Variant report

Variant	nsv960852
Chromosome Location	chr19:44890187-44921203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:984)
CpG islands
(count:671)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:44917786-44917800	K562	blood:	n/a	n/a
2	ATF1	chr19:44905595-44905930	K562	blood:	n/a	n/a
3	BACH1	chr19:44917598-44917627	K562	blood:	n/a	n/a
4	BATF	chr19:44914516-44914833	GM12878	blood:	n/a	n/a
5	BATF	chr19:44916806-44917020	GM12878	blood:	n/a	n/a
6	BATF	chr19:44914833-44915116	GM12878	blood:	n/a	n/a
7	BATF	chr19:44913634-44913897	GM12878	blood:	n/a	n/a
8	BATF	chr19:44918320-44918533	GM12878	blood:	n/a	n/a
9	BATF	chr19:44918337-44918531	GM12878	blood:	n/a	n/a
10	BATF	chr19:44919764-44919964	GM12878	blood:	n/a	n/a
11	BATF	chr19:44919178-44919458	GM12878	blood:	n/a	n/a
12	BATF	chr19:44913944-44914161	GM12878	blood:	n/a	n/a
13	BATF	chr19:44914580-44914824	GM12878	blood:	n/a	n/a
14	BATF	chr19:44914883-44915105	GM12878	blood:	n/a	n/a
15	BATF	chr19:44915147-44915853	GM12878	blood:	n/a	n/a
16	BATF	chr19:44919486-44919761	GM12878	blood:	n/a	n/a
17	BATF	chr19:44919536-44919764	GM12878	blood:	n/a	n/a
18	BATF	chr19:44913406-44913874	GM12878	blood:	n/a	n/a
19	BATF	chr19:44920132-44920324	GM12878	blood:	n/a	n/a
20	BATF	chr19:44915179-44915853	GM12878	blood:	n/a	n/a
21	BATF	chr19:44913939-44914167	GM12878	blood:	n/a	n/a
22	BATF	chr19:44913233-44913633	GM12878	blood:	n/a	n/a
23	BATF	chr19:44919167-44919405	GM12878	blood:	n/a	n/a
24	BATF	chr19:44917710-44918004	GM12878	blood:	n/a	n/a
25	BATF	chr19:44916804-44917060	GM12878	blood:	n/a	n/a
26	BCL11A	chr19:44914575-44914771	GM12878	blood:	n/a	n/a
27	BCL11A	chr19:44919484-44919989	GM12878	blood:	n/a	chr19:44919790-44919803
28	BCL11A	chr19:44917393-44917936	GM12878	blood:	n/a	n/a
29	BCL11A	chr19:44917718-44917903	GM12878	blood:	n/a	n/a
30	BCL11A	chr19:44920063-44920223	GM12878	blood:	n/a	n/a
31	BCL11A	chr19:44913357-44913876	GM12878	blood:	n/a	chr19:44913660-44913673
32	BCL11A	chr19:44918592-44918826	GM12878	blood:	n/a	n/a
33	BCL11A	chr19:44919161-44919353	GM12878	blood:	n/a	n/a
34	BCL11A	chr19:44914495-44914790	GM12878	blood:	n/a	n/a
35	BCL11A	chr19:44920248-44920439	GM12878	blood:	n/a	n/a
36	BCL11A	chr19:44918716-44919121	GM12878	blood:	n/a	n/a
37	BCL11A	chr19:44919508-44919981	GM12878	blood:	n/a	chr19:44919790-44919803
38	BCL11A	chr19:44915170-44915853	GM12878	blood:	n/a	n/a
39	BCL11A	chr19:44917413-44917654	GM12878	blood:	n/a	n/a
40	BCL11A	chr19:44913354-44913935	GM12878	blood:	n/a	chr19:44913660-44913673
41	BCL11A	chr19:44914264-44914471	GM12878	blood:	n/a	n/a
42	BCL11A	chr19:44914858-44915113	GM12878	blood:	n/a	n/a
43	BCL11A	chr19:44913947-44914143	GM12878	blood:	n/a	n/a
44	BCL11A	chr19:44916811-44917069	GM12878	blood:	n/a	n/a
45	BCL11A	chr19:44918909-44919142	GM12878	blood:	n/a	n/a
46	BCL11A	chr19:44919195-44919440	GM12878	blood:	n/a	n/a
47	BCL11A	chr19:44915158-44915851	GM12878	blood:	n/a	n/a
48	BCL11A	chr19:44914868-44915122	GM12878	blood:	n/a	n/a
49	BHLHE40	chr19:44917608-44917921	HepG2	liver:	n/a	n/a
50	BHLHE40	chr19:44920065-44920460	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:44905343-44905393	ProgFib	skin:	n/a
2	chr19:44905980-44906030	AoSMC	blood vessel:	n/a
3	chr19:44905980-44906030	ProgFib	skin:	n/a
4	chr19:44905782-44905832	K562	blood:	n/a
5	chr19:44906522-44906572	AoSMC	blood vessel:	n/a
6	chr19:44905782-44905832	H1-hESC	embryonic stem cell:	embryo
7	chr19:44906522-44906572	HRCEpiC	kidney:	n/a
8	chr19:44905343-44905393	BJ	skin:	n/a
9	chr19:44905980-44906030	RPTEC	kidney:	n/a
10	chr19:44890183-44890233	MCF-7	breast:	n/a
11	chr19:44905782-44905832	HAEpiC	amniotic membrane:	n/a
12	chr19:44905980-44906030	AG04449	skin:	fetal
13	chr19:44905980-44906030	GM12878	blood:	n/a
14	chr19:44906522-44906572	NH-A	brain:	n/a
15	chr19:44890183-44890233	PrEC	prostate:	n/a
16	chr19:44890183-44890233	MCF10A-Er-Src	breast:	n/a
17	chr19:44905782-44905832	BE2_C	brain:	n/a
18	chr19:44905782-44905832	AoSMC	blood vessel:	n/a
19	chr19:44905828-44905878	HRCEpiC	kidney:	n/a
20	chr19:44890183-44890233	BE2_C	brain:	n/a
21	chr19:44905782-44905832	HPAEpiC	pulmonary alveolar:	n/a
22	chr19:44905828-44905878	HCF	heart:	n/a
23	chr19:44905788-44905838	Jurkat	blood:	n/a
24	chr19:44905882-44905932	HIPEpiC	eye:	n/a
25	chr19:44905782-44905832	HepG2	liver:	n/a
26	chr19:44906522-44906572	HAEpiC	amniotic membrane:	n/a
27	chr19:44905343-44905393	BE2_C	brain:	n/a
28	chr19:44905916-44905966	MCF-7	breast:	n/a
29	chr19:44905882-44905932	Jurkat	blood:	n/a
30	chr19:44905882-44905932	RPTEC	kidney:	n/a
31	chr19:44905980-44906030	HUVEC	blood vessel:	n/a
32	chr19:44905980-44906030	HRCEpiC	kidney:	n/a
33	chr19:44906522-44906572	HNPCEpiC	eye:	n/a
34	chr19:44905828-44905878	HPAEpiC	pulmonary alveolar:	n/a
35	chr19:44905916-44905966	NHBE	bronchial:	n/a
36	chr19:44905788-44905838	SAEC	small airway:	n/a
