Variant report

Variant	nsv1058747
Chromosome Location	chr19:41334726-41376007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:565)
CpG islands
(count:305)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41337675-41338160	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41370633-41370945	K562	blood:	n/a	n/a
3	ATF1	chr19:41339642-41339915	K562	blood:	n/a	n/a
4	ATF1	chr19:41370536-41370948	K562	blood:	n/a	n/a
5	ATF3	chr19:41339265-41339474	K562	blood:	n/a	n/a
6	ATF3	chr19:41370620-41370877	K562	blood:	n/a	n/a
7	ATF3	chr19:41337642-41338304	A549	lung:	n/a	n/a
8	ATF3	chr19:41339727-41339986	K562	blood:	n/a	n/a
9	BCL3	chr19:41337399-41338400	A549	lung:	n/a	n/a
10	BCL3	chr19:41337271-41338291	A549	lung:	n/a	n/a
11	BHLHE40	chr19:41337782-41338177	HepG2	liver:	n/a	chr19:41337896-41337917
12	BHLHE40	chr19:41339267-41339464	K562	blood:	n/a	n/a
13	BHLHE40	chr19:41337685-41338115	K562	blood:	n/a	chr19:41337896-41337917
14	BHLHE40	chr19:41339813-41339844	K562	blood:	n/a	n/a
15	BHLHE40	chr19:41337763-41338048	HepG2	liver:	n/a	chr19:41337896-41337917
16	BHLHE40	chr19:41337595-41338254	HepG2	liver:	n/a	chr19:41337896-41337917
17	BHLHE40	chr19:41337704-41338087	A549	lung:	n/a	chr19:41337896-41337917
18	BRCA1	chr19:41337806-41338121	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr19:41349182-41350047	K562	blood:	n/a	n/a
20	CBX3	chr19:41339143-41339980	K562	blood:	n/a	n/a
21	CBX3	chr19:41370123-41371107	K562	blood:	n/a	n/a
22	CBX3	chr19:41347938-41348304	K562	blood:	n/a	n/a
23	CBX3	chr19:41347915-41348277	K562	blood:	n/a	n/a
24	CBX3	chr19:41337733-41338384	K562	blood:	n/a	n/a
25	CCNT2	chr19:41339675-41339875	K562	blood:	n/a	n/a
26	CCNT2	chr19:41370582-41370786	K562	blood:	n/a	n/a
27	CEBPB	chr19:41342862-41343338	A549	lung:	n/a	chr19:41343121-41343132
28	CEBPB	chr19:41337591-41338310	A549	lung:	n/a	n/a
29	CEBPB	chr19:41337501-41338297	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr19:41337708-41338253	MCF-7	breast:	n/a	n/a
31	CEBPB	chr19:41343053-41343247	H1-hESC	embryonic stem cell:	n/a	chr19:41343121-41343132
32	CEBPB	chr19:41370209-41371189	K562	blood:	n/a	chr19:41370433-41370441
33	CEBPB	chr19:41368480-41368982	A549	lung:	n/a	n/a
34	CEBPB	chr19:41368416-41368601	K562	blood:	n/a	n/a
35	CEBPB	chr19:41370543-41370910	K562	blood:	n/a	n/a
36	CEBPB	chr19:41337826-41338039	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:41373834-41374300	A549	lung:	n/a	n/a
38	CEBPB	chr19:41337684-41338241	A549	lung:	n/a	n/a
39	CEBPB	chr19:41368761-41369068	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:41367289-41367476	A549	lung:	n/a	n/a
41	CEBPB	chr19:41337608-41337699	K562	blood:	n/a	n/a
42	CEBPB	chr19:41334846-41335144	A549	lung:	n/a	chr19:41334912-41334923
43	CEBPB	chr19:41373920-41374208	K562	blood:	n/a	n/a
44	CEBPB	chr19:41362024-41362201	K562	blood:	n/a	n/a
45	CEBPB	chr19:41337619-41338177	A549	lung:	n/a	n/a
46	CEBPB	chr19:41337713-41338232	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:41343011-41343287	HepG2	liver:	n/a	chr19:41343121-41343132
48	CEBPB	chr19:41339359-41340046	K562	blood:	n/a	chr19:41339540-41339548
49	CEBPB	chr19:41337605-41338263	MCF-7	breast:	n/a	n/a
50	CEBPB	chr19:41343006-41343268	IMR90	lung:	n/a	chr19:41343121-41343132

