Variant report

Variant	nsv538213
Chromosome Location	chr6:45001948-45126730
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:122)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45017086-45017200	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:45090824-45091007	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:45011822-45012263	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:45017618-45017640	K562	blood:	n/a	n/a
5	ARID3A	chr6:45025490-45025613	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:45081891-45082077	HepG2	liver:	n/a	n/a
7	ATF1	chr6:45016978-45017291	K562	blood:	n/a	n/a
8	ATF1	chr6:45123102-45123463	K562	blood:	n/a	n/a
9	ATF1	chr6:45123857-45124210	K562	blood:	n/a	n/a
10	ATF1	chr6:45025523-45025589	K562	blood:	n/a	n/a
11	BHLHE40	chr6:45123836-45124198	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:45016926-45017297	K562	blood:	n/a	n/a
13	BHLHE40	chr6:45086708-45086783	K562	blood:	n/a	n/a
14	BRCA1	chr6:45011813-45011861	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr6:45109178-45109415	K562	blood:	n/a	n/a
16	CBX3	chr6:45016920-45017304	K562	blood:	n/a	n/a
17	CCNT2	chr6:45123918-45124143	K562	blood:	n/a	n/a
18	CCNT2	chr6:45003117-45003383	K562	blood:	n/a	n/a
19	CEBPB	chr6:45122501-45122512	K562	blood:	n/a	n/a
20	CEBPB	chr6:45042920-45043523	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:45074591-45074802	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:45039823-45040117	Hela-S3	cervix:	n/a	chr6:45039953-45039964 chr6:45039953-45039964 chr6:45039953-45039966 chr6:45039954-45039965 chr6:45039952-45039969
23	CEBPB	chr6:45122388-45122650	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:45115571-45115701	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:45039818-45040061	A549	lung:	n/a	chr6:45039953-45039964 chr6:45039953-45039964 chr6:45039953-45039966 chr6:45039954-45039965 chr6:45039952-45039969
26	CEBPB	chr6:45074584-45074778	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:45116509-45116712	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:45011885-45012095	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:45116441-45116743	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:45074722-45074725	K562	blood:	n/a	n/a
31	CEBPB	chr6:45039803-45040130	HepG2	liver:	n/a	chr6:45039953-45039964 chr6:45039953-45039964 chr6:45039953-45039966 chr6:45039954-45039965 chr6:45039952-45039969
32	CEBPB	chr6:45042969-45043439	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:45039808-45040092	K562	blood:	n/a	chr6:45039953-45039964 chr6:45039953-45039964 chr6:45039953-45039966 chr6:45039954-45039965 chr6:45039952-45039969
34	CEBPB	chr6:45122438-45122625	A549	lung:	n/a	n/a
35	CHD1	chr6:45124087-45124227	GM12878	blood:	n/a	n/a
36	CHD1	chr6:45088208-45088252	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr6:45123918-45124139	GM12878	blood:	n/a	n/a
38	CTCF	chr6:45054520-45054670	BE2_C	brain:	n/a	chr6:45054605-45054623 chr6:45054607-45054628 chr6:45054606-45054622 chr6:45054609-45054616
39	CTCF	chr6:45010098-45010160	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:45054420-45054570	HMEC	breast:	n/a	n/a
41	CTCF	chr6:45054540-45054690	HMF	breast:	n/a	chr6:45054605-45054623 chr6:45054607-45054628 chr6:45054606-45054622 chr6:45054609-45054616
42	CTCF	chr6:45054460-45054610	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr6:45042800-45042950	AG10803	skin:	n/a	n/a
44	CTCF	chr6:45054460-45054610	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr6:45010116-45010147	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:45054598-45054687	Hela-S3	cervix:	n/a	chr6:45054605-45054623 chr6:45054607-45054628 chr6:45054606-45054622 chr6:45054609-45054616
47	CTCF	chr6:45050676-45050714	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr6:45054380-45054530	AG09319	gingival:	n/a	n/a
49	CTCF	chr6:45054444-45054861	HCT-116	colon:	n/a	chr6:45054605-45054623 chr6:45054607-45054628 chr6:45054606-45054622 chr6:45054609-45054616
50	CTCF	chr6:45025167-45025218	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45030454-45030504	PrEC	prostate:	n/a
2	chr6:45079679-45079729	AoSMC	blood vessel:	n/a
3	chr6:45030454-45030504	ECC-1	luminal epithelium:	n/a
4	chr6:45030454-45030504	HAEpiC	amniotic membrane:	n/a
5	chr6:45030454-45030504	PANC-1	pancreas:	n/a
6	chr6:45079679-45079729	SAEC	small airway:	n/a
7	chr6:45079679-45079729	PrEC	prostate:	n/a
8	chr6:45079679-45079729	GM12892	blood:	n/a
9	chr6:45079679-45079729	NH-A	brain:	n/a
10	chr6:45030454-45030504	HCM	heart:	n/a
11	chr6:45030454-45030504	AoSMC	blood vessel:	n/a
12	chr6:45030454-45030504	HNPCEpiC	eye:	n/a
13	chr6:45030454-45030504	SK-N-SH	brain:	n/a
14	chr6:45079679-45079729	HRE	kidney:	n/a
15	chr6:45079679-45079729	AG09309	skin:	n/a
16	chr6:45079679-45079729	HNPCEpiC	eye:	n/a
17	chr6:45030454-45030504	BJ	skin:	n/a
18	chr6:45079679-45079729	SK-N-SH_RA	brain:	n/a
19	chr6:45079679-45079729	MCF10A-Er-Src	breast:	n/a
20	chr6:45079679-45079729	HRPEpiC	eye:	n/a
21	chr6:45030454-45030504	HL-60	blood:	n/a
22	chr6:45030454-45030504	HMEC	breast:	n/a
23	chr6:45079679-45079729	HepG2	liver:	n/a
24	chr6:45030454-45030504	GM19239	blood:	n/a
25	chr6:45079679-45079729	NB4	blood:	n/a
26	chr6:45030454-45030504	RPTEC	kidney:	n/a
27	chr6:45079679-45079729	HIPEpiC	eye:	n/a
28	chr6:45079679-45079729	GM12878	blood:	n/a
29	chr6:45030454-45030504	HUVEC	blood vessel:	n/a
30	chr6:45030454-45030504	CMK	blood:	n/a
