Variant report

Variant	nsv600658
Chromosome Location	chr5:178921861-178950814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 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	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	chr5:178922880-178923030	WI-38	lung:	n/a	n/a
8	CTCF	chr5:178922980-178923130	GM12872	blood:	n/a	chr5:178923029-178923037
9	CTCF	chr5:178923028-178923110	GM13976	blood:	n/a	chr5:178923029-178923037
10	CTCF	chr5:178923040-178923190	HCM	heart:	n/a	n/a
11	CTCF	chr5:178946486-178946625	GM19238	blood:	n/a	chr5:178946578-178946587
12	CTCF	chr5:178922960-178923110	Hela-S3	cervix:	n/a	chr5:178923029-178923037
13	CTCF	chr5:178922900-178923050	HFF	foreskin:	n/a	chr5:178923029-178923037
14	CTCF	chr5:178923020-178923170	HL-60	blood:	n/a	chr5:178923029-178923037
15	CTCF	chr5:178946500-178946650	GM12873	blood:	n/a	chr5:178946578-178946587
16	CTCF	chr5:178946453-178946609	MCF-7	breast:	n/a	chr5:178946578-178946587
17	CTCF	chr5:178922965-178923194	IMR90	lung:	n/a	chr5:178923029-178923037
18	CTCF	chr5:178923000-178923150	K562	blood:	n/a	chr5:178923029-178923037
19	CTCF	chr5:178946488-178946623	A549	lung:	n/a	chr5:178946578-178946587
20	CTCF	chr5:178922880-178923030	GM06990	blood:	n/a	n/a
21	CTCF	chr5:178922920-178923070	HRE	kidney:	n/a	chr5:178923029-178923037
22	CTCF	chr5:178922919-178923188	HepG2	liver:	n/a	chr5:178923029-178923037
23	CTCF	chr5:178946471-178946693	Spleen_OC	spleen:	n/a	chr5:178946578-178946587
24	CTCF	chr5:178946436-178946679	K562	blood:	n/a	chr5:178946578-178946587
25	CTCF	chr5:178922992-178923214	T-47D	breast:	n/a	chr5:178923029-178923037
26	CTCF	chr5:178946476-178946677	Pancreas_OC	pancreas:	n/a	chr5:178946578-178946587
27	CTCF	chr5:178946784-178946896	GM12878	blood:	n/a	n/a
28	CTCF	chr5:178921985-178922175	GM19239	blood:	n/a	n/a
29	CTCF	chr5:178922960-178923110	RPTEC	kidney:	n/a	chr5:178923029-178923037
30	CTCF	chr5:178931912-178932089	HepG2	liver:	n/a	n/a
31	CTCF	chr5:178922970-178923152	HepG2	liver:	n/a	chr5:178923029-178923037
32	CTCF	chr5:178946539-178946565	GM19240	blood:	n/a	n/a
33	CTCF	chr5:178946600-178946750	GM12872	blood:	n/a	n/a
34	CTCF	chr5:178946620-178946770	HCFaa	heart:	n/a	n/a
35	CTCF	chr5:178922960-178923110	BJ	skin:	n/a	chr5:178923029-178923037
36	CTCF	chr5:178944869-178944959	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:178921694-178921978	GM19239	blood:	n/a	n/a
38	CTCF	chr5:178922980-178923130	GM12874	blood:	n/a	chr5:178923029-178923037
39	CTCF	chr5:178946486-178946654	Medullo	brain:	n/a	chr5:178946578-178946587
40	CTCF	chr5:178946580-178946730	GM12864	blood:	n/a	n/a
41	CTCF	chr5:178922975-178923173	Hela-S3	cervix:	n/a	chr5:178923029-178923037
42	CTCF	chr5:178922720-178922870	GM12867	blood:	n/a	n/a
43	CTCF	chr5:178946580-178946730	WI-38	lung:	n/a	n/a
44	CTCF	chr5:178946465-178946658	K562	blood:	n/a	chr5:178946578-178946587
45	CTCF	chr5:178923013-178923162	Fibrobl	skin:	n/a	chr5:178923029-178923037
46	CTCF	chr5:178946433-178946677	GM12878	blood:	n/a	chr5:178946578-178946587
47	CTCF	chr5:178946600-178946750	NHLF	lung:	n/a	n/a
48	CTCF	chr5:178946600-178946750	HPF	lung:	n/a	n/a
49	CTCF	chr5:178946620-178946770	GM12873	blood:	n/a	n/a
50	CTCF	chr5:178922980-178923130	NB4	blood:	n/a	chr5:178923029-178923037

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178945540-178945590	HNPCEpiC	eye:	n/a
2	chr5:178945540-178945590	PFSK-1	brain:	n/a
3	chr5:178950795-178950845	HAEpiC	amniotic membrane:	n/a
4	chr5:178945540-178945590	Hela-S3	cervix:	n/a
5	chr5:178950795-178950845	HCM	heart:	n/a
6	chr5:178945540-178945590	HCT-116	colon:	n/a
7	chr5:178945540-178945590	GM19239	blood:	n/a
8	chr5:178945540-178945590	HepG2	liver:	n/a
9	chr5:178950795-178950845	MCF-7	breast:	n/a
10	chr5:178950795-178950845	Jurkat	blood:	n/a
11	chr5:178945540-178945590	T-47D	breast:	n/a
12	chr5:178945540-178945590	IMR90	lung:	fetal
13	chr5:178945540-178945590	Caco-2	colon:	n/a
14	chr5:178950795-178950845	SK-N-SH_RA	brain:	n/a
15	chr5:178945540-178945590	HRE	kidney:	n/a
16	chr5:178945540-178945590	AG09319	gingival:	n/a
17	chr5:178945540-178945590	NHDF-neo	bronchial:	n/a
18	chr5:178950795-178950845	ovcar-3	ovarian:	n/a
19	chr5:178945540-178945590	ovcar-3	ovarian:	n/a
20	chr5:178945540-178945590	HRPEpiC	eye:	n/a
21	chr5:178945540-178945590	GM06990	blood:	n/a
22	chr5:178950795-178950845	MCF10A-Er-Src	breast:	n/a
23	chr5:178950795-178950845	T-47D	breast:	n/a
24	chr5:178950795-178950845	HIPEpiC	eye:	n/a
25	chr5:178945540-178945590	HMEC	breast:	n/a
26	chr5:178945540-178945590	NT2-D1	testis:	n/a
27	chr5:178950795-178950845	GM19239	blood:	n/a
28	chr5:178945540-178945590	SKMC	muscle:	n/a
29	chr5:178945540-178945590	U87	brain:	n/a
30	chr5:178950795-178950845	HEEpiC	esophagus:	n/a
31	chr5:178950795-178950845	AG09309	skin:	n/a
