Variant report

Variant	esv3420290
Chromosome Location	chr19:21272477-21336432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:799)
CpG islands
(count:673)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21320974-21321431	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:21334536-21334657	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:21324511-21325033	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:21309568-21309872	K562	blood:	n/a	n/a
5	ARID3A	chr19:21326481-21326923	K562	blood:	n/a	n/a
6	ARID3A	chr19:21298266-21298592	K562	blood:	n/a	n/a
7	ARID3A	chr19:21310732-21311042	K562	blood:	n/a	n/a
8	ARID3A	chr19:21311642-21311836	K562	blood:	n/a	n/a
9	ARID3A	chr19:21324594-21324991	K562	blood:	n/a	n/a
10	ARID3A	chr19:21317764-21318041	HepG2	liver:	n/a	n/a
11	ATF1	chr19:21309871-21310055	K562	blood:	n/a	n/a
12	ATF1	chr19:21324532-21324958	K562	blood:	n/a	n/a
13	ATF1	chr19:21323783-21324152	K562	blood:	n/a	n/a
14	ATF1	chr19:21311655-21311901	K562	blood:	n/a	n/a
15	BACH1	chr19:21334389-21334437	K562	blood:	n/a	n/a
16	BATF	chr19:21284333-21284518	GM12878	blood:	n/a	chr19:21284437-21284448
17	BATF	chr19:21284292-21284552	GM12878	blood:	n/a	chr19:21284437-21284448
18	BHLHE40	chr19:21324578-21325040	K562	blood:	n/a	n/a
19	BHLHE40	chr19:21324647-21325001	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:21325755-21325765	K562	blood:	n/a	n/a
21	BHLHE40	chr19:21277600-21277808	GM12878	blood:	n/a	n/a
22	CBX3	chr19:21311545-21312525	K562	blood:	n/a	n/a
23	CBX3	chr19:21313134-21313546	K562	blood:	n/a	n/a
24	CBX3	chr19:21324429-21325106	K562	blood:	n/a	n/a
25	CBX3	chr19:21313141-21313522	K562	blood:	n/a	n/a
26	CBX3	chr19:21317713-21318138	K562	blood:	n/a	n/a
27	CCNT2	chr19:21324680-21324880	K562	blood:	n/a	n/a
28	CCNT2	chr19:21311599-21311941	K562	blood:	n/a	n/a
29	CCNT2	chr19:21298323-21298579	K562	blood:	n/a	n/a
30	CEBPB	chr19:21330138-21330368	IMR90	lung:	n/a	chr19:21330243-21330254
31	CEBPB	chr19:21287289-21287319	K562	blood:	n/a	n/a
32	CEBPB	chr19:21277976-21278043	K562	blood:	n/a	n/a
33	CEBPB	chr19:21309862-21309933	K562	blood:	n/a	n/a
34	CEBPB	chr19:21311395-21312007	K562	blood:	n/a	n/a
35	CEBPB	chr19:21326562-21327122	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:21309819-21310094	K562	blood:	n/a	n/a
37	CEBPB	chr19:21330144-21330361	K562	blood:	n/a	chr19:21330243-21330254
38	CEBPB	chr19:21311478-21311988	K562	blood:	n/a	n/a
39	CEBPB	chr19:21324525-21324869	K562	blood:	n/a	n/a
40	CEBPB	chr19:21324607-21324698	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr19:21324616-21324713	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:21324595-21324879	HepG2	liver:	n/a	n/a
43	CEBPB	chr19:21279665-21279786	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr19:21324597-21324775	A549	lung:	n/a	n/a
45	CEBPB	chr19:21317815-21318034	K562	blood:	n/a	n/a
46	CEBPB	chr19:21324542-21325274	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:21330247-21330280	HepG2	liver:	n/a	n/a
48	CEBPB	chr19:21287270-21287272	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPD	chr19:21324725-21325074	HepG2	liver:	n/a	n/a
50	CEBPD	chr19:21311549-21312059	K562	blood:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21323534-21323584	ovcar-3	ovarian:	n/a
2	chr19:21324750-21324800	HRE	kidney:	n/a
3	chr19:21323534-21323584	ovcar-3	ovarian:	n/a
4	chr19:21324750-21324800	HRE	kidney:	n/a
5	chr19:21324707-21324757	HMEC	breast:	n/a
6	chr19:21324707-21324757	NB4	blood:	n/a
7	chr19:21324833-21324883	AoSMC	blood vessel:	n/a
8	chr19:21324782-21324832	GM12878	blood:	n/a
