Variant report

Variant	esv2762746
Chromosome Location	chr2:99840143-99916898
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	BATF	chr2:99856950-99857204	GM12878	blood:	n/a	n/a
4	BATF	chr2:99856972-99857225	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:99895235-99895694	HepG2	liver:	n/a	n/a
6	BHLHE40	chr2:99856952-99857274	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:99854703-99854753	K562	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	chr2:99873103-99873596	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr2:99896759-99897060	MCF-7	breast:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
13	CEBPB	chr2:99898969-99899023	K562	blood:	n/a	n/a
14	CEBPB	chr2:99895210-99895580	A549	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
15	CEBPB	chr2:99895160-99895686	IMR90	lung:	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	chr2:99895140-99895648	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
18	CEBPB	chr2:99867010-99867376	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:99867003-99867374	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:99898960-99899066	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:99895309-99895544	K562	blood:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
22	CEBPB	chr2:99896754-99897198	Hela-S3	cervix:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
23	CEBPB	chr2:99867071-99867369	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr2:99895136-99895626	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
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	chr2:99895111-99895596	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
28	CEBPB	chr2:99896815-99897096	A549	lung:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
29	CEBPB	chr2:99895163-99895672	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
30	CEBPB	chr2:99895106-99895826	Hela-S3	cervix:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
31	CEBPB	chr2:99896793-99897128	HepG2	liver:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
32	CEBPB	chr2:99867094-99867402	ECC-1	luminal epithelium:	n/a	n/a
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	chr2:99862580-99862730	SAEC	small airway:	n/a	n/a
36	CTCF	chr2:99916716-99916755	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr2:99855860-99856010	NB4	blood:	n/a	n/a
38	CTCF	chr2:99855900-99856050	AG04450	lung:	n/a	n/a
39	CTCF	chr2:99855940-99856090	GM12875	blood:	n/a	n/a
40	CTCF	chr2:99862680-99862830	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr2:99855880-99856030	Caco-2	colon:	n/a	n/a
42	CTCF	chr2:99862230-99862379	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:99862139-99862340	HepG2	liver:	n/a	n/a
44	CTCF	chr2:99855797-99856043	GM12878	blood:	n/a	n/a
45	CTCF	chr2:99862560-99862710	HepG2	liver:	n/a	n/a
46	CTCF	chr2:99855900-99856050	GM12873	blood:	n/a	n/a
47	CTCF	chr2:99862500-99862650	GM12874	blood:	n/a	n/a
48	CTCF	chr2:99855940-99856090	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr2:99855820-99855970	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr2:99869107-99869145	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99858763-99858813	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:99858763-99858813	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:99871575-99871625	HAEpiC	amniotic membrane:	n/a
4	chr2:99908962-99909012	HMEC	breast:	n/a
5	chr2:99908962-99909012	PANC-1	pancreas:	n/a
6	chr2:99908962-99909012	HAEpiC	amniotic membrane:	n/a
7	chr2:99871738-99871788	ProgFib	skin:	n/a
8	chr2:99912152-99912202	GM12891	blood:	n/a
9	chr2:99858763-99858813	HCT-116	colon:	n/a
10	chr2:99872119-99872169	SAEC	small airway:	n/a
11	chr2:99867344-99867394	HUVEC	blood vessel:	n/a
12	chr2:99858763-99858813	HCPEpiC	choroid plexus:	n/a
13	chr2:99871270-99871320	HMEC	breast:	n/a
14	chr2:99871738-99871788	HCPEpiC	choroid plexus:	n/a
15	chr2:99867344-99867394	SK-N-MC	brain:	n/a
16	chr2:99867344-99867394	MCF10A-Er-Src	breast:	n/a
17	chr2:99871738-99871788	HMEC	breast:	n/a
18	chr2:99871575-99871625	NB4	blood:	n/a
19	chr2:99872119-99872169	PrEC	prostate:	n/a
20	chr2:99871738-99871788	NB4	blood:	n/a
21	chr2:99871575-99871625	SKMC	muscle:	n/a
22	chr2:99871270-99871320	RPTEC	kidney:	n/a
23	chr2:99871738-99871788	HUVEC	blood vessel:	n/a
24	chr2:99871575-99871625	NHBE	bronchial:	n/a
25	chr2:99908962-99909012	GM12891	blood:	n/a
26	chr2:99867344-99867394	K562	blood:	n/a
27	chr2:99872119-99872169	NB4	blood:	n/a
28	chr2:99867344-99867394	GM12878	blood:	n/a
29	chr2:99872119-99872169	HRPEpiC	eye:	n/a
30	chr2:99871270-99871320	HEEpiC	esophagus:	n/a
31	chr2:99871738-99871788	ovcar-3	ovarian:	n/a
32	chr2:99872119-99872169	GM12892	blood:	n/a
33	chr2:99867344-99867394	HEEpiC	esophagus:	n/a
34	chr2:99912152-99912202	RPTEC	kidney:	n/a
35	chr2:99912152-99912202	HRE	kidney:	n/a
36	chr2:99871575-99871625	K562	blood:	n/a
37	chr2:99871988-99872038	HL-60	blood:	n/a
38	chr2:99871575-99871625	HEK293	kidney:	embryo
39	chr2:99912152-99912202	PFSK-1	brain:	n/a
40	chr2:99871988-99872038	PANC-1	pancreas:	n/a
41	chr2:99872119-99872169	BE2_C	brain:	n/a
42	chr2:99871988-99872038	GM19239	blood:	n/a
43	chr2:99871988-99872038	Hela-S3	cervix:	n/a
44	chr2:99871988-99872038	IMR90	lung:	fetal
45	chr2:99908962-99909012	HCT-116	colon:	n/a
46	chr2:99908962-99909012	H1-hESC	embryonic stem cell:	embryo
47	chr2:99858763-99858813	SK-N-MC	brain:	n/a
48	chr2:99912152-99912202	K562	blood:	n/a
49	chr2:99871988-99872038	NHDF-neo	bronchial:	n/a
50	chr2:99871575-99871625	ProgFib	skin:	n/a

