Variant report

Variant	nsv583663
Chromosome Location	chr2:173287832-173307756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1127)
CpG islands
(count:1344)
Chromatin interactive
region (count:24)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr2:173296013-173296343	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:173307251-173307282	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:173295416-173295725	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:173293139-173293530	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:173306798-173307007	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:173292090-173292504	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	chr2:173291931-173292473	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:173292974-173293425	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr2:173306584-173307248	A549	lung:	n/a	n/a
13	BHLHE40	chr2:173302468-173302709	GM12878	blood:	n/a	n/a
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	chr2:173291690-173293224	HepG2	liver:	n/a	chr2:173292390-173292406 chr2:173292470-173292486
17	BHLHE40	chr2:173294161-173294743	HepG2	liver:	n/a	chr2:173294556-173294577 chr2:173294562-173294571 chr2:173294561-173294570 chr2:173294562-173294571
18	BRCA1	chr2:173306685-173307524	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr2:173292581-173292602	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr2:173303754-173304313	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr2:173292047-173292183	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:173291827-173292596	Hela-S3	cervix:	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	chr2:173303745-173304390	Hela-S3	cervix:	n/a	chr2:173304180-173304191 chr2:173304180-173304191
26	CEBPB	chr2:173291943-173292442	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:173295233-173295954	HCT-116	colon:	n/a	n/a
28	CEBPB	chr2:173300343-173300516	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:173298755-173298815	H1-hESC	embryonic stem cell:	n/a	chr2:173298788-173298799 chr2:173298788-173298801
30	CEBPB	chr2:173302343-173302496	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:173306696-173307298	A549	lung:	n/a	n/a
32	CEBPB	chr2:173300131-173300600	HepG2	liver:	n/a	chr2:173300184-173300197
33	CEBPB	chr2:173303651-173304380	A549	lung:	n/a	chr2:173304180-173304191 chr2:173304180-173304191
34	CEBPB	chr2:173295167-173295994	HCT-116	colon:	n/a	n/a
35	CEBPB	chr2:173295432-173295700	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:173295433-173295752	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:173306554-173307890	HCT-116	colon:	n/a	chr2:173307559-173307572
38	CEBPB	chr2:173306465-173307886	HCT-116	colon:	n/a	chr2:173307559-173307572
39	CEBPB	chr2:173299387-173299412	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:173306747-173307167	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:173298705-173298939	HepG2	liver:	n/a	chr2:173298788-173298799 chr2:173298788-173298801
42	CEBPB	chr2:173306665-173307748	Hela-S3	cervix:	n/a	chr2:173307559-173307572
43	CEBPB	chr2:173306789-173307145	A549	lung:	n/a	n/a
44	CEBPD	chr2:173292103-173292480	HepG2	liver:	n/a	n/a
45	CEBPD	chr2:173292046-173292727	HepG2	liver:	n/a	n/a
46	CHD1	chr2:173292906-173293164	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr2:173292320-173292658	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr2:173293408-173293833	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr2:173306571-173307595	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr2:173293198-173293538	HepG2	liver:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:173293392-173293442	IMR90	lung:	fetal
2	chr2:173294093-173294143	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:173293392-173293442	IMR90	lung:	fetal
4	chr2:173294093-173294143	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:173292978-173293028	AG10803	skin:	n/a
6	chr2:173291965-173292015	GM06990	blood:	n/a
7	chr2:173305865-173305915	HCF	heart:	n/a
8	chr2:173292579-173292629	K562	blood:	n/a
9	chr2:173292271-173292321	HIPEpiC	eye:	n/a
10	chr2:173298550-173298600	GM12878	blood:	n/a
11	chr2:173293182-173293232	HCPEpiC	choroid plexus:	n/a
12	chr2:173291908-173291958	RPTEC	kidney:	n/a
13	chr2:173292010-173292060	SK-N-MC	brain:	n/a
14	chr2:173305865-173305915	HIPEpiC	eye:	n/a
15	chr2:173291965-173292015	AoSMC	blood vessel:	n/a
16	chr2:173296469-173296519	HEEpiC	esophagus:	n/a
17	chr2:173293627-173293677	HCF	heart:	n/a
18	chr2:173296469-173296519	Hepatocyte	liver:	n/a
19	chr2:173293392-173293442	HRPEpiC	eye:	n/a
20	chr2:173291965-173292015	GM12892	blood:	n/a
21	chr2:173296469-173296519	HCPEpiC	choroid plexus:	n/a
22	chr2:173292207-173292257	ovcar-3	ovarian:	n/a
23	chr2:173289719-173289769	GM06990	blood:	n/a
24	chr2:173292010-173292060	HCT-116	colon:	n/a
25	chr2:173292207-173292257	NT2-D1	testis:	n/a
26	chr2:173292262-173292312	HRCEpiC	kidney:	n/a
27	chr2:173292277-173292327	SK-N-SH	brain:	n/a
28	chr2:173305865-173305915	PFSK-1	brain:	n/a
29	chr2:173291908-173291958	H1-hESC	embryonic stem cell:	embryo
30	chr2:173298550-173298600	IMR90	lung:	fetal
31	chr2:173293627-173293677	SK-N-MC	brain:	n/a
32	chr2:173293182-173293232	GM19239	blood:	n/a
33	chr2:173293392-173293442	AG09309	skin:	n/a
34	chr2:173292271-173292321	HEEpiC	esophagus:	n/a
35	chr2:173293182-173293232	GM12892	blood:	n/a
