Variant report

Variant	esv1811264
Chromosome Location	chr19:45162189-45170547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr19:45168794-45169603	A549	lung:	n/a	n/a
2	BCL3	chr19:45165688-45166981	A549	lung:	n/a	n/a
3	BCL3	chr19:45167680-45168684	A549	lung:	n/a	n/a
4	BCL3	chr19:45164659-45165657	A549	lung:	n/a	n/a
5	BHLHE40	chr19:45165333-45165533	K562	blood:	n/a	n/a
6	CTCF	chr19:45165000-45165150	AG04449	skin:	n/a	n/a
7	CTCF	chr19:45164980-45165130	K562	blood:	n/a	n/a
8	CTCF	chr19:45162060-45162210	GM06990	blood:	n/a	n/a
9	CTCF	chr19:45165000-45165150	A549	lung:	n/a	n/a
10	CTCF	chr19:45164980-45165130	AG10803	skin:	n/a	n/a
11	CTCF	chr19:45165000-45165150	HA-sp	spinal cord:	n/a	n/a
12	CTCF	chr19:45165100-45165250	HVMF	connective:	n/a	n/a
13	CTCF	chr19:45166220-45166370	GM12871	blood:	n/a	n/a
14	CTCF	chr19:45162560-45162710	HEK293	kidney:	n/a	n/a
15	CTCF	chr19:45164900-45165050	AG04450	lung:	n/a	n/a
16	CTCF	chr19:45166220-45166370	AG04450	lung:	n/a	n/a
17	CTCF	chr19:45164942-45165125	K562	blood:	n/a	n/a
18	CTCF	chr19:45166280-45166430	NHLF	lung:	n/a	n/a
19	CTCF	chr19:45165240-45165390	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr19:45165033-45165124	HepG2	liver:	n/a	n/a
21	CTCF	chr19:45164940-45165090	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr19:45164880-45165030	AG04450	lung:	n/a	n/a
23	CTCF	chr19:45165020-45165170	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr19:45164920-45165070	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr19:45164460-45164610	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr19:45164940-45165090	MCF-7	breast:	n/a	n/a
27	CTCF	chr19:45165028-45165112	GM12892	blood:	n/a	n/a
28	CTCF	chr19:45164940-45165090	AG04449	skin:	n/a	n/a
29	CTCF	chr19:45166280-45166430	HPF	lung:	n/a	n/a
30	CTCF	chr19:45164960-45165110	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr19:45164960-45165110	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr19:45165024-45165116	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:45164940-45165090	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr19:45165008-45165111	MCF-7	breast:	n/a	n/a
35	CTCF	chr19:45165021-45165109	K562	blood:	n/a	n/a
36	CTCF	chr19:45165020-45165134	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:45164920-45165070	HepG2	liver:	n/a	n/a
38	CTCF	chr19:45165021-45165096	MCF-7	breast:	n/a	n/a
39	CTCF	chr19:45165023-45165141	MCF-7	breast:	n/a	n/a
40	CTCF	chr19:45165000-45165150	HEK293	kidney:	n/a	n/a
41	CTCF	chr19:45166220-45166370	AG04449	skin:	n/a	n/a
42	E2F6	chr19:45165285-45165435	K562	blood:	n/a	n/a
43	ELF1	chr19:45169040-45169293	K562	blood:	n/a	chr19:45169159-45169172
44	ELF1	chr19:45169300-45169640	A549	lung:	n/a	n/a
45	EP300	chr19:45165305-45165470	K562	blood:	n/a	n/a
46	FOXA1	chr19:45168878-45169064	T-47D	breast:	n/a	n/a
47	GATA1	chr19:45168976-45169492	PBDE	blood:	n/a	n/a
48	GATA2	chr19:45165180-45165520	SH-SY5Y	brain:	n/a	n/a
49	GATA2	chr19:45165106-45165381	HUVEC	blood vessel:	n/a	n/a
50	GATA3	chr19:45165126-45165452	T-47D	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45165815-45165865	HCF	heart:	n/a
2	chr19:45165815-45165865	Hepatocyte	liver:	n/a
3	chr19:45165815-45165865	SKMC	muscle:	n/a
4	chr19:45165815-45165865	GM12878	blood:	n/a
5	chr19:45165815-45165865	HRPEpiC	eye:	n/a
