Variant report

Variant	nsv883268
Chromosome Location	chr5:178928962-178951106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178931255-178932227	HepG2	liver:	n/a	n/a
2	BATF	chr5:178945312-178945640	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:178945316-178945685	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:178932135-178932152	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:178931662-178931840	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:178931609-178932069	HepG2	liver:	n/a	n/a
7	CTCF	chr5:178946620-178946770	AG04450	lung:	n/a	n/a
8	CTCF	chr5:178946600-178946750	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr5:178946461-178946653	ProgFib	skin:	n/a	chr5:178946578-178946587
10	CTCF	chr5:178946464-178946667	Hela-S3	cervix:	n/a	chr5:178946578-178946587
11	CTCF	chr5:178946471-178946665	HUVEC	blood vessel:	n/a	chr5:178946578-178946587
12	CTCF	chr5:178946525-178946636	Kidney_OC	kidney:	n/a	chr5:178946578-178946587
13	CTCF	chr5:178946453-178946678	A549	lung:	n/a	chr5:178946578-178946587
14	CTCF	chr5:178946540-178946690	HVMF	connective:	n/a	chr5:178946578-178946587
15	CTCF	chr5:178946471-178946598	MCF-7	breast:	n/a	chr5:178946578-178946587
16	CTCF	chr5:178946560-178946710	GM12875	blood:	n/a	chr5:178946578-178946587
17	CTCF	chr5:178944801-178945016	K562	blood:	n/a	n/a
18	CTCF	chr5:178946500-178946650	GM12873	blood:	n/a	chr5:178946578-178946587
19	CTCF	chr5:178946600-178946750	HMF	breast:	n/a	n/a
20	CTCF	chr5:178946600-178946750	BJ	skin:	n/a	n/a
21	CTCF	chr5:178946620-178946770	HCFaa	heart:	n/a	n/a
22	CTCF	chr5:178946744-178946789	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:178946580-178946730	RPTEC	kidney:	n/a	n/a
24	CTCF	chr5:178946463-178946708	LNCaP	prostate:	n/a	chr5:178946578-178946587
25	CTCF	chr5:178931880-178932030	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr5:178946600-178946750	NHLF	lung:	n/a	n/a
27	CTCF	chr5:178946620-178946770	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr5:178946471-178946606	MCF-7	breast:	n/a	chr5:178946578-178946587
29	CTCF	chr5:178946547-178946591	A549	lung:	n/a	chr5:178946578-178946587
30	CTCF	chr5:178946600-178946750	AG09319	gingival:	n/a	n/a
31	CTCF	chr5:178946453-178946609	MCF-7	breast:	n/a	chr5:178946578-178946587
32	CTCF	chr5:178946539-178946565	GM19240	blood:	n/a	n/a
33	CTCF	chr5:178946493-178946639	GM19239	blood:	n/a	chr5:178946578-178946587
34	CTCF	chr5:178946460-178946669	Gliobla	brain:	n/a	chr5:178946578-178946587
35	CTCF	chr5:178946525-178946613	Fibrobl	skin:	n/a	chr5:178946578-178946587
36	CTCF	chr5:178945564-178945568	GM12891	blood:	n/a	n/a
37	CTCF	chr5:178946480-178946641	GM13976	blood:	n/a	chr5:178946578-178946587
38	CTCF	chr5:178946506-178946661	GM10266	blood:	n/a	chr5:178946578-178946587
39	CTCF	chr5:178946580-178946730	GM12864	blood:	n/a	n/a
40	CTCF	chr5:178946433-178946677	GM12878	blood:	n/a	chr5:178946578-178946587
41	CTCF	chr5:178946784-178946896	GM12878	blood:	n/a	n/a
42	CTCF	chr5:178931820-178931970	HRE	kidney:	n/a	n/a
43	CTCF	chr5:178946560-178946710	Hela-S3	cervix:	n/a	chr5:178946578-178946587
44	CTCF	chr5:178946436-178946679	K562	blood:	n/a	chr5:178946578-178946587
45	CTCF	chr5:178946600-178946750	HEK293	kidney:	n/a	n/a
46	CTCF	chr5:178946494-178946650	GM10248	blood:	n/a	chr5:178946578-178946587
47	CTCF	chr5:178944900-178945050	HepG2	liver:	n/a	n/a
48	CTCF	chr5:178946580-178946730	GM12873	blood:	n/a	n/a
49	CTCF	chr5:178944940-178945090	HEK293	kidney:	n/a	n/a
50	CTCF	chr5:178946560-178946710	BJ	skin:	n/a	chr5:178946578-178946587

