Variant report

Variant	esv1812853
Chromosome Location	chr19:45163671-45170547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:254)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:254 , 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	chr19:45165688-45166981	A549	lung:	n/a	n/a
2	BCL3	chr19:45167680-45168684	A549	lung:	n/a	n/a
3	BCL3	chr19:45168794-45169603	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	HA-sp	spinal cord:	n/a	n/a
7	CTCF	chr19:45165000-45165150	A549	lung:	n/a	n/a
8	CTCF	chr19:45164940-45165090	MCF-7	breast:	n/a	n/a
9	CTCF	chr19:45166220-45166370	AG04449	skin:	n/a	n/a
10	CTCF	chr19:45165100-45165250	HVMF	connective:	n/a	n/a
11	CTCF	chr19:45165020-45165170	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr19:45164900-45165050	AG04450	lung:	n/a	n/a
13	CTCF	chr19:45164940-45165090	AG04449	skin:	n/a	n/a
14	CTCF	chr19:45164980-45165130	K562	blood:	n/a	n/a
15	CTCF	chr19:45164920-45165070	HepG2	liver:	n/a	n/a
16	CTCF	chr19:45165020-45165134	MCF-7	breast:	n/a	n/a
17	CTCF	chr19:45164880-45165030	AG04450	lung:	n/a	n/a
18	CTCF	chr19:45166280-45166430	HPF	lung:	n/a	n/a
19	CTCF	chr19:45165033-45165124	HepG2	liver:	n/a	n/a
20	CTCF	chr19:45164940-45165090	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr19:45166220-45166370	AG04450	lung:	n/a	n/a
22	CTCF	chr19:45164942-45165125	K562	blood:	n/a	n/a
23	CTCF	chr19:45165008-45165111	MCF-7	breast:	n/a	n/a
24	CTCF	chr19:45164940-45165090	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr19:45164960-45165110	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr19:45164980-45165130	AG10803	skin:	n/a	n/a
27	CTCF	chr19:45165023-45165141	MCF-7	breast:	n/a	n/a
28	CTCF	chr19:45166220-45166370	GM12871	blood:	n/a	n/a
29	CTCF	chr19:45166280-45166430	NHLF	lung:	n/a	n/a
30	CTCF	chr19:45165000-45165150	HEK293	kidney:	n/a	n/a
31	CTCF	chr19:45164920-45165070	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr19:45165021-45165096	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:45165028-45165112	GM12892	blood:	n/a	n/a
34	CTCF	chr19:45164460-45164610	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr19:45164960-45165110	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr19:45165000-45165150	AG04449	skin:	n/a	n/a
37	CTCF	chr19:45165021-45165109	K562	blood:	n/a	n/a
38	CTCF	chr19:45165240-45165390	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr19:45165024-45165116	MCF-7	breast:	n/a	n/a
40	E2F6	chr19:45165285-45165435	K562	blood:	n/a	n/a
41	ELF1	chr19:45169040-45169293	K562	blood:	n/a	chr19:45169159-45169172
42	ELF1	chr19:45169300-45169640	A549	lung:	n/a	n/a
43	EP300	chr19:45165305-45165470	K562	blood:	n/a	n/a
44	FOXA1	chr19:45168878-45169064	T-47D	breast:	n/a	n/a
45	GATA1	chr19:45168976-45169492	PBDE	blood:	n/a	n/a
46	GATA2	chr19:45165106-45165381	HUVEC	blood vessel:	n/a	n/a
47	GATA2	chr19:45165180-45165520	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr19:45165110-45165533	MCF-7	breast:	n/a	n/a
49	GATA3	chr19:45165230-45165505	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr19:45165132-45165567	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	SK-N-SH	brain:	n/a
2	chr19:45165815-45165865	ECC-1	luminal epithelium:	n/a
3	chr19:45165815-45165865	AG04449	skin:	fetal
4	chr19:45165815-45165865	AG09309	skin:	n/a
5	chr19:45165815-45165865	HPAEpiC	pulmonary alveolar:	n/a
6	chr19:45165815-45165865	GM19239	blood:	n/a
7	chr19:45165815-45165865	BE2_C	brain:	n/a
8	chr19:45165815-45165865	SK-N-SH_RA	brain:	n/a
9	chr19:45165815-45165865	HRPEpiC	eye:	n/a
10	chr19:45165815-45165865	U87	brain:	n/a
11	chr19:45165815-45165865	K562	blood:	n/a
12	chr19:45165815-45165865	GM06990	blood:	n/a
13	chr19:45165815-45165865	T-47D	breast:	n/a
14	chr19:45165815-45165865	SKMC	muscle:	n/a
15	chr19:45165815-45165865	A549	lung:	n/a
16	chr19:45165815-45165865	SK-N-MC	brain:	n/a
17	chr19:45165815-45165865	NB4	blood:	n/a
18	chr19:45165815-45165865	SAEC	small airway:	n/a
19	chr19:45165815-45165865	Jurkat	blood:	n/a
20	chr19:45165815-45165865	AG09319	gingival:	n/a
21	chr19:45165815-45165865	HepG2	liver:	n/a
22	chr19:45165815-45165865	HNPCEpiC	eye:	n/a
23	chr19:45165815-45165865	NT2-D1	testis:	n/a
24	chr19:45165815-45165865	AG10803	skin:	n/a
25	chr19:45165815-45165865	HAEpiC	amniotic membrane:	n/a
26	chr19:45165815-45165865	HL-60	blood:	n/a
27	chr19:45165815-45165865	GM12892	blood:	n/a
28	chr19:45165815-45165865	HMEC	breast:	n/a
29	chr19:45165815-45165865	PANC-1	pancreas:	n/a
30	chr19:45165815-45165865	NHDF-neo	bronchial:	n/a
31	chr19:45165815-45165865	PrEC	prostate:	n/a
32	chr19:45165815-45165865	AG04450	lung:	fetal
33	chr19:45165815-45165865	Hepatocyte	liver:	n/a
34	chr19:45165815-45165865	HUVEC	blood vessel:	n/a
35	chr19:45165815-45165865	HEEpiC	esophagus:	n/a
36	chr19:45165815-45165865	Caco-2	colon:	n/a
37	chr19:45165815-45165865	PFSK-1	brain:	n/a
38	chr19:45165815-45165865	Hela-S3	cervix:	n/a
39	chr19:45165815-45165865	ProgFib	skin:	n/a
40	chr19:45165815-45165865	CMK	blood:	n/a
41	chr19:45165815-45165865	MCF10A-Er-Src	breast:	n/a
42	chr19:45165815-45165865	NHBE	bronchial:	n/a
43	chr19:45165815-45165865	GM12891	blood:	n/a
44	chr19:45165815-45165865	HCT-116	colon:	n/a
45	chr19:45165815-45165865	HIPEpiC	eye:	n/a
46	chr19:45165815-45165865	AoSMC	blood vessel:	n/a
47	chr19:45165815-45165865	HRE	kidney:	n/a
48	chr19:45165815-45165865	BJ	skin:	n/a
49	chr19:45165815-45165865	HCF	heart:	n/a
50	chr19:45165815-45165865	HEK293	kidney:	embryo

