Variant report

Variant	nsv1015103
Chromosome Location	chr3:69619879-69712504
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	ATF1	chr3:69701784-69702178	K562	blood:	n/a	n/a
2	CEBPB	chr3:69634687-69634976	K562	blood:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
3	CEBPB	chr3:69666599-69666853	IMR90	lung:	n/a	chr3:69666717-69666728
4	CEBPB	chr3:69637396-69637922	HepG2	liver:	n/a	chr3:69637794-69637805 chr3:69637795-69637806
5	CEBPB	chr3:69666554-69666767	HepG2	liver:	n/a	chr3:69666717-69666728
6	CEBPB	chr3:69697065-69697102	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr3:69634716-69634958	H1-hESC	embryonic stem cell:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
8	CEBPB	chr3:69684168-69684321	A549	lung:	n/a	n/a
9	CEBPB	chr3:69696982-69697192	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:69646344-69646636	IMR90	lung:	n/a	chr3:69646473-69646484
11	CEBPB	chr3:69634651-69634994	HepG2	liver:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
12	CEBPB	chr3:69696959-69697231	K562	blood:	n/a	n/a
13	CEBPB	chr3:69666612-69666872	A549	lung:	n/a	chr3:69666717-69666728
14	CEBPB	chr3:69646327-69646649	HepG2	liver:	n/a	chr3:69646473-69646484
15	CEBPB	chr3:69659531-69659560	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:69646319-69646614	A549	lung:	n/a	chr3:69646473-69646484
17	CEBPB	chr3:69634645-69634992	A549	lung:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
18	CEBPB	chr3:69696997-69697271	MCF-7	breast:	n/a	n/a
19	CEBPB	chr3:69637696-69637896	H1-hESC	embryonic stem cell:	n/a	chr3:69637794-69637805 chr3:69637795-69637806
20	CEBPB	chr3:69696932-69697239	IMR90	lung:	n/a	n/a
21	CEBPB	chr3:69634649-69634993	IMR90	lung:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
22	CEBPB	chr3:69674148-69674348	A549	lung:	n/a	chr3:69674222-69674233
23	CEBPB	chr3:69674162-69674362	HepG2	liver:	n/a	chr3:69674222-69674233
24	CEBPB	chr3:69696938-69697234	A549	lung:	n/a	n/a
25	CEBPB	chr3:69696927-69697264	HepG2	liver:	n/a	n/a
26	CTCF	chr3:69682758-69682810	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr3:69650757-69650882	Lung_OC	lung:	n/a	n/a
28	CTCF	chr3:69705940-69706090	MCF-7	breast:	n/a	n/a
29	CTCF	chr3:69698434-69698481	Lung_OC	lung:	n/a	n/a
30	CTCF	chr3:69706040-69706190	HEK293	kidney:	n/a	n/a
31	CTCF	chr3:69643282-69643328	LNCaP	prostate:	n/a	n/a
32	CTCF	chr3:69664897-69664959	GM10266	blood:	n/a	n/a
33	CTCF	chr3:69706040-69706190	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr3:69625515-69625551	GM10248	blood:	n/a	n/a
35	CTCF	chr3:69698280-69698430	HPF	lung:	n/a	n/a
36	CTCF	chr3:69705900-69706050	GM12866	blood:	n/a	n/a
37	CTCF	chr3:69626881-69626917	GM10248	blood:	n/a	n/a
38	CTCF	chr3:69666000-69666150	AG09319	gingival:	n/a	n/a
39	CTCF	chr3:69691019-69691083	LNCaP	prostate:	n/a	n/a
40	CTCF	chr3:69637357-69637414	GM20000	blood:	n/a	n/a
41	CTCF	chr3:69637440-69637590	Caco-2	colon:	n/a	n/a
42	E2F4	chr3:69673323-69673416	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr3:69664892-69665083	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr3:69672723-69672835	MCF10A-Er-Src	breast:	n/a	n/a
45	ELK4	chr3:69705868-69706058	HEK293	kidney:	n/a	n/a
46	EP300	chr3:69708391-69708685	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr3:69707611-69708995	SK-N-SH	brain:	n/a	chr3:69708918-69708927
48	EP300	chr3:69708405-69708663	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr3:69652967-69653005	GM12878	blood:	n/a	n/a
50	FOS	chr3:69699262-69699515	MCF10A-Er-Src	breast:	n/a	chr3:69699368-69699379

