Variant report

Variant	esv1822279
Chromosome Location	chr19:51332255-51339207
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:243)
CpG islands
(count:430)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:243 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:51338887-51339735	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:51339018-51339458	GM12878	blood:	n/a	chr19:51339112-51339128 chr19:51339352-51339368
3	BHLHE40	chr19:51338970-51339423	K562	blood:	n/a	chr19:51339112-51339128 chr19:51339352-51339368
4	BHLHE40	chr19:51339149-51339377	HepG2	liver:	n/a	chr19:51339352-51339368
5	BRCA1	chr19:51339039-51339530	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr19:51339092-51339589	GM12878	blood:	n/a	n/a
7	CBX3	chr19:51338890-51339610	K562	blood:	n/a	n/a
8	CCNT2	chr19:51338985-51339590	K562	blood:	n/a	chr19:51339375-51339384
9	CHD2	chr19:51339075-51339625	GM12878	blood:	n/a	n/a
10	CREB1	chr19:51338928-51339695	A549	lung:	n/a	n/a
11	CREB1	chr19:51338919-51339737	K562	blood:	n/a	n/a
12	CREB1	chr19:51338868-51339775	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr19:51338894-51339636	GM12878	blood:	n/a	n/a
14	CREB1	chr19:51338939-51339827	HepG2	liver:	n/a	n/a
15	CREB1	chr19:51339116-51339530	A549	lung:	n/a	n/a
16	CREB1	chr19:51338891-51339717	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr19:51339040-51339190	GM12871	blood:	n/a	n/a
18	CTCF	chr19:51339020-51339170	GM12864	blood:	n/a	n/a
19	CTCF	chr19:51339188-51339333	GM19238	blood:	n/a	n/a
20	CTCF	chr19:51339060-51339210	SAEC	small airway:	n/a	n/a
21	CTCF	chr19:51339186-51339676	GM12878	blood:	n/a	chr19:51339377-51339390 chr19:51339654-51339667
22	CTCF	chr19:51339200-51339350	GM12878	blood:	n/a	n/a
23	CTCF	chr19:51339163-51339410	GM12892	blood:	n/a	chr19:51339377-51339390
24	CTCF	chr19:51338680-51338830	NHEK	skin:	n/a	n/a
25	CTCF	chr19:51339056-51339077	GM12891	blood:	n/a	n/a
26	CTCF	chr19:51333400-51333550	GM12878	blood:	n/a	n/a
27	CTCF	chr19:51338960-51339110	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr19:51333040-51333190	HEK293	kidney:	n/a	n/a
29	CTCF	chr19:51339080-51339230	GM12871	blood:	n/a	n/a
30	CTCF	chr19:51333740-51333890	GM12871	blood:	n/a	chr19:51333789-51333802 chr19:51333783-51333796 chr19:51333770-51333783 chr19:51333800-51333813
31	CTCF	chr19:51339100-51339250	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr19:51333240-51333390	GM12878	blood:	n/a	n/a
33	E2F6	chr19:51338829-51339550	A549	lung:	n/a	chr19:51339375-51339384 chr19:51339146-51339157 chr19:51339094-51339109
34	E2F6	chr19:51338976-51339977	K562	blood:	n/a	chr19:51339375-51339384 chr19:51339146-51339157 chr19:51339094-51339109
35	E2F6	chr19:51338742-51340139	H1-hESC	embryonic stem cell:	n/a	chr19:51339375-51339384 chr19:51339146-51339157 chr19:51339094-51339109
36	E2F6	chr19:51338964-51339494	A549	lung:	n/a	chr19:51339375-51339384 chr19:51339146-51339157 chr19:51339094-51339109
37	E2F6	chr19:51338957-51339586	K562	blood:	n/a	chr19:51339375-51339384 chr19:51339146-51339157 chr19:51339094-51339109
38	EBF1	chr19:51339137-51339516	GM12878	blood:	n/a	chr19:51339341-51339350 chr19:51339340-51339351
39	EGR1	chr19:51339196-51339577	K562	blood:	n/a	chr19:51339376-51339389 chr19:51339346-51339356 chr19:51339376-51339386 chr19:51339373-51339387 chr19:51339496-51339506 chr19:51339374-51339384
40	ELF1	chr19:51338944-51339670	GM12878	blood:	n/a	n/a
41	ELF1	chr19:51339030-51339529	GM12878	blood:	n/a	n/a
42	ELK1	chr19:51339136-51339331	Hela-S3	cervix:	n/a	n/a
43	EP300	chr19:51339104-51339361	GM12878	blood:	n/a	n/a
44	EP300	chr19:51339133-51339552	K562	blood:	n/a	chr19:51339397-51339413
45	GATA2	chr19:51333094-51333497	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr19:51333191-51333488	SH-SY5Y	brain:	n/a	n/a
47	GTF2B	chr19:51339068-51339402	K562	blood:	n/a	n/a
48	GTF2F1	chr19:51339022-51339368	H1-hESC	embryonic stem cell:	n/a	n/a
49	GTF2F1	chr19:51339148-51339311	Hela-S3	cervix:	n/a	n/a
50	GTF2F1	chr19:51339135-51339308	K562	blood:	n/a	n/a

