Variant report

Variant	nsv879338
Chromosome Location	chr4:69414944-69556770
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:782)
CpG islands
(count:610)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:782 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
7	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
8	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
9	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
10	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
14	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
15	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
16	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
17	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
18	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
19	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
20	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
22	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
24	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
26	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
27	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
28	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
30	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
31	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
32	CTCF	chr4:69541318-69541394	Lung_OC	lung:	n/a	n/a
33	CTCF	chr4:69443470-69443502	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:69443447-69443535	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:69539060-69539210	GM12875	blood:	n/a	n/a
36	CTCF	chr4:69434856-69435015	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr4:69443417-69443543	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:69443400-69443550	NHEK	skin:	n/a	n/a
39	CTCF	chr4:69432120-69432270	GM12869	blood:	n/a	n/a
40	CTCF	chr4:69537061-69537242	Gliobla	brain:	n/a	n/a
41	CTCF	chr4:69443385-69443534	K562	blood:	n/a	n/a
42	CTCF	chr4:69537060-69537244	HepG2	liver:	n/a	n/a
43	CTCF	chr4:69443419-69443589	K562	blood:	n/a	n/a
44	CTCF	chr4:69539000-69539150	GM06990	blood:	n/a	n/a
45	CTCF	chr4:69537300-69537450	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr4:69443397-69443544	GM19240	blood:	n/a	n/a
47	CTCF	chr4:69537019-69537293	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:69523122-69523163	K562	blood:	n/a	n/a
49	CTCF	chr4:69434869-69435059	GM19240	blood:	n/a	n/a
50	CTCF	chr4:69419808-69419934	MCF-7	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69522639-69522689	HCT-116	colon:	n/a
2	chr4:69522639-69522689	ovcar-3	ovarian:	n/a
3	chr4:69514031-69514081	CMK	blood:	n/a
4	chr4:69537826-69537876	AG09319	gingival:	n/a
5	chr4:69434475-69434525	ECC-1	luminal epithelium:	n/a
6	chr4:69434475-69434525	GM12878	blood:	n/a
7	chr4:69435601-69435651	GM19239	blood:	n/a
8	chr4:69536319-69536369	NH-A	brain:	n/a
9	chr4:69537826-69537876	CMK	blood:	n/a
10	chr4:69536319-69536369	HCT-116	colon:	n/a
11	chr4:69537589-69537639	NT2-D1	testis:	n/a
12	chr4:69435593-69435643	Jurkat	blood:	n/a
13	chr4:69536319-69536369	BE2_C	brain:	n/a
14	chr4:69537826-69537876	T-47D	breast:	n/a
15	chr4:69435250-69435300	PFSK-1	brain:	n/a
16	chr4:69435593-69435643	BE2_C	brain:	n/a
17	chr4:69537806-69537856	GM19239	blood:	n/a
18	chr4:69435601-69435651	HCF	heart:	n/a
19	chr4:69537806-69537856	U87	brain:	n/a
20	chr4:69514031-69514081	GM06990	blood:	n/a
21	chr4:69435593-69435643	BJ	skin:	n/a
22	chr4:69435601-69435651	AG09319	gingival:	n/a
23	chr4:69514031-69514081	HCT-116	colon:	n/a
24	chr4:69435593-69435643	SK-N-SH_RA	brain:	n/a
25	chr4:69434475-69434525	BJ	skin:	n/a
26	chr4:69537589-69537639	GM12878	blood:	n/a
27	chr4:69434475-69434525	AoSMC	blood vessel:	n/a
28	chr4:69435601-69435651	PFSK-1	brain:	n/a
29	chr4:69537826-69537876	Jurkat	blood:	n/a
30	chr4:69435250-69435300	Hela-S3	cervix:	n/a
31	chr4:69537806-69537856	HEK293	kidney:	embryo
32	chr4:69537826-69537876	MCF10A-Er-Src	breast:	n/a
33	chr4:69537826-69537876	HCM	heart:	n/a
34	chr4:69537589-69537639	GM06990	blood:	n/a
35	chr4:69536319-69536369	ECC-1	luminal epithelium:	n/a
36	chr4:69536319-69536369	PFSK-1	brain:	n/a
37	chr4:69435601-69435651	SK-N-MC	brain:	n/a
38	chr4:69537826-69537876	H1-hESC	embryonic stem cell:	embryo
39	chr4:69514031-69514081	NHBE	bronchial:	n/a
40	chr4:69537826-69537876	ProgFib	skin:	n/a
41	chr4:69537826-69537876	HEK293	kidney:	embryo
42	chr4:69435593-69435643	MCF10A-Er-Src	breast:	n/a
43	chr4:69514031-69514081	ProgFib	skin:	n/a
44	chr4:69537826-69537876	SAEC	small airway:	n/a
45	chr4:69522639-69522689	ECC-1	luminal epithelium:	n/a
46	chr4:69435601-69435651	NT2-D1	testis:	n/a
47	chr4:69435593-69435643	NB4	blood:	n/a
48	chr4:69537826-69537876	HCPEpiC	choroid plexus:	n/a
49	chr4:69522639-69522689	BE2_C	brain:	n/a
50	chr4:69536319-69536369	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
2	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
3	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
4	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island

