Variant report

Variant	nsv535895
Chromosome Location	chr2:114015492-114037018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:916)
Chromatin interactive
region (count:7)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:114024089-114024236	K562	blood:	n/a	n/a
2	BACH1	chr2:114035511-114035512	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:114036189-114037046	ECC-1	luminal epithelium:	n/a	chr2:114036613-114036626
4	CEBPB	chr2:114023382-114023391	HepG2	liver:	n/a	n/a
5	CHD1	chr2:114036007-114036414	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr2:114035602-114035673	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr2:114034382-114035262	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr2:114030725-114030863	HepG2	liver:	n/a	n/a
9	CTBP2	chr2:114033409-114033857	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr2:114034159-114036770	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr2:114030740-114030890	GM12869	blood:	n/a	n/a
12	CTCF	chr2:114030671-114030679	Spleen_OC	spleen:	n/a	n/a
13	CTCF	chr2:114030800-114030950	GM12864	blood:	n/a	n/a
14	CTCF	chr2:114030740-114030890	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr2:114030620-114030870	NHDF-neo	bronchial:	n/a	n/a
16	CTCF	chr2:114030740-114030890	HEK293	kidney:	n/a	n/a
17	CTCF	chr2:114030720-114030870	GM12873	blood:	n/a	n/a
18	CTCF	chr2:114030720-114030870	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr2:114030740-114030890	HMF	breast:	n/a	n/a
20	CTCF	chr2:114030611-114030999	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr2:114030820-114030970	GM12872	blood:	n/a	n/a
22	CTCF	chr2:114017148-114017216	Lung_OC	lung:	n/a	n/a
23	CTCF	chr2:114030751-114030912	A549	lung:	n/a	n/a
24	CTCF	chr2:114030720-114030870	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr2:114030742-114030951	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr2:114030761-114030885	MCF-7	breast:	n/a	n/a
27	CTCF	chr2:114030720-114030870	GM12866	blood:	n/a	n/a
28	CTCF	chr2:114030800-114030950	GM12875	blood:	n/a	n/a
29	CTCF	chr2:114030740-114030890	GM12866	blood:	n/a	n/a
30	CTCF	chr2:114030740-114030890	HRE	kidney:	n/a	n/a
31	CTCF	chr2:114030720-114030870	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr2:114030720-114030870	AG09309	skin:	n/a	n/a
33	CTCF	chr2:114030760-114030910	AG09309	skin:	n/a	n/a
34	CTCF	chr2:114030800-114030950	HMF	breast:	n/a	n/a
35	CTCF	chr2:114030760-114030910	HepG2	liver:	n/a	n/a
36	CTCF	chr2:114030780-114030930	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr2:114030740-114030890	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:114030720-114030870	AG09319	gingival:	n/a	n/a
39	CTCF	chr2:114030700-114030850	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr2:114030690-114030922	HepG2	liver:	n/a	n/a
41	CTCF	chr2:114030760-114030910	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr2:114030740-114030890	AG04450	lung:	n/a	n/a
43	CTCF	chr2:114030718-114030910	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr2:114030800-114030950	GM12869	blood:	n/a	n/a
45	CTCF	chr2:114030700-114030850	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr2:114030748-114030905	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:114030784-114030835	GM19238	blood:	n/a	n/a
48	CTCF	chr2:114021280-114021430	NHDF-neo	bronchial:	n/a	chr2:114021298-114021311
49	CTCF	chr2:114030699-114030887	K562	blood:	n/a	n/a
50	CTCF	chr2:114030860-114031010	GM12867	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114036685-114036735	Hepatocyte	liver:	n/a
2	chr2:114036685-114036735	Hepatocyte	liver:	n/a
3	chr2:114033360-114033410	HRCEpiC	kidney:	n/a
4	chr2:114035193-114035243	ovcar-3	ovarian:	n/a
5	chr2:114033581-114033631	GM12891	blood:	n/a
6	chr2:114035193-114035243	Caco-2	colon:	n/a
7	chr2:114030824-114030874	PFSK-1	brain:	n/a
8	chr2:114033490-114033540	BE2_C	brain:	n/a
9	chr2:114035619-114035669	HRE	kidney:	n/a
10	chr2:114034595-114034645	AG04450	lung:	fetal
11	chr2:114033830-114033880	GM12878	blood:	n/a
12	chr2:114033490-114033540	HAEpiC	amniotic membrane:	n/a
13	chr2:114034595-114034645	SAEC	small airway:	n/a
14	chr2:114036571-114036621	HL-60	blood:	n/a
15	chr2:114033581-114033631	BE2_C	brain:	n/a
16	chr2:114033490-114033540	AG09309	skin:	n/a
17	chr2:114036444-114036494	GM12891	blood:	n/a
18	chr2:114036571-114036621	A549	lung:	n/a
19	chr2:114036685-114036735	HCF	heart:	n/a
20	chr2:114034534-114034584	Hepatocyte	liver:	n/a
21	chr2:114033830-114033880	NHBE	bronchial:	n/a
22	chr2:114034595-114034645	HepG2	liver:	n/a
23	chr2:114036571-114036621	SK-N-SH_RA	brain:	n/a
24	chr2:114036685-114036735	K562	blood:	n/a
25	chr2:114034534-114034584	SKMC	muscle:	n/a
26	chr2:114030824-114030874	HUVEC	blood vessel:	n/a
27	chr2:114035983-114036033	A549	lung:	n/a
28	chr2:114035619-114035669	HAEpiC	amniotic membrane:	n/a
29	chr2:114033490-114033540	GM12891	blood:	n/a
30	chr2:114030824-114030874	GM12878	blood:	n/a
31	chr2:114035619-114035669	PFSK-1	brain:	n/a
32	chr2:114036444-114036494	BJ	skin:	n/a
33	chr2:114036444-114036494	NT2-D1	testis:	n/a
34	chr2:114033360-114033410	CMK	blood:	n/a
35	chr2:114033581-114033631	Jurkat	blood:	n/a
36	chr2:114030824-114030874	HIPEpiC	eye:	n/a
37	chr2:114035983-114036033	HAEpiC	amniotic membrane:	n/a
38	chr2:114036685-114036735	MCF10A-Er-Src	breast:	n/a
39	chr2:114036571-114036621	HAEpiC	amniotic membrane:	n/a
40	chr2:114033830-114033880	T-47D	breast:	n/a
41	chr2:114034595-114034645	H1-hESC	embryonic stem cell:	embryo
42	chr2:114035193-114035243	NT2-D1	testis:	n/a
43	chr2:114033581-114033631	K562	blood:	n/a
