Variant report

Variant	nsv878719
Chromosome Location	chr4:15930961-15947493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:91)
CpG islands
(count:489)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:91 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:15939879-15940190	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr4:15939904-15939972	NHEK	skin:	n/a	n/a
3	CTCF	chr4:15938120-15938270	HEEpiC	esophagus:	n/a	n/a
4	CTCF	chr4:15936520-15936670	RPTEC	kidney:	n/a	n/a
5	CTCF	chr4:15942255-15942314	GM19239	blood:	n/a	n/a
6	CTCF	chr4:15938180-15938330	SAEC	small airway:	n/a	n/a
7	CTCF	chr4:15940160-15940310	SAEC	small airway:	n/a	n/a
8	CTCF	chr4:15940140-15940290	HMEC	breast:	n/a	n/a
9	CTCF	chr4:15945645-15945648	GM13977	blood:	n/a	n/a
10	CTCF	chr4:15938160-15938310	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr4:15940060-15940210	HEEpiC	esophagus:	n/a	n/a
12	CTCF	chr4:15945227-15945304	GM13977	blood:	n/a	n/a
13	EP300	chr4:15939569-15940619	ECC-1	luminal epithelium:	n/a	chr4:15940557-15940571
14	FOS	chr4:15939889-15940075	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr4:15939984-15940184	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr4:15936013-15936067	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr4:15935850-15936254	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr4:15931289-15931430	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr4:15931273-15931473	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr4:15939804-15940200	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr4:15938184-15938479	MCF10A-Er-Src	breast:	n/a	chr4:15938293-15938303 chr4:15938294-15938302 chr4:15938293-15938303
22	FOS	chr4:15938220-15938448	MCF10A-Er-Src	breast:	n/a	chr4:15938293-15938303 chr4:15938294-15938302 chr4:15938293-15938303
23	FOS	chr4:15935860-15936197	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr4:15938215-15938492	MCF10A-Er-Src	breast:	n/a	chr4:15938293-15938303 chr4:15938294-15938302 chr4:15938293-15938303
25	FOS	chr4:15938169-15938465	MCF10A-Er-Src	breast:	n/a	chr4:15938293-15938303 chr4:15938294-15938302 chr4:15938293-15938303
26	FOS	chr4:15935854-15936197	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr4:15939889-15940204	MCF10A-Er-Src	breast:	n/a	n/a
28	MAFF	chr4:15944025-15944267	K562	blood:	n/a	chr4:15944094-15944112
29	MAFF	chr4:15943929-15944286	HepG2	liver:	n/a	chr4:15944094-15944112
30	MAFK	chr4:15943935-15944282	IMR90	lung:	n/a	chr4:15944096-15944111
31	MAFK	chr4:15943945-15944268	HepG2	liver:	n/a	chr4:15944096-15944111
32	MAFK	chr4:15943928-15944280	HepG2	liver:	n/a	chr4:15944096-15944111
33	MAFK	chr4:15944019-15944267	K562	blood:	n/a	chr4:15944096-15944111
34	MAX	chr4:15947085-15947489	NB4	blood:	n/a	n/a
35	MAX	chr4:15939610-15940442	HCT-116	colon:	n/a	n/a
36	MAX	chr4:15939635-15940382	ECC-1	luminal epithelium:	n/a	n/a
37	MAX	chr4:15939699-15940347	ECC-1	luminal epithelium:	n/a	n/a
38	MAZ	chr4:15939880-15940096	Hela-S3	cervix:	n/a	n/a
39	MXI1	chr4:15939916-15940187	Hela-S3	cervix:	n/a	n/a
40	MYC	chr4:15931135-15931390	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr4:15938331-15938419	MCF10A-Er-Src	breast:	n/a	n/a
42	MYC	chr4:15939798-15940218	MCF10A-Er-Src	breast:	n/a	n/a
43	MYC	chr4:15947161-15947510	NB4	blood:	n/a	n/a
44	MYC	chr4:15942265-15942319	MCF-7	breast:	n/a	n/a
45	MYC	chr4:15938179-15938454	MCF10A-Er-Src	breast:	n/a	n/a
46	MYC	chr4:15939855-15940209	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr4:15942322-15942355	MCF-7	breast:	n/a	n/a
48	NFIC	chr4:15939701-15940436	ECC-1	luminal epithelium:	n/a	n/a
49	NFIC	chr4:15939667-15940481	ECC-1	luminal epithelium:	n/a	n/a
50	PBX3	chr4:15942069-15942240	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:15939862-15939912	NB4	blood:	n/a
2	chr4:15939862-15939912	NB4	blood:	n/a
3	chr4:15940541-15940591	Jurkat	blood:	n/a
4	chr4:15939889-15939939	U87	brain:	n/a
5	chr4:15939862-15939912	LNCaP	prostate:	n/a
6	chr4:15940033-15940083	MCF10A-Er-Src	breast:	n/a
7	chr4:15939862-15939912	HEK293	kidney:	embryo
8	chr4:15938093-15938143	HL-60	blood:	n/a
9	chr4:15940541-15940591	HCM	heart:	n/a
10	chr4:15940897-15940947	NHBE	bronchial:	n/a
11	chr4:15940058-15940108	SK-N-SH_RA	brain:	n/a
12	chr4:15938093-15938143	HCF	heart:	n/a
13	chr4:15939889-15939939	T-47D	breast:	n/a
14	chr4:15940897-15940947	HUVEC	blood vessel:	n/a
15	chr4:15940897-15940947	K562	blood:	n/a
16	chr4:15938093-15938143	HMEC	breast:	n/a
17	chr4:15938093-15938143	HRCEpiC	kidney:	n/a
18	chr4:15940033-15940083	AG04449	skin:	fetal
19	chr4:15940541-15940591	U87	brain:	n/a
20	chr4:15939889-15939939	HepG2	liver:	n/a
21	chr4:15940058-15940108	NB4	blood:	n/a
22	chr4:15939889-15939939	AoSMC	blood vessel:	n/a
23	chr4:15937298-15937348	GM12892	blood:	n/a