36	chr2:173292329-173292379	HRPEpiC	eye:	n/a
37	chr2:173292262-173292312	PrEC	prostate:	n/a
38	chr2:173292636-173292686	SAEC	small airway:	n/a
39	chr2:173292262-173292312	NHBE	bronchial:	n/a
40	chr2:173292010-173292060	HEK293	kidney:	embryo
41	chr2:173293328-173293378	HRCEpiC	kidney:	n/a
42	chr2:173293182-173293232	AG04449	skin:	fetal
43	chr2:173293627-173293677	HIPEpiC	eye:	n/a
44	chr2:173289719-173289769	PFSK-1	brain:	n/a
45	chr2:173291965-173292015	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:173292207-173292257	SAEC	small airway:	n/a
47	chr2:173293392-173293442	HRCEpiC	kidney:	n/a
48	chr2:173292978-173293028	HAEpiC	amniotic membrane:	n/a
49	chr2:173298550-173298600	AG09319	gingival:	n/a
50	chr2:173292268-173292318	MCF10A-Er-Src	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:173291662..173294325-chr2:173297442..173299980,3	MCF-7	breast:
2	chr2:173291261..173294444-chr2:173294873..173298615,3	K562	blood:
3	chr2:173297263..173301573-chr2:173305902..173308346,3	MCF-7	breast:
4	chr2:173297263..173301573-chr2:173305902..173308346,3	MCF-7	breast:
5	chr2:173291657..173293814-chr2:173297316..173300145,3	MCF-7	breast:
6	chr2:173290254..173291940-chr2:173293674..173296240,2	MCF-7	breast:
7	chr2:173291236..173294444-chr2:173296195..173299585,6	K562	blood:
8	chr2:173287551..173289075-chr2:173291560..173293629,2	K562	blood:
9	chr2:173292234..173292806-chr4:75230715..75231293,2	HCT-116	colon:
10	chr2:173294248..173297165-chr2:173302746..173304421,2	MCF-7	breast:
11	chr2:173290118..173293854-chr2:173304445..173308429,5	MCF-7	breast:
12	chr2:173290254..173291940-chr2:173293674..173296240,2	MCF-7	breast:
13	chr2:173278930..173282468-chr2:173284020..173288117,3	K562	blood:
14	chr2:173305610..173308515-chr2:173310023..173312671,2	MCF-7	breast:
15	chr12:98897396..98898383-chr2:173292432..173293421,2	Hela-S3	cervix:
16	chr2:173145139..173147717-chr2:173288396..173290436,2	MCF-7	breast:
17	chr2:173292559..173293271-chr2:173319543..173320061,2	MCF-7	breast:
18	chr2:173294248..173297165-chr2:173302746..173304421,2	MCF-7	breast:
19	chr2:173284765..173286767-chr2:173287351..173289106,2	MCF-7	breast:
20	chr2:173305651..173308111-chr2:173326516..173329013,2	MCF-7	breast:
21	chr2:173277939..173279825-chr2:173286825..173289513,2	MCF-7	breast:
22	chr2:173272055..173273820-chr2:173294658..173297401,2	MCF-7	breast:
23	chr2:173218614..173220137-chr2:173294190..173296145,2	K562	blood:
24	chr2:173307073..173308885-chr2:173311042..173312605,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 786 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11687010	chr2:173287832-173287833	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569931487	chr2:173287855-173287856	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563637748	chr2:173287875-173287876	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537362754	chr2:173287884-173287885	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs555353119	chr2:173287924-173287925	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs114038124	chr2:173287975-173287976	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374143488	chr2:173287994-173287995	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs564054582	chr2:173287995-173287996	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140040661	chr2:173288046-173288047	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553063207	chr2:173288068-173288069	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs188929076	chr2:173288113-173288114	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs543088187	chr2:173288115-173288116	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs374594335	chr2:173288119-173288120	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs192004700	chr2:173288122-173288123	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs144137633	chr2:173288127-173288128	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs147324402	chr2:173288128-173288129	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs182628545	chr2:173288146-173288147	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs560939308	chr2:173288158-173288159	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs528187712	chr2:173288193-173288194	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs566010455	chr2:173288203-173288204	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs375706045	chr2:173288211-173288212	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs531582549	chr2:173288247-173288248	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs376236855	chr2:173288308-173288309	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs148724177	chr2:173288319-173288320	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs2008518	chr2:173288337-173288338	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs532514388	chr2:173288414-173288415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs551521964	chr2:173288426-173288427	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569866598	chr2:173288436-173288437	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs530782039	chr2:173288438-173288439	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs374658773	chr2:173288473-173288474	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs1976943	chr2:173288474-173288475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567251202	chr2:173288484-173288485	