Variant report

Variant	nsv978807
Chromosome Location	chr19:35806669-35810074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:0)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:35807639-35807843	HepG2	liver:	n/a	n/a
2	ATF3	chr19:35809873-35810229	K562	blood:	n/a	n/a
3	ATF3	chr19:35808447-35808621	K562	blood:	n/a	n/a
4	BHLHE40	chr19:35809843-35810360	HepG2	liver:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
5	BHLHE40	chr19:35809614-35810369	K562	blood:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
6	BHLHE40	chr19:35808385-35808689	K562	blood:	n/a	n/a
7	BHLHE40	chr19:35806795-35807157	K562	blood:	n/a	n/a
8	BHLHE40	chr19:35809868-35810291	GM12878	blood:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
9	BHLHE40	chr19:35809901-35810260	A549	lung:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
10	BRCA1	chr19:35807607-35807721	HepG2	liver:	n/a	n/a
11	BRCA1	chr19:35809644-35810243	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr19:35809344-35810321	K562	blood:	n/a	n/a
13	CCNT2	chr19:35806853-35807065	K562	blood:	n/a	n/a
14	CEBPB	chr19:35809845-35810403	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr19:35806814-35807265	K562	blood:	n/a	n/a
16	CHD2	chr19:35809658-35810465	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr19:35809776-35809889	K562	blood:	n/a	n/a
18	CHD2	chr19:35807551-35807744	HepG2	liver:	n/a	n/a
19	CTCF	chr19:35806820-35806970	K562	blood:	n/a	n/a
20	CTCF	chr19:35806780-35806930	GM06990	blood:	n/a	n/a
21	CTCF	chr19:35806861-35806990	GM19239	blood:	n/a	n/a
22	CTCF	chr19:35806780-35806930	Caco-2	colon:	n/a	n/a
23	CTCF	chr19:35806633-35807065	K562	blood:	n/a	n/a
24	CTCF	chr19:35806813-35806955	GM10248	blood:	n/a	n/a
25	CTCF	chr19:35806820-35806970	GM06990	blood:	n/a	n/a
26	CTCF	chr19:35806860-35807010	GM12871	blood:	n/a	n/a
27	CTCF	chr19:35806840-35806990	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr19:35806809-35806995	GM12892	blood:	n/a	n/a
29	CTCF	chr19:35806820-35806970	GM12873	blood:	n/a	n/a
30	CTCF	chr19:35810034-35810109	GM19239	blood:	n/a	n/a
31	CTCF	chr19:35806820-35806970	GM12872	blood:	n/a	n/a
32	CTCF	chr19:35806845-35806912	GM19240	blood:	n/a	n/a
33	CTCF	chr19:35806790-35806993	HepG2	liver:	n/a	n/a
34	CTCF	chr19:35806800-35806950	GM12868	blood:	n/a	n/a
35	CTCF	chr19:35806820-35806970	GM12878	blood:	n/a	n/a
36	CTCF	chr19:35806716-35807062	GM12878	blood:	n/a	n/a
37	CTCF	chr19:35806700-35806850	GM12873	blood:	n/a	n/a
38	CTCF	chr19:35806690-35807037	K562	blood:	n/a	n/a
39	CTCF	chr19:35809960-35810110	HEK293	kidney:	n/a	n/a
40	CTCF	chr19:35806800-35806950	HepG2	liver:	n/a	n/a
41	CTCF	chr19:35806808-35806968	GM12878	blood:	n/a	n/a
42	CTCF	chr19:35806826-35806971	GM19238	blood:	n/a	n/a
43	CTCF	chr19:35806780-35806930	GM12872	blood:	n/a	n/a
44	CTCF	chr19:35806860-35807010	Caco-2	colon:	n/a	n/a
45	CTCF	chr19:35806720-35806870	GM12865	blood:	n/a	n/a
46	CTCF	chr19:35806875-35806990	GM12891	blood:	n/a	n/a
47	CTCF	chr19:35806840-35806990	GM12867	blood:	n/a	n/a
48	CTCF	chr19:35806780-35806930	BE2_C	brain:	n/a	n/a
49	CTCF	chr19:35806717-35807076	K562	blood:	n/a	n/a
50	CTCF	chr19:35806720-35806870	GM12869	blood:	n/a	n/a

