Variant report

Variant	nsv882395
Chromosome Location	chr5:96756689-96849023
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:398 , 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	BCL3	chr5:96831847-96832152	GM12878	blood:	n/a	n/a
2	BHLHE40	chr5:96830650-96830767	GM12878	blood:	n/a	n/a
3	BRCA1	chr5:96761275-96761538	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr5:96827337-96827579	HepG2	liver:	n/a	chr5:96827480-96827491 chr5:96827469-96827480
5	CEBPB	chr5:96769639-96770035	MCF-7	breast:	n/a	n/a
6	CEBPB	chr5:96767482-96767701	A549	lung:	n/a	chr5:96767561-96767572
7	CEBPB	chr5:96782630-96782690	HepG2	liver:	n/a	chr5:96782638-96782649
8	CEBPB	chr5:96835323-96835651	MCF-7	breast:	n/a	n/a
9	CEBPB	chr5:96767418-96767754	MCF-7	breast:	n/a	chr5:96767561-96767572
10	CEBPB	chr5:96767396-96767709	HepG2	liver:	n/a	chr5:96767561-96767572
11	CEBPB	chr5:96767484-96767678	Hela-S3	cervix:	n/a	chr5:96767561-96767572
12	CTCF	chr5:96761300-96761450	HAc	cerebellar:	n/a	n/a
13	CTCF	chr5:96763040-96763190	HMEC	breast:	n/a	n/a
14	CTCF	chr5:96763075-96763206	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:96761285-96761520	NHEK	skin:	n/a	n/a
16	CTCF	chr5:96831078-96831309	GM12878	blood:	n/a	n/a
17	CTCF	chr5:96761260-96761410	HCT-116	colon:	n/a	n/a
18	CTCF	chr5:96761291-96761490	GM12891	blood:	n/a	n/a
19	CTCF	chr5:96761380-96761530	GM12865	blood:	n/a	n/a
20	CTCF	chr5:96761300-96761450	MCF-7	breast:	n/a	n/a
21	CTCF	chr5:96804320-96804470	HEK293	kidney:	n/a	n/a
22	CTCF	chr5:96761320-96761470	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr5:96779580-96779730	GM12869	blood:	n/a	n/a
24	CTCF	chr5:96761231-96761595	IMR90	lung:	n/a	n/a
25	CTCF	chr5:96761300-96761450	GM12866	blood:	n/a	n/a
26	CTCF	chr5:96761340-96761490	GM12878	blood:	n/a	n/a
27	CTCF	chr5:96761340-96761490	AG09309	skin:	n/a	n/a
28	CTCF	chr5:96825338-96825358	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:96761280-96761430	HEK293	kidney:	n/a	n/a
30	CTCF	chr5:96763120-96763270	AG09319	gingival:	n/a	n/a
31	CTCF	chr5:96761387-96761452	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr5:96804360-96804510	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:96804260-96804410	NHEK	skin:	n/a	n/a
34	CTCF	chr5:96761320-96761470	GM12872	blood:	n/a	n/a
35	CTCF	chr5:96761281-96761511	GM19240	blood:	n/a	n/a
36	CTCF	chr5:96763092-96763192	NHEK	skin:	n/a	n/a
37	CTCF	chr5:96761340-96761490	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr5:96761314-96761506	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:96761360-96761510	A549	lung:	n/a	n/a
40	CTCF	chr5:96761280-96761430	GM12865	blood:	n/a	n/a
41	CTCF	chr5:96761268-96761529	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:96761319-96761518	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr5:96763126-96763159	ProgFib	skin:	n/a	n/a
44	CTCF	chr5:96763040-96763190	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr5:96761305-96761306	Medullo	brain:	n/a	n/a
46	CTCF	chr5:96761340-96761490	AG10803	skin:	n/a	n/a
47	CTCF	chr5:96761360-96761484	HepG2	liver:	n/a	n/a
48	CTCF	chr5:96804460-96804610	HMEC	breast:	n/a	n/a
49	CTCF	chr5:96761300-96761450	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr5:96761380-96761530	NHEK	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96789385-96789435	GM19239	blood:	n/a
2	chr5:96845117-96845167	HUVEC	blood vessel:	n/a
3	chr5:96789385-96789435	SK-N-SH	brain:	n/a
4	chr5:96789385-96789435	ECC-1	luminal epithelium:	n/a
5	chr5:96789385-96789435	GM12891	blood:	n/a
6	chr5:96845117-96845167	AoSMC	blood vessel:	n/a
7	chr5:96789385-96789435	NH-A	brain:	n/a
8	chr5:96789385-96789435	H1-hESC	embryonic stem cell:	embryo
9	chr5:96845117-96845167	HRCEpiC	kidney:	n/a
10	chr5:96845117-96845167	SK-N-SH	brain:	n/a
11	chr5:96845117-96845167	ovcar-3	ovarian:	n/a
12	chr5:96845117-96845167	HCM	heart:	n/a
13	chr5:96789385-96789435	AG10803	skin:	n/a
14	chr5:96845117-96845167	ECC-1	luminal epithelium:	n/a
15	chr5:96845117-96845167	NHBE	bronchial:	n/a
16	chr5:96789385-96789435	LNCaP	prostate:	n/a
17	chr5:96789385-96789435	PrEC	prostate:	n/a
18	chr5:96789385-96789435	AG09319	gingival:	n/a
19	chr5:96845117-96845167	PFSK-1	brain:	n/a
20	chr5:96845117-96845167	LNCaP	prostate:	n/a
21	chr5:96845117-96845167	HEEpiC	esophagus:	n/a
22	chr5:96845117-96845167	HIPEpiC	eye:	n/a
23	chr5:96845117-96845167	SK-N-SH_RA	brain:	n/a
24	chr5:96789385-96789435	SAEC	small airway:	n/a
25	chr5:96845117-96845167	HAEpiC	amniotic membrane:	n/a
26	chr5:96845117-96845167	SAEC	small airway:	n/a
27	chr5:96845117-96845167	HCPEpiC	choroid plexus:	n/a
28	chr5:96845117-96845167	CMK	blood:	n/a
29	chr5:96845117-96845167	AG10803	skin:	n/a
30	chr5:96789385-96789435	HNPCEpiC	eye:	n/a
31	chr5:96845117-96845167	SKMC	muscle:	n/a
