Variant report

Variant	nsv536070
Chromosome Location	chr2:183648083-183698793
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	chr2:183679569-183679767	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183648439-183648583	K562	blood:	n/a	n/a
3	ARID3A	chr2:183649467-183649783	K562	blood:	n/a	n/a
4	ARID3A	chr2:183668859-183669300	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:183649459-183649762	HepG2	liver:	n/a	n/a
6	BCL11A	chr2:183683644-183683969	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr2:183679511-183679776	HepG2	liver:	n/a	n/a
8	CCNT2	chr2:183650940-183651109	K562	blood:	n/a	n/a
9	CEBPB	chr2:183679659-183679922	HepG2	liver:	n/a	chr2:183679810-183679823 chr2:183679811-183679822
10	CEBPB	chr2:183651455-183651655	A549	lung:	n/a	n/a
11	CEBPB	chr2:183685030-183685198	A549	lung:	n/a	chr2:183685096-183685107
12	CEBPB	chr2:183684963-183685265	IMR90	lung:	n/a	chr2:183685096-183685107
13	CEBPB	chr2:183677460-183677521	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:183679609-183679973	HepG2	liver:	n/a	chr2:183679810-183679823 chr2:183679811-183679822
15	CEBPB	chr2:183684952-183685196	HepG2	liver:	n/a	chr2:183685096-183685107
16	CEBPB	chr2:183658874-183659067	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:183676867-183676952	HepG2	liver:	n/a	chr2:183676879-183676890
18	CEBPB	chr2:183676807-183676931	H1-hESC	embryonic stem cell:	n/a	chr2:183676879-183676890
19	CEBPB	chr2:183676829-183676918	K562	blood:	n/a	chr2:183676879-183676890
20	CHD2	chr2:183679559-183679605	HepG2	liver:	n/a	n/a
21	CTCF	chr2:183649500-183649650	GM12875	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
22	CTCF	chr2:183649620-183649770	GM12864	blood:	n/a	n/a
23	CTCF	chr2:183649580-183649730	HEEpiC	esophagus:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
24	CTCF	chr2:183649423-183649804	GM12878	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
25	CTCF	chr2:183649520-183649670	GM12873	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
26	CTCF	chr2:183649580-183649730	WI-38	lung:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
27	CTCF	chr2:183649540-183649690	GM12878	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
28	CTCF	chr2:183649560-183649710	HRE	kidney:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
29	CTCF	chr2:183649500-183649650	HA-sp	spinal cord:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
30	CTCF	chr2:183649520-183649670	HRPEpiC	eye:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
31	CTCF	chr2:183649495-183649759	HUVEC	blood vessel:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
32	CTCF	chr2:183649513-183649695	SK-N-SH_RA	brain:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
33	CTCF	chr2:183649560-183649710	AG09309	skin:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
34	CTCF	chr2:183648940-183649090	AG09319	gingival:	n/a	n/a
35	CTCF	chr2:183649365-183650093	SK-N-SH	brain:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
36	CTCF	chr2:183649540-183649690	HCT-116	colon:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
37	CTCF	chr2:183649435-183649755	SK-N-SH_RA	brain:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
38	CTCF	chr2:183649560-183649710	Caco-2	colon:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
39	CTCF	chr2:183649560-183649710	HMF	breast:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
40	CTCF	chr2:183649540-183649690	HEK293	kidney:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
41	CTCF	chr2:183649500-183649650	GM12870	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
42	CTCF	chr2:183649514-183649714	HepG2	liver:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
43	CTCF	chr2:183649516-183649697	GM13977	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
44	CTCF	chr2:183649520-183649670	AoAF	blood vessel:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
45	CTCF	chr2:183649540-183649690	HPF	lung:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
46	CTCF	chr2:183649480-183649630	MCF-7	breast:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
47	CTCF	chr2:183649480-183649630	GM12874	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
48	CTCF	chr2:183649580-183649730	GM12872	blood:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630
49	CTCF	chr2:183649060-183649210	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr2:183649408-183649802	MCF-7	breast:	n/a	chr2:183649607-183649625 chr2:183649608-183649624 chr2:183649609-183649630

