Variant report

Variant	nsv581748
Chromosome Location	chr2:46712759-46724016
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:350)
CpG islands
(count:184)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:46720481-46721121	GM12878	blood:	n/a	n/a
2	ATF2	chr2:46720531-46721087	GM12878	blood:	n/a	n/a
3	ATF2	chr2:46717670-46718108	GM12878	blood:	n/a	n/a
4	ATF3	chr2:46714867-46715087	K562	blood:	n/a	n/a
5	BATF	chr2:46720540-46720967	GM12878	blood:	n/a	n/a
6	BATF	chr2:46720571-46721001	GM12878	blood:	n/a	n/a
7	BCLAF1	chr2:46720475-46721012	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:46720623-46720994	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:46719385-46719598	HepG2	liver:	n/a	chr2:46719482-46719493
10	CEBPB	chr2:46719420-46719560	IMR90	lung:	n/a	chr2:46719482-46719493
11	CEBPB	chr2:46720714-46721066	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:46719420-46719542	K562	blood:	n/a	chr2:46719482-46719493
13	CEBPB	chr2:46715203-46715515	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:46720690-46721063	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:46720773-46721024	A549	lung:	n/a	n/a
16	CHD2	chr2:46715159-46715485	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr2:46720727-46720985	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr2:46721966-46722006	GM12878	blood:	n/a	n/a
19	CTCF	chr2:46715500-46715650	HCT-116	colon:	n/a	n/a
20	CTCF	chr2:46717760-46717910	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr2:46715666-46715736	K562	blood:	n/a	n/a
22	CTCF	chr2:46715360-46715510	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr2:46715640-46715790	RPTEC	kidney:	n/a	n/a
24	CTCF	chr2:46713734-46714043	GM12878	blood:	n/a	n/a
25	CTCF	chr2:46717780-46717930	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr2:46718180-46718330	AG04449	skin:	n/a	n/a
27	CTCF	chr2:46715660-46715810	AG09319	gingival:	n/a	n/a
28	CTCF	chr2:46715400-46715550	AG09319	gingival:	n/a	n/a
29	CTCF	chr2:46715660-46715810	BJ	skin:	n/a	n/a
30	CTCF	chr2:46715600-46715750	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr2:46718080-46718230	HAc	cerebellar:	n/a	n/a
32	CTCF	chr2:46717760-46717910	GM12872	blood:	n/a	n/a
33	CTCF	chr2:46715640-46715790	HMF	breast:	n/a	n/a
34	CTCF	chr2:46717720-46717870	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr2:46718080-46718230	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr2:46717760-46717910	GM12873	blood:	n/a	n/a
37	CTCF	chr2:46718140-46718290	BJ	skin:	n/a	n/a
38	CTCF	chr2:46715660-46715810	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr2:46715680-46715830	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr2:46718100-46718250	AG04450	lung:	n/a	n/a
41	CTCF	chr2:46713837-46713876	GM10266	blood:	n/a	n/a
42	CTCF	chr2:46715640-46715790	HMEC	breast:	n/a	n/a
43	CTCF	chr2:46715620-46715770	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr2:46717460-46717610	GM12865	blood:	n/a	n/a
45	CTCF	chr2:46717740-46717890	GM12864	blood:	n/a	n/a
46	CTCF	chr2:46715600-46715750	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr2:46717760-46717910	GM12870	blood:	n/a	n/a
48	CTCF	chr2:46717754-46717947	GM12878	blood:	n/a	n/a
49	CTCF	chr2:46713820-46713970	NHEK	skin:	n/a	n/a
50	CTCF	chr2:46717760-46717910	GM12867	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:46720801-46720851	ProgFib	skin:	n/a