9	chr19:21323534-21323584	U87	brain:	n/a
10	chr19:21324444-21324494	GM06990	blood:	n/a
11	chr19:21324130-21324180	AG04449	skin:	fetal
12	chr19:21323534-21323584	HRE	kidney:	n/a
13	chr19:21325005-21325055	Hela-S3	cervix:	n/a
14	chr19:21324796-21324846	SKMC	muscle:	n/a
15	chr19:21324750-21324800	U87	brain:	n/a
16	chr19:21324750-21324800	GM06990	blood:	n/a
17	chr19:21324782-21324832	SK-N-SH_RA	brain:	n/a
18	chr19:21325005-21325055	GM12878	blood:	n/a
19	chr19:21324750-21324800	AG04449	skin:	fetal
20	chr19:21305635-21305685	Hepatocyte	liver:	n/a
21	chr19:21325005-21325055	NT2-D1	testis:	n/a
22	chr19:21324833-21324883	AG04450	lung:	fetal
23	chr19:21323534-21323584	SK-N-SH	brain:	n/a
24	chr19:21324807-21324857	HNPCEpiC	eye:	n/a
25	chr19:21324782-21324832	HAEpiC	amniotic membrane:	n/a
26	chr19:21324130-21324180	SAEC	small airway:	n/a
27	chr19:21324444-21324494	LNCaP	prostate:	n/a
28	chr19:21323534-21323584	HNPCEpiC	eye:	n/a
29	chr19:21324833-21324883	AG09309	skin:	n/a
30	chr19:21324750-21324800	GM12892	blood:	n/a
31	chr19:21324796-21324846	PrEC	prostate:	n/a
32	chr19:21324796-21324846	AG04450	lung:	fetal
33	chr19:21324807-21324857	BE2_C	brain:	n/a
34	chr19:21305635-21305685	HCT-116	colon:	n/a
35	chr19:21305635-21305685	AG09319	gingival:	n/a
36	chr19:21324750-21324800	HUVEC	blood vessel:	n/a
37	chr19:21324444-21324494	BE2_C	brain:	n/a
38	chr19:21324796-21324846	NHBE	bronchial:	n/a
39	chr19:21324782-21324832	AG10803	skin:	n/a
40	chr19:21323534-21323584	GM12892	blood:	n/a
41	chr19:21324796-21324846	NH-A	brain:	n/a
42	chr19:21324833-21324883	PFSK-1	brain:	n/a
43	chr19:21324796-21324846	U87	brain:	n/a
44	chr19:21325005-21325055	HNPCEpiC	eye:	n/a
45	chr19:21324444-21324494	ECC-1	luminal epithelium:	n/a
46	chr19:21305635-21305685	HCF	heart:	n/a
47	chr19:21324833-21324883	GM12878	blood:	n/a
48	chr19:21324444-21324494	GM12892	blood:	n/a
49	chr19:21324444-21324494	SK-N-SH	brain:	n/a
50	chr19:21324707-21324757	HRPEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21324608..21326238-chr19:21328530..21331210,2	MCF-7	breast:
2	chr19:21312896..21314771-chr19:21323680..21326350,2	K562	blood:
3	chr19:21264288..21266539-chr19:21271478..21272991,2	MCF-7	breast:
4	chr19:21319136..21321232-chr19:21323817..21326389,2	K562	blood:
5	chr19:21264764..21267719-chr19:21267936..21273188,6	K562	blood:
6	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
7	chr14:39639460..39640068-chr19:21325033..21325860,2	Hela-S3	cervix:
8	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
9	chr19:21268213..21268800-chr19:21327512..21328424,2	MCF-7	breast:
10	chr19:21267358..21270716-chr19:21272495..21275149,3	MCF-7	breast:
11	chr19:21328122..21331831-chr19:21332882..21335579,3	K562	blood:
12	chr19:21266339..21268600-chr19:21281169..21284066,2	MCF-7	breast:
13	chr19:21329795..21332186-chr19:21344748..21346568,2	K562	blood:
14	chr19:21268071..21270842-chr19:21283139..21285114,2	K562	blood:
15	chr19:21325138..21326653-chr19:21327405..21328910,2	K562	blood:
16	chr19:21325138..21326653-chr19:21327405..21328910,2	K562	blood:
17	chr19:21263410..21266735-chr19:21269462..21274138,5	K562	blood:
18	chr19:21264016..21266575-chr19:21326485..21328797,2	MCF-7	breast:
19	chr19:21324747..21325334-chr19:21541551..21542092,2	Hela-S3	cervix:
20	chr19:21327774..21330342-chr19:21332349..21334379,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF714-2	chr19:21306620-21306991	NONHSAT063687
2	lnc-ZNF431-3	chr19:21301321-21301529	NONHSAT063686
3	lnc-ZNF430-2	chr19:21273717-21274564	NONHSAT063684
4	lnc-ZNF714-1	chr19:21307764-21307881	NONHSAT063683

