Variant report

Variant	nsv518076
Chromosome Location	chr19:19692579-19715794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:19701724-19701788	K562	blood:	n/a	n/a
2	ATF1	chr19:19708620-19708998	K562	blood:	n/a	n/a
3	ATF2	chr19:19701822-19702482	GM12878	blood:	n/a	n/a
4	ATF2	chr19:19709284-19709617	GM12878	blood:	n/a	n/a
5	ATF2	chr19:19709294-19709757	GM12878	blood:	n/a	n/a
6	ATF2	chr19:19701874-19702366	GM12878	blood:	n/a	n/a
7	ATF2	chr19:19708416-19709227	GM12878	blood:	n/a	n/a
8	ATF2	chr19:19708385-19709153	GM12878	blood:	n/a	n/a
9	BATF	chr19:19709251-19709773	GM12878	blood:	n/a	n/a
10	BATF	chr19:19701784-19702254	GM12878	blood:	n/a	chr19:19702037-19702047
11	BATF	chr19:19701888-19702196	GM12878	blood:	n/a	chr19:19702037-19702047
12	BATF	chr19:19708596-19709090	GM12878	blood:	n/a	chr19:19708795-19708806
13	BATF	chr19:19708611-19709090	GM12878	blood:	n/a	chr19:19708795-19708806
14	BATF	chr19:19709299-19709583	GM12878	blood:	n/a	n/a
15	BCL11A	chr19:19708658-19709020	GM12878	blood:	n/a	n/a
16	BCL11A	chr19:19701687-19702193	GM12878	blood:	n/a	chr19:19702024-19702033
17	BCL11A	chr19:19708497-19709079	GM12878	blood:	n/a	n/a
18	BCL3	chr19:19708556-19709068	GM12878	blood:	n/a	n/a
19	BCLAF1	chr19:19708360-19709227	GM12878	blood:	n/a	n/a
20	BCLAF1	chr19:19708349-19709134	GM12878	blood:	n/a	n/a
21	BHLHE40	chr19:19708486-19709152	GM12878	blood:	n/a	n/a
22	BHLHE40	chr19:19706095-19706110	K562	blood:	n/a	n/a
23	BHLHE40	chr19:19709432-19709840	GM12878	blood:	n/a	n/a
24	CEBPB	chr19:19705878-19706258	IMR90	lung:	n/a	chr19:19706060-19706069 chr19:19706058-19706071 chr19:19706060-19706071
25	CEBPB	chr19:19701921-19702439	MCF-7	breast:	n/a	n/a
26	CEBPB	chr19:19705940-19706165	Hela-S3	cervix:	n/a	chr19:19706060-19706069 chr19:19706058-19706071 chr19:19706060-19706071
27	CEBPB	chr19:19702006-19702290	HepG2	liver:	n/a	n/a
28	CEBPB	chr19:19701892-19702358	MCF-7	breast:	n/a	n/a
29	CEBPB	chr19:19701956-19702428	A549	lung:	n/a	n/a
30	CEBPB	chr19:19708306-19709831	GM12878	blood:	n/a	n/a
31	CEBPB	chr19:19701789-19702580	GM12878	blood:	n/a	n/a
32	CEBPB	chr19:19702105-19702196	K562	blood:	n/a	n/a
33	CEBPB	chr19:19702033-19702314	A549	lung:	n/a	n/a
34	CEBPB	chr19:19705980-19706156	A549	lung:	n/a	chr19:19706060-19706069 chr19:19706058-19706071 chr19:19706060-19706071
35	CEBPB	chr19:19705756-19706612	MCF-7	breast:	n/a	chr19:19706060-19706069 chr19:19706058-19706071 chr19:19706060-19706071
36	CEBPB	chr19:19701971-19702299	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr19:19701652-19702611	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:19701950-19702382	IMR90	lung:	n/a	n/a
39	CEBPB	chr19:19705919-19706230	HepG2	liver:	n/a	chr19:19706060-19706069 chr19:19706058-19706071 chr19:19706060-19706071
40	CEBPB	chr19:19705892-19706216	K562	blood:	n/a	chr19:19706060-19706069 chr19:19706058-19706071 chr19:19706060-19706071
41	CEBPB	chr19:19714360-19714484	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr19:19701901-19702539	GM12878	blood:	n/a	n/a
43	CHD2	chr19:19708537-19709071	GM12878	blood:	n/a	n/a
44	CHD2	chr19:19701936-19702466	GM12878	blood:	n/a	n/a
45	CREB1	chr19:19708474-19709183	GM12878	blood:	n/a	n/a
46	CREB1	chr19:19708493-19709164	GM12878	blood:	n/a	n/a
47	CTCF	chr19:19695344-19695397	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr19:19706437-19706596	MCF-7	breast:	n/a	chr19:19706506-19706522
49	CTCF	chr19:19695260-19695410	HEK293	kidney:	n/a	n/a
50	CTCF	chr19:19706461-19706533	H1-hESC	embryonic stem cell:	n/a	chr19:19706506-19706522

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19702508-19702558	HRE	kidney:	n/a
2	chr19:19702508-19702558	HMEC	breast:	n/a
3	chr19:19702508-19702558	H1-hESC	embryonic stem cell:	embryo
4	chr19:19702508-19702558	Hepatocyte	liver:	n/a
5	chr19:19702508-19702558	HCM	heart:	n/a
6	chr19:19702508-19702558	AG09319	gingival:	n/a
7	chr19:19702508-19702558	HCF	heart:	n/a
8	chr19:19702508-19702558	Hela-S3	cervix:	n/a
9	chr19:19702508-19702558	BJ	skin:	n/a
10	chr19:19702508-19702558	NHBE	bronchial:	n/a
11	chr19:19702508-19702558	HAEpiC	amniotic membrane:	n/a
12	chr19:19702508-19702558	IMR90	lung:	fetal