24	chr4:15939862-15939912	HRCEpiC	kidney:	n/a
25	chr4:15940541-15940591	HCT-116	colon:	n/a
26	chr4:15939889-15939939	NHDF-neo	bronchial:	n/a
27	chr4:15939862-15939912	AG04449	skin:	fetal
28	chr4:15937298-15937348	U87	brain:	n/a
29	chr4:15940541-15940591	A549	lung:	n/a
30	chr4:15938093-15938143	ProgFib	skin:	n/a
31	chr4:15940058-15940108	MCF10A-Er-Src	breast:	n/a
32	chr4:15940897-15940947	RPTEC	kidney:	n/a
33	chr4:15940058-15940108	T-47D	breast:	n/a
34	chr4:15939862-15939912	CMK	blood:	n/a
35	chr4:15940541-15940591	Hela-S3	cervix:	n/a
36	chr4:15937298-15937348	HRPEpiC	eye:	n/a
37	chr4:15937298-15937348	HRCEpiC	kidney:	n/a
38	chr4:15938093-15938143	HNPCEpiC	eye:	n/a
39	chr4:15940058-15940108	AG09319	gingival:	n/a
40	chr4:15940058-15940108	NHDF-neo	bronchial:	n/a
41	chr4:15940058-15940108	LNCaP	prostate:	n/a
42	chr4:15940541-15940591	NH-A	brain:	n/a
43	chr4:15938093-15938143	GM19239	blood:	n/a
44	chr4:15938093-15938143	HCT-116	colon:	n/a
45	chr4:15940897-15940947	AoSMC	blood vessel:	n/a
46	chr4:15939862-15939912	HAEpiC	amniotic membrane:	n/a
47	chr4:15939889-15939939	AG09309	skin:	n/a
48	chr4:15937298-15937348	Hepatocyte	liver:	n/a
49	chr4:15940058-15940108	ProgFib	skin:	n/a
50	chr4:15940033-15940083	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:15941251..15943362-chr4:15944391..15946203,2	K562	blood:
2	chr4:15938565..15940263-chr4:15946360..15948731,2	K562	blood:
3	chr4:15941251..15943362-chr4:15944391..15946203,2	K562	blood:
4	chr4:15919905..15922253-chr4:15932751..15934628,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FGFBP1	hsa-miR-124-3p	chr4:15937379-15937398

Variant related genes	Relation type
FGFBP1	TF binding region
FGFBP1	CpG island
ENSG00000137440	chromatin interactions

Extended variants
information (count: 748 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs876320	chr4:15930961-15930962	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149961041	chr4:15930987-15930988	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs192575986	chr4:15931025-15931026	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs183324760	chr4:15931040-15931041	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs188678232	chr4:15931054-15931055	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs192551483	chr4:15931077-15931078	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs559861906	chr4:15931094-15931095	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs144985054	chr4:15931129-15931130	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs548580071	chr4:15931162-15931163	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs184843214	chr4:15931191-15931192	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs188720457	chr4:15931208-15931209	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs536845746	chr4:15931282-15931283	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs567876583	chr4:15931312-15931313	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs531532286	chr4:15931346-15931347	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs377374196	chr4:15931406-15931407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs16892610	chr4:15931464-15931465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571433836	chr4:15931474-15931475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369639010	chr4:15931480-15931481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570397969	chr4:15931484-15931485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539315251	chr4:15931495-15931496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534033077	chr4:15931500-15931501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547607145	chr4:15931526-15931527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140507619	chr4:15931539-15931540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191181321	chr4:15931551-15931552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144261106	chr4:15931611-15931612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs887111	chr4:15931641-15931642	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs573114513	chr4:15931700-15931701	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537836693	chr4:15931771-15931772	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558470385	chr4:15931781-15931782	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542249103	chr4:15931788-15931789	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183743282	chr4:15931789-15931790	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74951208	chr4:15931807-15931808	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575719420	chr4:15931840-15931841	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573420968	chr4:15931852-15931853	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76293186	