Variant report

Variant	nsv1058936
Chromosome Location	chr19:43082848-43228161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1593)
CpG islands
(count:733)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:43208643-43208644	K562	blood:	n/a	n/a
2	BACH1	chr19:43082922-43083098	K562	blood:	n/a	n/a
3	BACH1	chr19:43100672-43101041	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:43139260-43139326	K562	blood:	n/a	n/a
5	BATF	chr19:43132976-43133178	GM12878	blood:	n/a	chr19:43133094-43133104
6	BATF	chr19:43179178-43179402	GM12878	blood:	n/a	n/a
7	BCL11A	chr19:43179101-43179287	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:43106732-43106880	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:43110839-43111090	K562	blood:	n/a	n/a
10	BHLHE40	chr19:43100628-43100974	K562	blood:	n/a	n/a
11	BHLHE40	chr19:43110883-43111176	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:43138971-43139294	HepG2	liver:	n/a	n/a
13	BHLHE40	chr19:43139176-43139401	K562	blood:	n/a	n/a
14	BRCA1	chr19:43111388-43111484	GM12878	blood:	n/a	n/a
15	BRCA1	chr19:43168346-43168356	GM12878	blood:	n/a	n/a
16	CBX3	chr19:43156238-43156476	K562	blood:	n/a	n/a
17	CBX3	chr19:43188032-43188426	HCT-116	colon:	n/a	n/a
18	CBX3	chr19:43190821-43191075	K562	blood:	n/a	n/a
19	CBX3	chr19:43190865-43191064	K562	blood:	n/a	n/a
20	CEBPB	chr19:43197922-43198219	A549	lung:	n/a	n/a
21	CEBPB	chr19:43150294-43150473	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr19:43127742-43127805	HepG2	liver:	n/a	chr19:43127762-43127773
23	CEBPB	chr19:43139178-43139417	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:43097951-43098246	HepG2	liver:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
25	CEBPB	chr19:43098008-43098186	IMR90	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
26	CEBPB	chr19:43128989-43129127	K562	blood:	n/a	n/a
27	CEBPB	chr19:43110761-43111081	HepG2	liver:	n/a	n/a
28	CEBPB	chr19:43139258-43139346	K562	blood:	n/a	n/a
29	CEBPB	chr19:43097919-43098273	A549	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
30	CEBPB	chr19:43156174-43156554	A549	lung:	n/a	chr19:43156349-43156360
31	CEBPB	chr19:43197904-43198224	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:43097979-43098209	K562	blood:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
33	CEBPB	chr19:43156216-43156522	HepG2	liver:	n/a	chr19:43156349-43156360
34	CEBPB	chr19:43197847-43198294	A549	lung:	n/a	n/a
35	CEBPB	chr19:43152306-43152361	IMR90	lung:	n/a	n/a
36	CHD2	chr19:43139100-43139262	K562	blood:	n/a	n/a
37	CTCF	chr19:43197760-43197910	AG10803	skin:	n/a	n/a
38	CTCF	chr19:43100760-43100910	GM12870	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
39	CTCF	chr19:43139220-43139370	GM12867	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
40	CTCF	chr19:43187986-43188511	A549	lung:	n/a	chr19:43188263-43188279 chr19:43188262-43188280 chr19:43188264-43188285
41	CTCF	chr19:43188180-43188330	HepG2	liver:	n/a	chr19:43188263-43188279 chr19:43188262-43188280 chr19:43188264-43188285
42	CTCF	chr19:43197753-43197834	GM12878	blood:	n/a	n/a
43	CTCF	chr19:43187912-43188025	GM12878	blood:	n/a	n/a
44	CTCF	chr19:43174860-43175010	A549	lung:	n/a	n/a
45	CTCF	chr19:43174832-43174940	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:43110380-43110530	GM12864	blood:	n/a	n/a
47	CTCF	chr19:43188240-43188390	WI-38	lung:	n/a	chr19:43188263-43188279 chr19:43188262-43188280 chr19:43188264-43188285
48	CTCF	chr19:43100740-43100890	GM12864	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
49	CTCF	chr19:43160200-43160350	NHEK	skin:	n/a	n/a
50	CTCF	chr19:43197980-43198130	HPF	lung:	n/a	chr19:43198076-43198097 chr19:43198074-43198092 chr19:43198023-43198031 chr19:43198071-43198089 chr19:43198075-43198091

