Variant report

Variant	nsv1010419
Chromosome Location	chr2:99857259-99897312
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	chr2:99870939-99870988	K562	blood:	n/a	n/a
2	ARID3A	chr2:99895164-99895764	HepG2	liver:	n/a	n/a
3	BHLHE40	chr2:99856952-99857274	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:99895235-99895694	HepG2	liver:	n/a	n/a
5	BRCA1	chr2:99897017-99897190	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr2:99887235-99887673	K562	blood:	n/a	n/a
7	CBX3	chr2:99887282-99887749	K562	blood:	n/a	n/a
8	CEBPB	chr2:99867010-99867376	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr2:99896793-99897128	HepG2	liver:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
10	CEBPB	chr2:99873103-99873596	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr2:99896815-99897096	A549	lung:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
12	CEBPB	chr2:99895106-99895826	Hela-S3	cervix:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
13	CEBPB	chr2:99895245-99895503	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
14	CEBPB	chr2:99867071-99867369	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr2:99895136-99895626	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
16	CEBPB	chr2:99895210-99895580	A549	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
17	CEBPB	chr2:99895163-99895672	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
18	CEBPB	chr2:99895160-99895686	IMR90	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
19	CEBPB	chr2:99895140-99895648	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
20	CEBPB	chr2:99867010-99867383	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:99867003-99867374	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:99896759-99897060	MCF-7	breast:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
23	CEBPB	chr2:99867094-99867402	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr2:99895111-99895596	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
25	CEBPB	chr2:99895309-99895544	K562	blood:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
26	CEBPB	chr2:99895144-99895666	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
27	CEBPB	chr2:99896754-99897198	Hela-S3	cervix:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
28	CHD2	chr2:99895156-99895749	Hela-S3	cervix:	n/a	n/a
29	CREB1	chr2:99867108-99867416	HepG2	liver:	n/a	n/a
30	CTCF	chr2:99862580-99862730	SAEC	small airway:	n/a	n/a
31	CTCF	chr2:99862540-99862690	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr2:99862157-99862784	K562	blood:	n/a	n/a
33	CTCF	chr2:99862140-99862290	AG04450	lung:	n/a	n/a
34	CTCF	chr2:99862560-99862710	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr2:99862600-99862750	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:99862149-99862388	GM12878	blood:	n/a	n/a
37	CTCF	chr2:99862560-99862710	GM12872	blood:	n/a	n/a
38	CTCF	chr2:99862550-99862764	HepG2	liver:	n/a	n/a
39	CTCF	chr2:99862180-99862330	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:99862543-99862739	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:99862620-99862770	NHLF	lung:	n/a	n/a
42	CTCF	chr2:99862580-99862730	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr2:99876568-99876597	GM13976	blood:	n/a	n/a
44	CTCF	chr2:99862620-99862770	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr2:99862140-99862290	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr2:99862560-99862710	HEK293	kidney:	n/a	n/a
47	CTCF	chr2:99863180-99863330	HepG2	liver:	n/a	n/a
48	CTCF	chr2:99862580-99862730	NB4	blood:	n/a	n/a
49	CTCF	chr2:99862580-99862730	HL-60	blood:	n/a	n/a
50	CTCF	chr2:99862600-99862750	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99872119-99872169	SK-N-SH_RA	brain:	n/a
2	chr2:99858763-99858813	PFSK-1	brain:	n/a
3	chr2:99871575-99871625	HUVEC	blood vessel:	n/a
4	chr2:99871988-99872038	Hepatocyte	liver:	n/a
5	chr2:99867344-99867394	HRE	kidney:	n/a
6	chr2:99872119-99872169	NHDF-neo	bronchial:	n/a
7	chr2:99872119-99872169	ECC-1	luminal epithelium:	n/a
8	chr2:99871988-99872038	PFSK-1	brain:	n/a
9	chr2:99871988-99872038	SK-N-SH_RA	brain:	n/a
10	chr2:99871738-99871788	HCT-116	colon:	n/a
11	chr2:99871988-99872038	SK-N-MC	brain:	n/a
12	chr2:99867344-99867394	Jurkat	blood:	n/a
13	chr2:99872119-99872169	AoSMC	blood vessel:	n/a
14	chr2:99871575-99871625	HEK293	kidney:	embryo
15	chr2:99872119-99872169	GM06990	blood:	n/a
16	chr2:99872119-99872169	MCF10A-Er-Src	breast:	n/a
17	chr2:99872119-99872169	HAEpiC	amniotic membrane:	n/a
18	chr2:99867344-99867394	PANC-1	pancreas:	n/a
19	chr2:99867344-99867394	SAEC	small airway:	n/a
20	chr2:99858763-99858813	BJ	skin:	n/a
21	chr2:99858763-99858813	A549	lung:	n/a
22	chr2:99871575-99871625	NB4	blood:	n/a
23	chr2:99872119-99872169	U87	brain:	n/a
24	chr2:99871270-99871320	MCF10A-Er-Src	breast:	n/a
