Variant report

Variant	esv3318773
Chromosome Location	chr19:39890112-39895210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:39891901-39893190	HepG2	liver:	n/a	n/a
2	ATF1	chr19:39892005-39892428	K562	blood:	n/a	n/a
3	ATF2	chr19:39894304-39895045	GM12878	blood:	n/a	chr19:39894575-39894589
4	ATF2	chr19:39892078-39893568	GM12878	blood:	n/a	n/a
5	ATF2	chr19:39891946-39893640	GM12878	blood:	n/a	n/a
6	ATF2	chr19:39894349-39895026	GM12878	blood:	n/a	chr19:39894575-39894589
7	ATF2	chr19:39894101-39894517	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:39893966-39894815	A549	lung:	n/a	chr19:39894673-39894693
9	ATF3	chr19:39893946-39894977	A549	lung:	n/a	chr19:39894673-39894693
10	ATF3	chr19:39893053-39893420	K562	blood:	n/a	n/a
11	ATF3	chr19:39891617-39893534	A549	lung:	n/a	n/a
12	ATF3	chr19:39894101-39894837	K562	blood:	n/a	chr19:39894673-39894693
13	ATF3	chr19:39892895-39893389	K562	blood:	n/a	n/a
14	ATF3	chr19:39894477-39894756	K562	blood:	n/a	chr19:39894673-39894693
15	ATF3	chr19:39891444-39893565	A549	lung:	n/a	n/a
16	BACH1	chr19:39892949-39893142	K562	blood:	n/a	n/a
17	BACH1	chr19:39893395-39893649	K562	blood:	n/a	n/a
18	BACH1	chr19:39892564-39894792	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr19:39894081-39894661	K562	blood:	n/a	n/a
20	BATF	chr19:39892000-39892367	GM12878	blood:	n/a	chr19:39892189-39892199 chr19:39892188-39892199
21	BATF	chr19:39894476-39894800	GM12878	blood:	n/a	n/a
22	BCL11A	chr19:39893187-39893605	GM12878	blood:	n/a	chr19:39893594-39893603 chr19:39893575-39893588 chr19:39893576-39893589 chr19:39893435-39893444
23	BCL11A	chr19:39894445-39894881	GM12878	blood:	n/a	chr19:39894737-39894746 chr19:39894609-39894618 chr19:39894729-39894738 chr19:39894667-39894680 chr19:39894700-39894709
24	BCL11A	chr19:39892276-39892651	GM12878	blood:	n/a	n/a
25	BCL11A	chr19:39892176-39892895	GM12878	blood:	n/a	n/a
26	BCL11A	chr19:39894499-39894822	GM12878	blood:	n/a	chr19:39894737-39894746 chr19:39894609-39894618 chr19:39894729-39894738 chr19:39894667-39894680 chr19:39894700-39894709
27	BCL3	chr19:39894419-39894926	GM12878	blood:	n/a	chr19:39894737-39894746 chr19:39894609-39894618 chr19:39894729-39894738 chr19:39894667-39894680 chr19:39894700-39894709
28	BCL3	chr19:39891503-39893841	A549	lung:	n/a	chr19:39893594-39893603 chr19:39893575-39893588 chr19:39893576-39893589 chr19:39893435-39893444
29	BCL3	chr19:39891947-39893730	GM12878	blood:	n/a	chr19:39893594-39893603 chr19:39893575-39893588 chr19:39893576-39893589 chr19:39893435-39893444
30	BCL3	chr19:39890154-39890902	A549	lung:	n/a	n/a
31	BCL3	chr19:39890114-39891402	A549	lung:	n/a	n/a
32	BCL3	chr19:39893904-39895106	A549	lung:	n/a	chr19:39894737-39894746 chr19:39894609-39894618 chr19:39894729-39894738 chr19:39894667-39894680 chr19:39894700-39894709
33	BCL3	chr19:39891530-39893804	A549	lung:	n/a	chr19:39893594-39893603 chr19:39893575-39893588 chr19:39893576-39893589 chr19:39893435-39893444
34	BCL3	chr19:39893964-39894999	A549	lung:	n/a	chr19:39894737-39894746 chr19:39894609-39894618 chr19:39894729-39894738 chr19:39894667-39894680 chr19:39894700-39894709
35	BCL3	chr19:39892172-39893541	GM12878	blood:	n/a	chr19:39893435-39893444
36	BCLAF1	chr19:39893031-39893480	K562	blood:	n/a	chr19:39893435-39893444
37	BCLAF1	chr19:39891650-39893742	GM12878	blood:	n/a	chr19:39893594-39893603 chr19:39893575-39893588 chr19:39893576-39893589 chr19:39893435-39893444
38	BCLAF1	chr19:39893997-39894919	GM12878	blood:	n/a	chr19:39894737-39894746 chr19:39894609-39894618 chr19:39894729-39894738 chr19:39894667-39894680 chr19:39894700-39894709
39	BCLAF1	chr19:39891847-39893779	GM12878	blood:	n/a	chr19:39893594-39893603 chr19:39893575-39893588 chr19:39893576-39893589 chr19:39893435-39893444
40	BCLAF1	chr19:39894277-39894995	GM12878	blood:	n/a	chr19:39894737-39894746 chr19:39894609-39894618 chr19:39894729-39894738 chr19:39894667-39894680 chr19:39894700-39894709
41	BHLHE40	chr19:39894169-39894985	A549	lung:	n/a	n/a
42	BHLHE40	chr19:39894065-39895014	K562	blood:	n/a	n/a
43	BHLHE40	chr19:39891954-39893240	HepG2	liver:	n/a	n/a
44	BHLHE40	chr19:39891951-39893694	A549	lung:	n/a	chr19:39893578-39893594
