Variant report

Variant	nsv459986
Chromosome Location	chr2:186297074-186413124
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:386)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:186340618-186340908	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
3	BCL3	chr2:186338970-186339324	GM12878	blood:	n/a	n/a
4	CBX3	chr2:186321328-186321586	HCT-116	colon:	n/a	n/a
5	CEBPB	chr2:186300444-186300644	H1-hESC	embryonic stem cell:	n/a	chr2:186300612-186300623
6	CEBPB	chr2:186319765-186320025	HepG2	liver:	n/a	chr2:186319845-186319856 chr2:186319872-186319885 chr2:186319845-186319858
7	CEBPB	chr2:186326140-186326258	A549	lung:	n/a	chr2:186326152-186326163
8	CEBPB	chr2:186328234-186328579	HepG2	liver:	n/a	chr2:186328405-186328416
9	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
10	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:186300587-186300787	HepG2	liver:	n/a	chr2:186300612-186300623
12	CEBPB	chr2:186330125-186330406	HepG2	liver:	n/a	chr2:186330266-186330277
13	CEBPB	chr2:186328274-186328568	A549	lung:	n/a	chr2:186328405-186328416
14	CEBPB	chr2:186321229-186321715	HCT-116	colon:	n/a	n/a
15	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:186301535-186301733	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:186301521-186301830	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
19	CEBPB	chr2:186338338-186338358	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
21	CEBPB	chr2:186313713-186313937	HepG2	liver:	n/a	chr2:186313826-186313837 chr2:186313826-186313839
22	CEBPB	chr2:186326049-186326249	HepG2	liver:	n/a	chr2:186326152-186326163
23	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr2:186387300-186387450	HCT-116	colon:	n/a	n/a
25	CTCF	chr2:186340560-186340710	RPTEC	kidney:	n/a	n/a
26	CTCF	chr2:186347600-186347681	MCF-7	breast:	n/a	n/a
27	CTCF	chr2:186340680-186340830	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr2:186387300-186387450	MCF-7	breast:	n/a	n/a
29	CTCF	chr2:186387240-186387390	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr2:186306420-186306570	HMEC	breast:	n/a	n/a
31	CTCF	chr2:186340680-186340830	HMEC	breast:	n/a	n/a
32	CTCF	chr2:186387280-186387430	HRE	kidney:	n/a	n/a
33	CTCF	chr2:186387201-186387561	GM12878	blood:	n/a	n/a
34	CTCF	chr2:186387260-186387410	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr2:186387300-186387450	RPTEC	kidney:	n/a	n/a
36	CTCF	chr2:186387380-186387530	GM12875	blood:	n/a	n/a
37	CTCF	chr2:186387280-186387430	GM12872	blood:	n/a	n/a
38	CTCF	chr2:186387220-186387370	GM12865	blood:	n/a	n/a
39	CTCF	chr2:186387280-186387430	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr2:186387244-186387623	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:186387401-186387475	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr2:186347614-186347651	NHEK	skin:	n/a	n/a
43	CTCF	chr2:186297860-186298010	GM06990	blood:	n/a	n/a
44	CTCF	chr2:186340780-186340930	HRE	kidney:	n/a	n/a
45	CTCF	chr2:186387320-186387470	SAEC	small airway:	n/a	n/a
46	CTCF	chr2:186306340-186306490	HepG2	liver:	n/a	chr2:186306416-186306424 chr2:186306417-186306425
47	CTCF	chr2:186387260-186387410	GM06990	blood:	n/a	n/a
48	CTCF	chr2:186387400-186387550	HepG2	liver:	n/a	n/a
49	CTCF	chr2:186340620-186340770	HVMF	connective:	n/a	n/a
50	CTCF	chr2:186411005-186411020	GM10248	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412073-186412123	PFSK-1	brain:	n/a
2	chr2:186412305-186412355	GM12878	blood:	n/a
3	chr2:186412305-186412355	GM12892	blood:	n/a
4	chr2:186412073-186412123	HCF	heart:	n/a
5	chr2:186412612-186412662	SK-N-MC	brain:	n/a
6	chr2:186412305-186412355	NHDF-neo	bronchial:	n/a
7	chr2:186412612-186412662	NH-A	brain:	n/a
8	chr2:186412073-186412123	AG04450	lung:	fetal
9	chr2:186412073-186412123	K562	blood:	n/a
10	chr2:186412305-186412355	AG10803	skin:	n/a
11	chr2:186412305-186412355	IMR90	lung:	fetal
12	chr2:186412612-186412662	U87	brain:	n/a
13	chr2:186412612-186412662	LNCaP	prostate:	n/a
14	chr2:186412612-186412662	HCPEpiC	choroid plexus:	n/a
15	chr2:186412612-186412662	HRCEpiC	kidney:	n/a
16	chr2:186412305-186412355	Hela-S3	cervix:	n/a
17	chr2:186412073-186412123	AG04449	skin:	fetal
18	chr2:186412305-186412355	ProgFib	skin:	n/a
19	chr2:186412073-186412123	HCT-116	colon:	n/a
20	chr2:186412073-186412123	HL-60	blood:	n/a
21	chr2:186412612-186412662	HCF	heart:	n/a
22	chr2:186412073-186412123	BE2_C	brain:	n/a
23	chr2:186412612-186412662	SK-N-SH_RA	brain:	n/a
24	chr2:186412073-186412123	HMEC	breast:	n/a
25	chr2:186412073-186412123	H1-hESC	embryonic stem cell:	embryo
26	chr2:186412073-186412123	PANC-1	pancreas:	n/a
27	chr2:186412305-186412355	A549	lung:	n/a
28	chr2:186412073-186412123	SK-N-SH_RA	brain:	n/a
29	chr2:186412305-186412355	BJ	skin:	n/a
30	chr2:186412612-186412662	HMEC	breast:	n/a
31	chr2:186412612-186412662	HEEpiC	esophagus:	n/a
32	chr2:186412305-186412355	AG04450	lung:	fetal
33	chr2:186412073-186412123	U87	brain:	n/a
34	chr2:186412612-186412662	ECC-1	luminal epithelium:	n/a
35	chr2:186412073-186412123	GM19239	blood:	n/a
36	chr2:186412612-186412662	GM12878	blood:	n/a
37	chr2:186412073-186412123	CMK	blood:	n/a
38	chr2:186412612-186412662	AG04449	skin:	fetal
39	chr2:186412073-186412123	ECC-1	luminal epithelium:	n/a
40	chr2:186412612-186412662	AG10803	skin:	n/a
41	chr2:186412305-186412355	HMEC	breast:	n/a
42	chr2:186412305-186412355	GM06990	blood:	n/a
