Variant report

Variant	nsv1018622
Chromosome Location	chr6:55297854-55320311
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	CEBPB	chr6:55298259-55298598	ECC-1	luminal epithelium:	n/a	chr6:55298389-55298400
2	CEBPB	chr6:55299688-55299810	HepG2	liver:	n/a	n/a
3	CEBPB	chr6:55298241-55298550	HepG2	liver:	n/a	chr6:55298389-55298400
4	CEBPB	chr6:55312755-55312946	A549	lung:	n/a	n/a
5	CEBPB	chr6:55298198-55298569	MCF-7	breast:	n/a	chr6:55298389-55298400
6	CEBPB	chr6:55298219-55298583	IMR90	lung:	n/a	chr6:55298389-55298400
7	CEBPB	chr6:55298209-55298577	H1-hESC	embryonic stem cell:	n/a	chr6:55298389-55298400
8	CEBPB	chr6:55298290-55298525	A549	lung:	n/a	chr6:55298389-55298400
9	CEBPB	chr6:55298214-55298564	Hela-S3	cervix:	n/a	chr6:55298389-55298400
10	CTCF	chr6:55310435-55310763	A549	lung:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
11	CTCF	chr6:55314160-55314310	AG09319	gingival:	n/a	n/a
12	CTCF	chr6:55310520-55310670	GM12865	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
13	CTCF	chr6:55310560-55310710	HAc	cerebellar:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
14	CTCF	chr6:55314120-55314270	A549	lung:	n/a	n/a
15	CTCF	chr6:55310580-55310730	BJ	skin:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
16	CTCF	chr6:55310560-55310710	HPF	lung:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
17	CTCF	chr6:55314100-55314250	HRE	kidney:	n/a	n/a
18	CTCF	chr6:55310540-55310690	Caco-2	colon:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
19	CTCF	chr6:55310619-55310679	NHEK	skin:	n/a	n/a
20	CTCF	chr6:55314100-55314250	HCT-116	colon:	n/a	n/a
21	CTCF	chr6:55310460-55310610	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr6:55310500-55310650	HRPEpiC	eye:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
23	CTCF	chr6:55314080-55314230	HVMF	connective:	n/a	n/a
24	CTCF	chr6:55310583-55310630	GM13976	blood:	n/a	chr6:55310608-55310626 chr6:55310609-55310625
25	CTCF	chr6:55314020-55314170	NHEK	skin:	n/a	n/a
26	CTCF	chr6:55310446-55310795	K562	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
27	CTCF	chr6:55310357-55310900	HCT-116	colon:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
28	CTCF	chr6:55310520-55310670	HA-sp	spinal cord:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
29	CTCF	chr6:55310520-55310670	Caco-2	colon:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
30	CTCF	chr6:55310526-55310707	LNCaP	prostate:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
31	CTCF	chr6:55310560-55310710	GM12864	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
32	CTCF	chr6:55310580-55310730	HA-sp	spinal cord:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
33	CTCF	chr6:55314182-55314255	GM19240	blood:	n/a	n/a
34	CTCF	chr6:55314160-55314310	HCT-116	colon:	n/a	n/a
35	CTCF	chr6:55310523-55310725	H1-hESC	embryonic stem cell:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
36	CTCF	chr6:55310540-55310690	HCFaa	heart:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
37	CTCF	chr6:55310280-55310430	AG09319	gingival:	n/a	n/a
38	CTCF	chr6:55314160-55314310	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr6:55310488-55310697	GM10266	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
40	CTCF	chr6:55310560-55310710	BE2_C	brain:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
41	CTCF	chr6:55310540-55310690	BJ	skin:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
42	CTCF	chr6:55310540-55310690	GM12874	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
43	CTCF	chr6:55310500-55310650	AoAF	blood vessel:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
44	CTCF	chr6:55314110-55314315	Gliobla	brain:	n/a	n/a
45	CTCF	chr6:55314160-55314310	AG04450	lung:	n/a	n/a
46	CTCF	chr6:55310549-55310683	SK-N-SH_RA	brain:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
47	CTCF	chr6:55310540-55310690	AG10803	skin:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
48	CTCF	chr6:55314079-55314347	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr6:55314100-55314250	GM12872	blood:	n/a	n/a
50	CTCF	chr6:55310560-55310710	HEEpiC	esophagus:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:55314478-55314528	AG04450	lung:	fetal
2	chr6:55298362-55298412	AG04450	lung:	fetal
3	chr6:55314478-55314528	AG09309	skin:	n/a
4	chr6:55298362-55298412	HUVEC	blood vessel:	n/a
5	chr6:55298362-55298412	GM12878	blood:	n/a
6	chr6:55298362-55298412	SK-N-MC	brain:	n/a
7	chr6:55314478-55314528	SAEC	small airway:	n/a
8	chr6:55314478-55314528	K562	blood:	n/a
9	chr6:55298362-55298412	HRPEpiC	eye:	n/a
10	chr6:55314478-55314528	ovcar-3	ovarian:	n/a
11	chr6:55298362-55298412	HepG2	liver:	n/a
12	chr6:55298362-55298412	SK-N-SH	brain:	n/a
13	chr6:55298362-55298412	HCM	heart:	n/a
14	chr6:55298362-55298412	SK-N-SH_RA	brain:	n/a
15	chr6:55298362-55298412	HCF	heart:	n/a
16	chr6:55314478-55314528	Jurkat	blood:	n/a
17	chr6:55298362-55298412	ProgFib	skin:	n/a
18	chr6:55298362-55298412	HNPCEpiC	eye:	n/a
19	chr6:55298362-55298412	SKMC	muscle:	n/a
20	chr6:55298362-55298412	HCT-116	colon:	n/a
21	chr6:55314478-55314528	IMR90	lung:	fetal
22	chr6:55298362-55298412	Hepatocyte	liver:	n/a
23	chr6:55314478-55314528	Caco-2	colon:	n/a
