Variant report

Variant	nsv1059094
Chromosome Location	chr19:40745377-40758235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:79)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:79 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:40758180-40758330	HCPEpiC	choroid plexus:	n/a	n/a
2	CTCF	chr19:40758160-40758310	A549	lung:	n/a	n/a
3	CTCF	chr19:40758220-40758370	HMEC	breast:	n/a	n/a
4	CTCF	chr19:40758000-40758150	HMEC	breast:	n/a	n/a
5	CTCF	chr19:40751080-40751230	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr19:40758180-40758330	NHEK	skin:	n/a	n/a
7	CTCF	chr19:40758180-40758330	A549	lung:	n/a	n/a
8	CTCF	chr19:40747860-40748010	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr19:40758120-40758270	BE2_C	brain:	n/a	n/a
10	CTCF	chr19:40758220-40758370	HEK293	kidney:	n/a	n/a
11	EBF1	chr19:40746578-40746709	GM12878	blood:	n/a	chr19:40746652-40746663 chr19:40746634-40746645
12	EBF1	chr19:40746542-40746729	GM12878	blood:	n/a	chr19:40746652-40746663 chr19:40746634-40746645
13	FOS	chr19:40747744-40748143	HUVEC	blood vessel:	n/a	n/a
14	GABPA	chr19:40754623-40755001	Hela-S3	cervix:	n/a	n/a
15	GATA2	chr19:40747733-40748176	HUVEC	blood vessel:	n/a	chr19:40748095-40748105
16	GATA2	chr19:40751413-40751615	SH-SY5Y	brain:	n/a	chr19:40751452-40751462
17	GATA3	chr19:40755611-40756165	MCF-7	breast:	n/a	n/a
18	GATA3	chr19:40758222-40758621	T-47D	breast:	n/a	n/a
19	HMGN3	chr19:40748477-40748488	K562	blood:	n/a	n/a
20	IRF4	chr19:40754653-40754954	GM12878	blood:	n/a	n/a
21	IRF4	chr19:40754550-40755071	GM12878	blood:	n/a	n/a
22	MAFF	chr19:40752226-40752549	HepG2	liver:	n/a	chr19:40752382-40752400
23	MAFF	chr19:40752243-40752572	K562	blood:	n/a	chr19:40752382-40752400
24	MAFK	chr19:40752231-40752567	HepG2	liver:	n/a	chr19:40752384-40752395 chr19:40752384-40752395 chr19:40752385-40752396 chr19:40752384-40752399 chr19:40752383-40752397
25	MAFK	chr19:40752344-40752497	Hela-S3	cervix:	n/a	chr19:40752384-40752395 chr19:40752384-40752395 chr19:40752385-40752396 chr19:40752384-40752399 chr19:40752383-40752397
26	MAFK	chr19:40752316-40752537	K562	blood:	n/a	chr19:40752384-40752395 chr19:40752384-40752395 chr19:40752385-40752396 chr19:40752384-40752399 chr19:40752383-40752397
27	MAFK	chr19:40752211-40752569	HepG2	liver:	n/a	chr19:40752384-40752395 chr19:40752384-40752395 chr19:40752385-40752396 chr19:40752384-40752399 chr19:40752383-40752397
28	MAFK	chr19:40752268-40752549	IMR90	lung:	n/a	chr19:40752384-40752395 chr19:40752384-40752395 chr19:40752385-40752396 chr19:40752384-40752399 chr19:40752383-40752397
29	MAX	chr19:40755609-40756168	MCF-7	breast:	n/a	n/a
30	MYC	chr19:40755715-40756070	MCF-7	breast:	n/a	n/a
31	MYC	chr19:40755736-40756062	MCF-7	breast:	n/a	n/a
32	MYC	chr19:40746781-40746832	HUVEC	blood vessel:	n/a	n/a
33	MYC	chr19:40747747-40748034	HUVEC	blood vessel:	n/a	n/a
34	MYC	chr19:40755829-40755850	MCF-7	breast:	n/a	n/a
35	MYC	chr19:40755817-40755827	MCF-7	breast:	n/a	n/a
36	MYC	chr19:40755744-40755917	MCF-7	breast:	n/a	n/a
37	NFIC	chr19:40758200-40758867	ECC-1	luminal epithelium:	n/a	n/a
38	NR3C1	chr19:40754506-40755076	A549	lung:	n/a	n/a
39	PAX5	chr19:40754522-40755175	GM12878	blood:	n/a	n/a
40	POLR2A	chr19:40753816-40754037	GM12878	blood:	n/a	n/a
41	POLR2A	chr19:40747550-40748176	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr19:40754443-40755181	GM12878	blood:	n/a	n/a
43	POLR2A	chr19:40731149-40781638	PANC-1	pancreas:	n/a	n/a
44	POLR2A	chr19:40747717-40747997	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr19:40747164-40747171	K562	blood:	n/a	n/a
46	POLR2A	chr19:40754424-40755149	GM12892	blood:	n/a	n/a
47	POLR2A	chr19:40754578-40755035	GM12878	blood:	n/a	n/a
48	POLR2A	chr19:40745821-40745926	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr19:40746231-40746521	K562	blood:	n/a	n/a
50	POLR2A	chr19:40747751-40748169	PFSK-1	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40751858-40751908	NHDF-neo	bronchial:	n/a