13	chr19:19702508-19702558	PANC-1	pancreas:	n/a
14	chr19:19702508-19702558	LNCaP	prostate:	n/a
15	chr19:19702508-19702558	GM12892	blood:	n/a
16	chr19:19702508-19702558	HEK293	kidney:	embryo
17	chr19:19702508-19702558	BE2_C	brain:	n/a
18	chr19:19702508-19702558	SK-N-SH_RA	brain:	n/a
19	chr19:19702508-19702558	AG04449	skin:	fetal
20	chr19:19702508-19702558	CMK	blood:	n/a
21	chr19:19702508-19702558	GM12878	blood:	n/a
22	chr19:19702508-19702558	SK-N-MC	brain:	n/a
23	chr19:19702508-19702558	U87	brain:	n/a
24	chr19:19702508-19702558	RPTEC	kidney:	n/a
25	chr19:19702508-19702558	T-47D	breast:	n/a
26	chr19:19702508-19702558	K562	blood:	n/a
27	chr19:19702508-19702558	Caco-2	colon:	n/a
28	chr19:19702508-19702558	PrEC	prostate:	n/a
29	chr19:19702508-19702558	ECC-1	luminal epithelium:	n/a
30	chr19:19702508-19702558	HUVEC	blood vessel:	n/a
31	chr19:19702508-19702558	MCF-7	breast:	n/a
32	chr19:19702508-19702558	NT2-D1	testis:	n/a
33	chr19:19702508-19702558	PFSK-1	brain:	n/a
34	chr19:19702508-19702558	ProgFib	skin:	n/a
35	chr19:19702508-19702558	GM19239	blood:	n/a
36	chr19:19702508-19702558	NB4	blood:	n/a
37	chr19:19702508-19702558	HEEpiC	esophagus:	n/a
38	chr19:19702508-19702558	NH-A	brain:	n/a
39	chr19:19702508-19702558	ovcar-3	ovarian:	n/a
40	chr19:19702508-19702558	HIPEpiC	eye:	n/a
41	chr19:19702508-19702558	GM12891	blood:	n/a
42	chr19:19702508-19702558	AoSMC	blood vessel:	n/a
43	chr19:19702508-19702558	HRCEpiC	kidney:	n/a
44	chr19:19702508-19702558	NHDF-neo	bronchial:	n/a
45	chr19:19702508-19702558	AG10803	skin:	n/a
46	chr19:19702508-19702558	GM06990	blood:	n/a
47	chr19:19702508-19702558	HRPEpiC	eye:	n/a
48	chr19:19702508-19702558	AG09309	skin:	n/a
49	chr19:19702508-19702558	A549	lung:	n/a
50	chr19:19702508-19702558	MCF10A-Er-Src	breast:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19660331..19661217-chr19:19705939..19706875,5	MCF-7	breast:
2	chr19:19706085..19710226-chr19:19714067..19716882,3	MCF-7	breast:
3	chr19:19707413..19710256-chr19:19720024..19721956,2	K562	blood:
4	chr19:19702026..19704512-chr19:19777801..19779336,2	MCF-7	breast:
5	chr19:19660297..19660827-chr19:19705920..19706825,2	MCF-7	breast:
6	chr19:19706003..19706852-chr19:19739305..19740113,2	MCF-7	breast:
7	chr19:19660487..19662090-chr19:19700692..19703512,2	MCF-7	breast:
8	chr19:19707335..19710149-chr19:19710538..19713142,3	MCF-7	breast:
9	chr19:19699647..19703848-chr19:19728208..19731865,4	MCF-7	breast:
10	chr19:19700624..19702587-chr19:19705452..19707616,2	MCF-7	breast:
11	chr19:19705848..19708142-chr19:19747423..19748977,2	MCF-7	breast:
12	chr19:19626874..19628418-chr19:19712468..19714125,2	K562	blood:
13	chr19:19660422..19661220-chr19:19705892..19706769,4	MCF-7	breast:
14	chr19:19701845..19703912-chr19:19706648..19708750,2	K562	blood:
15	chr19:19713434..19715276-chr19:19716951..19720317,3	K562	blood:
16	chr19:19705245..19708025-chr19:19737732..19740369,3	MCF-7	breast:
17	chr19:19702415..19703999-chr19:19742408..19743931,2	MCF-7	breast:
18	chr19:19701585..19704571-chr19:19749702..19751858,2	K562	blood:
19	chr19:19707335..19710149-chr19:19710538..19713142,3	MCF-7	breast:
20	chr19:19701845..19703912-chr19:19706648..19708750,2	K562	blood:
21	chr19:19695351..19697446-chr19:19737472..19739730,2	MCF-7	breast:
22	chr19:19685275..19686937-chr19:19695777..19697323,2	MCF-7	breast:
23	chr19:19661215..19662873-chr19:19705870..19708009,2	MCF-7	breast:
24	chr19:19626987..19628550-chr19:19704489..19706046,2	MCF-7	breast:
25	chr19:19700624..19702587-chr19:19705452..19707616,2	MCF-7	breast:
26	chr19:19684439..19686704-chr19:19692465..19694414,2	MCF-7	breast:
27	chr19:19699149..19708161-chr19:19735507..19742255,11	MCF-7	breast:
28	chr19:19703007..19704852-chr19:19716995..19718509,2	MCF-7	breast:
29	chr19:19706085..19710226-chr19:19714067..19716882,3	MCF-7	breast:
30	chr19:19713434..19715276-chr19:19716951..19719941,2	K562	blood:
31	chr19:19701600..19702494-chr19:19738189..19739163,2	MCF-7	breast:

No data

Variant related genes	Relation type
PBX4	TF binding region
PHF5CP	TF binding region
ENSG00000259242	TF binding region
PBX4	CpG island
PHF5CP	CpG island
ENSG00000259242	CpG island