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43203368-43203418	HCPEpiC	choroid plexus:	n/a
2	chr19:43203368-43203418	HCPEpiC	choroid plexus:	n/a
3	chr19:43099124-43099174	ProgFib	skin:	n/a
4	chr19:43200890-43200940	IMR90	lung:	fetal
5	chr19:43202122-43202172	Hela-S3	cervix:	n/a
6	chr19:43099124-43099174	HUVEC	blood vessel:	n/a
7	chr19:43198154-43198204	BE2_C	brain:	n/a
8	chr19:43202122-43202172	MCF10A-Er-Src	breast:	n/a
9	chr19:43198154-43198204	IMR90	lung:	fetal
10	chr19:43227392-43227442	HUVEC	blood vessel:	n/a
11	chr19:43099845-43099895	NT2-D1	testis:	n/a
12	chr19:43203368-43203418	PrEC	prostate:	n/a
13	chr19:43198154-43198204	GM12892	blood:	n/a
14	chr19:43099845-43099895	HCPEpiC	choroid plexus:	n/a
15	chr19:43099124-43099174	ECC-1	luminal epithelium:	n/a
16	chr19:43203368-43203418	HCF	heart:	n/a
17	chr19:43198154-43198204	T-47D	breast:	n/a
18	chr19:43099482-43099532	GM12891	blood:	n/a
19	chr19:43099795-43099845	Hepatocyte	liver:	n/a
20	chr19:43099124-43099174	HRE	kidney:	n/a
21	chr19:43099482-43099532	AG09309	skin:	n/a
22	chr19:43203368-43203418	U87	brain:	n/a
23	chr19:43099845-43099895	ECC-1	luminal epithelium:	n/a
24	chr19:43200890-43200940	HCT-116	colon:	n/a
25	chr19:43099482-43099532	MCF-7	breast:	n/a
26	chr19:43099124-43099174	MCF10A-Er-Src	breast:	n/a
27	chr19:43200890-43200940	Jurkat	blood:	n/a
28	chr19:43202312-43202362	GM06990	blood:	n/a
29	chr19:43202122-43202172	GM12891	blood:	n/a
30	chr19:43198154-43198204	AG04450	lung:	fetal
31	chr19:43202312-43202362	AG09319	gingival:	n/a
32	chr19:43085416-43085466	HRCEpiC	kidney:	n/a
33	chr19:43198154-43198204	HRCEpiC	kidney:	n/a
34	chr19:43200890-43200940	HCM	heart:	n/a
35	chr19:43099482-43099532	HRE	kidney:	n/a
36	chr19:43202312-43202362	HAEpiC	amniotic membrane:	n/a
37	chr19:43203368-43203418	HCT-116	colon:	n/a
38	chr19:43202312-43202362	HUVEC	blood vessel:	n/a
39	chr19:43227392-43227442	HCPEpiC	choroid plexus:	n/a
40	chr19:43099482-43099532	HCF	heart:	n/a
41	chr19:43198154-43198204	AG09309	skin:	n/a
42	chr19:43203368-43203418	Hela-S3	cervix:	n/a
43	chr19:43200890-43200940	AG04450	lung:	fetal
44	chr19:43202312-43202362	SK-N-SH	brain:	n/a
45	chr19:43198154-43198204	PFSK-1	brain:	n/a
46	chr19:43099124-43099174	AoSMC	blood vessel:	n/a
47	chr19:43099845-43099895	U87	brain:	n/a
48	chr19:43200890-43200940	SK-N-SH	brain:	n/a
49	chr19:43099795-43099845	Hela-S3	cervix:	n/a
50	chr19:43099124-43099174	HRPEpiC	eye:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:42633464..42636070-chr19:43108015..43110975,2	K562	blood:
2	chr19:42954441..42955205-chr19:43100309..43101289,2	MCF-7	breast:
3	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
4	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
5	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:
6	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
7	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
8	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
9	chr19:43139154..43139986-chr19:43246322..43246897,2	MCF-7	breast:
10	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
11	chr19:43149390..43151656-chr19:43158079..43159963,2	MCF-7	breast:
12	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
13	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
14	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
15	chr19:43070688..43071772-chr19:43100056..43100921,4	MCF-7	breast:
16	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
17	chr19:43067242..43067993-chr19:43100482..43101078,2	MCF-7	breast:
18	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
19	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
20	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:
21	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
22	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
23	chr19:43148558..43149434-chr20:53015100..53015659,2	MCF-7	breast:
24	chr19:43070787..43071783-chr19:43100383..43100953,3	MCF-7	breast:
25	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
26	chr19:43092830..43095599-chr19:43097248..43100120,2	K562	blood:
27	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
28	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
29	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066551
2	lnc-AC011497.1-2	chr19:43155239-43156171	ENSG00000213904.4
3	lnc-AC011497.1-2	chr19:43155869-43156816	NONHSAT066564
4	lnc-AC011497.1-2	chr19:43155388-43155602	NONHSAT066564
5	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066548
6	lnc-AC011497.1-2	chr19:43155239-43156507	ENSG00000213904.4

