Variant report

Variant	nsv885867
Chromosome Location	chr6:45936223-45982976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:45978885-45979622	GM12878	blood:	n/a	n/a
2	ATF2	chr6:45978991-45979643	GM12878	blood:	n/a	n/a
3	BATF	chr6:45978906-45979567	GM12878	blood:	n/a	n/a
4	BCLAF1	chr6:45979113-45979494	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:45979042-45979611	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:45978965-45979214	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:45980841-45981271	HepG2	liver:	n/a	chr6:45981043-45981055 chr6:45981124-45981135 chr6:45981124-45981137
8	CEBPB	chr6:45978453-45979470	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:45980435-45981271	Hela-S3	cervix:	n/a	chr6:45981043-45981055 chr6:45981124-45981135 chr6:45981124-45981137
10	CEBPB	chr6:45981027-45981240	A549	lung:	n/a	chr6:45981043-45981055 chr6:45981124-45981135 chr6:45981124-45981137
11	CHD2	chr6:45979174-45979660	GM12878	blood:	n/a	n/a
12	CHD2	chr6:45982854-45982975	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr6:45982115-45982437	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr6:45978794-45979416	Hela-S3	cervix:	n/a	n/a
15	CTBP2	chr6:45982874-45984194	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr6:45982383-45982479	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr6:45959000-45959150	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr6:45959020-45959170	GM12871	blood:	n/a	n/a
19	CTCF	chr6:45959020-45959170	Caco-2	colon:	n/a	n/a
20	CTCF	chr6:45959000-45959150	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr6:45982920-45983070	HepG2	liver:	n/a	chr6:45983015-45983028
22	CTCF	chr6:45959000-45959150	GM12864	blood:	n/a	n/a
23	CTCF	chr6:45959040-45959190	GM12867	blood:	n/a	n/a
24	CTCF	chr6:45959060-45959210	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr6:45959000-45959250	A549	lung:	n/a	n/a
26	CTCF	chr6:45959080-45959230	GM12878	blood:	n/a	n/a
27	CTCF	chr6:45982380-45982530	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr6:45959060-45959210	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr6:45982940-45983090	SAEC	small airway:	n/a	chr6:45983015-45983028
30	CTCF	chr6:45959054-45959135	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:45959159-45959204	Lung_OC	lung:	n/a	n/a
32	CTCF	chr6:45982920-45983070	Caco-2	colon:	n/a	chr6:45983015-45983028
33	CTCF	chr6:45959000-45959150	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr6:45959022-45959176	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:45959020-45959170	HAc	cerebellar:	n/a	n/a
36	CTCF	chr6:45962100-45962250	WI-38	lung:	n/a	n/a
37	CTCF	chr6:45959020-45959170	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr6:45959040-45959190	K562	blood:	n/a	n/a
39	CTCF	chr6:45959055-45959106	HepG2	liver:	n/a	n/a
40	CTCF	chr6:45958940-45959090	GM12867	blood:	n/a	n/a
41	CTCF	chr6:45959220-45959370	RPTEC	kidney:	n/a	n/a
42	CTCF	chr6:45982920-45983070	SAEC	small airway:	n/a	chr6:45983015-45983028
43	CTCF	chr6:45958840-45959130	K562	blood:	n/a	n/a
44	CTCF	chr6:45959000-45959150	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr6:45958940-45959090	GM12868	blood:	n/a	n/a
46	CTCF	chr6:45962697-45962734	GM20000	blood:	n/a	n/a
