Variant report

Variant	esv11293
Chromosome Location	chr3:52567550-52568100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:52567800-52568226	GM12878	blood:	n/a	n/a
2	ATF2	chr3:52567819-52568420	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr3:52567883-52568137	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:52567961-52568166	HepG2	liver:	n/a	n/a
5	CCNT2	chr3:52566580-52568816	K562	blood:	n/a	chr3:52566977-52566986 chr3:52567974-52567983 chr3:52567185-52567194 chr3:52567981-52567990
6	CEBPD	chr3:52567697-52568161	HepG2	liver:	n/a	n/a
7	CEBPD	chr3:52567923-52568175	HepG2	liver:	n/a	n/a
8	CHD1	chr3:52567392-52567726	GM12878	blood:	n/a	n/a
9	CHD1	chr3:52568030-52568179	GM12878	blood:	n/a	n/a
10	CHD2	chr3:52567828-52568191	K562	blood:	n/a	n/a
11	CHD2	chr3:52567348-52568163	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr3:52567513-52568198	GM12878	blood:	n/a	n/a
13	CHD2	chr3:52567981-52568162	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr3:52567987-52568178	HepG2	liver:	n/a	n/a
15	CREB1	chr3:52567301-52569320	HepG2	liver:	n/a	n/a
16	CREB1	chr3:52567776-52568113	A549	lung:	n/a	n/a
17	CTCF	chr3:52567920-52568070	K562	blood:	n/a	n/a
18	CTCF	chr3:52567991-52568033	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr3:52568060-52568210	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr3:52567912-52568167	IMR90	lung:	n/a	n/a
21	CTCF	chr3:52567930-52568132	GM19239	blood:	n/a	n/a
22	CTCF	chr3:52567940-52568090	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr3:52567960-52568110	GM12871	blood:	n/a	n/a
24	CTCF	chr3:52567920-52568070	HCM	heart:	n/a	n/a
25	CTCF	chr3:52567920-52568070	GM12865	blood:	n/a	n/a
26	CTCF	chr3:52567960-52568110	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr3:52567865-52568082	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr3:52567962-52568154	GM13976	blood:	n/a	n/a
29	CTCF	chr3:52567919-52568149	GM19240	blood:	n/a	n/a
30	CTCF	chr3:52567961-52568113	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr3:52567928-52568161	GM12891	blood:	n/a	n/a
32	CTCF	chr3:52567994-52568129	ProgFib	skin:	n/a	n/a
33	CTCF	chr3:52568040-52568190	Caco-2	colon:	n/a	n/a
34	CTCF	chr3:52567960-52568110	GM12875	blood:	n/a	n/a
35	CTCF	chr3:52567926-52568157	A549	lung:	n/a	n/a
36	CTCF	chr3:52567960-52568110	AG09309	skin:	n/a	n/a
37	CTCF	chr3:52568000-52568150	AG04450	lung:	n/a	n/a
38	CTCF	chr3:52567978-52568122	Fibrobl	skin:	n/a	n/a
39	CTCF	chr3:52567960-52568110	GM12864	blood:	n/a	n/a
40	CTCF	chr3:52567945-52568119	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:52568040-52568058	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr3:52567999-52568091	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:52567980-52568130	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr3:52567940-52568090	HFF	foreskin:	n/a	n/a
45	CTCF	chr3:52567954-52568124	K562	blood:	n/a	n/a
46	CTCF	chr3:52567940-52568090	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr3:52567940-52568090	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr3:52567980-52568130	Caco-2	colon:	n/a	n/a
49	CTCF	chr3:52567940-52568090	AG04450	lung:	n/a	n/a
50	CTCF	chr3:52567920-52568070	HMEC	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52567510-52567560	Hepatocyte	liver:	n/a
2	chr3:52567604-52567654	HRE	kidney:	n/a
3	chr3:52567510-52567560	CMK	blood:	n/a
4	chr3:52567604-52567654	BJ	skin:	n/a
5	chr3:52567510-52567560	RPTEC	kidney:	n/a
6	chr3:52567633-52567683	ECC-1	luminal epithelium:	n/a
