Variant report

Variant	nsv961858
Chromosome Location	chr2:110779013-110837772
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	BATF	chr2:110829579-110829796	GM12878	blood:	n/a	n/a
2	BHLHE40	chr2:110829505-110829790	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:110810820-110811025	HepG2	liver:	n/a	chr2:110810876-110810887
4	CEBPB	chr2:110810829-110810999	Hela-S3	cervix:	n/a	chr2:110810876-110810887
5	CEBPB	chr2:110810834-110810990	K562	blood:	n/a	chr2:110810876-110810887
6	CEBPB	chr2:110810802-110811002	A549	lung:	n/a	chr2:110810876-110810887
7	CEBPD	chr2:110813834-110814157	K562	blood:	n/a	n/a
8	CTCF	chr2:110835249-110835284	LNCaP	prostate:	n/a	n/a
9	CTCF	chr2:110805922-110805981	HepG2	liver:	n/a	chr2:110805968-110805976
10	CTCF	chr2:110789638-110789810	MCF-7	breast:	n/a	chr2:110789717-110789730
11	CTCF	chr2:110829402-110829510	GM12892	blood:	n/a	n/a
12	CTCF	chr2:110789712-110789795	GM13976	blood:	n/a	chr2:110789717-110789730
13	CTCF	chr2:110789665-110789800	GM12891	blood:	n/a	chr2:110789717-110789730
14	CTCF	chr2:110797587-110797807	MCF-7	breast:	n/a	chr2:110797699-110797717 chr2:110797694-110797715
15	CTCF	chr2:110789373-110789416	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr2:110829638-110829873	GM13977	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
17	CTCF	chr2:110822360-110822398	GM13976	blood:	n/a	n/a
18	CTCF	chr2:110789549-110789857	A549	lung:	n/a	chr2:110789717-110789730
19	CTCF	chr2:110789627-110789822	A549	lung:	n/a	chr2:110789717-110789730
20	CTCF	chr2:110797591-110797814	MCF-7	breast:	n/a	chr2:110797699-110797717 chr2:110797694-110797715
21	CTCF	chr2:110829459-110829873	A549	lung:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
22	CTCF	chr2:110829590-110829859	HUVEC	blood vessel:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
23	CTCF	chr2:110829650-110829844	GM10248	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
24	CTCF	chr2:110829483-110829860	K562	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
25	CTCF	chr2:110789639-110789645	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr2:110829640-110829875	LNCaP	prostate:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
27	CTCF	chr2:110829583-110829851	NHEK	skin:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
28	CTCF	chr2:110829403-110829498	GM19238	blood:	n/a	n/a
29	CTCF	chr2:110829561-110829861	GM19240	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
30	CTCF	chr2:110829577-110829863	K562	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
31	CTCF	chr2:110805980-110806130	HepG2	liver:	n/a	n/a
32	CTCF	chr2:110789607-110789837	A549	lung:	n/a	chr2:110789717-110789730
33	CTCF	chr2:110829604-110829853	GM19239	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
34	CTCF	chr2:110791714-110791743	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr2:110789859-110789875	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr2:110829668-110829843	GM20000	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
37	CTCF	chr2:110837269-110837339	GM13977	blood:	n/a	n/a
38	CTCF	chr2:110829571-110829852	MCF-7	breast:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
39	CTCF	chr2:110789649-110789814	MCF-7	breast:	n/a	chr2:110789717-110789730
40	CTCF	chr2:110829575-110829860	GM12891	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
41	CTCF	chr2:110829585-110829848	ProgFib	skin:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
42	CTCF	chr2:110789636-110789793	MCF-7	breast:	n/a	chr2:110789717-110789730
43	CTCF	chr2:110786166-110786225	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr2:110797594-110797790	NHEK	skin:	n/a	chr2:110797699-110797717 chr2:110797694-110797715
45	CTCF	chr2:110829588-110829846	Fibrobl	skin:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
46	CTCF	chr2:110818314-110818373	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr2:110829439-110829500	GM12891	blood:	n/a	n/a
48	CTCF	chr2:110829594-110829842	H1-hESC	embryonic stem cell:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
49	CTCF	chr2:110829606-110829879	Kidney_OC	kidney:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
50	CTCF	chr2:110789627-110789829	MCF-7	breast:	n/a	chr2:110789717-110789730