44	chr2:114034534-114034584	AoSMC	blood vessel:	n/a
45	chr2:114034534-114034584	HMEC	breast:	n/a
46	chr2:114036953-114037003	HRPEpiC	eye:	n/a
47	chr2:114036571-114036621	RPTEC	kidney:	n/a
48	chr2:114035193-114035243	T-47D	breast:	n/a
49	chr2:114030824-114030874	AG09319	gingival:	n/a
50	chr2:114036444-114036494	PANC-1	pancreas:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:114033208..114035776-chr2:114039656..114042402,2	K562	blood:
2	chr2:114031113..114032698-chr2:114037168..114039837,2	MCF-7	breast:
3	chr2:114023172..114025279-chr2:114025318..114027200,2	MCF-7	breast:
4	chr2:114026056..114028346-chr2:114029301..114030897,2	MCF-7	breast:
5	chr2:114026056..114028346-chr2:114029301..114030897,2	MCF-7	breast:
6	chr2:113996531..113999009-chr2:114030396..114033362,2	K562	blood:
7	chr2:114023172..114025279-chr2:114025318..114027200,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSD4-1	chr2:114023053-114023157	NONHSAT073773
2	lnc-PSD4-1	chr2:114016841-114017161	ENSG00000189223.9
3	lnc-PSD4-1	chr2:114016841-114017161	ENSG00000189223
4	lnc-PSD4-1	chr2:114020855-114021031	ENSG00000189223
5	lnc-PSD4-1	chr2:114023053-114023294	ENSG00000189223
6	lnc-PSD4-1	chr2:114030634-114030847	ENSG00000189223.9
7	lnc-PSD4-1	chr2:114016841-114017161	ENSG00000189223.9
8	lnc-PSD4-1	chr2:114020855-114021031	ENSG00000189223
9	lnc-PSD4-1	chr2:114020855-114020939	ENSG00000189223
10	lnc-PSD4-1	chr2:114020855-114021031	ENSG00000189223.9
11	lnc-PSD4-1	chr2:114023053-114023157	ENSG00000189223.9
12	lnc-PSD4-1	chr2:114023053-114034158	ENSG00000189223.9
13	lnc-PSD4-1	chr2:114016841-114017161	ENSG00000189223
14	lnc-PSD4-1	chr2:114023053-114024587	ENSG00000189223
15	lnc-PSD4-1	chr2:114023053-114024550	ENSG00000189223
16	lnc-PSD4-1	chr2:114020855-114020939	ENSG00000189223.9
17	lnc-PSD4-1	chr2:114020855-114021031	ENSG00000189223.9
18	lnc-PSD4-1	chr2:114029413-114029548	ENSG00000189223.9
19	lnc-AC016745.1-7	chr2:114031713-114033283	NONHSAT073774
20	lnc-PSD4-1	chr2:114020855-114021031	ENSG00000189223
21	lnc-PSD4-1	chr2:114020855-114021031	ENSG00000189223
22	lnc-PSD4-1	chr2:114016841-114017161	ENSG00000189223
23	lnc-PSD4-1	chr2:114023053-114023747	ENSG00000189223
24	lnc-PSD4-1	chr2:114020884-114021031	NONHSAT073773
25	lnc-PSD4-1	chr2:114027778-114027808	NONHSAT073773
26	lnc-PSD4-1	chr2:114027778-114027884	ENSG00000189223.9

No data

Variant related genes	Relation type
PAX8	TF binding region
PAX8	CpG island
ENSG00000258395	chromatin interactions
CXCL12	miRNA target sites
TMEM188	miRNA target sites
HIST2H2BE	miRNA target sites
C12orf35	miRNA target sites
SLC39A6	miRNA target sites
RPSA	miRNA target sites

Extended variants
information (count: 752 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:752 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530908972	chr2:114015611-114015612	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs11887525	chr2:114015692-114015693	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147083084	chr2:114015693-114015694	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs533367662	chr2:114015711-114015712	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs193133547	chr2:114015753-114015754	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs567059418	chr2:114015762-114015763	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529630740	chr2:114015774-114015775	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs548698788	chr2:114015779-114015780	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs568862973	chr2:114015815-114015816	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138427799	chr2:114015823-114015824	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557895822	chr2:114015864-114015865	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370510326	chr2:114015878-114015879	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571419967	chr2:114015885-114015886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561307430	chr2:114015919-114015920	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553998442	chr2:114015922-114015923	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185738047	chr2:114015954-114015955	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143924408	chr2:114015995-114015996	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189050718	chr2:114016000-114016001	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs575249213	chr2:114016008-114016009	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs544256114	chr2:114016014-114016015	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs180908497	chr2:114016070-114016071	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs6743571	chr2:114016071-114016072	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs540413078	chr2:114016105-114016106	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs560767127	chr2:114016118-114016119	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs185543375	chr2:114016119-114016120	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs77625234	chr2:114016158-114016159	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs562304308	chr2:114016159-114016160	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs531335222	chr2:114016206-114016207	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551472980	chr2:114016300-114016301	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571379204	chr2:114016308-114016309	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528688391	chr2:114016312-114016313	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150628515	