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534649751	chr2:173288487-173288488	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552712739	chr2:173288491-173288492	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs571295563	chr2:173288513-173288514	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs368166098	chr2:173288516-173288517	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs370693999	chr2:173288519-173288520	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs3856431	chr2:173288543-173288544	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs567672362	chr2:173288556-173288557	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs374747358	chr2:173288584-173288585	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs367859948	chr2:173288591-173288592	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs557093063	chr2:173288593-173288594	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs536651381	chr2:173288602-173288603	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs186978823	chr2:173288612-173288613	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs536545979	chr2:173288613-173288614	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs140189316	chr2:173288616-173288617	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs554869011	chr2:173288622-173288623	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs572885624	chr2:173288623-173288624	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs71015697	chr2:173288624-173288625	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs540586340	chr2:173288626-173288627	Weak transcription Enhancers	Chromatin interactive region lncRNA	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:1401 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173274600-173290200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:173285200-173291800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:173285200-173291800	Enhancers	Fetal Thymus	thymus
4	chr2:173286600-173290400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:173287200-173288600	Enhancers	Thymus	Thymus
6	chr2:173287200-173288600	Enhancers	Dnd41	blood
7	chr2:173287400-173288000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:173287400-173288400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:173287400-173289400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr2:173287600-173288200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:173287600-173288200	Enhancers	Primary T cells from cord blood	blood
12	chr2:173287600-173288400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr2:173287600-173288400	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr2:173287600-173290600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr2:173287800-173288000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr2:173287800-173288000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:173287800-173288200	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr2:173287800-173288400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr2:173287800-173288600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr2:173287800-173291000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr2:173288000-173288200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:173288000-173288200	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr2:173288000-173288200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr2:173288000-173288200	Enhancers	Fetal Kidney	kidney
25	chr2:173288000-173288400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr2:173288000-173288600	Enhancers	Primary T cells fromperipheralblood	blood
27	chr2:173288200-173288400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr2:173288200-173290400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr2:173288200-173290600	Weak transcription	Primary T cells from cord blood	blood
30	chr2:173288200-173290800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr2:173288400-173290200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr2:173288400-173290200	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr2:173288400-173290400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr2:173288400-173290800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr2:173288400-173291000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr2:173288400-173291800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:173288600-173289000	Weak transcription	Thymus	Thymus
38	chr2:173288600-173290600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr2:173288600-173290800	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr2:173289000-173289400	Enhancers	NHEK	skin
41	chr2:173289000-173289600	Enhancers	Thymus	Thymus
42	chr2:173289000-173291600	Weak transcription	Adipose Nuclei	Adipose
43	chr2:173289400-173289600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:173289400-173290200	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr2:173289400-173291400	Weak transcription	NHEK	skin
46	chr2:173289600-173290800	Weak transcription	Thymus	Thymus
47	chr2:173290200-173290400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:173290200-173290400	Enhancers	Psoas Muscle	Psoas
49	chr2:173290200-173290600	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr2:173290200-173291400	Enhancers	Primary T helper cells PMA-I stimulated	--

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