Variant report

Variant	esv3399851
Chromosome Location	chr19:35841723-35854402
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:977)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:35843673-35843997	K562	blood:	n/a	n/a
2	ARID3A	chr19:35843698-35844046	HepG2	liver:	n/a	n/a
3	ATF1	chr19:35849261-35849449	K562	blood:	n/a	n/a
4	ATF2	chr19:35843641-35844024	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:35843641-35844059	GM12878	blood:	n/a	n/a
6	ATF2	chr19:35843441-35844132	GM12878	blood:	n/a	n/a
7	BACH1	chr19:35851866-35852079	K562	blood:	n/a	n/a
8	BATF	chr19:35843521-35844065	GM12878	blood:	n/a	n/a
9	BATF	chr19:35845861-35846177	GM12878	blood:	n/a	n/a
10	BATF	chr19:35845812-35846219	GM12878	blood:	n/a	n/a
11	BCL11A	chr19:35845807-35846129	GM12878	blood:	n/a	n/a
12	BCL11A	chr19:35845807-35846119	GM12878	blood:	n/a	n/a
13	BCL3	chr19:35845771-35846177	GM12878	blood:	n/a	n/a
14	BCLAF1	chr19:35843466-35844148	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:35843500-35844067	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:35844722-35844918	K562	blood:	n/a	n/a
17	BHLHE40	chr19:35843412-35843999	K562	blood:	n/a	n/a
18	BHLHE40	chr19:35845830-35846158	GM12878	blood:	n/a	n/a
19	BRCA1	chr19:35843633-35843944	HepG2	liver:	n/a	n/a
20	CBX3	chr19:35843551-35844000	K562	blood:	n/a	n/a
21	CEBPB	chr19:35849017-35849385	IMR90	lung:	n/a	chr19:35849192-35849203
22	CEBPB	chr19:35849037-35849249	K562	blood:	n/a	chr19:35849192-35849203
23	CEBPB	chr19:35849083-35849292	H1-hESC	embryonic stem cell:	n/a	chr19:35849192-35849203
24	CEBPB	chr19:35849029-35849356	A549	lung:	n/a	chr19:35849192-35849203
25	CEBPB	chr19:35849025-35849368	K562	blood:	n/a	chr19:35849192-35849203
26	CEBPB	chr19:35849039-35849353	Hela-S3	cervix:	n/a	chr19:35849192-35849203
27	CEBPB	chr19:35844690-35844913	K562	blood:	n/a	n/a
28	CEBPB	chr19:35849027-35849357	HepG2	liver:	n/a	chr19:35849192-35849203
29	CHD2	chr19:35845832-35846195	GM12878	blood:	n/a	n/a
30	CHD2	chr19:35843569-35844066	GM12878	blood:	n/a	n/a
31	CREB1	chr19:35843675-35843986	A549	lung:	n/a	n/a
32	CREB1	chr19:35843592-35844040	A549	lung:	n/a	n/a
33	CREB1	chr19:35843595-35844026	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr19:35843582-35844081	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr19:35849891-35850044	NHEK	skin:	n/a	n/a
36	CTCF	chr19:35843760-35843910	AG09309	skin:	n/a	n/a
37	CTCF	chr19:35849798-35850068	GM13977	blood:	n/a	n/a
38	CTCF	chr19:35843760-35843910	HRE	kidney:	n/a	n/a
39	CTCF	chr19:35849864-35850076	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr19:35843800-35843950	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr19:35843709-35843979	ECC-1	luminal epithelium:	n/a	n/a
42	CTCF	chr19:35846962-35847134	HepG2	liver:	n/a	chr19:35847066-35847084
43	CTCF	chr19:35843760-35843910	HMEC	breast:	n/a	n/a
44	CTCF	chr19:35843780-35843930	HPF	lung:	n/a	n/a
45	CTCF	chr19:35843800-35843950	RPTEC	kidney:	n/a	n/a
46	CTCF	chr19:35844780-35844930	MCF-7	breast:	n/a	n/a
47	CTCF	chr19:35843718-35844007	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr19:35843780-35843930	AG04450	lung:	n/a	n/a
49	CTCF	chr19:35843760-35843910	GM12872	blood:	n/a	n/a
50	CTCF	chr19:35843649-35843981	ECC-1	luminal epithelium:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35849024-35849074	SK-N-MC	brain:	n/a
2	chr19:35849024-35849074	SK-N-MC	brain:	n/a
3	chr19:35843186-35843236	K562	blood:	n/a
4	chr19:35842448-35842498	HCM	heart:	n/a
5	chr19:35848801-35848851	BE2_C	brain:	n/a
6	chr19:35841676-35841726	H1-hESC	embryonic stem cell:	embryo
7	chr19:35849024-35849074	Hepatocyte	liver:	n/a
8	chr19:35842445-35842495	HIPEpiC	eye:	n/a
