Variant report

Variant	nsv1001733
Chromosome Location	chr2:112027610-112187721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1264)
CpG islands
(count:123)
Chromatin interactive
region (count:3)
LncRNA
region (count:43)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
2	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
3	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
4	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
6	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
7	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
8	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
9	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
10	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
11	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
12	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
13	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
14	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
15	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
16	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
17	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
18	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
19	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
20	BATF	chr2:112049811-112050042	GM12878	blood:	n/a	n/a
21	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
22	BATF	chr2:112029454-112029812	GM12878	blood:	n/a	chr2:112029663-112029674
23	BATF	chr2:112183233-112184090	GM12878	blood:	n/a	n/a
24	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
25	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
26	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a
27	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
28	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
29	BATF	chr2:112029496-112029836	GM12878	blood:	n/a	chr2:112029663-112029674
30	BATF	chr2:112169777-112169962	GM12878	blood:	n/a	chr2:112169903-112169914
31	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
32	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
33	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
34	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
35	BATF	chr2:112037291-112037501	GM12878	blood:	n/a	n/a
36	BATF	chr2:112049833-112050062	GM12878	blood:	n/a	n/a
37	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
38	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
39	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
40	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:112182331-112182639	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:112087560-112087812	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:112125764-112126223	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:112072806-112073106	GM12878	blood:	n/a	chr2:112072837-112072846
46	BCL11A	chr2:112072754-112073092	GM12878	blood:	n/a	chr2:112072837-112072846
47	BCL11A	chr2:112182226-112182918	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:112183223-112183810	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:112186983-112187434	GM12878	blood:	n/a	chr2:112187266-112187275
50	BCL3	chr2:112183366-112183629	GM12878	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124118-112124168	Hela-S3	cervix:	n/a
2	chr2:112124118-112124168	Hela-S3	cervix:	n/a
3	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
4	chr2:112124380-112124430	GM12878	blood:	n/a
5	chr2:112124118-112124168	HCF	heart:	n/a
6	chr2:112124380-112124430	ovcar-3	ovarian:	n/a
7	chr2:112124380-112124430	A549	lung:	n/a
8	chr2:112124380-112124430	AG09309	skin:	n/a
9	chr2:112124118-112124168	MCF-7	breast:	n/a
10	chr2:112124380-112124430	GM19239	blood:	n/a
11	chr2:112124380-112124430	AG10803	skin:	n/a
12	chr2:112124118-112124168	HIPEpiC	eye:	n/a
13	chr2:112124118-112124168	NT2-D1	testis:	n/a
14	chr2:112124118-112124168	HL-60	blood:	n/a
15	chr2:112124118-112124168	LNCaP	prostate:	n/a
16	chr2:112124118-112124168	AG04449	skin:	fetal
17	chr2:112124118-112124168	IMR90	lung:	fetal
18	chr2:112124380-112124430	HL-60	blood:	n/a
19	chr2:112124380-112124430	GM06990	blood:	n/a
20	chr2:112124380-112124430	RPTEC	kidney:	n/a
21	chr2:112124380-112124430	HepG2	liver:	n/a
22	chr2:112124380-112124430	AG04450	lung:	fetal
23	chr2:112124118-112124168	ProgFib	skin:	n/a
24	chr2:112124118-112124168	ECC-1	luminal epithelium:	n/a
25	chr2:112124118-112124168	HRCEpiC	kidney:	n/a
26	chr2:112124380-112124430	SK-N-SH_RA	brain:	n/a
27	chr2:112124380-112124430	HCF	heart:	n/a
28	chr2:112124380-112124430	MCF-7	breast:	n/a
29	chr2:112124118-112124168	HRE	kidney:	n/a
30	chr2:112124380-112124430	ECC-1	luminal epithelium:	n/a
31	chr2:112124380-112124430	HIPEpiC	eye:	n/a
32	chr2:112124380-112124430	AG04449	skin:	fetal
33	chr2:112124118-112124168	HNPCEpiC	eye:	n/a
34	chr2:112124118-112124168	NH-A	brain:	n/a
35	chr2:112124118-112124168	HCM	heart:	n/a
36	chr2:112124380-112124430	HEK293	kidney:	embryo
37	chr2:112124118-112124168	SKMC	muscle:	n/a
38	chr2:112124380-112124430	T-47D	breast:	n/a
39	chr2:112124118-112124168	AoSMC	blood vessel:	n/a
40	chr2:112124118-112124168	K562	blood:	n/a
41	chr2:112124118-112124168	MCF10A-Er-Src	breast:	n/a
42	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
43	chr2:112124380-112124430	NB4	blood:	n/a
44	chr2:112124380-112124430	HMEC	breast:	n/a
45	chr2:112124380-112124430	CMK	blood:	n/a
46	chr2:112124380-112124430	K562	blood:	n/a
47	chr2:112124380-112124430	Hela-S3	cervix:	n/a
48	chr2:112124118-112124168	HEEpiC	esophagus:	n/a
49	chr2:112124118-112124168	SK-N-SH	brain:	n/a
50	chr2:112124118-112124168	H1-hESC	embryonic stem cell:	embryo

