Variant report

Variant	nsv470061
Chromosome Location	chr4:99078105-99160699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:326)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:99153553-99153558	K562	blood:	n/a	n/a
2	ATF1	chr4:99153376-99153775	K562	blood:	n/a	n/a
3	ATF3	chr4:99153348-99153854	HCT-116	colon:	n/a	n/a
4	ATF3	chr4:99153321-99153783	K562	blood:	n/a	n/a
5	BATF	chr4:99124532-99124841	GM12878	blood:	n/a	n/a
6	BATF	chr4:99125451-99125672	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:99124533-99125120	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:99125383-99125694	GM12878	blood:	n/a	chr4:99125514-99125523
9	BHLHE40	chr4:99153453-99153676	K562	blood:	n/a	n/a
10	BHLHE40	chr4:99124431-99125689	GM12878	blood:	n/a	n/a
11	CBX3	chr4:99114602-99115008	K562	blood:	n/a	n/a
12	CBX3	chr4:99114621-99114898	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:99114607-99114961	K562	blood:	n/a	n/a
14	CEBPB	chr4:99153347-99153713	K562	blood:	n/a	chr4:99153553-99153564
15	CEBPB	chr4:99148245-99148444	K562	blood:	n/a	n/a
16	CEBPB	chr4:99130385-99130576	HepG2	liver:	n/a	chr4:99130445-99130458 chr4:99130447-99130458 chr4:99130445-99130456
17	CEBPB	chr4:99148210-99148436	A549	lung:	n/a	n/a
18	CEBPB	chr4:99153417-99153751	MCF-7	breast:	n/a	chr4:99153553-99153564
19	CEBPB	chr4:99148135-99148370	K562	blood:	n/a	n/a
20	CEBPB	chr4:99153372-99153737	A549	lung:	n/a	chr4:99153553-99153564
21	CEBPB	chr4:99148234-99148454	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:99153344-99153764	K562	blood:	n/a	chr4:99153553-99153564
23	CEBPB	chr4:99153384-99153746	HepG2	liver:	n/a	chr4:99153553-99153564
24	CEBPB	chr4:99153451-99153676	A549	lung:	n/a	chr4:99153553-99153564
25	CEBPB	chr4:99148091-99148450	MCF-7	breast:	n/a	n/a
26	CEBPB	chr4:99153387-99153751	IMR90	lung:	n/a	chr4:99153553-99153564
27	CEBPB	chr4:99130976-99131189	HepG2	liver:	n/a	chr4:99131088-99131099 chr4:99131088-99131101
28	CEBPB	chr4:99130337-99130476	H1-hESC	embryonic stem cell:	n/a	chr4:99130445-99130458 chr4:99130447-99130458 chr4:99130445-99130456
29	CEBPB	chr4:99153288-99153810	HCT-116	colon:	n/a	chr4:99153553-99153564
30	CEBPB	chr4:99130393-99130566	K562	blood:	n/a	chr4:99130445-99130458 chr4:99130447-99130458 chr4:99130445-99130456
31	CEBPB	chr4:99153302-99153930	HCT-116	colon:	n/a	chr4:99153553-99153564
32	CEBPB	chr4:99148141-99148464	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:99153382-99153768	Hela-S3	cervix:	n/a	chr4:99153553-99153564
34	CEBPB	chr4:99153414-99153726	H1-hESC	embryonic stem cell:	n/a	chr4:99153553-99153564
35	CEBPB	chr4:99153381-99153755	A549	lung:	n/a	chr4:99153553-99153564
36	CEBPB	chr4:99153274-99153808	K562	blood:	n/a	chr4:99153553-99153564
37	CEBPB	chr4:99148223-99148436	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPD	chr4:99153417-99153689	K562	blood:	n/a	chr4:99153554-99153565
39	CEBPD	chr4:99153396-99153705	K562	blood:	n/a	chr4:99153554-99153565
40	CHD2	chr4:99087693-99087766	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr4:99124518-99124978	GM12878	blood:	n/a	n/a
42	CHD2	chr4:99125211-99125750	GM12878	blood:	n/a	n/a
43	CREB1	chr4:99103047-99103359	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:99120440-99120590	AG10803	skin:	n/a	chr4:99120547-99120565
45	CTCF	chr4:99120537-99120627	GM12878	blood:	n/a	chr4:99120547-99120565
46	CTCF	chr4:99120448-99120703	MCF-7	breast:	n/a	chr4:99120547-99120565
47	CTCF	chr4:99120580-99120730	GM12874	blood:	n/a	n/a
48	CTCF	chr4:99120440-99120590	HCPEpiC	choroid plexus:	n/a	chr4:99120547-99120565
49	CTCF	chr4:99120460-99120610	AG09319	gingival:	n/a	chr4:99120547-99120565
50	CTCF	chr4:99120520-99120670	K562	blood:	n/a	chr4:99120547-99120565

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99159401-99159451	GM12892	blood:	n/a
2	chr4:99125084-99125134	PANC-1	pancreas:	n/a
3	chr4:99159401-99159451	SK-N-SH_RA	brain:	n/a
4	chr4:99159401-99159451	HRCEpiC	kidney:	n/a
5	chr4:99125084-99125134	HAEpiC	amniotic membrane:	n/a
6	chr4:99125084-99125134	HEEpiC	esophagus:	n/a
