Variant report

Variant	esv1793390
Chromosome Location	chr4:119294686-119390371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:119319359-119319713	GM12878	blood:	n/a	n/a
2	BATF	chr4:119340543-119341192	GM12878	blood:	n/a	chr4:119340900-119340911
3	BATF	chr4:119346684-119346850	GM12878	blood:	n/a	n/a
4	BATF	chr4:119340637-119341181	GM12878	blood:	n/a	chr4:119340900-119340911
5	BATF	chr4:119349910-119350272	GM12878	blood:	n/a	n/a
6	BATF	chr4:119319432-119319704	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:119366080-119366250	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:119345259-119345545	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:119340615-119341149	GM12878	blood:	n/a	chr4:119340900-119340909
10	BCL11A	chr4:119346839-119347055	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:119349658-119349869	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:119340729-119341128	GM12878	blood:	n/a	chr4:119340900-119340909
13	BCL11A	chr4:119347436-119347664	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:119357419-119357683	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:119348069-119348301	GM12878	blood:	n/a	n/a
16	BCL3	chr4:119382599-119382899	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:119319505-119319677	GM12878	blood:	n/a	n/a
18	CEBPB	chr4:119340970-119341155	Hela-S3	cervix:	n/a	chr4:119340996-119341007 chr4:119341094-119341111 chr4:119340996-119341009
19	CEBPB	chr4:119338475-119338816	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:119294969-119295325	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:119340964-119341126	HepG2	liver:	n/a	chr4:119340996-119341007 chr4:119341094-119341111 chr4:119340996-119341009
22	CEBPB	chr4:119382583-119382910	IMR90	lung:	n/a	chr4:119382722-119382733
23	CEBPB	chr4:119376054-119376279	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:119337044-119337239	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:119351771-119351934	K562	blood:	n/a	n/a
26	CEBPB	chr4:119331341-119331666	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:119340977-119341100	IMR90	lung:	n/a	chr4:119340996-119341007 chr4:119340996-119341009
28	CHD1	chr4:119318579-119318678	GM12878	blood:	n/a	n/a
29	CHD2	chr4:119345423-119345555	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:119345320-119345470	NB4	blood:	n/a	n/a
31	CTCF	chr4:119371620-119371770	GM06990	blood:	n/a	n/a
32	CTCF	chr4:119345212-119345645	A549	lung:	n/a	n/a
33	CTCF	chr4:119345300-119345450	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr4:119345230-119345616	IMR90	lung:	n/a	n/a
35	CTCF	chr4:119353280-119353430	GM12874	blood:	n/a	n/a
36	CTCF	chr4:119371640-119371790	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr4:119345300-119345450	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr4:119345308-119345509	GM19240	blood:	n/a	n/a
39	CTCF	chr4:119345320-119345470	NHLF	lung:	n/a	n/a
40	CTCF	chr4:119297289-119297362	Fibrobl	skin:	n/a	n/a
41	CTCF	chr4:119345380-119345530	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr4:119345380-119345530	GM12872	blood:	n/a	n/a
43	CTCF	chr4:119345285-119345535	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:119345290-119345507	GM12891	blood:	n/a	n/a
45	CTCF	chr4:119319440-119319590	GM12872	blood:	n/a	n/a
46	CTCF	chr4:119374118-119374125	LNCaP	prostate:	n/a	n/a
47	CTCF	chr4:119345380-119345530	GM12875	blood:	n/a	n/a
48	CTCF	chr4:119345300-119345450	AG09319	gingival:	n/a	n/a
49	CTCF	chr4:119387647-119387652	Medullo	brain:	n/a	n/a
50	CTCF	chr4:119358119-119358155	GM20000	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119295633-119295683	NHDF-neo	bronchial:	n/a
2	chr4:119318892-119318942	GM06990	blood:	n/a
3	chr4:119295633-119295683	GM12878	blood:	n/a
4	chr4:119295633-119295683	SAEC	small airway:	n/a
5	chr4:119295633-119295683	HIPEpiC	eye:	n/a
6	chr4:119295633-119295683	SKMC	muscle:	n/a
7	chr4:119295633-119295683	HepG2	liver:	n/a
8	chr4:119295633-119295683	MCF10A-Er-Src	breast:	n/a
9	chr4:119318892-119318942	A549	lung:	n/a
10	chr4:119318892-119318942	SK-N-MC	brain:	n/a
11	chr4:119295633-119295683	HEK293	kidney:	embryo
12	chr4:119295633-119295683	ProgFib	skin:	n/a
13	chr4:119318892-119318942	U87	brain:	n/a
14	chr4:119295633-119295683	HMEC	breast:	n/a
15	chr4:119295633-119295683	NB4	blood:	n/a
16	chr4:119295633-119295683	SK-N-SH_RA	brain:	n/a
17	chr4:119295633-119295683	HCPEpiC	choroid plexus:	n/a
18	chr4:119318892-119318942	AG09319	gingival:	n/a
19	chr4:119318892-119318942	T-47D	breast:	n/a
20	chr4:119295633-119295683	Jurkat	blood:	n/a
21	chr4:119295633-119295683	Hela-S3	cervix:	n/a
22	chr4:119318892-119318942	ProgFib	skin:	n/a
23	chr4:119295633-119295683	U87	brain:	n/a
24	chr4:119318892-119318942	AG09309	skin:	n/a
25	chr4:119318892-119318942	PrEC	prostate:	n/a
26	chr4:119318892-119318942	Caco-2	colon:	n/a
27	chr4:119318892-119318942	HAEpiC	amniotic membrane:	n/a
28	chr4:119318892-119318942	GM19239	blood:	n/a
29	chr4:119295633-119295683	AG09319	gingival:	n/a
30	chr4:119295633-119295683	HRCEpiC	kidney:	n/a
31	chr4:119295633-119295683	GM19239	blood:	n/a
32	chr4:119295633-119295683	ECC-1	luminal epithelium:	n/a
33	chr4:119295633-119295683	HCF	heart:	n/a