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:69710710-69710760	Jurkat	blood:	n/a
2	chr3:69710144-69710194	AG09309	skin:	n/a
3	chr3:69710586-69710636	AG04450	lung:	fetal
4	chr3:69710710-69710760	AoSMC	blood vessel:	n/a
5	chr3:69710710-69710760	AG10803	skin:	n/a
6	chr3:69710586-69710636	CMK	blood:	n/a
7	chr3:69710586-69710636	U87	brain:	n/a
8	chr3:69710144-69710194	GM12878	blood:	n/a
9	chr3:69710586-69710636	MCF-7	breast:	n/a
10	chr3:69710586-69710636	SKMC	muscle:	n/a
11	chr3:69710144-69710194	Caco-2	colon:	n/a
12	chr3:69710586-69710636	T-47D	breast:	n/a
13	chr3:69710144-69710194	HRE	kidney:	n/a
14	chr3:69710144-69710194	GM12891	blood:	n/a
15	chr3:69710586-69710636	HepG2	liver:	n/a
16	chr3:69710144-69710194	AG04449	skin:	fetal
17	chr3:69710710-69710760	HUVEC	blood vessel:	n/a
18	chr3:69710710-69710760	NHBE	bronchial:	n/a
19	chr3:69710144-69710194	NH-A	brain:	n/a
20	chr3:69710144-69710194	NB4	blood:	n/a
21	chr3:69710710-69710760	GM12892	blood:	n/a
22	chr3:69710144-69710194	SK-N-SH	brain:	n/a
23	chr3:69710710-69710760	IMR90	lung:	fetal
24	chr3:69710710-69710760	HCM	heart:	n/a
25	chr3:69710144-69710194	MCF10A-Er-Src	breast:	n/a
26	chr3:69710710-69710760	GM12878	blood:	n/a
27	chr3:69710586-69710636	SK-N-MC	brain:	n/a
28	chr3:69710144-69710194	H1-hESC	embryonic stem cell:	embryo
29	chr3:69710710-69710760	SK-N-SH	brain:	n/a
30	chr3:69710144-69710194	HRPEpiC	eye:	n/a
31	chr3:69710144-69710194	AG10803	skin:	n/a
32	chr3:69710710-69710760	HAEpiC	amniotic membrane:	n/a
33	chr3:69710710-69710760	AG04449	skin:	fetal
34	chr3:69710144-69710194	GM12892	blood:	n/a
35	chr3:69710144-69710194	HAEpiC	amniotic membrane:	n/a
36	chr3:69710144-69710194	SKMC	muscle:	n/a
37	chr3:69710710-69710760	HEEpiC	esophagus:	n/a
38	chr3:69710710-69710760	ECC-1	luminal epithelium:	n/a
39	chr3:69710710-69710760	T-47D	breast:	n/a
40	chr3:69710710-69710760	HMEC	breast:	n/a
41	chr3:69710710-69710760	GM06990	blood:	n/a
42	chr3:69710710-69710760	A549	lung:	n/a
43	chr3:69710586-69710636	HNPCEpiC	eye:	n/a
44	chr3:69710710-69710760	LNCaP	prostate:	n/a
45	chr3:69710710-69710760	HCF	heart:	n/a
46	chr3:69710586-69710636	A549	lung:	n/a
47	chr3:69710710-69710760	HL-60	blood:	n/a
48	chr3:69710586-69710636	Hela-S3	cervix:	n/a
49	chr3:69710144-69710194	BJ	skin:	n/a
50	chr3:69710586-69710636	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:69660815..69663559-chr3:69665701..69667253,2	K562	blood:
2	chr3:69704610..69707455-chr3:69833061..69835848,2	K562	blood:
3	chr3:69694033..69698273-chr3:69701406..69703258,4	K562	blood:
4	chr3:69660815..69663559-chr3:69665701..69667253,2	K562	blood:
5	chr3:69694033..69698273-chr3:69701406..69703258,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MITF-2	chr3:69641596-69642272	XLOC_002695
2	lnc-MITF-2	chr3:69640492-69640563	XLOC_002695

Variant related genes	Relation type
ENSG00000241667	TF binding region
ENSG00000240842	TF binding region
ENSG00000241667	CpG island
ENSG00000240842	CpG island
SMAD4	miRNA target sites
SPTY2D1	miRNA target sites