32	chr5:178950795-178950845	NB4	blood:	n/a
33	chr5:178950795-178950845	GM06990	blood:	n/a
34	chr5:178950795-178950845	SAEC	small airway:	n/a
35	chr5:178945540-178945590	NHBE	bronchial:	n/a
36	chr5:178945540-178945590	H1-hESC	embryonic stem cell:	embryo
37	chr5:178945540-178945590	HCF	heart:	n/a
38	chr5:178950795-178950845	HCF	heart:	n/a
39	chr5:178950795-178950845	H1-hESC	embryonic stem cell:	embryo
40	chr5:178950795-178950845	HL-60	blood:	n/a
41	chr5:178950795-178950845	AG10803	skin:	n/a
42	chr5:178950795-178950845	A549	lung:	n/a
43	chr5:178950795-178950845	BE2_C	brain:	n/a
44	chr5:178950795-178950845	HRCEpiC	kidney:	n/a
45	chr5:178945540-178945590	BE2_C	brain:	n/a
46	chr5:178945540-178945590	AG04449	skin:	fetal
47	chr5:178945540-178945590	Jurkat	blood:	n/a
48	chr5:178950795-178950845	HRPEpiC	eye:	n/a
49	chr5:178950795-178950845	AG04449	skin:	fetal
50	chr5:178950795-178950845	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:178946216..178946980-chr5:179095346..179096018,3	MCF-7	breast:
2	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
3	chr5:178923732..178926017-chr5:178977562..178979960,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPH1-3	chr5:178942465-178942580	ENSG00000253652
2	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652
3	lnc-RUFY1-4	chr5:178950418-178950475	NONHSAT105586
4	lnc-RUFY1-4	chr5:178949401-178949705	NONHSAT105586
5	lnc-RUFY1-4	chr5:178950374-178950475	NONHSAT105587
6	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
ENSG00000176783	chromatin interactions
GAPVD1	miRNA target sites

Extended variants
information (count: 1429 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11249631	chr5:178921861-178921862	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371961839	chr5:178921876-178921877	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111799451	chr5:178921898-178921899	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577099412	chr5:178921926-178921927	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184369894	chr5:178921939-178921940	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11249632	chr5:178921964-178921965	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs375283524	chr5:178921989-178921990	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376617164	chr5:178922039-178922040	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs187998485	chr5:178922057-178922058	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs11249633	chr5:178922058-178922059	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs370283623	chr5:178922073-178922074	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs11249634	chr5:178922091-178922092	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs553497525	chr5:178922112-178922113	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs191249824	chr5:178922115-178922116	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs76289951	chr5:178922116-178922117	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs565410879	chr5:178922121-178922122	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs572678624	chr5:178922133-178922134	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs544437491	chr5:178922137-178922138	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs11249635	chr5:178922141-178922142	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs556067007	chr5:178922168-178922169	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs375080736	chr5:178922195-178922196	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs568613633	chr5:178922241-178922242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527667077	chr5:178922287-178922288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368288642	chr5:178922297-178922298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552565730	chr5:178922351-178922352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76797273	chr5:178922354-178922355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73343117	chr5:178922388-178922389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148440439	chr5:178922454-178922455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567913422	chr5:178922468-178922469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535306663	chr5:178922502-178922503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553435960	chr5:178922553-178922554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184875216	chr5:178922563-178922564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112696921	chr5:178922570-178922571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557743495	chr5:178922579-178922580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577938057	chr5:178922653-178922654	