Variant report

Variant	esv3402814
Chromosome Location	chr19:56210240-56213138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:33)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:33 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA2	chr19:56212245-56212534	SH-SY5Y	brain:	n/a	n/a
2	POLR2A	chr19:56212058-56212570	GM12892	blood:	n/a	n/a
3	POLR2A	chr19:56212266-56212269	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr19:56210456-56210989	PFSK-1	brain:	n/a	n/a
5	POLR2A	chr19:56211106-56211147	HUVEC	blood vessel:	n/a	n/a
6	POLR2A	chr19:56210399-56211128	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr19:56213106-56213166	HepG2	liver:	n/a	n/a
8	POLR2A	chr19:56212092-56212565	PANC-1	pancreas:	n/a	n/a
9	POLR2A	chr19:56212235-56212393	K562	blood:	n/a	n/a
10	POLR2A	chr19:56212159-56212460	GM12878	blood:	n/a	n/a
11	POLR2A	chr19:56210868-56210918	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr19:56212964-56213296	K562	blood:	n/a	n/a
13	POLR2A	chr19:56212318-56212470	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr19:56210674-56211189	K562	blood:	n/a	n/a
15	POLR2A	chr19:56210940-56211060	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr19:56212451-56212690	GM12878	blood:	n/a	n/a
17	POLR2A	chr19:56212144-56212177	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr19:56212080-56212488	K562	blood:	n/a	n/a
19	POLR2A	chr19:56212451-56212460	K562	blood:	n/a	n/a
20	POLR2A	chr19:56212003-56212258	HepG2	liver:	n/a	n/a
21	POLR2A	chr19:56211739-56212372	HepG2	liver:	n/a	n/a
22	POLR2A	chr19:56210646-56210654	K562	blood:	n/a	n/a
23	POLR2A	chr19:56212465-56212651	HepG2	liver:	n/a	n/a
24	POLR2A	chr19:56212184-56212478	GM12878	blood:	n/a	n/a
25	POLR2A	chr19:56211786-56212439	PANC-1	pancreas:	n/a	n/a
26	POLR2A	chr19:56210645-56210736	HepG2	liver:	n/a	n/a
27	POLR2A	chr19:56211951-56212163	K562	blood:	n/a	n/a
28	POLR2A	chr19:56212319-56212357	MCF-7	breast:	n/a	n/a
29	POLR2A	chr19:56212145-56212564	HL-60	blood:	n/a	n/a
30	POLR2A	chr19:56212962-56213067	HepG2	liver:	n/a	n/a
31	POLR2A	chr19:56212401-56212432	K562	blood:	n/a	n/a
32	POLR2A	chr19:56212816-56213309	PANC-1	pancreas:	n/a	n/a
33	THAP1	chr19:56212267-56212451	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56212426-56212476	HRE	kidney:	n/a
2	chr19:56212426-56212476	ovcar-3	ovarian:	n/a
3	chr19:56212426-56212476	GM12892	blood:	n/a
4	chr19:56212426-56212476	SK-N-SH_RA	brain:	n/a
5	chr19:56212426-56212476	PANC-1	pancreas:	n/a
6	chr19:56212426-56212476	CMK	blood:	n/a
7	chr19:56212426-56212476	ECC-1	luminal epithelium:	n/a
