Variant report

Variant	nsv522096
Chromosome Location	chr6:147424880-147443480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:147428308-147428329	HepG2	liver:	n/a	n/a
2	CEBPB	chr6:147428148-147428494	HepG2	liver:	n/a	n/a
3	CEBPB	chr6:147428152-147428477	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:147428219-147428500	MCF-7	breast:	n/a	n/a
5	CEBPB	chr6:147428107-147428473	K562	blood:	n/a	n/a
6	CEBPB	chr6:147440467-147440831	HepG2	liver:	n/a	chr6:147440639-147440650
7	CEBPB	chr6:147440484-147440794	IMR90	lung:	n/a	chr6:147440639-147440650
8	CEBPB	chr6:147440482-147440806	A549	lung:	n/a	chr6:147440639-147440650
9	CEBPB	chr6:147428123-147428528	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:147428202-147428406	MCF-7	breast:	n/a	n/a
11	CEBPB	chr6:147428152-147428450	A549	lung:	n/a	n/a
12	CEBPB	chr6:147428151-147428520	K562	blood:	n/a	n/a
13	CEBPB	chr6:147440505-147440819	K562	blood:	n/a	chr6:147440639-147440650
14	CEBPB	chr6:147428132-147428425	K562	blood:	n/a	n/a
15	CTCF	chr6:147438860-147439010	BJ	skin:	n/a	n/a
16	CTCF	chr6:147427800-147427950	AG04450	lung:	n/a	n/a
17	CUX1	chr6:147428264-147428809	K562	blood:	n/a	n/a
18	E2F4	chr6:147432968-147433212	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr6:147428193-147428420	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr6:147438687-147439012	GM12878	blood:	n/a	chr6:147438853-147438863 chr6:147438852-147438863 chr6:147438853-147438862
21	EP300	chr6:147428228-147428437	K562	blood:	n/a	n/a
22	FOS	chr6:147428199-147428612	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr6:147428237-147428511	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr6:147428191-147428539	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr6:147428198-147428499	MCF10A-Er-Src	breast:	n/a	n/a
26	GATA3	chr6:147424720-147425306	SK-N-SH	brain:	n/a	chr6:147425005-147425015
27	GATA3	chr6:147424655-147425238	SK-N-SH	brain:	n/a	chr6:147425005-147425015
28	GATA3	chr6:147434216-147434379	SH-SY5Y	brain:	n/a	n/a
29	IRF1	chr6:147438761-147439091	K562	blood:	n/a	chr6:147438922-147438933 chr6:147438922-147438935 chr6:147438922-147438935 chr6:147438921-147438941 chr6:147438923-147438933 chr6:147438915-147438935 chr6:147438917-147438927 chr6:147438919-147438933 chr6:147438922-147438936 chr6:147438917-147438931 chr6:147438923-147438937 chr6:147438922-147438935
30	IRF1	chr6:147440227-147440251	K562	blood:	n/a	n/a
31	IRF1	chr6:147440216-147440307	K562	blood:	n/a	n/a
32	JUND	chr6:147428175-147428606	K562	blood:	n/a	n/a
33	KAP1	chr6:147427179-147427472	K562	blood:	n/a	n/a
34	MAFF	chr6:147426960-147427292	HepG2	liver:	n/a	n/a
35	MAFF	chr6:147426990-147427257	K562	blood:	n/a	n/a
36	MAFK	chr6:147428779-147428817	K562	blood:	n/a	n/a
37	MAFK	chr6:147426978-147427283	HepG2	liver:	n/a	n/a
38	MAFK	chr6:147426979-147427250	HepG2	liver:	n/a	n/a
39	MAFK	chr6:147426971-147427245	IMR90	lung:	n/a	n/a
40	MAFK	chr6:147427038-147427251	K562	blood:	n/a	n/a
41	MAZ	chr6:147428349-147428534	K562	blood:	n/a	n/a
42	MYC	chr6:147428053-147428438	K562	blood:	n/a	n/a
43	MYC	chr6:147437403-147437424	K562	blood:	n/a	n/a
44	MYC	chr6:147424800-147424968	NB4	blood:	n/a	n/a
45	POLR2A	chr6:147438042-147438574	HL-60	blood:	n/a	n/a
46	POLR2A	chr6:147437072-147437669	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr6:147429494-147429761	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr6:147438403-147438425	GM12878	blood:	n/a	n/a
49	POLR2A	chr6:147437110-147437750	H1-neurons	neurons:	n/a	n/a
50	RAD21	chr6:147428151-147428464	IMR90	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147428486-147428536	GM12878	blood:	n/a
2	chr6:147428486-147428536	HCPEpiC	choroid plexus:	n/a
3	chr6:147428486-147428536	LNCaP	prostate:	n/a
4	chr6:147428486-147428536	GM06990	blood:	n/a
5	chr6:147428486-147428536	Hela-S3	cervix:	n/a
6	chr6:147428486-147428536	GM12892	blood:	n/a
7	chr6:147428486-147428536	HCF	heart:	n/a
8	chr6:147428486-147428536	AG04450	lung:	fetal
9	chr6:147428486-147428536	HEK293	kidney:	embryo
10	chr6:147428486-147428536	U87	brain:	n/a
11	chr6:147428486-147428536	SK-N-MC	brain:	n/a
12	chr6:147428486-147428536	HCT-116	colon:	n/a
13	chr6:147428486-147428536	HRPEpiC	eye:	n/a
14	chr6:147428486-147428536	HCM	heart:	n/a
15	chr6:147428486-147428536	BE2_C	brain:	n/a
16	chr6:147428486-147428536	MCF10A-Er-Src	breast:	n/a
17	chr6:147428486-147428536	K562	blood:	n/a
18	chr6:147428486-147428536	AG09309	skin:	n/a
19	chr6:147428486-147428536	HL-60	blood:	n/a
20	chr6:147428486-147428536	CMK	blood:	n/a
21	chr6:147428486-147428536	ECC-1	luminal epithelium:	n/a
22	chr6:147428486-147428536	MCF-7	breast:	n/a
23	chr6:147428486-147428536	GM19239	blood:	n/a
24	chr6:147428486-147428536	IMR90	lung:	fetal
25	chr6:147428486-147428536	PFSK-1	brain:	n/a
26	chr6:147428486-147428536	RPTEC	kidney:	n/a
27	chr6:147428486-147428536	AoSMC	blood vessel:	n/a
28	chr6:147428486-147428536	SK-N-SH	brain:	n/a
29	chr6:147428486-147428536	ProgFib	skin:	n/a
30	chr6:147428486-147428536	H1-hESC	embryonic stem cell:	embryo
31	chr6:147428486-147428536	AG04449	skin:	fetal
32	chr6:147428486-147428536	PANC-1	pancreas:	n/a
33	chr6:147428486-147428536	HIPEpiC	eye:	n/a
34	chr6:147428486-147428536	HEEpiC	esophagus:	n/a
35	chr6:147428486-147428536	AG10803	skin:	n/a
36	chr6:147428486-147428536	NT2-D1	testis:	n/a
37	chr6:147428486-147428536	SKMC	muscle:	n/a
38	chr6:147428486-147428536	AG09319	gingival:	n/a
39	chr6:147428486-147428536	Caco-2	colon:	n/a
40	chr6:147428486-147428536	ovcar-3	ovarian:	n/a
41	chr6:147428486-147428536	BJ	skin:	n/a