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372333506	chr5:178922686-178922687	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189240965	chr5:178922734-178922735	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577416614	chr5:178922754-178922755	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544915193	chr5:178922794-178922795	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563213556	chr5:178922852-178922853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572347990	chr5:178922871-178922872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375391664	chr5:178922888-178922889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141681653	chr5:178922890-178922891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200506237	chr5:178922904-178922905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560545039	chr5:178923016-178923017	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527802753	chr5:178923023-178923024	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552250821	chr5:178923026-178923027	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114650956	chr5:178923101-178923102	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531656304	chr5:178923117-178923118	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369078340	chr5:178923122-178923123	Weak transcription Bivalent/Poised TSS Enhancers	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:150 , 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	chr5:178918400-178925400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:178921600-178922200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:178921800-178922000	Bivalent/Poised TSS	Fetal Lung	lung
5	chr5:178921800-178922000	Enhancers	Spleen	Spleen
6	chr5:178921800-178922200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:178921800-178922200	ZNF genes & repeats	Fetal Kidney	kidney
8	chr5:178921800-178922200	ZNF genes & repeats	Pancreas	Pancrea
9	chr5:178922000-178922200	Bivalent Enhancer	Fetal Brain Male	brain
10	chr5:178922000-178922200	Enhancers	Gastric	stomach
11	chr5:178922000-178922400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:178922000-178923000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr5:178922000-178925200	Weak transcription	Spleen	Spleen
14	chr5:178922200-178931400	Weak transcription	Pancreas	Pancrea
15	chr5:178922600-178922800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:178923000-178923200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr5:178923000-178923600	Enhancers	Fetal Brain Female	brain
18	chr5:178923600-178923800	Bivalent Enhancer	HepG2	liver
19	chr5:178923600-178924800	Weak transcription	Fetal Brain Female	brain
20	chr5:178924200-178925200	Enhancers	Fetal Brain Male	brain
21	chr5:178924600-178925000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:178924600-178925400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:178924600-178925600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:178924800-178925200	Enhancers	Brain Germinal Matrix	brain
25	chr5:178924800-178925200	Bivalent Enhancer	Fetal Stomach	stomach
26	chr5:178924800-178925200	Bivalent Enhancer	HepG2	liver
27	chr5:178924800-178925400	Enhancers	Fetal Muscle Leg	muscle
28	chr5:178924800-178925600	Enhancers	Fetal Brain Female	brain
29	chr5:178924800-178925600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr5:178924800-178925600	Enhancers	NHDF-Ad	bronchial
31	chr5:178925000-178925400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr5:178925000-178925600	Enhancers	Adipose Nuclei	Adipose
33	chr5:178925200-178925600	Active TSS	Spleen	Spleen
34	chr5:178925400-178925600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:178925400-178925800	Enhancers	Esophagus	oesophagus
36	chr5:178925600-178935000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:178926200-178926400	Enhancers	Esophagus	oesophagus
38	chr5:178926200-178926400	Enhancers	Fetal Stomach	stomach
39	chr5:178928600-178931400	Weak transcription	Fetal Stomach	stomach
40	chr5:178931200-178931400	Enhancers	HepG2	liver
41	chr5:178931200-178932400	Enhancers	Liver	Liver
42	chr5:178931200-178932800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr5:178931400-178931600	Enhancers	Fetal Stomach	stomach
44	chr5:178931400-178931600	Enhancers	Pancreas	Pancrea
45	chr5:178931400-178931800	Enhancers	Fetal Kidney	kidney
46	chr5:178931400-178932800	Flanking Active TSS	HepG2	liver
47	chr5:178931600-178931800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:178931600-178931800	Enhancers	Fetal Lung	lung
49	chr5:178931600-178932000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:178931600-178932200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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