Variant report

Variant	nsv875414
Chromosome Location	chr2:173267081-173307756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1231)
CpG islands
(count:1343)
Chromatin interactive
region (count:37)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:173300084-173300259	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:173307251-173307282	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:173292090-173292504	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:173296013-173296343	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:173293139-173293530	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:173295416-173295725	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:173306798-173307007	HepG2	liver:	n/a	n/a
8	ATF2	chr2:173291667-173292184	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr2:173306723-173307267	A549	lung:	n/a	n/a
10	BACH1	chr2:173292974-173293425	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:173291931-173292473	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr2:173306584-173307248	A549	lung:	n/a	n/a
13	BHLHE40	chr2:173291690-173293224	HepG2	liver:	n/a	chr2:173292390-173292406 chr2:173292470-173292486
14	BHLHE40	chr2:173294498-173294698	K562	blood:	n/a	chr2:173294556-173294577 chr2:173294562-173294571 chr2:173294561-173294570 chr2:173294562-173294571
15	BHLHE40	chr2:173292946-173293146	A549	lung:	n/a	n/a
16	BHLHE40	chr2:173294161-173294743	HepG2	liver:	n/a	chr2:173294556-173294577 chr2:173294562-173294571 chr2:173294561-173294570 chr2:173294562-173294571
17	BHLHE40	chr2:173302468-173302709	GM12878	blood:	n/a	n/a
18	BRCA1	chr2:173292047-173292183	HepG2	liver:	n/a	n/a
19	BRCA1	chr2:173303754-173304313	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr2:173306685-173307524	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr2:173291827-173292596	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr2:173292581-173292602	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr2:173303476-173304570	HCT-116	colon:	n/a	n/a
24	CCNT2	chr2:173292200-173292608	K562	blood:	n/a	chr2:173292384-173292393 chr2:173292257-173292266
25	CEBPB	chr2:173298705-173298939	HepG2	liver:	n/a	chr2:173298788-173298799 chr2:173298788-173298801
26	CEBPB	chr2:173300343-173300516	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:173295433-173295752	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:173300131-173300600	HepG2	liver:	n/a	chr2:173300184-173300197
29	CEBPB	chr2:173276215-173276245	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:173295167-173295994	HCT-116	colon:	n/a	n/a
31	CEBPB	chr2:173298755-173298815	H1-hESC	embryonic stem cell:	n/a	chr2:173298788-173298799 chr2:173298788-173298801
32	CEBPB	chr2:173306554-173307890	HCT-116	colon:	n/a	chr2:173307559-173307572
33	CEBPB	chr2:173306465-173307886	HCT-116	colon:	n/a	chr2:173307559-173307572
34	CEBPB	chr2:173281387-173281518	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:173291943-173292442	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr2:173302343-173302496	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:173306747-173307167	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:173306665-173307748	Hela-S3	cervix:	n/a	chr2:173307559-173307572
39	CEBPB	chr2:173295233-173295954	HCT-116	colon:	n/a	n/a
40	CEBPB	chr2:173306696-173307298	A549	lung:	n/a	n/a
41	CEBPB	chr2:173299387-173299412	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:173269706-173270033	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:173295432-173295700	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:173303651-173304380	A549	lung:	n/a	chr2:173304180-173304191 chr2:173304180-173304191
45	CEBPB	chr2:173306789-173307145	A549	lung:	n/a	n/a
46	CEBPB	chr2:173303745-173304390	Hela-S3	cervix:	n/a	chr2:173304180-173304191 chr2:173304180-173304191
47	CEBPD	chr2:173292046-173292727	HepG2	liver:	n/a	n/a
48	CEBPD	chr2:173292103-173292480	HepG2	liver:	n/a	n/a
49	CEBPZ	chr2:173286414-173286422	HepG2	liver:	n/a	n/a
50	CHD1	chr2:173292906-173293164	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:173293627-173293677	ProgFib	skin:	n/a
2	chr2:173293627-173293677	ProgFib	skin:	n/a
3	chr2:173292329-173292379	HL-60	blood:	n/a
4	chr2:173291965-173292015	HL-60	blood:	n/a
5	chr2:173292978-173293028	ProgFib	skin:	n/a
6	chr2:173291908-173291958	HMEC	breast:	n/a
7	chr2:173291908-173291958	T-47D	breast:	n/a
8	chr2:173293627-173293677	HL-60	blood:	n/a
9	chr2:173292579-173292629	NH-A	brain:	n/a
