Variant report

Variant	nsv960862
Chromosome Location	chr19:52780307-52785546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:52782222-52782242	Kidney_OC	kidney:	n/a	n/a
2	EGR1	chr19:52780851-52781245	MCF-7	breast:	n/a	n/a
3	GATA3	chr19:52780675-52781073	MCF-7	breast:	n/a	n/a
4	GATA3	chr19:52780811-52781078	T-47D	breast:	n/a	n/a
5	GATA3	chr19:52780794-52781038	T-47D	breast:	n/a	n/a
6	MAFK	chr19:52784924-52785432	HepG2	liver:	n/a	chr19:52785256-52785271
7	MAFK	chr19:52785171-52785371	HepG2	liver:	n/a	chr19:52785256-52785271
8	POLR2A	chr19:52784990-52785028	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr19:52780757-52781170	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52785044-52785094	HNPCEpiC	eye:	n/a
2	chr19:52784208-52784258	PrEC	prostate:	n/a
3	chr19:52784799-52784849	RPTEC	kidney:	n/a
4	chr19:52784499-52784549	LNCaP	prostate:	n/a
5	chr19:52785044-52785094	NB4	blood:	n/a
6	chr19:52785044-52785094	GM06990	blood:	n/a
7	chr19:52784493-52784543	HNPCEpiC	eye:	n/a
8	chr19:52785044-52785094	K562	blood:	n/a
9	chr19:52784208-52784258	RPTEC	kidney:	n/a
10	chr19:52784493-52784543	AoSMC	blood vessel:	n/a
11	chr19:52784493-52784543	GM12892	blood:	n/a
12	chr19:52785044-52785094	HCM	heart:	n/a
13	chr19:52784499-52784549	HCPEpiC	choroid plexus:	n/a
14	chr19:52784493-52784543	Jurkat	blood:	n/a
15	chr19:52784493-52784543	HRCEpiC	kidney:	n/a
16	chr19:52785044-52785094	HL-60	blood:	n/a
17	chr19:52784499-52784549	GM12878	blood:	n/a
18	chr19:52784799-52784849	HMEC	breast:	n/a
19	chr19:52784499-52784549	AG10803	skin:	n/a
20	chr19:52784799-52784849	K562	blood:	n/a
21	chr19:52784208-52784258	GM06990	blood:	n/a
22	chr19:52784493-52784543	HL-60	blood:	n/a
23	chr19:52785044-52785094	HUVEC	blood vessel:	n/a
24	chr19:52784208-52784258	NHDF-neo	bronchial:	n/a
25	chr19:52785044-52785094	HepG2	liver:	n/a
26	chr19:52784799-52784849	HEEpiC	esophagus:	n/a
27	chr19:52784493-52784543	HAEpiC	amniotic membrane:	n/a
28	chr19:52784208-52784258	AoSMC	blood vessel:	n/a
29	chr19:52784799-52784849	HRCEpiC	kidney:	n/a
30	chr19:52784499-52784549	AoSMC	blood vessel:	n/a
31	chr19:52785044-52785094	ProgFib	skin:	n/a
32	chr19:52785044-52785094	T-47D	breast:	n/a
33	chr19:52784208-52784258	HL-60	blood:	n/a
34	chr19:52784799-52784849	AG04449	skin:	fetal
35	chr19:52784499-52784549	AG04450	lung:	fetal
36	chr19:52784799-52784849	HUVEC	blood vessel:	n/a
37	chr19:52784499-52784549	HRE	kidney:	n/a
38	chr19:52784493-52784543	HUVEC	blood vessel:	n/a
39	chr19:52784499-52784549	NHBE	bronchial:	n/a
40	chr19:52784208-52784258	Caco-2	colon:	n/a
41	chr19:52784499-52784549	HRCEpiC	kidney:	n/a
42	chr19:52784499-52784549	HCM	heart:	n/a
43	chr19:52784499-52784549	HEK293	kidney:	embryo
44	chr19:52784493-52784543	Hepatocyte	liver:	n/a
45	chr19:52784493-52784543	PrEC	prostate:	n/a
46	chr19:52784493-52784543	NHDF-neo	bronchial:	n/a
47	chr19:52785044-52785094	GM12892	blood:	n/a
48	chr19:52784493-52784543	HPAEpiC	pulmonary alveolar:	n/a
49	chr19:52784493-52784543	HepG2	liver:	n/a
50	chr19:52784208-52784258	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:52772381..52778282-chr19:52778346..52783668,9	MCF-7	breast:
2	chr19:52785054..52786730-chr19:52799548..52801904,2	K562	blood:
3	chr19:52772026..52776261-chr19:52781637..52786393,5	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-643	chr19:52785110-52785131	MIMAT0003313

No data

Variant related genes	Relation type
MIR643	TF binding region
ZNF766	TF binding region
MIR643	CpG island
ZNF766	CpG island
ENSG00000269102	chromatin interactions
ENSG00000198464	chromatin interactions
ENSG00000196214	chromatin interactions