9	chr19:35841676-35841726	U87	brain:	n/a
10	chr19:35843282-35843332	HCPEpiC	choroid plexus:	n/a
11	chr19:35843132-35843182	AG04449	skin:	fetal
12	chr19:35849393-35849443	HAEpiC	amniotic membrane:	n/a
13	chr19:35842445-35842495	ProgFib	skin:	n/a
14	chr19:35846383-35846433	PANC-1	pancreas:	n/a
15	chr19:35842171-35842221	AG09319	gingival:	n/a
16	chr19:35850463-35850513	BJ	skin:	n/a
17	chr19:35842171-35842221	H1-hESC	embryonic stem cell:	embryo
18	chr19:35849024-35849074	Jurkat	blood:	n/a
19	chr19:35842431-35842481	CMK	blood:	n/a
20	chr19:35842586-35842636	NT2-D1	testis:	n/a
21	chr19:35843282-35843332	U87	brain:	n/a
22	chr19:35842586-35842636	Hepatocyte	liver:	n/a
23	chr19:35841676-35841726	NB4	blood:	n/a
24	chr19:35848801-35848851	NHDF-neo	bronchial:	n/a
25	chr19:35842853-35842903	HCT-116	colon:	n/a
26	chr19:35841676-35841726	Caco-2	colon:	n/a
27	chr19:35843186-35843236	GM06990	blood:	n/a
28	chr19:35846383-35846433	SAEC	small airway:	n/a
29	chr19:35846383-35846433	HMEC	breast:	n/a
30	chr19:35842586-35842636	HCF	heart:	n/a
31	chr19:35843186-35843236	HUVEC	blood vessel:	n/a
32	chr19:35848801-35848851	HCPEpiC	choroid plexus:	n/a
33	chr19:35850463-35850513	NH-A	brain:	n/a
34	chr19:35842171-35842221	HNPCEpiC	eye:	n/a
35	chr19:35842171-35842221	U87	brain:	n/a
36	chr19:35843132-35843182	PFSK-1	brain:	n/a
37	chr19:35842431-35842481	HAEpiC	amniotic membrane:	n/a
38	chr19:35846383-35846433	Hepatocyte	liver:	n/a
39	chr19:35849176-35849226	Jurkat	blood:	n/a
40	chr19:35849176-35849226	HEEpiC	esophagus:	n/a
41	chr19:35841676-35841726	GM12891	blood:	n/a
42	chr19:35848801-35848851	AG09309	skin:	n/a
43	chr19:35842171-35842221	BE2_C	brain:	n/a
44	chr19:35849393-35849443	HIPEpiC	eye:	n/a
45	chr19:35849024-35849074	HRPEpiC	eye:	n/a
46	chr19:35849176-35849226	HEK293	kidney:	embryo
47	chr19:35849024-35849074	GM12878	blood:	n/a
48	chr19:35849393-35849443	PrEC	prostate:	n/a
49	chr19:35849024-35849074	RPTEC	kidney:	n/a
50	chr19:35849176-35849226	Hepatocyte	liver:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35738565..35740290-chr19:35840353..35842474,2	MCF-7	breast:
2	chr19:35843424..35844251-chr19:36207480..36208456,3	MCF-7	breast:
3	chr19:35843603..35844331-chr19:35959340..35959868,2	K562	blood:
4	chr19:35760138..35760948-chr19:35843260..35843943,2	MCF-7	breast:
5	chr19:35843785..35844301-chr19:35986298..35986858,2	MCF-7	breast:
6	chr19:35797242..35798191-chr19:35843391..35844009,2	MCF-7	breast:
7	chr19:35738586..35740249-chr19:35841328..35842901,2	MCF-7	breast:
8	chr19:35758781..35763844-chr19:35840402..35843897,5	K562	blood:
9	chr19:35843407..35844387-chr19:35985269..35986971,10	K562	blood:
10	chr19:35843321..35844375-chr19:35959230..35959949,5	MCF-7	breast:
11	chr19:35842803..35847555-chr19:35958346..35962291,5	MCF-7	breast:
12	chr19:35768943..35770953-chr19:35842158..35843798,2	K562	blood:
13	chr19:35839659..35842221-chr19:36034910..36036786,2	MCF-7	breast:
14	chr19:35759344..35762217-chr19:35841314..35843989,4	MCF-7	breast:
15	chr19:35843276..35843934-chr19:35986292..35986832,2	MCF-7	breast:
16	chr19:35843772..35844323-chr8:129916469..129916969,2	MCF-7	breast:
17	chr19:35843479..35844366-chr19:35970362..35970878,2	MCF-7	breast:
18	chr19:35842321..35845191-chr19:35845202..35847710,3	MCF-7	breast:
19	chr19:35842680..35845070-chr19:36207201..36209915,2	K562	blood:
20	chr19:35843622..35844283-chr19:35963657..35964335,2	MCF-7	breast:
21	chr19:35843359..35844349-chr19:36000937..36001943,6	K562	blood:
22	chr19:35843378..35844331-chr19:35959313..35960316,8	MCF-7	breast:
23	chr19:35842337..35844746-chr19:35937975..35940888,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FFAR1-1	chr19:35843326-35844764	NONHSAT065829

