Variant report

Variant	nsv963706
Chromosome Location	chr2:114144729-114162579
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	ARID3A	chr2:114147934-114148353	K562	blood:	n/a	n/a
2	ARID3A	chr2:114147862-114148323	HepG2	liver:	n/a	n/a
3	ATF2	chr2:114147524-114148275	GM12878	blood:	n/a	n/a
4	ATF3	chr2:114147873-114148254	GM12878	blood:	n/a	n/a
5	BATF	chr2:114147663-114148035	GM12878	blood:	n/a	n/a
6	BATF	chr2:114147578-114148177	GM12878	blood:	n/a	n/a
7	BCLAF1	chr2:114147751-114148357	GM12878	blood:	n/a	chr2:114147920-114147927
8	BHLHE40	chr2:114147990-114148308	K562	blood:	n/a	n/a
9	BHLHE40	chr2:114147870-114148423	GM12878	blood:	n/a	n/a
10	BRCA1	chr2:114147927-114148172	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr2:114147881-114148337	K562	blood:	n/a	n/a
12	CEBPB	chr2:114145910-114146103	A549	lung:	n/a	n/a
13	CEBPB	chr2:114145953-114146153	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:114145875-114146124	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:114147911-114148242	Hela-S3	cervix:	n/a	n/a
16	CHD1	chr2:114147965-114148165	GM12878	blood:	n/a	n/a
17	CHD2	chr2:114147764-114148319	GM12878	blood:	n/a	n/a
18	CTCF	chr2:114147820-114147970	A549	lung:	n/a	n/a
19	CTCF	chr2:114148100-114148250	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr2:114148008-114148137	MCF-7	breast:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148009-114148025
21	CTCF	chr2:114147980-114148130	SK-N-SH_RA	brain:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
22	CTCF	chr2:114148000-114148150	HRE	kidney:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
23	CTCF	chr2:114147781-114148333	K562	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
24	CTCF	chr2:114147945-114148190	MCF-7	breast:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
25	CTCF	chr2:114147980-114148130	AoAF	blood vessel:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
26	CTCF	chr2:114147720-114147870	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr2:114155816-114155851	Lung_OC	lung:	n/a	n/a
28	CTCF	chr2:114147980-114148130	GM12869	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
29	CTCF	chr2:114147960-114148110	GM12868	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
30	CTCF	chr2:114147980-114148130	GM12874	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
31	CTCF	chr2:114147925-114148206	MCF-7	breast:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
32	CTCF	chr2:114147980-114148130	HPF	lung:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
33	CTCF	chr2:114147980-114148130	Caco-2	colon:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
34	CTCF	chr2:114148000-114148150	GM12869	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
35	CTCF	chr2:114148040-114148190	Caco-2	colon:	n/a	chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094
36	CTCF	chr2:114147980-114148130	HEK293	kidney:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
37	CTCF	chr2:114147783-114148435	MCF-7	breast:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
38	CTCF	chr2:114147908-114148207	SK-N-SH_RA	brain:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
39	CTCF	chr2:114147980-114148130	GM12870	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
40	CTCF	chr2:114147873-114148223	Pancreas_OC	pancreas:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
41	CTCF	chr2:114147980-114148130	HBMEC	blood vessel:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
42	CTCF	chr2:114147960-114148110	HAc	cerebellar:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
43	CTCF	chr2:114147835-114148277	ECC-1	luminal epithelium:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
44	CTCF	chr2:114148020-114148170	GM12865	blood:	n/a	chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094
45	CTCF	chr2:114147940-114148090	HCM	heart:	n/a	chr2:114148008-114148026 chr2:114148081-114148089 chr2:114148003-114148024 chr2:114148009-114148025
46	CTCF	chr2:114147941-114148178	SK-N-SH_RA	brain:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
47	CTCF	chr2:114148020-114148170	HCM	heart:	n/a	chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094
48	CTCF	chr2:114147980-114148130	NB4	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
49	CTCF	chr2:114147833-114148223	Lung_OC	lung:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025
50	CTCF	chr2:114147980-114148130	GM12801	blood:	n/a	chr2:114148008-114148026 chr2:114148071-114148092 chr2:114148081-114148089 chr2:114148076-114148094 chr2:114148003-114148024 chr2:114148009-114148025

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114151353-114151403	IMR90	lung:	fetal
2	chr2:114151353-114151403	RPTEC	kidney:	n/a
3	chr2:114151353-114151403	Caco-2	colon:	n/a
4	chr2:114151353-114151403	ovcar-3	ovarian:	n/a
5	chr2:114151353-114151403	MCF-7	breast:	n/a
6	chr2:114151353-114151403	Jurkat	blood:	n/a
7	chr2:114151353-114151403	Hela-S3	cervix:	n/a
8	chr2:114151353-114151403	LNCaP	prostate:	n/a
9	chr2:114151353-114151403	HIPEpiC	eye:	n/a
10	chr2:114151353-114151403	HCF	heart:	n/a
11	chr2:114151353-114151403	HepG2	liver:	n/a
12	chr2:114151353-114151403	HNPCEpiC	eye:	n/a
13	chr2:114151353-114151403	CMK	blood:	n/a
14	chr2:114151353-114151403	GM12891	blood:	n/a
15	chr2:114151353-114151403	HEEpiC	esophagus:	n/a
16	chr2:114151353-114151403	NB4	blood:	n/a
17	chr2:114151353-114151403	GM12878	blood:	n/a
18	chr2:114151353-114151403	BJ	skin:	n/a
