Variant report

Variant	nsv523271
Chromosome Location	chr8:19215390-19226335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:19217237-19217465	A549	lung:	n/a	n/a
2	CEBPB	chr8:19217141-19217443	HepG2	liver:	n/a	n/a
3	CTCF	chr8:19217440-19217590	HepG2	liver:	n/a	n/a
4	E2F4	chr8:19221083-19221259	MCF10A-Er-Src	breast:	n/a	n/a
5	EP300	chr8:19214559-19215694	SK-N-SH	brain:	n/a	chr8:19214876-19214890
6	EP300	chr8:19214885-19215424	SK-N-SH_RA	brain:	n/a	n/a
7	FOS	chr8:19223662-19223862	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr8:19223748-19223910	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr8:19220370-19220598	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr8:19221022-19221371	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr8:19220370-19220581	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr8:19223746-19223945	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr8:19220997-19221390	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr8:19221011-19221323	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr8:19220340-19220610	MCF10A-Er-Src	breast:	n/a	n/a
16	FOXA1	chr8:19216897-19217303	HepG2	liver:	n/a	n/a
17	FOXA1	chr8:19216907-19217321	HepG2	liver:	n/a	n/a
18	FOXA1	chr8:19216932-19217329	HepG2	liver:	n/a	n/a
19	FOXA1	chr8:19216831-19217314	HepG2	liver:	n/a	n/a
20	GATA2	chr8:19214888-19215457	SH-SY5Y	brain:	n/a	n/a
21	GATA3	chr8:19218867-19219060	SH-SY5Y	brain:	n/a	n/a
22	KAP1	chr8:19222602-19223227	U2OS	brain:	n/a	n/a
23	KAP1	chr8:19222718-19223220	HEK293	kidney:	n/a	n/a
24	MAX	chr8:19216868-19217292	HepG2	liver:	n/a	n/a
25	MXI1	chr8:19214661-19215912	SK-N-SH	brain:	n/a	n/a
26	MYC	chr8:19221058-19221278	MCF10A-Er-Src	breast:	n/a	n/a
27	NR3C1	chr8:19226170-19226537	A549	lung:	n/a	n/a
28	POLR2A	chr8:19220995-19221355	U87	brain:	n/a	n/a
29	POLR2A	chr8:19224170-19224178	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr8:19223866-19223908	ProgFib	skin:	n/a	n/a
31	POLR2A	chr8:19220426-19220564	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr8:19220999-19221355	U87	brain:	n/a	n/a
33	POLR2A	chr8:19224231-19224309	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr8:19217478-19217643	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr8:19221112-19221983	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr8:19222828-19222875	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr8:19220923-19221420	U87	brain:	n/a	n/a
38	POLR2A	chr8:19220899-19220911	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr8:19222983-19223036	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr8:19224380-19224451	Hela-S3	cervix:	n/a	n/a
41	SPI1	chr8:19226080-19226433	HL-60	blood:	n/a	n/a
42	SPI1	chr8:19226154-19226550	HL-60	blood:	n/a	n/a
43	SPI1	chr8:19226192-19226395	GM12891	blood:	n/a	n/a
44	SPI1	chr8:19222109-19222516	HL-60	blood:	n/a	chr8:19222305-19222318 chr8:19222306-19222319 chr8:19222307-19222316