(count:16 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 277 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	rs561411038	chr19:45163735-45163736	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs564413585	chr19:45163751-45163752	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs114089140	chr19:45163848-45163849	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs549911790	chr19:45163880-45163881	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs569094902	chr19:45163906-45163907	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs185386090	chr19:45163909-45163910	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs551525920	chr19:45163914-45163915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs571088297	chr19:45163915-45163916	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs188555960	chr19:45163938-45163939	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs553446409	chr19:45163940-45163941	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs118049609	chr19:45163947-45163948	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs536202602	chr19:45163971-45163972	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs376947649	chr19:45163976-45163977	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs146936825	chr19:45163988-45163989	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs117224367	chr19:45163992-45163993	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs545352471	chr19:45164033-45164034	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs137962107	chr19:45164036-45164037	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs143534060	chr19:45164051-45164052	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs117545741	chr19:45164083-45164084	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs145928510	chr19:45164098-45164099	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs530228917	chr19:45164113-45164114	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs181281870	chr19:45164141-45164142	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138615096	chr19:45164185-45164186	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs376913210	chr19:45164208-45164209	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs532567624	chr19:45164277-45164278	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs371147280	chr19:45164281-45164282	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs551376348	chr19:45164296-45164297	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs62119316	chr19:45164345-45164346	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs115951903	chr19:45164358-45164359	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs527435998	chr19:45164363-45164364	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs149317616	chr19:45164395-45164396	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs376428727	chr19:45164396-45164397	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs568148100	chr19:45164411-45164412	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs566986246	chr19:45164413-45164414	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs144642740	chr19:45164414-45164415	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs369677696	chr19:45164437-45164438	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs201876233	chr19:45164526-45164527	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs35357621	chr19:45164540-45164541	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs373411447	chr19:45164575-45164576	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs139862252	chr19:45164576-45164577	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs143321959	chr19:45164577-45164578	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369178432	chr19:45164578-45164579	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs569531982	chr19:45164611-45164612	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs116395038	chr19:45164616-45164617	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376217571	chr19:45164632-45164633	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs370210721	chr19:45164633-45164634	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs369364306	chr19:45164638-45164639	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs538672075	chr19:45164660-45164661	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	3 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:288 , 50 per page) page: 1 2 3 4 5 6

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	chr19:45152600-45164400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr19:45152600-45165000	Strong transcription	Muscle Satellite Cultured Cells	--
21	chr19:45152600-45165200	Weak transcription	Right Atrium	heart
22	chr19:45152600-45166800	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr19:45152600-45167000	Strong transcription	HUVEC	blood vessel
24	chr19:45152600-45169200	Strong transcription	Osteobl	bone
25	chr19:45152600-45178200	Weak transcription	Fetal Heart	heart
26	chr19:45152800-45165600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:45153000-45165600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr19:45153000-45167000	Strong transcription	Gastric	stomach
29	chr19:45153000-45168600	Strong transcription	NH-A	brain
30	chr19:45153400-45168600	Strong transcription	Lung	lung
31	chr19:45154000-45173400	Weak transcription	Small Intestine	intestine
32	chr19:45155000-45168400	Weak transcription	Primary T cells from cord blood	blood
33	chr19:45156000-45166800	Strong transcription	HepG2	liver
34	chr19:45156200-45165400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:45157000-45165400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr19:45157000-45167600	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr19:45157800-45168400	Strong transcription	Left Ventricle	heart
38	chr19:45158200-45166400	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr19:45158600-45164800	Strong transcription	HSMM	muscle
40	chr19:45158600-45166800	Strong transcription	Duodenum Mucosa	Duodenum
41	chr19:45158600-45167400	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr19:45159000-45165600	Strong transcription	NHDF-Ad	bronchial
43	chr19:45159200-45165600	Strong transcription	Fetal Kidney	kidney
44	chr19:45159400-45163800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr19:45159400-45167800	Strong transcription	Pancreas	Pancrea
46	chr19:45160600-45166400	Strong transcription	Adipose Nuclei	Adipose
47	chr19:45160600-45166800	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr19:45160600-45170800	Strong transcription	Fetal Intestine Small	intestine
49	chr19:45160800-45163800	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr19:45160800-45165400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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