Variant report

Variant	esv19087
Chromosome Location	chr19:55607778-55609493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:55 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:55607660-55607810	GM06990	blood:	n/a	n/a
2	CTCF	chr19:55608620-55608678	GM19239	blood:	n/a	n/a
3	CTCF	chr19:55608595-55608635	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr19:55608687-55608755	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr19:55607486-55607808	H1-hESC	embryonic stem cell:	n/a	n/a
6	EBF1	chr19:55607799-55607980	GM12878	blood:	n/a	n/a
7	MAX	chr19:55609383-55609679	NB4	blood:	n/a	n/a
8	MAX	chr19:55607560-55607972	H1-hESC	embryonic stem cell:	n/a	chr19:55607896-55607905 chr19:55607897-55607904
9	MYC	chr19:55609316-55609659	NB4	blood:	n/a	n/a
10	MYC	chr19:55608984-55608993	MCF-7	breast:	n/a	n/a
11	MYC	chr19:55608507-55608830	MCF-7	breast:	n/a	n/a
12	MYC	chr19:55608836-55608981	MCF-7	breast:	n/a	n/a
13	MYC	chr19:55608169-55608276	H1-hESC	embryonic stem cell:	n/a	n/a
14	NR3C1	chr19:55608008-55609133	A549	lung:	n/a	n/a
15	POLR2A	chr19:55608419-55608557	ProgFib	skin:	n/a	n/a
16	POLR2A	chr19:55608469-55608562	MCF-7	breast:	n/a	n/a
17	POLR2A	chr19:55608383-55608711	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr19:55608438-55608709	HepG2	liver:	n/a	n/a
19	POLR2A	chr19:55607763-55607956	K562	blood:	n/a	n/a
20	POLR2A	chr19:55607962-55608022	K562	blood:	n/a	n/a
21	POLR2A	chr19:55608433-55608737	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr19:55608589-55608714	MCF-7	breast:	n/a	n/a
23	POLR2A	chr19:55608933-55608962	MCF-7	breast:	n/a	n/a
24	POLR2A	chr19:55607965-55609131	GM12878	blood:	n/a	n/a
25	POLR2A	chr19:55607995-55609121	GM12891	blood:	n/a	n/a
26	POLR2A	chr19:55609123-55610750	HL-60	blood:	n/a	n/a
27	POLR2A	chr19:55608246-55608424	K562	blood:	n/a	n/a
28	POLR2A	chr19:55608797-55609002	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr19:55608049-55609093	GM12878	blood:	n/a	n/a
30	POLR2A	chr19:55608986-55609024	MCF-7	breast:	n/a	n/a
31	POLR2A	chr19:55607846-55608080	K562	blood:	n/a	n/a
32	POLR2A	chr19:55609185-55609363	HepG2	liver:	n/a	n/a
33	POLR2A	chr19:55609219-55609340	HUVEC	blood vessel:	n/a	n/a
34	POLR2A	chr19:55608097-55609120	GM12892	blood:	n/a	n/a
35	POLR2A	chr19:55609210-55610131	K562	blood:	n/a	n/a
36	POLR2A	chr19:55608368-55608905	K562	blood:	n/a	n/a
37	POLR2A	chr19:55608001-55609101	A549	lung:	n/a	n/a
38	POLR2A	chr19:55608672-55608931	MCF-7	breast:	n/a	n/a
39	POLR2A	chr19:55608249-55609010	GM12892	blood:	n/a	n/a
40	POLR2A	chr19:55608387-55608782	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr19:55609358-55609605	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr19:55608264-55609035	A549	lung:	n/a	n/a
43	POLR2A	chr19:55608744-55609263	K562	blood:	n/a	n/a
44	POLR2A	chr19:55608977-55609354	K562	blood:	n/a	n/a
45	POLR2A	chr19:55608005-55609181	GM12891	blood:	n/a	n/a
46	POLR2A	chr19:55608590-55608645	ProgFib	skin:	n/a	n/a
47	POLR2A	chr19:55608020-55609113	GM12878	blood:	n/a	n/a
48	POLR2A	chr19:55608347-55608777	GM12892	blood:	n/a	n/a
49	POLR2A	chr19:55608006-55609100	H1-hESC	embryonic stem cell:	n/a	n/a
50	RAD21	chr19:55607423-55607866	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:55609047-55609097	Hepatocyte	liver:	n/a
2	chr19:55607746-55607796	U87	brain:	n/a
3	chr19:55609047-55609097	SKMC	muscle:	n/a
4	chr19:55609047-55609097	HMEC	breast:	n/a
5	chr19:55607746-55607796	HIPEpiC	eye:	n/a
6	chr19:55607746-55607796	RPTEC	kidney:	n/a
7	chr19:55607746-55607796	PrEC	prostate:	n/a
8	chr19:55607746-55607796	NHBE	bronchial:	n/a
9	chr19:55607746-55607796	SK-N-SH_RA	brain:	n/a
10	chr19:55609047-55609097	ProgFib	skin:	n/a
11	chr19:55607746-55607796	H1-hESC	embryonic stem cell:	embryo
12	chr19:55609047-55609097	AG09309	skin:	n/a
13	chr19:55609047-55609097	AG09319	gingival:	n/a
14	chr19:55607746-55607796	HCT-116	colon:	n/a
15	chr19:55607746-55607796	AG09309	skin:	n/a
16	chr19:55609047-55609097	AG04450	lung:	fetal
17	chr19:55609047-55609097	H1-hESC	embryonic stem cell:	embryo
18	chr19:55609047-55609097	PFSK-1	brain:	n/a
19	chr19:55607746-55607796	HRCEpiC	kidney:	n/a
20	chr19:55609047-55609097	NB4	blood:	n/a
21	chr19:55609047-55609097	HCF	heart:	n/a
22	chr19:55609047-55609097	Jurkat	blood:	n/a
23	chr19:55609047-55609097	BJ	skin:	n/a
24	chr19:55609047-55609097	HCT-116	colon:	n/a
25	chr19:55607746-55607796	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:55609047-55609097	HCPEpiC	choroid plexus:	n/a
27	chr19:55609047-55609097	NT2-D1	testis:	n/a
28	chr19:55607746-55607796	MCF-7	breast:	n/a
29	chr19:55607746-55607796	HCPEpiC	choroid plexus:	n/a
30	chr19:55607746-55607796	PFSK-1	brain:	n/a
31	chr19:55607746-55607796	CMK	blood:	n/a
32	chr19:55607746-55607796	GM06990	blood:	n/a
33	chr19:55609047-55609097	LNCaP	prostate:	n/a
34	chr19:55607746-55607796	HRPEpiC	eye:	n/a
35	chr19:55609047-55609097	GM12878	blood:	n/a
