Variant report

Variant	nsv1054156
Chromosome Location	chr14:44429845-44659931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:44479441-44480344	HepG2	liver:	n/a	n/a
2	BACH1	chr14:44632100-44632238	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:44435424-44435438	GM12878	blood:	n/a	n/a
4	BRCA1	chr14:44618833-44619126	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr14:44560924-44561243	H1-hESC	embryonic stem cell:	n/a	chr14:44561060-44561071
6	CEBPB	chr14:44479378-44479560	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
7	CEBPB	chr14:44572581-44572713	HepG2	liver:	n/a	chr14:44572646-44572657 chr14:44572645-44572658
8	CEBPB	chr14:44599593-44600126	A549	lung:	n/a	chr14:44599949-44599960
9	CEBPB	chr14:44560929-44561184	K562	blood:	n/a	chr14:44561060-44561071
10	CEBPB	chr14:44479333-44479685	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
11	CEBPB	chr14:44484998-44485226	HepG2	liver:	n/a	chr14:44485063-44485074
12	CEBPB	chr14:44499069-44499521	Hela-S3	cervix:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
13	CEBPB	chr14:44605865-44606139	A549	lung:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
14	CEBPB	chr14:44498838-44499445	A549	lung:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
15	CEBPB	chr14:44448312-44448448	HepG2	liver:	n/a	chr14:44448367-44448378
16	CEBPB	chr14:44560911-44561241	HepG2	liver:	n/a	chr14:44561060-44561071
17	CEBPB	chr14:44605817-44606143	HepG2	liver:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
18	CEBPB	chr14:44560911-44561219	IMR90	lung:	n/a	chr14:44561060-44561071
19	CEBPB	chr14:44595881-44596093	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:44479304-44479659	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
21	CEBPB	chr14:44498824-44499447	IMR90	lung:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
22	CEBPB	chr14:44606738-44606986	HepG2	liver:	n/a	chr14:44606862-44606873
23	CEBPB	chr14:44657629-44657829	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr14:44450644-44451128	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:44541354-44541571	HepG2	liver:	n/a	chr14:44541425-44541436
26	CEBPB	chr14:44487331-44487496	A549	lung:	n/a	n/a
27	CEBPB	chr14:44560981-44561240	A549	lung:	n/a	chr14:44561060-44561071
28	CEBPB	chr14:44478929-44479169	A549	lung:	n/a	n/a
29	CEBPB	chr14:44452992-44453227	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr14:44582232-44582510	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:44499216-44499416	H1-hESC	embryonic stem cell:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
32	CEBPB	chr14:44499135-44499425	MCF-7	breast:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
33	CEBPB	chr14:44478922-44479578	IMR90	lung:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
34	CEBPB	chr14:44487307-44487471	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:44444697-44444949	HepG2	liver:	n/a	chr14:44444844-44444855
36	CEBPB	chr14:44498807-44499464	HepG2	liver:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
37	CEBPB	chr14:44595859-44595978	A549	lung:	n/a	n/a
38	CEBPB	chr14:44479371-44479562	MCF-7	breast:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
39	CEBPB	chr14:44633192-44633496	Hela-S3	cervix:	n/a	chr14:44633351-44633362
40	CEBPB	chr14:44478922-44479645	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
41	CEBPB	chr14:44618834-44619117	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr14:44606767-44606976	H1-hESC	embryonic stem cell:	n/a	chr14:44606862-44606873
43	CEBPB	chr14:44605796-44606154	Hela-S3	cervix:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
44	CEBPB	chr14:44599875-44600120	HepG2	liver:	n/a	chr14:44599949-44599960
45	CEBPB	chr14:44633186-44633505	HepG2	liver:	n/a	chr14:44633351-44633362
46	CHD2	chr14:44618838-44619102	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr14:44618879-44618881	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr14:44618900-44619050	GM12869	blood:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
49	CTCF	chr14:44457406-44457439	Lung_OC	lung:	n/a	n/a
50	CTCF	chr14:44618860-44619010	AG04450	lung:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958

No.	Distal block	Cell Line	Cell type
1	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
2	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
3	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
4	chr14:44370246..44372256-chr14:44617257..44619025,2	MCF-7	breast:
5	chr14:44659162..44661192-chr14:44662497..44664945,3	MCF-7	breast:
6	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
7	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
8	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
9	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
10	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
11	chr14:44429802..44430574-chr20:39327036..39327797,2	MCF-7	breast:
12	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
13	chr14:44569949..44570449-chr8:101630587..101631141,2	MCF-7	breast:
14	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
15	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-8	chr14:44477505-44479523	ucscGeneNc_uc001wvs_1
2	lnc-FSCB-6	chr14:44621821-44621918	l_977_chr14:44621312-44622966_testes
3	lnc-FSCB-6	chr14:44621313-44621629	l_977_chr14:44621312-44622966_testes
4	lnc-FSCB-7	chr14:44546737-44547087	NONHSAT036603
5	lnc-FSCB-6	chr14:44622425-44622966	l_977_chr14:44621312-44622966_testes
6	lnc-FSCB-2	chr14:44518586-44518710	ENSG00000258969
7	lnc-FSCB-6	chr14:44622029-44622354	l_977_chr14:44621312-44622966_testes
8	lnc-FSCB-2	chr14:44464984-44465046	ENSG00000258969