ENSG00000258674	chromatin interactions
ENSG00000089639	chromatin interactions
ENSG00000105717	chromatin interactions
ENSG00000186010	chromatin interactions
ENSG00000259242	chromatin interactions
ENSG00000064547	chromatin interactions

Extended variants
information (count: 817 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7252981	chr19:19692579-19692580	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141932641	chr19:19692654-19692655	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557376172	chr19:19692655-19692656	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570712800	chr19:19692685-19692686	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540136467	chr19:19692698-19692699	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551976199	chr19:19692718-19692719	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553217230	chr19:19692765-19692766	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573125059	chr19:19692780-19692781	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35024830	chr19:19692808-19692809	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184975262	chr19:19692809-19692810	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543316827	chr19:19692867-19692868	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575343432	chr19:19692892-19692893	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112107493	chr19:19692960-19692961	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564117874	chr19:19692965-19692966	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577529413	chr19:19692985-19692986	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189777906	chr19:19692987-19692988	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560472052	chr19:19693022-19693023	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs529188647	chr19:19693053-19693054	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs549241961	chr19:19693081-19693082	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs554484387	chr19:19693141-19693142	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs562673054	chr19:19693144-19693145	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs531039855	chr19:19693161-19693162	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs573931579	chr19:19693193-19693194	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs536259660	chr19:19693236-19693237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181057144	chr19:19693242-19693243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556903857	chr19:19693252-19693253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539423481	chr19:19693255-19693256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371722547	chr19:19693258-19693259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140789220	chr19:19693267-19693268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12977917	chr19:19693299-19693300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs185483408	chr19:19693321-19693322	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs191609940	chr19:19693335-19693336	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs143115527	chr19:19693426-19693427	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs557537673	chr19:19693460-19693461	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs576711616	chr19:19693535-19693536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577643582	chr19:19693545-19693546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540264227	chr19:19693548-19693549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560183150	chr19:19693553-19693554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12462757	chr19:19693581-19693582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542898724	chr19:19693588-19693589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562714895	chr19:19693599-19693600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34981178	chr19:19693610-19693611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368166138	chr19:19693625-19693626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370110648	