36	chr19:55607746-55607796	K562	blood:	n/a
37	chr19:55607746-55607796	SK-N-SH	brain:	n/a
38	chr19:55609047-55609097	NHDF-neo	bronchial:	n/a
39	chr19:55609047-55609097	ECC-1	luminal epithelium:	n/a
40	chr19:55609047-55609097	GM06990	blood:	n/a
41	chr19:55609047-55609097	HEEpiC	esophagus:	n/a
42	chr19:55609047-55609097	HIPEpiC	eye:	n/a
43	chr19:55609047-55609097	RPTEC	kidney:	n/a
44	chr19:55607746-55607796	ECC-1	luminal epithelium:	n/a
45	chr19:55607746-55607796	HCF	heart:	n/a
46	chr19:55609047-55609097	NH-A	brain:	n/a
47	chr19:55609047-55609097	HRPEpiC	eye:	n/a
48	chr19:55607746-55607796	HRE	kidney:	n/a
49	chr19:55609047-55609097	NHBE	bronchial:	n/a
50	chr19:55609047-55609097	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:55606186..55608004-chr19:55668541..55670350,2	K562	blood:
2	chr19:55593783..55596973-chr19:55605739..55609072,3	MCF-7	breast:
3	chr19:55602817..55605063-chr19:55607847..55611978,5	K562	blood:
4	chr19:55602846..55604950-chr19:55605722..55608309,2	MCF-7	breast:
5	chr19:55609257..55613232-chr19:55613674..55618222,6	K562	blood:
6	chr19:55549659..55551205-chr19:55608941..55611105,2	K562	blood:
7	chr19:55591561..55594163-chr19:55604044..55608526,4	K562	blood:
8	chr19:55606533..55609893-chr19:55627288..55629671,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RDH13-2	chr19:55608731-55608751	NONHSAT067992
2	lnc-RDH13-2	chr19:55608844-55609398	NONHSAT067992

No data

Variant related genes	Relation type
PPP1R12C	TF binding region
PPP1R12C	CpG island
ENSG00000267577	chromatin interactions
ENSG00000129991	chromatin interactions
ENSG00000131037	chromatin interactions
ENSG00000125503	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528396596	chr19:55607820-55607821	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs115452929	chr19:55607885-55607886	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs186772450	chr19:55607900-55607901	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs549367196	chr19:55607901-55607902	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs569595243	chr19:55607918-55607919	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs191337120	chr19:55607930-55607931	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs549037350	chr19:55607935-55607936	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs183159711	chr19:55607960-55607961	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs534830133	chr19:55607993-55607994	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs546544767	chr19:55608001-55608002	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs557947071	chr19:55608038-55608039	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs372061043	chr19:55608040-55608041	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs2532053	chr19:55608054-55608055	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs2532054	chr19:55608068-55608069	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs187991819	chr19:55608091-55608092	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs199758330	chr19:55608100-55608101	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs537589053	chr19:55608113-55608114	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs200731891	chr19:55608115-55608116	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs193025346	chr19:55608137-55608138	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs201384553	chr19:55608141-55608142	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs56222528	chr19:55608143-55608144	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs542985403	chr19:55608148-55608149	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs71367146	chr19:55608175-55608176	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs199891373	chr19:55608179-55608180	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs375061961	chr19:55608185-55608186	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs112906934	chr19:55608207-55608208	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs367764706	chr19:55608217-55608218	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs553412270	chr19:55608236-55608237	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs111514549	chr19:55608239-55608240	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs36197554	chr19:55608247-55608248	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs200659525	chr19:55608248-55608249	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs36195463	chr19:55608249-55608250	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs74177902	chr19:55608251-55608252	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs74170786	chr19:55608269-55608270	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs2532056	chr19:55608299-55608300	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
