Variant report

Variant	nsv469569
Chromosome Location	chr15:31886000-31974400
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	chr15:31931274-31931549	HepG2	liver:	n/a	n/a
2	BATF	chr15:31942586-31942812	GM12878	blood:	n/a	n/a
3	BCL11A	chr15:31942588-31942835	GM12878	blood:	n/a	n/a
4	BRCA1	chr15:31897757-31899408	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr15:31901506-31901800	IMR90	lung:	n/a	n/a
6	CEBPB	chr15:31899930-31900147	HepG2	liver:	n/a	n/a
7	CEBPB	chr15:31972095-31972264	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:31931258-31931592	HepG2	liver:	n/a	chr15:31931452-31931463
9	CEBPB	chr15:31908263-31908457	K562	blood:	n/a	chr15:31908327-31908338
10	CEBPB	chr15:31897659-31899611	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr15:31931278-31931622	H1-hESC	embryonic stem cell:	n/a	chr15:31931452-31931463
12	CEBPB	chr15:31931269-31931571	HepG2	liver:	n/a	chr15:31931452-31931463
13	CEBPB	chr15:31898181-31898720	MCF-7	breast:	n/a	n/a
14	CEBPB	chr15:31898244-31898622	MCF-7	breast:	n/a	n/a
15	CEBPB	chr15:31931277-31931549	A549	lung:	n/a	chr15:31931452-31931463
16	CEBPB	chr15:31897668-31899067	A549	lung:	n/a	n/a
17	CEBPB	chr15:31908180-31908480	HepG2	liver:	n/a	chr15:31908327-31908338
18	CEBPB	chr15:31931279-31931549	MCF-7	breast:	n/a	chr15:31931452-31931463
19	CEBPB	chr15:31901523-31901788	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr15:31931263-31931645	HepG2	liver:	n/a	chr15:31931452-31931463
21	CEBPB	chr15:31931202-31931649	Hela-S3	cervix:	n/a	chr15:31931452-31931463
22	CEBPB	chr15:31897767-31898924	A549	lung:	n/a	n/a
23	CEBPB	chr15:31931325-31931534	K562	blood:	n/a	chr15:31931452-31931463
24	CEBPB	chr15:31931268-31931680	A549	lung:	n/a	chr15:31931452-31931463
25	CEBPB	chr15:31931264-31931579	IMR90	lung:	n/a	chr15:31931452-31931463
26	CEBPB	chr15:31897770-31899026	IMR90	lung:	n/a	n/a
27	CEBPB	chr15:31899887-31900221	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:31897804-31898156	MCF-7	breast:	n/a	n/a
29	CEBPB	chr15:31931265-31931648	A549	lung:	n/a	chr15:31931452-31931463
30	CEBPB	chr15:31897783-31898053	HepG2	liver:	n/a	n/a
31	CEBPB	chr15:31931263-31931553	MCF-7	breast:	n/a	chr15:31931452-31931463
32	CEBPB	chr15:31899883-31900229	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:31931269-31931505	HepG2	liver:	n/a	chr15:31931452-31931463
34	CEBPB	chr15:31897741-31898150	MCF-7	breast:	n/a	n/a
35	CEBPD	chr15:31931258-31931526	HepG2	liver:	n/a	n/a
36	CHD2	chr15:31897666-31898106	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr15:31901627-31901782	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr15:31942495-31942512	GM10266	blood:	n/a	n/a
39	CTCF	chr15:31941940-31942090	AG09319	gingival:	n/a	n/a
40	CTCF	chr15:31942034-31942035	GM12892	blood:	n/a	n/a
41	CTCF	chr15:31941904-31942110	GM12891	blood:	n/a	n/a
42	CTCF	chr15:31897677-31897874	GM19238	blood:	n/a	chr15:31897787-31897803 chr15:31897786-31897804
43	CTCF	chr15:31897700-31897850	GM12864	blood:	n/a	chr15:31897787-31897803 chr15:31897786-31897804
44	CTCF	chr15:31897685-31897887	MCF-7	breast:	n/a	chr15:31897787-31897803 chr15:31897786-31897804
45	CTCF	chr15:31897700-31897850	K562	blood:	n/a	chr15:31897787-31897803 chr15:31897786-31897804
46	CTCF	chr15:31897660-31897810	AG04449	skin:	n/a	chr15:31897787-31897803 chr15:31897786-31897804
47	CTCF	chr15:31931300-31931450	AG04449	skin:	n/a	n/a
48	CTCF	chr15:31941891-31942115	GM19238	blood:	n/a	n/a
49	CTCF	chr15:31897752-31897857	GM10266	blood:	n/a	chr15:31897787-31897803 chr15:31897786-31897804
50	CTCF	chr15:31897720-31897870	BE2_C	brain:	n/a	chr15:31897787-31897803 chr15:31897786-31897804