32	chr5:96789385-96789435	HCT-116	colon:	n/a
33	chr5:96789385-96789435	Hepatocyte	liver:	n/a
34	chr5:96789385-96789435	SKMC	muscle:	n/a
35	chr5:96789385-96789435	HEEpiC	esophagus:	n/a
36	chr5:96845117-96845167	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:96789385-96789435	HRE	kidney:	n/a
38	chr5:96789385-96789435	ovcar-3	ovarian:	n/a
39	chr5:96789385-96789435	HCF	heart:	n/a
40	chr5:96789385-96789435	AG04449	skin:	fetal
41	chr5:96789385-96789435	PANC-1	pancreas:	n/a
42	chr5:96845117-96845167	AG09319	gingival:	n/a
43	chr5:96845117-96845167	AG09309	skin:	n/a
44	chr5:96789385-96789435	A549	lung:	n/a
45	chr5:96789385-96789435	U87	brain:	n/a
46	chr5:96845117-96845167	Hela-S3	cervix:	n/a
47	chr5:96789385-96789435	NHBE	bronchial:	n/a
48	chr5:96845117-96845167	Jurkat	blood:	n/a
49	chr5:96789385-96789435	Jurkat	blood:	n/a
50	chr5:96845117-96845167	ProgFib	skin:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:96757244..96760010-chr5:96764877..96766486,2	MCF-7	breast:
2	chr5:96757244..96760010-chr5:96764877..96766486,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-1	chr5:96772257-96772921	ENSG00000251513.1
2	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	NR_105028
3	lnc-CTD-2215E18.1.1-1	chr5:96767448-96767604	ENSG00000251513.1
4	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	XLOC_004483
5	lnc-RIOK2-4	chr5:96786031-96786319	NONHSAT102930
6	lnc-CTD-2215E18.1.1-2	chr5:96840399-96840496	NONHSAT102931
7	lnc-RIOK2-3	chr5:96785062-96785445	NONHSAT102929

No data

Variant related genes	Relation type
ENSG00000249977	TF binding region
ENSG00000250331	TF binding region
ENSG00000249977	CpG island
ENSG00000250331	CpG island

Extended variants
information (count: 1721 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1721 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146689	chr5:96756689-96756690	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376952448	chr5:96756750-96756751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7719981	chr5:96756758-96756759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150874338	chr5:96756804-96756805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529328877	chr5:96756809-96756810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9314206	chr5:96756812-96756813	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs187777178	chr5:96756858-96756859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139539218	chr5:96756881-96756882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113312766	chr5:96756912-96756913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146184191	chr5:96756913-96756914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189565673	chr5:96756962-96756963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370996961	chr5:96756964-96756965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139052367	chr5:96756980-96756981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556274053	chr5:96756983-96756984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529504364	chr5:96756993-96756994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs291826	chr5:96757038-96757039	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs144158691	chr5:96757048-96757049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572334192	chr5:96757066-96757067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546151436	chr5:96757087-96757088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564247934	chr5:96757154-96757155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531580611	chr5:96757172-96757173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543541586	chr5:96757186-96757187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34605451	chr5:96757190-96757191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6889289	chr5:96757253-96757254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182263088	chr5:96757323-96757324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532453601	chr5:96757351-96757352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186903304	chr5:96757354-96757355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186076229	chr5:96767459-96767460	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs190483841	chr5:96767465-96767466	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs116055115	chr5:96767467-96767468	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs183090618	chr5:96767508-96767509	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs574962880	chr5:96767514-96767515	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs75736057	chr5:96767516-96767517	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs554137051	chr5:96767558-96767559	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs551649381	