Variant report

Variant	esv33134
Chromosome Location	chr2:191318791-191365710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:546)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:191333834-191334379	K562	blood:	n/a	n/a
2	ARID3A	chr2:191324271-191324420	K562	blood:	n/a	n/a
3	ARID3A	chr2:191327384-191327693	K562	blood:	n/a	n/a
4	ARID3A	chr2:191342333-191342599	K562	blood:	n/a	n/a
5	ARID3A	chr2:191329810-191330124	K562	blood:	n/a	n/a
6	ATF1	chr2:191324700-191325011	K562	blood:	n/a	n/a
7	ATF1	chr2:191333965-191334272	K562	blood:	n/a	n/a
8	ATF2	chr2:191329491-191330341	GM12878	blood:	n/a	n/a
9	ATF3	chr2:191362301-191362530	K562	blood:	n/a	n/a
10	BCLAF1	chr2:191329760-191330340	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:191327288-191327671	K562	blood:	n/a	n/a
12	BHLHE40	chr2:191324672-191325571	K562	blood:	n/a	chr2:191325398-191325407 chr2:191325397-191325406 chr2:191325398-191325407
13	BHLHE40	chr2:191323080-191323155	K562	blood:	n/a	n/a
14	BHLHE40	chr2:191342404-191342604	K562	blood:	n/a	n/a
15	BRCA1	chr2:191346809-191346816	GM12878	blood:	n/a	n/a
16	CBX3	chr2:191324539-191325015	K562	blood:	n/a	n/a
17	CBX3	chr2:191327272-191327771	K562	blood:	n/a	n/a
18	CBX3	chr2:191356631-191356886	K562	blood:	n/a	n/a
19	CCNT2	chr2:191324648-191324999	K562	blood:	n/a	chr2:191324843-191324863
20	CCNT2	chr2:191325208-191325408	K562	blood:	n/a	n/a
21	CCNT2	chr2:191329884-191330038	K562	blood:	n/a	n/a
22	CCNT2	chr2:191333987-191334325	K562	blood:	n/a	n/a
23	CCNT2	chr2:191359626-191359974	K562	blood:	n/a	n/a
24	CCNT2	chr2:191342398-191342594	K562	blood:	n/a	n/a
25	CCNT2	chr2:191327313-191327808	K562	blood:	n/a	chr2:191327522-191327542
26	CEBPB	chr2:191362223-191362569	MCF-7	breast:	n/a	chr2:191362394-191362405
27	CEBPB	chr2:191321347-191321377	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:191327000-191327276	K562	blood:	n/a	chr2:191327137-191327148 chr2:191327108-191327119
29	CEBPB	chr2:191325326-191325543	K562	blood:	n/a	n/a
30	CEBPB	chr2:191362271-191362526	K562	blood:	n/a	chr2:191362394-191362405
31	CEBPB	chr2:191362251-191362544	A549	lung:	n/a	chr2:191362394-191362405
32	CEBPB	chr2:191324704-191325033	K562	blood:	n/a	n/a
33	CEBPB	chr2:191357884-191358175	HepG2	liver:	n/a	chr2:191358052-191358063
34	CEBPB	chr2:191362277-191362482	HepG2	liver:	n/a	chr2:191362394-191362405
35	CEBPB	chr2:191364967-191365286	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:191362223-191362575	HepG2	liver:	n/a	chr2:191362394-191362405
37	CEBPB	chr2:191333769-191334217	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:191362296-191362496	Hela-S3	cervix:	n/a	chr2:191362394-191362405
39	CEBPB	chr2:191357976-191358173	A549	lung:	n/a	chr2:191358052-191358063
40	CEBPB	chr2:191365050-191365250	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:191365075-191365207	A549	lung:	n/a	n/a
42	CEBPB	chr2:191362227-191362560	K562	blood:	n/a	chr2:191362394-191362405
43	CEBPB	chr2:191362150-191362678	MCF-7	breast:	n/a	chr2:191362394-191362405
44	CEBPB	chr2:191365056-191365170	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:191333746-191334271	A549	lung:	n/a	n/a
46	CEBPB	chr2:191327026-191327221	HepG2	liver:	n/a	chr2:191327137-191327148 chr2:191327108-191327119
47	CEBPB	chr2:191324628-191325063	K562	blood:	n/a	n/a
48	CEBPB	chr2:191333833-191334274	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr2:191362236-191362521	H1-hESC	embryonic stem cell:	n/a	chr2:191362394-191362405
50	CEBPB	chr2:191358064-191358065	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:191343262-191343312	SK-N-SH	brain:	n/a
2	chr2:191365138-191365188	ECC-1	luminal epithelium:	n/a
3	chr2:191365138-191365188	HRPEpiC	eye:	n/a
4	chr2:191365138-191365188	AG04449	skin:	fetal
5	chr2:191343262-191343312	SK-N-SH_RA	brain:	n/a
6	chr2:191343262-191343312	HMEC	breast:	n/a
7	chr2:191343262-191343312	AG10803	skin:	n/a
8	chr2:191365138-191365188	HMEC	breast:	n/a
9	chr2:191343262-191343312	RPTEC	kidney:	n/a
10	chr2:191343262-191343312	LNCaP	prostate:	n/a
11	chr2:191365138-191365188	ovcar-3	ovarian:	n/a
12	chr2:191365138-191365188	HRCEpiC	kidney:	n/a
13	chr2:191365138-191365188	PFSK-1	brain:	n/a
