Variant report

Variant	nsv9720
Chromosome Location	chr19:39277331-39283376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:226)
CpG islands
(count:491)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr19:39283347-39283518	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr19:39282186-39282336	Lung_OC	lung:	n/a	n/a
3	CTCF	chr19:39283198-39283616	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr19:39283320-39283470	AG04450	lung:	n/a	n/a
5	CTCF	chr19:39282256-39282292	GM20000	blood:	n/a	n/a
6	CTCF	chr19:39283300-39283450	HCM	heart:	n/a	n/a
7	CTCF	chr19:39283347-39283544	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr19:39283300-39283450	HPF	lung:	n/a	n/a
9	CTCF	chr19:39283371-39283518	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr19:39283300-39283450	SAEC	small airway:	n/a	n/a
11	CTCF	chr19:39282160-39282341	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr19:39283300-39283450	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr19:39283240-39283390	GM12869	blood:	n/a	n/a
14	CTCF	chr19:39283320-39283470	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr19:39283316-39283529	GM19239	blood:	n/a	n/a
16	CTCF	chr19:39283320-39283470	AG10803	skin:	n/a	n/a
17	CTCF	chr19:39283320-39283470	HepG2	liver:	n/a	n/a
18	CTCF	chr19:39282120-39282385	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr19:39283340-39283490	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr19:39282094-39282129	GM12878	blood:	n/a	n/a
21	CTCF	chr19:39281684-39281719	GM19239	blood:	n/a	n/a
22	CTCF	chr19:39283376-39283511	Gliobla	brain:	n/a	n/a
23	CTCF	chr19:39282512-39282669	GM12891	blood:	n/a	chr19:39282629-39282637
24	CTCF	chr19:39283300-39283450	GM12878	blood:	n/a	n/a
25	CTCF	chr19:39283300-39283450	NHLF	lung:	n/a	n/a
26	CTCF	chr19:39283329-39283552	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr19:39283360-39283510	HMF	breast:	n/a	n/a
28	CTCF	chr19:39283360-39283510	GM12864	blood:	n/a	n/a
29	CTCF	chr19:39283325-39283526	GM19240	blood:	n/a	n/a
30	CTCF	chr19:39283340-39283490	GM12866	blood:	n/a	n/a
31	CTCF	chr19:39283091-39283099	GM13977	blood:	n/a	n/a
32	CTCF	chr19:39282674-39282682	GM12891	blood:	n/a	n/a
33	CTCF	chr19:39283300-39283450	AG09319	gingival:	n/a	n/a
34	CTCF	chr19:39282584-39282634	GM13976	blood:	n/a	n/a
35	CTCF	chr19:39282001-39282094	Lung_OC	lung:	n/a	n/a
36	CTCF	chr19:39281203-39281390	GM13976	blood:	n/a	n/a
37	CTCF	chr19:39282238-39282295	GM12892	blood:	n/a	n/a
38	CTCF	chr19:39283300-39283450	HVMF	connective:	n/a	n/a
39	CTCF	chr19:39283300-39283450	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr19:39283320-39283470	HPF	lung:	n/a	n/a
41	CTCF	chr19:39283300-39283450	GM12872	blood:	n/a	n/a
42	CTCF	chr19:39283327-39283561	Lung_OC	lung:	n/a	n/a
43	CTCF	chr19:39283353-39283522	Fibrobl	skin:	n/a	n/a
44	CTCF	chr19:39283340-39283490	HCM	heart:	n/a	n/a
45	CTCF	chr19:39283320-39283470	RPTEC	kidney:	n/a	n/a
46	CTCF	chr19:39283300-39283450	HFF	foreskin:	n/a	n/a
47	CTCF	chr19:39282182-39282335	GM19239	blood:	n/a	n/a
48	CTCF	chr19:39283360-39283510	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr19:39283360-39283510	GM12873	blood:	n/a	n/a
50	CTCF	chr19:39283340-39283490	GM12868	blood:	n/a	n/a