6	chr19:45165815-45165865	GM06990	blood:	n/a
7	chr19:45165815-45165865	HNPCEpiC	eye:	n/a
8	chr19:45165815-45165865	CMK	blood:	n/a
9	chr19:45165815-45165865	ovcar-3	ovarian:	n/a
10	chr19:45165815-45165865	PANC-1	pancreas:	n/a
11	chr19:45165815-45165865	AG04450	lung:	fetal
12	chr19:45165815-45165865	BE2_C	brain:	n/a
13	chr19:45165815-45165865	AG04449	skin:	fetal
14	chr19:45165815-45165865	K562	blood:	n/a
15	chr19:45165815-45165865	HCPEpiC	choroid plexus:	n/a
16	chr19:45165815-45165865	GM12891	blood:	n/a
17	chr19:45165815-45165865	HEEpiC	esophagus:	n/a
18	chr19:45165815-45165865	MCF10A-Er-Src	breast:	n/a
19	chr19:45165815-45165865	AoSMC	blood vessel:	n/a
20	chr19:45165815-45165865	ProgFib	skin:	n/a
21	chr19:45165815-45165865	IMR90	lung:	fetal
22	chr19:45165815-45165865	MCF-7	breast:	n/a
23	chr19:45165815-45165865	GM19239	blood:	n/a
24	chr19:45165815-45165865	NHBE	bronchial:	n/a
25	chr19:45165815-45165865	PrEC	prostate:	n/a
26	chr19:45165815-45165865	AG10803	skin:	n/a
27	chr19:45165815-45165865	NT2-D1	testis:	n/a
28	chr19:45165815-45165865	A549	lung:	n/a
29	chr19:45165815-45165865	Caco-2	colon:	n/a
30	chr19:45165815-45165865	HAEpiC	amniotic membrane:	n/a
31	chr19:45165815-45165865	HepG2	liver:	n/a
32	chr19:45165815-45165865	NB4	blood:	n/a
33	chr19:45165815-45165865	HUVEC	blood vessel:	n/a
34	chr19:45165815-45165865	Hela-S3	cervix:	n/a
35	chr19:45165815-45165865	HCM	heart:	n/a
36	chr19:45165815-45165865	HL-60	blood:	n/a
37	chr19:45165815-45165865	SK-N-MC	brain:	n/a
38	chr19:45165815-45165865	HIPEpiC	eye:	n/a
39	chr19:45165815-45165865	NHDF-neo	bronchial:	n/a
40	chr19:45165815-45165865	RPTEC	kidney:	n/a
41	chr19:45165815-45165865	HMEC	breast:	n/a
42	chr19:45165815-45165865	AG09309	skin:	n/a
43	chr19:45165815-45165865	H1-hESC	embryonic stem cell:	embryo
44	chr19:45165815-45165865	HCT-116	colon:	n/a
45	chr19:45165815-45165865	HEK293	kidney:	embryo
46	chr19:45165815-45165865	SK-N-SH_RA	brain:	n/a
47	chr19:45165815-45165865	PFSK-1	brain:	n/a
48	chr19:45165815-45165865	SK-N-SH	brain:	n/a
49	chr19:45165815-45165865	ECC-1	luminal epithelium:	n/a
50	chr19:45165815-45165865	HRE	kidney:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:45162255..45163987-chr8:146016275..146018293,2	MCF-7	breast:
2	chr19:45160009..45162203-chr19:45167891..45170574,2	MCF-7	breast:
3	chr19:45165424..45170809-chr19:45174095..45176705,6	MCF-7	breast:
4	chr19:45166812..45168963-chr19:45171333..45172963,2	K562	blood:
5	chr19:45164861..45166953-chr19:45250378..45253353,2	MCF-7	breast:
6	chr19:45145777..45147294-chr19:45168783..45170918,2	MCF-7	breast:
7	chr19:45163762..45165442-chr19:45167441..45169595,3	K562	blood:
8	chr19:45160009..45162203-chr19:45167891..45170574,2	MCF-7	breast:
9	chr19:45163507..45165937-chr19:45174707..45176258,2	MCF-7	breast:
10	chr19:45163762..45165442-chr19:45167441..45169595,3	K562	blood:
11	chr19:45167841..45169722-chr19:45250819..45253279,2	MCF-7	breast:
12	chr19:45165601..45167675-chr19:45169237..45171055,2	MCF-7	breast:
13	chr19:45071084..45073228-chr19:45167120..45169999,2	MCF-7	breast:
14	chr19:45168616..45170129-chr19:45175364..45177317,2	K562	blood:
15	chr19:45165601..45167675-chr19:45169237..45171055,2	MCF-7	breast:
16	chr19:45055613..45057790-chr19:45168454..45170638,2	K562	blood:
17	chr19:45163718..45166142-chr19:45347949..45350163,2	MCF-7	breast:

No data

Variant related genes	Relation type
CEACAM19	TF binding region
CEACAM19	CpG island
ENSG00000130202	chromatin interactions
ENSG00000069399	chromatin interactions
ENSG00000073008	chromatin interactions
ENSG00000161016	chromatin interactions
ENSG00000186567	chromatin interactions

Extended variants
information (count: 317 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35385129	chr19:45162189-45162190	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372262577	chr19:45162214-45162215	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs369725394	chr19:45162238-45162239	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537683327	chr19:45162321-45162322	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs146565995	chr19:45162325-45162326	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs112064707	chr19:45162335-45162336	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs140080540	chr19:45162369-45162370	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372134533	chr19:45162370-45162371	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs143760407	chr19:45162486-45162487	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574111080	chr19:45162505-45162506	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs375071119	chr19:45162528-45162529	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552118628	chr19:45162555-45162556	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs542898951	chr19:45162594-45162595	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs563080381	chr19:45162664-45162665	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs10405025	chr19:45162667-45162668	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541180932	chr19:45162684-45162685	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs551686962	chr19:45162705-45162706	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145836076	chr19:45162712-45162713	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs76615629	chr19:45162785-45162786	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371604375	chr19:45162901-45162902	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs181025374	chr19:45162946-45162947	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149006679	chr19:45162947-45162948	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs567645938	chr19:45162949-45162950	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs10411273	chr19:45162955-45162956	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549247947	chr19:45162991-45162992	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569101764	chr19:45162996-45162997	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537997051	chr19:45163208-45163209	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112380004	chr19:45163274-45163275	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs573768318	chr19:45163395-45163396	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs747093	chr19:45163438-45163439	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs5828218	chr19:45163440-45163441	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113880192	chr19:45163441-45163442	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533662868	chr19:45163450-45163451	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs737100	chr19:45163451-45163452	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs369836414	chr19:45163466-45163467	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs151139288	chr19:45163485-45163486	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563151259	chr19:45163487-45163488	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs576675554	chr19:45163510-45163511	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs545546797	chr19:45163516-45163517	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs565357557	chr19:45163635-45163636	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs754340	chr19:45163671-45163672	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs73048353	chr19:45163718-45163719	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs561411038	chr19:45163735-45163736	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs564413585	chr19:45163751-45163752	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs114089140	chr19:45163848-45163849	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs549911790	chr19:45163880-45163881	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs569094902	chr19:45163906-45163907	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs185386090	chr19:45163909-45163910	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs551525920	chr19:45163914-45163915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs571088297	chr19:45163915-45163916	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Adrenocortical carcinoma	18281524	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45148000-45165000	Weak transcription	K562	blood
2	chr19:45148200-45170200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr19:45149200-45167000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr19:45149400-45167200	Strong transcription	HUES6 Cell Line	embryonic stem cell
5	chr19:45150200-45167200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr19:45150600-45167200	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr19:45150600-45167200	Strong transcription	Brain Germinal Matrix	brain
8	chr19:45150600-45167400	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr19:45150600-45167400	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr19:45150600-45167400	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr19:45151000-45167800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:45151200-45166400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr19:45151200-45166400	Strong transcription	Cortex derived primary cultured neurospheres	brain
14	chr19:45151400-45167000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr19:45152000-45167800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr19:45152400-45163800	Strong transcription	NHLF	lung
17	chr19:45152400-45165000	Strong transcription	NHEK	skin
18	chr19:45152400-45166600	Strong transcription	Stomach Smooth Muscle	stomach
19	chr19:45152600-45163400	Strong transcription	HSMMtube	muscle
20	chr19:45152600-45164400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr19:45152600-45165000	Strong transcription	Muscle Satellite Cultured Cells	--
22	chr19:45152600-45165200	Weak transcription	Right Atrium	heart
23	chr19:45152600-45166800	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr19:45152600-45167000	Strong transcription	HUVEC	blood vessel
25	chr19:45152600-45169200	Strong transcription	Osteobl	bone
26	chr19:45152600-45178200	Weak transcription	Fetal Heart	heart
27	chr19:45152800-45165600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr19:45153000-45165600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr19:45153000-45167000	Strong transcription	Gastric	stomach
30	chr19:45153000-45168600	Strong transcription	NH-A	brain
31	chr19:45153400-45168600	Strong transcription	Lung	lung
32	chr19:45154000-45173400	Weak transcription	Small Intestine	intestine
33	chr19:45155000-45162200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr19:45155000-45168400	Weak transcription	Primary T cells from cord blood	blood
35	chr19:45156000-45166800	Strong transcription	HepG2	liver
36	chr19:45156200-45165400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr19:45157000-45163000	Weak transcription	Brain Substantia Nigra	brain
38	chr19:45157000-45165400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr19:45157000-45167600	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr19:45157200-45162200	Weak transcription	Brain Angular Gyrus	brain
41	chr19:45157800-45168400	Strong transcription	Left Ventricle	heart
42	chr19:45158200-45163000	Strong transcription	A549	lung
43	chr19:45158200-45166400	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr19:45158600-45164800	Strong transcription	HSMM	muscle
45	chr19:45158600-45166800	Strong transcription	Duodenum Mucosa	Duodenum
46	chr19:45158600-45167400	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr19:45158800-45162200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr19:45159000-45165600	Strong transcription	NHDF-Ad	bronchial
49	chr19:45159200-45165600	Strong transcription	Fetal Kidney	kidney
50	chr19:45159400-45163800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain

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