7	chr4:99125084-99125134	H1-hESC	embryonic stem cell:	embryo
8	chr4:99125084-99125134	SK-N-SH_RA	brain:	n/a
9	chr4:99125084-99125134	Hepatocyte	liver:	n/a
10	chr4:99159401-99159451	HAEpiC	amniotic membrane:	n/a
11	chr4:99159401-99159451	GM12878	blood:	n/a
12	chr4:99125084-99125134	HepG2	liver:	n/a
13	chr4:99125084-99125134	SAEC	small airway:	n/a
14	chr4:99125084-99125134	Jurkat	blood:	n/a
15	chr4:99125084-99125134	ECC-1	luminal epithelium:	n/a
16	chr4:99159401-99159451	NT2-D1	testis:	n/a
17	chr4:99125084-99125134	PFSK-1	brain:	n/a
18	chr4:99125084-99125134	AG10803	skin:	n/a
19	chr4:99159401-99159451	HEEpiC	esophagus:	n/a
20	chr4:99159401-99159451	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:99125084-99125134	HEK293	kidney:	embryo
22	chr4:99125084-99125134	RPTEC	kidney:	n/a
23	chr4:99125084-99125134	AG09319	gingival:	n/a
24	chr4:99159401-99159451	U87	brain:	n/a
25	chr4:99159401-99159451	HRPEpiC	eye:	n/a
26	chr4:99125084-99125134	HRPEpiC	eye:	n/a
27	chr4:99125084-99125134	MCF10A-Er-Src	breast:	n/a
28	chr4:99159401-99159451	AoSMC	blood vessel:	n/a
29	chr4:99159401-99159451	HL-60	blood:	n/a
30	chr4:99125084-99125134	MCF-7	breast:	n/a
31	chr4:99125084-99125134	HNPCEpiC	eye:	n/a
32	chr4:99125084-99125134	NH-A	brain:	n/a
33	chr4:99125084-99125134	HRE	kidney:	n/a
34	chr4:99125084-99125134	Hela-S3	cervix:	n/a
35	chr4:99159401-99159451	HCM	heart:	n/a
36	chr4:99159401-99159451	BE2_C	brain:	n/a
37	chr4:99159401-99159451	Jurkat	blood:	n/a
38	chr4:99125084-99125134	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:99159401-99159451	HMEC	breast:	n/a
40	chr4:99159401-99159451	ECC-1	luminal epithelium:	n/a
41	chr4:99125084-99125134	AoSMC	blood vessel:	n/a
42	chr4:99125084-99125134	HL-60	blood:	n/a
43	chr4:99125084-99125134	AG04449	skin:	fetal
44	chr4:99125084-99125134	K562	blood:	n/a
45	chr4:99159401-99159451	AG04449	skin:	fetal
46	chr4:99125084-99125134	BE2_C	brain:	n/a
47	chr4:99159401-99159451	MCF-7	breast:	n/a
48	chr4:99159401-99159451	HCT-116	colon:	n/a
49	chr4:99125084-99125134	SKMC	muscle:	n/a
50	chr4:99159401-99159451	HCPEpiC	choroid plexus:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:99120152..99122281-chr4:99124783..99127768,2	K562	blood:
2	chr4:99064189..99066561-chr4:99135372..99138314,2	MCF-7	breast:
3	chr4:99077205..99079531-chr4:99181198..99183165,2	MCF-7	breast:
4	chr4:99092058..99095008-chr4:99098244..99101009,2	MCF-7	breast:
5	chr4:99083174..99085665-chr4:99180019..99182924,2	MCF-7	breast:
6	chr4:99118953..99122803-chr4:99123376..99126878,4	MCF-7	breast:
7	chr4:99105475..99108210-chr4:99112091..99113844,2	MCF-7	breast:
8	chr1:6706577..6707089-chr4:99143310..99144015,2	MCF-7	breast:
9	chr4:99157632..99160467-chr4:99160653..99163373,3	K562	blood:
10	chr4:99157632..99160467-chr4:99160653..99163373,3	K562	blood:
11	chr4:99071301..99072792-chr4:99120456..99121365,4	MCF-7	breast:
12	chr4:99134719..99136619-chr4:99142724..99145033,2	K562	blood:
13	chr4:99153861..99155781-chr4:99155970..99158168,2	K562	blood:
14	chr4:99093723..99096153-chr4:99098147..99099856,2	K562	blood:
15	chr4:99105475..99108210-chr4:99112091..99113844,2	MCF-7	breast:
16	chr4:99153861..99155781-chr4:99155970..99158168,2	K562	blood:
17	chr4:99139397..99141906-chr4:99171269..99172909,2	K562	blood:
18	chr4:99120152..99122281-chr4:99124783..99127768,2	K562	blood:
19	chr4:99086672..99088660-chr4:99180652..99182426,2	MCF-7	breast:
20	chr4:99126049..99128565-chr4:99168371..99171053,2	K562	blood:
21	chr4:99157087..99159312-chr4:99180098..99182981,3	MCF-7	breast:
22	chr4:99134906..99136728-chr4:99181753..99183514,2	K562	blood:
23	chr4:99134719..99136619-chr4:99142724..99145033,2	K562	blood:
24	chr4:99118953..99122803-chr4:99123376..99126878,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf37-1	chr4:99106282-99106355	XLOC_004020
2	lnc-C4orf37-1	chr4:99104226-99104923	XLOC_004020
3	lnc-RAP1GDS1-2	chr4:99090440-99090451	NONHSAT097482
4	lnc-RAP1GDS1-2	chr4:99090441-99090451	XLOC_003613

No data

Variant related genes	Relation type
ENSG00000200658	TF binding region