42	chr6:147428486-147428536	GM12891	blood:	n/a
43	chr6:147428486-147428536	HRCEpiC	kidney:	n/a
44	chr6:147428486-147428536	NHBE	bronchial:	n/a
45	chr6:147428486-147428536	HNPCEpiC	eye:	n/a
46	chr6:147428486-147428536	HAEpiC	amniotic membrane:	n/a
47	chr6:147428486-147428536	NHDF-neo	bronchial:	n/a
48	chr6:147428486-147428536	HMEC	breast:	n/a
49	chr6:147428486-147428536	A549	lung:	n/a
50	chr6:147428486-147428536	SAEC	small airway:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:147437032..147439799-chr6:147479756..147483330,3	K562	blood:
2	chr6:147420588..147422113-chr6:147425783..147427483,2	K562	blood:
3	chr6:147427313..147429430-chr6:147435405..147437072,2	K562	blood:
4	chr6:147426845..147428573-chr6:147517289..147519124,2	K562	blood:
5	chr6:147427313..147429430-chr6:147435405..147437072,2	K562	blood:
6	chr6:147426207..147429085-chr6:147439279..147441613,3	K562	blood:
7	chr6:147424959..147428934-chr6:147429472..147432018,4	MCF-7	breast:
8	chr6:147436472..147438342-chr6:147524210..147525806,2	K562	blood:
9	chr6:147425896..147428449-chr6:147432490..147434531,2	K562	blood:
10	chr6:147431206..147434248-chr6:147448632..147451102,3	K562	blood:
11	chr6:147442930..147446294-chr6:147532679..147536475,3	K562	blood:
12	chr6:147430213..147433528-chr6:147478461..147482182,3	K562	blood:
13	chr6:147206418..147208548-chr6:147443169..147444927,2	K562	blood:
14	chr6:147415331..147417181-chr6:147425131..147427562,2	K562	blood:
15	chr6:147439196..147441349-chr6:147442627..147444720,2	K562	blood:
16	chr6:147442873..147445423-chr6:147447092..147450084,3	K562	blood:
17	chr6:147232453..147234855-chr6:147426627..147429327,2	K562	blood:
18	chr6:147425896..147428449-chr6:147432490..147434531,2	K562	blood:
19	chr6:147443197..147445695-chr6:147447092..147449198,3	K562	blood:
20	chr6:147420322..147423479-chr6:147424445..147428438,5	K562	blood:
21	chr6:147419431..147422088-chr6:147424854..147426764,2	MCF-7	breast:
22	chr6:147424959..147428934-chr6:147429472..147432018,4	MCF-7	breast:
23	chr6:147408861..147411040-chr6:147429825..147431994,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452
2	lnc-SHPRH-2	chr6:147440553-147440613	NONHSAT115433
3	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452
4	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452
5	lnc-SHPRH-2	chr6:147440553-147440613	NONHSAT115441
6	lnc-SHPRH-2	chr6:147440553-147440599	ENSG00000233452
7	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452

No data

Variant related genes	Relation type
STXBP5-AS1	TF binding region
STXBP5-AS1	CpG island
ENSG00000164506	chromatin interactions
ENSG00000233452	chromatin interactions
ENSG00000196634	chromatin interactions
MTMR4	miRNA target sites
ADAM12	miRNA target sites
TMEM161B	miRNA target sites
PPP1CB	miRNA target sites
HAND1	miRNA target sites

Extended variants
information (count: 654 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6908011	chr6:147424880-147424881	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374635011	chr6:147424903-147424904	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547449452	chr6:147424926-147424927	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs567936737	chr6:147424934-147424935	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs564522924	chr6:147424940-147424941	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs374001230	chr6:147425059-147425060	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547009775	chr6:147425118-147425119	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs371370168	chr6:147425125-147425126	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs566751131	chr6:147425140-147425141	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs377638241	chr6:147425149-147425150	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs549252933	chr6:147425166-147425167	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs34845068	chr6:147425212-147425213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544644942	chr6:147425221-147425222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550362904	chr6:147425244-147425245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115076034	chr6:147425256-147425257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111363719	chr6:147425257-147425258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534214160	chr6:147425262-147425263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570173743	chr6:147425315-147425316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192074970	chr6:147425318-147425319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370798185	chr6:147425383-147425384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552961072	chr6:147425385-147425386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114061128	chr6:147425390-147425391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542123345	chr6:147425393-147425394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79662964	chr6:147425398-147425399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575510248	chr6:147425408-147425409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570164863	chr6:147425417-147425418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564262059	chr6:147425478-147425479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs578081467	chr6:147425491-147425492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562754620	chr6:147425532-147425533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368285258	chr6:147425544-147425545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540352112	