Extended variants
information (count: 2511 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2511 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560205444	chr3:69620201-69620202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532116427	chr3:69620243-69620244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552303265	chr3:69620244-69620245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193261138	chr3:69620325-69620326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538950946	chr3:69620335-69620336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185368747	chr3:69620378-69620379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567824225	chr3:69620499-69620500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370553718	chr3:69620537-69620538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557604842	chr3:69620552-69620553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9879369	chr3:69620573-69620574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577654025	chr3:69620582-69620583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546863994	chr3:69620590-69620591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150329530	chr3:69620594-69620595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538609993	chr3:69620602-69620603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs288514	chr3:69620621-69620622	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs138374439	chr3:69620649-69620650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368847703	chr3:69620652-69620653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538315696	chr3:69620694-69620695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189033527	chr3:69620698-69620699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192982815	chr3:69620715-69620716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540554195	chr3:69620749-69620750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556215362	chr3:69620767-69620768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34750928	chr3:69620783-69620784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs288513	chr3:69620791-69620792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs576918195	chr3:69620795-69620796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573637679	chr3:69620804-69620805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4855416	chr3:69620828-69620829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs142945984	chr3:69620883-69620884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531333421	chr3:69620886-69620887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548250656	chr3:69620935-69620936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561345924	chr3:69620974-69620975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6549239	chr3:69621052-69621053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs9828225	chr3:69621067-69621068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs145133561	chr3:69621082-69621083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139003569	chr3:69621093-69621094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79033750	chr3:69621101-69621102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552181996	chr3:69621102-69621103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs288512	chr3:69621130-69621131	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537971029	chr3:69621132-69621133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111865006	chr3:69621143-69621144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552468725	chr3:69621199-69621200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533934427	chr3:69621215-69621216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553999662	chr3:69621224-69621225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367890453	chr3:69621231-69621232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531038011	chr3:69621243-69621244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550622217	chr3:69621250-69621251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371759428	chr3:69621306-69621307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529490423	chr3:69621354-69621355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546095073	chr3:69621360-69621361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72943517	chr3:69621361-69621362	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69620200-69622200	Weak transcription	Aorta	Aorta
2	chr3:69627600-69628400	Enhancers	Fetal Lung	lung
3	chr3:69628000-69629400	Enhancers	Fetal Muscle Leg	muscle
4	chr3:69628000-69629600	Enhancers	Fetal Brain Male	brain
5	chr3:69628200-69628400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:69628200-69629000	Enhancers	Adipose Nuclei	Adipose
7	chr3:69628200-69629600	Enhancers	Fetal Brain Female	brain
8	chr3:69628200-69629800	Enhancers	Brain Germinal Matrix	brain
9	chr3:69628400-69628600	Enhancers	Brain Angular Gyrus	brain
10	chr3:69628400-69628600	Enhancers	Brain Hippocampus Middle	brain
11	chr3:69628400-69628600	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr3:69628400-69628800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:69628400-69628800	Enhancers	Fetal Kidney	kidney
14	chr3:69628400-69629400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr3:69628400-69629400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:69628400-69629600	Flanking Active TSS	Fetal Lung	lung
17	chr3:69628600-69628800	Flanking Active TSS	Brain Angular Gyrus	brain
18	chr3:69628600-69628800	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
19	chr3:69628600-69629000	Enhancers	Brain Cingulate Gyrus	brain
20	chr3:69628600-69629000	Flanking Active TSS	Brain Hippocampus Middle	brain
21	chr3:69628600-69629200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr3:69628600-69629400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:69628600-69629400	Enhancers	Brain Substantia Nigra	brain
24	chr3:69628600-69629400	Enhancers	Fetal Stomach	stomach
25	chr3:69628800-69629000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:69628800-69629000	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
27	chr3:69628800-69629200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr3:69628800-69629200	Enhancers	Psoas Muscle	Psoas
29	chr3:69628800-69629400	Active TSS	Brain Angular Gyrus	brain
30	chr3:69628800-69629400	Enhancers	Ovary	ovary
31	chr3:69629000-69629200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
32	chr3:69629000-69629400	Bivalent Enhancer	Adipose Nuclei	Adipose
33	chr3:69629000-69629600	Enhancers	Brain Hippocampus Middle	brain
34	chr3:69629200-69629600	Bivalent Enhancer	Psoas Muscle	Psoas
35	chr3:69629400-69629600	Enhancers	Lung	lung
36	chr3:69629400-69630800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:69629400-69630800	Weak transcription	Ovary	ovary
38	chr3:69629600-69630800	Weak transcription	Lung	lung
39	chr3:69629600-69631000	Enhancers	Fetal Lung	lung
40	chr3:69629800-69630800	Weak transcription	Brain Germinal Matrix	brain
41	chr3:69630600-69631000	Enhancers	Spleen	Spleen
42	chr3:69630800-69631000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:69630800-69631000	Enhancers	Brain Germinal Matrix	brain
44	chr3:69630800-69631000	Enhancers	Lung	lung
45	chr3:69630800-69631000	Enhancers	Ovary	ovary
46	chr3:69630800-69631400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:69631000-69632000	Weak transcription	Fetal Lung	lung
48	chr3:69632000-69632200	Enhancers	Fetal Lung	lung
49	chr3:69638800-69639000	Enhancers	Fetal Brain Male	brain
50	chr3:69639000-69644200	Weak transcription	Fetal Brain Male	brain

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