Variant report

Variant	nsv1005118
Chromosome Location	chr2:99841951-99924543
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	chr2:99895164-99895764	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99870939-99870988	K562	blood:	n/a	n/a
3	BATF	chr2:99856972-99857225	GM12878	blood:	n/a	n/a
4	BATF	chr2:99856950-99857204	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:99895235-99895694	HepG2	liver:	n/a	n/a
6	BHLHE40	chr2:99854703-99854753	K562	blood:	n/a	n/a
7	BHLHE40	chr2:99856952-99857274	GM12878	blood:	n/a	n/a
8	BRCA1	chr2:99897017-99897190	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr2:99887235-99887673	K562	blood:	n/a	n/a
10	CBX3	chr2:99887282-99887749	K562	blood:	n/a	n/a
11	CEBPB	chr2:99895140-99895648	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
12	CEBPB	chr2:99895210-99895580	A549	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
13	CEBPB	chr2:99895111-99895596	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
14	CEBPB	chr2:99867003-99867374	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:99895106-99895826	Hela-S3	cervix:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
16	CEBPB	chr2:99895245-99895503	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
17	CEBPB	chr2:99896815-99897096	A549	lung:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
18	CEBPB	chr2:99895136-99895626	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
19	CEBPB	chr2:99895160-99895686	IMR90	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
20	CEBPB	chr2:99867094-99867402	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr2:99896793-99897128	HepG2	liver:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
22	CEBPB	chr2:99895309-99895544	K562	blood:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
23	CEBPB	chr2:99898969-99899023	K562	blood:	n/a	n/a
24	CEBPB	chr2:99898960-99899066	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:99867010-99867383	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:99895144-99895666	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
27	CEBPB	chr2:99867010-99867376	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:99867071-99867369	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr2:99895163-99895672	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
30	CEBPB	chr2:99873103-99873596	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr2:99896754-99897198	Hela-S3	cervix:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
32	CEBPB	chr2:99896759-99897060	MCF-7	breast:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
33	CHD2	chr2:99895156-99895749	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr2:99867108-99867416	HepG2	liver:	n/a	n/a
35	CTCF	chr2:99923592-99923639	Lung_OC	lung:	n/a	n/a
36	CTCF	chr2:99862580-99862730	HMF	breast:	n/a	n/a
37	CTCF	chr2:99862157-99862784	K562	blood:	n/a	n/a
38	CTCF	chr2:99855840-99855990	HPF	lung:	n/a	n/a
39	CTCF	chr2:99862560-99862710	GM12872	blood:	n/a	n/a
40	CTCF	chr2:99862164-99862382	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:99862560-99862710	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr2:99855980-99856130	GM12865	blood:	n/a	n/a
43	CTCF	chr2:99855847-99856039	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr2:99862230-99862379	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:99855860-99856010	HMF	breast:	n/a	n/a
46	CTCF	chr2:99903599-99903627	GM13976	blood:	n/a	n/a
47	CTCF	chr2:99855862-99856001	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr2:99863180-99863330	HepG2	liver:	n/a	n/a
49	CTCF	chr2:99855860-99856010	SAEC	small airway:	n/a	n/a
50	CTCF	chr2:99862606-99862682	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99871270-99871320	AG10803	skin:	n/a
2	chr2:99908962-99909012	HRPEpiC	eye:	n/a
3	chr2:99918042-99918092	NT2-D1	testis:	n/a
4	chr2:99871738-99871788	ovcar-3	ovarian:	n/a
5	chr2:99918767-99918817	A549	lung:	n/a
6	chr2:99872119-99872169	HRPEpiC	eye:	n/a
7	chr2:99918042-99918092	A549	lung:	n/a
8	chr2:99912152-99912202	HEK293	kidney:	embryo
9	chr2:99918767-99918817	H1-hESC	embryonic stem cell:	embryo
10	chr2:99858763-99858813	PrEC	prostate:	n/a
11	chr2:99917669-99917719	PrEC	prostate:	n/a
12	chr2:99918603-99918653	PFSK-1	brain:	n/a
13	chr2:99871270-99871320	HepG2	liver:	n/a
14	chr2:99918042-99918092	BE2_C	brain:	n/a
15	chr2:99872119-99872169	PFSK-1	brain:	n/a
16	chr2:99871575-99871625	HMEC	breast:	n/a
17	chr2:99867344-99867394	Caco-2	colon:	n/a
18	chr2:99917669-99917719	SK-N-MC	brain:	n/a
19	chr2:99858763-99858813	MCF10A-Er-Src	breast:	n/a
20	chr2:99871988-99872038	HL-60	blood:	n/a
21	chr2:99918767-99918817	AG04449	skin:	fetal
22	chr2:99871988-99872038	CMK	blood:	n/a
23	chr2:99871270-99871320	HCPEpiC	choroid plexus:	n/a
24	chr2:99918767-99918817	Caco-2	colon:	n/a
25	chr2:99858763-99858813	GM06990	blood:	n/a
26	chr2:99871575-99871625	H1-hESC	embryonic stem cell:	embryo
27	chr2:99871988-99872038	BE2_C	brain:	n/a
28	chr2:99918042-99918092	CMK	blood:	n/a
29	chr2:99917669-99917719	RPTEC	kidney:	n/a
30	chr2:99871988-99872038	PFSK-1	brain:	n/a
31	chr2:99858763-99858813	ECC-1	luminal epithelium:	n/a
32	chr2:99871575-99871625	AG04450	lung:	fetal
33	chr2:99871575-99871625	HL-60	blood:	n/a
34	chr2:99871270-99871320	H1-hESC	embryonic stem cell:	embryo
