Variant report

Variant	nsv1021917
Chromosome Location	chr6:45879064-45898314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45890705-45890713	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:45898191-45898481	HepG2	liver:	n/a	n/a
3	ATF2	chr6:45891623-45892285	GM12878	blood:	n/a	n/a
4	ATF2	chr6:45888487-45889088	GM12878	blood:	n/a	n/a
5	ATF2	chr6:45888459-45888973	GM12878	blood:	n/a	n/a
6	ATF2	chr6:45891752-45892199	GM12878	blood:	n/a	n/a
7	BATF	chr6:45888464-45889068	GM12878	blood:	n/a	chr6:45888726-45888736 chr6:45888725-45888736
8	BATF	chr6:45888477-45888970	GM12878	blood:	n/a	chr6:45888726-45888736 chr6:45888725-45888736
9	BATF	chr6:45891559-45892218	GM12878	blood:	n/a	chr6:45891913-45891924
10	BATF	chr6:45891765-45892170	GM12878	blood:	n/a	chr6:45891913-45891924
11	BCL11A	chr6:45888416-45889028	GM12878	blood:	n/a	chr6:45888729-45888738 chr6:45888728-45888737
12	BCL11A	chr6:45888639-45888963	GM12878	blood:	n/a	chr6:45888729-45888738 chr6:45888728-45888737
13	BCL11A	chr6:45891715-45892190	GM12878	blood:	n/a	n/a
14	BCL3	chr6:45891683-45892212	GM12878	blood:	n/a	n/a
15	BCL3	chr6:45888520-45888982	GM12878	blood:	n/a	chr6:45888729-45888738 chr6:45888728-45888737
16	BCLAF1	chr6:45891671-45892218	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:45888586-45889159	GM12878	blood:	n/a	chr6:45888729-45888738 chr6:45888728-45888737
18	BCLAF1	chr6:45888478-45889034	GM12878	blood:	n/a	chr6:45888729-45888738 chr6:45888728-45888737
19	BCLAF1	chr6:45891743-45892090	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:45888537-45888977	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:45898212-45898517	K562	blood:	n/a	n/a
22	BHLHE40	chr6:45898217-45898473	GM12878	blood:	n/a	n/a
23	BRCA1	chr6:45898206-45898455	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr6:45891583-45891824	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:45891678-45892205	GM12878	blood:	n/a	n/a
26	CEBPB	chr6:45888428-45889111	GM12878	blood:	n/a	chr6:45888753-45888764
27	CEBPB	chr6:45891807-45892083	GM12878	blood:	n/a	n/a
28	CEBPB	chr6:45884307-45884520	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:45891527-45892054	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:45888103-45888202	HepG2	liver:	n/a	chr6:45888125-45888136
31	CHD2	chr6:45888431-45889128	GM12878	blood:	n/a	n/a
32	CREB1	chr6:45891638-45892231	GM12878	blood:	n/a	n/a
33	CREB1	chr6:45888576-45888957	GM12878	blood:	n/a	n/a
34	CREB1	chr6:45891531-45892217	GM12878	blood:	n/a	n/a
35	CTCF	chr6:45898194-45898504	GM12891	blood:	n/a	chr6:45898346-45898364 chr6:45898349-45898362 chr6:45898415-45898422 chr6:45898348-45898369
36	CTCF	chr6:45898280-45898430	WI-38	lung:	n/a	chr6:45898346-45898364 chr6:45898349-45898362 chr6:45898415-45898422 chr6:45898348-45898369
37	CTCF	chr6:45898280-45898430	HCT-116	colon:	n/a	chr6:45898346-45898364 chr6:45898349-45898362 chr6:45898415-45898422 chr6:45898348-45898369
38	CTCF	chr6:45890436-45890922	A549	lung:	n/a	chr6:45890699-45890715 chr6:45890698-45890716 chr6:45890693-45890714
39	CTCF	chr6:45898300-45898450	MCF-7	breast:	n/a	chr6:45898346-45898364 chr6:45898349-45898362 chr6:45898415-45898422 chr6:45898348-45898369
40	CTCF	chr6:45890620-45890770	MCF-7	breast:	n/a	chr6:45890699-45890715 chr6:45890698-45890716 chr6:45890693-45890714
41	CTCF	chr6:45883680-45883830	AG10803	skin:	n/a	chr6:45883722-45883743 chr6:45883727-45883745 chr6:45883729-45883742
42	CTCF	chr6:45898260-45898410	MCF-7	breast:	n/a	chr6:45898346-45898364 chr6:45898349-45898362 chr6:45898348-45898369
43	CTCF	chr6:45890617-45890776	HepG2	liver:	n/a	chr6:45890699-45890715 chr6:45890698-45890716 chr6:45890693-45890714
44	CTCF	chr6:45898121-45898186	GM12891	blood:	n/a	n/a
45	CTCF	chr6:45894520-45894670	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr6:45898174-45898506	Gliobla	brain:	n/a	chr6:45898346-45898364 chr6:45898349-45898362 chr6:45898415-45898422 chr6:45898348-45898369
47	CTCF	chr6:45898076-45898124	GM19239	blood:	n/a	n/a
