Variant report

Variant	nsv874856
Chromosome Location	chr2:112189642-112333936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2518)
CpG islands
(count:184)
Chromatin interactive
region (count:4)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2518 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112286629-112286892	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:112279969-112280556	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
4	ARID3A	chr2:112221794-112221988	HepG2	liver:	n/a	n/a
5	ATF1	chr2:112252616-112252812	K562	blood:	n/a	n/a
6	ATF1	chr2:112251003-112251203	K562	blood:	n/a	n/a
7	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
8	ATF2	chr2:112236677-112236938	GM12878	blood:	n/a	n/a
9	ATF3	chr2:112292952-112293475	HepG2	liver:	n/a	chr2:112293252-112293272 chr2:112293263-112293272
10	BACH1	chr2:112251425-112251440	K562	blood:	n/a	n/a
11	BATF	chr2:112238764-112238956	GM12878	blood:	n/a	n/a
12	BATF	chr2:112209363-112210356	GM12878	blood:	n/a	n/a
13	BATF	chr2:112251368-112251781	GM12878	blood:	n/a	chr2:112251535-112251545 chr2:112251573-112251582
14	BATF	chr2:112206432-112206650	GM12878	blood:	n/a	n/a
15	BATF	chr2:112236417-112237152	GM12878	blood:	n/a	n/a
16	BATF	chr2:112209629-112210364	GM12878	blood:	n/a	n/a
17	BATF	chr2:112290657-112291078	GM12878	blood:	n/a	chr2:112290906-112290916 chr2:112290905-112290916
18	BATF	chr2:112195321-112195643	GM12878	blood:	n/a	chr2:112195574-112195583
19	BATF	chr2:112220893-112221142	GM12878	blood:	n/a	n/a
20	BATF	chr2:112251898-112252984	GM12878	blood:	n/a	chr2:112252692-112252702 chr2:112252678-112252688
21	BATF	chr2:112211973-112212259	GM12878	blood:	n/a	n/a
22	BATF	chr2:112327815-112328182	GM12878	blood:	n/a	n/a
23	BATF	chr2:112236428-112237126	GM12878	blood:	n/a	n/a
24	BATF	chr2:112285351-112285619	GM12878	blood:	n/a	n/a
25	BATF	chr2:112221520-112221892	GM12878	blood:	n/a	n/a
26	BATF	chr2:112282643-112283006	GM12878	blood:	n/a	n/a
27	BATF	chr2:112211976-112212278	GM12878	blood:	n/a	n/a
28	BATF	chr2:112303348-112304091	GM12878	blood:	n/a	chr2:112303735-112303744
29	BATF	chr2:112305421-112305663	GM12878	blood:	n/a	chr2:112305590-112305600 chr2:112305586-112305596
30	BATF	chr2:112303521-112304031	GM12878	blood:	n/a	chr2:112303735-112303744
31	BATF	chr2:112193854-112194550	GM12878	blood:	n/a	chr2:112194264-112194272
32	BATF	chr2:112267135-112267389	GM12878	blood:	n/a	n/a
33	BATF	chr2:112264388-112264857	GM12878	blood:	n/a	n/a
34	BATF	chr2:112195246-112195683	GM12878	blood:	n/a	chr2:112195574-112195583
35	BATF	chr2:112195688-112196162	GM12878	blood:	n/a	n/a
36	BATF	chr2:112250963-112251779	GM12878	blood:	n/a	chr2:112251535-112251545 chr2:112251573-112251582
37	BATF	chr2:112251972-112252940	GM12878	blood:	n/a	chr2:112252692-112252702 chr2:112252678-112252688
38	BATF	chr2:112248667-112249139	GM12878	blood:	n/a	n/a
39	BATF	chr2:112285289-112285637	GM12878	blood:	n/a	n/a
40	BATF	chr2:112327786-112328223	GM12878	blood:	n/a	n/a
41	BATF	chr2:112250737-112250940	GM12878	blood:	n/a	n/a
42	BATF	chr2:112282646-112282952	GM12878	blood:	n/a	n/a
43	BATF	chr2:112198041-112198360	GM12878	blood:	n/a	n/a
44	BATF	chr2:112237987-112238183	GM12878	blood:	n/a	n/a
45	BATF	chr2:112264445-112264864	GM12878	blood:	n/a	n/a
46	BATF	chr2:112190544-112190853	GM12878	blood:	n/a	n/a
47	BATF	chr2:112258184-112258454	GM12878	blood:	n/a	n/a
48	BATF	chr2:112248607-112249357	GM12878	blood:	n/a	n/a
49	BATF	chr2:112190573-112190841	GM12878	blood:	n/a	n/a
50	BATF	chr2:112193934-112194446	GM12878	blood:	n/a	chr2:112194264-112194272

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112293267-112293317	HIPEpiC	eye:	n/a
2	chr2:112293267-112293317	HIPEpiC	eye:	n/a
3	chr2:112252254-112252304	HCF	heart:	n/a
4	chr2:112280286-112280336	U87	brain:	n/a
5	chr2:112252254-112252304	SK-N-MC	brain:	n/a
6	chr2:112293267-112293317	Hepatocyte	liver:	n/a
7	chr2:112293267-112293317	GM06990	blood:	n/a
8	chr2:112293267-112293317	HEK293	kidney:	embryo
9	chr2:112293267-112293317	Hela-S3	cervix:	n/a
10	chr2:112293267-112293317	HepG2	liver:	n/a
11	chr2:112252254-112252304	SAEC	small airway:	n/a
12	chr2:112280286-112280336	HEEpiC	esophagus:	n/a
13	chr2:112280286-112280336	MCF10A-Er-Src	breast:	n/a