2	chr2:46720801-46720851	ProgFib	skin:	n/a
3	chr2:46715231-46715281	AG09319	gingival:	n/a
4	chr2:46720801-46720851	AG04450	lung:	fetal
5	chr2:46715231-46715281	SK-N-SH	brain:	n/a
6	chr2:46715231-46715281	HIPEpiC	eye:	n/a
7	chr2:46715231-46715281	NT2-D1	testis:	n/a
8	chr2:46720801-46720851	PANC-1	pancreas:	n/a
9	chr2:46717839-46717889	NH-A	brain:	n/a
10	chr2:46715231-46715281	GM12878	blood:	n/a
11	chr2:46720801-46720851	K562	blood:	n/a
12	chr2:46715231-46715281	HMEC	breast:	n/a
13	chr2:46717839-46717889	HIPEpiC	eye:	n/a
14	chr2:46720801-46720851	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:46715231-46715281	PFSK-1	brain:	n/a
16	chr2:46715231-46715281	MCF10A-Er-Src	breast:	n/a
17	chr2:46717839-46717889	SAEC	small airway:	n/a
18	chr2:46720801-46720851	T-47D	breast:	n/a
19	chr2:46717839-46717889	SK-N-SH	brain:	n/a
20	chr2:46715231-46715281	ovcar-3	ovarian:	n/a
21	chr2:46717839-46717889	AG10803	skin:	n/a
22	chr2:46715231-46715281	T-47D	breast:	n/a
23	chr2:46717839-46717889	ovcar-3	ovarian:	n/a
24	chr2:46720801-46720851	BE2_C	brain:	n/a
25	chr2:46717839-46717889	NB4	blood:	n/a
26	chr2:46715231-46715281	Jurkat	blood:	n/a
27	chr2:46715231-46715281	ECC-1	luminal epithelium:	n/a
28	chr2:46717839-46717889	SK-N-SH_RA	brain:	n/a
29	chr2:46715231-46715281	HCM	heart:	n/a
30	chr2:46720801-46720851	SK-N-SH_RA	brain:	n/a
31	chr2:46720801-46720851	HIPEpiC	eye:	n/a
32	chr2:46717839-46717889	ECC-1	luminal epithelium:	n/a
33	chr2:46715231-46715281	PANC-1	pancreas:	n/a
34	chr2:46717839-46717889	BJ	skin:	n/a
35	chr2:46720801-46720851	LNCaP	prostate:	n/a
36	chr2:46717839-46717889	PANC-1	pancreas:	n/a
37	chr2:46717839-46717889	GM12891	blood:	n/a
38	chr2:46717839-46717889	HL-60	blood:	n/a
39	chr2:46720801-46720851	NB4	blood:	n/a
40	chr2:46715231-46715281	H1-hESC	embryonic stem cell:	embryo
41	chr2:46717839-46717889	HEEpiC	esophagus:	n/a
42	chr2:46720801-46720851	AoSMC	blood vessel:	n/a
43	chr2:46717839-46717889	AG04449	skin:	fetal
44	chr2:46717839-46717889	T-47D	breast:	n/a
45	chr2:46715231-46715281	HNPCEpiC	eye:	n/a
46	chr2:46715231-46715281	PrEC	prostate:	n/a
47	chr2:46715231-46715281	HRCEpiC	kidney:	n/a
48	chr2:46720801-46720851	AG10803	skin:	n/a
49	chr2:46720801-46720851	H1-hESC	embryonic stem cell:	embryo
50	chr2:46720801-46720851	ECC-1	luminal epithelium:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:46713674..46717376-chr2:46717590..46719594,3	K562	blood:
2	chr2:46721184..46729524-chr2:46766976..46775977,14	K562	blood:
3	chr2:46712457..46718126-chr2:46724421..46727428,6	K562	blood:
4	chr2:46713674..46716471-chr2:46717649..46719594,2	K562	blood:
5	chr2:46721452..46724242-chr2:46727690..46730244,3	MCF-7	breast:
6	chr2:46714508..46716993-chr2:46724518..46727090,2	K562	blood:
7	chr2:46707494..46710484-chr2:46718946..46721502,2	K562	blood:
8	chr2:46713674..46717376-chr2:46717590..46719594,3	K562	blood:
9	chr2:46710349..46713099-chr2:46769270..46771905,2	MCF-7	breast:
10	chr2:46693283..46695227-chr2:46712341..46714395,2	K562	blood:
11	chr2:46715260..46716783-chr2:46718663..46721578,2	MCF-7	breast:
12	chr2:46716484..46718309-chr2:46842742..46845548,2	K562	blood:
13	chr2:46713674..46716471-chr2:46717649..46719594,2	K562	blood:
14	chr2:46715260..46716783-chr2:46718663..46721578,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1E2-5	chr2:46717889-46717970	NONHSAT070501