37	chr19:44905882-44905932	ECC-1	luminal epithelium:	n/a
38	chr19:44905343-44905393	AoSMC	blood vessel:	n/a
39	chr19:44905830-44905880	RPTEC	kidney:	n/a
40	chr19:44891400-44891450	HCF	heart:	n/a
41	chr19:44905830-44905880	AG10803	skin:	n/a
42	chr19:44906522-44906572	SAEC	small airway:	n/a
43	chr19:44905828-44905878	HepG2	liver:	n/a
44	chr19:44905788-44905838	BJ	skin:	n/a
45	chr19:44905830-44905880	HNPCEpiC	eye:	n/a
46	chr19:44905882-44905932	SK-N-MC	brain:	n/a
47	chr19:44905788-44905838	GM12878	blood:	n/a
48	chr19:44905882-44905932	AG10803	skin:	n/a
49	chr19:44905980-44906030	HIPEpiC	eye:	n/a
50	chr19:44905828-44905878	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:44895650..44897507-chr2:133068550..133071124,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF229-1	chr19:44905734-44905767	NONHSAT066696
2	lnc-ZNF229-1	chr19:44901364-44901421	ENSG00000267188.1
3	lnc-ZNF229-1	chr19:44896603-44896630	ENSG00000267188.1
4	lnc-ZNF229-1	chr19:44900827-44901421	NONHSAT066696

No data

Variant related genes	Relation type
ENSG00000267173	TF binding region
ZNF285	TF binding region
ENSG00000267173	CpG island
ZNF285	CpG island

Extended variants
information (count: 1887 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1887 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10409019	chr19:44890200-44890201	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs180853730	chr19:44890240-44890241	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569531714	chr19:44890266-44890267	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186080034	chr19:44890268-44890269	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558931318	chr19:44890275-44890276	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141320090	chr19:44890288-44890289	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535040997	chr19:44890340-44890341	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191325992	chr19:44890442-44890443	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574760693	chr19:44890447-44890448	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537048833	chr19:44890464-44890465	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146849454	chr19:44890487-44890488	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576966217	chr19:44890503-44890504	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546277397	chr19:44890518-44890519	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182847893	chr19:44890519-44890520	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568721073	chr19:44890521-44890522	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540835537	chr19:44890527-44890528	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561189319	chr19:44890545-44890546	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537018592	chr19:44890547-44890548	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549812630	chr19:44890548-44890549	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563268816	chr19:44890559-44890560	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57875747	chr19:44890569-44890570	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367713759	chr19:44890597-44890598	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371234807	chr19:44890608-44890609	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs535239931	chr19:44890618-44890619	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs548325464	chr19:44890625-44890626	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs549713544	chr19:44890631-44890632	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs138364822	chr19:44890652-44890653	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs149238831	chr19:44890654-44890655	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs150036734	chr19:44890662-44890663	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs145386319	chr19:44890671-44890672	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs148795043	chr19:44890674-44890675	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs73039936	chr19:44890685-44890686	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs147871364	chr19:44890689-44890690	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs1836280	chr19:44890697-44890698	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs369315997	chr19:44890699-44890700	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs147054008	chr19:44890722-44890723	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs151063377	chr19:44890727-44890728	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs376214387	chr19:44890738-44890739	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs573229458	chr19:44890752-44890753	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs541224546	chr19:44890783-44890784	