Variant related genes	Relation type
ENSG00000259137	TF binding region
ENSG00000259019	TF binding region
ENSG00000253740	chromatin interactions
ENSG00000229771	chromatin interactions
ENSG00000174226	chromatin interactions

Extended variants
information (count: 1901 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1901 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565246706	chr14:44429845-44429846	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148030928	chr14:44429916-44429917	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550587730	chr14:44429983-44429984	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568992351	chr14:44429989-44429990	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530175471	chr14:44430030-44430031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183461594	chr14:44430044-44430045	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117323629	chr14:44430054-44430055	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534467599	chr14:44430060-44430061	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559001989	chr14:44430112-44430113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs17309204	chr14:44430137-44430138	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs537819913	chr14:44430168-44430169	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs10132432	chr14:44430243-44430244	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs117663219	chr14:44430255-44430256	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116328293	chr14:44430258-44430259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551846581	chr14:44430259-44430260	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541948335	chr14:44430273-44430274	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553890343	chr14:44430284-44430285	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572160441	chr14:44430286-44430287	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs143675784	chr14:44430344-44430345	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs564201656	chr14:44430358-44430359	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111422501	chr14:44430379-44430380	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371577617	chr14:44430411-44430412	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs559315335	chr14:44430438-44430439	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs544192949	chr14:44430446-44430447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562592866	chr14:44430460-44430461	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530091447	chr14:44430470-44430471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528346486	chr14:44430561-44430562	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs547316201	chr14:44443801-44443802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533215469	chr14:44443816-44443817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182153746	chr14:44443820-44443821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559014705	chr14:44443931-44443932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543877483	chr14:44443976-44443977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563823960	chr14:44443984-44443985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10137617	chr14:44443996-44443997	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs545143863	chr14:44444047-44444048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546039836	chr14:44444100-44444101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563348928	chr14:44444109-44444110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530801679	chr14:44444114-44444115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186801820	chr14:44444126-44444127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112482777	chr14:44447815-44447816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183351162	chr14:44447874-44447875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544789174	chr14:44447910-44447911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188813715	chr14:44447921-44447922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs941944	chr14:44447955-44447956	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs370540110	chr14:44448067-44448068	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs374176455	chr14:44448068-44448069	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs33953097	chr14:44448069-44448070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs3035452	chr14:44448071-44448072	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs374568920	chr14:44448072-44448073	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs368575282	chr14:44448073-44448074	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44443800-44444200	Enhancers	Fetal Brain Male	brain
2	chr14:44447800-44448000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:44448000-44449800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:44450400-44450800	Enhancers	Fetal Intestine Small	intestine
5	chr14:44450400-44451200	Enhancers	Liver	Liver
6	chr14:44450400-44451200	Enhancers	Fetal Intestine Large	intestine
7	chr14:44450600-44451200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr14:44450600-44451200	Enhancers	HepG2	liver
9	chr14:44450800-44451400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:44464800-44465000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:44472800-44473000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:44473600-44473800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:44478400-44481000	Enhancers	Liver	Liver
14	chr14:44479000-44480800	Enhancers	HepG2	liver
15	chr14:44496600-44497000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:44497000-44498800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr14:44497600-44497800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr14:44498800-44499800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr14:44498800-44500600	Enhancers	Fetal Intestine Large	intestine
20	chr14:44499600-44500000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr14:44499600-44500200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr14:44499600-44500400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr14:44499600-44500800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr14:44499800-44500600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr14:44499800-44500600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr14:44499800-44500600	Enhancers	Fetal Intestine Small	intestine
27	chr14:44499800-44501000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr14:44500000-44500200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr14:44500000-44500400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr14:44500000-44500400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:44500000-44500400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr14:44500000-44500400	Enhancers	Fetal Heart	heart
33	chr14:44500000-44500600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr14:44500000-44500600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr14:44500000-44500600	Enhancers	Fetal Stomach	stomach
36	chr14:44500000-44500800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr14:44500000-44500800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr14:44500000-44501000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr14:44500000-44501000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr14:44500200-44500600	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr14:44500200-44500800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr14:44500200-44500800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr14:44500200-44501400	Enhancers	Brain Germinal Matrix	brain
44	chr14:44500400-44500600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr14:44500600-44500800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr14:44507600-44509200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:44508400-44508600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:44508600-44509200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:44510000-44510200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:44514000-44514400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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