48	CTCF	chr6:45890640-45890790	GM12868	blood:	n/a	chr6:45890699-45890715 chr6:45890698-45890716 chr6:45890693-45890714
49	CTCF	chr6:45890620-45890770	HRE	kidney:	n/a	chr6:45890699-45890715 chr6:45890698-45890716 chr6:45890693-45890714
50	CTCF	chr6:45898211-45898492	Kidney_OC	kidney:	n/a	chr6:45898346-45898364 chr6:45898349-45898362 chr6:45898415-45898422 chr6:45898348-45898369

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45891455-45891505	AG09319	gingival:	n/a
2	chr6:45891455-45891505	ECC-1	luminal epithelium:	n/a
3	chr6:45895069-45895119	HRPEpiC	eye:	n/a
4	chr6:45891455-45891505	HCF	heart:	n/a
5	chr6:45895069-45895119	IMR90	lung:	fetal
6	chr6:45895069-45895119	HRCEpiC	kidney:	n/a
7	chr6:45895069-45895119	HUVEC	blood vessel:	n/a
8	chr6:45895069-45895119	HAEpiC	amniotic membrane:	n/a
9	chr6:45895069-45895119	SK-N-MC	brain:	n/a
10	chr6:45895069-45895119	AG10803	skin:	n/a
11	chr6:45895069-45895119	HIPEpiC	eye:	n/a
12	chr6:45895069-45895119	T-47D	breast:	n/a
13	chr6:45891455-45891505	HEK293	kidney:	embryo
14	chr6:45891455-45891505	HNPCEpiC	eye:	n/a
15	chr6:45891455-45891505	NT2-D1	testis:	n/a
16	chr6:45891455-45891505	LNCaP	prostate:	n/a
17	chr6:45891455-45891505	Hela-S3	cervix:	n/a
18	chr6:45891455-45891505	MCF10A-Er-Src	breast:	n/a
19	chr6:45891455-45891505	PrEC	prostate:	n/a
20	chr6:45891455-45891505	SK-N-MC	brain:	n/a
21	chr6:45895069-45895119	Hela-S3	cervix:	n/a
22	chr6:45895069-45895119	ovcar-3	ovarian:	n/a
23	chr6:45895069-45895119	NH-A	brain:	n/a
24	chr6:45891455-45891505	AG09309	skin:	n/a
25	chr6:45891455-45891505	NHBE	bronchial:	n/a
26	chr6:45895069-45895119	Hepatocyte	liver:	n/a
27	chr6:45895069-45895119	LNCaP	prostate:	n/a
28	chr6:45895069-45895119	SKMC	muscle:	n/a
29	chr6:45891455-45891505	U87	brain:	n/a
30	chr6:45891455-45891505	HCM	heart:	n/a
31	chr6:45891455-45891505	GM19239	blood:	n/a
32	chr6:45895069-45895119	ECC-1	luminal epithelium:	n/a
33	chr6:45891455-45891505	H1-hESC	embryonic stem cell:	embryo
34	chr6:45895069-45895119	GM19239	blood:	n/a
35	chr6:45891455-45891505	Caco-2	colon:	n/a
36	chr6:45895069-45895119	CMK	blood:	n/a
37	chr6:45891455-45891505	K562	blood:	n/a
38	chr6:45891455-45891505	AG04449	skin:	fetal
39	chr6:45895069-45895119	SAEC	small airway:	n/a
40	chr6:45891455-45891505	HepG2	liver:	n/a
41	chr6:45891455-45891505	HEEpiC	esophagus:	n/a
42	chr6:45895069-45895119	AG04449	skin:	fetal
43	chr6:45891455-45891505	NB4	blood:	n/a
44	chr6:45891455-45891505	A549	lung:	n/a
45	chr6:45895069-45895119	HepG2	liver:	n/a
46	chr6:45891455-45891505	MCF-7	breast:	n/a
47	chr6:45891455-45891505	AoSMC	blood vessel:	n/a
48	chr6:45891455-45891505	IMR90	lung:	fetal
49	chr6:45895069-45895119	PANC-1	pancreas:	n/a
50	chr6:45891455-45891505	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:45897865..45898727-chr6:45982870..45983433,2	MCF-7	breast:
2	chr6:45896169..45897673-chr6:45900583..45902413,2	K562	blood:
3	chr6:45879897..45882120-chr6:45883023..45885109,2	MCF-7	breast:
4	chr6:45898210..45898759-chr6:45913836..45914644,2	MCF-7	breast:
5	chr6:45623457..45625814-chr6:45890186..45892755,2	MCF-7	breast:
6	chr6:44598184..44598870-chr6:45890670..45891186,2	K562	blood:
7	chr6:44620218..44622571-chr6:45890865..45893250,2	MCF-7	breast:
8	chr6:45898314..45898956-chr6:46593729..46594636,2	MCF-7	breast:
9	chr6:45756761..45757645-chr6:45890500..45891157,2	MCF-7	breast:
10	chr6:45896173..45899025-chr6:45900583..45902149,3	K562	blood:
11	chr6:45897955..45898801-chr6:46057521..46058514,3	MCF-7	breast:
12	chr6:44623182..44623933-chr6:45889938..45891174,4	K562	blood:
13	chr6:44560942..44561805-chr6:45890244..45890927,2	MCF-7	breast:
14	chr6:45879897..45882120-chr6:45883023..45885109,2	MCF-7	breast:
15	chr6:45897904..45898920-chr6:46377652..46378792,5	K562	blood:
16	chr6:44443149..44444048-chr6:45890206..45890910,3	K562	blood:
17	chr6:44648875..44649699-chr6:45894327..45895186,2	K562	blood:
18	chr6:45897935..45898821-chr6:46377732..46378655,2	MCF-7	breast:

Variant related genes	Relation type
CLIC5	TF binding region
CLIC5	CpG island