No data

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35807878..35810423-chr19:36035383..36039227,3	MCF-7	breast:
2	chr19:35740175..35741891-chr19:35807694..35809845,2	MCF-7	breast:
3	chr19:35762082..35763038-chr19:35808102..35809008,5	MCF-7	breast:
4	chr19:35788326..35791177-chr19:35803354..35807024,3	MCF-7	breast:
5	chr19:35604701..35607129-chr19:35809231..35811359,2	MCF-7	breast:
6	chr19:35758596..35761330-chr19:35808386..35811398,6	MCF-7	breast:
7	chr19:35757351..35762248-chr19:35804679..35808319,5	MCF-7	breast:
8	chr19:35607895..35610299-chr19:35808518..35810247,2	MCF-7	breast:
9	chr19:35782451..35783179-chr19:35808099..35808940,2	MCF-7	breast:
10	chr19:35801834..35808584-chr19:35810190..35813576,7	MCF-7	breast:
11	chr19:35614004..35615566-chr19:35808376..35809985,2	MCF-7	breast:
12	chr19:35801054..35803091-chr19:35805182..35806855,2	MCF-7	breast:
13	chr19:35807993..35809012-chr19:36044708..36045631,5	MCF-7	breast:
14	chr19:35778338..35780262-chr19:35804621..35807184,2	MCF-7	breast:
15	chr19:35807993..35809012-chr19:36044708..36045631,4	MCF-7	breast:
16	chr19:35808141..35808673-chr19:35999936..36000808,2	MCF-7	breast:
17	chr19:35491237..35491794-chr19:35808497..35809009,2	MCF-7	breast:
18	chr19:35738973..35741505-chr19:35806828..35808599,2	MCF-7	breast:
19	chr19:35771719..35773722-chr19:35808312..35810561,2	K562	blood:
20	chr19:35760384..35761203-chr19:35808161..35809024,2	MCF-7	breast:
21	chr19:35759827..35760405-chr19:35809677..35810195,2	MCF-7	breast:
22	chr19:35762082..35763038-chr19:35808435..35809008,4	MCF-7	breast:
23	chr19:35807998..35809046-chr19:40971871..40972634,3	MCF-7	breast:
24	chr19:35807787..35809317-chr19:35810235..35812842,2	K562	blood:
25	chr19:35755149..35764508-chr19:35799437..35813142,44	MCF-7	breast:
26	chr19:35490912..35491745-chr19:35808049..35808930,2	MCF-7	breast:
27	chr19:35808228..35808955-chr19:36059823..36060624,3	MCF-7	breast:
28	chr19:35808879..35811383-chr19:35819038..35823207,3	K562	blood:
29	chr19:35782103..35783478-chr19:35808039..35808940,5	MCF-7	breast:
30	chr19:35760570..35761203-chr19:35808161..35808860,2	MCF-7	breast:

No data

Variant related genes	Relation type
CD22	TF binding region
ENSG00000089351	chromatin interactions
ENSG00000269303	chromatin interactions
ENSG00000105677	chromatin interactions
ENSG00000105698	chromatin interactions
ENSG00000236144	chromatin interactions
ENSG00000105697	chromatin interactions
ENSG00000269553	chromatin interactions
ENSG00000105695	chromatin interactions
ENSG00000160460	chromatin interactions
ENSG00000105699	chromatin interactions
ENSG00000012124	chromatin interactions
ENSG00000089356	chromatin interactions