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

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

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
2	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
3	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
4	lnc-AC108463.1-3	chr2:112033908-112033997	ENSG00000172965.6
5	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
6	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
7	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
8	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
9	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
10	lnc-BCL2L11-2	chr2:112037022-112037457	XLOC_001624
11	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
12	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
13	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
14	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
15	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
16	lnc-BCL2L11-2	chr2:112043757-112044842	XLOC_001624
17	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
18	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
19	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
20	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
21	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
22	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
23	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
24	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
25	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
26	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
27	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
28	lnc-BCL2L11-2	chr2:112037444-112037486	XLOC_001624
29	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
30	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
31	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
32	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
33	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
34	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
35	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
36	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
37	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
38	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
39	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
40	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
41	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
42	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
43	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639

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

No data

Variant related genes	Relation type
ENSG00000270190	TF binding region
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
ENSG00000270190	CpG island
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions
KLHL24	miRNA target sites
ASCC3	miRNA target sites
ITSN2	miRNA target sites

Extended variants
information (count: 4012 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4012 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1715175	chr2:112027610-112027611	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547899680	chr2:112027675-112027676	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs568276375	chr2:112027798-112027799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537253317	chr2:112027855-112027856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550812296	chr2:112027872-112027873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200173416	chr2:112027963-112027964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573154553	chr2:112028330-112028331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138358233	chr2:112028357-112028358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186895480	chr2:112028358-112028359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575516143	chr2:112028391-112028392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535916495	chr2:112028442-112028443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555906010	chr2:112028552-112028553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574638363	chr2:112028553-112028554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543639340	chr2:112028568-112028569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563536859	chr2:112028571-112028572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577043862	chr2:112028581-112028582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546104353	chr2:112028620-112028621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559056831	chr2:112028718-112028719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528100489	chr2:112028726-112028727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547836638	chr2:112028743-112028744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150180142	chr2:112028766-112028767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192426033	chr2:112028824-112028825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550746968	chr2:112028834-112028835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571054581	chr2:112028855-112028856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539717275	chr2:112028856-112028857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547286179	chr2:112028940-112028941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566710445	chr2:112028943-112028944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138725326	chr2:112028952-112028953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535853026	chr2:112028963-112028964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555844608	chr2:112028976-112028977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74543152	chr2:112028980-112028981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184401572	chr2:112028994-112028995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374971390	chr2:112029025-112029026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556855336	chr2:112029060-112029061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115005368	chr2:112029062-112029063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140480416	chr2:112029064-112029065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545741255	chr2:112029177-112029178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559603257	chr2:112029198-112029199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542281571	chr2:112029226-112029227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188936104	chr2:112029239-112029240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572851030	chr2:112029243-112029244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541418583	chr2:112029273-112029274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142825073	chr2:112029317-112029318	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs193249996	chr2:112029321-112029322	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs530501081	chr2:112029322-112029323	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs544318107	chr2:112029352-112029353	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs564488604	chr2:112029431-112029432	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs185378714	chr2:112029530-112029531	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs533580518	chr2:112029539-112029540	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs908881	chr2:112029546-112029547	Weak transcription Enhancers	TF binding region	1 gene(s)	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:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112008600-112048600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:112016600-112029000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:112019200-112032600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:112020600-112048000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr2:112022800-112031200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:112023400-112046400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:112025000-112034400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:112025400-112031000	Weak transcription	Pancreas	Pancrea
9	chr2:112025600-112116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:112025800-112037800	Weak transcription	HSMM	muscle
11	chr2:112028800-112029200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:112028800-112029400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr2:112028800-112029800	Enhancers	HMEC	breast
14	chr2:112028800-112029800	Enhancers	NHEK	skin
15	chr2:112029000-112029800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:112029400-112032000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:112031000-112031200	Enhancers	Adipose Nuclei	Adipose
18	chr2:112031000-112031200	Enhancers	Spleen	Spleen
19	chr2:112031000-112031400	Enhancers	Pancreas	Pancrea
20	chr2:112031200-112031400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:112031400-112032600	Weak transcription	Adipose Nuclei	Adipose
22	chr2:112031400-112036000	Weak transcription	Pancreas	Pancrea
23	chr2:112032600-112032800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:112032600-112032800	Enhancers	Left Ventricle	heart
25	chr2:112032600-112033000	Enhancers	Adipose Nuclei	Adipose
26	chr2:112032600-112033000	Enhancers	Psoas Muscle	Psoas
27	chr2:112032600-112033000	Enhancers	Right Atrium	heart
28	chr2:112032600-112033200	Enhancers	Liver	Liver
29	chr2:112032600-112033400	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr2:112032800-112033200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr2:112032800-112033400	Weak transcription	Left Ventricle	heart
32	chr2:112033400-112034200	Enhancers	Left Ventricle	heart
33	chr2:112034200-112034800	Weak transcription	Left Ventricle	heart
34	chr2:112034800-112035000	Enhancers	Left Ventricle	heart
35	chr2:112036000-112036200	Enhancers	Pancreas	Pancrea
36	chr2:112044400-112046600	Weak transcription	Pancreas	Pancrea
37	chr2:112045400-112045600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr2:112045400-112045800	Enhancers	NHEK	skin
39	chr2:112045400-112046000	Enhancers	HMEC	breast
40	chr2:112045600-112046200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:112045800-112047600	Weak transcription	NHEK	skin
42	chr2:112046000-112046400	Weak transcription	HMEC	breast
43	chr2:112046200-112046400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr2:112046400-112046600	Enhancers	HMEC	breast
45	chr2:112046400-112046800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:112046400-112047000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:112046400-112047800	Enhancers	Placenta	Placenta
48	chr2:112046400-112048600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr2:112046400-112057400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:112046600-112047800	Weak transcription	HMEC	breast

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