Variant report

Variant	nsv569443
Chromosome Location	chr15:53936907-53972798
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	chr15:53947832-53947856	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53958161-53958371	HepG2	liver:	n/a	n/a
3	CEBPB	chr15:53971377-53971565	HepG2	liver:	n/a	chr15:53971439-53971450
4	CEBPB	chr15:53971315-53971562	A549	lung:	n/a	chr15:53971439-53971450
5	CHD1	chr15:53947735-53947742	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr15:53947740-53947890	HBMEC	blood vessel:	n/a	n/a
7	CTCF	chr15:53947740-53947890	Caco-2	colon:	n/a	n/a
8	CTCF	chr15:53958318-53958350	Gliobla	brain:	n/a	n/a
9	CTCF	chr15:53947716-53947912	HepG2	liver:	n/a	n/a
10	CTCF	chr15:53947820-53947970	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr15:53947760-53947910	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr15:53958180-53958330	GM12878	blood:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
13	CTCF	chr15:53947740-53947890	RPTEC	kidney:	n/a	n/a
14	CTCF	chr15:53958360-53958510	HAc	cerebellar:	n/a	n/a
15	CTCF	chr15:53947780-53947930	RPTEC	kidney:	n/a	n/a
16	CTCF	chr15:53958224-53958413	LNCaP	prostate:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
17	CTCF	chr15:53958200-53958350	SAEC	small airway:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
18	CTCF	chr15:53958200-53958350	HRE	kidney:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
19	CTCF	chr15:53958060-53958210	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr15:53947858-53947922	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr15:53958269-53958373	GM12878	blood:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
22	CTCF	chr15:53961920-53962070	AG10803	skin:	n/a	n/a
23	CTCF	chr15:53947760-53947910	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr15:53957783-53957830	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:53958220-53958370	HCT-116	colon:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
26	CTCF	chr15:53958289-53958337	Spleen_OC	spleen:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
27	CTCF	chr15:53947681-53947912	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr15:53947680-53947830	A549	lung:	n/a	n/a
29	CTCF	chr15:53961161-53961215	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr15:53957792-53957813	GM13977	blood:	n/a	n/a
31	CTCF	chr15:53947680-53947830	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr15:53958220-53958370	A549	lung:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
33	CTCF	chr15:53958240-53958390	GM12871	blood:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
34	CTCF	chr15:53947800-53947950	GM06990	blood:	n/a	n/a
35	CTCF	chr15:53946372-53946415	Medullo	brain:	n/a	n/a
36	CTCF	chr15:53958080-53958230	GM06990	blood:	n/a	n/a
37	CTCF	chr15:53958220-53958370	HMEC	breast:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
38	CTCF	chr15:53947731-53947970	MCF-7	breast:	n/a	n/a
39	CTCF	chr15:53958194-53958378	HepG2	liver:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
40	CTCF	chr15:53958200-53958350	Caco-2	colon:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
41	CTCF	chr15:53947800-53947950	GM12872	blood:	n/a	n/a
42	CTCF	chr15:53947769-53947942	MCF-7	breast:	n/a	n/a
43	CTCF	chr15:53970760-53970910	A549	lung:	n/a	n/a
44	CTCF	chr15:53958260-53958410	HMEC	breast:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
45	CTCF	chr15:53947943-53947945	MCF-7	breast:	n/a	n/a
46	CTCF	chr15:53958174-53958462	GM12878	blood:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
47	CTCF	chr15:53958220-53958370	AG04449	skin:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
48	CTCF	chr15:53971320-53971470	GM12874	blood:	n/a	n/a
49	CTCF	chr15:53958180-53958330	HAc	cerebellar:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
50	CTCF	chr15:53958300-53958450	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53943590-53943640	HCPEpiC	choroid plexus:	n/a
2	chr15:53943590-53943640	HepG2	liver:	n/a
3	chr15:53943590-53943640	T-47D	breast:	n/a
4	chr15:53943590-53943640	HUVEC	blood vessel:	n/a
5	chr15:53943590-53943640	AG09319	gingival:	n/a
6	chr15:53943590-53943640	HEEpiC	esophagus:	n/a
7	chr15:53943590-53943640	MCF-7	breast:	n/a
8	chr15:53943590-53943640	GM19239	blood:	n/a
9	chr15:53943590-53943640	GM06990	blood:	n/a
10	chr15:53943590-53943640	SK-N-SH	brain:	n/a
11	chr15:53943590-53943640	AG09309	skin:	n/a
12	chr15:53943590-53943640	HRPEpiC	eye:	n/a
13	chr15:53943590-53943640	AG04449	skin:	fetal
14	chr15:53943590-53943640	AoSMC	blood vessel:	n/a
15	chr15:53943590-53943640	IMR90	lung:	fetal
16	chr15:53943590-53943640	ovcar-3	ovarian:	n/a
17	chr15:53943590-53943640	BJ	skin:	n/a
18	chr15:53943590-53943640	MCF10A-Er-Src	breast:	n/a
19	chr15:53943590-53943640	HL-60	blood:	n/a
20	chr15:53943590-53943640	SKMC	muscle:	n/a
21	chr15:53943590-53943640	NHDF-neo	bronchial:	n/a
22	chr15:53943590-53943640	AG04450	lung:	fetal
23	chr15:53943590-53943640	GM12878	blood:	n/a
24	chr15:53943590-53943640	U87	brain:	n/a