Extended variants
information (count: 3910 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3910 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7435827	chr4:69414944-69414945	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150917744	chr4:69415027-69415028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528362517	chr4:69415064-69415065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs5859132	chr4:69415065-69415066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397766650	chr4:69415079-69415080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184193098	chr4:69415086-69415087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560467681	chr4:69415126-69415127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139405862	chr4:69415142-69415143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187535515	chr4:69415148-69415149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549010021	chr4:69415218-69415219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75179908	chr4:69415226-69415227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531463568	chr4:69415241-69415242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551084463	chr4:69415277-69415278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570679026	chr4:69415355-69415356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535757348	chr4:69415375-69415376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539656773	chr4:69415381-69415382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192792938	chr4:69415393-69415394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370369705	chr4:69415533-69415534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7436962	chr4:69415555-69415556	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs149623767	chr4:69415568-69415569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182800993	chr4:69415569-69415570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187178490	chr4:69415570-69415571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9996186	chr4:69415607-69415608	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs192032503	chr4:69415672-69415673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184593981	chr4:69415710-69415711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577871733	chr4:69415729-69415730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189205947	chr4:69415735-69415736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540430356	chr4:69415794-69415795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548546722	chr4:69415961-69415962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560464823	chr4:69415993-69415994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537119867	chr4:69416023-69416024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193056632	chr4:69416051-69416052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185869646	chr4:69416065-69416066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562476986	chr4:69416328-69416329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376071081	chr4:69416353-69416354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374994336	chr4:69416382-69416383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201282859	chr4:69416396-69416397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368859012	chr4:69416425-69416426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143750013	chr4:69416430-69416431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201957986	chr4:69416439-69416440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371644681	chr4:69416448-69416449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374869749	chr4:69416466-69416467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377204498	chr4:69416515-69416516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571014866	chr4:69416542-69416543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147227030	chr4:69416547-69416548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13102139	chr4:69416556-69416557	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs145097129	chr4:69416569-69416570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201344972	chr4:69416625-69416626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567039489	chr4:69416640-69416641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200882210	chr4:69416663-69416664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69409200-69418800	Weak transcription	Liver	Liver
2	chr4:69413600-69418800	Strong transcription	Rectal Mucosa Donor 31	rectum
3	chr4:69417200-69418400	Enhancers	NHEK	skin
4	chr4:69417800-69418200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:69417800-69419200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:69417800-69420600	Enhancers	HepG2	liver
7	chr4:69418600-69419200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:69418800-69419200	Enhancers	Liver	Liver
9	chr4:69418800-69421800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr4:69420600-69421000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:69421000-69423400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:69421600-69423000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr4:69421800-69422200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:69421800-69422600	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr4:69422200-69430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:69422400-69422800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:69422600-69431200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr4:69427200-69427400	Enhancers	Liver	Liver
19	chr4:69427400-69433200	Weak transcription	Liver	Liver
20	chr4:69429200-69439800	Weak transcription	Right Atrium	heart
21	chr4:69430400-69430800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:69431200-69431400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr4:69431200-69431600	Enhancers	HMEC	breast
24	chr4:69431400-69434600	Active TSS	Rectal Mucosa Donor 31	rectum
25	chr4:69432800-69434200	Active TSS	Duodenum Mucosa	Duodenum
26	chr4:69433200-69433400	Flanking Active TSS	Liver	Liver
27	chr4:69433400-69434000	Active TSS	Liver	Liver
28	chr4:69434000-69435000	Weak transcription	Liver	Liver
29	chr4:69434200-69439200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr4:69434600-69435200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr4:69435000-69436200	Enhancers	Liver	Liver
32	chr4:69435200-69435800	Enhancers	Small Intestine	intestine
33	chr4:69435200-69436000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:69435200-69438000	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr4:69435400-69435800	Enhancers	Primary B cells from peripheral blood	blood
36	chr4:69435600-69436200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr4:69435800-69436800	Weak transcription	Primary B cells from peripheral blood	blood
38	chr4:69436000-69441800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:69436200-69446600	Weak transcription	Liver	Liver
40	chr4:69436800-69439000	Enhancers	Primary B cells from peripheral blood	blood
41	chr4:69438000-69438400	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr4:69438400-69439800	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr4:69439000-69441000	Weak transcription	Primary B cells from peripheral blood	blood
44	chr4:69439200-69439400	Enhancers	Duodenum Mucosa	Duodenum
45	chr4:69439400-69448200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:69439600-69440000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr4:69441000-69443000	Enhancers	Primary B cells from peripheral blood	blood
48	chr4:69441800-69442000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:69446600-69448000	Enhancers	Liver	Liver
50	chr4:69447400-69448000	Enhancers	NHEK	skin

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