8	chr19:56212426-56212476	IMR90	lung:	fetal
9	chr19:56212426-56212476	HCT-116	colon:	n/a
10	chr19:56212426-56212476	NT2-D1	testis:	n/a
11	chr19:56212426-56212476	Hepatocyte	liver:	n/a
12	chr19:56212426-56212476	SKMC	muscle:	n/a
13	chr19:56212426-56212476	AG09309	skin:	n/a
14	chr19:56212426-56212476	MCF10A-Er-Src	breast:	n/a
15	chr19:56212426-56212476	SK-N-SH	brain:	n/a
16	chr19:56212426-56212476	HRPEpiC	eye:	n/a
17	chr19:56212426-56212476	GM12891	blood:	n/a
18	chr19:56212426-56212476	NH-A	brain:	n/a
19	chr19:56212426-56212476	GM19239	blood:	n/a
20	chr19:56212426-56212476	SAEC	small airway:	n/a
21	chr19:56212426-56212476	K562	blood:	n/a
22	chr19:56212426-56212476	HAEpiC	amniotic membrane:	n/a
23	chr19:56212426-56212476	GM12878	blood:	n/a
24	chr19:56212426-56212476	HUVEC	blood vessel:	n/a
25	chr19:56212426-56212476	HMEC	breast:	n/a
26	chr19:56212426-56212476	HEK293	kidney:	embryo
27	chr19:56212426-56212476	HIPEpiC	eye:	n/a
28	chr19:56212426-56212476	GM06990	blood:	n/a
29	chr19:56212426-56212476	NHDF-neo	bronchial:	n/a
30	chr19:56212426-56212476	HPAEpiC	pulmonary alveolar:	n/a
31	chr19:56212426-56212476	Caco-2	colon:	n/a
32	chr19:56212426-56212476	HRCEpiC	kidney:	n/a
33	chr19:56212426-56212476	NB4	blood:	n/a
34	chr19:56212426-56212476	AG04450	lung:	fetal
35	chr19:56212426-56212476	U87	brain:	n/a
36	chr19:56212426-56212476	A549	lung:	n/a
37	chr19:56212426-56212476	NHBE	bronchial:	n/a
38	chr19:56212426-56212476	Jurkat	blood:	n/a
39	chr19:56212426-56212476	LNCaP	prostate:	n/a
40	chr19:56212426-56212476	PFSK-1	brain:	n/a
41	chr19:56212426-56212476	HEEpiC	esophagus:	n/a
42	chr19:56212426-56212476	BE2_C	brain:	n/a
43	chr19:56212426-56212476	RPTEC	kidney:	n/a
44	chr19:56212426-56212476	AG10803	skin:	n/a
45	chr19:56212426-56212476	T-47D	breast:	n/a
46	chr19:56212426-56212476	HNPCEpiC	eye:	n/a
47	chr19:56212426-56212476	SK-N-MC	brain:	n/a
48	chr19:56212426-56212476	PrEC	prostate:	n/a
49	chr19:56212426-56212476	BJ	skin:	n/a
50	chr19:56212426-56212476	HepG2	liver:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56194595..56204961-chr19:56206160..56210902,10	K562	blood:
2	chr19:56163850..56167887-chr19:56212407..56215372,3	K562	blood:
3	chr19:56207047..56209791-chr19:56212188..56214555,3	K562	blood:
4	chr19:56185419..56191490-chr19:56212273..56216664,6	K562	blood:
5	chr19:56110891..56112606-chr19:56211484..56213987,2	K562	blood:
6	chr19:56188121..56189803-chr19:56212346..56215225,2	K562	blood:
7	chr19:56204403..56206705-chr19:56209102..56212375,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPN1-4	chr19:56211415-56212585	NONHSAT068074