ENSG00000200658	CpG island
ENSG00000138698	chromatin interactions
ENSG00000200658	chromatin interactions
ENSG00000163116	chromatin interactions
ENSG00000214559	chromatin interactions

Extended variants
information (count: 1985 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1985 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17027299	chr4:99078105-99078106	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75127325	chr4:99078129-99078130	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531629301	chr4:99078152-99078153	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144652345	chr4:99078162-99078163	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs191523322	chr4:99078244-99078245	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569064972	chr4:99078274-99078275	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs535797493	chr4:99078279-99078280	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377659434	chr4:99078295-99078296	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs72894382	chr4:99078343-99078344	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs183353062	chr4:99078357-99078358	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs558254768	chr4:99078410-99078411	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187249483	chr4:99078414-99078415	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577335841	chr4:99078495-99078496	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575960571	chr4:99078545-99078546	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544492255	chr4:99078566-99078567	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563153144	chr4:99078580-99078581	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs190578641	chr4:99078590-99078591	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371209458	chr4:99078615-99078616	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544051877	chr4:99078625-99078626	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376242231	chr4:99078628-99078629	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs543776930	chr4:99078697-99078698	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147451236	chr4:99078737-99078738	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs555784695	chr4:99078755-99078756	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183066659	chr4:99078792-99078793	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs565072738	chr4:99078794-99078795	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187789408	chr4:99078847-99078848	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576784813	chr4:99078889-99078890	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs79223005	chr4:99078942-99078943	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs550504413	chr4:99079018-99079019	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191241558	chr4:99079049-99079050	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs35038202	chr4:99079113-99079114	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs536125872	chr4:99079153-99079154	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs548107930	chr4:99079169-99079170	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs566104633	chr4:99079182-99079183	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533559728	chr4:99079223-99079224	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs7656233	chr4:99079237-99079238	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs576871341	chr4:99079266-99079267	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs184667964	chr4:99079274-99079275	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574039102	chr4:99079315-99079316	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs12502398	chr4:99079344-99079345	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143276441	chr4:99079351-99079352	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs76903803	chr4:99079352-99079353	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529841749	chr4:99079356-99079357	