25	chr15:53943590-53943640	HRCEpiC	kidney:	n/a
26	chr15:53943590-53943640	PFSK-1	brain:	n/a
27	chr15:53943590-53943640	K562	blood:	n/a
28	chr15:53943590-53943640	GM12891	blood:	n/a
29	chr15:53943590-53943640	SK-N-SH_RA	brain:	n/a
30	chr15:53943590-53943640	NT2-D1	testis:	n/a
31	chr15:53943590-53943640	Jurkat	blood:	n/a
32	chr15:53943590-53943640	HEK293	kidney:	embryo
33	chr15:53943590-53943640	HNPCEpiC	eye:	n/a
34	chr15:53943590-53943640	GM12892	blood:	n/a
35	chr15:53943590-53943640	BE2_C	brain:	n/a
36	chr15:53943590-53943640	HCM	heart:	n/a
37	chr15:53943590-53943640	SK-N-MC	brain:	n/a
38	chr15:53943590-53943640	PrEC	prostate:	n/a
39	chr15:53943590-53943640	RPTEC	kidney:	n/a
40	chr15:53943590-53943640	NH-A	brain:	n/a
41	chr15:53943590-53943640	HCF	heart:	n/a
42	chr15:53943590-53943640	NHBE	bronchial:	n/a
43	chr15:53943590-53943640	ProgFib	skin:	n/a
44	chr15:53943590-53943640	HIPEpiC	eye:	n/a
45	chr15:53943590-53943640	LNCaP	prostate:	n/a
46	chr15:53943590-53943640	CMK	blood:	n/a
47	chr15:53943590-53943640	HMEC	breast:	n/a
48	chr15:53943590-53943640	Hepatocyte	liver:	n/a
49	chr15:53943590-53943640	ECC-1	luminal epithelium:	n/a
50	chr15:53943590-53943640	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:53057704..53058252-chr15:53950484..53951446,2	MCF-7	breast:
2	chr15:53057663..53058643-chr15:53947402..53948111,2	MCF-7	breast:
3	chr15:53072427..53073417-chr15:53957937..53958702,5	MCF-7	breast:
4	chr15:53945998..53946891-chr15:54009249..54010202,2	MCF-7	breast:
5	chr15:53676366..53677226-chr15:53947378..53948497,3	MCF-7	breast:
6	chr15:53958809..53961070-chr15:53966400..53969207,2	MCF-7	breast:
7	chr15:53958809..53961070-chr15:53966400..53969207,2	MCF-7	breast:
8	chr15:53949957..53952071-chr15:53952352..53954072,2	MCF-7	breast:
9	chr15:53676762..53677326-chr15:53957733..53958557,2	MCF-7	breast:
10	chr15:53949957..53952071-chr15:53952352..53954072,2	MCF-7	breast:
11	chr15:53072550..53073539-chr15:53947412..53948347,3	MCF-7	breast:

Variant related genes	Relation type
RNU2-53P	TF binding region
RNU2-53P	CpG island
ENSG00000169856	chromatin interactions

Extended variants
information (count: 1495 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4776168	chr15:53936907-53936908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532627746	chr15:53936943-53936944	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs12593967	chr15:53936948-53936949	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs138270660	chr15:53936967-53936968	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs539929011	chr15:53936999-53937000	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs113561604	chr15:53937038-53937039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547157914	chr15:53937051-53937052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567491041	chr15:53937077-53937078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558227755	chr15:53937079-53937080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536447673	chr15:53937080-53937081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573131133	chr15:53937100-53937101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556347094	chr15:53937138-53937139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117433756	chr15:53937140-53937141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78434728	chr15:53937171-53937172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558939496	chr15:53937180-53937181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74891855	chr15:53937196-53937197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572335558	chr15:53937224-53937225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541555670	chr15:53937255-53937256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554763450	chr15:53937293-53937294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574832164	chr15:53937391-53937392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555347649	chr15:53937456-53937457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563508599	chr15:53937495-53937496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114669624	chr15:53937499-53937500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs690610	chr15:53937518-53937519	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs564927411	chr15:53937519-53937520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527278879	chr15:53937537-53937538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188306089	chr15:53937580-53937581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376221706	chr15:53937581-53937582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7170810	chr15:53937597-53937598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs141844796	chr15:53937610-53937611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550014482	chr15:53937721-53937722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181828579	chr15:53937722-53937723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559649741	