14	chr2:112252254-112252304	HEEpiC	esophagus:	n/a
15	chr2:112252254-112252304	BJ	skin:	n/a
16	chr2:112280286-112280336	NHBE	bronchial:	n/a
17	chr2:112252254-112252304	AG09319	gingival:	n/a
18	chr2:112293267-112293317	NH-A	brain:	n/a
19	chr2:112252254-112252304	ProgFib	skin:	n/a
20	chr2:112252254-112252304	SK-N-SH_RA	brain:	n/a
21	chr2:112280286-112280336	A549	lung:	n/a
22	chr2:112252254-112252304	HUVEC	blood vessel:	n/a
23	chr2:112252254-112252304	HRPEpiC	eye:	n/a
24	chr2:112293267-112293317	AG09309	skin:	n/a
25	chr2:112252254-112252304	SKMC	muscle:	n/a
26	chr2:112293267-112293317	BJ	skin:	n/a
27	chr2:112252254-112252304	GM12892	blood:	n/a
28	chr2:112280286-112280336	AG04449	skin:	fetal
29	chr2:112280286-112280336	PrEC	prostate:	n/a
30	chr2:112293267-112293317	ProgFib	skin:	n/a
31	chr2:112252254-112252304	GM12891	blood:	n/a
32	chr2:112280286-112280336	HAEpiC	amniotic membrane:	n/a
33	chr2:112252254-112252304	T-47D	breast:	n/a
34	chr2:112280286-112280336	Jurkat	blood:	n/a
35	chr2:112252254-112252304	AG04450	lung:	fetal
36	chr2:112252254-112252304	ovcar-3	ovarian:	n/a
37	chr2:112293267-112293317	SK-N-SH_RA	brain:	n/a
38	chr2:112293267-112293317	A549	lung:	n/a
39	chr2:112293267-112293317	AoSMC	blood vessel:	n/a
40	chr2:112280286-112280336	HCF	heart:	n/a
41	chr2:112252254-112252304	CMK	blood:	n/a
42	chr2:112293267-112293317	SK-N-SH	brain:	n/a
43	chr2:112252254-112252304	HMEC	breast:	n/a
44	chr2:112252254-112252304	GM19239	blood:	n/a
45	chr2:112293267-112293317	LNCaP	prostate:	n/a
46	chr2:112252254-112252304	NT2-D1	testis:	n/a
47	chr2:112280286-112280336	LNCaP	prostate:	n/a
48	chr2:112280286-112280336	HCPEpiC	choroid plexus:	n/a
49	chr2:112252254-112252304	Hela-S3	cervix:	n/a
50	chr2:112252254-112252304	PFSK-1	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111877393..111879713-chr2:112235053..112237981,2	K562	blood:
2	chr2:111878764..111880387-chr2:112231090..112233888,2	MCF-7	breast:
3	chr2:111877705..111880008-chr2:112211679..112213711,2	MCF-7	breast:
4	chr2:112239413..112241217-chr2:112461159..112463413,2	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112227180-112227564	ENSG00000172965.6
2	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
3	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
4	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
5	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
6	lnc-AC108463.1-3	chr2:112252462-112252597	ENSG00000172965.6
7	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073642
8	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073656
9	lnc-ANAPC1-3	chr2:112315990-112317514	NONHSAT073659
10	lnc-AC108463.1-3	chr2:112252462-112252677	ENSG00000172965.6
11	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073658
12	lnc-AC108463.1-3	chr2:112227364-112227564	ENSG00000172965.6
13	lnc-AC108463.1-3	chr2:112252462-112252540	NONHSAT073639
14	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073654
15	lnc-AC108463.1-3	chr2:112227215-112227564	ENSG00000172965.6
16	lnc-AC108463.1-3	chr2:112237484-112237657	NONHSAT073639
17	lnc-AC108463.1-3	chr2:112227364-112227376	NONHSAT073639
18	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
19	lnc-AC108463.1-3	chr2:112252462-112252602	ENSG00000172965.6
20	lnc-AC108463.1-2	chr2:112249520-112250145	ENSG00000224959
21	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073656
22	lnc-BCL2L11-3	chr2:112268201-112268567	XLOC_001625
23	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
24	lnc-BCL2L11-3	chr2:112248850-112249239	XLOC_001625
25	lnc-AC108463.1-3	chr2:112252462-112252631	ENSG00000172965.6
26	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073640
27	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073622
28	lnc-AC108463.1-3	chr2:112199085-112199198	ENSG00000172965.6
29	lnc-AC108463.1-3	chr2:112252462-112252611	ENSG00000172965.6
30	lnc-AC108463.1-3	chr2:112252462-112252610	ENSG00000172965.6
31	lnc-AC108463.1-2	chr2:112252134-112252388	ENSG00000224959
32	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
33	lnc-AC108463.1-3	chr2:112227095-112227564	ENSG00000172965.6
34	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6

No data

Variant related genes	Relation type
MIR4435-1HG	TF binding region
ENSG00000271635	TF binding region