10	chr2:173293627-173293677	Hepatocyte	liver:	n/a
11	chr2:173294093-173294143	NH-A	brain:	n/a
12	chr2:173296469-173296519	NHBE	bronchial:	n/a
13	chr2:173289719-173289769	T-47D	breast:	n/a
14	chr2:173292268-173292318	ECC-1	luminal epithelium:	n/a
15	chr2:173292207-173292257	HEK293	kidney:	embryo
16	chr2:173292262-173292312	HepG2	liver:	n/a
17	chr2:173291908-173291958	ProgFib	skin:	n/a
18	chr2:173292271-173292321	AG09319	gingival:	n/a
19	chr2:173293328-173293378	ProgFib	skin:	n/a
20	chr2:173289719-173289769	GM12892	blood:	n/a
21	chr2:173296469-173296519	K562	blood:	n/a
22	chr2:173293182-173293232	Jurkat	blood:	n/a
23	chr2:173292579-173292629	HL-60	blood:	n/a
24	chr2:173298550-173298600	HRPEpiC	eye:	n/a
25	chr2:173293392-173293442	ProgFib	skin:	n/a
26	chr2:173289719-173289769	SKMC	muscle:	n/a
27	chr2:173305865-173305915	GM12892	blood:	n/a
28	chr2:173292262-173292312	AG09309	skin:	n/a
29	chr2:173293328-173293378	U87	brain:	n/a
30	chr2:173292329-173292379	LNCaP	prostate:	n/a
31	chr2:173293392-173293442	Jurkat	blood:	n/a
32	chr2:173292978-173293028	CMK	blood:	n/a
33	chr2:173293328-173293378	SK-N-MC	brain:	n/a
34	chr2:173298550-173298600	NT2-D1	testis:	n/a
35	chr2:173292636-173292686	T-47D	breast:	n/a
36	chr2:173293392-173293442	MCF-7	breast:	n/a
37	chr2:173292010-173292060	AG10803	skin:	n/a
38	chr2:173292262-173292312	HMEC	breast:	n/a
39	chr2:173293328-173293378	K562	blood:	n/a
40	chr2:173292268-173292318	HRPEpiC	eye:	n/a
41	chr2:173298550-173298600	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:173292262-173292312	SK-N-MC	brain:	n/a
43	chr2:173292262-173292312	GM06990	blood:	n/a
44	chr2:173292216-173292266	Hepatocyte	liver:	n/a
45	chr2:173298550-173298600	HIPEpiC	eye:	n/a
46	chr2:173305865-173305915	ovcar-3	ovarian:	n/a
47	chr2:173291908-173291958	NHBE	bronchial:	n/a
48	chr2:173294093-173294143	HAEpiC	amniotic membrane:	n/a
49	chr2:173296469-173296519	HIPEpiC	eye:	n/a
50	chr2:173292271-173292321	HIPEpiC	eye:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:173277939..173279825-chr2:173286825..173289513,2	MCF-7	breast:
2	chr2:173278930..173282468-chr2:173284020..173288117,3	K562	blood:
3	chr2:173290118..173293854-chr2:173304445..173308429,5	MCF-7	breast:
4	chr2:173307073..173308885-chr2:173311042..173312605,2	MCF-7	breast:
5	chr2:173272055..173273820-chr2:173294658..173297401,2	MCF-7	breast:
6	chr2:173294248..173297165-chr2:173302746..173304421,2	MCF-7	breast:
7	chr2:173218614..173220137-chr2:173294190..173296145,2	K562	blood:
8	chr2:173291662..173294325-chr2:173297442..173299980,3	MCF-7	breast:
9	chr2:173290254..173291940-chr2:173293674..173296240,2	MCF-7	breast:
10	chr2:173305610..173308515-chr2:173310023..173312671,2	MCF-7	breast:
11	chr2:173287551..173289075-chr2:173291560..173293629,2	K562	blood:
12	chr2:173272055..173273820-chr2:173294658..173297401,2	MCF-7	breast:
13	chr2:173290254..173291940-chr2:173293674..173296240,2	MCF-7	breast:
14	chr2:173265324..173267931-chr2:173283487..173286402,2	MCF-7	breast:
15	chr2:173292234..173292806-chr4:75230715..75231293,2	HCT-116	colon:
16	chr2:173277939..173279825-chr2:173286825..173289513,2	MCF-7	breast:
17	chr2:173305651..173308111-chr2:173326516..173329013,2	MCF-7	breast:
18	chr2:173268443..173272799-chr2:173274089..173275875,3	K562	blood:
19	chr2:173266015..173268775-chr2:173291252..173293915,2	MCF-7	breast:
20	chr2:173297263..173301573-chr2:173305902..173308346,3	MCF-7	breast:
21	chr2:173278303..173281188-chr2:173318534..173320264,2	MCF-7	breast:
22	chr2:173291236..173294444-chr2:173296195..173299585,6	K562	blood:
23	chr2:173291261..173294444-chr2:173294873..173298615,3	K562	blood:
24	chr2:173294248..173297165-chr2:173302746..173304421,2	MCF-7	breast:
25	chr2:173291657..173293814-chr2:173297316..173300145,3	MCF-7	breast:
26	chr2:173265324..173267931-chr2:173283487..173286402,2	MCF-7	breast:
27	chr2:173278930..173282468-chr2:173284020..173288117,3	K562	blood:
28	chr2:173284765..173286767-chr2:173287351..173289106,2	MCF-7	breast:
29	chr2:173277577..173279810-chr2:173280486..173283402,2	MCF-7	breast:
30	chr2:173284264..173284881-chrX:54068900..54069545,2	MCF-7	breast:
31	chr12:98897396..98898383-chr2:173292432..173293421,2	Hela-S3	cervix:
32	chr2:173284765..173286767-chr2:173287351..173289106,2	MCF-7	breast:
33	chr2:173277577..173279810-chr2:173280486..173283402,2	MCF-7	breast:
34	chr2:173292559..173293271-chr2:173319543..173320061,2	MCF-7	breast:
35	chr2:173297263..173301573-chr2:173305902..173308346,3	MCF-7	breast:
36	chr2:173268443..173272799-chr2:173274089..173275875,3	K562	blood:
37	chr2:173145139..173147717-chr2:173288396..173290436,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLX2-7	chr2:173288542-173288901	NONHSAT075502
2	lnc-DLX2-9	chr2:173296163-173300407	ucscGeneNc_uc002uht_1
3	lnc-DLX2-9	chr2:173307279-173307407	ucscGeneNc_uc002uht_1
4	lnc-DLX2-2	chr2:173292948-173293331	ENSG00000226963.1
5	lnc-DLX2-2	chr2:173292502-173292675	ENSG00000226963.1

No data

Variant related genes	Relation type
ITGA6	TF binding region
ENSG00000226963	TF binding region
ITGA6	CpG island
ENSG00000226963	CpG island
ENSG00000245017	chromatin interactions
ENSG00000172943	chromatin interactions
ENSG00000226963	chromatin interactions
ENSG00000091409	chromatin interactions
ENSG00000124882	chromatin interactions

Extended variants
information (count: 1604 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:1604 , 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	rs10930554	chr2:173267081-173267082	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558360420	chr2:173267107-173267108	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570276606	chr2:173267128-173267129	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs544483394	chr2:173267179-173267180	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537697223	chr2:173267186-173267187	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs557789021	chr2:173267253-173267254	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372645135	chr2:173267284-173267285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs556096208	chr2:173267353-173267354	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs60820657	chr2:173267365-173267366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574077145	chr2:173267409-173267410	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs187366327	chr2:173267424-173267425	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs150144452	chr2:173267426-173267427	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs192470683	chr2:173267429-173267430	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs578068845	chr2:173267434-173267435	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184063543	chr2:173267472-173267473	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs566424027	chr2:173267474-173267475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs187802449	chr2:173267486-173267487	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192428177	chr2:173267493-173267494	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs147563406	chr2:173267503-173267504	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs73033940	chr2:173267523-173267524	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs184562660	chr2:173267608-173267609	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7597542	chr2:173267613-173267614	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs559163825	chr2:173267645-173267646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75476623	chr2:173267694-173267695	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs551508073	chr2:173267765-173267766	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570215097	chr2:173267779-173267780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187023100	chr2:173267780-173267781	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs549686682	chr2:173267795-173267796	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191797322	chr2:173267813-173267814	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs73976785	chr2:173267833-173267834	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73033942	chr2:173267839-173267840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs577971608	chr2:173267863-173267864	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142135003	chr2:173267877-173267878	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs557039956	chr2:173267926-173267927	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs74949171	chr2:173267954-173267955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs573299795	chr2:173267979-173267980	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540063811	chr2:173268022-173268023	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540797263	chr2:173268065-173268066	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs575829459	chr2:173268084-173268085	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs117476190	chr2:173268097-173268098	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559794984	chr2:173268108-173268109	