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39278997-39279047	AG04449	skin:	fetal
2	chr19:39281374-39281424	AoSMC	blood vessel:	n/a
3	chr19:39279408-39279458	HCF	heart:	n/a
4	chr19:39278997-39279047	AG04449	skin:	fetal
5	chr19:39281374-39281424	AoSMC	blood vessel:	n/a
6	chr19:39279408-39279458	HCF	heart:	n/a
7	chr19:39279324-39279374	HCM	heart:	n/a
8	chr19:39279408-39279458	K562	blood:	n/a
9	chr19:39282077-39282127	GM12878	blood:	n/a
10	chr19:39279703-39279753	A549	lung:	n/a
11	chr19:39281374-39281424	SK-N-SH	brain:	n/a
12	chr19:39282077-39282127	NT2-D1	testis:	n/a
13	chr19:39281374-39281424	SK-N-SH_RA	brain:	n/a
14	chr19:39279703-39279753	GM12891	blood:	n/a
15	chr19:39283334-39283384	SK-N-SH_RA	brain:	n/a
16	chr19:39278997-39279047	ECC-1	luminal epithelium:	n/a
17	chr19:39279324-39279374	HNPCEpiC	eye:	n/a
18	chr19:39282077-39282127	HCM	heart:	n/a
19	chr19:39279703-39279753	HRCEpiC	kidney:	n/a
20	chr19:39278997-39279047	H1-hESC	embryonic stem cell:	embryo
21	chr19:39279408-39279458	HCT-116	colon:	n/a
22	chr19:39279266-39279316	HCPEpiC	choroid plexus:	n/a
23	chr19:39279408-39279458	Caco-2	colon:	n/a
24	chr19:39279703-39279753	AG04449	skin:	fetal
25	chr19:39279324-39279374	MCF10A-Er-Src	breast:	n/a
26	chr19:39279266-39279316	RPTEC	kidney:	n/a
27	chr19:39281374-39281424	AG09319	gingival:	n/a
28	chr19:39281374-39281424	AG10803	skin:	n/a
29	chr19:39279324-39279374	CMK	blood:	n/a
30	chr19:39278997-39279047	HAEpiC	amniotic membrane:	n/a
31	chr19:39279266-39279316	PANC-1	pancreas:	n/a
32	chr19:39279408-39279458	GM12878	blood:	n/a
33	chr19:39279266-39279316	NHBE	bronchial:	n/a
34	chr19:39278997-39279047	MCF-7	breast:	n/a
35	chr19:39278997-39279047	AG10803	skin:	n/a
36	chr19:39283334-39283384	SK-N-MC	brain:	n/a
37	chr19:39283334-39283384	NHBE	bronchial:	n/a
38	chr19:39278997-39279047	LNCaP	prostate:	n/a
39	chr19:39278997-39279047	U87	brain:	n/a
40	chr19:39279324-39279374	Hepatocyte	liver:	n/a
41	chr19:39278997-39279047	AG09309	skin:	n/a
42	chr19:39282077-39282127	LNCaP	prostate:	n/a
43	chr19:39282077-39282127	T-47D	breast:	n/a
44	chr19:39279703-39279753	Hela-S3	cervix:	n/a
45	chr19:39282077-39282127	GM12892	blood:	n/a
46	chr19:39279703-39279753	HIPEpiC	eye:	n/a
47	chr19:39279703-39279753	NHDF-neo	bronchial:	n/a
48	chr19:39279324-39279374	NHDF-neo	bronchial:	n/a
49	chr19:39278997-39279047	Hela-S3	cervix:	n/a
50	chr19:39279266-39279316	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:39263336..39266472-chr19:39281321..39283014,3	K562	blood:
2	chr19:39277481..39279141-chr19:39336896..39339737,2	K562	blood:
3	chr19:39278557..39281313-chr19:39305805..39307829,2	MCF-7	breast:

No data

Variant related genes	Relation type
LGALS7B	TF binding region
LGALS7B	CpG island
ENSG00000104824	chromatin interactions
ENSG00000205076	chromatin interactions
ENSG00000104823	chromatin interactions