No data

Variant related genes	Relation type
ENSG00000253515	TF binding region
ENSG00000253515	CpG island
ENSG00000250565	chromatin interactions
ENSG00000119878	chromatin interactions
ENSG00000151665	chromatin interactions
ENSG00000119729	chromatin interactions
ENSG00000253515	chromatin interactions

Extended variants
information (count: 484 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2276555	chr2:46712759-46712760	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572926208	chr2:46712764-46712765	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs144614961	chr2:46712783-46712784	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs138546410	chr2:46712785-46712786	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs575342053	chr2:46712811-46712812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs544224731	chr2:46712819-46712820	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs577968335	chr2:46712895-46712896	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs563868969	chr2:46712897-46712898	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs182864354	chr2:46712908-46712909	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs542906209	chr2:46712935-46712936	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs559918413	chr2:46712937-46712938	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs141523569	chr2:46712943-46712944	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs370524864	chr2:46712944-46712945	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs116095607	chr2:46712969-46712970	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs144416258	chr2:46712977-46712978	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs575304587	chr2:46713002-46713003	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs148365072	chr2:46713062-46713063	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs141527322	chr2:46713082-46713083	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs116317073	chr2:46713114-46713115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs115417850	chr2:46713135-46713136	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114270675	chr2:46713187-46713188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187464113	chr2:46713197-46713198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4953388	chr2:46713201-46713202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs575402157	chr2:46713209-46713210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150868977	chr2:46713219-46713220	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554554353	chr2:46713298-46713299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574322632	chr2:46713306-46713307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs4953389	chr2:46713321-46713322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs541729619	chr2:46713370-46713371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192370615	chr2:46713429-46713430	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183755962	chr2:46713458-46713459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7573688	chr2:46713478-46713479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs17035179	chr2:46713523-46713524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs113759174	chr2:46713538-46713539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111412238	chr2:46713546-46713547	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs34748421	chr2:46713556-46713557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566403136	chr2:46713557-46713558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs397984478	chr2:46713575-46713576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200328306	chr2:46713576-46713577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs76991791	chr2:46713595-46713596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113540871	chr2:46713596-46713597	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140754382	chr2:46713605-46713606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78178954	chr2:46713640-46713641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs112622817	chr2:46713663-46713664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531429894	chr2:46713673-46713674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569028395	chr2:46713704-46713705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188974165	chr2:46713709-46713710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs145626032	chr2:46713731-46713732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs574407317	chr2:46713740-46713741	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533531703	chr2:46713742-46713743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Myelofibrosis	22110671	CNVD
Hypotonia	17579669	CNVD
Hypotonia-Cystinuria syndrome	16385448	CNVD
Glioblastoma multiforme	17002787	CNVD
Cystinuria	17625506	CNVD
Breast cancer	16272173	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46689200-46714800	Weak transcription	Right Atrium	heart
2	chr2:46700200-46714800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr2:46705000-46716600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:46708400-46714800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:46708400-46714800	Weak transcription	Lung	lung
6	chr2:46709000-46713000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:46709200-46714600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:46709200-46714800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:46709400-46714600	Weak transcription	NHDF-Ad	bronchial
10	chr2:46709600-46714600	Weak transcription	HUVEC	blood vessel
11	chr2:46709600-46714600	Weak transcription	Osteobl	bone
12	chr2:46709600-46715000	Weak transcription	A549	lung
13	chr2:46710000-46713600	Weak transcription	Hela-S3	cervix
14	chr2:46710000-46714600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:46710000-46714600	Weak transcription	NHLF	lung
16	chr2:46710800-46714800	Weak transcription	Right Ventricle	heart
17	chr2:46711800-46713200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr2:46712000-46714000	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr2:46712400-46712800	Weak transcription	Psoas Muscle	Psoas
20	chr2:46712600-46714600	Weak transcription	Left Ventricle	heart
21	chr2:46712800-46713000	Enhancers	Psoas Muscle	Psoas
22	chr2:46713000-46714400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr2:46713000-46714600	Weak transcription	Psoas Muscle	Psoas
24	chr2:46713200-46714600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr2:46713600-46717600	Enhancers	Hela-S3	cervix
26	chr2:46713800-46714000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr2:46713800-46714000	Enhancers	Colon Smooth Muscle	Colon
28	chr2:46713800-46714400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr2:46713800-46718800	Enhancers	Spleen	Spleen
30	chr2:46714000-46714400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr2:46714000-46714600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:46714000-46714800	Weak transcription	Colon Smooth Muscle	Colon
33	chr2:46714000-46714800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr2:46714400-46714800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr2:46714400-46714800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr2:46714400-46714800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:46714600-46715000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr2:46714600-46715200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:46714600-46715200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr2:46714600-46715400	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr2:46714600-46715400	Enhancers	HUVEC	blood vessel
42	chr2:46714600-46715600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:46714600-46715600	Enhancers	Fetal Stomach	stomach
44	chr2:46714600-46715600	Enhancers	NH-A	brain
45	chr2:46714600-46715800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:46714600-46715800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr2:46714600-46715800	Enhancers	Stomach Smooth Muscle	stomach
48	chr2:46714600-46715800	Enhancers	HSMM	muscle
49	chr2:46714600-46716000	Enhancers	NHDF-Ad	bronchial
50	chr2:46714600-46716000	Enhancers	Osteobl	bone

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