45	BHLHE40	chr19:39891779-39895197	GM12878	blood:	n/a	chr19:39893578-39893594
46	BHLHE40	chr19:39891979-39893689	K562	blood:	n/a	chr19:39893578-39893594
47	BRCA1	chr19:39894219-39894845	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr19:39892946-39893095	HepG2	liver:	n/a	n/a
49	BRCA1	chr19:39892272-39892606	HepG2	liver:	n/a	n/a
50	BRCA1	chr19:39894318-39894601	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39894666-39894716	NHBE	bronchial:	n/a
2	chr19:39894764-39894814	MCF10A-Er-Src	breast:	n/a
3	chr19:39892799-39892849	Hepatocyte	liver:	n/a
4	chr19:39894666-39894716	MCF-7	breast:	n/a
5	chr19:39892799-39892849	CMK	blood:	n/a
6	chr19:39893195-39893245	Jurkat	blood:	n/a
7	chr19:39894666-39894716	HCPEpiC	choroid plexus:	n/a
8	chr19:39894764-39894814	HIPEpiC	eye:	n/a
9	chr19:39894764-39894814	Jurkat	blood:	n/a
10	chr19:39893195-39893245	SKMC	muscle:	n/a
11	chr19:39894559-39894609	H1-hESC	embryonic stem cell:	embryo
12	chr19:39893195-39893245	ovcar-3	ovarian:	n/a
13	chr19:39894666-39894716	PrEC	prostate:	n/a
14	chr19:39894764-39894814	HRCEpiC	kidney:	n/a
15	chr19:39892799-39892849	AG09319	gingival:	n/a
16	chr19:39892799-39892849	A549	lung:	n/a
17	chr19:39894764-39894814	MCF-7	breast:	n/a
18	chr19:39894767-39894817	U87	brain:	n/a
19	chr19:39894764-39894814	K562	blood:	n/a
20	chr19:39892799-39892849	HCM	heart:	n/a
21	chr19:39894764-39894814	HCM	heart:	n/a
22	chr19:39893195-39893245	ECC-1	luminal epithelium:	n/a
23	chr19:39894767-39894817	BE2_C	brain:	n/a
24	chr19:39894559-39894609	HMEC	breast:	n/a
25	chr19:39890911-39890961	HUVEC	blood vessel:	n/a
26	chr19:39893195-39893245	SAEC	small airway:	n/a
27	chr19:39894764-39894814	GM19239	blood:	n/a
28	chr19:39893195-39893245	AoSMC	blood vessel:	n/a
29	chr19:39894666-39894716	HepG2	liver:	n/a
30	chr19:39894559-39894609	HRE	kidney:	n/a
31	chr19:39894767-39894817	HRPEpiC	eye:	n/a
32	chr19:39894764-39894814	PrEC	prostate:	n/a
33	chr19:39894764-39894814	HUVEC	blood vessel:	n/a
34	chr19:39893195-39893245	SK-N-SH	brain:	n/a
35	chr19:39893195-39893245	AG04449	skin:	fetal
36	chr19:39890911-39890961	AG04449	skin:	fetal
37	chr19:39894666-39894716	BJ	skin:	n/a
38	chr19:39890911-39890961	GM06990	blood:	n/a
39	chr19:39894559-39894609	BJ	skin:	n/a
40	chr19:39894666-39894716	HPAEpiC	pulmonary alveolar:	n/a
41	chr19:39894767-39894817	HCPEpiC	choroid plexus:	n/a
42	chr19:39894559-39894609	GM12892	blood:	n/a
43	chr19:39894559-39894609	HCF	heart:	n/a
44	chr19:39892799-39892849	HAEpiC	amniotic membrane:	n/a
45	chr19:39894767-39894817	GM12891	blood:	n/a
46	chr19:39893195-39893245	NH-A	brain:	n/a
47	chr19:39894767-39894817	Hepatocyte	liver:	n/a
48	chr19:39890911-39890961	SK-N-MC	brain:	n/a
49	chr19:39892799-39892849	HL-60	blood:	n/a
50	chr19:39893195-39893245	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:39892567..39894706-chr19:40016383..40018403,2	K562	blood:
2	chr19:39699475..39701716-chr19:39889022..39890849,2	MCF-7	breast:
3	chr19:39892099..39894899-chr20:45988132..45989899,2	MCF-7	breast:
4	chr19:39894110..39895108-chr2:121832156..121833021,2	Hela-S3	cervix:
5	chr19:39887866..39890343-chr19:40030809..40032954,2	MCF-7	breast:
6	chr19:39837705..39840014-chr19:39891010..39893848,2	MCF-7	breast:
7	chr1:45241109..45241631-chr19:39894426..39894926,2	HCT-116	colon:
8	chr19:39891894..39893517-chr19:39962020..39964082,2	K562	blood:
9	chr1:3817339..3817901-chr19:39893395..39894216,2	Hela-S3	cervix:
10	chr19:39893196..39895716-chr19:39934783..39936652,2	MCF-7	breast:
11	chr19:39615977..39618241-chr19:39893024..39896089,3	MCF-7	breast:
12	chr19:39836712..39838528-chr19:39893059..39894655,2	K562	blood:
13	chr19:39891586..39893179-chr19:40030915..40033387,2	MCF-7	breast:
14	chr1:201979450..201979955-chr19:39892907..39893652,2	HCT-116	colon:
15	chr19:39890843..39892874-chr19:40028629..40030722,2	MCF-7	breast:
16	chr19:39849513..39851836-chr19:39891478..39893245,2	K562	blood:
17	chr19:39891472..39894356-chr19:39969884..39972397,2	K562	blood:
18	chr19:39615245..39617740-chr19:39889549..39891116,2	MCF-7	breast:

Variant related genes	Relation type
ZFP36	TF binding region
ZFP36	CpG island
ENSG00000105197	chromatin interactions
ENSG00000264294	chromatin interactions