35	chr2:99918603-99918653	HIPEpiC	eye:	n/a
36	chr2:99917669-99917719	NHBE	bronchial:	n/a
37	chr2:99908962-99909012	ECC-1	luminal epithelium:	n/a
38	chr2:99871575-99871625	HUVEC	blood vessel:	n/a
39	chr2:99917669-99917719	MCF-7	breast:	n/a
40	chr2:99871988-99872038	Caco-2	colon:	n/a
41	chr2:99872119-99872169	SK-N-SH_RA	brain:	n/a
42	chr2:99872119-99872169	AG10803	skin:	n/a
43	chr2:99858763-99858813	NT2-D1	testis:	n/a
44	chr2:99871575-99871625	HNPCEpiC	eye:	n/a
45	chr2:99871738-99871788	HCPEpiC	choroid plexus:	n/a
46	chr2:99872119-99872169	NT2-D1	testis:	n/a
47	chr2:99871738-99871788	AoSMC	blood vessel:	n/a
48	chr2:99867344-99867394	PFSK-1	brain:	n/a
49	chr2:99908962-99909012	MCF-7	breast:	n/a
50	chr2:99918767-99918817	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:99771253..99773056-chr2:99921350..99922897,2	K562	blood:
2	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
3	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
4	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
5	chr2:99918821..99920555-chr2:99920714..99922754,2	MCF-7	breast:
6	chr2:99795164..99797878-chr2:99854234..99856098,2	K562	blood:
7	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
8	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
9	chr2:99866201..99868659-chr2:99869387..99872001,2	K562	blood:
10	chr2:99919697..99922118-chr2:99951528..99953553,2	K562	blood:
11	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
12	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
13	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
14	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
15	chr2:99860434..99863311-chr2:99975532..99977093,2	MCF-7	breast:
16	chr2:99845973..99846811-chr6:105648996..105649854,2	MCF-7	breast:
17	chr2:99895187..99896703-chr2:99951053..99953668,2	MCF-7	breast:
18	chr2:99905599..99909122-chr2:99945751..99948599,3	MCF-7	breast:
19	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
20	chr2:99855888..99858243-chr2:99952048..99955134,3	MCF-7	breast:

Variant related genes	Relation type
LYG2	TF binding region
C2orf15	TF binding region
LYG1	TF binding region
LYG2	CpG island
C2orf15	CpG island
LYG1	CpG island
ENSG00000115514	chromatin interactions
ENSG00000144182	chromatin interactions
ENSG00000158411	chromatin interactions
ENSG00000185674	chromatin interactions
ENSG00000273155	chromatin interactions
ENSG00000241962	chromatin interactions
ENSG00000185414	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000135951	chromatin interactions
ENSG00000144214	chromatin interactions

Extended variants
information (count: 2856 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2856 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562687285	chr2:99841956-99841957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180925794	chr2:99841977-99841978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371965912	chr2:99842035-99842036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544289678	chr2:99842061-99842062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185853681	chr2:99842127-99842128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2707623	chr2:99842156-99842157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192367755	chr2:99842178-99842179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547150475	chr2:99842187-99842188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139127665	chr2:99842196-99842197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368145679	chr2:99842211-99842212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539045415	chr2:99842226-99842227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74944102	chr2:99842256-99842257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184045679	chr2:99842260-99842261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552823000	chr2:99842265-99842266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569458245	chr2:99842266-99842267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537798814	chr2:99842283-99842284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554287727	chr2:99842299-99842300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568116754	chr2:99842306-99842307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375971538	chr2:99842311-99842312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533630899	chr2:99842324-99842325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553480916	chr2:99842340-99842341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576626757	chr2:99842367-99842368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186424754	chr2:99842426-99842427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545635498	chr2:99842428-99842429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556382569	chr2:99842452-99842453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190789215	chr2:99842453-99842454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6711981	chr2:99842500-99842501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs561110162	chr2:99842577-99842578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199508228	chr2:99842584-99842585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147068497	