Extended variants
information (count: 173 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:173 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188988454	chr19:39277396-39277397	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs533416189	chr19:39277404-39277405	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs372598418	chr19:39277441-39277442	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs375509653	chr19:39277459-39277460	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552053064	chr19:39277474-39277475	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs560287407	chr19:39277509-39277510	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs375247512	chr19:39277516-39277517	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs368367935	chr19:39277527-39277528	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs527898537	chr19:39277542-39277543	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549052652	chr19:39277590-39277591	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192228136	chr19:39277627-39277628	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs538235294	chr19:39277652-39277653	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs12151271	chr19:39277655-39277656	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs571626054	chr19:39277820-39277821	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539324261	chr19:39277872-39277873	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558047219	chr19:39277924-39277925	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573057999	chr19:39277943-39277944	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111310299	chr19:39278009-39278010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs62121413	chr19:39278019-39278020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs369982398	chr19:39278059-39278060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs73040747	chr19:39278069-39278070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544302399	chr19:39278077-39278078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs62121414	chr19:39278124-39278125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113880630	chr19:39278137-39278138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561676675	chr19:39278145-39278146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560449574	chr19:39278147-39278148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs183895154	chr19:39278177-39278178	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs549212155	chr19:39278209-39278210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs7259749	chr19:39278229-39278230	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs145924848	chr19:39278233-39278234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs550252608	chr19:39278246-39278247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545988458	chr19:39278253-39278254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369862408	chr19:39278277-39278278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539056898	chr19:39278288-39278289	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372954538	chr19:39278333-39278334	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112187733	chr19:39278334-39278335	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374832202	chr19:39278339-39278340	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566819873	chr19:39278382-39278383	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113063179	chr19:39278393-39278394	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369223521	chr19:39278433-39278434	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188724474	chr19:39278475-39278476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529471494	chr19:39278496-39278497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555559313	chr19:39278633-39278634	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs567456745	chr19:39278646-39278647	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs537514259	chr19:39278662-39278663	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556241251	chr19:39278673-39278674	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs537735141	chr19:39278697-39278698	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs180831687	chr19:39278702-39278703	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs545017599	chr19:39278708-39278709	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs572522237	chr19:39278731-39278732	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39265600-39283000	Weak transcription	Spleen	Spleen
2	chr19:39269800-39277600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:39272600-39277400	Weak transcription	K562	blood
4	chr19:39274200-39279200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:39275400-39277400	Weak transcription	A549	lung
6	chr19:39275600-39279000	Weak transcription	HepG2	liver
7	chr19:39275600-39279200	Weak transcription	Fetal Intestine Small	intestine
8	chr19:39275600-39279200	Weak transcription	Stomach Mucosa	stomach
9	chr19:39276000-39277600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr19:39276200-39277400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr19:39276200-39279000	Weak transcription	Fetal Intestine Large	intestine
12	chr19:39276200-39283000	Weak transcription	Pancreas	Pancrea
13	chr19:39276400-39277600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr19:39276800-39278200	Enhancers	HMEC	breast
15	chr19:39277000-39278000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr19:39277200-39277400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr19:39277200-39277400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr19:39277200-39277400	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr19:39277200-39277600	Flanking Active TSS	NHEK	skin
20	chr19:39277200-39278000	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr19:39277200-39283200	Weak transcription	NH-A	brain
22	chr19:39277400-39277600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr19:39277400-39277600	Enhancers	Fetal Muscle Leg	muscle
24	chr19:39277400-39277600	Enhancers	K562	blood
25	chr19:39277400-39277800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
26	chr19:39277400-39277800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:39277400-39277800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:39277400-39277800	Enhancers	Right Ventricle	heart
29	chr19:39277400-39277800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr19:39277400-39277800	Enhancers	A549	lung
31	chr19:39277400-39278000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr19:39277400-39278200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr19:39277600-39277800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr19:39277600-39277800	Enhancers	Placenta	Placenta
35	chr19:39277600-39277800	Enhancers	Fetal Thymus	thymus
36	chr19:39277600-39278000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:39277600-39278000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr19:39277600-39278200	Enhancers	Esophagus	oesophagus
39	chr19:39277600-39278200	Enhancers	NHEK	skin
40	chr19:39277600-39279400	Weak transcription	Fetal Muscle Leg	muscle
41	chr19:39277800-39278000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr19:39277800-39278000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr19:39277800-39278200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:39277800-39278800	Weak transcription	Fetal Thymus	thymus
45	chr19:39277800-39278800	Weak transcription	A549	lung
46	chr19:39277800-39279200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr19:39277800-39279200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr19:39277800-39282800	Weak transcription	Placenta	Placenta
49	chr19:39277800-39283000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr19:39277800-39283000	Weak transcription	Right Ventricle	heart

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