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51334972-51335022	HAEpiC	amniotic membrane:	n/a
2	chr19:51336166-51336216	ECC-1	luminal epithelium:	n/a
3	chr19:51336166-51336216	HL-60	blood:	n/a
4	chr19:51334972-51335022	HAEpiC	amniotic membrane:	n/a
5	chr19:51336166-51336216	ECC-1	luminal epithelium:	n/a
6	chr19:51336166-51336216	HL-60	blood:	n/a
7	chr19:51334432-51334482	A549	lung:	n/a
8	chr19:51334972-51335022	AG04450	lung:	fetal
9	chr19:51336166-51336216	PFSK-1	brain:	n/a
10	chr19:51334890-51334940	HMEC	breast:	n/a
11	chr19:51334432-51334482	HCPEpiC	choroid plexus:	n/a
12	chr19:51334432-51334482	NH-A	brain:	n/a
13	chr19:51334496-51334546	SAEC	small airway:	n/a
14	chr19:51334972-51335022	HRCEpiC	kidney:	n/a
15	chr19:51336166-51336216	HPAEpiC	pulmonary alveolar:	n/a
16	chr19:51336166-51336216	HNPCEpiC	eye:	n/a
17	chr19:51334890-51334940	NHBE	bronchial:	n/a
18	chr19:51338987-51339037	NHDF-neo	bronchial:	n/a
19	chr19:51336102-51336152	IMR90	lung:	fetal
20	chr19:51334890-51334940	HPAEpiC	pulmonary alveolar:	n/a
21	chr19:51334890-51334940	PFSK-1	brain:	n/a
22	chr19:51336102-51336152	CMK	blood:	n/a
23	chr19:51334890-51334940	SAEC	small airway:	n/a
24	chr19:51334496-51334546	NB4	blood:	n/a
25	chr19:51334972-51335022	Jurkat	blood:	n/a
26	chr19:51334496-51334546	ProgFib	skin:	n/a
27	chr19:51336102-51336152	NT2-D1	testis:	n/a
28	chr19:51334972-51335022	SK-N-SH	brain:	n/a
29	chr19:51334890-51334940	PrEC	prostate:	n/a
30	chr19:51338987-51339037	PANC-1	pancreas:	n/a
31	chr19:51334972-51335022	T-47D	breast:	n/a
32	chr19:51334432-51334482	ProgFib	skin:	n/a
33	chr19:51334972-51335022	HCPEpiC	choroid plexus:	n/a
34	chr19:51336102-51336152	ECC-1	luminal epithelium:	n/a
35	chr19:51334890-51334940	H1-hESC	embryonic stem cell:	embryo
36	chr19:51336102-51336152	HUVEC	blood vessel:	n/a
37	chr19:51334432-51334482	HCT-116	colon:	n/a
38	chr19:51336166-51336216	ovcar-3	ovarian:	n/a
39	chr19:51334890-51334940	HRPEpiC	eye:	n/a
40	chr19:51334496-51334546	SK-N-SH_RA	brain:	n/a
41	chr19:51334496-51334546	MCF-7	breast:	n/a
42	chr19:51334432-51334482	Hepatocyte	liver:	n/a
43	chr19:51336166-51336216	CMK	blood:	n/a
44	chr19:51336102-51336152	PrEC	prostate:	n/a
45	chr19:51336166-51336216	RPTEC	kidney:	n/a
46	chr19:51338987-51339037	NH-A	brain:	n/a
47	chr19:51336102-51336152	SAEC	small airway:	n/a
48	chr19:51334972-51335022	PrEC	prostate:	n/a
49	chr19:51334972-51335022	HL-60	blood:	n/a
50	chr19:51334496-51334546	ECC-1	luminal epithelium:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51317814..51320322-chr19:51337524..51339862,2	K562	blood:
2	chr19:51336643..51338613-chr19:51344192..51347019,2	K562	blood:
3	chr19:51306173..51309320-chr19:51331029..51336004,5	MCF-7	breast:
4	chr19:51324739..51330198-chr19:51333522..51340343,9	K562	blood:
5	chr19:51321294..51329149-chr19:51334672..51341529,13	K562	blood:
6	chr19:51306397..51309290-chr19:51336512..51339467,5	MCF-7	breast:
7	chr19:51321080..51324665-chr19:51336622..51339226,4	K562	blood:
8	chr19:51301551..51303392-chr19:51334103..51335973,2	K562	blood:
9	chr19:51305738..51308360-chr19:51337101..51338971,2	K562	blood:
10	chr19:51329123..51330696-chr19:51332372..51334623,3	K562	blood:
11	chr19:51332534..51334303-chr19:51338291..51340341,2	MCF-7	breast:
12	chr19:51338317..51340292-chr19:51344781..51347697,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLK3-1	chr19:51333786-51333820	ENSG00000267968.1
2	lnc-KLK3-1	chr19:51334372-51334549	ENSG00000267968.1

No data

Variant related genes	Relation type
ENSG00000267968	TF binding region
KLK15	TF binding region
ENSG00000267968	CpG island
KLK15	CpG island
ENSG00000167748	chromatin interactions
ENSG00000267968	chromatin interactions
ENSG00000167747	chromatin interactions
ENSG00000221241	chromatin interactions
ENSG00000180279	chromatin interactions
ENSG00000174562	chromatin interactions
ENSG00000221381	chromatin interactions

Extended variants