24	chr6:55314478-55314528	CMK	blood:	n/a
25	chr6:55314478-55314528	HCT-116	colon:	n/a
26	chr6:55314478-55314528	SK-N-MC	brain:	n/a
27	chr6:55314478-55314528	HMEC	breast:	n/a
28	chr6:55298362-55298412	MCF-7	breast:	n/a
29	chr6:55314478-55314528	HEEpiC	esophagus:	n/a
30	chr6:55298362-55298412	HEK293	kidney:	embryo
31	chr6:55298362-55298412	HMEC	breast:	n/a
32	chr6:55298362-55298412	SAEC	small airway:	n/a
33	chr6:55314478-55314528	GM06990	blood:	n/a
34	chr6:55298362-55298412	AG10803	skin:	n/a
35	chr6:55314478-55314528	MCF-7	breast:	n/a
36	chr6:55298362-55298412	GM06990	blood:	n/a
37	chr6:55298362-55298412	Hela-S3	cervix:	n/a
38	chr6:55314478-55314528	T-47D	breast:	n/a
39	chr6:55298362-55298412	NHDF-neo	bronchial:	n/a
40	chr6:55314478-55314528	H1-hESC	embryonic stem cell:	embryo
41	chr6:55298362-55298412	U87	brain:	n/a
42	chr6:55298362-55298412	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:55314478-55314528	AG09319	gingival:	n/a
44	chr6:55298362-55298412	AG09309	skin:	n/a
45	chr6:55314478-55314528	ECC-1	luminal epithelium:	n/a
46	chr6:55298362-55298412	HCPEpiC	choroid plexus:	n/a
47	chr6:55314478-55314528	Hela-S3	cervix:	n/a
48	chr6:55298362-55298412	NT2-D1	testis:	n/a
49	chr6:55314478-55314528	SKMC	muscle:	n/a
50	chr6:55314478-55314528	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:55313718..55314729-chr6:55817986..55818869,4	MCF-7	breast:
2	chr6:55296640..55298261-chr6:55299680..55302209,2	K562	blood:
3	chr6:55309906..55311058-chr6:55817976..55819297,5	MCF-7	breast:
4	chr6:55300666..55302654-chr6:55304305..55306294,2	MCF-7	breast:
5	chr6:55296640..55298261-chr6:55299680..55302209,2	K562	blood:
6	chr6:55310627..55311224-chr6:55806307..55806968,2	MCF-7	breast:
7	chr6:55313873..55314721-chr6:55806208..55806737,2	MCF-7	breast:
8	chr6:55313181..55315342-chr6:55800874..55802800,2	MCF-7	breast:
9	chr6:55313762..55314282-chr6:56157199..56157825,2	MCF-7	breast:
10	chr6:55310143..55310712-chr6:55818032..55818931,2	MCF-7	breast:
11	chr6:55313713..55314676-chr6:55750196..55751674,4	MCF-7	breast:
12	chr6:55310131..55310914-chr6:55750826..55751625,3	MCF-7	breast:
13	chr6:55314098..55314636-chr6:55750998..55751586,2	MCF-7	breast:
14	chr6:55310142..55311120-chr6:56157237..56158075,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMP5-4	chr6:55310232-55312709	NONHSAT113233

Variant related genes	Relation type
HMGCLL1	TF binding region
HMGCLL1	CpG island
ENSG00000146151	chromatin interactions

Extended variants
information (count: 884 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:884 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539797038	chr6:55297866-55297867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115400224	chr6:55297868-55297869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570156112	chr6:55297882-55297883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138322823	chr6:55297897-55297898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555251996	chr6:55297898-55297899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17750698	chr6:55297903-55297904	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs116174701	chr6:55297921-55297922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558001505	chr6:55297938-55297939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115087464	chr6:55297947-55297948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181887059	chr6:55297948-55297949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542972906	chr6:55297956-55297957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563083402	chr6:55297973-55297974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573398472	chr6:55298003-55298004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373626311	chr6:55298007-55298008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144302355	chr6:55298008-55298009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs59500889	chr6:55298009-55298010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376799765	chr6:55298063-55298064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569227416	chr6:55298126-55298127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149204412	chr6:55298143-55298144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114409877	chr6:55298152-55298153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs36119453	chr6:55298224-55298225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376451635	chr6:55298228-55298229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547778721	chr6:55298264-55298265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112622991	chr6:55298275-55298276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73744288	chr6:55298278-55298279	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs533409415	chr6:55298286-55298287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1502206	chr6:55298348-55298349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572012408	chr6:55298362-55298363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534665782	chr6:55298396-55298397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143319052	chr6:55298427-55298428	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377730304	