2	chr19:40751858-40751908	HMEC	breast:	n/a
3	chr19:40751858-40751908	GM12892	blood:	n/a
4	chr19:40751858-40751908	CMK	blood:	n/a
5	chr19:40751858-40751908	HCT-116	colon:	n/a
6	chr19:40751858-40751908	Jurkat	blood:	n/a
7	chr19:40751858-40751908	HEEpiC	esophagus:	n/a
8	chr19:40751858-40751908	BE2_C	brain:	n/a
9	chr19:40751858-40751908	SK-N-SH	brain:	n/a
10	chr19:40751858-40751908	AG04450	lung:	fetal
11	chr19:40751858-40751908	Hela-S3	cervix:	n/a
12	chr19:40751858-40751908	AG04449	skin:	fetal
13	chr19:40751858-40751908	HCF	heart:	n/a
14	chr19:40751858-40751908	HRPEpiC	eye:	n/a
15	chr19:40751858-40751908	HepG2	liver:	n/a
16	chr19:40751858-40751908	HNPCEpiC	eye:	n/a
17	chr19:40751858-40751908	BJ	skin:	n/a
18	chr19:40751858-40751908	H1-hESC	embryonic stem cell:	embryo
19	chr19:40751858-40751908	K562	blood:	n/a
20	chr19:40751858-40751908	Hepatocyte	liver:	n/a
21	chr19:40751858-40751908	GM12878	blood:	n/a
22	chr19:40751858-40751908	NT2-D1	testis:	n/a
23	chr19:40751858-40751908	SAEC	small airway:	n/a
24	chr19:40751858-40751908	PANC-1	pancreas:	n/a
25	chr19:40751858-40751908	Caco-2	colon:	n/a
26	chr19:40751858-40751908	SK-N-SH_RA	brain:	n/a
27	chr19:40751858-40751908	IMR90	lung:	fetal
28	chr19:40751858-40751908	HPAEpiC	pulmonary alveolar:	n/a
29	chr19:40751858-40751908	GM12891	blood:	n/a
30	chr19:40751858-40751908	HUVEC	blood vessel:	n/a
31	chr19:40751858-40751908	GM06990	blood:	n/a
32	chr19:40751858-40751908	HCM	heart:	n/a
33	chr19:40751858-40751908	LNCaP	prostate:	n/a
34	chr19:40751858-40751908	RPTEC	kidney:	n/a
35	chr19:40751858-40751908	AG09319	gingival:	n/a
36	chr19:40751858-40751908	T-47D	breast:	n/a
37	chr19:40751858-40751908	PFSK-1	brain:	n/a
38	chr19:40751858-40751908	ProgFib	skin:	n/a
39	chr19:40751858-40751908	AG09309	skin:	n/a
40	chr19:40751858-40751908	NB4	blood:	n/a
41	chr19:40751858-40751908	HIPEpiC	eye:	n/a
42	chr19:40751858-40751908	U87	brain:	n/a
43	chr19:40751858-40751908	HEK293	kidney:	embryo
44	chr19:40751858-40751908	MCF-7	breast:	n/a
45	chr19:40751858-40751908	NH-A	brain:	n/a
46	chr19:40751858-40751908	HCPEpiC	choroid plexus:	n/a
47	chr19:40751858-40751908	HRE	kidney:	n/a
48	chr19:40751858-40751908	HAEpiC	amniotic membrane:	n/a
49	chr19:40751858-40751908	PrEC	prostate:	n/a
50	chr19:40751858-40751908	NHBE	bronchial:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40757637..40759923-chr19:40784996..40787780,2	K562	blood:
2	chr19:40746507..40749034-chr19:40749901..40751932,2	K562	blood:
3	chr19:40730457..40732107-chr19:40746793..40748406,2	MCF-7	breast:
4	chr19:40753793..40756540-chr19:40760904..40762760,3	K562	blood:
5	chr19:40757204..40758764-chr19:40774239..40776253,2	K562	blood:
6	chr19:40746123..40749034-chr19:40749509..40752053,3	K562	blood:
7	chr19:40746507..40749034-chr19:40749901..40751932,2	K562	blood:
8	chr19:40732755..40733312-chr19:40755398..40756094,2	MCF-7	breast:
9	chr19:40742212..40745152-chr19:40750527..40752389,2	MCF-7	breast:
10	chr19:40754146..40755800-chr19:40763608..40765954,2	K562	blood:
11	chr19:40735147..40737446-chr19:40752058..40754215,2	MCF-7	breast:
12	chr19:40749209..40752062-chr19:40757715..40759395,2	K562	blood:
13	chr19:40746123..40749034-chr19:40749509..40752053,3	K562	blood:
14	chr19:40746630..40748490-chr19:40790537..40793116,2	MCF-7	breast:
15	chr19:40752594..40756116-chr19:40758257..40762594,4	K562	blood:
16	chr19:40736321..40741961-chr19:40743077..40747922,9	K562	blood:

No data

Variant related genes	Relation type
AKT2	TF binding region
AKT2	CpG island
ENSG00000105221	chromatin interactions
ENSG00000105219	chromatin interactions

Extended variants