31	chr6:45079679-45079729	NT2-D1	testis:	n/a
32	chr6:45030454-45030504	GM12891	blood:	n/a
33	chr6:45030454-45030504	MCF10A-Er-Src	breast:	n/a
34	chr6:45079679-45079729	Hela-S3	cervix:	n/a
35	chr6:45030454-45030504	HRE	kidney:	n/a
36	chr6:45030454-45030504	HCT-116	colon:	n/a
37	chr6:45030454-45030504	AG09309	skin:	n/a
38	chr6:45079679-45079729	HEK293	kidney:	embryo
39	chr6:45030454-45030504	HCPEpiC	choroid plexus:	n/a
40	chr6:45079679-45079729	Hepatocyte	liver:	n/a
41	chr6:45030454-45030504	Hepatocyte	liver:	n/a
42	chr6:45079679-45079729	NHBE	bronchial:	n/a
43	chr6:45030454-45030504	HIPEpiC	eye:	n/a
44	chr6:45079679-45079729	HCM	heart:	n/a
45	chr6:45079679-45079729	HL-60	blood:	n/a
46	chr6:45030454-45030504	A549	lung:	n/a
47	chr6:45079679-45079729	K562	blood:	n/a
48	chr6:45030454-45030504	AG04450	lung:	fetal
49	chr6:45030454-45030504	MCF-7	breast:	n/a
50	chr6:45079679-45079729	HRCEpiC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
2	chr6:45054220..45054815-chr6:45386791..45387562,3	MCF-7	breast:
3	chr6:45083331..45086142-chr6:45155794..45158780,2	K562	blood:
4	chr6:45092014..45095175-chr6:45095501..45098870,4	K562	blood:
5	chr6:45119653..45122627-chr6:45134013..45136661,2	MCF-7	breast:
6	chr12:48357281..48357866-chr6:45012051..45012551,2	Hela-S3	cervix:
7	chr6:45061664..45064501-chr6:45066770..45068668,2	K562	blood:
8	chr6:45117043..45119503-chr6:45122120..45124121,2	K562	blood:
9	chr6:45091825..45094517-chr6:45344694..45347186,2	MCF-7	breast:
10	chr6:45061664..45064501-chr6:45066770..45068668,2	K562	blood:
11	chr6:45093713..45096382-chr6:45127644..45129447,2	K562	blood:
12	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
13	chr6:45120420..45122464-chr6:45122631..45125594,2	K562	blood:
14	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
15	chr6:45124236..45126557-chr6:45137066..45139205,2	MCF-7	breast:
16	chr19:27731523..27732363-chr6:45117749..45118249,2	MCF-7	breast:
17	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
18	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
19	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
20	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
21	chr6:45092014..45095175-chr6:45095501..45098870,4	K562	blood:
22	chr6:45054176..45055264-chr6:45386958..45387535,3	MCF-7	breast:
23	chr6:45117043..45119503-chr6:45122120..45124121,2	K562	blood:
24	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
25	chr6:45120420..45122464-chr6:45122631..45125594,2	K562	blood:
26	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
27	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
28	chr6:44443174..44444085-chr6:45053756..45054587,2	MCF-7	breast:
29	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-4	chr6:45126607-45127248	NONHSAT112972

No data

Variant related genes	Relation type
ENSG00000219384	TF binding region
ENSG00000219384	CpG island
ENSG00000196284	chromatin interactions
ENSG00000134291	chromatin interactions

Extended variants
information (count: 3986 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3986 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556572336	chr6:45001949-45001950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142677425	chr6:45002080-45002081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144209915	chr6:45002095-45002096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542172319	chr6:45002164-45002165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560447259	chr6:45002192-45002193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111853733	chr6:45002197-45002198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116174616	chr6:45002221-45002222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566788308	chr6:45002255-45002256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140218541	chr6:45002278-45002279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550408352	chr6:45002281-45002282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568907583	chr6:45002352-45002353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141091335	chr6:45002374-45002375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371764396	chr6:45002378-45002379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370806367	chr6:45002443-45002444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184595721	chr6:45002474-45002475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568311174	chr6:45002558-45002559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187836266	chr6:45002589-45002590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566803707	chr6:45002623-45002624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534067617	chr6:45002641-45002642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558848334	chr6:45002655-45002656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192611488	chr6:45002666-45002667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538011667	chr6:45002714-45002715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556405420	chr6:45002752-45002753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574854719	chr6:45002881-45002882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149640160	chr6:45002893-45002894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553741002	chr6:45002979-45002980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572452391	chr6:45003026-45003027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557148926	