Variant report

Variant	nsv882381
Chromosome Location	chr5:92576494-92649716
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	chr5:92581525-92582684	HepG2	liver:	n/a	chr5:92582527-92582543 chr5:92582528-92582544
2	BHLHE40	chr5:92607827-92607942	GM12878	blood:	n/a	n/a
3	BHLHE40	chr5:92582030-92582487	HepG2	liver:	n/a	n/a
4	CBX3	chr5:92593184-92593787	HCT-116	colon:	n/a	n/a
5	CEBPB	chr5:92637237-92637566	Hela-S3	cervix:	n/a	chr5:92637416-92637427
6	CEBPB	chr5:92637271-92637564	HepG2	liver:	n/a	chr5:92637416-92637427
7	CEBPB	chr5:92582064-92582441	A549	lung:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
8	CEBPB	chr5:92619673-92619984	HepG2	liver:	n/a	chr5:92619817-92619828
9	CEBPB	chr5:92643327-92643643	MCF-7	breast:	n/a	n/a
10	CEBPB	chr5:92635103-92636207	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr5:92582049-92582491	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
12	CEBPB	chr5:92616410-92616574	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:92629814-92630170	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:92582101-92582482	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
15	CEBPB	chr5:92609049-92609380	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:92582194-92582394	IMR90	lung:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
17	CEBPB	chr5:92581970-92582541	ECC-1	luminal epithelium:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
18	CEBPB	chr5:92637257-92637589	IMR90	lung:	n/a	chr5:92637416-92637427
19	CEBPB	chr5:92635034-92635321	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:92635064-92635340	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:92643367-92643630	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:92582034-92582543	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
23	CEBPB	chr5:92615098-92615172	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:92629733-92630237	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:92635459-92636120	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr5:92610520-92610580	HepG2	liver:	n/a	chr5:92610557-92610568 chr5:92610557-92610570
27	CEBPB	chr5:92582117-92582354	H1-hESC	embryonic stem cell:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
28	CEBPB	chr5:92610027-92610405	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:92582054-92582496	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
30	CEBPB	chr5:92593461-92593556	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:92643226-92643703	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:92582017-92582417	A549	lung:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
33	CEBPB	chr5:92582053-92582506	ECC-1	luminal epithelium:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
34	CEBPD	chr5:92582084-92582432	HepG2	liver:	n/a	n/a
35	CEBPD	chr5:92582061-92582426	HepG2	liver:	n/a	n/a
36	CEBPZ	chr5:92582242-92582332	HepG2	liver:	n/a	n/a
37	CHD2	chr5:92581987-92582384	HepG2	liver:	n/a	n/a
38	CTCF	chr5:92587980-92588130	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:92587910-92588154	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:92588000-92588150	HMF	breast:	n/a	n/a
41	CTCF	chr5:92609460-92609610	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr5:92625760-92625910	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr5:92625892-92625895	LNCaP	prostate:	n/a	n/a