chr19:19693632-19693633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139249988	chr19:19693666-19693667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183387136	chr19:19693695-19693696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533451800	chr19:19693780-19693781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149995758	chr19:19693808-19693809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188791380	chr19:19693836-19693837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541739789	chr19:19693876-19693877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19671600-19701800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr19:19672000-19704800	Weak transcription	Brain Angular Gyrus	brain
3	chr19:19674200-19699800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr19:19676200-19701600	Weak transcription	GM12878-XiMat	blood
5	chr19:19678800-19693000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr19:19681200-19701600	Weak transcription	NHLF	lung
7	chr19:19681400-19701600	Weak transcription	Fetal Lung	lung
8	chr19:19681600-19693000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr19:19681600-19701600	Weak transcription	Esophagus	oesophagus
10	chr19:19681600-19703200	Weak transcription	Dnd41	blood
11	chr19:19681800-19692800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr19:19682000-19692800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr19:19682000-19702200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr19:19682400-19692800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr19:19682600-19692800	Weak transcription	Spleen	Spleen
16	chr19:19682600-19700600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr19:19686600-19700600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr19:19687000-19693000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr19:19687000-19701600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:19688400-19692800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr19:19688400-19699000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:19689400-19692800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr19:19689400-19693000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:19689600-19693000	Strong transcription	Fetal Stomach	stomach
25	chr19:19689800-19698800	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr19:19689800-19700600	Weak transcription	Thymus	Thymus
27	chr19:19689800-19701800	Weak transcription	Fetal Brain Female	brain
28	chr19:19690200-19694000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr19:19690600-19693400	Enhancers	Stomach Mucosa	stomach
30	chr19:19690600-19693800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr19:19691000-19698600	Weak transcription	Brain Germinal Matrix	brain
32	chr19:19691200-19693200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr19:19691200-19699600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr19:19691200-19700600	Weak transcription	Primary T cells from cord blood	blood
35	chr19:19691400-19692600	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr19:19691400-19699200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr19:19691400-19699400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr19:19691600-19692600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr19:19692000-19692600	Enhancers	Fetal Heart	heart
40	chr19:19692200-19692600	Enhancers	Right Ventricle	heart
41	chr19:19692200-19693200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:19692200-19693200	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr19:19692400-19692600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr19:19692400-19693200	Enhancers	Duodenum Mucosa	Duodenum
45	chr19:19692400-19693200	Enhancers	Gastric	stomach
46	chr19:19692400-19693400	Enhancers	Colonic Mucosa	Colon
47	chr19:19692400-19693400	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr19:19692400-19693800	Enhancers	Primary T cells fromperipheralblood	blood
49	chr19:19692400-19693800	Enhancers	Fetal Muscle Trunk	muscle
50	chr19:19692600-19693000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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