14	chr2:191365138-191365188	HUVEC	blood vessel:	n/a
15	chr2:191365138-191365188	HIPEpiC	eye:	n/a
16	chr2:191365138-191365188	NH-A	brain:	n/a
17	chr2:191343262-191343312	U87	brain:	n/a
18	chr2:191365138-191365188	ProgFib	skin:	n/a
19	chr2:191365138-191365188	HEK293	kidney:	embryo
20	chr2:191343262-191343312	NT2-D1	testis:	n/a
21	chr2:191365138-191365188	Jurkat	blood:	n/a
22	chr2:191343262-191343312	HEEpiC	esophagus:	n/a
23	chr2:191365138-191365188	HEEpiC	esophagus:	n/a
24	chr2:191365138-191365188	HCM	heart:	n/a
25	chr2:191365138-191365188	AG09309	skin:	n/a
26	chr2:191343262-191343312	HEK293	kidney:	embryo
27	chr2:191343262-191343312	CMK	blood:	n/a
28	chr2:191343262-191343312	Jurkat	blood:	n/a
29	chr2:191365138-191365188	HCF	heart:	n/a
30	chr2:191343262-191343312	AG09309	skin:	n/a
31	chr2:191343262-191343312	HL-60	blood:	n/a
32	chr2:191343262-191343312	A549	lung:	n/a
33	chr2:191343262-191343312	HCF	heart:	n/a
34	chr2:191343262-191343312	SKMC	muscle:	n/a
35	chr2:191343262-191343312	HRCEpiC	kidney:	n/a
36	chr2:191365138-191365188	H1-hESC	embryonic stem cell:	embryo
37	chr2:191365138-191365188	NHDF-neo	bronchial:	n/a
38	chr2:191365138-191365188	T-47D	breast:	n/a
39	chr2:191343262-191343312	IMR90	lung:	fetal
40	chr2:191343262-191343312	PrEC	prostate:	n/a
41	chr2:191343262-191343312	NHDF-neo	bronchial:	n/a
42	chr2:191365138-191365188	HNPCEpiC	eye:	n/a
43	chr2:191365138-191365188	NHBE	bronchial:	n/a
44	chr2:191365138-191365188	GM12891	blood:	n/a
45	chr2:191343262-191343312	AG04450	lung:	fetal
46	chr2:191365138-191365188	A549	lung:	n/a
47	chr2:191365138-191365188	GM19239	blood:	n/a
48	chr2:191343262-191343312	GM12892	blood:	n/a
49	chr2:191365138-191365188	HL-60	blood:	n/a
50	chr2:191365138-191365188	MCF10A-Er-Src	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:191271631..191274450-chr2:191332507..191334267,2	MCF-7	breast:
2	chr2:191352866..191353470-chr2:191362410..191363076,2	MCF-7	breast:
3	chr2:191271518..191274523-chr2:191322577..191324895,3	K562	blood:
4	chr2:191332610..191334392-chr2:191512174..191513999,2	K562	blood:
5	chr2:191323309..191325277-chr2:191325283..191326874,2	MCF-7	breast:
6	chr2:191272262..191274939-chr2:191333629..191335814,2	MCF-7	breast:
7	chr2:191271856..191274509-chr2:191327501..191329614,2	MCF-7	breast:
8	chr2:191323309..191325277-chr2:191325283..191326874,2	MCF-7	breast:
9	chr2:191318515..191323057-chr2:191332501..191335066,4	MCF-7	breast:
10	chr2:191183320..191185607-chr2:191359830..191362891,3	K562	blood:
11	chr2:191346074..191348706-chr2:191348723..191351195,2	MCF-7	breast:
12	chr2:191362897..191364895-chr2:191367365..191369091,2	MCF-7	breast:
13	chr2:191352866..191353470-chr2:191362410..191363076,2	MCF-7	breast:
14	chr2:191362838..191365518-chr2:191369727..191371363,2	K562	blood:
15	chr2:191319837..191321780-chr2:191409480..191411973,2	K562	blood:
16	chr2:191362419..191364235-chr2:191364760..191367673,2	MCF-7	breast:
17	chr2:191318515..191323057-chr2:191332501..191335066,4	MCF-7	breast:
18	chr2:191270853..191273774-chr2:191346461..191348908,2	MCF-7	breast:
19	chr2:191346074..191348706-chr2:191348723..191351195,2	MCF-7	breast:
20	chr2:191324546..191326612-chr2:191328587..191331332,2	K562	blood:
21	chr2:191272256..191273819-chr2:191346015..191348019,2	K562	blood:
22	chr2:191324546..191326612-chr2:191328587..191331332,2	K562	blood:
23	chr2:191244163..191247100-chr2:191325958..191329938,4	K562	blood:
24	chr2:191329948..191335204-chr2:191345053..191349333,4	MCF-7	breast:
25	chr2:191362419..191364235-chr2:191364760..191367673,2	MCF-7	breast:
26	chr2:191322695..191327408-chr2:191328013..191334645,7	K562	blood:
27	chr2:191317071..191321557-chr2:191322471..191325941,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM194B-3	chr2:191318818-191319247	ENSG00000272979.1
2	lnc-INPP1-1	chr2:191334484-191334581	NONHSAT076085

No data

Variant related genes	Relation type
ENSG00000272979	TF binding region
MFSD6	TF binding region
ENSG00000272979	CpG island
MFSD6	CpG island
ENSG00000198130	chromatin interactions
ENSG00000151690	chromatin interactions
ENSG00000138386	chromatin interactions
ENSG00000272979	chromatin interactions