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41355973-41356023	HIPEpiC	eye:	n/a
2	chr19:41354682-41354732	ProgFib	skin:	n/a
3	chr19:41354553-41354603	PFSK-1	brain:	n/a
4	chr19:41354142-41354192	MCF10A-Er-Src	breast:	n/a
5	chr19:41354553-41354603	HCM	heart:	n/a
6	chr19:41354682-41354732	K562	blood:	n/a
7	chr19:41354142-41354192	PANC-1	pancreas:	n/a
8	chr19:41355973-41356023	SAEC	small airway:	n/a
9	chr19:41354142-41354192	SAEC	small airway:	n/a
10	chr19:41354553-41354603	AG09309	skin:	n/a
11	chr19:41354553-41354603	SK-N-SH	brain:	n/a
12	chr19:41354142-41354192	HCT-116	colon:	n/a
13	chr19:41354553-41354603	H1-hESC	embryonic stem cell:	embryo
14	chr19:41354142-41354192	RPTEC	kidney:	n/a
15	chr19:41351924-41351974	GM12891	blood:	n/a
16	chr19:41354553-41354603	SK-N-MC	brain:	n/a
17	chr19:41354142-41354192	HRE	kidney:	n/a
18	chr19:41351924-41351974	HUVEC	blood vessel:	n/a
19	chr19:41354142-41354192	HUVEC	blood vessel:	n/a
20	chr19:41351924-41351974	RPTEC	kidney:	n/a
21	chr19:41354142-41354192	HL-60	blood:	n/a
22	chr19:41355973-41356023	HAEpiC	amniotic membrane:	n/a
23	chr19:41351924-41351974	HRE	kidney:	n/a
24	chr19:41354553-41354603	ovcar-3	ovarian:	n/a
25	chr19:41354142-41354192	HNPCEpiC	eye:	n/a
26	chr19:41355973-41356023	RPTEC	kidney:	n/a
27	chr19:41354142-41354192	HCM	heart:	n/a
28	chr19:41351924-41351974	BJ	skin:	n/a
29	chr19:41354682-41354732	HRPEpiC	eye:	n/a
30	chr19:41354553-41354603	GM12891	blood:	n/a
31	chr19:41354553-41354603	A549	lung:	n/a
32	chr19:41354142-41354192	HEEpiC	esophagus:	n/a
33	chr19:41354553-41354603	GM12878	blood:	n/a
34	chr19:41354142-41354192	AG09309	skin:	n/a
35	chr19:41351924-41351974	T-47D	breast:	n/a
36	chr19:41351924-41351974	PFSK-1	brain:	n/a
37	chr19:41354142-41354192	AG09319	gingival:	n/a
38	chr19:41354553-41354603	NHDF-neo	bronchial:	n/a
39	chr19:41355973-41356023	AoSMC	blood vessel:	n/a
40	chr19:41354682-41354732	PrEC	prostate:	n/a
41	chr19:41354142-41354192	T-47D	breast:	n/a
42	chr19:41354682-41354732	HL-60	blood:	n/a
43	chr19:41354142-41354192	ovcar-3	ovarian:	n/a
44	chr19:41354553-41354603	Hepatocyte	liver:	n/a
45	chr19:41354142-41354192	GM06990	blood:	n/a
46	chr19:41354682-41354732	HCM	heart:	n/a
47	chr19:41354142-41354192	Hela-S3	cervix:	n/a
48	chr19:41354142-41354192	NHDF-neo	bronchial:	n/a
49	chr19:41355973-41356023	T-47D	breast:	n/a
50	chr19:41351924-41351974	HCPEpiC	choroid plexus:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
2	chr19:41309668..41312632-chr19:41335922..41337729,2	MCF-7	breast:
3	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
4	chr19:41168873..41171001-chr19:41337568..41339858,2	MCF-7	breast:
5	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
6	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
7	chr19:41195484..41197379-chr19:41368669..41371255,2	K562	blood:
8	chr16:4474827..4477394-chr19:41351022..41353007,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2A6-1	chr19:41342991-41343115	ENSG00000269843.1
2	lnc-CYP2A6-1	chr19:41337126-41337482	ENSG00000269843.1

No data

Variant related genes	Relation type
ENSG00000269843	TF binding region
CYP2F2P	TF binding region
CYP2A6	TF binding region
ENSG00000269843	CpG island
CYP2F2P	CpG island
CYP2A6	CpG island
ENSG00000105245	chromatin interactions
ENSG00000103423	chromatin interactions
ENSG00000269858	chromatin interactions
ENSG00000262246	chromatin interactions