45	STAT3	chr8:19220400-19220545	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr8:19221213-19221315	MCF10A-Er-Src	breast:	n/a	n/a
47	TCF7L2	chr8:19216944-19217208	HepG2	liver:	n/a	chr8:19217128-19217142 chr8:19217130-19217139 chr8:19217129-19217139
48	USF2	chr8:19216087-19216187	Hela-S3	cervix:	n/a	n/a
49	USF2	chr8:19216036-19216081	HepG2	liver:	n/a	n/a
50	ZNF143	chr8:19223421-19223432	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19215409-19215459	Hela-S3	cervix:	n/a
2	chr8:19215409-19215459	MCF-7	breast:	n/a
3	chr8:19215409-19215459	HNPCEpiC	eye:	n/a
4	chr8:19215409-19215459	PANC-1	pancreas:	n/a
5	chr8:19215409-19215459	AG10803	skin:	n/a
6	chr8:19215409-19215459	SK-N-SH	brain:	n/a
7	chr8:19215409-19215459	ECC-1	luminal epithelium:	n/a
8	chr8:19215409-19215459	HCPEpiC	choroid plexus:	n/a
9	chr8:19215409-19215459	ProgFib	skin:	n/a
10	chr8:19215409-19215459	NH-A	brain:	n/a
11	chr8:19215409-19215459	IMR90	lung:	fetal
12	chr8:19215409-19215459	Hepatocyte	liver:	n/a
13	chr8:19215409-19215459	ovcar-3	ovarian:	n/a
14	chr8:19215409-19215459	AG09319	gingival:	n/a
15	chr8:19215409-19215459	T-47D	breast:	n/a
16	chr8:19215409-19215459	PFSK-1	brain:	n/a
17	chr8:19215409-19215459	HCF	heart:	n/a
18	chr8:19215409-19215459	GM19239	blood:	n/a
19	chr8:19215409-19215459	HEEpiC	esophagus:	n/a
20	chr8:19215409-19215459	NHDF-neo	bronchial:	n/a
21	chr8:19215409-19215459	NT2-D1	testis:	n/a
22	chr8:19215409-19215459	SAEC	small airway:	n/a
23	chr8:19215409-19215459	LNCaP	prostate:	n/a
24	chr8:19215409-19215459	RPTEC	kidney:	n/a
25	chr8:19215409-19215459	K562	blood:	n/a
26	chr8:19215409-19215459	MCF10A-Er-Src	breast:	n/a
27	chr8:19215409-19215459	HL-60	blood:	n/a
28	chr8:19215409-19215459	GM12878	blood:	n/a
29	chr8:19215409-19215459	CMK	blood:	n/a
30	chr8:19215409-19215459	HRCEpiC	kidney:	n/a
31	chr8:19215409-19215459	NHBE	bronchial:	n/a
32	chr8:19215409-19215459	HMEC	breast:	n/a
33	chr8:19215409-19215459	HIPEpiC	eye:	n/a
34	chr8:19215409-19215459	SK-N-SH_RA	brain:	n/a
35	chr8:19215409-19215459	HRPEpiC	eye:	n/a
36	chr8:19215409-19215459	NB4	blood:	n/a
37	chr8:19215409-19215459	BJ	skin:	n/a
38	chr8:19215409-19215459	HCM	heart:	n/a
39	chr8:19215409-19215459	H1-hESC	embryonic stem cell:	embryo
40	chr8:19215409-19215459	HAEpiC	amniotic membrane:	n/a
41	chr8:19215409-19215459	GM06990	blood:	n/a
42	chr8:19215409-19215459	Caco-2	colon:	n/a
43	chr8:19215409-19215459	AG04449	skin:	fetal
44	chr8:19215409-19215459	AG09309	skin:	n/a
45	chr8:19215409-19215459	HCT-116	colon:	n/a
46	chr8:19215409-19215459	PrEC	prostate:	n/a
47	chr8:19215409-19215459	A549	lung:	n/a
48	chr8:19215409-19215459	SKMC	muscle:	n/a
49	chr8:19215409-19215459	HepG2	liver:	n/a
50	chr8:19215409-19215459	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:19225560..19227761-chr8:19271454..19274357,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTS10-3	chr8:19221583-19221610	NONHSAT125374
2	lnc-INTS10-3	chr8:19218299-19218839	NONHSAT125374