Extended variants
information (count: 128 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140523122	chr19:35806677-35806678	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs7254669	chr19:35806699-35806700	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs375972371	chr19:35806708-35806709	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs149918559	chr19:35806738-35806739	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs186781163	chr19:35806754-35806755	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs114688239	chr19:35806755-35806756	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs547486990	chr19:35806768-35806769	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs548174195	chr19:35806831-35806832	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs191156950	chr19:35806841-35806842	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs145005416	chr19:35806842-35806843	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs149102472	chr19:35806871-35806872	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs559390257	chr19:35806876-35806877	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs12463142	chr19:35806889-35806890	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs569928239	chr19:35806921-35806922	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs146115890	chr19:35806951-35806952	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs570354844	chr19:35806989-35806990	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs36106949	chr19:35806999-35807000	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs556353997	chr19:35807008-35807009	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs576205140	chr19:35807086-35807087	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs553273643	chr19:35807093-35807094	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs138965227	chr19:35807106-35807107	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs117190650	chr19:35807109-35807110	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs141115879	chr19:35807122-35807123	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs371377106	chr19:35807132-35807133	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs146943328	chr19:35807148-35807149	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs34559517	chr19:35807189-35807190	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs182616342	chr19:35807218-35807219	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs147995872	chr19:35807240-35807241	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs141688825	chr19:35807249-35807250	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs549787489	chr19:35807351-35807352	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs548235444	chr19:35807397-35807398	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs561860743	chr19:35807404-35807405	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs527655607	chr19:35807431-35807432	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs11673191	chr19:35807444-35807445	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs547795539	chr19:35807460-35807461	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs150869208	chr19:35807483-35807484	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs368840173	chr19:35807497-35807498	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs138285301	chr19:35807521-35807522	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs550105582	chr19:35807529-35807530	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs569829188	chr19:35807532-35807533	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs535663954	chr19:35807543-35807544	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs187786589	chr19:35807587-35807588	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs116028289	chr19:35807593-35807594	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs534308977	chr19:35807641-35807642	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs568070574	chr19:35807672-35807673	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs577465074	chr19:35807688-35807689	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs531079331	chr19:35807717-35807718	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs11673522	chr19:35807727-35807728	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs142983498	chr19:35807729-35807730	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs16970218	chr19:35807756-35807757	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

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

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35774800-35809600	Weak transcription	Right Atrium	heart
2	chr19:35794400-35810000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr19:35797800-35809600	Weak transcription	Brain Angular Gyrus	brain
4	chr19:35798200-35811400	Weak transcription	Liver	Liver
5	chr19:35801000-35809400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr19:35803000-35808600	Weak transcription	Fetal Thymus	thymus
7	chr19:35803200-35808200	Weak transcription	Brain Anterior Caudate	brain
8	chr19:35803200-35808400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr19:35803200-35809600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr19:35803200-35809600	Weak transcription	Fetal Lung	lung
11	chr19:35803400-35809800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr19:35803400-35809800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr19:35804200-35809800	Weak transcription	Fetal Kidney	kidney
14	chr19:35804200-35811000	Enhancers	Primary B cells from peripheral blood	blood
15	chr19:35804600-35809400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr19:35804600-35809800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:35804800-35806800	Weak transcription	Primary B cells from cord blood	blood
18	chr19:35804800-35806800	Weak transcription	Brain Hippocampus Middle	brain
19	chr19:35804800-35808000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr19:35804800-35808800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr19:35805000-35807800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr19:35805000-35808200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr19:35805000-35808400	Weak transcription	Spleen	Spleen
24	chr19:35805000-35809200	Weak transcription	NHEK	skin
25	chr19:35805000-35809600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:35805200-35806800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr19:35805200-35809400	Weak transcription	HMEC	breast
28	chr19:35805200-35809600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr19:35805400-35808000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr19:35805400-35808400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr19:35805600-35811400	Enhancers	K562	blood
32	chr19:35806000-35807600	Strong transcription	Brain Substantia Nigra	brain
33	chr19:35806600-35807000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:35806600-35807000	Genic enhancers	Ovary	ovary
35	chr19:35806600-35808000	Flanking Active TSS	HepG2	liver
36	chr19:35806600-35809400	Enhancers	Hela-S3	cervix
37	chr19:35806800-35807000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr19:35806800-35807000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr19:35806800-35807200	Strong transcription	Brain Hippocampus Middle	brain
40	chr19:35806800-35809400	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr19:35806800-35810600	Enhancers	Primary B cells from cord blood	blood
42	chr19:35807000-35807200	Strong transcription	Ovary	ovary
43	chr19:35807000-35808000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr19:35807000-35809600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr19:35807200-35808000	Weak transcription	Brain Hippocampus Middle	brain
46	chr19:35807200-35808400	Weak transcription	Ovary	ovary
47	chr19:35807400-35808000	Enhancers	GM12878-XiMat	blood
48	chr19:35807400-35808400	Enhancers	Duodenum Mucosa	Duodenum
49	chr19:35807400-35808400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr19:35807600-35807800	Enhancers	Fetal Muscle Trunk	muscle

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