chr6:147425561-147425562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184340350	chr6:147425566-147425567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558780585	chr6:147425593-147425594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549291495	chr6:147425607-147425608	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs562796368	chr6:147425615-147425616	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs531798322	chr6:147425616-147425617	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs551600890	chr6:147425620-147425621	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs114602253	chr6:147425700-147425701	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs539552259	chr6:147425701-147425702	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs558415204	chr6:147425707-147425708	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs189813883	chr6:147425785-147425786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs115359699	chr6:147425786-147425787	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs530031152	chr6:147425838-147425839	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs200317549	chr6:147425845-147425846	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs184498666	chr6:147425879-147425880	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs555705868	chr6:147425889-147425890	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs141515328	chr6:147425927-147425928	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs575276841	chr6:147425994-147425995	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs189073044	chr6:147426046-147426047	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs558014849	chr6:147426112-147426113	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147421800-147427800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:147422000-147427800	Weak transcription	Osteobl	bone
3	chr6:147422000-147428000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:147423800-147426000	Enhancers	Primary T cells from cord blood	blood
5	chr6:147424400-147425400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr6:147424400-147425800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr6:147424400-147426400	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr6:147424600-147425600	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr6:147424600-147425800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr6:147424600-147425800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr6:147424600-147425800	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr6:147424600-147425800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr6:147424600-147425800	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr6:147424600-147425800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:147424600-147425800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:147424600-147425800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:147424600-147426400	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr6:147424800-147425200	Enhancers	Dnd41	blood
19	chr6:147424800-147425200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr6:147424800-147425800	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr6:147424800-147425800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr6:147424800-147429400	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr6:147425000-147425200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:147425000-147425200	Enhancers	Fetal Thymus	thymus
25	chr6:147425000-147425800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr6:147425200-147425600	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr6:147425200-147429800	Weak transcription	Fetal Thymus	thymus
28	chr6:147425200-147430600	Weak transcription	Dnd41	blood
29	chr6:147425400-147428000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr6:147425600-147425800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr6:147425600-147426400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr6:147425600-147428000	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr6:147425600-147428200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:147425800-147427800	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr6:147425800-147427800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr6:147425800-147428000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr6:147425800-147428000	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr6:147425800-147428000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr6:147425800-147428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr6:147425800-147428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr6:147425800-147428200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:147425800-147429600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr6:147425800-147430000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr6:147426000-147428000	Weak transcription	Primary T cells from cord blood	blood
45	chr6:147426400-147426600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr6:147426400-147428000	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr6:147426400-147428000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr6:147426600-147427800	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr6:147427800-147428000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:147427800-147428000	Enhancers	NHLF	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links