44	CTCF	chr5:92588035-92588099	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr5:92625757-92625870	LNCaP	prostate:	n/a	n/a
46	CTCF	chr5:92587902-92588310	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:92588060-92588210	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr5:92588060-92588210	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr5:92588000-92588150	HepG2	liver:	n/a	n/a
50	CTCF	chr5:92587860-92588010	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:92635711-92635761	AG04449	skin:	fetal
2	chr5:92597063-92597113	AG09309	skin:	n/a
3	chr5:92635711-92635761	AG04449	skin:	fetal
4	chr5:92597063-92597113	AG09309	skin:	n/a
5	chr5:92635711-92635761	ovcar-3	ovarian:	n/a
6	chr5:92603424-92603474	GM12892	blood:	n/a
7	chr5:92582155-92582205	GM19239	blood:	n/a
8	chr5:92603169-92603219	AG09319	gingival:	n/a
9	chr5:92615296-92615346	HUVEC	blood vessel:	n/a
10	chr5:92603043-92603093	GM12878	blood:	n/a
11	chr5:92603169-92603219	ProgFib	skin:	n/a
12	chr5:92603169-92603219	SKMC	muscle:	n/a
13	chr5:92635711-92635761	HCM	heart:	n/a
14	chr5:92582155-92582205	SAEC	small airway:	n/a
15	chr5:92597063-92597113	Caco-2	colon:	n/a
16	chr5:92635711-92635761	SK-N-SH	brain:	n/a
17	chr5:92615296-92615346	ovcar-3	ovarian:	n/a
18	chr5:92641165-92641215	NHDF-neo	bronchial:	n/a
19	chr5:92615296-92615346	GM19239	blood:	n/a
20	chr5:92615296-92615346	AG09319	gingival:	n/a
21	chr5:92615296-92615346	AG04450	lung:	fetal
22	chr5:92641165-92641215	LNCaP	prostate:	n/a
23	chr5:92641165-92641215	AG10803	skin:	n/a
24	chr5:92603424-92603474	AG09319	gingival:	n/a
25	chr5:92641165-92641215	SAEC	small airway:	n/a
26	chr5:92597063-92597113	HRE	kidney:	n/a
27	chr5:92615296-92615346	BJ	skin:	n/a
28	chr5:92597063-92597113	SK-N-MC	brain:	n/a
29	chr5:92582155-92582205	HAEpiC	amniotic membrane:	n/a
30	chr5:92582155-92582205	HNPCEpiC	eye:	n/a
31	chr5:92641165-92641215	HCF	heart:	n/a
32	chr5:92641165-92641215	NH-A	brain:	n/a
33	chr5:92597063-92597113	Hela-S3	cervix:	n/a
34	chr5:92641165-92641215	HIPEpiC	eye:	n/a
35	chr5:92603169-92603219	AG04449	skin:	fetal
36	chr5:92615296-92615346	HEK293	kidney:	embryo
37	chr5:92597063-92597113	AG04449	skin:	fetal
38	chr5:92641165-92641215	HL-60	blood:	n/a
39	chr5:92603043-92603093	AG10803	skin:	n/a
40	chr5:92603424-92603474	HEEpiC	esophagus:	n/a
41	chr5:92615296-92615346	SK-N-MC	brain:	n/a
42	chr5:92603043-92603093	NHDF-neo	bronchial:	n/a
43	chr5:92603424-92603474	HCM	heart:	n/a
44	chr5:92603169-92603219	HUVEC	blood vessel:	n/a
45	chr5:92615296-92615346	AoSMC	blood vessel:	n/a
46	chr5:92582155-92582205	PANC-1	pancreas:	n/a
47	chr5:92603169-92603219	HNPCEpiC	eye:	n/a
48	chr5:92603043-92603093	BJ	skin:	n/a
49	chr5:92603424-92603474	ECC-1	luminal epithelium:	n/a
50	chr5:92597063-92597113	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:92611705..92613694-chr5:92615359..92617784,2	K562	blood:
2	chr5:92614535..92617070-chr5:92627594..92629532,2	MCF-7	breast:
3	chr5:92607951..92610447-chr5:92611670..92614154,2	K562	blood:
4	chr5:92572759..92575011-chr5:92577902..92579568,2	MCF-7	breast:
5	chr5:92614535..92617070-chr5:92627594..92629532,2	MCF-7	breast:
6	chr5:92607951..92610447-chr5:92611670..92614154,2	K562	blood:
7	chr5:92245272..92245812-chr5:92587648..92588348,2	MCF-7	breast:
8	chr5:92611705..92613694-chr5:92615359..92617784,2	K562	blood:

