Variant report

Variant	esv3413868
Chromosome Location	chr19:40130700-40184720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:797)
CpG islands
(count:366)
Chromatin interactive
region (count:19)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:40177332-40177734	GM12878	blood:	n/a	n/a
2	ATF2	chr19:40166454-40167085	GM12878	blood:	n/a	n/a
3	ATF2	chr19:40169169-40171721	GM12878	blood:	n/a	n/a
4	ATF2	chr19:40182800-40183815	GM12878	blood:	n/a	n/a
5	ATF2	chr19:40166517-40167044	GM12878	blood:	n/a	n/a
6	ATF2	chr19:40182851-40183369	GM12878	blood:	n/a	n/a
7	ATF2	chr19:40169348-40171215	GM12878	blood:	n/a	n/a
8	BACH1	chr19:40181595-40181848	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr19:40166440-40167020	GM12878	blood:	n/a	n/a
10	BATF	chr19:40169465-40170751	GM12878	blood:	n/a	n/a
11	BATF	chr19:40164543-40164840	GM12878	blood:	n/a	n/a
12	BATF	chr19:40182871-40183555	GM12878	blood:	n/a	chr19:40183116-40183126
13	BATF	chr19:40166542-40166952	GM12878	blood:	n/a	n/a
14	BCL11A	chr19:40169661-40170751	GM12878	blood:	n/a	n/a
15	BCL11A	chr19:40166534-40167022	GM12878	blood:	n/a	chr19:40166845-40166854
16	BCL3	chr19:40170081-40170842	GM12878	blood:	n/a	n/a
17	BCL3	chr19:40177478-40177702	GM12878	blood:	n/a	chr19:40177575-40177584
18	BCL3	chr19:40182720-40183232	GM12878	blood:	n/a	chr19:40183115-40183124 chr19:40183114-40183123
19	BCL3	chr19:40169586-40170952	GM12878	blood:	n/a	chr19:40169623-40169631
20	BCL3	chr19:40166516-40167084	GM12878	blood:	n/a	chr19:40166845-40166854
21	BCL3	chr19:40166584-40167009	GM12878	blood:	n/a	chr19:40166845-40166854
22	BCL3	chr19:40182662-40183301	GM12878	blood:	n/a	chr19:40183115-40183124 chr19:40183114-40183123
23	BCLAF1	chr19:40166547-40167019	GM12878	blood:	n/a	chr19:40166845-40166854
24	BCLAF1	chr19:40169381-40171764	GM12878	blood:	n/a	chr19:40169623-40169631
25	BCLAF1	chr19:40169441-40171302	GM12878	blood:	n/a	chr19:40169623-40169631
26	BHLHE40	chr19:40171344-40171662	GM12878	blood:	n/a	n/a
27	BHLHE40	chr19:40183715-40183926	GM12878	blood:	n/a	n/a
28	BHLHE40	chr19:40169675-40171090	GM12878	blood:	n/a	n/a
29	BRCA1	chr19:40169254-40169347	GM12878	blood:	n/a	n/a
30	BRCA1	chr19:40169819-40170833	GM12878	blood:	n/a	n/a
31	BRCA1	chr19:40172330-40172407	GM12878	blood:	n/a	n/a
32	CEBPB	chr19:40169429-40170617	GM12878	blood:	n/a	n/a
33	CEBPB	chr19:40140585-40140785	HepG2	liver:	n/a	chr19:40140634-40140645
34	CEBPB	chr19:40136019-40136106	HepG2	liver:	n/a	chr19:40136071-40136082 chr19:40136071-40136082 chr19:40136072-40136083
35	CEBPB	chr19:40151350-40151658	Hela-S3	cervix:	n/a	chr19:40151501-40151514
36	CEBPB	chr19:40174793-40175365	Hela-S3	cervix:	n/a	n/a
37	CHD1	chr19:40162625-40162903	GM12878	blood:	n/a	n/a
38	CHD1	chr19:40169671-40171710	GM12878	blood:	n/a	n/a
39	CHD2	chr19:40171410-40171603	GM12878	blood:	n/a	n/a
40	CHD2	chr19:40172217-40172294	GM12878	blood:	n/a	n/a
41	CHD2	chr19:40169141-40171016	GM12878	blood:	n/a	n/a
42	CTCF	chr19:40162618-40162997	K562	blood:	n/a	n/a
43	CTCF	chr19:40162720-40162870	Caco-2	colon:	n/a	n/a
44	CTCF	chr19:40162740-40162890	SAEC	small airway:	n/a	n/a
45	CTCF	chr19:40164600-40164750	HEK293	kidney:	n/a	n/a
46	CTCF	chr19:40163040-40163190	HMF	breast:	n/a	n/a
47	CTCF	chr19:40162722-40162919	GM13976	blood:	n/a	n/a
48	CTCF	chr19:40162760-40162910	GM12871	blood:	n/a	n/a
49	CTCF	chr19:40162722-40162925	GM10266	blood:	n/a	n/a
50	CTCF	chr19:40164534-40164804	A549	lung:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40168876-40168926	NB4	blood:	n/a
2	chr19:40174352-40174402	HAEpiC	amniotic membrane:	n/a
3	chr19:40169912-40169962	NT2-D1	testis:	n/a
4	chr19:40169912-40169962	GM12892	blood:	n/a
5	chr19:40168558-40168608	ovcar-3	ovarian:	n/a
6	chr19:40169418-40169468	SK-N-SH_RA	brain:	n/a
7	chr19:40174352-40174402	BJ	skin:	n/a
8	chr19:40174352-40174402	NHBE	bronchial:	n/a
9	chr19:40174352-40174402	Hela-S3	cervix:	n/a
10	chr19:40169418-40169468	HEEpiC	esophagus:	n/a
11	chr19:40174352-40174402	T-47D	breast:	n/a
12	chr19:40169418-40169468	PFSK-1	brain:	n/a
13	chr19:40169839-40169889	GM19239	blood:	n/a
14	chr19:40169839-40169889	NHBE	bronchial:	n/a
15	chr19:40169912-40169962	ovcar-3	ovarian:	n/a