19	chr2:114151353-114151403	SK-N-SH_RA	brain:	n/a
20	chr2:114151353-114151403	HEK293	kidney:	embryo
21	chr2:114151353-114151403	SK-N-MC	brain:	n/a
22	chr2:114151353-114151403	PANC-1	pancreas:	n/a
23	chr2:114151353-114151403	SK-N-SH	brain:	n/a
24	chr2:114151353-114151403	HMEC	breast:	n/a
25	chr2:114151353-114151403	NHDF-neo	bronchial:	n/a
26	chr2:114151353-114151403	AG09319	gingival:	n/a
27	chr2:114151353-114151403	AG04449	skin:	fetal
28	chr2:114151353-114151403	HAEpiC	amniotic membrane:	n/a
29	chr2:114151353-114151403	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:114151353-114151403	GM19239	blood:	n/a
31	chr2:114151353-114151403	ProgFib	skin:	n/a
32	chr2:114151353-114151403	PFSK-1	brain:	n/a
33	chr2:114151353-114151403	GM06990	blood:	n/a
34	chr2:114151353-114151403	AG04450	lung:	fetal
35	chr2:114151353-114151403	SAEC	small airway:	n/a
36	chr2:114151353-114151403	K562	blood:	n/a
37	chr2:114151353-114151403	HCT-116	colon:	n/a
38	chr2:114151353-114151403	HCM	heart:	n/a
39	chr2:114151353-114151403	Hepatocyte	liver:	n/a
40	chr2:114151353-114151403	SKMC	muscle:	n/a
41	chr2:114151353-114151403	HL-60	blood:	n/a
42	chr2:114151353-114151403	HRPEpiC	eye:	n/a
43	chr2:114151353-114151403	GM12892	blood:	n/a
44	chr2:114151353-114151403	HUVEC	blood vessel:	n/a
45	chr2:114151353-114151403	HCPEpiC	choroid plexus:	n/a
46	chr2:114151353-114151403	U87	brain:	n/a
47	chr2:114151353-114151403	AG09309	skin:	n/a
48	chr2:114151353-114151403	PrEC	prostate:	n/a
49	chr2:114151353-114151403	MCF10A-Er-Src	breast:	n/a
50	chr2:114151353-114151403	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:97777932..97778642-chr2:114147602..114148330,3	MCF-7	breast:
2	chr2:114006461..114007910-chr2:114147631..114148371,4	K562	blood:
3	chr2:97778139..97778659-chr2:114147598..114148210,2	K562	blood:
4	chr2:114140085..114141972-chr2:114145675..114147776,2	K562	blood:
5	chr2:113837351..113838104-chr2:114147540..114148341,3	K562	blood:
6	chr2:113961603..113962131-chr2:114147652..114148320,2	K562	blood:
7	chr2:113958498..113959276-chr2:114147736..114148311,2	K562	blood:
8	chr2:113961183..113962044-chr2:114147703..114148314,2	MCF-7	breast:
9	chr2:113894600..113895171-chr2:114147816..114148753,2	MCF-7	breast:
10	chr2:114159767..114162349-chr2:114163621..114165460,2	MCF-7	breast:
11	chr2:113895658..113897096-chr2:114147534..114148565,6	K562	blood:
12	chr12:808962..809943-chr2:114147779..114148497,2	MCF-7	breast:
13	chr2:97778136..97778658-chr2:114147633..114148424,9	MCF-7	breast:

Variant related genes	Relation type
IGKV1OR2-108	TF binding region
IGKV1OR2-108	CpG island
ENSG00000231292	chromatin interactions

Extended variants
information (count: 632 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573968716	chr2:114144733-114144734	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs142494283	chr2:114144736-114144737	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs192797954	chr2:114144768-114144769	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs536579418	chr2:114144816-114144817	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143941894	chr2:114144819-114144820	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs112560446	chr2:114144820-114144821	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs548426650	chr2:114144822-114144823	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs568369356	chr2:114144875-114144876	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs11686610	chr2:114144913-114144914	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs184750344	chr2:114144929-114144930	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs6728162	chr2:114144936-114144937	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs539153481	chr2:114144938-114144939	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs35097808	chr2:114144962-114144963	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs558807060	chr2:114144972-114144973	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs566231759	chr2:114144979-114144980	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs188787466	chr2:114145023-114145024	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554795432	chr2:114145028-114145029	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs192105593	chr2:114145033-114145034	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs542999088	chr2:114145034-114145035	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs184410713	chr2:114145065-114145066	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543807460	chr2:114145082-114145083	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs113648209	chr2:114145091-114145092	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs545847233	chr2:114145189-114145190	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs369255798	chr2:114145190-114145191	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs111996483	chr2:114145222-114145223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371818820	chr2:114145270-114145271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559190044	chr2:114145306-114145307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528240664	chr2:114145313-114145314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11123183	chr2:114145320-114145321	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs11123184	chr2:114145327-114145328	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs561178017	