47	CTCF	chr6:45958960-45959110	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:45959020-45959170	GM12873	blood:	n/a	n/a
49	CTCF	chr6:45982360-45982510	HEK293	kidney:	n/a	n/a
50	CTCF	chr6:45959020-45959170	HMEC	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45982569-45982619	SAEC	small airway:	n/a
2	chr6:45982653-45982703	Hela-S3	cervix:	n/a
3	chr6:45979349-45979399	NT2-D1	testis:	n/a
4	chr6:45982653-45982703	HL-60	blood:	n/a
5	chr6:45979349-45979399	HEK293	kidney:	embryo
6	chr6:45982421-45982471	SK-N-SH	brain:	n/a
7	chr6:45982421-45982471	ECC-1	luminal epithelium:	n/a
8	chr6:45979349-45979399	HRE	kidney:	n/a
9	chr6:45982653-45982703	HUVEC	blood vessel:	n/a
10	chr6:45982569-45982619	Jurkat	blood:	n/a
11	chr6:45982653-45982703	BJ	skin:	n/a
12	chr6:45979349-45979399	ProgFib	skin:	n/a
13	chr6:45979349-45979399	AoSMC	blood vessel:	n/a
14	chr6:45979349-45979399	Caco-2	colon:	n/a
15	chr6:45982653-45982703	GM12891	blood:	n/a
16	chr6:45982421-45982471	RPTEC	kidney:	n/a
17	chr6:45982421-45982471	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:45982569-45982619	Hela-S3	cervix:	n/a
19	chr6:45982421-45982471	Hela-S3	cervix:	n/a
20	chr6:45982653-45982703	Jurkat	blood:	n/a
21	chr6:45982653-45982703	A549	lung:	n/a
22	chr6:45982421-45982471	HL-60	blood:	n/a
23	chr6:45979349-45979399	AG09309	skin:	n/a
24	chr6:45982421-45982471	HCPEpiC	choroid plexus:	n/a
25	chr6:45982569-45982619	HCT-116	colon:	n/a
26	chr6:45979349-45979399	AG04450	lung:	fetal
27	chr6:45982653-45982703	NHDF-neo	bronchial:	n/a
28	chr6:45982653-45982703	K562	blood:	n/a
29	chr6:45982653-45982703	H1-hESC	embryonic stem cell:	embryo
30	chr6:45982421-45982471	NHBE	bronchial:	n/a
31	chr6:45982421-45982471	HCT-116	colon:	n/a
32	chr6:45982653-45982703	SKMC	muscle:	n/a
33	chr6:45982421-45982471	Caco-2	colon:	n/a
34	chr6:45982421-45982471	SK-N-MC	brain:	n/a
35	chr6:45982569-45982619	NB4	blood:	n/a
36	chr6:45982421-45982471	HNPCEpiC	eye:	n/a
37	chr6:45982569-45982619	PANC-1	pancreas:	n/a
38	chr6:45982569-45982619	NHDF-neo	bronchial:	n/a
39	chr6:45982569-45982619	AG09319	gingival:	n/a
40	chr6:45982653-45982703	ECC-1	luminal epithelium:	n/a
41	chr6:45982653-45982703	GM06990	blood:	n/a
42	chr6:45982653-45982703	CMK	blood:	n/a
43	chr6:45982569-45982619	T-47D	breast:	n/a
44	chr6:45982421-45982471	K562	blood:	n/a
45	chr6:45982569-45982619	H1-hESC	embryonic stem cell:	embryo
46	chr6:45982653-45982703	HEK293	kidney:	embryo
47	chr6:45982653-45982703	HCT-116	colon:	n/a
48	chr6:45982653-45982703	NHBE	bronchial:	n/a
49	chr6:45982421-45982471	HEK293	kidney:	embryo
50	chr6:45982421-45982471	HCM	heart:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:45978565..45981449-chr6:45989773..45991611,2	K562	blood:
2	chr6:45980539..45983062-chr6:45983993..45986730,2	K562	blood:
3	chr6:45972108..45974934-chr6:45976922..45979622,2	K562	blood:
4	chr10:12382244..12382792-chr6:45978181..45978798,2	MCF-7	breast:
5	chr6:45965967..45967545-chr6:45976025..45978546,2	K562	blood:
6	chr6:45972108..45974934-chr6:45976922..45979622,2	K562	blood:
7	chr6:45942534..45945438-chr6:45953727..45956305,2	MCF-7	breast:
8	chr6:45965967..45967545-chr6:45976025..45978546,2	K562	blood:
9	chr6:45942534..45945438-chr6:45953727..45956305,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ENPP5-1	chr6:45982020-45982451	NONHSAT113001