Extended variants
information (count: 1613 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184861533	chr2:191318810-191318811	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs28620277	chr2:191318934-191318935	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs530339467	chr2:191318981-191318982	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs77936516	chr2:191318994-191318995	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs569916381	chr2:191319000-191319001	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs189659767	chr2:191319030-191319031	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs552640099	chr2:191319038-191319039	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs13410179	chr2:191319061-191319062	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs151202063	chr2:191319084-191319085	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs114763811	chr2:191319109-191319110	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs531903327	chr2:191319145-191319146	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs568335557	chr2:191319215-191319216	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs535753304	chr2:191319238-191319239	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs140252377	chr2:191319239-191319240	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs575500392	chr2:191319246-191319247	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs73979252	chr2:191319260-191319261	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs180888158	chr2:191319261-191319262	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145244682	chr2:191319282-191319283	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141244742	chr2:191319338-191319339	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572884365	chr2:191319356-191319357	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540189281	chr2:191319413-191319414	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184424112	chr2:191319476-191319477	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs530281554	chr2:191319530-191319531	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190564588	chr2:191319570-191319571	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374653357	chr2:191319613-191319614	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113730731	chr2:191319618-191319619	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs71863671	chr2:191319659-191319660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs147326871	chr2:191319692-191319693	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563687289	chr2:191319693-191319694	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148949934	chr2:191319694-191319695	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs367869498	chr2:191319702-191319703	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200434851	chr2:191319708-191319709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201705798	chr2:191319709-191319710	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs531113668	chr2:191319712-191319713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368805771	chr2:191319713-191319714	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377412166	chr2:191319719-191319720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552533664	chr2:191319726-191319727	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577092514	chr2:191319727-191319728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570891009	chr2:191319753-191319754	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181835088	chr2:191319770-191319771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562165432	chr2:191319812-191319813	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546970623	chr2:191319822-191319823	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568476019	chr2:191319827-191319828	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs535890733	chr2:191319870-191319871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550890484	chr2:191319875-191319876	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569203248	chr2:191319919-191319920	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138793878	chr2:191319924-191319925	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529454371	chr2:191319944-191319945	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs142267925	chr2:191319978-191319979	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201038149	chr2:191319980-191319981	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Ovarian cancer	21720365	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1301 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191302200-191319200	Weak transcription	Fetal Intestine Small	intestine