7	chr3:52567510-52567560	AG10803	skin:	n/a
8	chr3:52567633-52567683	AG04450	lung:	fetal
9	chr3:52567633-52567683	NHDF-neo	bronchial:	n/a
10	chr3:52567604-52567654	NT2-D1	testis:	n/a
11	chr3:52567604-52567654	IMR90	lung:	fetal
12	chr3:52567633-52567683	HRE	kidney:	n/a
13	chr3:52567633-52567683	T-47D	breast:	n/a
14	chr3:52567633-52567683	H1-hESC	embryonic stem cell:	embryo
15	chr3:52567510-52567560	NHBE	bronchial:	n/a
16	chr3:52567604-52567654	GM06990	blood:	n/a
17	chr3:52567510-52567560	HRE	kidney:	n/a
18	chr3:52567604-52567654	T-47D	breast:	n/a
19	chr3:52567510-52567560	ECC-1	luminal epithelium:	n/a
20	chr3:52567633-52567683	SK-N-SH	brain:	n/a
21	chr3:52567633-52567683	NH-A	brain:	n/a
22	chr3:52567510-52567560	H1-hESC	embryonic stem cell:	embryo
23	chr3:52567510-52567560	SK-N-SH	brain:	n/a
24	chr3:52567510-52567560	HUVEC	blood vessel:	n/a
25	chr3:52567510-52567560	BE2_C	brain:	n/a
26	chr3:52567633-52567683	GM06990	blood:	n/a
27	chr3:52567604-52567654	HEEpiC	esophagus:	n/a
28	chr3:52567633-52567683	AG04449	skin:	fetal
29	chr3:52567510-52567560	SKMC	muscle:	n/a
30	chr3:52567604-52567654	A549	lung:	n/a
31	chr3:52567633-52567683	AG09309	skin:	n/a
32	chr3:52567604-52567654	HCF	heart:	n/a
33	chr3:52567510-52567560	AoSMC	blood vessel:	n/a
34	chr3:52567604-52567654	HL-60	blood:	n/a
35	chr3:52567510-52567560	HCT-116	colon:	n/a
36	chr3:52567604-52567654	NHBE	bronchial:	n/a
37	chr3:52567604-52567654	AoSMC	blood vessel:	n/a
38	chr3:52567604-52567654	HUVEC	blood vessel:	n/a
39	chr3:52567510-52567560	Caco-2	colon:	n/a
40	chr3:52567633-52567683	MCF10A-Er-Src	breast:	n/a
41	chr3:52567604-52567654	PANC-1	pancreas:	n/a
42	chr3:52567633-52567683	SAEC	small airway:	n/a
43	chr3:52567604-52567654	H1-hESC	embryonic stem cell:	embryo
44	chr3:52567510-52567560	A549	lung:	n/a
45	chr3:52567510-52567560	ovcar-3	ovarian:	n/a
46	chr3:52567633-52567683	GM12892	blood:	n/a
47	chr3:52567510-52567560	U87	brain:	n/a
48	chr3:52567510-52567560	HAEpiC	amniotic membrane:	n/a
49	chr3:52567510-52567560	Jurkat	blood:	n/a
50	chr3:52567510-52567560	PFSK-1	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:52567106..52571736-chr3:52712759..52716604,4	K562	blood:
2	chr3:52487897..52490713-chr3:52565636..52568320,3	K562	blood:
3	chr3:52567315..52569798-chr3:52739141..52741499,3	MCF-7	breast:
4	chr3:52566165..52568026-chr3:52648479..52651083,2	K562	blood:
5	chr3:52567128..52569011-chr3:52738941..52741649,3	K562	blood:
6	chr3:52527250..52529955-chr3:52567199..52569414,2	MCF-7	breast:
7	chr3:52504515..52506973-chr3:52565446..52568302,2	MCF-7	breast:
8	chr3:52567779..52572340-chr3:52718708..52722750,6	K562	blood:
9	chr3:52444067..52446922-chr3:52566590..52568238,2	K562	blood:
10	chr3:52567015..52567802-chr3:186500888..186501659,2	Hela-S3	cervix:
11	chr3:52554843..52559532-chr3:52566910..52570402,7	MCF-7	breast:
12	chr22:47133970..47134516-chr3:52567792..52568293,2	HCT-116	colon:
13	chr3:52567230..52568070-chr9:131218351..131218852,2	Hela-S3	cervix:
14	chr3:52567553..52570571-chr3:52718365..52721514,3	MCF-7	breast:
15	chr15:65596638..65597519-chr3:52567379..52568024,2	HCT-116	colon:
16	chr3:52566406..52569677-chr3:52718507..52721358,5	MCF-7	breast:
17	chr3:52503525..52506168-chr3:52566167..52568849,2	MCF-7	breast:
18	chr3:52311763..52314254-chr3:52566006..52568592,3	K562	blood:
19	chr3:52551484..52554158-chr3:52567066..52569157,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf78-1	chr3:52568052-52568164	NONHSAT089937

