Variant report

Variant	esv2762286
Chromosome Location	chr2:151351927-151395632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:305)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 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	ATF2	chr2:151385379-151385856	GM12878	blood:	n/a	n/a
2	ATF3	chr2:151383317-151383694	A549	lung:	n/a	n/a
3	BACH1	chr2:151385902-151386352	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:151385876-151386338	GM12878	blood:	n/a	n/a
5	BATF	chr2:151385475-151385786	GM12878	blood:	n/a	chr2:151385636-151385649
6	BCL11A	chr2:151385503-151385795	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:151385812-151386285	GM12878	blood:	n/a	chr2:151386170-151386179
8	BCL3	chr2:151383267-151383823	A549	lung:	n/a	n/a
9	BRCA1	chr2:151352174-151352862	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:151373419-151373907	A549	lung:	n/a	n/a
11	CEBPB	chr2:151352231-151353097	A549	lung:	n/a	chr2:151352446-151352455
12	CEBPB	chr2:151384063-151384473	MCF-7	breast:	n/a	n/a
13	CEBPB	chr2:151385834-151386409	A549	lung:	n/a	n/a
14	CEBPB	chr2:151386054-151386326	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:151352304-151352928	IMR90	lung:	n/a	chr2:151352446-151352455
16	CEBPB	chr2:151354005-151354110	K562	blood:	n/a	chr2:151354068-151354079
17	CEBPB	chr2:151388547-151388876	IMR90	lung:	n/a	chr2:151388683-151388694
18	CEBPB	chr2:151385908-151386425	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:151383248-151383878	A549	lung:	n/a	n/a
20	CEBPB	chr2:151383371-151383787	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr2:151373338-151373647	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:151352253-151353043	Hela-S3	cervix:	n/a	chr2:151352446-151352455
23	CEBPB	chr2:151383371-151383734	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:151383360-151383766	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:151385936-151386344	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:151383435-151383792	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr2:151383335-151383797	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:151353914-151354239	IMR90	lung:	n/a	chr2:151354068-151354079
29	CEBPB	chr2:151385798-151386451	A549	lung:	n/a	n/a
30	CEBPB	chr2:151389467-151389767	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:151388633-151388743	K562	blood:	n/a	chr2:151388683-151388694
32	CEBPB	chr2:151385562-151386361	A549	lung:	n/a	n/a
33	CEBPB	chr2:151352356-151352895	A549	lung:	n/a	chr2:151352446-151352455
34	CEBPB	chr2:151352420-151352877	A549	lung:	n/a	chr2:151352446-151352455
35	CEBPB	chr2:151385839-151386464	MCF-7	breast:	n/a	n/a
36	CEBPB	chr2:151386038-151386278	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:151377570-151378002	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:151353930-151354239	HepG2	liver:	n/a	chr2:151354068-151354079
39	CEBPB	chr2:151383345-151383767	A549	lung:	n/a	n/a
40	CEBPB	chr2:151383248-151383848	MCF-7	breast:	n/a	n/a
41	CEBPB	chr2:151353941-151354239	Hela-S3	cervix:	n/a	chr2:151354068-151354079
42	CEBPB	chr2:151388603-151388774	Hela-S3	cervix:	n/a	chr2:151388683-151388694
43	CEBPB	chr2:151384097-151384527	MCF-7	breast:	n/a	n/a
44	CEBPB	chr2:151370189-151370672	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:151373338-151373633	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:151353959-151354234	A549	lung:	n/a	chr2:151354068-151354079
47	CHD1	chr2:151386036-151386144	GM12878	blood:	n/a	n/a
48	CHD2	chr2:151383321-151383715	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr2:151352478-151353028	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr2:151379052-151379060	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:151389355-151389405	NHBE	bronchial:	n/a