25	chr2:99871988-99872038	AG09319	gingival:	n/a
26	chr2:99858763-99858813	ProgFib	skin:	n/a
27	chr2:99871575-99871625	GM12892	blood:	n/a
28	chr2:99867344-99867394	HepG2	liver:	n/a
29	chr2:99867344-99867394	AG09309	skin:	n/a
30	chr2:99871575-99871625	RPTEC	kidney:	n/a
31	chr2:99858763-99858813	NHBE	bronchial:	n/a
32	chr2:99871738-99871788	GM12878	blood:	n/a
33	chr2:99871575-99871625	AG04449	skin:	fetal
34	chr2:99871575-99871625	HRPEpiC	eye:	n/a
35	chr2:99871988-99872038	ovcar-3	ovarian:	n/a
36	chr2:99872119-99872169	PFSK-1	brain:	n/a
37	chr2:99867344-99867394	GM12892	blood:	n/a
38	chr2:99872119-99872169	A549	lung:	n/a
39	chr2:99871575-99871625	Caco-2	colon:	n/a
40	chr2:99871738-99871788	NB4	blood:	n/a
41	chr2:99867344-99867394	HCM	heart:	n/a
42	chr2:99858763-99858813	BE2_C	brain:	n/a
43	chr2:99858763-99858813	NHDF-neo	bronchial:	n/a
44	chr2:99871270-99871320	AG04450	lung:	fetal
45	chr2:99872119-99872169	HNPCEpiC	eye:	n/a
46	chr2:99871738-99871788	GM06990	blood:	n/a
47	chr2:99871738-99871788	AG04449	skin:	fetal
48	chr2:99871270-99871320	SK-N-MC	brain:	n/a
49	chr2:99871270-99871320	NHDF-neo	bronchial:	n/a
50	chr2:99871988-99872038	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:99855888..99858243-chr2:99952048..99955134,3	MCF-7	breast:
2	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
3	chr2:99860434..99863311-chr2:99975532..99977093,2	MCF-7	breast:
4	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
5	chr2:99866201..99868659-chr2:99869387..99872001,2	K562	blood:
6	chr2:99895187..99896703-chr2:99951053..99953668,2	MCF-7	breast:
7	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
8	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
9	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:

Variant related genes	Relation type
LYG2	TF binding region
LYG2	CpG island
ENSG00000158417	chromatin interactions
ENSG00000185674	chromatin interactions
ENSG00000115514	chromatin interactions

Extended variants
information (count: 1409 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1409 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570746262	chr2:99857276-99857277	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs191469547	chr2:99857322-99857323	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs184259839	chr2:99857346-99857347	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs75340268	chr2:99857353-99857354	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544716487	chr2:99857430-99857431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs555107973	chr2:99857499-99857500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs377319274	chr2:99857636-99857637	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574886399	chr2:99857650-99857651	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375275330	chr2:99857651-99857652	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7579999	chr2:99857670-99857671	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs532824811	chr2:99857688-99857689	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs546116768	chr2:99857757-99857758	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562139902	chr2:99857795-99857796	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150554804	chr2:99857802-99857803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs547842402	chr2:99857848-99857849	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568151143	chr2:99857863-99857864	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527467470	chr2:99857864-99857865	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs190475240	chr2:99857900-99857901	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs995617	chr2:99857904-99857905	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs570592225	chr2:99857925-99857926	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539723993	chr2:99857954-99857955	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs139570891	chr2:99858000-99858001	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs149787418	chr2:99858036-99858037	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs539342422	chr2:99858117-99858118	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145782106	chr2:99858164-99858165	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs555069244	chr2:99858176-99858177	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs374740708	chr2:99858188-99858189	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs574889317	chr2:99858237-99858238	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534067788	chr2:99858265-99858266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554321362	chr2:99858298-99858299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17020585	chr2:99858326-99858327	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs375315760	chr2:99858353-99858354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546078046	