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110829661-110829711	A549	lung:	n/a
2	chr2:110827645-110827695	Hepatocyte	liver:	n/a
3	chr2:110827645-110827695	PANC-1	pancreas:	n/a
4	chr2:110833739-110833789	HUVEC	blood vessel:	n/a
5	chr2:110829661-110829711	HEEpiC	esophagus:	n/a
6	chr2:110833739-110833789	IMR90	lung:	fetal
7	chr2:110833739-110833789	AG04450	lung:	fetal
8	chr2:110833739-110833789	SAEC	small airway:	n/a
9	chr2:110827645-110827695	PFSK-1	brain:	n/a
10	chr2:110829661-110829711	MCF-7	breast:	n/a
11	chr2:110827645-110827695	HEK293	kidney:	embryo
12	chr2:110827645-110827695	HAEpiC	amniotic membrane:	n/a
13	chr2:110827645-110827695	AG10803	skin:	n/a
14	chr2:110827645-110827695	HCM	heart:	n/a
15	chr2:110827645-110827695	GM06990	blood:	n/a
16	chr2:110829661-110829711	SKMC	muscle:	n/a
17	chr2:110827645-110827695	HRCEpiC	kidney:	n/a
18	chr2:110827645-110827695	GM12878	blood:	n/a
19	chr2:110833739-110833789	HEK293	kidney:	embryo
20	chr2:110833739-110833789	ECC-1	luminal epithelium:	n/a
21	chr2:110829661-110829711	BJ	skin:	n/a
22	chr2:110827645-110827695	BJ	skin:	n/a
23	chr2:110829661-110829711	ovcar-3	ovarian:	n/a
24	chr2:110829661-110829711	HRCEpiC	kidney:	n/a
25	chr2:110829661-110829711	SK-N-SH	brain:	n/a
26	chr2:110833739-110833789	HRCEpiC	kidney:	n/a
27	chr2:110827645-110827695	HL-60	blood:	n/a
28	chr2:110827645-110827695	SKMC	muscle:	n/a
29	chr2:110829661-110829711	SAEC	small airway:	n/a
30	chr2:110829661-110829711	HCPEpiC	choroid plexus:	n/a
31	chr2:110829661-110829711	AG09319	gingival:	n/a
32	chr2:110827645-110827695	HCT-116	colon:	n/a
33	chr2:110827645-110827695	HCF	heart:	n/a
34	chr2:110827645-110827695	HIPEpiC	eye:	n/a
35	chr2:110833739-110833789	SK-N-MC	brain:	n/a
36	chr2:110833739-110833789	HCM	heart:	n/a
37	chr2:110829661-110829711	HAEpiC	amniotic membrane:	n/a
38	chr2:110827645-110827695	U87	brain:	n/a
39	chr2:110829661-110829711	SK-N-MC	brain:	n/a
40	chr2:110833739-110833789	H1-hESC	embryonic stem cell:	embryo
41	chr2:110829661-110829711	U87	brain:	n/a
42	chr2:110829661-110829711	HCM	heart:	n/a
43	chr2:110827645-110827695	HEEpiC	esophagus:	n/a
44	chr2:110829661-110829711	CMK	blood:	n/a
45	chr2:110833739-110833789	Hepatocyte	liver:	n/a
46	chr2:110829661-110829711	IMR90	lung:	fetal
47	chr2:110833739-110833789	AoSMC	blood vessel:	n/a
48	chr2:110833739-110833789	HCT-116	colon:	n/a
49	chr2:110827645-110827695	HMEC	breast:	n/a
50	chr2:110833739-110833789	Jurkat	blood:	n/a

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4267	chr2:110827594-110827609	MIMAT0016893