ENSG00000240350	TF binding region
ENSG00000224959	TF binding region
MIR4435-1HG	CpG island
ENSG00000271635	CpG island
ENSG00000240350	CpG island
ENSG00000224959	CpG island
ENSG00000153094	chromatin interactions

Extended variants
information (count: 3793 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3793 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55888240	chr2:112189642-112189643	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs541148825	chr2:112189643-112189644	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs559880108	chr2:112189672-112189673	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs187452076	chr2:112189680-112189681	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs58628601	chr2:112189706-112189707	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542438825	chr2:112189712-112189713	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs562795433	chr2:112189715-112189716	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs531545886	chr2:112189784-112189785	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551313504	chr2:112189785-112189786	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs189846559	chr2:112189786-112189787	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148112559	chr2:112189829-112189830	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs113416340	chr2:112189900-112189901	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547502344	chr2:112189914-112189915	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs182469783	chr2:112189963-112189964	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs538687429	chr2:112189971-112189972	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs536836509	chr2:112190038-112190039	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs550148951	chr2:112190055-112190056	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs570291131	chr2:112190065-112190066	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs538967549	chr2:112190091-112190092	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558882225	chr2:112190135-112190136	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572122192	chr2:112190170-112190171	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs534731626	chr2:112190252-112190253	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554621370	chr2:112190296-112190297	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574636052	chr2:112190329-112190330	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149528480	chr2:112190331-112190332	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575458694	chr2:112190357-112190358	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs562549199	chr2:112190494-112190495	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs576238617	chr2:112190543-112190544	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs377203112	chr2:112190639-112190640	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544993122	chr2:112190697-112190698	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs565220632	chr2:112190698-112190699	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs527260273	chr2:112190731-112190732	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs565110556	chr2:112190771-112190772	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs547465388	chr2:112190779-112190780	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs538109940	chr2:112190797-112190798	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs554490300	chr2:112190817-112190818	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs574321857	chr2:112190831-112190832	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560956817	chr2:112190832-112190833	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs529823794	chr2:112190833-112190834	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs981965	chr2:112190858-112190859	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs111277180	chr2:112190882-112190883	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570177398	chr2:112190912-112190913	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539283915	chr2:112190918-112190919	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs146227989	