Variant report

Variant	esv2830033
Chromosome Location	chr17:50462226-50506926
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	chr17:50488269-50488506	HepG2	liver:	n/a	n/a
2	CTCF	chr17:50479640-50479790	MCF-7	breast:	n/a	n/a
3	CTCF	chr17:50486609-50486667	GM20000	blood:	n/a	n/a
4	CTCF	chr17:50473403-50473416	MCF-7	breast:	n/a	n/a
5	EP300	chr17:50496355-50497084	T-47D	breast:	n/a	chr17:50496785-50496794 chr17:50496791-50496801 chr17:50496924-50496934
6	EP300	chr17:50496355-50497154	T-47D	breast:	n/a	chr17:50496785-50496794 chr17:50496791-50496801 chr17:50496924-50496934
7	ESR1	chr17:50496434-50497016	T-47D	breast:	n/a	n/a
8	FOSL2	chr17:50488133-50488487	HepG2	liver:	n/a	chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488376-50488383 chr17:50488375-50488383 chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488375-50488383
9	FOSL2	chr17:50488148-50488530	HepG2	liver:	n/a	chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488376-50488383 chr17:50488375-50488383 chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488375-50488383
10	FOXA1	chr17:50488125-50488555	HepG2	liver:	n/a	chr17:50488362-50488374
11	FOXA1	chr17:50496335-50497177	T-47D	breast:	n/a	n/a
12	FOXA1	chr17:50496630-50497119	HepG2	liver:	n/a	n/a
13	FOXA1	chr17:50488087-50488535	HepG2	liver:	n/a	chr17:50488362-50488374
14	FOXA1	chr17:50486478-50486927	HepG2	liver:	n/a	n/a
15	FOXA1	chr17:50488112-50488490	HepG2	liver:	n/a	chr17:50488362-50488374
16	FOXA1	chr17:50496400-50497082	HepG2	liver:	n/a	n/a
17	FOXA1	chr17:50496535-50497059	HepG2	liver:	n/a	n/a
18	FOXA1	chr17:50496193-50497114	T-47D	breast:	n/a	n/a
19	FOXA1	chr17:50496576-50497099	HepG2	liver:	n/a	n/a
20	FOXA1	chr17:50488110-50488543	HepG2	liver:	n/a	chr17:50488362-50488374
21	FOXA2	chr17:50488147-50488488	HepG2	liver:	n/a	chr17:50488362-50488374
22	FOXA2	chr17:50486412-50487087	A549	lung:	n/a	n/a
23	FOXA2	chr17:50496474-50497079	HepG2	liver:	n/a	n/a
24	GATA2	chr17:50468519-50468791	SH-SY5Y	brain:	n/a	n/a
25	GATA2	chr17:50472656-50473148	SH-SY5Y	brain:	n/a	n/a
26	GATA2	chr17:50462176-50462496	SH-SY5Y	brain:	n/a	chr17:50462354-50462363 chr17:50462350-50462366
27	GATA3	chr17:50496064-50497166	T-47D	breast:	n/a	n/a
28	GATA3	chr17:50496109-50497174	T-47D	breast:	n/a	n/a
29	GATA3	chr17:50462335-50462543	SH-SY5Y	brain:	n/a	chr17:50462354-50462363 chr17:50462350-50462366
30	GATA3	chr17:50472610-50473153	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr17:50496436-50497067	MCF-7	breast:	n/a	n/a
32	GATA3	chr17:50472669-50472993	T-47D	breast:	n/a	n/a
33	GATA3	chr17:50496325-50497216	MCF-7	breast:	n/a	n/a
34	GATA3	chr17:50506648-50506720	SH-SY5Y	brain:	n/a	chr17:50506669-50506682
35	HDAC2	chr17:50496563-50497133	MCF-7	breast:	n/a	chr17:50497049-50497063 chr17:50496925-50496934 chr17:50497051-50497065 chr17:50496791-50496800
36	HDAC2	chr17:50496527-50496873	MCF-7	breast:	n/a	chr17:50496791-50496800
37	JUN	chr17:50488258-50488487	HepG2	liver:	n/a	chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488376-50488383 chr17:50488375-50488383 chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488375-50488383
38	JUND	chr17:50489127-50489372	HepG2	liver:	n/a	n/a
39	JUND	chr17:50496360-50497220	T-47D	breast:	n/a	n/a
40	JUND	chr17:50496350-50497115	T-47D	breast:	n/a	n/a
41	JUND	chr17:50488266-50488411	HepG2	liver:	n/a	chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488376-50488383 chr17:50488373-50488384 chr17:50488375-50488383 chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488375-50488383
42	JUND	chr17:50496062-50496874	HepG2	liver:	n/a	chr17:50496114-50496124 chr17:50496115-50496124 chr17:50496114-50496123 chr17:50496116-50496123
43	JUND	chr17:50488187-50488552	HepG2	liver:	n/a	chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488376-50488383 chr17:50488373-50488384 chr17:50488375-50488383 chr17:50488374-50488384 chr17:50488374-50488384 chr17:50488375-50488383
44	MAFK	chr17:50478560-50478813	HepG2	liver:	n/a	n/a
45	MAFK	chr17:50498799-50498816	HepG2	liver:	n/a	n/a
46	MAFK	chr17:50478586-50478839	HepG2	liver:	n/a	n/a
47	MYC	chr17:50475465-50475665	MCF10A-Er-Src	breast:	n/a	n/a
48	NR2F2	chr17:50496491-50497161	MCF-7	breast:	n/a	n/a
49	POLR2A	chr17:50486776-50486860	A549	lung:	n/a	n/a
50	POLR2A	chr17:50486662-50486838	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:50487054-50487104	SAEC	small airway:	n/a
2	chr17:50487054-50487104	BE2_C	brain:	n/a
3	chr17:50487054-50487104	SK-N-SH_RA	brain:	n/a
4	chr17:50487054-50487104	HCPEpiC	choroid plexus:	n/a
5	chr17:50487054-50487104	HEK293	kidney:	embryo
6	chr17:50487054-50487104	Jurkat	blood:	n/a
7	chr17:50487054-50487104	NHDF-neo	bronchial:	n/a
8	chr17:50487054-50487104	HRPEpiC	eye:	n/a
9	chr17:50487054-50487104	HepG2	liver:	n/a
10	chr17:50487054-50487104	BJ	skin:	n/a
11	chr17:50487054-50487104	AoSMC	blood vessel:	n/a
12	chr17:50487054-50487104	HUVEC	blood vessel:	n/a
13	chr17:50487054-50487104	SK-N-SH	brain:	n/a
14	chr17:50487054-50487104	ECC-1	luminal epithelium:	n/a