information (count: 329 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3077973	chr19:51332307-51332308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs34600671	chr19:51332310-51332311	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs367832244	chr19:51332311-51332312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371395870	chr19:51332319-51332320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs4802749	chr19:51332333-51332334	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs4802750	chr19:51332335-51332336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546434081	chr19:51332343-51332344	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543906527	chr19:51332348-51332349	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs571468363	chr19:51332352-51332353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538345807	chr19:51332355-51332356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73585068	chr19:51332368-51332369	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73585071	chr19:51332401-51332402	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs536227933	chr19:51332410-51332411	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs143962377	chr19:51332412-51332413	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs148210673	chr19:51332462-51332463	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs266113	chr19:51332481-51332482	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186872857	chr19:51332494-51332495	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs141193565	chr19:51332520-51332521	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs73585073	chr19:51332563-51332564	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562969401	chr19:51332578-51332579	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576458687	chr19:51332613-51332614	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574607059	chr19:51332660-51332661	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs266114	chr19:51332670-51332671	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs377395172	chr19:51332680-51332681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs191719471	chr19:51332712-51332713	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs528369427	chr19:51332738-51332739	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs150725583	chr19:51332776-51332777	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs181265664	chr19:51332813-51332814	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185877613	chr19:51332818-51332819	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs111994810	chr19:51332893-51332894	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190255704	chr19:51332897-51332898	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529815686	chr19:51332926-51332927	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555720815	chr19:51332935-51332936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113839453	chr19:51332954-51332955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs368922590	chr19:51332968-51332969	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570888308	chr19:51333000-51333001	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs374408036	chr19:51333004-51333005	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574040531	chr19:51333051-51333052	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs571077372	chr19:51333052-51333053	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs538398819	chr19:51333059-51333060	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs182120411	chr19:51333074-51333075	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs574547822	chr19:51333075-51333076	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs146017451	chr19:51333085-51333086	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs560056928	chr19:51333113-51333114	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs74725213	chr19:51333173-51333174	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs266115	chr19:51333238-51333239	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs545571047	chr19:51333293-51333294	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs565160250	chr19:51333306-51333307	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs8101564	chr19:51333343-51333344	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs8100734	chr19:51333354-51333355	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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	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
