Variant report

Variant	esv1846322
Chromosome Location	chr19:40350730-40404261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1048)
CpG islands
(count:1650)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1048 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40388564-40388584	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40372209-40372386	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
4	ATF1	chr19:40372283-40372483	K562	blood:	n/a	n/a
5	ATF2	chr19:40372199-40372449	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:40372203-40372491	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr19:40404210-40404647	GM12878	blood:	n/a	chr19:40404401-40404414
8	BCL11A	chr19:40372229-40372663	GM12878	blood:	n/a	chr19:40372417-40372430
9	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:40353783-40353941	K562	blood:	n/a	chr19:40353876-40353885 chr19:40353876-40353885 chr19:40353874-40353887 chr19:40353870-40353891 chr19:40353877-40353886
11	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
12	BHLHE40	chr19:40393689-40394027	HepG2	liver:	n/a	n/a
13	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
14	BHLHE40	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
15	BHLHE40	chr19:40404194-40404362	GM12878	blood:	n/a	n/a
16	CBX3	chr19:40404078-40404473	K562	blood:	n/a	n/a
17	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
18	CEBPB	chr19:40402703-40402726	H1-hESC	embryonic stem cell:	n/a	chr19:40402707-40402718
19	CEBPB	chr19:40402641-40402841	A549	lung:	n/a	chr19:40402707-40402718
20	CEBPB	chr19:40354800-40355128	K562	blood:	n/a	n/a
21	CEBPB	chr19:40369307-40369516	HepG2	liver:	n/a	n/a
22	CEBPB	chr19:40402571-40402768	K562	blood:	n/a	chr19:40402707-40402718
23	CEBPB	chr19:40354817-40355067	K562	blood:	n/a	n/a
24	CEBPB	chr19:40354870-40355111	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:40402564-40402888	HepG2	liver:	n/a	chr19:40402707-40402718
26	CEBPB	chr19:40354824-40355043	K562	blood:	n/a	n/a
27	CEBPB	chr19:40353775-40353778	K562	blood:	n/a	n/a
28	CEBPB	chr19:40354843-40355101	A549	lung:	n/a	n/a
29	CEBPB	chr19:40388532-40388555	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr19:40402580-40402849	IMR90	lung:	n/a	chr19:40402707-40402718
31	CHD2	chr19:40404120-40404312	GM12878	blood:	n/a	n/a
32	CHD2	chr19:40388541-40388748	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr19:40388522-40388673	ProgFib	skin:	n/a	n/a
34	CTCF	chr19:40388520-40388670	HMEC	breast:	n/a	n/a
35	CTCF	chr19:40372123-40372643	K562	blood:	n/a	chr19:40372450-40372463
36	CTCF	chr19:40366361-40366462	K562	blood:	n/a	n/a
37	CTCF	chr19:40372151-40372680	A549	lung:	n/a	chr19:40372450-40372463
38	CTCF	chr19:40372260-40372410	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr19:40372280-40372430	NHLF	lung:	n/a	n/a
40	CTCF	chr19:40388496-40388723	GM13976	blood:	n/a	n/a
41	CTCF	chr19:40404240-40404390	NHEK	skin:	n/a	n/a
42	CTCF	chr19:40388500-40388650	HRE	kidney:	n/a	n/a
43	CTCF	chr19:40403980-40404130	HEK293	kidney:	n/a	n/a
44	CTCF	chr19:40388520-40388670	HCM	heart:	n/a	n/a
45	CTCF	chr19:40372280-40372430	GM12870	blood:	n/a	n/a
46	CTCF	chr19:40404212-40404465	GM12891	blood:	n/a	n/a
47	CTCF	chr19:40404217-40404475	GM19239	blood:	n/a	n/a
48	CTCF	chr19:40388500-40388650	GM12865	blood:	n/a	n/a
49	CTCF	chr19:40404244-40404419	Fibrobl	skin:	n/a	n/a