chr2:114145335-114145336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530863197	chr2:114145358-114145359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11123185	chr2:114145395-114145396	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs570039810	chr2:114145419-114145420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532418448	chr2:114145424-114145425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552600628	chr2:114145457-114145458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147723212	chr2:114145507-114145508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185473864	chr2:114145509-114145510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546612068	chr2:114145518-114145519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10194893	chr2:114145542-114145543	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532358257	chr2:114145612-114145613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537319466	chr2:114145614-114145615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10194994	chr2:114145639-114145640	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs576729994	chr2:114145641-114145642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368203491	chr2:114145679-114145680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545481880	chr2:114145683-114145684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553026762	chr2:114145699-114145700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189165161	chr2:114145718-114145719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73955025	chr2:114145749-114145750	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs569246603	chr2:114145774-114145775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114128800-114147400	Weak transcription	A549	lung
2	chr2:114143800-114145800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr2:114144200-114145200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr2:114145200-114145800	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr2:114145400-114147600	Weak transcription	NHEK	skin
6	chr2:114145800-114147000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr2:114145800-114147200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr2:114146400-114147600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr2:114146400-114147600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr2:114146800-114147600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:114147000-114147600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr2:114147200-114147600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr2:114147400-114147600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:114147400-114147600	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr2:114147400-114147600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr2:114147400-114147600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr2:114147400-114147600	Enhancers	Dnd41	blood
18	chr2:114147400-114147600	Enhancers	GM12878-XiMat	blood
19	chr2:114147400-114148400	Enhancers	A549	lung
20	chr2:114147600-114147800	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr2:114147600-114147800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
22	chr2:114147600-114147800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
23	chr2:114147600-114147800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
24	chr2:114147600-114147800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:114147600-114147800	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr2:114147600-114147800	Flanking Active TSS	Rectal Smooth Muscle	rectum
27	chr2:114147600-114147800	Flanking Active TSS	Dnd41	blood
28	chr2:114147600-114147800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr2:114147600-114148000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:114147600-114148000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:114147600-114148000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr2:114147600-114148000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr2:114147600-114148000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
34	chr2:114147600-114148000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
35	chr2:114147600-114148000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr2:114147600-114148000	Active TSS	Muscle Satellite Cultured Cells	--
37	chr2:114147600-114148000	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr2:114147600-114148000	Active TSS	Fetal Thymus	thymus
39	chr2:114147600-114148000	Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr2:114147600-114148000	Active TSS	Stomach Smooth Muscle	stomach
41	chr2:114147600-114148000	Active TSS	Thymus	Thymus
42	chr2:114147600-114148000	Active TSS	NHDF-Ad	bronchial
43	chr2:114147600-114148200	Active TSS	Primary monocytes fromperipheralblood	blood
44	chr2:114147600-114148200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr2:114147600-114148200	Active TSS	Primary T cells from cord blood	blood
46	chr2:114147600-114148200	Active TSS	Primary T cells fromperipheralblood	blood
47	chr2:114147600-114148200	Active TSS	Primary hematopoietic stem cells	blood
48	chr2:114147600-114148200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr2:114147600-114148200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr2:114147600-114148200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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