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs113469099	chr4:99079364-99079365	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs35117645	chr4:99079365-99079366	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547770609	chr4:99079370-99079371	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373602838	chr4:99079379-99079380	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538334046	chr4:99079380-99079381	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs377012258	chr4:99079381-99079382	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs370968052	chr4:99079382-99079383	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99080600-99081000	Enhancers	Dnd41	blood
2	chr4:99083800-99084200	Enhancers	Fetal Heart	heart
3	chr4:99084200-99087600	Weak transcription	Fetal Heart	heart
4	chr4:99086800-99087200	Enhancers	A549	lung
5	chr4:99087000-99088200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:99087200-99087600	Flanking Active TSS	A549	lung
7	chr4:99087200-99087800	Enhancers	Right Atrium	heart
8	chr4:99087200-99088200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:99087200-99088200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:99087200-99088200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:99087200-99088200	Enhancers	HMEC	breast
12	chr4:99087200-99088200	Enhancers	NHEK	skin
13	chr4:99087200-99088400	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr4:99087200-99088600	Enhancers	Liver	Liver
15	chr4:99087400-99087800	Enhancers	Left Ventricle	heart
16	chr4:99087400-99088200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr4:99087400-99088200	Enhancers	Esophagus	oesophagus
18	chr4:99087400-99088200	Enhancers	Hela-S3	cervix
19	chr4:99087600-99088000	Enhancers	Fetal Heart	heart
20	chr4:99087600-99088400	Enhancers	A549	lung
21	chr4:99087800-99088000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr4:99087800-99088200	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr4:99088000-99091800	Weak transcription	Fetal Heart	heart
24	chr4:99088200-99098200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr4:99088400-99088800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:99088800-99092000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr4:99090000-99090200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:99090000-99091800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:99090400-99091400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr4:99091000-99092400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr4:99091400-99092400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:99091400-99092600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:99091600-99092400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:99091800-99092200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:99091800-99092200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:99091800-99092200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:99091800-99092200	Enhancers	Fetal Heart	heart
38	chr4:99091800-99092600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr4:99091800-99092600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr4:99091800-99092800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:99092000-99092400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:99092000-99092600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:99092200-99097000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr4:99092400-99092800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:99092400-99097400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr4:99092600-99097200	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr4:99092600-99097200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr4:99092600-99097200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:99092600-99097600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr4:99092800-99093000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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