No data

Variant related genes	Relation type
CEACAMP1	TF binding region
RPS10P28	TF binding region
CEACAM8	TF binding region
CEACAMP5	TF binding region
CEACAMP1	CpG island
RPS10P28	CpG island
CEACAM8	CpG island
CEACAMP5	CpG island
ENSG00000124469	chromatin interactions
ENSG00000231561	chromatin interactions

Extended variants
information (count: 3835 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3835 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10402361	chr19:43082848-43082849	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375516154	chr19:43082909-43082910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192486457	chr19:43082952-43082953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150843491	chr19:43082963-43082964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185287658	chr19:43082964-43082965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376968180	chr19:43082973-43082974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74940545	chr19:43082996-43082997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564964573	chr19:43083016-43083017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572442777	chr19:43083019-43083020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541551747	chr19:43083028-43083029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs45595831	chr19:43083043-43083044	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs111266523	chr19:43083067-43083068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530342100	chr19:43083074-43083075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550464128	chr19:43083112-43083113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548404542	chr19:43083126-43083127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190180238	chr19:43083165-43083166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532886944	chr19:43083166-43083167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10403065	chr19:43083171-43083172	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs10403856	chr19:43083227-43083228	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566996722	chr19:43083266-43083267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533611346	chr19:43083362-43083363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547471277	chr19:43083365-43083366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181523890	chr19:43083450-43083451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139262529	chr19:43083504-43083505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375369775	chr19:43083612-43083613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142802005	chr19:43083694-43083695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs386809432	chr19:43083703-43083704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs80225363	chr19:43083716-43083717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538593312	chr19:43083834-43083835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558515464	chr19:43083883-43083884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572411700	chr19:43083935-43083936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111903477	chr19:43084134-43084135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541140354	chr19:43084143-43084144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563218698	chr19:43084162-43084163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73932731	chr19:43084235-43084236	Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs113795833	chr19:43084241-43084242	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544012425	chr19:43084280-43084281	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs45459094	chr19:43084292-43084293	Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs146053787	chr19:43084301-43084302	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564888540	chr19:43084315-43084316	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184895640	chr19:43084406-43084407	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564680114	chr19:43084408-43084409	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527302962	chr19:43084430-43084431	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189408163	chr19:43084475-43084476	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139996497	chr19:43084481-43084482	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374171388	chr19:43084546-43084547	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529765618	chr19:43084579-43084580	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549560814	chr19:43084604-43084605	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143477715	chr19:43084616-43084617	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117250901	chr19:43084617-43084618	Genic enhancers Weak transcription	n/a	n/a	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
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
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
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	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
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164920	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43072400-43084200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr19:43081400-43100600	Weak transcription	Spleen	Spleen
3	chr19:43082600-43083600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr19:43083600-43083800	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr19:43084200-43084800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
6	chr19:43084800-43085400	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr19:43085400-43086200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr19:43086200-43088000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
9	chr19:43088000-43092200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr19:43088400-43088800	Bivalent Enhancer	Primary B cells from cord blood	blood
11	chr19:43088400-43089400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr19:43088800-43089400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr19:43090200-43091200	Bivalent Enhancer	Primary B cells from cord blood	blood
14	chr19:43092200-43094400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
15	chr19:43094200-43094400	Enhancers	Primary B cells from cord blood	blood
16	chr19:43094400-43095400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr19:43094400-43100200	Weak transcription	Primary B cells from cord blood	blood
18	chr19:43095400-43096400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
19	chr19:43096400-43096800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr19:43096800-43097400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr19:43096800-43099000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr19:43097400-43097800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr19:43097800-43099200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr19:43099200-43099600	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr19:43099600-43100800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr19:43099800-43100200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr19:43100200-43100800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr19:43100200-43100800	Enhancers	Primary B cells from cord blood	blood
29	chr19:43100400-43100800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr19:43100400-43101000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr19:43100400-43101000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr19:43100400-43101200	Enhancers	Adipose Nuclei	Adipose
33	chr19:43100600-43100800	Bivalent Enhancer	Placenta	Placenta
34	chr19:43100600-43101000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr19:43100600-43101000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr19:43100600-43101000	Enhancers	Right Ventricle	heart
37	chr19:43100600-43101000	Enhancers	Spleen	Spleen
38	chr19:43100600-43101200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
39	chr19:43100600-43101200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr19:43100600-43101200	Enhancers	Brain Cingulate Gyrus	brain
41	chr19:43100600-43101200	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr19:43100600-43101200	Bivalent Enhancer	HepG2	liver
43	chr19:43100800-43101000	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr19:43100800-43101000	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr19:43100800-43101000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr19:43100800-43101200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr19:43100800-43101200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:43100800-43101200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
49	chr19:43100800-43101200	Enhancers	Esophagus	oesophagus
50	chr19:43100800-43101200	Enhancers	Pancreas	Pancrea

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