ENSG00000130669	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000176396	chromatin interactions
ENSG00000225721	chromatin interactions
ENSG00000142937	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000196235	chromatin interactions

Extended variants
information (count: 169 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:169 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553103627	chr19:39890140-39890141	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574591730	chr19:39890153-39890154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs542007613	chr19:39890182-39890183	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs374787634	chr19:39890246-39890247	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185752989	chr19:39890248-39890249	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs146374303	chr19:39890258-39890259	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189683263	chr19:39890262-39890263	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139593249	chr19:39890267-39890268	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs532392224	chr19:39890305-39890306	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs548922381	chr19:39890310-39890311	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs182859715	chr19:39890322-39890323	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs559374196	chr19:39890381-39890382	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530143528	chr19:39890393-39890394	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560723880	chr19:39890403-39890404	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562858628	chr19:39890459-39890460	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs548346133	chr19:39890466-39890467	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570129280	chr19:39890480-39890481	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576932334	chr19:39890526-39890527	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531170552	chr19:39890541-39890542	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs117687643	chr19:39890545-39890546	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571171438	chr19:39890607-39890608	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534554391	chr19:39890610-39890611	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs188758948	chr19:39890726-39890727	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs193293164	chr19:39890733-39890734	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535564040	chr19:39890736-39890737	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557045200	chr19:39890773-39890774	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201125461	chr19:39890793-39890794	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144312899	chr19:39890800-39890801	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546018292	chr19:39890808-39890809	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112947797	chr19:39890836-39890837	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557764387	chr19:39890886-39890887	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs376148851	chr19:39890958-39890959	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541042108	chr19:39890975-39890976	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534809630	chr19:39891024-39891025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373366483	chr19:39891068-39891069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs73547948	chr19:39891128-39891129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10414216	chr19:39891161-39891162	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs146048872	chr19:39891163-39891164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs28750116	chr19:39891175-39891176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571398573	chr19:39891199-39891200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10412877	chr19:39891219-39891220	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs34947393	chr19:39891220-39891221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531010294	chr19:39891222-39891223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76140040	