16	chr19:40168558-40168608	ProgFib	skin:	n/a
17	chr19:40168876-40168926	ECC-1	luminal epithelium:	n/a
18	chr19:40168876-40168926	HCT-116	colon:	n/a
19	chr19:40169912-40169962	AG09309	skin:	n/a
20	chr19:40168558-40168608	Hela-S3	cervix:	n/a
21	chr19:40168558-40168608	IMR90	lung:	fetal
22	chr19:40169912-40169962	AG10803	skin:	n/a
23	chr19:40168558-40168608	SK-N-SH	brain:	n/a
24	chr19:40168558-40168608	U87	brain:	n/a
25	chr19:40169839-40169889	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:40169839-40169889	ovcar-3	ovarian:	n/a
27	chr19:40169912-40169962	HAEpiC	amniotic membrane:	n/a
28	chr19:40168558-40168608	HAEpiC	amniotic membrane:	n/a
29	chr19:40168558-40168608	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:40169839-40169889	HCM	heart:	n/a
31	chr19:40169418-40169468	GM06990	blood:	n/a
32	chr19:40168558-40168608	GM12878	blood:	n/a
33	chr19:40168558-40168608	AG04449	skin:	fetal
34	chr19:40174352-40174402	BE2_C	brain:	n/a
35	chr19:40168558-40168608	PrEC	prostate:	n/a
36	chr19:40169912-40169962	H1-hESC	embryonic stem cell:	embryo
37	chr19:40169418-40169468	AG04449	skin:	fetal
38	chr19:40168876-40168926	HIPEpiC	eye:	n/a
39	chr19:40169418-40169468	K562	blood:	n/a
40	chr19:40169912-40169962	NB4	blood:	n/a
41	chr19:40169912-40169962	Caco-2	colon:	n/a
42	chr19:40168558-40168608	ECC-1	luminal epithelium:	n/a
43	chr19:40174352-40174402	HCM	heart:	n/a
44	chr19:40169839-40169889	HCT-116	colon:	n/a
45	chr19:40169418-40169468	SAEC	small airway:	n/a
46	chr19:40169839-40169889	Caco-2	colon:	n/a
47	chr19:40169418-40169468	SK-N-SH	brain:	n/a
48	chr19:40168876-40168926	HUVEC	blood vessel:	n/a
49	chr19:40169839-40169889	HEK293	kidney:	embryo
50	chr19:40169912-40169962	HUVEC	blood vessel:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40168776..40170659-chr19:40171070..40173926,2	MCF-7	breast:
2	chr19:40168776..40170659-chr19:40171070..40173926,2	MCF-7	breast:
3	chr19:39925057..39927468-chr19:40150682..40153479,2	K562	blood:
4	chr12:31226694..31227233-chr19:40172228..40172728,2	HCT-116	colon:
5	chr19:40164188..40165085-chr19:40256246..40256847,2	MCF-7	breast:
6	chr19:40166260..40168931-chr19:40253973..40255544,2	MCF-7	breast:
7	chr19:40172219..40174410-chr19:40181019..40183380,2	MCF-7	breast:
8	chr19:40055301..40057183-chr19:40147250..40149926,2	MCF-7	breast:
9	chr19:40041798..40042719-chr19:40162291..40163385,9	MCF-7	breast:
10	chr19:40172219..40174410-chr19:40181019..40183380,2	MCF-7	breast:
11	chr19:40166471..40169299-chr19:40170755..40172585,2	K562	blood:
12	chr19:39988438..39989161-chr19:40162366..40162932,2	K562	blood:
13	chr19:40164964..40166897-chr19:40168193..40170501,2	K562	blood:
14	chr19:40041783..40042891-chr19:40162333..40163330,4	K562	blood:
15	chr19:40163659..40164641-chr19:40256992..40257878,2	MCF-7	breast:
16	chr19:40163210..40165073-chr19:40333318..40334922,2	MCF-7	breast:
17	chr19:40041871..40042653-chr19:40162390..40162892,2	MCF-7	breast:
18	chr19:39988198..39988763-chr19:40162454..40163227,2	MCF-7	breast:
19	chr19:40164310..40165291-chr19:40476366..40477083,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS16-1	chr19:40131114-40131324	NONHSAT066318
2	lnc-LGALS14-1	chr19:40175884-40176058	ENSG00000226025
3	lnc-LGALS14-1	chr19:40175942-40176058	NR_034156
4	lnc-LGALS14-1	chr19:40170014-40170074	NR_034156
5	lnc-LGALS14-1	chr19:40176193-40176292	NR_034156
6	lnc-LGALS14-1	chr19:40172073-40172149	NR_034156
7	lnc-LGALS16-1	chr19:40132792-40133041	NONHSAT066318
8	lnc-LGALS14-1	chr19:40176825-40177013	NR_034156
9	lnc-LGALS16-1	chr19:40131461-40131546	NONHSAT066318
10	lnc-LGALS14-1	chr19:40172638-40172848	NR_034156
11	lnc-LGALS14-1	chr19:40174127-40174403	NR_034156
12	lnc-LGALS14-1	chr19:40175350-40175447	NR_034156

No data

Variant related genes	Relation type
LGALS16	TF binding region
ENSG00000268088	TF binding region
ENSG00000226025	TF binding region
ENSG00000240320	TF binding region
ENSG00000268243	TF binding region
ENSG00000269460	TF binding region
LGALS16	CpG island
ENSG00000268088	CpG island
ENSG00000226025	CpG island
ENSG00000240320	CpG island
ENSG00000268243	CpG island
ENSG00000269460	CpG island
ENSG00000013573	chromatin interactions