information (count: 448 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190750610	chr19:40745402-40745403	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs149420215	chr19:40745417-40745418	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs556084970	chr19:40745436-40745437	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577404981	chr19:40745440-40745441	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144848866	chr19:40745447-40745448	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538951106	chr19:40745540-40745541	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs148132838	chr19:40745546-40745547	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs142934627	chr19:40745581-40745582	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540731003	chr19:40745639-40745640	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs561888227	chr19:40745646-40745647	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs184173571	chr19:40745698-40745699	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371852405	chr19:40745722-40745723	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs544914914	chr19:40745740-40745741	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs563211543	chr19:40745771-40745772	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551301156	chr19:40745772-40745773	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs56245956	chr19:40745778-40745779	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560751036	chr19:40745843-40745844	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527353928	chr19:40745844-40745845	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528488515	chr19:40745885-40745886	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs375236349	chr19:40745906-40745907	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs566917128	chr19:40745914-40745915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12980468	chr19:40745923-40745924	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs367714258	chr19:40745941-40745942	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs35817154	chr19:40745968-40745969	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549648922	chr19:40745971-40745972	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs571234560	chr19:40745985-40745986	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs538944575	chr19:40745994-40745995	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371943261	chr19:40745999-40746000	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs553646470	chr19:40746032-40746033	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536203851	chr19:40746033-40746034	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545754921	chr19:40746039-40746040	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs193200414	chr19:40746072-40746073	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555870471	chr19:40746080-40746081	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs574069264	chr19:40746106-40746107	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140072476	chr19:40746235-40746236	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562894145	chr19:40746257-40746258	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs578240866	chr19:40746277-40746278	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143744952	chr19:40746326-40746327	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560431977	chr19:40746400-40746401	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527930463	chr19:40746417-40746418	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146288687	chr19:40746423-40746424	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs139257531	chr19:40746430-40746431	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149948043	chr19:40746620-40746621	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs182954706	chr19:40746637-40746638	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187008970	chr19:40746677-40746678	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs548486162	chr19:40746683-40746684	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs113908342	chr19:40746697-40746698	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs77270135	chr19:40746700-40746701	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538511726	chr19:40746733-40746734	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs145112246	chr19:40746842-40746843	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Lung cancer	21569311	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