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

Variant related genes	Relation type
LYG2	TF binding region
LYG2	CpG island
ENSG00000158411	chromatin interactions
ENSG00000241962	chromatin interactions
ENSG00000185414	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000185674	chromatin interactions
ENSG00000115514	chromatin interactions

Extended variants
information (count: 2664 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2664 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537205042	chr2:99840168-99840169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557556182	chr2:99840186-99840187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184122447	chr2:99840211-99840212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530948626	chr2:99840242-99840243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6747601	chr2:99840270-99840271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs553731797	chr2:99840273-99840274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572873056	chr2:99840308-99840309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377427313	chr2:99840309-99840310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567685180	chr2:99840342-99840343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190720425	chr2:99840397-99840398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576119422	chr2:99840424-99840425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149836949	chr2:99840429-99840430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371702011	chr2:99840460-99840461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529874202	chr2:99840472-99840473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562764189	chr2:99840474-99840475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181965015	chr2:99840480-99840481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560054298	chr2:99840497-99840498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185620876	chr2:99840527-99840528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189052414	chr2:99840532-99840533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571382209	chr2:99840615-99840616	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537569898	chr2:99840642-99840643	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550832357	chr2:99840668-99840669	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181550101	chr2:99840680-99840681	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145961729	chr2:99840682-99840683	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542123166	chr2:99840719-99840720	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4851195	chr2:99840748-99840749	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs535719506	chr2:99840806-99840807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527679718	chr2:99840816-99840817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538610141	chr2:99840828-99840829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558601597	chr2:99840847-99840848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575164613	chr2:99840918-99840919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76348155	chr2:99840950-99840951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10205632	chr2:99841030-99841031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560864302	chr2:99841041-99841042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574563408	chr2:99841057-99841058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12477438	chr2:99841085-99841086	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs369527488	chr2:99841094-99841095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6736885	chr2:99841108-99841109	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs532297883	chr2:99841143-99841144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146656561	chr2:99841146-99841147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1586433	chr2:99841213-99841214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1586434	chr2:99841233-99841234	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530840400	chr2:99841248-99841249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148824426	chr2:99841271-99841272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567695363	chr2:99841282-99841283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142650510	chr2:99841292-99841293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1586435	chr2:99841294-99841295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151021087	chr2:99841302-99841303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1586436	chr2:99841366-99841367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531850527	chr2:99841393-99841394	Weak transcription Strong 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:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr2:99814800-99840600	Weak transcription	Brain Hippocampus Middle	brain
4	chr2:99815000-99840600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:99815000-99840800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr2:99815000-99841800	Weak transcription	Pancreas	Pancrea
7	chr2:99815000-99842400	Weak transcription	Fetal Lung	lung
8	chr2:99815200-99840600	Weak transcription	Aorta	Aorta
9	chr2:99815200-99841800	Weak transcription	Spleen	Spleen
10	chr2:99815200-99842000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr2:99815200-99842400	Weak transcription	Brain Substantia Nigra	brain
12	chr2:99815600-99842000	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr2:99815600-99842200	Weak transcription	Fetal Stomach	stomach
14	chr2:99815600-99843400	Weak transcription	Fetal Brain Female	brain
15	chr2:99818200-99854600	Weak transcription	Left Ventricle	heart
16	chr2:99818600-99842200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:99818800-99843600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr2:99819000-99843200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr2:99825200-99843200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:99825400-99841800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:99827600-99842800	Weak transcription	Fetal Brain Male	brain
22	chr2:99829600-99844400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:99832600-99842800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr2:99833200-99841400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr2:99833200-99842600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:99833400-99843400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr2:99834800-99842400	Weak transcription	Brain Anterior Caudate	brain
28	chr2:99836000-99842600	Weak transcription	Psoas Muscle	Psoas
29	chr2:99836200-99847600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr2:99838600-99840600	Weak transcription	Liver	Liver
31	chr2:99839600-99842000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr2:99840600-99840800	ZNF genes & repeats	Aorta	Aorta
33	chr2:99840600-99841000	Strong transcription	Liver	Liver
34	chr2:99840600-99841200	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr2:99840600-99841400	Strong transcription	Brain Hippocampus Middle	brain
36	chr2:99840800-99874400	Weak transcription	Aorta	Aorta
37	chr2:99841000-99843000	Weak transcription	Liver	Liver
38	chr2:99841200-99843200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr2:99841400-99843000	Weak transcription	Brain Hippocampus Middle	brain
40	chr2:99853600-99863200	Weak transcription	Esophagus	oesophagus
41	chr2:99854600-99854800	Enhancers	Left Ventricle	heart
42	chr2:99854600-99855200	Enhancers	K562	blood
43	chr2:99854800-99865800	Weak transcription	Left Ventricle	heart
44	chr2:99855200-99855600	Flanking Active TSS	K562	blood
45	chr2:99855600-99855800	Enhancers	K562	blood
46	chr2:99858200-99859200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr2:99858400-99859200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr2:99858800-99864800	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr2:99860400-99899800	Weak transcription	Psoas Muscle	Psoas
50	chr2:99860800-99864400	Weak transcription	Lung	lung

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