36	rs113960122	chr19:55608309-55608310	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs67907312	chr19:55608320-55608321	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs11668800	chr19:55608322-55608323	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs11672675	chr19:55608329-55608330	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs62124200	chr19:55608354-55608355	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs112303742	chr19:55608361-55608362	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs67395660	chr19:55608371-55608372	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs111960953	chr19:55608372-55608373	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs111365066	chr19:55608387-55608388	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs79964275	chr19:55608393-55608394	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs565087423	chr19:55608396-55608397	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs62124201	chr19:55608401-55608402	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs113852915	chr19:55608425-55608426	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs202003479	chr19:55608434-55608435	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs372611347	chr19:55608435-55608436	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung squamous cell carcinoma	20842114	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55593800-55620400	Weak transcription	HMEC	breast
2	chr19:55599200-55626600	Weak transcription	Fetal Kidney	kidney
3	chr19:55599200-55627200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr19:55599400-55614800	Weak transcription	GM12878-XiMat	blood
5	chr19:55599800-55626000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr19:55600000-55610600	Weak transcription	NHDF-Ad	bronchial
7	chr19:55600000-55612800	Weak transcription	HSMMtube	muscle
8	chr19:55600000-55613400	Weak transcription	Fetal Lung	lung
9	chr19:55600000-55613800	Weak transcription	NH-A	brain
10	chr19:55600000-55614600	Weak transcription	HSMM	muscle
11	chr19:55600000-55626600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr19:55600000-55627000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr19:55600200-55609800	Weak transcription	Stomach Mucosa	stomach
14	chr19:55600200-55610800	Strong transcription	NHLF	lung
15	chr19:55600200-55612600	Weak transcription	K562	blood
16	chr19:55600200-55614600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr19:55600400-55608200	Strong transcription	Fetal Stomach	stomach
18	chr19:55600600-55614600	Weak transcription	HUVEC	blood vessel
19	chr19:55600800-55607800	Strong transcription	Fetal Intestine Small	intestine
20	chr19:55600800-55608000	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr19:55600800-55608000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr19:55600800-55608000	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr19:55600800-55608200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr19:55601000-55607800	Strong transcription	Fetal Muscle Leg	muscle
25	chr19:55601000-55608200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr19:55601000-55608200	Strong transcription	Adipose Nuclei	Adipose
27	chr19:55601200-55608000	Strong transcription	Colon Smooth Muscle	Colon
28	chr19:55601200-55608000	Strong transcription	Thymus	Thymus
29	chr19:55601400-55607800	Strong transcription	Left Ventricle	heart
30	chr19:55601400-55611000	Weak transcription	Right Atrium	heart
31	chr19:55601400-55626400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr19:55601800-55608200	Strong transcription	Fetal Brain Female	brain
33	chr19:55601800-55609800	Strong transcription	Colonic Mucosa	Colon
34	chr19:55602000-55608000	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr19:55602000-55608200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr19:55602000-55613800	Strong transcription	Gastric	stomach
37	chr19:55602000-55615400	Strong transcription	Lung	lung
38	chr19:55602000-55618400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr19:55602200-55608000	Strong transcription	Fetal Intestine Large	intestine
40	chr19:55602400-55608000	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr19:55602800-55614200	Weak transcription	Psoas Muscle	Psoas
42	chr19:55602800-55626400	Weak transcription	Hela-S3	cervix
43	chr19:55603400-55608000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr19:55603600-55609400	Weak transcription	NHEK	skin
45	chr19:55603800-55612600	Weak transcription	Small Intestine	intestine
46	chr19:55604000-55608400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr19:55605600-55607800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr19:55605600-55607800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr19:55605600-55607800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr19:55605600-55607800	Strong transcription	Brain Cingulate Gyrus	brain

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