No data

Variant related genes	Relation type
SH2D4A	TF binding region
SH2D4A	CpG island

Extended variants
information (count: 527 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11991640	chr8:19215390-19215391	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147027506	chr8:19215391-19215392	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs58228214	chr8:19215393-19215394	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs551812980	chr8:19215450-19215451	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs548669493	chr8:19215460-19215461	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs565427853	chr8:19215475-19215476	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs372557685	chr8:19215501-19215502	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs186467886	chr8:19215505-19215506	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs548147889	chr8:19215522-19215523	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs567998293	chr8:19215600-19215601	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs559003016	chr8:19215601-19215602	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs138131529	chr8:19215617-19215618	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs35804693	chr8:19215636-19215637	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs577233389	chr8:19215648-19215649	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs541189367	chr8:19215697-19215698	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368939224	chr8:19215703-19215704	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs373157190	chr8:19215729-19215730	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs559243596	chr8:19215733-19215734	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs75705990	chr8:19215809-19215810	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs76735233	chr8:19215810-19215811	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572482186	chr8:19215859-19215860	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs534843783	chr8:19215863-19215864	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs10101035	chr8:19215871-19215872	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs574760764	chr8:19215884-19215885	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149597272	chr8:19215953-19215954	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560695609	chr8:19215954-19215955	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563249689	chr8:19215966-19215967	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576765641	chr8:19216033-19216034	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376422145	chr8:19216078-19216079	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs559148110	chr8:19216080-19216081	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs7839534	chr8:19216104-19216105	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs528173743	chr8:19216110-19216111	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs73667645	chr8:19216115-19216116	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs76273535	chr8:19216188-19216189	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543073200	chr8:19216218-19216219	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10089751	chr8:19216219-19216220	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs10104268	chr8:19216228-19216229	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs571496787	chr8:19216245-19216246	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559477579	chr8:19216276-19216277	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148467682	chr8:19216298-19216299	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566160083	chr8:19216311-19216312	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535092182	chr8:19216321-19216322	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541225004	chr8:19216343-19216344	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532320697	chr8:19216450-19216451	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13439427	chr8:19216459-19216460	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs141709163	chr8:19216468-19216469	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201520575	chr8:19216482-19216483	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568960409	chr8:19216595-19216596	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533251523	chr8:19216600-19216601	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10503654	chr8:19216622-19216623	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19173600-19254800	Weak transcription	Colonic Mucosa	Colon
2	chr8:19174000-19223600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr8:19174200-19220400	Weak transcription	HSMM	muscle
4	chr8:19186200-19229800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr8:19195600-19231200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr8:19196400-19220400	Weak transcription	HMEC	breast
7	chr8:19203000-19218200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:19205600-19220600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:19205600-19221000	Weak transcription	Stomach Mucosa	stomach
10	chr8:19205800-19219000	Weak transcription	Adipose Nuclei	Adipose
11	chr8:19205800-19220800	Weak transcription	Lung	lung
12	chr8:19205800-19221000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:19206600-19223800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr8:19208400-19216000	Weak transcription	Esophagus	oesophagus
15	chr8:19208400-19221200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr8:19208400-19231200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:19208800-19215400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:19210600-19216800	Weak transcription	Small Intestine	intestine
19	chr8:19211400-19224600	Strong transcription	A549	lung
20	chr8:19211600-19219600	Strong transcription	NHDF-Ad	bronchial
21	chr8:19212200-19220400	Weak transcription	Ovary	ovary
22	chr8:19213800-19215600	Enhancers	Fetal Lung	lung
23	chr8:19213800-19216400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr8:19213800-19216600	Strong transcription	Fetal Intestine Small	intestine
25	chr8:19214000-19215600	Enhancers	Fetal Muscle Trunk	muscle
26	chr8:19214000-19215600	Enhancers	Fetal Muscle Leg	muscle
27	chr8:19214000-19216200	Genic enhancers	Fetal Stomach	stomach
28	chr8:19214200-19216000	Strong transcription	HepG2	liver
29	chr8:19214400-19216400	Enhancers	Fetal Brain Male	brain
30	chr8:19214400-19216600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr8:19214400-19216600	Strong transcription	Fetal Intestine Large	intestine
32	chr8:19214400-19266200	Weak transcription	Aorta	Aorta
33	chr8:19214600-19215600	Enhancers	Fetal Heart	heart
34	chr8:19214600-19220000	Strong transcription	Hela-S3	cervix
35	chr8:19214800-19215400	Enhancers	Fetal Kidney	kidney
36	chr8:19214800-19215400	Genic enhancers	NHLF	lung
37	chr8:19214800-19215600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:19214800-19215600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:19214800-19215600	Enhancers	HSMMtube	muscle
40	chr8:19214800-19216200	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr8:19214800-19216200	Strong transcription	Osteobl	bone
42	chr8:19214800-19216400	Strong transcription	Liver	Liver
43	chr8:19215000-19215600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr8:19215000-19216600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:19215000-19216600	Strong transcription	Gastric	stomach
46	chr8:19215000-19216600	Strong transcription	Pancreas	Pancrea
47	chr8:19215000-19216800	Strong transcription	Duodenum Mucosa	Duodenum
48	chr8:19215000-19217000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:19215200-19215400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:19215200-19215400	Enhancers	Placenta	Placenta

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