34	chr4:119318892-119318942	HepG2	liver:	n/a
35	chr4:119295633-119295683	NHBE	bronchial:	n/a
36	chr4:119318892-119318942	BE2_C	brain:	n/a
37	chr4:119295633-119295683	HEEpiC	esophagus:	n/a
38	chr4:119318892-119318942	GM12892	blood:	n/a
39	chr4:119318892-119318942	LNCaP	prostate:	n/a
40	chr4:119295633-119295683	CMK	blood:	n/a
41	chr4:119318892-119318942	ovcar-3	ovarian:	n/a
42	chr4:119295633-119295683	K562	blood:	n/a
43	chr4:119318892-119318942	Jurkat	blood:	n/a
44	chr4:119318892-119318942	NB4	blood:	n/a
45	chr4:119318892-119318942	K562	blood:	n/a
46	chr4:119318892-119318942	NT2-D1	testis:	n/a
47	chr4:119318892-119318942	NH-A	brain:	n/a
48	chr4:119295633-119295683	AG04449	skin:	fetal
49	chr4:119318892-119318942	HUVEC	blood vessel:	n/a
50	chr4:119295633-119295683	HCT-116	colon:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:119311600..119313151-chr4:119317635..119319995,2	MCF-7	breast:
2	chr4:119198536..119201399-chr4:119334515..119337557,3	MCF-7	breast:
3	chr4:119297227..119299368-chr4:119300296..119302370,2	K562	blood:
4	chr4:119292842..119294538-chr4:119297260..119300160,2	MCF-7	breast:
5	chr4:119199853..119201646-chr4:119293860..119297820,3	MCF-7	breast:
6	chr4:119204030..119205775-chr4:119295374..119296879,2	K562	blood:
7	chr4:119199281..119200962-chr4:119368800..119371509,2	MCF-7	breast:
8	chr4:119311600..119313151-chr4:119317635..119319995,2	MCF-7	breast:
9	chr4:119297227..119299368-chr4:119300296..119302370,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDST3-3	chr4:119349734-119350000	XLOC_003661
2	lnc-PRSS12-1	chr4:119321669-119321989	NONHSAT097980
3	lnc-NDST3-3	chr4:119348948-119349038	XLOC_003661
4	lnc-NDST3-3	chr4:119350138-119350584	XLOC_003661

No data

Variant related genes	Relation type
CEP170P1	TF binding region
NDUFS5P5	TF binding region
CEP170P1	CpG island
NDUFS5P5	CpG island
ENSG00000269893	chromatin interactions

Extended variants
information (count: 2039 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2039 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549816200	chr4:119294691-119294692	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372822584	chr4:119294702-119294703	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569685576	chr4:119294719-119294720	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538616589	chr4:119294730-119294731	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs183489739	chr4:119294741-119294742	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572362805	chr4:119294805-119294806	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144715392	chr4:119294806-119294807	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554588370	chr4:119294810-119294811	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570542106	chr4:119294813-119294814	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539929987	chr4:119294837-119294838	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574540619	chr4:119294841-119294842	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376420785	chr4:119294849-119294850	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543286532	chr4:119294866-119294867	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188171369	chr4:119294889-119294890	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113584865	chr4:119294940-119294941	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181145708	chr4:119294960-119294961	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545780829	chr4:119295016-119295017	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148543796	chr4:119295067-119295068	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141248141	chr4:119295122-119295123	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542483986	chr4:119295164-119295165	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs17516575	chr4:119295170-119295171	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs531121444	chr4:119295171-119295172	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146257347	chr4:119295246-119295247	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372676093	chr4:119295322-119295323	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs186492558	chr4:119295359-119295360	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139998393	chr4:119295390-119295391	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569730652	chr4:119295425-119295426	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532287557	chr4:119295434-119295435	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190154161	chr4:119295439-119295440	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs373282070	chr4:119295442-119295443	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372171119	chr4:119295615-119295616	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs78974785	chr4:119295629-119295630	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553361708	chr4:119295717-119295718	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534616844	chr4:119295757-119295758	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186400401	chr4:119295763-119295764	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554832704	chr4:119295787-119295788	