung:	n/a	n/a
41	EP300	chr12:63154448-63155084	HepG2	liver:	n/a	n/a
42	EP300	chr12:63153948-63155377	A549	lung:	n/a	n/a
43	EP300	chr12:63151698-63152645	A549	lung:	n/a	n/a
44	EP300	chr12:63144437-63145727	A549	lung:	n/a	chr12:63144892-63144906
45	EP300	chr12:63150975-63151066	K562	blood:	n/a	n/a
46	EP300	chr12:63154550-63154955	HepG2	liver:	n/a	n/a
47	EP300	chr12:63154794-63154917	K562	blood:	n/a	n/a
48	ESRRA	chr12:63154316-63155091	GM12878	blood:	n/a	n/a
49	ETS1	chr12:63154513-63154977	A549	lung:	n/a	n/a
50	FOS	chr12:63156446-63156838	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63150899-63150949	HUVEC	blood vessel:	n/a
2	chr12:63144886-63144936	ovcar-3	ovarian:	n/a
3	chr12:63150899-63150949	Caco-2	colon:	n/a
4	chr12:63144886-63144936	HIPEpiC	eye:	n/a
5	chr12:63144886-63144936	ECC-1	luminal epithelium:	n/a
6	chr12:63150899-63150949	NH-A	brain:	n/a
7	chr12:63150899-63150949	SK-N-SH_RA	brain:	n/a
8	chr12:63150899-63150949	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:63144886-63144936	HNPCEpiC	eye:	n/a
10	chr12:63150899-63150949	SAEC	small airway:	n/a
11	chr12:63150899-63150949	Hepatocyte	liver:	n/a
12	chr12:63150899-63150949	ProgFib	skin:	n/a
13	chr12:63150899-63150949	PrEC	prostate:	n/a
14	chr12:63150899-63150949	GM12878	blood:	n/a
15	chr12:63150899-63150949	HRCEpiC	kidney:	n/a
16	chr12:63144886-63144936	IMR90	lung:	fetal
17	chr12:63144886-63144936	PFSK-1	brain:	n/a
18	chr12:63144886-63144936	GM12878	blood:	n/a
19	chr12:63144886-63144936	HCM	heart:	n/a
20	chr12:63150899-63150949	Hela-S3	cervix:	n/a
21	chr12:63150899-63150949	HCT-116	colon:	n/a
22	chr12:63150899-63150949	HL-60	blood:	n/a
23	chr12:63144886-63144936	NT2-D1	testis:	n/a
24	chr12:63144886-63144936	PANC-1	pancreas:	n/a
25	chr12:63144886-63144936	NB4	blood:	n/a
26	chr12:63144886-63144936	Hela-S3	cervix:	n/a
27	chr12:63150899-63150949	SK-N-SH	brain:	n/a
28	chr12:63150899-63150949	K562	blood:	n/a
29	chr12:63144886-63144936	SK-N-SH	brain:	n/a
30	chr12:63144886-63144936	BJ	skin:	n/a
31	chr12:63150899-63150949	HEEpiC	esophagus:	n/a
32	chr12:63150899-63150949	T-47D	breast:	n/a
33	chr12:63144886-63144936	AG10803	skin:	n/a
34	chr12:63150899-63150949	CMK	blood:	n/a
35	chr12:63150899-63150949	BJ	skin:	n/a
36	chr12:63150899-63150949	HNPCEpiC	eye:	n/a
37	chr12:63144886-63144936	CMK	blood:	n/a
38	chr12:63150899-63150949	HRPEpiC	eye:	n/a
39	chr12:63144886-63144936	SAEC	small airway:	n/a
40	chr12:63150899-63150949	NHBE	bronchial:	n/a
41	chr12:63144886-63144936	AG09319	gingival:	n/a
42	chr12:63150899-63150949	GM12892	blood:	n/a
43	chr12:63144886-63144936	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:63150899-63150949	NHDF-neo	bronchial:	n/a
45	chr12:63144886-63144936	HCT-116	colon:	n/a
46	chr12:63144886-63144936	RPTEC	kidney:	n/a
47	chr12:63144886-63144936	AG04450	lung:	fetal
48	chr12:63144886-63144936	SK-N-SH_RA	brain:	n/a
49	chr12:63144886-63144936	AoSMC	blood vessel:	n/a
50	chr12:63144886-63144936	U87	brain:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63153929..63156518-chr12:63158042..63160004,2	K562	blood:
2	chr12:63155609..63159608-chr12:63162125..63165442,4	K562	blood:
3	chr12:63154137..63156513-chr12:63157546..63160196,2	MCF-7	breast:
4	chr12:62995824..62997393-chr12:63146838..63148876,2	MCF-7	breast:
5	chr12:62995291..62997610-chr12:63154157..63156822,2	K562	blood:
6	chr12:63158098..63159608-chr12:63162604..63165458,2	K562	blood:
7	chr12:63153929..63156518-chr12:63158042..63160004,2	K562	blood:
8	chr12:63158098..63159608-chr12:63162604..63165458,2	K562	blood:
9	chr12:62995414..62998835-chr12:63156967..63159768,4	MCF-7	breast:
10	chr12:63155609..63159608-chr12:63162125..63165442,4	K562	blood:
11	chr12:63131484..63133718-chr12:63162471..63164846,2	MCF-7	breast:
12	chr12:62990224..62992773-chr12:63153301..63155013,2	K562	blood:
13	chr12:62995380..62997043-chr12:63160693..63163072,2	MCF-7	breast:
14	chr12:63154137..63156513-chr12:63157546..63160196,2	MCF-7	breast:
15	chr12:62997413..63000389-chr12:63154055..63157053,2	MCF-7	breast:
16	chr12:63129686..63132741-chr12:63143731..63146913,3	MCF-7	breast:

No data

Variant related genes	Relation type
GAPDHP44	TF binding region
GAPDHP44	CpG island
ENSG00000199179	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000257354	chromatin interactions

Extended variants
information (count: 817 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7297618	chr12:63142592-63142593	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs367599460	chr12:63142648-63142649	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116318274	chr12:63142741-63142742	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556668247	chr12:63142768-63142769	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs17098259	chr12:63142785-63142786	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs408671	chr12:63142828-63142829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191705873	chr12:63142842-63142843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374909590	chr12:63142867-63142868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184117169	chr12:63142900-63142901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559106119	chr12:63142921-63142922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528039738	chr12:63142931-63142932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs58490000	chr12:63142947-63142948	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs116904210	chr12:63142950-63142951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117294696	chr12:63142951-63142952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs80138146	chr12:63142954-63142955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571024413	chr12:63142970-63142971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533487151	chr12:63142981-63142982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547741709	chr12:63143005-63143006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547026162	chr12:63143013-63143014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560862653	chr12:63143056-63143057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148546031	chr12:63143065-63143066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554616755	chr12:63143070-63143071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142872134	chr12:63143071-63143072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567994935	chr12:63143148-63143149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529752374	chr12:63143186-63143187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536883014	chr12:63143266-63143267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556750021	chr12:63143276-63143277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549518474	chr12:63143277-63143278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545581877	chr12:63143280-63143281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569708025	chr12:63143359-63143360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572789996	chr12:63143453-63143454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146594625	chr12:63143481-63143482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77948767	chr12:63143485-63143486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141357380	chr12:63143544-63143545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531214200	chr12:63143587-63143588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143871257	chr12:63143615-63143616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75752879	chr12:63143662-63143663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117013221	chr12:63143664-63143665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546820519	chr12:63143712-63143713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs199552409	chr12:63143743-63143744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529300877	chr12:63143746-63143747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549345918	chr12:63143750-63143751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565963159	chr12:63143760-63143761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568874908	chr12:63143768-63143769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536967879	chr12:63143769-63143770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376288764	chr12:63143817-63143818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370324322	chr12:63143823-63143824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs68143437	chr12:63143848-63143849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs397820691	chr12:63143861-63143862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572433333	chr12:63143862-63143863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63096600-63157000	Weak transcription	Pancreas	Pancrea
2	chr12:63123000-63152000	Weak transcription	Gastric	stomach
3	chr12:63124200-63145400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:63125800-63143000	Weak transcription	Psoas Muscle	Psoas
5	chr12:63126000-63149200	Weak transcription	Lung	lung
6	chr12:63126200-63155600	Weak transcription	Aorta	Aorta
7	chr12:63130200-63153200	Weak transcription	Fetal Intestine Large	intestine
8	chr12:63131400-63148000	Weak transcription	Fetal Intestine Small	intestine
9	chr12:63132600-63145400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:63133600-63144800	Weak transcription	Brain Anterior Caudate	brain
11	chr12:63133800-63143000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:63134200-63145000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:63134200-63150600	Weak transcription	Right Atrium	heart
14	chr12:63134400-63144600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr12:63134400-63160600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr12:63135600-63145000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:63136000-63142600	Weak transcription	Brain Angular Gyrus	brain
18	chr12:63136000-63145000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:63136400-63144600	Weak transcription	Brain Substantia Nigra	brain
20	chr12:63138800-63149200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:63139000-63144600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr12:63139000-63144800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr12:63139400-63150400	Weak transcription	Left Ventricle	heart
24	chr12:63139600-63142600	Weak transcription	HSMMtube	muscle
25	chr12:63139600-63143000	Weak transcription	Brain Hippocampus Middle	brain
26	chr12:63139800-63142600	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr12:63139800-63143000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:63139800-63148400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:63140000-63149200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr12:63140000-63150800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:63140000-63168600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr12:63140600-63145000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr12:63140800-63145600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:63141800-63147800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr12:63142000-63144400	Enhancers	A549	lung
36	chr12:63142200-63142800	Strong transcription	HepG2	liver
37	chr12:63142200-63143200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:63142200-63143400	Enhancers	Osteobl	bone
39	chr12:63142200-63144600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr12:63142400-63142600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr12:63142400-63143000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:63142400-63143200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr12:63142400-63143400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr12:63142400-63143800	Enhancers	HSMM	muscle
45	chr12:63142400-63145200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:63142600-63143000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:63142600-63143200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:63142600-63143200	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr12:63142600-63143800	Enhancers	HSMMtube	muscle
50	chr12:63142600-63145800	Enhancers	Brain Angular Gyrus	brain

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