chr15:53937741-53937742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538970246	chr15:53937800-53937801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150184487	chr15:53937805-53937806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566113301	chr15:53937837-53937838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113488100	chr15:53937848-53937849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534713979	chr15:53937881-53937882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562334883	chr15:53937896-53937897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184797828	chr15:53937908-53937909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574611038	chr15:53937914-53937915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62005954	chr15:53937942-53937943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs557158600	chr15:53937960-53937961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367858440	chr15:53937976-53937977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79898680	chr15:53938041-53938042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376216939	chr15:53938047-53938048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559789809	chr15:53938065-53938066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62005955	chr15:53938118-53938119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs75452646	chr15:53938173-53938174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78709093	chr15:53938179-53938180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53927200-53951400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:53927600-53941200	Weak transcription	Liver	Liver
3	chr15:53936600-53937200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr15:53936800-53937000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr15:53936800-53937200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:53936800-53937200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr15:53936800-53937400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr15:53936800-53937400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr15:53937000-53937600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr15:53937000-53937600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr15:53941200-53943400	Enhancers	Liver	Liver
12	chr15:53943400-53953000	Weak transcription	Liver	Liver
13	chr15:53948800-53949000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr15:53949000-53950800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr15:53949800-53951200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr15:53950000-53950200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:53950000-53951800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr15:53950200-53951600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:53950400-53951600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr15:53950400-53951800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr15:53950600-53950800	Enhancers	Pancreas	Pancrea
22	chr15:53950600-53951200	Enhancers	Brain Germinal Matrix	brain
23	chr15:53950600-53951400	Enhancers	HepG2	liver
24	chr15:53950600-53951800	Enhancers	Fetal Heart	heart
25	chr15:53950600-53951800	Enhancers	Fetal Lung	lung
26	chr15:53950800-53951200	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr15:53950800-53951400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr15:53950800-53951800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr15:53951000-53951800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr15:53951000-53951800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr15:53951000-53951800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr15:53951200-53951600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:53951200-53951600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:53951200-53951800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr15:53951400-53951600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:53951400-53959200	Weak transcription	HepG2	liver
37	chr15:53951600-53951800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:53951600-53951800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:53951600-53973000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:53953000-53953600	Strong transcription	Liver	Liver
41	chr15:53953600-53955400	Weak transcription	Liver	Liver
42	chr15:53955400-53957800	Strong transcription	Liver	Liver
43	chr15:53957800-53972800	Weak transcription	Liver	Liver
44	chr15:53958000-53958600	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr15:53959200-53959600	Enhancers	HepG2	liver
46	chr15:53959400-53959600	Enhancers	Pancreas	Pancrea
47	chr15:53959600-53986200	Weak transcription	Pancreas	Pancrea
48	chr15:53961400-53961600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr15:53962600-53962800	Enhancers	Aorta	Aorta
50	chr15:53962800-53963800	Weak transcription	Aorta	Aorta

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