Extended variants
information (count: 1974 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1974 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563677580	chr19:41334782-41334783	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142135809	chr19:41334786-41334787	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs552893427	chr19:41334807-41334808	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185034796	chr19:41334861-41334862	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs528697878	chr19:41334882-41334883	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs570293120	chr19:41334888-41334889	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs547129468	chr19:41334889-41334890	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs192436678	chr19:41334934-41334935	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs535509493	chr19:41334940-41334941	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs183780316	chr19:41334950-41334951	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs568500103	chr19:41334991-41334992	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539391032	chr19:41335063-41335064	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs7255471	chr19:41335066-41335067	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs150715260	chr19:41335079-41335080	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs139055970	chr19:41335159-41335160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573930024	chr19:41335169-41335170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555503662	chr19:41335175-41335176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574863814	chr19:41335245-41335246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542293865	chr19:41335265-41335266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144002017	chr19:41335269-41335270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368038805	chr19:41335327-41335328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530923805	chr19:41335333-41335334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375543775	chr19:41335386-41335387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs202226624	chr19:41335476-41335477	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs146868784	chr19:41335494-41335495	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564777117	chr19:41335506-41335507	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs117313429	chr19:41335585-41335586	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs546898000	chr19:41335589-41335590	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs568620614	chr19:41335610-41335611	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs571910871	chr19:41335617-41335618	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs140716932	chr19:41335645-41335646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550643650	chr19:41335678-41335679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568561342	chr19:41335696-41335697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539050367	chr19:41335742-41335743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545553605	chr19:41335769-41335770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564116401	chr19:41335778-41335779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144393139	chr19:41335788-41335789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74719953	chr19:41335799-41335800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145373180	chr19:41335818-41335819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187051210	chr19:41335828-41335829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115767583	chr19:41335926-41335927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs377610328	chr19:41336089-41336090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149160241	chr19:41336090-41336091	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572311210	chr19:41336112-41336113	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78929108	chr19:41336171-41336172	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546233185	chr19:41336179-41336180	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs116064259	chr19:41336223-41336224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs561756838	chr19:41336224-41336225	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528824902	chr19:41336227-41336228	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375975761	chr19:41336238-41336239	Weak transcription	Chromatin interactive region	1 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
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
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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	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
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41324800-41337400	Weak transcription	Colonic Mucosa	Colon
2	chr19:41324800-41339200	Weak transcription	Brain Germinal Matrix	brain
3	chr19:41325000-41337400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr19:41325600-41337400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr19:41326000-41339800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr19:41328800-41337400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr19:41329000-41335400	Weak transcription	Fetal Muscle Leg	muscle
8	chr19:41329200-41335000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr19:41329200-41337200	Weak transcription	A549	lung
10	chr19:41330000-41337800	Weak transcription	Colon Smooth Muscle	Colon
11	chr19:41330000-41339800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr19:41330200-41335000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr19:41330200-41349400	Weak transcription	Right Ventricle	heart
14	chr19:41330400-41337200	Weak transcription	HepG2	liver
15	chr19:41331000-41335000	Weak transcription	Lung	lung
16	chr19:41331600-41337800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr19:41331600-41339800	Weak transcription	Fetal Lung	lung
18	chr19:41332600-41335200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:41332600-41335600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr19:41332600-41336200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr19:41332800-41337600	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr19:41333000-41337400	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr19:41333200-41335800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr19:41333200-41337400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr19:41333400-41335000	Weak transcription	Fetal Kidney	kidney
26	chr19:41333400-41335000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr19:41333400-41335200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr19:41333400-41335200	Weak transcription	Primary B cells from cord blood	blood
29	chr19:41333400-41335600	Weak transcription	Esophagus	oesophagus
30	chr19:41333400-41335800	Weak transcription	Dnd41	blood
31	chr19:41333400-41336400	Weak transcription	Fetal Brain Male	brain
32	chr19:41333400-41336800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr19:41333400-41336800	Weak transcription	Brain Anterior Caudate	brain
34	chr19:41333400-41337200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr19:41333400-41337200	Weak transcription	HSMM	muscle
36	chr19:41333400-41337200	Weak transcription	HSMMtube	muscle
37	chr19:41333400-41337200	Weak transcription	NHDF-Ad	bronchial
38	chr19:41333400-41337200	Weak transcription	Osteobl	bone
39	chr19:41333400-41337400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr19:41333400-41337400	Weak transcription	Pancreas	Pancrea
41	chr19:41333400-41337400	Weak transcription	K562	blood
42	chr19:41333400-41337600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:41333400-41337600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr19:41333400-41338000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr19:41333400-41338400	Weak transcription	Primary T cells from cord blood	blood
46	chr19:41333400-41339200	Weak transcription	Brain Angular Gyrus	brain
47	chr19:41333400-41339200	Weak transcription	Brain Substantia Nigra	brain
48	chr19:41333600-41334800	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr19:41333600-41336600	Weak transcription	Ovary	ovary
50	chr19:41333600-41337200	Weak transcription	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links