Anaplastic thyroid cancer	18753363	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40732800-40759000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr19:40735600-40757600	Weak transcription	Stomach Mucosa	stomach
3	chr19:40735800-40748200	Weak transcription	Psoas Muscle	Psoas
4	chr19:40737600-40748600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr19:40737600-40749600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:40737600-40751200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:40738000-40746600	Strong transcription	Ovary	ovary
8	chr19:40738000-40747000	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr19:40738000-40748600	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr19:40738000-40748800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:40738000-40749000	Strong transcription	Thymus	Thymus
12	chr19:40738000-40751600	Strong transcription	Dnd41	blood
13	chr19:40738000-40763800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr19:40738200-40748200	Strong transcription	Pancreas	Pancrea
15	chr19:40738200-40748600	Strong transcription	NHLF	lung
16	chr19:40738200-40748800	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr19:40738200-40749000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:40738200-40756200	Strong transcription	Primary B cells from peripheral blood	blood
19	chr19:40738400-40746800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr19:40738400-40749400	Strong transcription	Fetal Thymus	thymus
21	chr19:40738400-40749600	Strong transcription	Fetal Brain Female	brain
22	chr19:40738600-40747200	Strong transcription	Brain Cingulate Gyrus	brain
23	chr19:40738600-40747200	Strong transcription	Skeletal Muscle Male	skeletal muscle
24	chr19:40738600-40747600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr19:40738600-40747600	Strong transcription	Lung	lung
26	chr19:40738600-40748600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr19:40738800-40747200	Strong transcription	Brain Hippocampus Middle	brain
28	chr19:40738800-40747600	Weak transcription	Right Atrium	heart
29	chr19:40738800-40748400	Strong transcription	Colonic Mucosa	Colon
30	chr19:40738800-40748600	Strong transcription	Duodenum Mucosa	Duodenum
31	chr19:40738800-40748800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr19:40738800-40749600	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr19:40738800-40750800	Weak transcription	Fetal Heart	heart
34	chr19:40738800-40758000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr19:40739000-40746400	Strong transcription	Brain Angular Gyrus	brain
36	chr19:40739000-40747400	Strong transcription	Right Ventricle	heart
37	chr19:40739000-40747600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr19:40739000-40747600	Strong transcription	Brain Germinal Matrix	brain
39	chr19:40739000-40747600	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr19:40739000-40747600	Strong transcription	Stomach Smooth Muscle	stomach
41	chr19:40739000-40748000	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr19:40739000-40748600	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr19:40739000-40748600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr19:40739000-40748600	Strong transcription	Gastric	stomach
45	chr19:40739000-40749000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr19:40739000-40749400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr19:40739000-40751200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr19:40739200-40747200	Strong transcription	Adipose Nuclei	Adipose
49	chr19:40739200-40747400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr19:40739200-40747600	Strong transcription	Esophagus	oesophagus

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