chr6:45003046-45003047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536339425	chr6:45003067-45003068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564398218	chr6:45003070-45003071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534138165	chr6:45003116-45003117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183773127	chr6:45003134-45003135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs16873088	chr6:45003167-45003168	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs570658427	chr6:45003188-45003189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180901848	chr6:45003191-45003192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529778100	chr6:45003240-45003241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144360098	chr6:45003250-45003251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555072921	chr6:45003253-45003254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs117980719	chr6:45003254-45003255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527243716	chr6:45003313-45003314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368183965	chr6:45003318-45003319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1329714	chr6:45003335-45003336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs184758940	chr6:45003380-45003381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62436438	chr6:45003438-45003439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537673348	chr6:45003455-45003456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79498798	chr6:45003532-45003533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568501875	chr6:45003541-45003542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572775960	chr6:45003557-45003558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189631465	chr6:45003580-45003581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372259998	chr6:45003617-45003618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44974800-45004600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:44995200-45004400	Weak transcription	Aorta	Aorta
3	chr6:45000800-45003800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr6:45001400-45002000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr6:45002000-45003800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr6:45003800-45004200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:45003800-45004200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr6:45007800-45009200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:45011200-45012600	Enhancers	HepG2	liver
10	chr6:45011600-45012200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:45011800-45012200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:45011800-45012600	Enhancers	Fetal Intestine Large	intestine
13	chr6:45012000-45012200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:45012000-45013800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr6:45012200-45017000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr6:45012200-45022000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr6:45012600-45016800	Weak transcription	HepG2	liver
18	chr6:45013800-45020000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr6:45016400-45018000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:45016400-45019200	Enhancers	Dnd41	blood
21	chr6:45016400-45019600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:45016600-45017600	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr6:45016600-45017600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:45016600-45017600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr6:45016600-45018600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:45016600-45019000	Enhancers	HUVEC	blood vessel
27	chr6:45016800-45017400	Enhancers	Primary B cells from peripheral blood	blood
28	chr6:45016800-45017600	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr6:45016800-45017600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:45016800-45018000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr6:45016800-45018200	Enhancers	Primary T cells from cord blood	blood
32	chr6:45016800-45018200	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr6:45016800-45018200	Enhancers	HepG2	liver
34	chr6:45016800-45018200	Enhancers	K562	blood
35	chr6:45016800-45018600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:45016800-45019000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr6:45017000-45017200	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr6:45017000-45017400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr6:45017000-45017400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr6:45017000-45017400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:45017000-45017400	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr6:45017000-45017400	Enhancers	Primary T cells fromperipheralblood	blood
43	chr6:45017000-45017400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:45017000-45017400	Enhancers	HMEC	breast
45	chr6:45017000-45017400	Enhancers	NH-A	brain
46	chr6:45017000-45017400	Enhancers	NHEK	skin
47	chr6:45017000-45017600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:45017000-45017600	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr6:45017000-45017600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:45017000-45017800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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