Variant report

Variant	nsv1003262
Chromosome Location	chr2:99858556-99924543
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	chr2:99895235-99895694	HepG2	liver:	n/a	n/a
4	BRCA1	chr2:99897017-99897190	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr2:99887235-99887673	K562	blood:	n/a	n/a
6	CBX3	chr2:99887282-99887749	K562	blood:	n/a	n/a
7	CEBPB	chr2:99896759-99897060	MCF-7	breast:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
8	CEBPB	chr2:99895140-99895648	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
9	CEBPB	chr2:99898969-99899023	K562	blood:	n/a	n/a
10	CEBPB	chr2:99867003-99867374	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:99895106-99895826	Hela-S3	cervix:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
12	CEBPB	chr2:99873103-99873596	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr2:99895160-99895686	IMR90	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
14	CEBPB	chr2:99895144-99895666	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
15	CEBPB	chr2:99867010-99867383	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:99867071-99867369	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr2:99898960-99899066	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:99896815-99897096	A549	lung:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
19	CEBPB	chr2:99895136-99895626	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
20	CEBPB	chr2:99895210-99895580	A549	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
21	CEBPB	chr2:99895309-99895544	K562	blood:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
22	CEBPB	chr2:99895111-99895596	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
23	CEBPB	chr2:99896793-99897128	HepG2	liver:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
24	CEBPB	chr2:99867094-99867402	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr2:99896754-99897198	Hela-S3	cervix:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
26	CEBPB	chr2:99895163-99895672	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
27	CEBPB	chr2:99895245-99895503	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
28	CEBPB	chr2:99867010-99867376	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr2:99895156-99895749	Hela-S3	cervix:	n/a	n/a
30	CREB1	chr2:99867108-99867416	HepG2	liver:	n/a	n/a
31	CTCF	chr2:99862560-99862710	HepG2	liver:	n/a	n/a
32	CTCF	chr2:99862540-99862690	GM12871	blood:	n/a	n/a
33	CTCF	chr2:99862580-99862730	GM12864	blood:	n/a	n/a
34	CTCF	chr2:99903599-99903627	GM13976	blood:	n/a	n/a
35	CTCF	chr2:99862446-99862541	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:99862620-99862770	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr2:99862520-99862670	GM12872	blood:	n/a	n/a
38	CTCF	chr2:99862560-99862710	HAc	cerebellar:	n/a	n/a
39	CTCF	chr2:99862546-99862818	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr2:99862550-99862764	HepG2	liver:	n/a	n/a
41	CTCF	chr2:99862540-99862690	HRE	kidney:	n/a	n/a
42	CTCF	chr2:99862580-99862730	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr2:99862540-99862690	HPF	lung:	n/a	n/a
44	CTCF	chr2:99862600-99862750	GM12873	blood:	n/a	n/a
45	CTCF	chr2:99862160-99862310	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:99916880-99917030	HepG2	liver:	n/a	n/a
47	CTCF	chr2:99862539-99862759	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:99862540-99862690	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr2:99862157-99862784	K562	blood:	n/a	n/a
50	CTCF	chr2:99862540-99862690	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99918767-99918817	PrEC	prostate:	n/a
2	chr2:99908962-99909012	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:99917669-99917719	NHBE	bronchial:	n/a
4	chr2:99871988-99872038	HAEpiC	amniotic membrane:	n/a
5	chr2:99871270-99871320	SAEC	small airway:	n/a
6	chr2:99867344-99867394	PrEC	prostate:	n/a
7	chr2:99872119-99872169	U87	brain:	n/a
8	chr2:99918603-99918653	ovcar-3	ovarian:	n/a
9	chr2:99917669-99917719	BE2_C	brain:	n/a
10	chr2:99858763-99858813	CMK	blood:	n/a
11	chr2:99858763-99858813	GM06990	blood:	n/a
12	chr2:99912152-99912202	HCT-116	colon:	n/a
13	chr2:99908962-99909012	SK-N-SH	brain:	n/a
14	chr2:99867344-99867394	HIPEpiC	eye:	n/a
15	chr2:99918042-99918092	K562	blood:	n/a
16	chr2:99871270-99871320	AG10803	skin:	n/a
17	chr2:99908962-99909012	SAEC	small airway:	n/a
18	chr2:99918767-99918817	AG04449	skin:	fetal
19	chr2:99918603-99918653	NH-A	brain:	n/a
20	chr2:99918767-99918817	Hepatocyte	liver:	n/a
21	chr2:99858763-99858813	K562	blood:	n/a
22	chr2:99858763-99858813	BJ	skin:	n/a
23	chr2:99867344-99867394	BJ	skin:	n/a
24	chr2:99917669-99917719	SK-N-MC	brain:	n/a
25	chr2:99908962-99909012	HIPEpiC	eye:	n/a
26	chr2:99918042-99918092	A549	lung:	n/a
27	chr2:99917669-99917719	PrEC	prostate:	n/a
28	chr2:99871575-99871625	SAEC	small airway:	n/a
29	chr2:99918664-99918714	Caco-2	colon:	n/a
30	chr2:99871270-99871320	HCF	heart:	n/a
31	chr2:99858763-99858813	AoSMC	blood vessel:	n/a
32	chr2:99858763-99858813	Caco-2	colon:	n/a
33	chr2:99872119-99872169	SK-N-MC	brain:	n/a
34	chr2:99918603-99918653	AG10803	skin:	n/a
35	chr2:99918603-99918653	Jurkat	blood:	n/a
36	chr2:99917669-99917719	GM12891	blood:	n/a
37	chr2:99918767-99918817	HCF	heart:	n/a
38	chr2:99871988-99872038	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:99918042-99918092	PrEC	prostate:	n/a
40	chr2:99858763-99858813	ovcar-3	ovarian:	n/a
41	chr2:99918042-99918092	GM06990	blood:	n/a
42	chr2:99918603-99918653	HRPEpiC	eye:	n/a
43	chr2:99918603-99918653	ECC-1	luminal epithelium:	n/a
44	chr2:99918664-99918714	IMR90	lung:	fetal
45	chr2:99871575-99871625	HRCEpiC	kidney:	n/a
46	chr2:99918603-99918653	ProgFib	skin:	n/a
47	chr2:99871738-99871788	NHBE	bronchial:	n/a
48	chr2:99918042-99918092	Jurkat	blood:	n/a
49	chr2:99867344-99867394	NHBE	bronchial:	n/a
50	chr2:99918042-99918092	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
2	chr2:99860434..99863311-chr2:99975532..99977093,2	MCF-7	breast:
3	chr2:99919697..99922118-chr2:99951528..99953553,2	K562	blood:
4	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
5	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
6	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
7	chr2:99895187..99896703-chr2:99951053..99953668,2	MCF-7	breast:
8	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
9	chr2:99905599..99909122-chr2:99945751..99948599,3	MCF-7	breast:
10	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
11	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
12	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
13	chr2:99918821..99920555-chr2:99920714..99922754,2	MCF-7	breast:
14	chr2:99866201..99868659-chr2:99869387..99872001,2	K562	blood:
15	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
16	chr2:99771253..99773056-chr2:99921350..99922897,2	K562	blood:

Variant related genes	Relation type
C2orf15	TF binding region
LYG1	TF binding region
LYG2	TF binding region
C2orf15	CpG island
LYG1	CpG island
LYG2	CpG island
ENSG00000144214	chromatin interactions
ENSG00000144182	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000185674	chromatin interactions
ENSG00000135951	chromatin interactions
ENSG00000273155	chromatin interactions

Extended variants
information (count: 2293 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2293 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4851196	chr2:99858556-99858557	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372735201	chr2:99858560-99858561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190358132	chr2:99858584-99858585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533204663	chr2:99858631-99858632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375698571	chr2:99858686-99858687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554549006	chr2:99858727-99858728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550051165	chr2:99858744-99858745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146631159	chr2:99858763-99858764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79919264	chr2:99858764-99858765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202072872	chr2:99858781-99858782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141392354	chr2:99858802-99858803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199699326	chr2:99858864-99858865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368752128	chr2:99858877-99858878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569037546	chr2:99858883-99858884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370131623	chr2:99858896-99858897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201233687	chr2:99858897-99858898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143389707	chr2:99858911-99858912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142825471	chr2:99858946-99858947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138810405	chr2:99858947-99858948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200397476	chr2:99859002-99859003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554013558	chr2:99859014-99859015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576982419	chr2:99859031-99859032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112498361	chr2:99859090-99859091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539649086	chr2:99859093-99859094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556412738	chr2:99859105-99859106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17022405	chr2:99859139-99859140	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs542153122	chr2:99859159-99859160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143405751	chr2:99859187-99859188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148339550	chr2:99859208-99859209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541114981	chr2:99859250-99859251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62153807	chr2:99859279-99859280	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs75042409	chr2:99859317-99859318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181552208	chr2:99859327-99859328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79636153	chr2:99859357-99859358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529180153	chr2:99859408-99859409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549053080	chr2:99859444-99859445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568433182	chr2:99859464-99859465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185498642	chr2:99859474-99859475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533949519	chr2:99859581-99859582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140556776	chr2:99859663-99859664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34865835	chr2:99859665-99859666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570633314	chr2:99859678-99859679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78516855	chr2:99859686-99859687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539611349	chr2:99859692-99859693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556324107	chr2:99859705-99859706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188354400	chr2:99859758-99859759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150112375	chr2:99859782-99859783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555829614	chr2:99859795-99859796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17760953	chr2:99859863-99859864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs561293710	chr2:99859895-99859896	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:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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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