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178945540-178945590	SK-N-SH_RA	brain:	n/a
2	chr5:178950855-178950905	MCF10A-Er-Src	breast:	n/a
3	chr5:178950855-178950905	AoSMC	blood vessel:	n/a
4	chr5:178950855-178950905	HCF	heart:	n/a
5	chr5:178950795-178950845	SAEC	small airway:	n/a
6	chr5:178950855-178950905	AG09319	gingival:	n/a
7	chr5:178950855-178950905	HepG2	liver:	n/a
8	chr5:178945540-178945590	MCF-7	breast:	n/a
9	chr5:178950795-178950845	A549	lung:	n/a
10	chr5:178950795-178950845	ProgFib	skin:	n/a
11	chr5:178950795-178950845	PFSK-1	brain:	n/a
12	chr5:178945540-178945590	BE2_C	brain:	n/a
13	chr5:178945540-178945590	SAEC	small airway:	n/a
14	chr5:178950855-178950905	SKMC	muscle:	n/a
15	chr5:178945540-178945590	ovcar-3	ovarian:	n/a
16	chr5:178950795-178950845	AoSMC	blood vessel:	n/a
17	chr5:178945540-178945590	HRE	kidney:	n/a
18	chr5:178950795-178950845	SK-N-SH	brain:	n/a
19	chr5:178950795-178950845	GM12878	blood:	n/a
20	chr5:178945540-178945590	ECC-1	luminal epithelium:	n/a
21	chr5:178945540-178945590	NT2-D1	testis:	n/a
22	chr5:178950855-178950905	HRE	kidney:	n/a
23	chr5:178950855-178950905	PrEC	prostate:	n/a
24	chr5:178950795-178950845	PANC-1	pancreas:	n/a
25	chr5:178945540-178945590	AG04450	lung:	fetal
26	chr5:178950855-178950905	U87	brain:	n/a
27	chr5:178950855-178950905	PANC-1	pancreas:	n/a
28	chr5:178950855-178950905	HEEpiC	esophagus:	n/a
29	chr5:178950855-178950905	BE2_C	brain:	n/a
30	chr5:178945540-178945590	AG04449	skin:	fetal
31	chr5:178950855-178950905	HIPEpiC	eye:	n/a
32	chr5:178945540-178945590	GM12891	blood:	n/a
33	chr5:178950855-178950905	HAEpiC	amniotic membrane:	n/a
34	chr5:178945540-178945590	AG10803	skin:	n/a
35	chr5:178950855-178950905	HCT-116	colon:	n/a
36	chr5:178950795-178950845	MCF10A-Er-Src	breast:	n/a
37	chr5:178950795-178950845	HIPEpiC	eye:	n/a
38	chr5:178950855-178950905	MCF-7	breast:	n/a
39	chr5:178950855-178950905	HRPEpiC	eye:	n/a
40	chr5:178950855-178950905	RPTEC	kidney:	n/a
41	chr5:178950795-178950845	AG04450	lung:	fetal
42	chr5:178945540-178945590	SKMC	muscle:	n/a
43	chr5:178950795-178950845	HUVEC	blood vessel:	n/a
44	chr5:178950855-178950905	SK-N-SH_RA	brain:	n/a
45	chr5:178950795-178950845	HL-60	blood:	n/a
46	chr5:178945540-178945590	HepG2	liver:	n/a
47	chr5:178950855-178950905	SAEC	small airway:	n/a
48	chr5:178950855-178950905	PFSK-1	brain:	n/a
49	chr5:178945540-178945590	HCF	heart:	n/a
50	chr5:178945540-178945590	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:178946216..178946980-chr5:179095346..179096018,3	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUFY1-4	chr5:178951021-178952136	NONHSAT105587
2	lnc-RUFY1-4	chr5:178950418-178950475	NONHSAT105586
3	lnc-RUFY1-4	chr5:178950374-178950475	NONHSAT105587
4	lnc-RUFY1-4	chr5:178951021-178952136	NONHSAT105586
5	lnc-HNRNPH1-3	chr5:178942465-178942580	ENSG00000253652
6	lnc-RUFY1-4	chr5:178949401-178949705	NONHSAT105586
7	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652
8	lnc-HNRNPH1-2	chr5:178949497-178950926	ENSG00000251657

No data

Variant related genes	Relation type
ENSG00000251545	TF binding region
ENSG00000253652	TF binding region
ENSG00000251545	CpG island
ENSG00000253652	CpG island
GAPVD1	miRNA target sites