chr2:112190940-112190941	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs374154009	chr2:112190945-112190946	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs111897091	chr2:112190976-112190977	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs552578404	chr2:112191012-112191013	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs566059835	chr2:112191031-112191032	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs534693674	chr2:112191058-112191059	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs530320181	chr2:112191059-112191060	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1848 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112113800-112191600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:112176000-112194800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:112176000-112197400	Weak transcription	Osteobl	bone
4	chr2:112176000-112199000	Weak transcription	NH-A	brain
5	chr2:112178800-112193200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:112179400-112191400	Weak transcription	HMEC	breast
7	chr2:112179400-112199000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:112181800-112192400	Enhancers	Primary B cells from peripheral blood	blood
9	chr2:112182800-112189800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:112183000-112190800	Weak transcription	Fetal Muscle Leg	muscle
11	chr2:112183200-112189800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr2:112183200-112189800	Weak transcription	Dnd41	blood
13	chr2:112183200-112191400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:112183200-112191400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:112183200-112207200	Weak transcription	HUVEC	blood vessel
16	chr2:112184000-112193200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr2:112184000-112196600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr2:112185000-112191600	Enhancers	Primary B cells from cord blood	blood
19	chr2:112185400-112191400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr2:112185400-112192000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:112185400-112199800	Weak transcription	HSMM	muscle
22	chr2:112185400-112220200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr2:112186800-112190800	Weak transcription	HSMMtube	muscle
24	chr2:112187000-112191800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr2:112187000-112199600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:112187200-112190000	Weak transcription	GM12878-XiMat	blood
27	chr2:112187200-112197600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:112187400-112191200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr2:112187600-112190400	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr2:112187800-112191600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:112187800-112199400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr2:112188200-112191800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr2:112188400-112190200	Enhancers	HepG2	liver
34	chr2:112188600-112190000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:112188600-112192400	Enhancers	K562	blood
36	chr2:112188800-112190000	Weak transcription	Adipose Nuclei	Adipose
37	chr2:112189400-112190200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr2:112189400-112190200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr2:112189400-112190600	Enhancers	Fetal Thymus	thymus
40	chr2:112189600-112190000	Enhancers	Spleen	Spleen
41	chr2:112189600-112190400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:112189600-112199400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:112189800-112190400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr2:112189800-112191000	Enhancers	Primary T cells fromperipheralblood	blood
45	chr2:112189800-112191000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:112189800-112193400	Enhancers	Dnd41	blood
47	chr2:112190000-112190200	Enhancers	GM12878-XiMat	blood
48	chr2:112190000-112190400	Enhancers	Primary hematopoietic stem cells	blood
49	chr2:112190000-112190400	Enhancers	Adipose Nuclei	Adipose
50	chr2:112190000-112191000	Enhancers	Primary T killer memory cells from peripheral blood	blood

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