ENSG00000196235	chromatin interactions
ENSG00000013275	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000105193	chromatin interactions
ENSG00000226025	chromatin interactions

Extended variants
information (count: 1934 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1934 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76579664	chr19:40130701-40130702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6508892	chr19:40130713-40130714	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533952640	chr19:40130717-40130718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555382311	chr19:40130747-40130748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553884627	chr19:40130765-40130766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7250911	chr19:40130767-40130768	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs544512100	chr19:40130788-40130789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139268916	chr19:40130805-40130806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575690164	chr19:40130813-40130814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546350025	chr19:40130829-40130830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7254051	chr19:40130843-40130844	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528696376	chr19:40130939-40130940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547131903	chr19:40130994-40130995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2108390	chr19:40131001-40131002	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187885912	chr19:40131002-40131003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62623438	chr19:40131024-40131025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568541059	chr19:40131085-40131086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532738774	chr19:40131098-40131099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551202387	chr19:40131112-40131113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566519329	chr19:40131125-40131126	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs144922276	chr19:40131130-40131131	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs192554393	chr19:40131146-40131147	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs546046642	chr19:40131157-40131158	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs567457129	chr19:40131167-40131168	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs538174275	chr19:40131189-40131190	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs556479226	chr19:40131207-40131208	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs575732652	chr19:40131213-40131214	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs546146960	chr19:40131220-40131221	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs557982115	chr19:40131229-40131230	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs573244127	chr19:40131233-40131234	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs540368713	chr19:40131300-40131301	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs116958647	chr19:40131346-40131347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113822147	chr19:40131395-40131396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142133897	chr19:40131494-40131495	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs562806763	chr19:40131510-40131511	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs532774001	chr19:40131661-40131662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533288021	chr19:40131672-40131673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551309122	chr19:40131683-40131684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566339756	chr19:40131716-40131717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184993426	chr19:40131721-40131722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374781627	chr19:40131814-40131815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs717348	chr19:40131820-40131821	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs377497438	chr19:40131839-40131840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147769935	chr19:40131840-40131841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556516078	chr19:40131842-40131843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571528758	chr19:40131864-40131865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539454100	chr19:40131876-40131877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558180116	chr19:40131879-40131880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573147142	chr19:40131927-40131928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540755515	chr19:40131996-40131997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40127600-40131800	Enhancers	Placenta	Placenta