chr2:99842585-99842586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538311578	chr2:99842688-99842689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372061827	chr2:99842751-99842752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540726347	chr2:99842841-99842842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560606856	chr2:99842859-99842860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532710771	chr2:99842909-99842910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556295451	chr2:99842956-99842957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574680906	chr2:99842966-99842967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542063516	chr2:99842982-99842983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563165565	chr2:99843001-99843002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371686619	chr2:99843041-99843042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199822426	chr2:99843063-99843064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531930051	chr2:99843099-99843100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200942076	chr2:99843120-99843121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201742216	chr2:99843164-99843165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200033725	chr2:99843166-99843167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200907873	chr2:99843173-99843174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs202165445	chr2:99843175-99843176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548901663	chr2:99843194-99843195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567698786	chr2:99843195-99843196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200111268	chr2:99843212-99843213	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:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99814400-99842200	Weak transcription	Ovary	ovary
2	chr2:99814400-99842800	Weak transcription	Colon Smooth Muscle	Colon
3	chr2:99815000-99842400	Weak transcription	Fetal Lung	lung
4	chr2:99815200-99842000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr2:99815200-99842400	Weak transcription	Brain Substantia Nigra	brain
6	chr2:99815600-99842000	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr2:99815600-99842200	Weak transcription	Fetal Stomach	stomach
8	chr2:99815600-99843400	Weak transcription	Fetal Brain Female	brain
9	chr2:99818200-99854600	Weak transcription	Left Ventricle	heart
10	chr2:99818600-99842200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:99818800-99843600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:99819000-99843200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr2:99825200-99843200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:99827600-99842800	Weak transcription	Fetal Brain Male	brain
15	chr2:99829600-99844400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:99832600-99842800	Weak transcription	Stomach Smooth Muscle	stomach
17	chr2:99833200-99842600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr2:99833400-99843400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:99834800-99842400	Weak transcription	Brain Anterior Caudate	brain
20	chr2:99836000-99842600	Weak transcription	Psoas Muscle	Psoas
21	chr2:99836200-99847600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr2:99839600-99842000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr2:99840800-99874400	Weak transcription	Aorta	Aorta
24	chr2:99841000-99843000	Weak transcription	Liver	Liver
25	chr2:99841200-99843200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr2:99841400-99843000	Weak transcription	Brain Hippocampus Middle	brain
27	chr2:99853600-99863200	Weak transcription	Esophagus	oesophagus
28	chr2:99854600-99854800	Enhancers	Left Ventricle	heart
29	chr2:99854600-99855200	Enhancers	K562	blood
30	chr2:99854800-99865800	Weak transcription	Left Ventricle	heart
31	chr2:99855200-99855600	Flanking Active TSS	K562	blood
32	chr2:99855600-99855800	Enhancers	K562	blood
33	chr2:99858200-99859200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr2:99858400-99859200	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr2:99858800-99864800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr2:99860400-99899800	Weak transcription	Psoas Muscle	Psoas
37	chr2:99860800-99864400	Weak transcription	Lung	lung
38	chr2:99861200-99879200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr2:99861200-99900800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr2:99861800-99871200	Weak transcription	Colon Smooth Muscle	Colon
41	chr2:99861800-99899400	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr2:99862000-99863600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr2:99862000-99879200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr2:99862200-99864200	Enhancers	HepG2	liver
45	chr2:99862600-99863200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:99863000-99863400	Enhancers	Gastric	stomach
47	chr2:99863200-99863400	ZNF genes & repeats	Esophagus	oesophagus
48	chr2:99864200-99867200	Weak transcription	HepG2	liver
49	chr2:99867200-99867400	Enhancers	HepG2	liver
50	chr2:99867200-99867600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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