2	chr2:151389355-151389405	GM12878	blood:	n/a
3	chr2:151389355-151389405	HepG2	liver:	n/a
4	chr2:151352580-151352630	NH-A	brain:	n/a
5	chr2:151377525-151377575	HCT-116	colon:	n/a
6	chr2:151377525-151377575	Caco-2	colon:	n/a
7	chr2:151389355-151389405	GM12891	blood:	n/a
8	chr2:151389355-151389405	PrEC	prostate:	n/a
9	chr2:151377525-151377575	AoSMC	blood vessel:	n/a
10	chr2:151386104-151386154	Caco-2	colon:	n/a
11	chr2:151352580-151352630	HCT-116	colon:	n/a
12	chr2:151386104-151386154	NHDF-neo	bronchial:	n/a
13	chr2:151389355-151389405	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:151386104-151386154	AG09319	gingival:	n/a
15	chr2:151377525-151377575	HepG2	liver:	n/a
16	chr2:151377525-151377575	K562	blood:	n/a
17	chr2:151377525-151377575	HEEpiC	esophagus:	n/a
18	chr2:151377525-151377575	GM12892	blood:	n/a
19	chr2:151386104-151386154	HNPCEpiC	eye:	n/a
20	chr2:151352580-151352630	Caco-2	colon:	n/a
21	chr2:151395457-151395507	SK-N-SH_RA	brain:	n/a
22	chr2:151386104-151386154	SAEC	small airway:	n/a
23	chr2:151395457-151395507	GM12892	blood:	n/a
24	chr2:151377525-151377575	SKMC	muscle:	n/a
25	chr2:151389355-151389405	ProgFib	skin:	n/a
26	chr2:151386104-151386154	H1-hESC	embryonic stem cell:	embryo
27	chr2:151389355-151389405	HRPEpiC	eye:	n/a
28	chr2:151377525-151377575	NB4	blood:	n/a
29	chr2:151386104-151386154	HL-60	blood:	n/a
30	chr2:151377525-151377575	Hepatocyte	liver:	n/a
31	chr2:151352580-151352630	HRE	kidney:	n/a
32	chr2:151352580-151352630	SKMC	muscle:	n/a
33	chr2:151386104-151386154	HMEC	breast:	n/a
34	chr2:151389355-151389405	A549	lung:	n/a
35	chr2:151395457-151395507	HMEC	breast:	n/a
36	chr2:151377525-151377575	A549	lung:	n/a
37	chr2:151377525-151377575	HAEpiC	amniotic membrane:	n/a
38	chr2:151389355-151389405	HMEC	breast:	n/a
39	chr2:151377525-151377575	SAEC	small airway:	n/a
40	chr2:151352580-151352630	NHDF-neo	bronchial:	n/a
41	chr2:151389355-151389405	HEEpiC	esophagus:	n/a
42	chr2:151395457-151395507	Caco-2	colon:	n/a
43	chr2:151352580-151352630	NB4	blood:	n/a
44	chr2:151377525-151377575	HUVEC	blood vessel:	n/a
45	chr2:151386104-151386154	MCF-7	breast:	n/a
46	chr2:151377525-151377575	Jurkat	blood:	n/a
47	chr2:151389355-151389405	Caco-2	colon:	n/a
48	chr2:151389355-151389405	U87	brain:	n/a
49	chr2:151377525-151377575	GM19239	blood:	n/a
50	chr2:151389355-151389405	GM12892	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:151380440..151382886-chr2:151384300..151385802,2	MCF-7	breast:
2	chr2:151343363..151344946-chr2:151394476..151396500,2	MCF-7	breast:
3	chr2:151384979..151386756-chr2:151443074..151444971,2	MCF-7	breast:
4	chr2:151342260..151345348-chr2:151358491..151361400,3	MCF-7	breast:
5	chr2:151340012..151345676-chr2:151379784..151387560,12	MCF-7	breast:
6	chr2:151376610..151379421-chr2:151457834..151460059,2	MCF-7	breast:
7	chr2:151376819..151380137-chr2:151381497..151383418,3	MCF-7	breast:
8	chr2:151377855..151379453-chr2:151381453..151383648,2	MCF-7	breast:
9	chr2:151342650..151345471-chr2:151380012..151385936,6	MCF-7	breast:
10	chr2:151341583..151344657-chr2:151352840..151355389,3	MCF-7	breast:
11	chr2:151383148..151383912-chr2:151466904..151467549,2	MCF-7	breast:
12	chr2:151342490..151344318-chr2:151365459..151367655,3	MCF-7	breast:
13	chr2:151342213..151344471-chr2:151377706..151379728,2	MCF-7	breast:
14	chr2:151377855..151379453-chr2:151381453..151383648,2	MCF-7	breast:
15	chr2:151342012..151344983-chr2:151388815..151393204,4	MCF-7	breast:
16	chr2:151376610..151379497-chr2:151451017..151452892,2	MCF-7	breast:
17	chr2:151334640..151336393-chr2:151360591..151362874,2	MCF-7	breast:
18	chr2:151376819..151380137-chr2:151381497..151383418,3	MCF-7	breast:
19	chr2:151380440..151382886-chr2:151384300..151385802,2	MCF-7	breast:

No data

Variant related genes	Relation type
RND3	TF binding region
RND3	CpG island
ENSG00000115963	chromatin interactions

Extended variants
information (count: 1560 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1560 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1569158	chr2:151351927-151351928	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530373466	chr2:151351961-151351962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555301143	chr2:151351991-151351992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs36040274	chr2:151351999-151352000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572111754	chr2:151352026-151352027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs12624003	chr2:151352033-151352034	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs541296539	chr2:151352055-151352056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs534785088	chr2:151352061-151352062	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs533491624	chr2:151352067-151352068	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs145135671	chr2:151352115-151352116	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs181460664	chr2:151352139-151352140	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs12692720	chr2:151352154-151352155	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574237370	chr2:151352192-151352193	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs376601778	chr2:151352193-151352194	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs373604129	chr2:151352197-151352198	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs369032995	chr2:151352208-151352209	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531425315	chr2:151352213-151352214	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185713245	chr2:151352283-151352284	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568016260	chr2:151352290-151352291	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527307946	chr2:151352374-151352375	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547342768	chr2:151352436-151352437	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570701603	chr2:151352442-151352443	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530693507	chr2:151352449-151352450	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149756948	chr2:151352473-151352474	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189457219	chr2:151352502-151352503	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530982347	chr2:151352568-151352569	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115206914	chr2:151352639-151352640	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs7561737	chr2:151352765-151352766	Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs555463120	chr2:151352771-151352772	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs572073941	chr2:151352776-151352777	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs541010128	chr2:151352849-151352850	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs76247232	chr2:151352861-151352862	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs199777994	chr2:151352862-151352863	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113758259	chr2:151352960-151352961	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369717034	chr2:151352976-151352977	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563865560	chr2:151353005-151353006	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs180965522	chr2:151353014-151353015	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12692722	chr2:151353052-151353053	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561784483	chr2:151353068-151353069	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377626413	chr2:151353162-151353163	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535495873	chr2:151353204-151353205	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568051835	chr2:151353227-151353228	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185888519	chr2:151353243-151353244	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547363464	chr2:151353335-151353336	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563964624	chr2:151353340-151353341	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533210182	chr2:151353349-151353350	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549807503	chr2:151353366-151353367	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs207462552	chr2:151353372-151353373	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192504600	chr2:151353385-151353386	Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535761329	chr2:151353409-151353410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151344000-151352000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:151344200-151352600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:151344400-151352000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:151344600-151352000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:151348200-151352200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr2:151349200-151352000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:151349200-151352200	Weak transcription	HSMMtube	muscle
8	chr2:151349200-151352400	Weak transcription	HUVEC	blood vessel
9	chr2:151350000-151352800	Enhancers	Osteobl	bone
10	chr2:151350600-151352000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr2:151350600-151352200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:151350600-151352200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr2:151350600-151352200	Enhancers	Hela-S3	cervix
14	chr2:151350600-151352800	Enhancers	NHDF-Ad	bronchial
15	chr2:151350600-151353000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:151350800-151352200	Enhancers	A549	lung
17	chr2:151350800-151352800	Enhancers	NHLF	lung
18	chr2:151351200-151352000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:151351200-151352200	Enhancers	HSMM	muscle
20	chr2:151351200-151352800	Enhancers	NHEK	skin
21	chr2:151351400-151352200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:151351400-151352400	Weak transcription	Fetal Lung	lung
23	chr2:151351400-151353400	Enhancers	Fetal Heart	heart
24	chr2:151351800-151352200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:151351800-151353400	Enhancers	HMEC	breast
26	chr2:151351800-151353600	Enhancers	NH-A	brain
27	chr2:151352000-151352400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:151352000-151352400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:151352000-151353000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:151352000-151353000	Enhancers	Placenta Amnion	Placenta Amnion
31	chr2:151352000-151353600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:151352000-151354200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:151352200-151352400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr2:151352200-151352400	Flanking Active TSS	HSMM	muscle
35	chr2:151352200-151352600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:151352200-151352600	Enhancers	HSMMtube	muscle
37	chr2:151352200-151353200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr2:151352200-151353200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:151352200-151353200	Flanking Active TSS	Hela-S3	cervix
40	chr2:151352200-151353400	Flanking Active TSS	A549	lung
41	chr2:151352200-151353600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr2:151352400-151352800	Active TSS	Muscle Satellite Cultured Cells	--
43	chr2:151352400-151352800	Enhancers	HSMM	muscle
44	chr2:151352400-151352800	Enhancers	HUVEC	blood vessel
45	chr2:151352400-151353000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:151352400-151353000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr2:151352400-151353000	Enhancers	Fetal Lung	lung
48	chr2:151352600-151352800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr2:151352600-151352800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr2:151352600-151353400	Flanking Active TSS	HSMMtube	muscle

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