No data

Variant related genes	Relation type
RNU6-754P	TF binding region
RNU6-754P	CpG island
ENSG00000212468	chromatin interactions

Extended variants
information (count: 1978 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1978 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3777595	chr6:45936223-45936224	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148586360	chr6:45936288-45936289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533193974	chr6:45936306-45936307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529155582	chr6:45936339-45936340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182500040	chr6:45936432-45936433	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs551576940	chr6:45936452-45936453	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs9472632	chr6:45936523-45936524	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs369490007	chr6:45936574-45936575	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs142953629	chr6:45936578-45936579	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs557092957	chr6:45936579-45936580	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs151100629	chr6:45936599-45936600	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs572750186	chr6:45936611-45936612	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs536493323	chr6:45936627-45936628	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs76991950	chr6:45936639-45936640	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs573292419	chr6:45936658-45936659	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140914538	chr6:45936676-45936677	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs1538331	chr6:45936679-45936680	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs577962705	chr6:45936702-45936703	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs545329214	chr6:45936828-45936829	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs186126234	chr6:45936848-45936849	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs530727021	chr6:45936879-45936880	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs190800123	chr6:45936901-45936902	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs183033218	chr6:45936912-45936913	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs528187537	chr6:45936918-45936919	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs34254847	chr6:45937129-45937130	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs546142062	chr6:45937163-45937164	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570920777	chr6:45937194-45937195	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs532021134	chr6:45937201-45937202	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188888329	chr6:45937254-45937255	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs569480311	chr6:45937271-45937272	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs536839235	chr6:45937275-45937276	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs548516862	chr6:45937307-45937308	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs9395140	chr6:45937320-45937321	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs370278084	chr6:45937339-45937340	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs374102733	chr6:45937342-45937343	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs116771117	chr6:45937373-45937374	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs577299954	chr6:45937395-45937396	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs9395141	chr6:45937403-45937404	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs193238494	chr6:45937422-45937423	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182640718	chr6:45937429-45937430	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551288706	chr6:45937469-45937470	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs538044225	chr6:45937470-45937471	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs7756444	chr6:45937472-45937473	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs542772906	chr6:45937474-45937475	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs560947941	chr6:45937506-45937507	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs572564129	chr6:45937539-45937540	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs187768429	chr6:45937544-45937545	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs397779323	chr6:45937556-45937557	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs564686677	chr6:45937592-45937593	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs116896066	chr6:45937601-45937602	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45918800-45938400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr6:45928200-45936400	Weak transcription	Fetal Kidney	kidney
3	chr6:45932600-45937800	Weak transcription	Fetal Intestine Large	intestine
4	chr6:45933600-45941400	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr6:45934400-45937200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:45934400-45937200	Weak transcription	Small Intestine	intestine
7	chr6:45934400-45938600	Enhancers	Right Atrium	heart
8	chr6:45934600-45936800	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr6:45934600-45937600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:45934800-45936800	Weak transcription	Ovary	ovary
11	chr6:45934800-45937400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:45934800-45937600	Weak transcription	Fetal Intestine Small	intestine
13	chr6:45935000-45936400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr6:45935000-45937600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:45935000-45938400	Weak transcription	Lung	lung
16	chr6:45935200-45936800	Weak transcription	Colonic Mucosa	Colon
17	chr6:45935200-45937800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr6:45935600-45936800	Weak transcription	Psoas Muscle	Psoas
19	chr6:45935800-45937000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr6:45935800-45938000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:45936000-45936400	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr6:45936000-45936800	Weak transcription	Left Ventricle	heart
23	chr6:45936000-45937000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr6:45936000-45941200	Enhancers	Fetal Heart	heart
25	chr6:45936200-45936800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr6:45936200-45937600	Weak transcription	Right Ventricle	heart
27	chr6:45936400-45936800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr6:45936400-45936800	Enhancers	Fetal Kidney	kidney
29	chr6:45936400-45936800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
30	chr6:45936400-45937000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr6:45936400-45937600	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr6:45936800-45937000	Enhancers	Adipose Nuclei	Adipose
33	chr6:45936800-45937000	Enhancers	Psoas Muscle	Psoas
34	chr6:45936800-45937000	Active TSS	Rectal Mucosa Donor 31	rectum
35	chr6:45936800-45937000	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
36	chr6:45936800-45937000	Enhancers	Spleen	Spleen
37	chr6:45936800-45937600	Active TSS	Colonic Mucosa	Colon
38	chr6:45936800-45938000	Active TSS	Rectal Smooth Muscle	rectum
39	chr6:45936800-45938600	Enhancers	Left Ventricle	heart
40	chr6:45936800-45938600	Enhancers	Ovary	ovary
41	chr6:45936800-45942000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr6:45937000-45937200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr6:45937000-45937400	Weak transcription	Psoas Muscle	Psoas
44	chr6:45937000-45937600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr6:45937000-45937800	Weak transcription	Adipose Nuclei	Adipose
46	chr6:45937000-45938200	Active TSS	Sigmoid Colon	Sigmoid Colon
47	chr6:45937000-45940000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:45937200-45937400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr6:45937200-45937800	Enhancers	Small Intestine	intestine
50	chr6:45937200-45938400	Active TSS	Rectal Mucosa Donor 31	rectum

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