ENSG00000112782	chromatin interactions

Extended variants
information (count: 919 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9367228	chr6:45879064-45879065	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564747838	chr6:45879128-45879129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190888990	chr6:45879206-45879207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570555865	chr6:45879241-45879242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182683750	chr6:45879252-45879253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187804631	chr6:45879278-45879279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148539503	chr6:45879401-45879402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs3179832	chr6:45879402-45879403	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142844679	chr6:45879409-45879410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554089846	chr6:45879430-45879431	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191252246	chr6:45879435-45879436	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183162650	chr6:45879461-45879462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557804621	chr6:45879464-45879465	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576499399	chr6:45879488-45879489	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146549232	chr6:45879496-45879497	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3088356	chr6:45879527-45879528	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs35261495	chr6:45879559-45879560	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs145606105	chr6:45879560-45879561	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550096254	chr6:45879595-45879596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527460803	chr6:45879607-45879608	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552422362	chr6:45879611-45879612	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563991086	chr6:45879654-45879655	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531444839	chr6:45879656-45879657	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187540533	chr6:45879684-45879685	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192311535	chr6:45879714-45879715	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146510313	chr6:45879722-45879723	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199687499	chr6:45879738-45879739	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566057594	chr6:45879743-45879744	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539613327	chr6:45879776-45879777	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558342250	chr6:45879783-45879784	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184521047	chr6:45879791-45879792	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188001371	chr6:45879794-45879795	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34951069	chr6:45879804-45879805	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs193235434	chr6:45879808-45879809	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs184398918	chr6:45879811-45879812	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs115341689	chr6:45879812-45879813	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs560458748	chr6:45879818-45879819	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs572385521	chr6:45879865-45879866	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs545979128	chr6:45879866-45879867	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs564308029	chr6:45879908-45879909	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs181296240	chr6:45879915-45879916	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs543493833	chr6:45879922-45879923	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs79157994	chr6:45879928-45879929	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs34208595	chr6:45879936-45879937	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs547008899	chr6:45880005-45880006	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565995804	chr6:45880028-45880029	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565751731	chr6:45880057-45880058	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111377022	chr6:45880076-45880077	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72871427	chr6:45880173-45880174	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138574937	chr6:45880181-45880182	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45866400-45880000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr6:45866600-45898400	Weak transcription	Colonic Mucosa	Colon