50	CTCF	chr19:40372260-40372410	GM12873	blood:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40397977-40398027	HRPEpiC	eye:	n/a
2	chr19:40393119-40393169	HIPEpiC	eye:	n/a
3	chr19:40366607-40366657	PrEC	prostate:	n/a
4	chr19:40397977-40398027	HRPEpiC	eye:	n/a
5	chr19:40393119-40393169	HIPEpiC	eye:	n/a
6	chr19:40366607-40366657	PrEC	prostate:	n/a
7	chr19:40362928-40362978	PFSK-1	brain:	n/a
8	chr19:40388677-40388727	U87	brain:	n/a
9	chr19:40396032-40396082	PrEC	prostate:	n/a
10	chr19:40379680-40379730	HIPEpiC	eye:	n/a
11	chr19:40366394-40366444	BE2_C	brain:	n/a
12	chr19:40376883-40376933	SK-N-SH_RA	brain:	n/a
13	chr19:40396032-40396082	ProgFib	skin:	n/a
14	chr19:40372977-40373027	HMEC	breast:	n/a
15	chr19:40362928-40362978	K562	blood:	n/a
16	chr19:40391320-40391370	HMEC	breast:	n/a
17	chr19:40396538-40396588	HRCEpiC	kidney:	n/a
18	chr19:40377434-40377484	HIPEpiC	eye:	n/a
19	chr19:40375973-40376023	SKMC	muscle:	n/a
20	chr19:40372977-40373027	NT2-D1	testis:	n/a
21	chr19:40364151-40364201	HNPCEpiC	eye:	n/a
22	chr19:40366607-40366657	HCM	heart:	n/a
23	chr19:40377434-40377484	U87	brain:	n/a
24	chr19:40372977-40373027	SK-N-SH_RA	brain:	n/a
25	chr19:40396538-40396588	PrEC	prostate:	n/a
26	chr19:40392568-40392618	IMR90	lung:	fetal
27	chr19:40376883-40376933	PFSK-1	brain:	n/a
28	chr19:40396538-40396588	ProgFib	skin:	n/a
29	chr19:40366088-40366138	AG10803	skin:	n/a
30	chr19:40396032-40396082	HRCEpiC	kidney:	n/a
31	chr19:40391320-40391370	BE2_C	brain:	n/a
32	chr19:40396538-40396588	PFSK-1	brain:	n/a
33	chr19:40398384-40398434	H1-hESC	embryonic stem cell:	embryo
34	chr19:40372977-40373027	GM12892	blood:	n/a
35	chr19:40399454-40399504	HCT-116	colon:	n/a
36	chr19:40375973-40376023	AG09319	gingival:	n/a
37	chr19:40368363-40368413	ovcar-3	ovarian:	n/a
38	chr19:40368830-40368880	HCT-116	colon:	n/a
39	chr19:40399454-40399504	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:40375973-40376023	Hela-S3	cervix:	n/a
41	chr19:40392568-40392618	AG10803	skin:	n/a
42	chr19:40366607-40366657	NHDF-neo	bronchial:	n/a
43	chr19:40368830-40368880	HMEC	breast:	n/a
44	chr19:40372977-40373027	HRE	kidney:	n/a
45	chr19:40368363-40368413	SK-N-SH_RA	brain:	n/a
46	chr19:40380853-40380903	T-47D	breast:	n/a
47	chr19:40391320-40391370	MCF-7	breast:	n/a
48	chr19:40368363-40368413	HL-60	blood:	n/a
49	chr19:40396538-40396588	HNPCEpiC	eye:	n/a
50	chr19:40359249-40359299	HPAEpiC	pulmonary alveolar:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40338036..40340893-chr19:40348527..40351769,3	MCF-7	breast:
2	chr19:40337506..40339114-chr19:40356435..40358897,2	MCF-7	breast:
3	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
4	chr19:40350892..40352430-chr19:40476216..40478037,2	K562	blood:
5	chr19:40371880..40372846-chr19:40476486..40477439,2	MCF-7	breast:
6	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
7	chr19:40333922..40335627-chr19:40352940..40355252,2	K562	blood:
8	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
9	chr19:40337126..40339206-chr19:40352976..40355937,2	K562	blood:
10	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
11	chr19:40403844..40404724-chr19:40476336..40477181,3	MCF-7	breast:
12	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
13	chr19:40345236..40348068-chr19:40350382..40353367,3	K562	blood:
14	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
15	chr19:40335567..40338351-chr19:40347856..40350907,4	MCF-7	breast:

No data

Variant related genes	Relation type
FCGBP	TF binding region
FCGBP	CpG island
ENSG00000013275	chromatin interactions
ENSG00000105202	chromatin interactions

Extended variants
information (count: 2225 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2225 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556071071	chr19:40350741-40350742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs150379531	chr19:40350775-40350776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35240257	chr19:40350795-40350796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551580535	chr19:40350834-40350835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537880729	chr19:40350851-40350852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560369386	chr19:40350875-40350876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs80083819	chr19:40350936-40350937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577680982	chr19:40350970-40350971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200070234	chr19:40350984-40350985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs58538017	chr19:40350996-40350997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs61424284	chr19:40351001-40351002	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2009348	chr19:40351028-40351029	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs193145645	chr19:40351029-40351030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185187087	chr19:40351090-40351091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542437691	chr19:40351110-40351111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs561273985	chr19:40351124-40351125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs57994656	chr19:40351144-40351145	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543285089	chr19:40351154-40351155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562546554	chr19:40351167-40351168	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533117558	chr19:40351177-40351178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs146009245	chr19:40351184-40351185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs377149809	chr19:40351207-40351208	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566847767	chr19:40351232-40351233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527912244	chr19:40351235-40351236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138563006	chr19:40351239-40351240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542167472	chr19:40351276-40351277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376262711	chr19:40351277-40351278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12462650	chr19:40351331-40351332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549307785	chr19:40351350-40351351	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556846702	chr19:40351456-40351457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562459744	chr19:40351481-40351482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4802061	chr19:40351487-40351488	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs141659613	chr19:40351497-40351498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144416585	chr19:40351559-40351560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572034158	chr19:40351572-40351573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542674934	chr19:40351611-40351612	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375922168	chr19:40351670-40351671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs148404704	chr19:40351681-40351682	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34091726	chr19:40351699-40351700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546711532	chr19:40351712-40351713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs10419882	chr19:40351746-40351747	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs543323694	chr19:40351757-40351758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs10412687	chr19:40351831-40351832	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375622748	chr19:40351870-40351871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs74646898	chr19:40351875-40351876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376023614	chr19:40351881-40351882	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370033079	chr19:40351884-40351885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs373765258	chr19:40351918-40351919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376341853	chr19:40351921-40351922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs5828050	chr19:40351925-40351926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40349400-40354400	Weak transcription	Colonic Mucosa	Colon
2	chr19:40349800-40353600	Weak transcription	Primary T cells from cord blood	blood
3	chr19:40349800-40356000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr19:40349800-40357400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
6	chr19:40350200-40353400	Weak transcription	Fetal Intestine Small	intestine
7	chr19:40350400-40372200	Weak transcription	Dnd41	blood
8	chr19:40350600-40365200	Weak transcription	Placenta	Placenta
9	chr19:40350800-40351000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
10	chr19:40350800-40353400	Weak transcription	Fetal Stomach	stomach
11	chr19:40351000-40361000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr19:40351200-40353600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr19:40351400-40353400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr19:40351600-40353400	Weak transcription	Stomach Mucosa	stomach
15	chr19:40351600-40353800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr19:40351600-40357200	Weak transcription	Primary B cells from cord blood	blood
17	chr19:40352000-40357000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr19:40352000-40357200	Weak transcription	Fetal Muscle Leg	muscle
19	chr19:40352000-40363200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr19:40352000-40364200	Weak transcription	Fetal Muscle Trunk	muscle
21	chr19:40352000-40372600	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr19:40352200-40356400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr19:40352400-40372400	Weak transcription	Fetal Intestine Large	intestine
24	chr19:40352600-40364000	Weak transcription	Rectal Smooth Muscle	rectum
25	chr19:40352800-40360600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr19:40352800-40360600	Weak transcription	Spleen	Spleen
27	chr19:40353200-40354200	Weak transcription	Gastric	stomach
28	chr19:40353400-40354600	Strong transcription	Fetal Intestine Small	intestine
29	chr19:40353400-40354600	Strong transcription	Stomach Mucosa	stomach
30	chr19:40353400-40354800	Strong transcription	Fetal Stomach	stomach
31	chr19:40353400-40366000	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr19:40353600-40355000	Strong transcription	Primary T cells from cord blood	blood
33	chr19:40353600-40360000	Strong transcription	Rectal Mucosa Donor 31	rectum
34	chr19:40353800-40354600	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr19:40354200-40354400	ZNF genes & repeats	Gastric	stomach
36	chr19:40354200-40370800	Weak transcription	Fetal Brain Female	brain
37	chr19:40354400-40354600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:40354400-40354600	Strong transcription	Colonic Mucosa	Colon
39	chr19:40354400-40354800	Enhancers	A549	lung
40	chr19:40354400-40355400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr19:40354400-40362600	Weak transcription	Gastric	stomach
42	chr19:40354600-40356000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr19:40354600-40356200	Weak transcription	Colonic Mucosa	Colon
44	chr19:40354600-40356200	Weak transcription	Fetal Intestine Small	intestine
45	chr19:40354600-40357200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr19:40354600-40362800	Weak transcription	Stomach Mucosa	stomach
47	chr19:40354600-40372200	Weak transcription	HepG2	liver
48	chr19:40354800-40356200	Weak transcription	Fetal Stomach	stomach
49	chr19:40355000-40355800	Weak transcription	Primary T cells from cord blood	blood
50	chr19:40355200-40372200	Weak transcription	Primary T helper cells PMA-I stimulated	--

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