43	chr2:186412305-186412355	GM12891	blood:	n/a
44	chr2:186412305-186412355	SK-N-MC	brain:	n/a
45	chr2:186412305-186412355	HNPCEpiC	eye:	n/a
46	chr2:186412612-186412662	SKMC	muscle:	n/a
47	chr2:186412612-186412662	GM19239	blood:	n/a
48	chr2:186412305-186412355	SK-N-SH	brain:	n/a
49	chr2:186412073-186412123	GM12878	blood:	n/a
50	chr2:186412305-186412355	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
2	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
3	chr2:186291344..186293651-chr2:186297486..186299914,2	K562	blood:
4	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
5	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
6	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
7	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
8	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
9	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
10	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
11	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:
12	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
13	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
14	chr15:50184826..50185646-chr2:186340212..186341106,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSIP2-5	chr2:186370427-186370468	NONHSAT075962
2	lnc-FSIP2-5	chr2:186369880-186375991	NONHSAT075963
3	lnc-FSIP2-5	chr2:186408484-186409210	NONHSAT075962
4	lnc-FSIP2-5	chr2:186370211-186370365	NONHSAT075962
5	lnc-ZSWIM2-15	chr2:186311542-186311686	ucscGeneNc_uc002upi_2
6	lnc-FSIP2-5	chr2:186410628-186411001	NONHSAT075962
7	lnc-ZSWIM2-15	chr2:186302301-186302409	ucscGeneNc_uc002upi_2
8	lnc-ZSWIM2-15	chr2:186309034-186309104	ucscGeneNc_uc002upi_2
9	lnc-FSIP2-5	chr2:186411316-186411619	NONHSAT075962
10	lnc-FSIP2-5	chr2:186347761-186347818	NONHSAT075962
11	lnc-FSIP2-5	chr2:186411283-186411299	NONHSAT075962
12	lnc-FSIP2-5	chr2:186298824-186298920	NONHSAT075962
13	lnc-FSIP2-5	chr2:186371629-186371957	NONHSAT075962
14	lnc-FSIP2-5	chr2:186410448-186410599	NONHSAT075962
15	lnc-FSIP2-5	chr2:186369727-186370202	NONHSAT075962
16	lnc-FSIP2-5	chr2:186366772-186369632	NONHSAT075963
17	lnc-FSIP2-5	chr2:186327396-186327672	NONHSAT075962
18	lnc-FSIP2-5	chr2:186386989-186387497	NONHSAT075962
19	lnc-FSIP2-5	chr2:186403858-186404073	NONHSAT075962

No data

Variant related genes	Relation type
ENSG00000225406	TF binding region
ENSG00000225406	CpG island
ENSG00000226747	chromatin interactions
ENSG00000188738	chromatin interactions

Extended variants
information (count: 4306 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4306 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2113533	chr2:186297074-186297075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530965050	chr2:186297084-186297085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535614450	chr2:186297135-186297136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144028220	chr2:186297152-186297153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13014885	chr2:186297215-186297216	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs565626700	chr2:186297252-186297253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373993567	chr2:186297257-186297258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376960333	chr2:186297261-186297262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139943924	chr2:186297329-186297330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13015110	chr2:186297338-186297339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546754032	chr2:186297346-186297347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13014616	chr2:186297357-186297358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs184093841	chr2:186297401-186297402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541594554	chr2:186297422-186297423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563168344	chr2:186297460-186297461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146503093	chr2:186297491-186297492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35336042	chr2:186297547-186297548	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs386653474	chr2:186297548-186297549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13015569	chr2:186297549-186297550	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs35282538	chr2:186297550-186297551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575504810	chr2:186297554-186297555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542598214	chr2:186297612-186297613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143671033	chr2:186297631-186297632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546981460	chr2:186297652-186297653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568633594	chr2:186297657-186297658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377585435	chr2:186297689-186297690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562465770	chr2:186297690-186297691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557574864	chr2:186297691-186297692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77082678	chr2:186297704-186297705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376298567	chr2:186297712-186297713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370126775	chr2:186297728-186297729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370797814	