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs75529119	chr2:173268132-173268133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141061839	chr2:173268142-173268143	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540991181	chr2:173268164-173268165	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559258513	chr2:173268177-173268178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573029815	chr2:173268211-173268212	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs551495623	chr2:173268273-173268274	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs528908122	chr2:173268318-173268319	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184525620	chr2:173268319-173268320	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs531110060	chr2:173268320-173268321	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:45)

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
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
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
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173259000-173268400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr2:173262200-173269600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:173262600-173268000	Weak transcription	Esophagus	oesophagus
4	chr2:173262800-173267400	Weak transcription	NHEK	skin
5	chr2:173263400-173268000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:173263400-173268200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:173263400-173273000	Weak transcription	Right Atrium	heart
8	chr2:173263600-173272800	Weak transcription	Fetal Muscle Leg	muscle
9	chr2:173264600-173268000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:173264600-173268200	Weak transcription	Lung	lung
11	chr2:173264800-173267600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:173264800-173268000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr2:173266600-173267200	Enhancers	HUVEC	blood vessel
14	chr2:173266800-173267200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:173266800-173267600	Enhancers	Fetal Thymus	thymus
16	chr2:173266800-173268600	Enhancers	Left Ventricle	heart
17	chr2:173266800-173268600	Enhancers	Right Ventricle	heart
18	chr2:173266800-173268800	Enhancers	Adipose Nuclei	Adipose
19	chr2:173267000-173267200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:173267000-173267400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:173267200-173268200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr2:173267200-173268200	Weak transcription	HUVEC	blood vessel
23	chr2:173267400-173268400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr2:173267400-173268400	Enhancers	NHEK	skin
25	chr2:173267400-173268600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr2:173267600-173268000	Weak transcription	Fetal Thymus	thymus
27	chr2:173267600-173270600	Enhancers	HMEC	breast
28	chr2:173267600-173275600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:173267800-173274600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:173268000-173268200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr2:173268000-173268600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:173268000-173268600	Enhancers	Esophagus	oesophagus
33	chr2:173268000-173268600	Enhancers	Fetal Thymus	thymus
34	chr2:173268000-173270400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:173268000-173270600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:173268200-173268600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr2:173268200-173268600	Enhancers	Lung	lung
38	chr2:173268200-173269600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:173268200-173270000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:173268200-173270000	Enhancers	HUVEC	blood vessel
41	chr2:173268200-173270000	Enhancers	NH-A	brain
42	chr2:173268200-173270400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:173268400-173268800	Flanking Active TSS	NHEK	skin
44	chr2:173268400-173270000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr2:173268400-173270000	Enhancers	Fetal Kidney	kidney
46	chr2:173268400-173270400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr2:173268600-173270000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:173268600-173272800	Weak transcription	Esophagus	oesophagus
49	chr2:173268600-173272800	Weak transcription	Fetal Thymus	thymus
50	chr2:173268600-173272800	Weak transcription	Left Ventricle	heart

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