15	chr17:50487054-50487104	GM12892	blood:	n/a
16	chr17:50487054-50487104	HPAEpiC	pulmonary alveolar:	n/a
17	chr17:50487054-50487104	LNCaP	prostate:	n/a
18	chr17:50487054-50487104	HCM	heart:	n/a
19	chr17:50487054-50487104	SK-N-MC	brain:	n/a
20	chr17:50487054-50487104	AG04450	lung:	fetal
21	chr17:50487054-50487104	HRE	kidney:	n/a
22	chr17:50487054-50487104	HNPCEpiC	eye:	n/a
23	chr17:50487054-50487104	K562	blood:	n/a
24	chr17:50487054-50487104	GM19239	blood:	n/a
25	chr17:50487054-50487104	A549	lung:	n/a
26	chr17:50487054-50487104	NB4	blood:	n/a
27	chr17:50487054-50487104	H1-hESC	embryonic stem cell:	embryo
28	chr17:50487054-50487104	U87	brain:	n/a
29	chr17:50487054-50487104	Hepatocyte	liver:	n/a
30	chr17:50487054-50487104	MCF-7	breast:	n/a
31	chr17:50487054-50487104	HCT-116	colon:	n/a
32	chr17:50487054-50487104	SKMC	muscle:	n/a
33	chr17:50487054-50487104	GM06990	blood:	n/a
34	chr17:50487054-50487104	T-47D	breast:	n/a
35	chr17:50487054-50487104	IMR90	lung:	fetal
36	chr17:50487054-50487104	HIPEpiC	eye:	n/a
37	chr17:50487054-50487104	HRCEpiC	kidney:	n/a
38	chr17:50487054-50487104	HL-60	blood:	n/a
39	chr17:50487054-50487104	RPTEC	kidney:	n/a
40	chr17:50487054-50487104	CMK	blood:	n/a
41	chr17:50487054-50487104	Caco-2	colon:	n/a
42	chr17:50487054-50487104	HMEC	breast:	n/a
43	chr17:50487054-50487104	ovcar-3	ovarian:	n/a
44	chr17:50487054-50487104	MCF10A-Er-Src	breast:	n/a
45	chr17:50487054-50487104	NT2-D1	testis:	n/a
46	chr17:50487054-50487104	GM12878	blood:	n/a
47	chr17:50487054-50487104	HCF	heart:	n/a
48	chr17:50487054-50487104	ProgFib	skin:	n/a
49	chr17:50487054-50487104	HEEpiC	esophagus:	n/a
50	chr17:50487054-50487104	PFSK-1	brain:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC102948.1.1-3	chr17:50467875-50467950	ENSG00000263317.1

Variant related genes	Relation type
ENSG00000263317	TF binding region
ENSG00000263317	CpG island

Extended variants
information (count: 430 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4794340	chr17:50462226-50462227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143459601	chr17:50462263-50462264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566583707	chr17:50462274-50462275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374572083	chr17:50462310-50462311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535567133	chr17:50462318-50462319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562344503	chr17:50462329-50462330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548935910	chr17:50462379-50462380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151230745	chr17:50462388-50462389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538274744	chr17:50462405-50462406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557760480	chr17:50462421-50462422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577918026	chr17:50462439-50462440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117560666	chr17:50462443-50462444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12453008	chr17:50462528-50462529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12451238	chr17:50462529-50462530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140401361	chr17:50462580-50462581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367954254	chr17:50462583-50462584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34875392	chr17:50462615-50462616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573743846	chr17:50462622-50462623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557426950	chr17:50462713-50462714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35495225	chr17:50462764-50462765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs3898324	chr17:50462776-50462777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73989309	chr17:50462778-50462779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7502269	chr17:50462808-50462809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4058273	chr17:50462823-50462824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545034132	chr17:50462833-50462834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564575192	chr17:50462856-50462857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544741918	chr17:50462896-50462897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533684960	chr17:50462904-50462905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546753539	chr17:50462920-50462921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560332640	chr17:50462999-50463000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368945040	chr17:50463006-50463007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529475722	chr17:50463051-50463052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375546915	chr17:50463061-50463062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527900186	chr17:50463063-50463064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532810586	