No data

Variant related genes	Relation type
FFAR3	TF binding region
FFAR1	TF binding region
FFAR3	CpG island
FFAR1	CpG island
ENSG00000105699	chromatin interactions
ENSG00000105677	chromatin interactions
ENSG00000126266	chromatin interactions
ENSG00000236144	chromatin interactions
ENSG00000126262	chromatin interactions
ENSG00000272333	chromatin interactions
ENSG00000161249	chromatin interactions
ENSG00000188508	chromatin interactions
ENSG00000105698	chromatin interactions

Extended variants
information (count: 567 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546465427	chr19:35841730-35841731	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs563082535	chr19:35841746-35841747	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs186641429	chr19:35841761-35841762	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs200493786	chr19:35841762-35841763	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs562283774	chr19:35841791-35841792	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs374289937	chr19:35841795-35841796	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs146050843	chr19:35841816-35841817	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs377654595	chr19:35841817-35841818	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs113233684	chr19:35841824-35841825	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs547937786	chr19:35841855-35841856	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs1978013	chr19:35841857-35841858	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs1978014	chr19:35841858-35841859	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs191823138	chr19:35841924-35841925	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs183854951	chr19:35841949-35841950	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs535754610	chr19:35841962-35841963	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs189018229	chr19:35841975-35841976	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs565563771	chr19:35841977-35841978	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs534395668	chr19:35842011-35842012	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs562734694	chr19:35842034-35842035	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs377137174	chr19:35842047-35842048	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs536594764	chr19:35842052-35842053	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs556925904	chr19:35842066-35842067	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs191882409	chr19:35842149-35842150	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs542531070	chr19:35842158-35842159	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs10418569	chr19:35842241-35842242	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs572713749	chr19:35842263-35842264	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs553346205	chr19:35842275-35842276	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs564618036	chr19:35842278-35842279	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs533470248	chr19:35842289-35842290	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs544387917	chr19:35842298-35842299	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs185716928	chr19:35842322-35842323	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs560681691	chr19:35842324-35842325	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs112380079	chr19:35842334-35842335	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs529149169	chr19:35842340-35842341	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs548895443	chr19:35842341-35842342	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs565527204	chr19:35842360-35842361	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs369386290	chr19:35842371-35842372	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs182374629	chr19:35842385-35842386	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs374114764	chr19:35842442-35842443	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs148545938	chr19:35842449-35842450	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376838337	chr19:35842466-35842467	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs375966117	chr19:35842485-35842486	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs75455784	chr19:35842490-35842491	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs138336486	chr19:35842526-35842527	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs536139569	chr19:35842558-35842559	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs200173092	chr19:35842564-35842565	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs368886663	chr19:35842574-35842575	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs372221350	chr19:35842684-35842685	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs375191494	chr19:35842685-35842686	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs572675476	chr19:35842724-35842725	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Pleomorphic liposarcoma	18784837	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	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35817600-35844000	Weak transcription	Brain Angular Gyrus	brain
2	chr19:35836800-35843800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr19:35836800-35848000	Weak transcription	Brain Substantia Nigra	brain
4	chr19:35837600-35843600	Weak transcription	Brain Anterior Caudate	brain
5	chr19:35838200-35849200	Weak transcription	Brain Hippocampus Middle	brain
6	chr19:35838400-35842200	Enhancers	Primary B cells from peripheral blood	blood
7	chr19:35838600-35843600	Weak transcription	K562	blood
8	chr19:35839000-35842600	Enhancers	Primary B cells from cord blood	blood
9	chr19:35839000-35843600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr19:35839000-35843600	Enhancers	GM12878-XiMat	blood
11	chr19:35839200-35843600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr19:35839200-35843600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr19:35839200-35843600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr19:35839200-35843600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr19:35839200-35843600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr19:35839200-35843800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr19:35839200-35848600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr19:35839200-35848800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr19:35839600-35843600	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr19:35839800-35843600	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr19:35840200-35843400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr19:35840400-35843600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr19:35840600-35843400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr19:35840600-35843600	Weak transcription	HepG2	liver
25	chr19:35840800-35846200	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr19:35840800-35848400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr19:35841000-35843200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr19:35841200-35843200	Weak transcription	Spleen	Spleen
29	chr19:35841200-35843600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:35841600-35841800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr19:35841600-35843600	Weak transcription	Ovary	ovary
32	chr19:35841800-35842600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr19:35842200-35843400	Weak transcription	Primary B cells from peripheral blood	blood
34	chr19:35842600-35843000	Weak transcription	Primary B cells from cord blood	blood
35	chr19:35842600-35843800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:35842800-35843200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr19:35843000-35844200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr19:35843000-35844200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr19:35843000-35844600	Enhancers	Primary B cells from cord blood	blood
40	chr19:35843200-35843400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr19:35843200-35843600	Bivalent Enhancer	Fetal Stomach	stomach
42	chr19:35843200-35844000	Enhancers	Spleen	Spleen
43	chr19:35843200-35844200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr19:35843200-35844200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:35843400-35843600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:35843400-35843600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr19:35843400-35843600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr19:35843400-35843800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr19:35843400-35843800	Enhancers	Adipose Nuclei	Adipose
50	chr19:35843400-35844200	Enhancers	Primary B cells from peripheral blood	blood

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