chr19:39891300-39891301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564586102	chr19:39891320-39891321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376749345	chr19:39891328-39891329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546588942	chr19:39891350-39891351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569527229	chr19:39891357-39891358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187277065	chr19:39891358-39891359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142298188	chr19:39891401-39891402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39883000-39891800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:39883200-39891600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:39883200-39892400	Weak transcription	Fetal Brain Male	brain
4	chr19:39883200-39892400	Weak transcription	Fetal Kidney	kidney
5	chr19:39885000-39892600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr19:39886200-39892000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr19:39886200-39892400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr19:39886800-39893400	Weak transcription	Aorta	Aorta
9	chr19:39886800-39893400	Weak transcription	Ovary	ovary
10	chr19:39887800-39890600	Genic enhancers	Fetal Thymus	thymus
11	chr19:39888000-39890400	Genic enhancers	Placenta	Placenta
12	chr19:39888000-39890600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:39888000-39891000	Genic enhancers	Fetal Intestine Small	intestine
14	chr19:39888000-39892400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr19:39888000-39893600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr19:39888000-39893600	Enhancers	Stomach Mucosa	stomach
17	chr19:39888200-39890400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:39888200-39892000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr19:39888200-39892000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr19:39888200-39892600	Weak transcription	Fetal Brain Female	brain
21	chr19:39888400-39890600	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr19:39888800-39890200	Enhancers	K562	blood
23	chr19:39888800-39892000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:39888800-39892000	Weak transcription	Brain Substantia Nigra	brain
25	chr19:39888800-39892200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr19:39888800-39892200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr19:39888800-39892200	Weak transcription	Fetal Heart	heart
28	chr19:39888800-39892400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr19:39888800-39892400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr19:39889000-39890400	Genic enhancers	Primary hematopoietic stem cells	blood
31	chr19:39889000-39890600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr19:39889000-39890600	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr19:39889000-39890800	Strong transcription	Brain Anterior Caudate	brain
34	chr19:39889000-39891000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr19:39889000-39891600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr19:39889000-39891800	Weak transcription	Right Atrium	heart
37	chr19:39889000-39892000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr19:39889000-39892000	Enhancers	Primary T cells from cord blood	blood
39	chr19:39889000-39892000	Enhancers	Adipose Nuclei	Adipose
40	chr19:39889000-39892200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr19:39889000-39893000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr19:39889200-39890400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr19:39889200-39890600	Genic enhancers	Primary B cells from peripheral blood	blood
44	chr19:39889200-39890600	Enhancers	Esophagus	oesophagus
45	chr19:39889200-39891600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr19:39889200-39891800	Enhancers	Duodenum Mucosa	Duodenum
47	chr19:39889200-39892000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr19:39889200-39892000	Weak transcription	Brain Hippocampus Middle	brain
49	chr19:39889200-39892200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr19:39889200-39892400	Weak transcription	HUVEC	blood vessel

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