Variant report

Variant	nsv583664
Chromosome Location	chr2:173289239-173307756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1126)
CpG islands
(count:1344)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1126 , 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	chr2:173293139-173293530	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:173292090-173292504	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:173295416-173295725	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:173300084-173300259	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:173306798-173307007	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:173296013-173296343	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:173307251-173307282	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	chr2:173291690-173293224	HepG2	liver:	n/a	chr2:173292390-173292406 chr2:173292470-173292486
14	BHLHE40	chr2:173294161-173294743	HepG2	liver:	n/a	chr2:173294556-173294577 chr2:173294562-173294571 chr2:173294561-173294570 chr2:173294562-173294571
15	BHLHE40	chr2:173294498-173294698	K562	blood:	n/a	chr2:173294556-173294577 chr2:173294562-173294571 chr2:173294561-173294570 chr2:173294562-173294571
16	BHLHE40	chr2:173292946-173293146	A549	lung:	n/a	n/a
17	BHLHE40	chr2:173302468-173302709	GM12878	blood:	n/a	n/a
18	BRCA1	chr2:173291827-173292596	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr2:173306685-173307524	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr2:173292047-173292183	HepG2	liver:	n/a	n/a
21	BRCA1	chr2:173292581-173292602	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr2:173303754-173304313	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	chr2:173295233-173295954	HCT-116	colon:	n/a	n/a
26	CEBPB	chr2:173302343-173302496	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:173291943-173292442	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:173306747-173307167	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:173295433-173295752	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:173295167-173295994	HCT-116	colon:	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	chr2:173306665-173307748	Hela-S3	cervix:	n/a	chr2:173307559-173307572
34	CEBPB	chr2:173303651-173304380	A549	lung:	n/a	chr2:173304180-173304191 chr2:173304180-173304191
35	CEBPB	chr2:173298705-173298939	HepG2	liver:	n/a	chr2:173298788-173298799 chr2:173298788-173298801
36	CEBPB	chr2:173306789-173307145	A549	lung:	n/a	n/a
37	CEBPB	chr2:173300343-173300516	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:173295432-173295700	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:173299387-173299412	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:173298755-173298815	H1-hESC	embryonic stem cell:	n/a	chr2:173298788-173298799 chr2:173298788-173298801
41	CEBPB	chr2:173306465-173307886	HCT-116	colon:	n/a	chr2:173307559-173307572
42	CEBPB	chr2:173306554-173307890	HCT-116	colon:	n/a	chr2:173307559-173307572
43	CEBPB	chr2:173303745-173304390	Hela-S3	cervix:	n/a	chr2:173304180-173304191 chr2:173304180-173304191
44	CEBPD	chr2:173292046-173292727	HepG2	liver:	n/a	n/a
45	CEBPD	chr2:173292103-173292480	HepG2	liver:	n/a	n/a
46	CHD1	chr2:173293408-173293833	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	chr2:173292906-173293164	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr2:173306571-173307595	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr2:173292952-173293703	H1-hESC	embryonic stem cell:	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	chr2:173296469-173296519	Hela-S3	cervix:	n/a
2	chr2:173293328-173293378	Hepatocyte	liver:	n/a
3	chr2:173296469-173296519	Hela-S3	cervix:	n/a
4	chr2:173293328-173293378	Hepatocyte	liver:	n/a
5	chr2:173292277-173292327	NHDF-neo	bronchial:	n/a
6	chr2:173293182-173293232	AG10803	skin:	n/a
7	chr2:173292636-173292686	MCF-7	breast:	n/a
8	chr2:173298550-173298600	HepG2	liver:	n/a
9	chr2:173292277-173292327	HRPEpiC	eye:	n/a
10	chr2:173292010-173292060	AG10803	skin:	n/a
11	chr2:173298550-173298600	HMEC	breast:	n/a
12	chr2:173298550-173298600	HRCEpiC	kidney:	n/a
13	chr2:173305865-173305915	HCT-116	colon:	n/a
14	chr2:173292216-173292266	SK-N-SH_RA	brain:	n/a
15	chr2:173293328-173293378	LNCaP	prostate:	n/a
16	chr2:173292579-173292629	GM12892	blood:	n/a
17	chr2:173292207-173292257	GM12892	blood:	n/a
18	chr2:173292579-173292629	IMR90	lung:	fetal
19	chr2:173292277-173292327	HCF	heart:	n/a
20	chr2:173291908-173291958	AoSMC	blood vessel:	n/a
21	chr2:173292207-173292257	PrEC	prostate:	n/a
22	chr2:173292268-173292318	AoSMC	blood vessel:	n/a
23	chr2:173305865-173305915	MCF-7	breast:	n/a
24	chr2:173293392-173293442	PrEC	prostate:	n/a
25	chr2:173292277-173292327	BE2_C	brain:	n/a
26	chr2:173293627-173293677	IMR90	lung:	fetal
27	chr2:173292216-173292266	AG09319	gingival:	n/a
28	chr2:173305865-173305915	SAEC	small airway:	n/a
29	chr2:173292271-173292321	Jurkat	blood:	n/a
30	chr2:173305865-173305915	RPTEC	kidney:	n/a
31	chr2:173292010-173292060	NHDF-neo	bronchial:	n/a
32	chr2:173291965-173292015	HCT-116	colon:	n/a
33	chr2:173292268-173292318	ProgFib	skin:	n/a
34	chr2:173292271-173292321	GM19239	blood:	n/a
35	chr2:173293392-173293442	ovcar-3	ovarian:	n/a
36	chr2:173292636-173292686	HCPEpiC	choroid plexus:	n/a
37	chr2:173292579-173292629	AG04449	skin:	fetal
38	chr2:173293328-173293378	PANC-1	pancreas:	n/a
39	chr2:173296469-173296519	SK-N-SH_RA	brain:	n/a
40	chr2:173292579-173292629	HepG2	liver:	n/a
41	chr2:173292262-173292312	SK-N-SH_RA	brain:	n/a
42	chr2:173292579-173292629	HRPEpiC	eye:	n/a
43	chr2:173293328-173293378	ovcar-3	ovarian:	n/a
44	chr2:173296469-173296519	PANC-1	pancreas:	n/a
45	chr2:173289719-173289769	SK-N-SH_RA	brain:	n/a
46	chr2:173291908-173291958	NT2-D1	testis:	n/a
47	chr2:173296469-173296519	LNCaP	prostate:	n/a
48	chr2:173292277-173292327	GM19239	blood:	n/a
49	chr2:173291965-173292015	NHBE	bronchial:	n/a
50	chr2:173289719-173289769	HUVEC	blood vessel:	n/a