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183658977-183659027	H1-hESC	embryonic stem cell:	embryo
2	chr2:183658977-183659027	H1-hESC	embryonic stem cell:	embryo
3	chr2:183658977-183659027	PANC-1	pancreas:	n/a
4	chr2:183683268-183683318	ECC-1	luminal epithelium:	n/a
5	chr2:183683268-183683318	GM12878	blood:	n/a
6	chr2:183658977-183659027	HNPCEpiC	eye:	n/a
7	chr2:183658977-183659027	Jurkat	blood:	n/a
8	chr2:183667124-183667174	GM12892	blood:	n/a
9	chr2:183658977-183659027	BJ	skin:	n/a
10	chr2:183683268-183683318	GM12892	blood:	n/a
11	chr2:183658977-183659027	PFSK-1	brain:	n/a
12	chr2:183683268-183683318	ProgFib	skin:	n/a
13	chr2:183683268-183683318	AoSMC	blood vessel:	n/a
14	chr2:183683268-183683318	AG09319	gingival:	n/a
15	chr2:183683268-183683318	GM06990	blood:	n/a
16	chr2:183683268-183683318	SKMC	muscle:	n/a
17	chr2:183658977-183659027	HRCEpiC	kidney:	n/a
18	chr2:183667124-183667174	PrEC	prostate:	n/a
19	chr2:183667124-183667174	T-47D	breast:	n/a
20	chr2:183658977-183659027	IMR90	lung:	fetal
21	chr2:183683268-183683318	HEK293	kidney:	embryo
22	chr2:183658977-183659027	HAEpiC	amniotic membrane:	n/a
23	chr2:183667124-183667174	MCF-7	breast:	n/a
24	chr2:183683268-183683318	NH-A	brain:	n/a
25	chr2:183667124-183667174	HAEpiC	amniotic membrane:	n/a
26	chr2:183683268-183683318	HL-60	blood:	n/a
27	chr2:183658977-183659027	AG10803	skin:	n/a
28	chr2:183667124-183667174	U87	brain:	n/a
29	chr2:183658977-183659027	HMEC	breast:	n/a
30	chr2:183683268-183683318	PFSK-1	brain:	n/a
31	chr2:183658977-183659027	HCT-116	colon:	n/a
32	chr2:183667124-183667174	NH-A	brain:	n/a
33	chr2:183658977-183659027	MCF10A-Er-Src	breast:	n/a
34	chr2:183667124-183667174	GM12878	blood:	n/a
35	chr2:183683268-183683318	HNPCEpiC	eye:	n/a
36	chr2:183658977-183659027	HCM	heart:	n/a
37	chr2:183658977-183659027	HCPEpiC	choroid plexus:	n/a
38	chr2:183667124-183667174	IMR90	lung:	fetal
39	chr2:183658977-183659027	GM12891	blood:	n/a
40	chr2:183683268-183683318	NHDF-neo	bronchial:	n/a
41	chr2:183667124-183667174	A549	lung:	n/a
42	chr2:183658977-183659027	GM12878	blood:	n/a
43	chr2:183658977-183659027	GM19239	blood:	n/a
44	chr2:183683268-183683318	HUVEC	blood vessel:	n/a
45	chr2:183658977-183659027	SK-N-MC	brain:	n/a
46	chr2:183667124-183667174	HCPEpiC	choroid plexus:	n/a
47	chr2:183683268-183683318	HMEC	breast:	n/a
48	chr2:183667124-183667174	HepG2	liver:	n/a
49	chr2:183658977-183659027	HCF	heart:	n/a
50	chr2:183667124-183667174	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:183676835..183678660-chr2:183680847..183683198,2	K562	blood:
2	chr2:183658306..183660291-chr2:183661982..183664789,2	K562	blood:
3	chr2:183686694..183689194-chr2:183689476..183692268,2	K562	blood:
4	chr2:183666474..183669367-chr2:183675559..183677309,2	K562	blood:
5	chr2:183676117..183678247-chr2:183702144..183703855,2	MCF-7	breast:
6	chr2:183695751..183697908-chr2:183701079..183703543,2	K562	blood:
7	chr2:183649264..183650285-chr2:183734657..183735584,4	MCF-7	breast:
8	chr2:183686694..183689194-chr2:183689476..183692268,2	K562	blood:
9	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:
10	chr2:183659213..183661128-chr2:183664377..183666463,2	MCF-7	breast:
11	chr2:183659213..183661128-chr2:183664377..183666463,2	MCF-7	breast:
12	chr2:183653144..183655094-chr2:183658549..183660271,2	K562	blood:
13	chr2:183658306..183660291-chr2:183661982..183664789,2	K562	blood:
14	chr2:183676835..183678660-chr2:183680847..183683198,2	K562	blood:
15	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
16	chr2:183660311..183663383-chr2:183663723..183666825,3	K562	blood:
17	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
18	chr2:183666474..183669367-chr2:183675559..183677309,2	K562	blood:
19	chr2:183653144..183655094-chr2:183658549..183660271,2	K562	blood:
20	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
21	chr2:183666072..183668811-chr2:183672766..183675135,2	MCF-7	breast:
22	chr2:183666072..183668811-chr2:183672766..183675135,2	MCF-7	breast:
23	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
24	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:
25	chr2:183691013..183692579-chr2:183710091..183711908,2	MCF-7	breast:
26	chr2:183648396..183651176-chr2:183657370..183660801,3	K562	blood:
27	chr2:183648396..183651176-chr2:183657370..183660801,3	K562	blood:
28	chr2:183660311..183663383-chr2:183663723..183666825,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNAJC10-2	chr2:183654087-183659706	NONHSAT075921
2	lnc-DUSP19-4	chr2:183650679-183652638	NONHSAT075919
3	lnc-DUSP19-3	chr2:183652825-183653162	NONHSAT075920