chr4:15931885-15931886	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147808501	chr4:15931900-15931901	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544801932	chr4:15931949-15931950	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562223858	chr4:15931954-15931955	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189189915	chr4:15931965-15931966	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531368611	chr4:15931974-15931975	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1107782	chr4:15932007-15932008	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs1107781	chr4:15932013-15932014	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs527542805	chr4:15932032-15932033	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs34288492	chr4:15932033-15932034	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs377371363	chr4:15932046-15932047	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs540883872	chr4:15932089-15932090	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs547622567	chr4:15932114-15932115	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs182472265	chr4:15932117-15932118	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs535974440	chr4:15932156-15932157	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs549525504	chr4:15932164-15932165	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15920600-15937600	Weak transcription	Esophagus	oesophagus
2	chr4:15924200-15931400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:15924400-15936200	Weak transcription	HMEC	breast
4	chr4:15927600-15932200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:15928600-15931200	Weak transcription	Adipose Nuclei	Adipose
6	chr4:15928600-15931400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:15928800-15931200	Weak transcription	NHEK	skin
8	chr4:15930400-15931200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:15930600-15931400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:15930800-15931400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr4:15931200-15931600	Enhancers	NHEK	skin
12	chr4:15931200-15932200	Enhancers	Fetal Muscle Leg	muscle
13	chr4:15931200-15932600	Enhancers	Adipose Nuclei	Adipose
14	chr4:15931400-15931600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:15931400-15931800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:15931400-15932600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:15931400-15932600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr4:15931600-15933400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:15931600-15935600	Weak transcription	NHEK	skin
20	chr4:15931800-15932000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:15931800-15932200	Enhancers	HSMMtube	muscle
22	chr4:15931800-15932600	Enhancers	Fetal Thymus	thymus
23	chr4:15932000-15932400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:15932000-15932400	Enhancers	Thymus	Thymus
25	chr4:15932000-15932600	Bivalent Enhancer	GM12878-XiMat	blood
26	chr4:15932200-15932400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:15932200-15932400	Bivalent Enhancer	Fetal Muscle Leg	muscle
28	chr4:15932200-15933200	Enhancers	Primary B cells from peripheral blood	blood
29	chr4:15932400-15932600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:15932400-15933400	Weak transcription	Thymus	Thymus
31	chr4:15932400-15935400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:15933200-15934600	Weak transcription	Primary B cells from peripheral blood	blood
33	chr4:15933400-15936200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:15934400-15934800	Enhancers	GM12878-XiMat	blood
35	chr4:15934600-15934800	Enhancers	Primary B cells from peripheral blood	blood
36	chr4:15935400-15935800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:15935600-15935800	Enhancers	NHEK	skin
38	chr4:15935800-15936200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:15935800-15936200	Genic enhancers	NHEK	skin
40	chr4:15935800-15936400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:15936200-15937200	Genic enhancers	HMEC	breast
42	chr4:15936200-15938600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr4:15936200-15939800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:15936200-15939800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:15936200-15939800	Transcr. at gene 5' and 3'	NHEK	skin
46	chr4:15936400-15937000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:15937000-15937600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:15937200-15937600	Enhancers	Aorta	Aorta
49	chr4:15937200-15937800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:15937200-15938400	Enhancers	Fetal Muscle Leg	muscle

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