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31898033-31898083	HMEC	breast:	n/a
2	chr15:31898033-31898083	HMEC	breast:	n/a
3	chr15:31948632-31948682	AoSMC	blood vessel:	n/a
4	chr15:31948632-31948682	HUVEC	blood vessel:	n/a
5	chr15:31948632-31948682	PFSK-1	brain:	n/a
6	chr15:31948632-31948682	RPTEC	kidney:	n/a
7	chr15:31898033-31898083	MCF-7	breast:	n/a
8	chr15:31948632-31948682	ovcar-3	ovarian:	n/a
9	chr15:31948632-31948682	NH-A	brain:	n/a
10	chr15:31948632-31948682	HRE	kidney:	n/a
11	chr15:31948632-31948682	AG04450	lung:	fetal
12	chr15:31898033-31898083	NHBE	bronchial:	n/a
13	chr15:31898033-31898083	BJ	skin:	n/a
14	chr15:31898033-31898083	Hepatocyte	liver:	n/a
15	chr15:31948632-31948682	Hepatocyte	liver:	n/a
16	chr15:31948632-31948682	LNCaP	prostate:	n/a
17	chr15:31898033-31898083	PFSK-1	brain:	n/a
18	chr15:31948075-31948125	T-47D	breast:	n/a
19	chr15:31948075-31948125	ProgFib	skin:	n/a
20	chr15:31948075-31948125	NHBE	bronchial:	n/a
21	chr15:31948632-31948682	T-47D	breast:	n/a
22	chr15:31948632-31948682	HNPCEpiC	eye:	n/a
23	chr15:31948632-31948682	HCM	heart:	n/a
24	chr15:31948632-31948682	HCPEpiC	choroid plexus:	n/a
25	chr15:31948632-31948682	AG10803	skin:	n/a
26	chr15:31948075-31948125	Hepatocyte	liver:	n/a
27	chr15:31948075-31948125	PANC-1	pancreas:	n/a
28	chr15:31948075-31948125	HCF	heart:	n/a
29	chr15:31898033-31898083	HEEpiC	esophagus:	n/a
30	chr15:31898033-31898083	HIPEpiC	eye:	n/a
31	chr15:31898033-31898083	GM06990	blood:	n/a
32	chr15:31898033-31898083	NB4	blood:	n/a
33	chr15:31898033-31898083	ovcar-3	ovarian:	n/a
34	chr15:31948632-31948682	GM12891	blood:	n/a
35	chr15:31898033-31898083	HCT-116	colon:	n/a
36	chr15:31948075-31948125	HL-60	blood:	n/a
37	chr15:31898033-31898083	SK-N-SH	brain:	n/a
38	chr15:31898033-31898083	HCM	heart:	n/a
39	chr15:31948075-31948125	HPAEpiC	pulmonary alveolar:	n/a
40	chr15:31948075-31948125	Caco-2	colon:	n/a
41	chr15:31948075-31948125	GM06990	blood:	n/a
42	chr15:31898033-31898083	SK-N-MC	brain:	n/a
43	chr15:31898033-31898083	HNPCEpiC	eye:	n/a
44	chr15:31898033-31898083	T-47D	breast:	n/a
45	chr15:31948632-31948682	K562	blood:	n/a
46	chr15:31948075-31948125	AG04449	skin:	fetal
47	chr15:31948075-31948125	Hela-S3	cervix:	n/a
48	chr15:31948075-31948125	K562	blood:	n/a
49	chr15:31948075-31948125	RPTEC	kidney:	n/a
50	chr15:31898033-31898083	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31860388..31862871-chr15:31898549..31900652,2	MCF-7	breast:
2	chr1:149222127..149223797-chr15:31897038..31899511,2	MCF-7	breast:

Variant related genes	Relation type
OTUD7A	TF binding region
OTUD7A	CpG island

Extended variants
information (count: 3300 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3300 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550361388	chr15:31886002-31886003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113028236	chr15:31886012-31886013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539410661	chr15:31886049-31886050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553019743	chr15:31886053-31886054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189902869	chr15:31886059-31886060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534985381	chr15:31886101-31886102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149779929	chr15:31886108-31886109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75322799	chr15:31886121-31886122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs180757936	chr15:31886168-31886169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138659812	chr15:31886207-31886208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544005508	chr15:31886265-31886266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374332158	chr15:31886284-31886285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563397700	chr15:31886312-31886313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11854539	chr15:31886335-31886336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs376697817	chr15:31886350-31886351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185323541	chr15:31886438-31886439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190859786	chr15:31886450-31886451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181890752	chr15:31886476-31886477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545878368	chr15:31886483-31886484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548176592	chr15:31886540-31886541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149331491	chr15:31886569-31886570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9806655	chr15:31886584-31886585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550815596	chr15:31886664-31886665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187659687	chr15:31886675-31886676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539524840	chr15:31886721-31886722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546745900	chr15:31886864-31886865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566472453	chr15:31886887-31886888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138151585	chr15:31886951-31886952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368219890	chr15:31886957-31886958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115875366	chr15:31887020-31887021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537221462	chr15:31887025-31887026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74318383	chr15:31887038-31887039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545644779	chr15:31887133-31887134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554173554	chr15:31887142-31887143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576347512	chr15:31887162-31887163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191487703	chr15:31887216-31887217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573112392	chr15:31887229-31887230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542207413	chr15:31887237-31887238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568708448	chr15:31887325-31887326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143519781	chr15:31887330-31887331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147167086	chr15:31887331-31887332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564251610	chr15:31887346-31887347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148600605	chr15:31887358-31887359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76448792	chr15:31887382-31887383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566572283	chr15:31887417-31887418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528837564	chr15:31887419-31887420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141157893	chr15:31887428-31887429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572454281	chr15:31887431-31887432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542804946	chr15:31887565-31887566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537335776	chr15:31887587-31887588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Renal cell carcinoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Autism	21865298	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31862400-31897000	Weak transcription	Gastric	stomach
2	chr15:31872200-31886600	Weak transcription	Brain Anterior Caudate	brain
3	chr15:31877400-31886800	Weak transcription	Brain Angular Gyrus	brain
4	chr15:31877800-31900800	Weak transcription	Pancreas	Pancrea
5	chr15:31879000-31886600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr15:31883800-31886600	Weak transcription	Fetal Stomach	stomach
7	chr15:31883800-31887000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr15:31883800-31889600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr15:31883800-31897000	Weak transcription	Right Atrium	heart
10	chr15:31885400-31886200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr15:31886200-31887000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr15:31886600-31887200	Enhancers	Fetal Stomach	stomach
13	chr15:31886600-31887400	Enhancers	Brain Anterior Caudate	brain
14	chr15:31886600-31887400	Enhancers	Brain Cingulate Gyrus	brain
15	chr15:31886800-31887000	Enhancers	Psoas Muscle	Psoas
16	chr15:31886800-31888000	Enhancers	Brain Angular Gyrus	brain
17	chr15:31887000-31887400	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr15:31887000-31887400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr15:31887400-31897400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr15:31887400-31897600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr15:31888000-31898000	Weak transcription	Brain Angular Gyrus	brain
22	chr15:31889600-31889800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr15:31889600-31890600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr15:31889600-31891000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:31889800-31890400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr15:31889800-31891400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr15:31890200-31891600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr15:31890400-31890800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr15:31890400-31891000	Enhancers	Hela-S3	cervix
30	chr15:31890400-31891200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr15:31890400-31891600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr15:31890400-31891600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr15:31890400-31891600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr15:31890600-31891000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr15:31890600-31891000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr15:31890600-31891200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr15:31890600-31891600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:31890600-31891600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr15:31890800-31891000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr15:31890800-31891000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr15:31890800-31891200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr15:31890800-31891200	Enhancers	Fetal Muscle Trunk	muscle
43	chr15:31890800-31891200	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr15:31890800-31891200	Enhancers	HepG2	liver
45	chr15:31890800-31891400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:31890800-31891400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:31890800-31891600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr15:31890800-31891600	Enhancers	Lung	lung
49	chr15:31891000-31891200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:31891000-31891200	Enhancers	HUES6 Cell Line	embryonic stem cell

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