2	chr19:40131800-40132600	Weak transcription	Placenta	Placenta
3	chr19:40131800-40133600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr19:40132000-40133400	Enhancers	HepG2	liver
5	chr19:40132200-40133000	Bivalent Enhancer	A549	lung
6	chr19:40132600-40133200	Enhancers	Placenta	Placenta
7	chr19:40133200-40151200	Weak transcription	Placenta	Placenta
8	chr19:40146800-40147000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr19:40147000-40147200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr19:40148600-40149400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:40150600-40151200	Bivalent Enhancer	GM12878-XiMat	blood
12	chr19:40152200-40153000	Enhancers	Primary T cells from cord blood	blood
13	chr19:40161200-40162600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr19:40161200-40162600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr19:40161200-40162600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr19:40161200-40162600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr19:40161200-40162800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr19:40161200-40162800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr19:40161200-40162800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr19:40161200-40162800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr19:40161400-40162600	Enhancers	H1 Cell Line	embryonic stem cell
22	chr19:40161400-40162800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr19:40161800-40162000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr19:40162400-40162600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:40162400-40162600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
26	chr19:40162400-40162600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr19:40162400-40162600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr19:40162400-40162600	Enhancers	Brain Hippocampus Middle	brain
29	chr19:40162400-40162800	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr19:40162400-40163200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr19:40162400-40163200	Enhancers	GM12878-XiMat	blood
32	chr19:40162400-40164600	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr19:40162400-40164600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr19:40162600-40162800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr19:40162600-40162800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr19:40162600-40163600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr19:40162600-40164200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr19:40162600-40164600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr19:40162600-40164600	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr19:40162600-40169600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr19:40162800-40163000	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr19:40162800-40163000	Bivalent Enhancer	A549	lung
43	chr19:40162800-40163800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr19:40162800-40164200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr19:40162800-40164400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr19:40162800-40164600	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr19:40162800-40166800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr19:40163000-40164200	Enhancers	Primary T cells fromperipheralblood	blood
49	chr19:40163200-40163400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr19:40163200-40164200	Weak transcription	GM12878-XiMat	blood

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