Extended variants
information (count: 232 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:232 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527237938	chr19:52780319-52780320	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551776419	chr19:52780337-52780338	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558637948	chr19:52780390-52780391	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144421672	chr19:52780434-52780435	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182014190	chr19:52780435-52780436	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187116483	chr19:52780437-52780438	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568244132	chr19:52780438-52780439	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs62110400	chr19:52780439-52780440	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191543536	chr19:52780441-52780442	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566066463	chr19:52780450-52780451	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573378793	chr19:52780451-52780452	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183450932	chr19:52780461-52780462	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs372493852	chr19:52780504-52780505	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534776170	chr19:52780528-52780529	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544870425	chr19:52780545-52780546	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs147815149	chr19:52780550-52780551	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574933785	chr19:52780576-52780577	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185543087	chr19:52780580-52780581	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542057241	chr19:52780636-52780637	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559784833	chr19:52780698-52780699	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189906816	chr19:52780706-52780707	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577345037	chr19:52780711-52780712	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs79554348	chr19:52780712-52780713	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs76855708	chr19:52780713-52780714	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs551886329	chr19:52780720-52780721	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538474785	chr19:52780743-52780744	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs376859755	chr19:52780756-52780757	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563715631	chr19:52780758-52780759	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542307851	chr19:52780789-52780790	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs368703702	chr19:52780790-52780791	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141669779	chr19:52780793-52780794	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs147057284	chr19:52780798-52780799	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568275268	chr19:52780849-52780850	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535590256	chr19:52780854-52780855	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138171032	chr19:52780863-52780864	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566939971	chr19:52780883-52780884	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs115762707	chr19:52780886-52780887	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs116814122	chr19:52780900-52780901	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs570813933	chr19:52780960-52780961	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35307376	chr19:52780968-52780969	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs375190606	chr19:52780971-52780972	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575051040	chr19:52780979-52780980	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs2247844	chr19:52781007-52781008	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553930871	chr19:52781044-52781045	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182162268	chr19:52781059-52781060	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545490257	chr19:52781101-52781102	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs564068605	chr19:52781107-52781108	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs531297049	chr19:52781119-52781120	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543053586	chr19:52781156-52781157	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149136418	chr19:52781159-52781160	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52774000-52786600	Weak transcription	Right Ventricle	heart
2	chr19:52774000-52787200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr19:52774200-52786600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr19:52774200-52797400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:52774200-52799600	Weak transcription	Hela-S3	cervix
6	chr19:52774400-52781000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr19:52774400-52782000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr19:52774400-52786600	Weak transcription	Osteobl	bone
9	chr19:52774400-52787000	Weak transcription	HUVEC	blood vessel
10	chr19:52774400-52787400	Weak transcription	NHDF-Ad	bronchial
11	chr19:52774600-52780400	ZNF genes & repeats	Primary B cells from cord blood	blood
12	chr19:52774600-52781200	ZNF genes & repeats	GM12878-XiMat	blood
13	chr19:52774600-52782000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr19:52774600-52782600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr19:52774600-52783600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr19:52774600-52783800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
17	chr19:52774600-52786400	Weak transcription	Brain Angular Gyrus	brain
18	chr19:52774600-52786600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr19:52774600-52795800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
20	chr19:52774800-52780400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr19:52774800-52782400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:52774800-52786400	Weak transcription	Brain Substantia Nigra	brain
23	chr19:52775000-52785400	Weak transcription	Gastric	stomach
24	chr19:52775000-52786400	Weak transcription	Brain Hippocampus Middle	brain
25	chr19:52775000-52786400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr19:52775000-52787400	Weak transcription	HepG2	liver
27	chr19:52775200-52786600	Weak transcription	Left Ventricle	heart
28	chr19:52775600-52780400	ZNF genes & repeats	Fetal Brain Female	brain
29	chr19:52775600-52781800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
30	chr19:52775600-52782000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
31	chr19:52776000-52783600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr19:52776000-52783800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:52776800-52781400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
34	chr19:52777000-52780400	ZNF genes & repeats	Primary T cells from cord blood	blood
35	chr19:52777000-52782000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr19:52777200-52782800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr19:52777200-52784800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr19:52777200-52787400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr19:52777200-52794000	Weak transcription	Psoas Muscle	Psoas
40	chr19:52777400-52786400	Weak transcription	Small Intestine	intestine
41	chr19:52777400-52787400	Weak transcription	Fetal Brain Male	brain
42	chr19:52777600-52784800	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr19:52777600-52785400	Weak transcription	Adipose Nuclei	Adipose
44	chr19:52777600-52786000	Weak transcription	NH-A	brain
45	chr19:52777600-52786800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr19:52777800-52780400	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr19:52777800-52780800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr19:52777800-52785400	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr19:52777800-52785600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr19:52777800-52785800	Weak transcription	K562	blood

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