chr17:50463064-50463065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569051729	chr17:50463089-50463090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199717620	chr17:50463090-50463091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537850868	chr17:50463092-50463093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186208678	chr17:50463163-50463164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577275191	chr17:50463179-50463180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534110375	chr17:50463191-50463192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4474737	chr17:50463192-50463193	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs575099616	chr17:50463195-50463196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567452981	chr17:50463201-50463202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550965671	chr17:50463219-50463220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556289727	chr17:50463228-50463229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs8071812	chr17:50463252-50463253	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs544635681	chr17:50463253-50463254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117208956	chr17:50463256-50463257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571983417	chr17:50463299-50463300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	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
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chordoma	18071362	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myeloproliferative neoplasm	20015882	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:50457600-50466600	Weak transcription	Stomach Mucosa	stomach
2	chr17:50463000-50463400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr17:50466000-50466800	Enhancers	Duodenum Mucosa	Duodenum
4	chr17:50466200-50466800	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr17:50466400-50467200	Enhancers	Aorta	Aorta
6	chr17:50466600-50467000	Enhancers	Stomach Mucosa	stomach
7	chr17:50466800-50467000	Flanking Active TSS	Duodenum Mucosa	Duodenum
8	chr17:50466800-50467000	Enhancers	Ovary	ovary
9	chr17:50466800-50467000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
10	chr17:50466800-50467200	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr17:50467000-50467400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr17:50467000-50467400	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr17:50467000-50467600	Active TSS	Duodenum Mucosa	Duodenum
14	chr17:50467000-50467600	Active TSS	Ovary	ovary
15	chr17:50467000-50467600	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr17:50467000-50467800	Active TSS	Stomach Mucosa	stomach
17	chr17:50467200-50467600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr17:50467200-50467600	Active TSS	Adipose Nuclei	Adipose
19	chr17:50467200-50467600	Active TSS	Aorta	Aorta
20	chr17:50467200-50467600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
21	chr17:50467200-50467600	Active TSS	Rectal Smooth Muscle	rectum
22	chr17:50467200-50467600	Active TSS	Right Atrium	heart
23	chr17:50467200-50467800	Active TSS	Colon Smooth Muscle	Colon
24	chr17:50467400-50467600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr17:50467400-50467600	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
26	chr17:50467600-50468000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr17:50467600-50468000	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr17:50468600-50469400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr17:50472600-50473400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr17:50487400-50488200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr17:50487800-50488800	Enhancers	HepG2	liver
32	chr17:50494600-50494800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr17:50495000-50496200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr17:50496200-50496600	Enhancers	Gastric	stomach
35	chr17:50496200-50496600	Enhancers	Pancreas	Pancrea
36	chr17:50496200-50496600	Enhancers	Psoas Muscle	Psoas
37	chr17:50496200-50496800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr17:50496200-50496800	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr17:50496200-50497400	Enhancers	HepG2	liver
40	chr17:50496200-50497600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr17:50496200-50497600	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr17:50496200-50497600	Enhancers	Liver	Liver
43	chr17:50496400-50496800	Enhancers	Brain Angular Gyrus	brain
44	chr17:50496400-50497000	Enhancers	Adipose Nuclei	Adipose
45	chr17:50496600-50497000	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr17:50496600-50497400	Weak transcription	Gastric	stomach
47	chr17:50497000-50497400	Enhancers	Brain Germinal Matrix	brain
48	chr17:50497400-50497800	Enhancers	Gastric	stomach
49	chr17:50497800-50498000	Weak transcription	Gastric	stomach
50	chr17:50498000-50498400	Enhancers	Gastric	stomach

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