chr5:96767576-96767577	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs539852907	chr5:96767580-96767581	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs115536477	chr5:96772334-96772335	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs186893725	chr5:96772338-96772339	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs369896884	chr5:96772403-96772404	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs535662499	chr5:96772406-96772407	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs191785165	chr5:96772415-96772416	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs183598900	chr5:96772416-96772417	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs150843809	chr5:96772466-96772467	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs555304763	chr5:96772475-96772476	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs574438421	chr5:96772579-96772580	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs116800683	chr5:96772595-96772596	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs573640263	chr5:96772601-96772602	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs548275861	chr5:96772649-96772650	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs139295622	chr5:96772692-96772693	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs559083506	chr5:96772716-96772717	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96753200-96757000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr5:96753400-96757000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:96755600-96756800	Weak transcription	Ovary	ovary
4	chr5:96756400-96756800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:96756400-96757000	Enhancers	Fetal Lung	lung
6	chr5:96756800-96757000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:96756800-96757000	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr5:96756800-96757400	Enhancers	Ovary	ovary
9	chr5:96785000-96785400	Enhancers	GM12878-XiMat	blood
10	chr5:96787800-96788400	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr5:96787800-96789400	Enhancers	Brain Angular Gyrus	brain
12	chr5:96787800-96789800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:96787800-96790000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:96787800-96790000	Enhancers	Brain Hippocampus Middle	brain
15	chr5:96787800-96790200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr5:96788000-96789800	Enhancers	Brain Substantia Nigra	brain
17	chr5:96788000-96790000	Enhancers	Brain Cingulate Gyrus	brain
18	chr5:96788000-96790600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr5:96788200-96788800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:96788400-96788800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
21	chr5:96788400-96789000	Enhancers	Colon Smooth Muscle	Colon
22	chr5:96788400-96789400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:96788400-96790000	Enhancers	Brain Germinal Matrix	brain
24	chr5:96788600-96788800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:96788600-96789200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr5:96788600-96789200	Enhancers	Brain Anterior Caudate	brain
27	chr5:96788600-96789400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:96788800-96789600	Enhancers	Fetal Brain Female	brain
29	chr5:96788800-96789800	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr5:96789000-96789400	Enhancers	Fetal Kidney	kidney
31	chr5:96791800-96794600	Weak transcription	Pancreas	Pancrea
32	chr5:96794200-96794400	Enhancers	GM12878-XiMat	blood
33	chr5:96794400-96794800	Flanking Active TSS	GM12878-XiMat	blood
34	chr5:96794600-96794800	ZNF genes & repeats	Pancreas	Pancrea
35	chr5:96794800-96795400	Enhancers	GM12878-XiMat	blood
36	chr5:96797400-96798400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:96801600-96802600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:96802600-96803200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr5:96806000-96808000	ZNF genes & repeats	Pancreas	Pancrea
40	chr5:96807000-96808000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:96808000-96808200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:96811800-96812400	Enhancers	GM12878-XiMat	blood
43	chr5:96812200-96813000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr5:96812400-96812800	Enhancers	NHEK	skin
45	chr5:96812400-96813000	Flanking Active TSS	GM12878-XiMat	blood
46	chr5:96813000-96815600	Enhancers	GM12878-XiMat	blood
47	chr5:96814000-96814600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:96814200-96814600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:96814200-96814600	Enhancers	Fetal Lung	lung
50	chr5:96814200-96814600	Enhancers	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links