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
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	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
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51320800-51338800	Weak transcription	Right Atrium	heart
2	chr19:51328000-51333400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr19:51331000-51338800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:51332800-51334400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr19:51333000-51333800	Enhancers	HSMM	muscle
6	chr19:51333200-51333800	Enhancers	Fetal Heart	heart
7	chr19:51333400-51333600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr19:51333400-51333600	Enhancers	A549	lung
9	chr19:51333400-51333600	Bivalent Enhancer	HepG2	liver
10	chr19:51333400-51333800	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr19:51333400-51334800	Enhancers	Colonic Mucosa	Colon
12	chr19:51333600-51333800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr19:51333800-51334000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr19:51333800-51338400	Weak transcription	Fetal Heart	heart
15	chr19:51334000-51334200	Bivalent Enhancer	HSMMtube	muscle
16	chr19:51334200-51338200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr19:51334400-51335800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr19:51334600-51334800	Bivalent/Poised TSS	Hela-S3	cervix
19	chr19:51334800-51338200	Weak transcription	A549	lung
20	chr19:51334800-51338600	Weak transcription	Colonic Mucosa	Colon
21	chr19:51335800-51336800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr19:51336000-51336400	Enhancers	K562	blood
23	chr19:51336400-51338200	Weak transcription	K562	blood
24	chr19:51338200-51338400	Flanking Active TSS	GM12878-XiMat	blood
25	chr19:51338200-51338400	Active TSS	K562	blood
26	chr19:51338200-51338600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
27	chr19:51338200-51338600	Enhancers	Pancreas	Pancrea
28	chr19:51338200-51338600	Active TSS	Rectal Mucosa Donor 31	rectum
29	chr19:51338200-51338600	Enhancers	A549	lung
30	chr19:51338200-51338600	Enhancers	NHEK	skin
31	chr19:51338200-51338800	Enhancers	Primary B cells from peripheral blood	blood
32	chr19:51338200-51338800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr19:51338200-51338800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr19:51338400-51338600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr19:51338400-51338600	Bivalent/Poised TSS	Primary B cells from cord blood	blood
36	chr19:51338400-51338600	Bivalent/Poised TSS	Primary T cells from cord blood	blood
37	chr19:51338400-51338600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
38	chr19:51338400-51338600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
39	chr19:51338400-51338600	Bivalent Enhancer	Colon Smooth Muscle	Colon
40	chr19:51338400-51338600	Enhancers	Duodenum Mucosa	Duodenum
41	chr19:51338400-51338600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr19:51338400-51338600	Enhancers	Fetal Brain Female	brain
43	chr19:51338400-51338600	Active TSS	GM12878-XiMat	blood
44	chr19:51338400-51338600	Bivalent Enhancer	Hela-S3	cervix
45	chr19:51338400-51338800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr19:51338400-51338800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
47	chr19:51338400-51338800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr19:51338400-51338800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
49	chr19:51338400-51338800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
50	chr19:51338400-51338800	Enhancers	Fetal Heart	heart

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