Variant related genes	Relation type
POLD2P1	TF binding region
POLD2P1	CpG island

Extended variants
information (count: 2363 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2363 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7448746	chr5:92576494-92576495	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115498171	chr5:92576511-92576512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576940196	chr5:92576515-92576516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538962893	chr5:92576551-92576552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541875368	chr5:92576552-92576553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184189587	chr5:92576581-92576582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561967585	chr5:92576642-92576643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4479828	chr5:92576679-92576680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535903589	chr5:92576681-92576682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551292855	chr5:92576697-92576698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75243785	chr5:92576726-92576727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532992561	chr5:92576820-92576821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546611683	chr5:92576825-92576826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566438244	chr5:92576840-92576841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535544019	chr5:92576877-92576878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555471721	chr5:92576899-92576900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188557598	chr5:92576906-92576907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72784442	chr5:92576939-92576940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs558059431	chr5:92576973-92576974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150691292	chr5:92577000-92577001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116137207	chr5:92577007-92577008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112903208	chr5:92577028-92577029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139936292	chr5:92577040-92577041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539890002	chr5:92577123-92577124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181092405	chr5:92577124-92577125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541936748	chr5:92577273-92577274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149880384	chr5:92577308-92577309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79402095	chr5:92577371-92577372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145930220	chr5:92577412-92577413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558568742	chr5:92577447-92577448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564842369	chr5:92577471-92577472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139878601	chr5:92577516-92577517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540209562	chr5:92577620-92577621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547271216	chr5:92577707-92577708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72784444	chr5:92577776-92577777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs528857382	chr5:92577809-92577810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549131732	chr5:92577811-92577812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527335257	chr5:92577974-92577975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184407664	chr5:92578060-92578061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189588225	chr5:92578095-92578096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374308755	chr5:92578098-92578099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180850658	chr5:92578121-92578122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571378944	chr5:92578138-92578139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200150575	chr5:92578168-92578169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10607895	chr5:92578169-92578170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs62366839	chr5:92578179-92578180	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs368946652	chr5:92578185-92578186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572936805	chr5:92578215-92578216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535437346	chr5:92578231-92578232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12521348	chr5:92578270-92578271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

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
Esophageal adenocarcinoma	18519675	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
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92573000-92579000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr5:92573000-92581000	Weak transcription	NHLF	lung
3	chr5:92573600-92581000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr5:92573600-92585400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:92577400-92578000	Enhancers	Fetal Kidney	kidney
6	chr5:92577400-92578200	Enhancers	Fetal Lung	lung
7	chr5:92577600-92577800	Enhancers	Fetal Stomach	stomach
8	chr5:92578000-92578200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr5:92578000-92578800	Weak transcription	Fetal Kidney	kidney
10	chr5:92578200-92578600	Weak transcription	Fetal Lung	lung
11	chr5:92578200-92579000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:92578600-92579400	Weak transcription	Fetal Stomach	stomach
13	chr5:92578600-92579800	Enhancers	Fetal Lung	lung
14	chr5:92578800-92579600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:92578800-92579600	Enhancers	Fetal Kidney	kidney
16	chr5:92578800-92579800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr5:92578800-92579800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:92578800-92579800	Enhancers	HUVEC	blood vessel
19	chr5:92578800-92584000	Enhancers	HepG2	liver
20	chr5:92579000-92579200	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr5:92579000-92579800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:92579000-92579800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr5:92579000-92581000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:92579200-92579400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr5:92579200-92580200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr5:92579400-92579600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr5:92579400-92582600	Enhancers	Fetal Stomach	stomach
28	chr5:92579600-92579800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:92579600-92580600	Weak transcription	Fetal Kidney	kidney
30	chr5:92579600-92581400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:92579600-92581800	Enhancers	Stomach Smooth Muscle	stomach
32	chr5:92579600-92582000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr5:92579800-92580800	Weak transcription	Fetal Lung	lung
34	chr5:92579800-92581000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:92579800-92582000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:92579800-92584600	Weak transcription	HUVEC	blood vessel
37	chr5:92580200-92582200	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr5:92580200-92582600	Enhancers	Colon Smooth Muscle	Colon
39	chr5:92580600-92583200	Enhancers	Fetal Kidney	kidney
40	chr5:92580800-92585000	Enhancers	Fetal Lung	lung
41	chr5:92581000-92581400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:92581000-92581400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr5:92581000-92581600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr5:92581000-92582400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:92581000-92582400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:92581000-92582400	Enhancers	Adipose Nuclei	Adipose
47	chr5:92581000-92582400	Enhancers	Fetal Muscle Leg	muscle
48	chr5:92581000-92582400	Enhancers	Ovary	ovary
49	chr5:92581000-92582600	Enhancers	Brain Cingulate Gyrus	brain
50	chr5:92581000-92582600	Enhancers	NHLF	lung

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