No data

Variant related genes	Relation type
NT5DC2	TF binding region
SMIM4	TF binding region
NT5DC2	CpG island
SMIM4	CpG island
ENSG00000200156	chromatin interactions
ENSG00000016864	chromatin interactions
ENSG00000114902	chromatin interactions
ENSG00000010318	chromatin interactions
ENSG00000100422	chromatin interactions
ENSG00000136811	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000010322	chromatin interactions
ENSG00000114854	chromatin interactions
ENSG00000010327	chromatin interactions
ENSG00000163939	chromatin interactions
ENSG00000168268	chromatin interactions
ENSG00000163930	chromatin interactions
ENSG00000164091	chromatin interactions
ENSG00000163938	chromatin interactions

Extended variants
information (count: 14 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs66782572	chr3:52567617-52567618	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376765486	chr3:52567630-52567631	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
3	rs558970437	chr3:52567646-52567647	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
4	rs112562394	chr3:52567779-52567780	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
5	rs558765554	chr3:52567793-52567794	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
6	rs192855409	chr3:52567794-52567795	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	mRNA abundance
7	rs183793563	chr3:52567819-52567820	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
8	rs541612392	chr3:52567968-52567969	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
9	rs28380177	chr3:52567998-52567999	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
10	rs28396446	chr3:52568005-52568006	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
11	rs555216056	chr3:52568026-52568027	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs575168334	chr3:52568030-52568031	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
13	rs369120098	chr3:52568042-52568043	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
14	rs112769777	chr3:52568049-52568050	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Lung cancer	16618734	CNVD
Neuroblastoma	19686582	CNVD
Renal cell carcinoma	18765545	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52566200-52567600	Flanking Active TSS	Adipose Nuclei	Adipose
2	chr3:52566200-52569000	Active TSS	H9 Cell Line	embryonic stem cell
3	chr3:52566200-52571600	Active TSS	Fetal Kidney	kidney
4	chr3:52566400-52568600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:52566400-52568600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:52566400-52569000	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr3:52566600-52567600	Flanking Active TSS	Colonic Mucosa	Colon
8	chr3:52566600-52567600	Flanking Active TSS	Placenta	Placenta
9	chr3:52566600-52567600	Flanking Active TSS	Right Ventricle	heart
10	chr3:52566600-52567800	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr3:52566600-52567800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr3:52566600-52568400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
13	chr3:52566600-52568400	Active TSS	Brain Angular Gyrus	brain
14	chr3:52566600-52568600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:52566600-52568600	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr3:52566600-52568600	Active TSS	A549	lung
17	chr3:52566600-52568800	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr3:52566800-52567600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
19	chr3:52566800-52567600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
20	chr3:52566800-52568200	Active TSS	Duodenum Smooth Muscle	Duodenum
21	chr3:52566800-52568200	Active TSS	Sigmoid Colon	Sigmoid Colon
22	chr3:52566800-52568400	Active TSS	NH-A	brain
23	chr3:52566800-52568600	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr3:52566800-52568600	Active TSS	HSMMtube	muscle
25	chr3:52566800-52568800	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr3:52566800-52568800	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr3:52566800-52568800	Active TSS	Rectal Smooth Muscle	rectum
28	chr3:52566800-52569000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr3:52566800-52569200	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr3:52566800-52569200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:52566800-52569400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr3:52567000-52567600	Flanking Active TSS	Primary B cells from cord blood	blood
33	chr3:52567000-52567600	Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr3:52567000-52567600	Enhancers	Fetal Brain Male	brain
35	chr3:52567000-52567600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr3:52567000-52567800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:52567000-52568000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr3:52567000-52568200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr3:52567000-52568200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr3:52567000-52568200	Active TSS	Primary T cells from cord blood	blood
41	chr3:52567000-52568200	Active TSS	Muscle Satellite Cultured Cells	--
42	chr3:52567000-52568200	Active TSS	Brain Anterior Caudate	brain
43	chr3:52567000-52568200	Active TSS	Duodenum Mucosa	Duodenum
44	chr3:52567000-52568200	Active TSS	Esophagus	oesophagus
45	chr3:52567000-52568200	Active TSS	Fetal Stomach	stomach
46	chr3:52567000-52568200	Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr3:52567000-52568200	Active TSS	Small Intestine	intestine
48	chr3:52567000-52568200	Active TSS	GM12878-XiMat	blood
49	chr3:52567000-52568200	Active TSS	Hela-S3	cervix
50	chr3:52567000-52568200	Active TSS	HepG2	liver

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