chr2:99858372-99858373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147865199	chr2:99858433-99858434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185506331	chr2:99858457-99858458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571562768	chr2:99858507-99858508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144217798	chr2:99858524-99858525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561594672	chr2:99858538-99858539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527366930	chr2:99858540-99858541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4851196	chr2:99858556-99858557	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs372735201	chr2:99858560-99858561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190358132	chr2:99858584-99858585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533204663	chr2:99858631-99858632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375698571	chr2:99858686-99858687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554549006	chr2:99858727-99858728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550051165	chr2:99858744-99858745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146631159	chr2:99858763-99858764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79919264	chr2:99858764-99858765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202072872	chr2:99858781-99858782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141392354	chr2:99858802-99858803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99840800-99874400	Weak transcription	Aorta	Aorta
2	chr2:99853600-99863200	Weak transcription	Esophagus	oesophagus
3	chr2:99854800-99865800	Weak transcription	Left Ventricle	heart
4	chr2:99858200-99859200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:99858400-99859200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:99858800-99864800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:99860400-99899800	Weak transcription	Psoas Muscle	Psoas
8	chr2:99860800-99864400	Weak transcription	Lung	lung
9	chr2:99861200-99879200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr2:99861200-99900800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:99861800-99871200	Weak transcription	Colon Smooth Muscle	Colon
12	chr2:99861800-99899400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:99862000-99863600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:99862000-99879200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr2:99862200-99864200	Enhancers	HepG2	liver
16	chr2:99862600-99863200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:99863000-99863400	Enhancers	Gastric	stomach
18	chr2:99863200-99863400	ZNF genes & repeats	Esophagus	oesophagus
19	chr2:99864200-99867200	Weak transcription	HepG2	liver
20	chr2:99867200-99867400	Enhancers	HepG2	liver
21	chr2:99867200-99867600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:99869800-99880000	Weak transcription	Right Ventricle	heart
23	chr2:99870600-99871200	Enhancers	Stomach Mucosa	stomach
24	chr2:99872000-99872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:99872000-99873200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr2:99872000-99873800	Enhancers	HMEC	breast
27	chr2:99872200-99872400	Bivalent Enhancer	HepG2	liver
28	chr2:99872200-99872600	Enhancers	NHEK	skin
29	chr2:99872200-99872800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:99872200-99873000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr2:99872200-99873600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr2:99872400-99872800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr2:99872400-99873000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:99872400-99873000	Enhancers	Esophagus	oesophagus
35	chr2:99872400-99873200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:99872400-99873600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:99872600-99873000	Flanking Active TSS	NHEK	skin
38	chr2:99872600-99873200	Enhancers	NH-A	brain
39	chr2:99872800-99873200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:99872800-99873400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:99873000-99873800	Enhancers	NHEK	skin
42	chr2:99873000-99877600	Weak transcription	Esophagus	oesophagus
43	chr2:99873200-99875600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr2:99873400-99877600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:99873600-99877800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:99873800-99877600	Weak transcription	HMEC	breast
47	chr2:99873800-99900600	Weak transcription	Ovary	ovary
48	chr2:99874400-99874600	ZNF genes & repeats	Aorta	Aorta
49	chr2:99874600-99879400	Weak transcription	Aorta	Aorta
50	chr2:99876200-99882400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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