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs561026253	chr19:44890788-44890789	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs12610859	chr19:44890801-44890802	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs543718218	chr19:44890810-44890811	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs73039937	chr19:44890817-44890818	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs369555191	chr19:44890822-44890823	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs138614800	chr19:44890824-44890825	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs148896964	chr19:44890825-44890826	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs372788610	chr19:44890839-44890840	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs59953894	chr19:44890841-44890842	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138001522	chr19:44890848-44890849	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	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
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
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44886400-44890400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr19:44887800-44890200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr19:44888200-44893800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr19:44888200-44904800	Weak transcription	Fetal Brain Male	brain
5	chr19:44888400-44890400	Weak transcription	Brain Anterior Caudate	brain
6	chr19:44888400-44891000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr19:44888600-44890400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr19:44888600-44893800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr19:44888800-44890400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr19:44889000-44890400	Weak transcription	Brain Substantia Nigra	brain
11	chr19:44889000-44893800	Weak transcription	Fetal Intestine Large	intestine
12	chr19:44889000-44894000	Weak transcription	Fetal Stomach	stomach
13	chr19:44889000-44905000	Weak transcription	Right Ventricle	heart
14	chr19:44889200-44890400	Weak transcription	Pancreas	Pancrea
15	chr19:44889200-44890800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr19:44889200-44893000	Weak transcription	Fetal Heart	heart
17	chr19:44889200-44896200	Strong transcription	Skeletal Muscle Female	skeletal muscle
18	chr19:44889400-44892000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:44889600-44890800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
20	chr19:44889600-44892400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr19:44889600-44892600	Strong transcription	Brain Hippocampus Middle	brain
22	chr19:44889600-44892600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
23	chr19:44889600-44896800	Strong transcription	Fetal Brain Female	brain
24	chr19:44889600-44897600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
25	chr19:44889600-44899600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:44889800-44890400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr19:44889800-44890400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:44889800-44890600	ZNF genes & repeats	Left Ventricle	heart
29	chr19:44889800-44891000	ZNF genes & repeats	Primary B cells from cord blood	blood
30	chr19:44889800-44892400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr19:44889800-44892400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr19:44889800-44893000	Strong transcription	Brain Germinal Matrix	brain
33	chr19:44889800-44893600	ZNF genes & repeats	Stomach Smooth Muscle	stomach
34	chr19:44889800-44894600	ZNF genes & repeats	Adipose Nuclei	Adipose
35	chr19:44889800-44897800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr19:44889800-44904800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr19:44890000-44890200	Weak transcription	Primary B cells from peripheral blood	blood
38	chr19:44890000-44891400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
39	chr19:44890000-44891800	ZNF genes & repeats	Aorta	Aorta
40	chr19:44890000-44892600	Strong transcription	Fetal Lung	lung
41	chr19:44890000-44892600	Strong transcription	Fetal Muscle Leg	muscle
42	chr19:44890000-44896200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr19:44890000-44897600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr19:44890200-44890400	ZNF genes & repeats	Primary B cells from peripheral blood	blood
45	chr19:44890200-44894200	Strong transcription	Skeletal Muscle Male	skeletal muscle
46	chr19:44890200-44894400	Weak transcription	Brain Angular Gyrus	brain
47	chr19:44890200-44904800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr19:44890200-44904800	Weak transcription	HSMMtube	muscle
49	chr19:44890400-44890600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
50	chr19:44890400-44890600	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links