Variant report

Variant	nsv874854
Chromosome Location	chr2:112069814-112189642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1058)
CpG islands
(count:124)
Chromatin interactive
region (count:3)
LncRNA
region (count:37)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
2	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
3	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
5	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
6	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
7	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
8	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
9	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
10	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
11	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
12	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
13	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
14	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
15	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
16	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
17	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
18	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
19	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
20	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
21	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
22	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
23	BATF	chr2:112188947-112189209	GM12878	blood:	n/a	n/a
24	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
25	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a
26	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
27	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
28	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
29	BATF	chr2:112169777-112169962	GM12878	blood:	n/a	chr2:112169903-112169914
30	BATF	chr2:112183233-112184090	GM12878	blood:	n/a	n/a
31	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
32	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
33	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
34	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
35	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
36	BATF	chr2:112188889-112189327	GM12878	blood:	n/a	n/a
37	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
38	BCL11A	chr2:112125764-112126223	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:112186983-112187434	GM12878	blood:	n/a	chr2:112187266-112187275
40	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:112182331-112182639	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:112072806-112073106	GM12878	blood:	n/a	chr2:112072837-112072846
43	BCL11A	chr2:112188940-112189225	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:112072754-112073092	GM12878	blood:	n/a	chr2:112072837-112072846
45	BCL11A	chr2:112182226-112182918	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:112188884-112189288	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:112183223-112183810	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:112087560-112087812	GM12878	blood:	n/a	n/a
49	BCL3	chr2:112183366-112183629	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:112165402-112165622	K562	blood:	n/a	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124118-112124168	SK-N-SH	brain:	n/a
2	chr2:112124118-112124168	AoSMC	blood vessel:	n/a
3	chr2:112124118-112124168	SK-N-SH	brain:	n/a
4	chr2:112124118-112124168	AoSMC	blood vessel:	n/a
5	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
6	chr2:112124380-112124430	K562	blood:	n/a
7	chr2:112124380-112124430	T-47D	breast:	n/a
8	chr2:112124118-112124168	T-47D	breast:	n/a
9	chr2:112124118-112124168	HEK293	kidney:	embryo
10	chr2:112124118-112124168	PrEC	prostate:	n/a
11	chr2:112124380-112124430	GM19239	blood:	n/a
12	chr2:112124118-112124168	CMK	blood:	n/a
13	chr2:112124118-112124168	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:112124380-112124430	ProgFib	skin:	n/a
15	chr2:112124380-112124430	SAEC	small airway:	n/a
16	chr2:112124118-112124168	NHDF-neo	bronchial:	n/a
17	chr2:112124380-112124430	U87	brain:	n/a
18	chr2:112124380-112124430	HCT-116	colon:	n/a
19	chr2:112124380-112124430	SKMC	muscle:	n/a
20	chr2:112124380-112124430	Jurkat	blood:	n/a
21	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
22	chr2:112124118-112124168	BJ	skin:	n/a
23	chr2:112124380-112124430	H1-hESC	embryonic stem cell:	embryo
24	chr2:112124118-112124168	IMR90	lung:	fetal
25	chr2:112124380-112124430	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:112124380-112124430	IMR90	lung:	fetal
27	chr2:112124118-112124168	PFSK-1	brain:	n/a
28	chr2:112124118-112124168	HCM	heart:	n/a
29	chr2:112124380-112124430	HRE	kidney:	n/a
30	chr2:112124380-112124430	LNCaP	prostate:	n/a
31	chr2:112124380-112124430	HCPEpiC	choroid plexus:	n/a
32	chr2:112124380-112124430	Hela-S3	cervix:	n/a
33	chr2:112124118-112124168	HNPCEpiC	eye:	n/a
34	chr2:112124118-112124168	SAEC	small airway:	n/a
35	chr2:112124118-112124168	NH-A	brain:	n/a
36	chr2:112124380-112124430	HNPCEpiC	eye:	n/a
37	chr2:112124118-112124168	HMEC	breast:	n/a
38	chr2:112124118-112124168	AG04449	skin:	fetal
39	chr2:112124380-112124430	ovcar-3	ovarian:	n/a
40	chr2:112124118-112124168	NT2-D1	testis:	n/a
41	chr2:112124118-112124168	AG09309	skin:	n/a
42	chr2:112124118-112124168	ovcar-3	ovarian:	n/a
43	chr2:112124380-112124430	HCF	heart:	n/a
44	chr2:112124118-112124168	SKMC	muscle:	n/a
45	chr2:112124380-112124430	NB4	blood:	n/a
46	chr2:112124118-112124168	Caco-2	colon:	n/a
47	chr2:112124380-112124430	GM12878	blood:	n/a
48	chr2:112124118-112124168	HRPEpiC	eye:	n/a
49	chr2:112124118-112124168	GM12891	blood:	n/a
50	chr2:112124118-112124168	PANC-1	pancreas:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:
2	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:
3	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
2	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
3	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
4	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
5	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
6	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
7	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
8	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
9	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
10	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
11	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
12	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
13	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
14	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639
15	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
16	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
17	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
18	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
19	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
20	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
22	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
23	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
24	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
25	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
26	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
27	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
28	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
29	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
30	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
31	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
32	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
33	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
34	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
35	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
36	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
37	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
MIR4435-1HG	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
MIR4435-1HG	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions

Extended variants
information (count: 2889 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2889 , 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	rs2333912	chr2:112069814-112069815	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112083854	chr2:112069825-112069826	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565820694	chr2:112069852-112069853	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs62161634	chr2:112069880-112069881	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71413065	chr2:112069923-112069924	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12614461	chr2:112069961-112069962	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547610121	chr2:112069988-112069989	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561215534	chr2:112070014-112070015	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150834373	chr2:112070018-112070019	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557981854	chr2:112070024-112070025	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201932769	chr2:112070038-112070039	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550107453	chr2:112070050-112070051	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569953410	chr2:112070051-112070052	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539069119	chr2:112070080-112070081	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375472759	chr2:112070083-112070084	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368521592	chr2:112070093-112070094	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560272518	chr2:112070098-112070099	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552379627	chr2:112070105-112070106	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566213905	chr2:112070112-112070113	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72627498	chr2:112070126-112070127	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs537503633	chr2:112070144-112070145	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs870672	chr2:112070149-112070150	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377621554	chr2:112070187-112070188	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557409869	chr2:112070207-112070208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs885212	chr2:112070210-112070211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192384323	chr2:112070214-112070215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183943352	chr2:112070225-112070226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187708587	chr2:112070228-112070229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs59996630	chr2:112070253-112070254	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs368931058	chr2:112070320-112070321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201354076	chr2:112070326-112070327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545021727	chr2:112070327-112070328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558345316	chr2:112070332-112070333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571827449	chr2:112070412-112070413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541189990	chr2:112070532-112070533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542630560	chr2:112070550-112070551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58475388	chr2:112070553-112070554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192326672	chr2:112070556-112070557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs151150304	chr2:112070570-112070571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543755549	chr2:112070578-112070579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184662208	chr2:112070588-112070589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4399729	chr2:112070640-112070641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs59912265	chr2:112070647-112070648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4268930	chr2:112070685-112070686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552569902	chr2:112070737-112070738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4643548	chr2:112070754-112070755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566150825	chr2:112070788-112070789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191882972	chr2:112070814-112070815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373405464	chr2:112070815-112070816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184437288	chr2:112070832-112070833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112025600-112116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:112055000-112070600	Weak transcription	NHLF	lung
3	chr2:112058200-112071000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:112060400-112079200	Weak transcription	HSMMtube	muscle
5	chr2:112062400-112070200	Weak transcription	Osteobl	bone
6	chr2:112062800-112070600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:112062800-112070600	Weak transcription	NH-A	brain
8	chr2:112063600-112070000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:112063600-112086200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:112067400-112070400	Weak transcription	Fetal Muscle Leg	muscle
11	chr2:112068000-112072800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr2:112068600-112071600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr2:112068800-112070000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr2:112068800-112072200	Enhancers	Liver	Liver
15	chr2:112069600-112070200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:112069600-112070800	Enhancers	Brain Hippocampus Middle	brain
17	chr2:112069600-112070800	Enhancers	Brain Substantia Nigra	brain
18	chr2:112069600-112071400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:112069600-112071400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr2:112069600-112071600	Enhancers	NHDF-Ad	bronchial
21	chr2:112069600-112072000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:112069600-112072200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:112069600-112074800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:112069800-112070000	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr2:112069800-112070200	Enhancers	Brain Angular Gyrus	brain
26	chr2:112069800-112070800	Weak transcription	Brain Anterior Caudate	brain
27	chr2:112069800-112070800	Enhancers	Fetal Lung	lung
28	chr2:112069800-112071600	Enhancers	Placenta	Placenta
29	chr2:112070000-112070200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:112070000-112070200	Enhancers	Adipose Nuclei	Adipose
31	chr2:112070000-112070800	Enhancers	HMEC	breast
32	chr2:112070000-112071000	Enhancers	Fetal Muscle Trunk	muscle
33	chr2:112070000-112071400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:112070000-112071400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr2:112070000-112071400	Enhancers	Fetal Heart	heart
36	chr2:112070000-112071600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:112070200-112070600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:112070200-112071200	Weak transcription	Adipose Nuclei	Adipose
39	chr2:112070200-112071600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr2:112070200-112071600	Enhancers	Osteobl	bone
41	chr2:112070400-112071000	Enhancers	Fetal Muscle Leg	muscle
42	chr2:112070600-112070800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:112070600-112070800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:112070600-112070800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:112070600-112070800	Enhancers	A549	lung
46	chr2:112070600-112071000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr2:112070600-112071000	Enhancers	Left Ventricle	heart
48	chr2:112070600-112071400	Enhancers	Lung	lung
49	chr2:112070600-112071400	Enhancers	NH-A	brain
50	chr2:112070600-112071600	Enhancers	NHLF	lung

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