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568289612	chr4:119295800-119295801	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs542205889	chr4:119295827-119295828	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556914840	chr4:119295902-119295903	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576634490	chr4:119295923-119295924	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139402250	chr4:119295928-119295929	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs9997615	chr4:119295954-119295955	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs146518562	chr4:119295984-119295985	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541895504	chr4:119296014-119296015	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562384999	chr4:119296097-119296098	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs531157180	chr4:119296117-119296118	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544783687	chr4:119296135-119296136	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139798771	chr4:119296153-119296154	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557939801	chr4:119296162-119296163	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111524745	chr4:119296170-119296171	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Esophageal squamous carcinoma	18350619	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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	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
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119294400-119294800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr4:119294400-119295000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:119294400-119296400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr4:119294600-119295800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:119294800-119295200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:119295200-119295400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr4:119295400-119295600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr4:119295600-119295800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr4:119296400-119297800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:119297800-119298000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:119308000-119308200	Bivalent/Poised TSS	Right Atrium	heart
12	chr4:119310600-119310800	Enhancers	NHDF-Ad	bronchial
13	chr4:119310600-119310800	Enhancers	NHLF	lung
14	chr4:119310600-119311000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:119310800-119311000	Flanking Active TSS	NHDF-Ad	bronchial
16	chr4:119311000-119311200	Active TSS	NHDF-Ad	bronchial
17	chr4:119311200-119318200	Weak transcription	NHDF-Ad	bronchial
18	chr4:119313600-119315400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:119315200-119316800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:119315400-119315600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:119315400-119315800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
22	chr4:119315400-119316000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:119315400-119316800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr4:119315400-119317200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr4:119315400-119317400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:119315800-119317000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:119316000-119316800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr4:119316000-119318000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:119316200-119320000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr4:119316200-119320800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:119316600-119316800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr4:119316800-119317000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr4:119316800-119318000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:119316800-119318000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr4:119316800-119321600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:119317000-119317800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr4:119317000-119318200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr4:119317000-119318600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:119317000-119319600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
40	chr4:119317200-119317600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr4:119317600-119318400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr4:119317600-119318400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:119317600-119319200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr4:119317600-119319600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:119317600-119319800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr4:119317800-119318400	Enhancers	Placenta	Placenta
47	chr4:119317800-119318600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:119317800-119320000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr4:119317800-119320200	Enhancers	HMEC	breast
50	chr4:119318000-119318200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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