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF714	hsa-miR-222-3p	chr19:21304966-21304986

Variant related genes	Relation type
ZNF431	TF binding region
RNA5SP469	TF binding region
VN1R81P	TF binding region
ENSG00000256240	TF binding region
RPL7AP10	TF binding region
ZNF431	CpG island
RNA5SP469	CpG island
VN1R81P	CpG island
ENSG00000256240	CpG island
RPL7AP10	CpG island
ENSG00000172687	chromatin interactions
ENSG00000240522	chromatin interactions
ENSG00000160352	chromatin interactions
ENSG00000196705	chromatin interactions
ENSG00000182400	chromatin interactions

Extended variants
information (count: 2535 )
Associated
traits (count: 40 )

Variant overlapped rSNPs/rCNVs (count:2535 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181393944	chr19:21272485-21272486	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs575666629	chr19:21272492-21272493	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541625509	chr19:21272522-21272523	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs117878541	chr19:21272580-21272581	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35907046	chr19:21272599-21272600	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs76737776	chr19:21272601-21272602	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs74999014	chr19:21272602-21272603	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34179128	chr19:21272606-21272607	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574079263	chr19:21272613-21272614	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10416058	chr19:21272628-21272629	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs12972715	chr19:21272635-21272636	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs199863428	chr19:21272640-21272641	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10415482	chr19:21272641-21272642	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10417213	chr19:21272649-21272650	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10415838	chr19:21272661-21272662	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs10415659	chr19:21272670-21272671	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs113060938	chr19:21272673-21272674	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376440286	chr19:21272674-21272675	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs202150079	chr19:21272679-21272680	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113578184	chr19:21272682-21272683	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs10417366	chr19:21272687-21272688	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs71333806	chr19:21272691-21272692	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs10415673	chr19:21272694-21272695	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs10415875	chr19:21272707-21272708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs112420525	chr19:21272717-21272718	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531887125	chr19:21272765-21272766	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551983640	chr19:21272853-21272854	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13346419	chr19:21272985-21272986	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537383935	chr19:21273032-21273033	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547864478	chr19:21273038-21273039	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570251141	chr19:21273047-21273048	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567673763	chr19:21273054-21273055	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs73535730	chr19:21273073-21273074	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556207145	chr19:21273074-21273075	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs377000377	chr19:21273134-21273135	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569963197	chr19:21273166-21273167	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538542127	chr19:21273182-21273183	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558757565	chr19:21273186-21273187	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571908725	chr19:21273211-21273212	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113486391	chr19:21273272-21273273	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138110898	chr19:21273275-21273276	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376794303	chr19:21273289-21273290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs571283947	chr19:21273389-21273390	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142119136	chr19:21273392-21273393	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs59499960	chr19:21273457-21273458	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs10424283	chr19:21273470-21273471	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs145972895	chr19:21273567-21273568	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375882422	chr19:21273583-21273584	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs36127444	chr19:21273608-21273609	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558485211	chr19:21273618-21273619	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:40)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1934 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21247400-21289600	Weak transcription	Aorta	Aorta
2	chr19:21265400-21274800	Weak transcription	Lung	lung
3	chr19:21265600-21273400	Weak transcription	Left Ventricle	heart
4	chr19:21265600-21273800	Weak transcription	Esophagus	oesophagus
5	chr19:21265600-21275000	Weak transcription	Pancreas	Pancrea
6	chr19:21265600-21286400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr19:21265600-21295800	Weak transcription	Small Intestine	intestine
8	chr19:21265600-21300000	Weak transcription	Brain Angular Gyrus	brain
9	chr19:21265600-21305200	Weak transcription	Psoas Muscle	Psoas
10	chr19:21265800-21275000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr19:21265800-21275000	Weak transcription	Primary B cells from cord blood	blood
12	chr19:21265800-21275000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr19:21265800-21275400	Weak transcription	Brain Hippocampus Middle	brain
14	chr19:21265800-21282600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr19:21265800-21289800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr19:21265800-21290600	Weak transcription	Adipose Nuclei	Adipose
17	chr19:21265800-21297200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr19:21265800-21297200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr19:21265800-21299600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr19:21265800-21299800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr19:21265800-21302200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr19:21265800-21302800	Weak transcription	Fetal Muscle Trunk	muscle
23	chr19:21265800-21303000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr19:21266000-21274000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr19:21266000-21275000	Weak transcription	Fetal Heart	heart
26	chr19:21266000-21276400	Weak transcription	Fetal Intestine Small	intestine
27	chr19:21266000-21278800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:21266000-21286000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr19:21266000-21287600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr19:21266000-21287800	Weak transcription	Duodenum Mucosa	Duodenum
31	chr19:21266000-21288400	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr19:21266000-21289400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr19:21266000-21290800	Weak transcription	Brain Anterior Caudate	brain
34	chr19:21266000-21290800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr19:21266000-21290800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr19:21266000-21292600	Weak transcription	Fetal Kidney	kidney
37	chr19:21266000-21297400	Weak transcription	HUVEC	blood vessel
38	chr19:21266200-21273400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr19:21266200-21273800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr19:21266200-21274600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr19:21266200-21274600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr19:21266200-21275000	Weak transcription	Fetal Stomach	stomach
43	chr19:21266200-21276400	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr19:21266200-21288600	Weak transcription	Thymus	Thymus
45	chr19:21266200-21288800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr19:21266200-21289800	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr19:21266200-21292400	Weak transcription	Primary T cells from cord blood	blood
48	chr19:21266200-21296600	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr19:21266200-21301600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr19:21266400-21272800	Weak transcription	Fetal Thymus	thymus

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