chr6:55298428-55298429	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534494595	chr6:55298540-55298541	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186913391	chr6:55298583-55298584	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549421519	chr6:55298587-55298588	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528388718	chr6:55298596-55298597	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534766090	chr6:55298604-55298605	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138736991	chr6:55298627-55298628	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577505324	chr6:55298633-55298634	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555101307	chr6:55298790-55298791	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146572424	chr6:55298791-55298792	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536694006	chr6:55298794-55298795	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142734281	chr6:55298831-55298832	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1546298	chr6:55298959-55298960	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs191010076	chr6:55298989-55298990	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559353780	chr6:55299107-55299108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs41271316	chr6:55299126-55299127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558129212	chr6:55299156-55299157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541607110	chr6:55299172-55299173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1546299	chr6:55299220-55299221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs181782875	chr6:55299259-55299260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22581003	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55296000-55298400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:55297800-55299000	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr6:55298000-55298600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:55298200-55298600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:55298200-55298800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr6:55298200-55298800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr6:55298200-55298800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:55298200-55298800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:55298200-55299000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr6:55298200-55299000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:55298200-55299000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr6:55298200-55299000	Enhancers	HMEC	breast
13	chr6:55298200-55299200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:55298200-55299200	Enhancers	NHLF	lung
15	chr6:55298400-55298800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr6:55298400-55299000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:55298400-55299000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr6:55298400-55299000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:55298400-55299000	Enhancers	NHDF-Ad	bronchial
20	chr6:55298400-55299000	Enhancers	Osteobl	bone
21	chr6:55298400-55299200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:55298600-55299000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:55298600-55299000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:55298600-55299200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:55298800-55299200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:55299000-55301600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr6:55299000-55303000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:55299800-55300000	Enhancers	Fetal Heart	heart
29	chr6:55300000-55301000	Weak transcription	Fetal Heart	heart
30	chr6:55301000-55302600	Enhancers	Fetal Heart	heart
31	chr6:55302600-55307000	Weak transcription	Fetal Heart	heart
32	chr6:55303000-55303800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:55303000-55303800	Enhancers	Brain Germinal Matrix	brain
34	chr6:55306800-55308600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:55307000-55309400	Enhancers	Fetal Heart	heart
36	chr6:55307200-55308400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr6:55307200-55308800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:55307400-55308200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:55307800-55308200	Enhancers	Adipose Nuclei	Adipose
40	chr6:55307800-55309000	Enhancers	Liver	Liver
41	chr6:55308000-55308400	Flanking Active TSS	Osteobl	bone
42	chr6:55308200-55308600	Enhancers	Fetal Lung	lung
43	chr6:55308200-55309400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr6:55308200-55313600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:55308200-55314000	Weak transcription	Adipose Nuclei	Adipose
46	chr6:55308600-55310400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:55308600-55310400	Weak transcription	Fetal Lung	lung
48	chr6:55308800-55312400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:55309000-55310600	Weak transcription	Liver	Liver
50	chr6:55309400-55312200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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