No data

Variant related genes	Relation type
ENSG00000267117	TF binding region
ENSG00000267117	CpG island
ENSG00000203305	chromatin interactions
ENSG00000211571	chromatin interactions
ENSG00000267183	chromatin interactions
ENSG00000267523	chromatin interactions
ENSG00000267018	chromatin interactions
ENSG00000179943	chromatin interactions
ENSG00000267117	chromatin interactions
ENSG00000063245	chromatin interactions
ENSG00000171443	chromatin interactions
ENSG00000063244	chromatin interactions

Extended variants
information (count: 166 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:166 , 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	rs537347307	chr19:56210256-56210257	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs11384864	chr19:56210278-56210279	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs397964334	chr19:56210287-56210288	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs189293708	chr19:56210331-56210332	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs28449839	chr19:56210352-56210353	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs561885889	chr19:56210353-56210354	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs527547820	chr19:56210362-56210363	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs181758907	chr19:56210368-56210369	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs186347594	chr19:56210405-56210406	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs189572203	chr19:56210428-56210429	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs536657162	chr19:56210430-56210431	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs6509952	chr19:56210471-56210472	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569690289	chr19:56210473-56210474	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs181021273	chr19:56210474-56210475	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs534463679	chr19:56210501-56210502	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs186255457	chr19:56210515-56210516	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs533691210	chr19:56210519-56210520	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs375097852	chr19:56210520-56210521	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs191609702	chr19:56210530-56210531	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs547293851	chr19:56210531-56210532	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs552601348	chr19:56210547-56210548	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs117361361	chr19:56210590-56210591	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs183387511	chr19:56210604-56210605	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs543760171	chr19:56210606-56210607	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs572646616	chr19:56210675-56210676	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs187379602	chr19:56210676-56210677	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs190645824	chr19:56210690-56210691	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs527509709	chr19:56210704-56210705	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs567107035	chr19:56210713-56210714	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs547709236	chr19:56210724-56210725	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs373293470	chr19:56210726-56210727	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs183285492	chr19:56210732-56210733	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs533083026	chr19:56210745-56210746	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs549701345	chr19:56210803-56210804	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs569568835	chr19:56210846-56210847	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs535520520	chr19:56210851-56210852	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs548699795	chr19:56210856-56210857	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs565932897	chr19:56210885-56210886	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs4801261	chr19:56210928-56210929	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557939916	chr19:56210950-56210951	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs578161659	chr19:56211001-56211002	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537366088	chr19:56211014-56211015	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111438319	chr19:56211038-56211039	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573984758	chr19:56211039-56211040	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369254407	chr19:56211061-56211062	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559932235	chr19:56211063-56211064	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs111700424	chr19:56211107-56211108	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541184255	chr19:56211114-56211115	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs544086699	chr19:56211123-56211124	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs564274191	chr19:56211151-56211152	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56188200-56218200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr19:56188400-56211200	Strong transcription	Cortex derived primary cultured neurospheres	brain
3	chr19:56188400-56213600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:56188600-56212400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:56188600-56215600	Weak transcription	Fetal Brain Male	brain
6	chr19:56188800-56212400	Strong transcription	Thymus	Thymus
7	chr19:56189200-56212600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr19:56189400-56212400	Strong transcription	Brain Germinal Matrix	brain
9	chr19:56189600-56213200	Strong transcription	Primary T cells from cord blood	blood
10	chr19:56190000-56212600	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr19:56190200-56212400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr19:56191000-56212400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:56191800-56218800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr19:56192000-56214600	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr19:56192200-56211200	Strong transcription	Skeletal Muscle Male	skeletal muscle
16	chr19:56192400-56212400	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr19:56192800-56213200	Strong transcription	Adipose Nuclei	Adipose
18	chr19:56193200-56214000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr19:56193600-56213200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr19:56193800-56212000	Weak transcription	HSMM	muscle
21	chr19:56195000-56212400	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr19:56195400-56217600	Weak transcription	Right Atrium	heart
23	chr19:56197600-56212600	Strong transcription	Lung	lung
24	chr19:56197800-56212400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr19:56199000-56212400	Strong transcription	Liver	Liver
26	chr19:56199200-56210800	Strong transcription	Pancreas	Pancrea
27	chr19:56199200-56214600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr19:56199600-56213200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr19:56199800-56210600	Strong transcription	Right Ventricle	heart
30	chr19:56199800-56212400	Strong transcription	Aorta	Aorta
31	chr19:56200000-56212400	Strong transcription	Duodenum Smooth Muscle	Duodenum
32	chr19:56200000-56212600	Strong transcription	Stomach Smooth Muscle	stomach
33	chr19:56200000-56213200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr19:56200000-56216000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:56200200-56210800	Strong transcription	Brain Inferior Temporal Lobe	brain
36	chr19:56200400-56212600	Strong transcription	Esophagus	oesophagus
37	chr19:56200600-56212200	Strong transcription	Gastric	stomach
38	chr19:56200600-56212600	Strong transcription	Fetal Stomach	stomach
39	chr19:56200800-56212600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr19:56200800-56212600	Strong transcription	Placenta	Placenta
41	chr19:56200800-56212600	Strong transcription	Ovary	ovary
42	chr19:56201000-56213000	Weak transcription	K562	blood
43	chr19:56201400-56212200	Strong transcription	Duodenum Mucosa	Duodenum
44	chr19:56201400-56212400	Strong transcription	Fetal Muscle Leg	muscle
45	chr19:56201400-56212600	Strong transcription	Fetal Muscle Trunk	muscle
46	chr19:56201400-56212800	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr19:56202000-56212400	Strong transcription	Colonic Mucosa	Colon
48	chr19:56202000-56212400	Strong transcription	Spleen	Spleen
49	chr19:56202200-56212600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr19:56202400-56213000	Strong transcription	Fetal Intestine Small	intestine

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