chr2:114016342-114016343	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547252118	chr2:114016343-114016344	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567497263	chr2:114016358-114016359	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72831838	chr2:114016401-114016402	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs565599815	chr2:114016407-114016408	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188830439	chr2:114016502-114016503	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181586711	chr2:114016506-114016507	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537866736	chr2:114016569-114016570	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557765733	chr2:114016616-114016617	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531260171	chr2:114016620-114016621	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78479394	chr2:114016640-114016641	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540769564	chr2:114016642-114016643	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186231492	chr2:114016660-114016661	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574186255	chr2:114016682-114016683	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542904422	chr2:114016739-114016740	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563197330	chr2:114016754-114016755	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531297688	chr2:114016782-114016783	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551379516	chr2:114016811-114016812	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564899824	chr2:114016837-114016838	Genic enhancers Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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	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
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
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113998200-114020600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr2:113999600-114016400	Weak transcription	Fetal Stomach	stomach
3	chr2:113999600-114028400	Weak transcription	Ovary	ovary
4	chr2:114006600-114016200	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr2:114006600-114016200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr2:114006800-114015800	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr2:114007200-114016800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:114008400-114016000	Enhancers	Primary T cells fromperipheralblood	blood
9	chr2:114009800-114019000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr2:114010000-114016200	Enhancers	Primary T cells from cord blood	blood
11	chr2:114010000-114016200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr2:114010200-114015800	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr2:114010200-114030400	Weak transcription	GM12878-XiMat	blood
14	chr2:114010400-114022400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr2:114011200-114016200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:114013000-114015600	Strong transcription	Duodenum Mucosa	Duodenum
17	chr2:114013000-114016400	Weak transcription	Dnd41	blood
18	chr2:114013200-114015600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:114013200-114016200	Enhancers	HSMMtube	muscle
20	chr2:114013200-114016400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr2:114013200-114019600	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr2:114013400-114017600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:114013400-114018200	Weak transcription	Fetal Kidney	kidney
24	chr2:114013600-114016000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:114013600-114020000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:114013800-114016000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr2:114013800-114016200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr2:114013800-114016200	Enhancers	Psoas Muscle	Psoas
29	chr2:114013800-114016200	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr2:114013800-114019800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr2:114014000-114018400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:114014400-114016600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:114014600-114016000	Weak transcription	Placenta	Placenta
34	chr2:114014800-114015600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:114014800-114015600	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr2:114014800-114015600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr2:114014800-114015800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:114014800-114015800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr2:114014800-114015800	Enhancers	Lung	lung
40	chr2:114014800-114015800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr2:114014800-114016200	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr2:114014800-114016400	Enhancers	Fetal Heart	heart
43	chr2:114015000-114016000	Enhancers	Primary hematopoietic stem cells	blood
44	chr2:114015000-114016200	Enhancers	Fetal Muscle Leg	muscle
45	chr2:114015200-114015600	Weak transcription	HSMM	muscle
46	chr2:114015200-114015800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:114015200-114015800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr2:114015200-114016000	Enhancers	A549	lung
49	chr2:114015200-114016800	Weak transcription	Adipose Nuclei	Adipose
50	chr2:114015200-114018600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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