(count:21 , 50 per page) page: 1

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

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLX2-2	chr2:173292502-173292675	ENSG00000226963.1
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

No data

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

Extended variants
information (count: 711 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1001926	chr2:173289239-173289240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77117084	chr2:173289272-173289273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368210730	chr2:173289296-173289297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530419046	chr2:173289317-173289318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535721214	chr2:173289336-173289337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542816747	chr2:173289396-173289397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs60202603	chr2:173289425-173289426	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs78307320	chr2:173289435-173289436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78696407	chr2:173289436-173289437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139319401	chr2:173289480-173289481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372719373	chr2:173289542-173289543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546620458	chr2:173289547-173289548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564895368	chr2:173289584-173289585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577636087	chr2:173289607-173289608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78582092	chr2:173289625-173289626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550243803	chr2:173289661-173289662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548870760	chr2:173289692-173289693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193048561	chr2:173289719-173289720	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs10930555	chr2:173289736-173289737	Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566961495	chr2:173289790-173289791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534497110	chr2:173289798-173289799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559032798	chr2:173289829-173289830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570801799	chr2:173289845-173289846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538209649	chr2:173289849-173289850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185231476	chr2:173289924-173289925	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs62167765	chr2:173289968-173289969	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs144245656	chr2:173289971-173289972	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs73023468	chr2:173290115-173290116	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573002333	chr2:173290216-173290217	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs111825325	chr2:173290227-173290228	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs540500161	chr2:173290280-173290281	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs2272496	chr2:173290287-173290288	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs2141698	chr2:173290395-173290396	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs190472550	chr2:173290427-173290428	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs562144137	chr2:173290443-173290444	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs553816749	chr2:173290517-173290518	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs76058534	chr2:173290562-173290563	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs547922197	chr2:173290565-173290566	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs567050193	chr2:173290586-173290587	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs527907245	chr2:173290678-173290679	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs71415298	chr2:173290774-173290775	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs140999787	chr2:173290783-173290784	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs73023472	chr2:173290795-173290796	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549963231	chr2:173290835-173290836	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs34148532	chr2:173290836-173290837	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs556557024	chr2:173290868-173290869	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs568509682	chr2:173290905-173290906	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs535952240	chr2:173290908-173290909	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs146750086	chr2:173290921-173290922	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs148833435	chr2:173291037-173291038	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	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:1380 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

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	chr2:173287400-173289400	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr2:173287600-173290600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr2:173287800-173291000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:173288200-173290400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr2:173288200-173290600	Weak transcription	Primary T cells from cord blood	blood
10	chr2:173288200-173290800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr2:173288400-173290200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr2:173288400-173290200	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr2:173288400-173290400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr2:173288400-173290800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr2:173288400-173291000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr2:173288400-173291800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:173288600-173290600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr2:173288600-173290800	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr2:173289000-173289400	Enhancers	NHEK	skin
20	chr2:173289000-173289600	Enhancers	Thymus	Thymus
21	chr2:173289000-173291600	Weak transcription	Adipose Nuclei	Adipose
22	chr2:173289400-173289600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:173289400-173290200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr2:173289400-173291400	Weak transcription	NHEK	skin
25	chr2:173289600-173290800	Weak transcription	Thymus	Thymus
26	chr2:173290200-173290400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:173290200-173290400	Enhancers	Psoas Muscle	Psoas
28	chr2:173290200-173290600	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr2:173290200-173291400	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr2:173290200-173291400	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr2:173290200-173291600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr2:173290200-173291600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr2:173290200-173291600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr2:173290200-173291800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr2:173290200-173291800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:173290200-173292000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
37	chr2:173290400-173290800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:173290400-173291000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:173290400-173291400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
40	chr2:173290400-173291400	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr2:173290400-173291400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:173290400-173291800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr2:173290600-173291000	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr2:173290600-173291200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr2:173290600-173291400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr2:173290600-173291600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr2:173290600-173291600	Enhancers	Primary T cells from cord blood	blood
48	chr2:173290600-173291800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:173290600-173291800	Weak transcription	Psoas Muscle	Psoas
50	chr2:173290800-173291000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell

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