Variant related genes	Relation type
MIR4267	TF binding region
MIR4267	CpG island

Extended variants
information (count: 236 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:236 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565180888	chr2:110783876-110783877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1972810	chr2:110783884-110783885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577318078	chr2:110783915-110783916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539970087	chr2:110784109-110784110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141473006	chr2:110784119-110784120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559701968	chr2:110784128-110784129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528898543	chr2:110784139-110784140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371847735	chr2:110784160-110784161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376854971	chr2:110784183-110784184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368696583	chr2:110784206-110784207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546688534	chr2:110784207-110784208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs406115	chr2:110784224-110784225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549233318	chr2:110784305-110784306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562644349	chr2:110784309-110784310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113660456	chr2:110784377-110784378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370164758	chr2:110784380-110784381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373168391	chr2:110784523-110784524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571510723	chr2:110784545-110784546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534261562	chr2:110785548-110785549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547945701	chr2:110785566-110785567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146681801	chr2:110785634-110785635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536271763	chr2:110785674-110785675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556768588	chr2:110785676-110785677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576655433	chr2:110785690-110785691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539367379	chr2:110785694-110785695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558705337	chr2:110785711-110785712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572339410	chr2:110785721-110785722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539908978	chr2:110785750-110785751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559839391	chr2:110785777-110785778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201533161	chr2:110785796-110785797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143984605	chr2:110785805-110785806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542265895	chr2:110785810-110785811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562543760	chr2:110785827-110785828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531501378	chr2:110785839-110785840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545347773	chr2:110785870-110785871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565058085	chr2:110785872-110785873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527497641	chr2:110785923-110785924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547882918	chr2:110785973-110785974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567656530	chr2:110786003-110786004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs336776	chr2:110786008-110786009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549905422	chr2:110786010-110786011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62160479	chr2:110786078-110786079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570060545	chr2:110786104-110786105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538931735	chr2:110786107-110786108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558842186	chr2:110786118-110786119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565909541	chr2:110786132-110786133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534894184	chr2:110786134-110786135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553413284	chr2:110786152-110786153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573642652	chr2:110786252-110786253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542752375	chr2:110786254-110786255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110783800-110784000	Enhancers	Fetal Intestine Large	intestine
2	chr2:110783800-110786000	Weak transcription	Pancreas	Pancrea
3	chr2:110785800-110792600	Weak transcription	Fetal Intestine Large	intestine
4	chr2:110786000-110786400	Enhancers	Fetal Muscle Trunk	muscle
5	chr2:110792600-110793000	Enhancers	Pancreas	Pancrea
6	chr2:110805800-110806600	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr2:110805800-110806600	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr2:110806000-110806600	Enhancers	Pancreas	Pancrea
9	chr2:110806000-110807600	Enhancers	Fetal Muscle Trunk	muscle
10	chr2:110806000-110807600	Enhancers	HepG2	liver
11	chr2:110806200-110806600	Enhancers	HSMMtube	muscle
12	chr2:110806400-110807000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr2:110810400-110811000	Enhancers	HUVEC	blood vessel
14	chr2:110810600-110810800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:110810600-110810800	Enhancers	Fetal Heart	heart
16	chr2:110810600-110810800	Enhancers	A549	lung
17	chr2:110810600-110810800	Enhancers	NHEK	skin
18	chr2:110810600-110811000	Enhancers	Fetal Lung	lung
19	chr2:110810600-110811000	Enhancers	Dnd41	blood
20	chr2:110811000-110812000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr2:110811000-110812000	Weak transcription	Fetal Heart	heart
22	chr2:110811000-110812000	Weak transcription	Fetal Lung	lung
23	chr2:110811000-110812000	Weak transcription	A549	lung
24	chr2:110811000-110812000	Weak transcription	HUVEC	blood vessel
25	chr2:110811000-110812000	Weak transcription	NHEK	skin
26	chr2:110812000-110812200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:110812000-110812200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:110812000-110812200	Enhancers	Fetal Brain Male	brain
29	chr2:110812000-110812200	Enhancers	Fetal Lung	lung
30	chr2:110812000-110812400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr2:110812000-110812400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr2:110812000-110812400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:110812000-110812400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:110812000-110812400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:110812000-110812400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:110812000-110812400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:110812000-110812400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:110812000-110812400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:110812000-110812400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:110812000-110812400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:110812000-110812400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr2:110812000-110812400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:110812000-110812400	Enhancers	Brain Hippocampus Middle	brain
44	chr2:110812000-110812400	Enhancers	Fetal Heart	heart
45	chr2:110812000-110812400	Enhancers	Fetal Intestine Large	intestine
46	chr2:110812000-110812400	Enhancers	Fetal Intestine Small	intestine
47	chr2:110812000-110812400	Enhancers	Fetal Stomach	stomach
48	chr2:110812000-110812400	Enhancers	Left Ventricle	heart
49	chr2:110812000-110812400	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr2:110812000-110812400	Enhancers	A549	lung

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