3	chr6:45867800-45884200	Weak transcription	Fetal Heart	heart
4	chr6:45868800-45889600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:45869000-45879600	Weak transcription	Adipose Nuclei	Adipose
6	chr6:45870000-45881800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr6:45870200-45879600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:45870400-45880600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:45870800-45881200	Weak transcription	Placenta	Placenta
10	chr6:45871000-45879400	Weak transcription	Right Ventricle	heart
11	chr6:45871000-45879400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr6:45871000-45881800	Weak transcription	Lung	lung
13	chr6:45871200-45879200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:45871200-45884400	Weak transcription	Psoas Muscle	Psoas
15	chr6:45871200-45885600	Weak transcription	Spleen	Spleen
16	chr6:45876200-45882200	Strong transcription	Skeletal Muscle Female	skeletal muscle
17	chr6:45876400-45881800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr6:45877200-45882000	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr6:45877400-45882400	Strong transcription	Left Ventricle	heart
20	chr6:45878000-45879600	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr6:45878400-45880000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:45878400-45880000	Strong transcription	Fetal Intestine Small	intestine
23	chr6:45878400-45882400	Strong transcription	Skeletal Muscle Male	skeletal muscle
24	chr6:45878600-45882400	Strong transcription	Fetal Intestine Large	intestine
25	chr6:45878800-45879600	Weak transcription	Right Atrium	heart
26	chr6:45879200-45882200	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr6:45879400-45879600	Enhancers	Stomach Smooth Muscle	stomach
28	chr6:45879400-45881400	Strong transcription	Right Ventricle	heart
29	chr6:45879400-45882000	Strong transcription	Sigmoid Colon	Sigmoid Colon
30	chr6:45879600-45879800	Enhancers	Fetal Muscle Trunk	muscle
31	chr6:45879600-45880000	Enhancers	Right Atrium	heart
32	chr6:45879600-45880600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:45879600-45881400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:45879600-45882000	Strong transcription	Adipose Nuclei	Adipose
35	chr6:45879600-45882200	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr6:45879800-45880000	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr6:45879800-45889600	Weak transcription	Fetal Muscle Trunk	muscle
38	chr6:45880000-45880800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:45880000-45881200	Weak transcription	Fetal Intestine Small	intestine
40	chr6:45880000-45882000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr6:45880000-45884600	Weak transcription	Right Atrium	heart
42	chr6:45880000-45884800	Weak transcription	Fetal Muscle Leg	muscle
43	chr6:45880200-45880600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:45880600-45881200	Strong transcription	Duodenum Mucosa	Duodenum
45	chr6:45880600-45883400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:45880600-45883800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:45880800-45882400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr6:45881200-45882200	Strong transcription	Placenta	Placenta
49	chr6:45881200-45882600	Strong transcription	Fetal Intestine Small	intestine
50	chr6:45881200-45908000	Weak transcription	Duodenum Mucosa	Duodenum

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