Extended variants
information (count: 1117 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368698715	chr5:178929048-178929049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561860500	chr5:178929060-178929061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140153572	chr5:178929086-178929087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529055757	chr5:178929091-178929092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547288824	chr5:178929174-178929175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565728129	chr5:178929225-178929226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532886177	chr5:178929255-178929256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200971676	chr5:178929383-178929384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397947910	chr5:178929419-178929420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4555781	chr5:178929507-178929508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369554523	chr5:178929570-178929571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71596422	chr5:178929601-178929602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199762971	chr5:178929633-178929634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116587013	chr5:178929634-178929635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184390153	chr5:178929696-178929697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542981512	chr5:178929708-178929709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569658040	chr5:178929710-178929711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375847155	chr5:178929711-178929712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537075945	chr5:178929722-178929723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs56281148	chr5:178929778-178929779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112900666	chr5:178929870-178929871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200451836	chr5:178929908-178929909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201452980	chr5:178929964-178929965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376027836	chr5:178930013-178930014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200054029	chr5:178930016-178930017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9686812	chr5:178930069-178930070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs55965418	chr5:178930144-178930145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371415473	chr5:178930304-178930305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556875607	chr5:178930666-178930667	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs568684582	chr5:178930672-178930673	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs536016000	chr5:178930687-178930688	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs372790984	chr5:178930794-178930795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377401291	chr5:178930816-178930817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554085192	chr5:178930833-178930834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188753818	chr5:178930861-178930862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571634572	chr5:178930870-178930871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545891303	chr5:178930871-178930872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6870908	chr5:178930892-178930893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs28427497	chr5:178930933-178930934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs543432211	chr5:178930936-178930937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111451404	chr5:178930962-178930963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529182982	chr5:178930974-178930975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541170457	chr5:178931043-178931044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559277191	chr5:178931054-178931055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533202375	chr5:178931056-178931057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551485280	chr5:178931067-178931068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149851916	chr5:178931071-178931072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530491872	chr5:178931072-178931073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183840428	chr5:178931089-178931090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189626264	chr5:178931106-178931107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178913800-178935200	Weak transcription	Right Atrium	heart
2	chr5:178922200-178931400	Weak transcription	Pancreas	Pancrea
3	chr5:178925600-178935000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178928600-178931400	Weak transcription	Fetal Stomach	stomach
5	chr5:178931200-178931400	Enhancers	HepG2	liver
6	chr5:178931200-178932400	Enhancers	Liver	Liver
7	chr5:178931200-178932800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:178931400-178931600	Enhancers	Fetal Stomach	stomach
9	chr5:178931400-178931600	Enhancers	Pancreas	Pancrea
10	chr5:178931400-178931800	Enhancers	Fetal Kidney	kidney
11	chr5:178931400-178932800	Flanking Active TSS	HepG2	liver
12	chr5:178931600-178931800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:178931600-178931800	Enhancers	Fetal Lung	lung
14	chr5:178931600-178932000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr5:178931600-178932200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:178931600-178935200	Weak transcription	Fetal Stomach	stomach
17	chr5:178931800-178933000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr5:178931800-178936000	Weak transcription	Fetal Kidney	kidney
19	chr5:178931800-178936400	Weak transcription	Fetal Lung	lung
20	chr5:178932800-178933400	Enhancers	HepG2	liver
21	chr5:178933000-178943200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:178933400-178935200	Weak transcription	HepG2	liver
23	chr5:178934600-178936800	Enhancers	Primary B cells from cord blood	blood
24	chr5:178934600-178937000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr5:178934800-178935000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr5:178934800-178935000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:178934800-178935200	Active TSS	Monocytes-CD14+_RO01746	blood
28	chr5:178934800-178936400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:178934800-178937000	Enhancers	Primary hematopoietic stem cells	blood
30	chr5:178935000-178935400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
31	chr5:178935000-178935400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:178935000-178937000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr5:178935200-178935400	Enhancers	Fetal Stomach	stomach
34	chr5:178935200-178935400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr5:178935200-178935600	Enhancers	HepG2	liver
36	chr5:178935400-178936000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:178935400-178936200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr5:178935400-178936400	Weak transcription	Fetal Stomach	stomach
39	chr5:178935400-178937200	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr5:178936000-178936800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:178936000-178936800	Enhancers	Fetal Kidney	kidney
42	chr5:178936200-178936400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr5:178936400-178936600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr5:178936400-178936600	Enhancers	Fetal Stomach	stomach
45	chr5:178936400-178936600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr5:178936400-178936800	Enhancers	Primary B cells from peripheral blood	blood
47	chr5:178936400-178936800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr5:178936400-178936800	Enhancers	Thymus	Thymus
49	chr5:178936400-178937000	Enhancers	Fetal Lung	lung
50	chr5:178936600-178936800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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