chr2:186297771-186297772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537142894	chr2:186297779-186297780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35630311	chr2:186297783-186297784	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs186943047	chr2:186297809-186297810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377462895	chr2:186297826-186297827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541634607	chr2:186297874-186297875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140925120	chr2:186297908-186297909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559946595	chr2:186297918-186297919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572163321	chr2:186297962-186297963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552953168	chr2:186297965-186297966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77126608	chr2:186297979-186297980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs541754787	chr2:186298000-186298001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545691286	chr2:186298037-186298038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541154538	chr2:186298088-186298089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140327599	chr2:186298096-186298097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530664711	chr2:186298106-186298107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572987642	chr2:186298144-186298145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541116202	chr2:186298160-186298161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371393825	chr2:186298161-186298162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Autism	22543975	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186291200-186297800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:186292000-186297800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:186292000-186297800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr2:186292000-186298000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:186292000-186298200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr2:186292000-186298200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:186293000-186298200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:186293000-186298200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr2:186293200-186297600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr2:186293200-186297800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:186296000-186298200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:186296200-186298200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:186297600-186298600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr2:186297800-186298000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr2:186297800-186298200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:186297800-186298400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:186297800-186298400	Enhancers	HMEC	breast
18	chr2:186297800-186298600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr2:186297800-186298600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr2:186297800-186298600	Enhancers	NHEK	skin
21	chr2:186297800-186299200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:186297800-186299200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr2:186298000-186298600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:186298000-186298800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr2:186298000-186299000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr2:186298200-186298400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr2:186298200-186298600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:186298200-186298600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:186298200-186298600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:186298200-186298800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:186298200-186299000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:186298200-186299200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:186298200-186315800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:186298400-186298600	Flanking Active TSS	HMEC	breast
35	chr2:186298400-186298600	Enhancers	NH-A	brain
36	chr2:186298600-186298800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:186298600-186298800	Flanking Active TSS	NHEK	skin
38	chr2:186298600-186299200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr2:186298600-186299600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr2:186298600-186300400	Active TSS	HMEC	breast
41	chr2:186298600-186315800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:186298800-186299200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:186298800-186300000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:186298800-186300200	Active TSS	NHEK	skin
45	chr2:186298800-186314800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr2:186299000-186299200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr2:186299200-186299400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr2:186299200-186299600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr2:186299200-186299600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr2:186299200-186301400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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