Variant related genes	Relation type
RPL31P15	TF binding region
ENSG00000212404	TF binding region
RPL31P15	CpG island
ENSG00000212404	CpG island

Extended variants
information (count: 1569 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1569 , 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	rs34476308	chr2:183648137-183648138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532005146	chr2:183648164-183648165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552170136	chr2:183648166-183648167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562407951	chr2:183648183-183648184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186613502	chr2:183648215-183648216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189831876	chr2:183648221-183648222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549684241	chr2:183648258-183648259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182945890	chr2:183648278-183648279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567904466	chr2:183648279-183648280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536936211	chr2:183648288-183648289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547351948	chr2:183648297-183648298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187811484	chr2:183648325-183648326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371350658	chr2:183648366-183648367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567454256	chr2:183648467-183648468	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs541251328	chr2:183648494-183648495	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs574066085	chr2:183648497-183648498	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558926717	chr2:183648530-183648531	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs575610653	chr2:183648597-183648598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192915191	chr2:183648631-183648632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536754520	chr2:183648659-183648660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538342015	chr2:183648661-183648662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538106008	chr2:183648707-183648708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554341670	chr2:183648722-183648723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56844297	chr2:183648761-183648762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114498451	chr2:183648794-183648795	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs540123359	chr2:183648797-183648798	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs150133579	chr2:183648866-183648867	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577080063	chr2:183648877-183648878	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs545439313	chr2:183648909-183648910	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs112209483	chr2:183648939-183648940	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs373320878	chr2:183648965-183648966	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs532207290	chr2:183648994-183648995	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs548344410	chr2:183649023-183649024	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561451263	chr2:183649032-183649033	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs569317484	chr2:183649047-183649048	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs75867858	chr2:183649068-183649069	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs547236742	chr2:183649082-183649083	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs567135940	chr2:183649098-183649099	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs288313	chr2:183649154-183649155	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs138655359	chr2:183649214-183649215	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs187643343	chr2:183649254-183649255	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs288312	chr2:183649266-183649267	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs6726219	chr2:183649296-183649297	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559502558	chr2:183649297-183649298	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548103731	chr2:183649299-183649300	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs568233677	chr2:183649346-183649347	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs141888980	chr2:183649369-183649370	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs534150693	chr2:183649370-183649371	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs146266247	chr2:183649395-183649396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs6726555	chr2:183649422-183649423	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:52)

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
Intellectual disability	22102821	CNVD
Autism	18522746	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
low-grade B-cell lymphoma tumor	18367492	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183581800-183655600	Weak transcription	Pancreas	Pancrea
2	chr2:183623200-183651400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:183625000-183650600	Weak transcription	Stomach Mucosa	stomach
4	chr2:183627200-183652600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr2:183627200-183657800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:183627400-183652400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr2:183631000-183652800	Weak transcription	NHLF	lung
8	chr2:183631600-183653400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr2:183632400-183648200	Weak transcription	Fetal Heart	heart
10	chr2:183633800-183652800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:183633800-183657800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr2:183638000-183652400	Weak transcription	Brain Anterior Caudate	brain
13	chr2:183639800-183653400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr2:183639800-183654600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:183641200-183652400	Weak transcription	Brain Germinal Matrix	brain
16	chr2:183641400-183649800	Weak transcription	Fetal Brain Female	brain
17	chr2:183642400-183648800	Weak transcription	Liver	Liver
18	chr2:183642600-183649000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr2:183643800-183649400	Weak transcription	Fetal Lung	lung
20	chr2:183643800-183656600	Weak transcription	HUVEC	blood vessel
21	chr2:183644200-183652800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:183645200-183657800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:183645400-183654200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr2:183645400-183655000	Weak transcription	Fetal Intestine Small	intestine
25	chr2:183645600-183652600	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr2:183645600-183657200	Weak transcription	Adipose Nuclei	Adipose
27	chr2:183645800-183650400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr2:183645800-183652200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:183645800-183652600	Weak transcription	Fetal Intestine Large	intestine
30	chr2:183645800-183652800	Weak transcription	A549	lung
31	chr2:183645800-183653800	Weak transcription	Fetal Muscle Leg	muscle
32	chr2:183645800-183655000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr2:183645800-183657200	Weak transcription	NHEK	skin
34	chr2:183645800-183657800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:183646000-183649600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr2:183646000-183653400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr2:183646000-183653600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr2:183646000-183653800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:183646000-183654400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:183646000-183658800	Weak transcription	Left Ventricle	heart
41	chr2:183646000-183659400	Weak transcription	Aorta	Aorta
42	chr2:183646200-183652000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:183646200-183653200	Weak transcription	Primary B cells from cord blood	blood
44	chr2:183646200-183654400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:183646200-183657200	Weak transcription	Primary hematopoietic stem cells	blood
46	chr2:183646200-183657800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr2:183646400-183649600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:183647800-183648200	Enhancers	K562	blood
49	chr2:183648200-183649400	Weak transcription	K562	blood
50	chr2:183648800-183650000	Enhancers	Liver	Liver

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