2	chr2:191302200-191321200	Weak transcription	Esophagus	oesophagus
3	chr2:191302400-191331000	Weak transcription	A549	lung
4	chr2:191302800-191319400	Weak transcription	Fetal Brain Female	brain
5	chr2:191302800-191320200	Weak transcription	Fetal Thymus	thymus
6	chr2:191302800-191321200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr2:191303400-191321000	Weak transcription	Thymus	Thymus
8	chr2:191303400-191321200	Weak transcription	Dnd41	blood
9	chr2:191303600-191321000	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr2:191303800-191321000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr2:191303800-191331600	Weak transcription	Brain Germinal Matrix	brain
12	chr2:191303800-191332600	Weak transcription	Fetal Intestine Large	intestine
13	chr2:191306600-191321000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr2:191306600-191351000	Weak transcription	Pancreas	Pancrea
15	chr2:191307600-191322600	Weak transcription	Aorta	Aorta
16	chr2:191308000-191328800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr2:191308800-191319000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr2:191308800-191320000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr2:191308800-191327200	Weak transcription	Right Atrium	heart
20	chr2:191309200-191322400	Weak transcription	Fetal Muscle Leg	muscle
21	chr2:191309400-191331400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr2:191310200-191323600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr2:191310400-191331600	Weak transcription	Stomach Mucosa	stomach
24	chr2:191311400-191324200	Weak transcription	Fetal Heart	heart
25	chr2:191311600-191321400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:191311600-191321400	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr2:191311600-191331400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr2:191311800-191324600	Weak transcription	Left Ventricle	heart
29	chr2:191311800-191331400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:191311800-191331400	Weak transcription	Rectal Smooth Muscle	rectum
31	chr2:191311800-191331600	Weak transcription	Ovary	ovary
32	chr2:191312000-191332400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr2:191312200-191321200	Weak transcription	Fetal Stomach	stomach
34	chr2:191312200-191324400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr2:191313000-191321200	Weak transcription	Gastric	stomach
36	chr2:191313000-191331400	Weak transcription	HSMMtube	muscle
37	chr2:191313000-191333600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr2:191313800-191323600	Weak transcription	Brain Anterior Caudate	brain
39	chr2:191314000-191331600	Weak transcription	Fetal Kidney	kidney
40	chr2:191315800-191327400	Weak transcription	Spleen	Spleen
41	chr2:191316200-191318800	Enhancers	Brain Hippocampus Middle	brain
42	chr2:191316200-191319200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr2:191316400-191321400	Weak transcription	Lung	lung
44	chr2:191316600-191321800	Weak transcription	Primary B cells from cord blood	blood
45	chr2:191316600-191323400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr2:191316600-191324600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr2:191316600-191325200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:191316600-191331200	Weak transcription	NHLF	lung
49	chr2:191317000-191323600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr2:191317200-191319400	Strong transcription	Primary T cells from cord blood	blood

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