Variant report

Variant	esv3421336
Chromosome Location	chr8:6421944-6427042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6421737-6422437	HepG2	liver:	n/a	chr8:6422337-6422353
2	CTCF	chr8:6424644-6424787	GM19239	blood:	n/a	n/a
3	CTCF	chr8:6424331-6424355	GM12878	blood:	n/a	n/a
4	CTCF	chr8:6424203-6424360	GM19239	blood:	n/a	n/a
5	CTCF	chr8:6424026-6424131	GM19239	blood:	n/a	n/a
6	CTCF	chr8:6424597-6424648	GM12892	blood:	n/a	n/a
7	CTCF	chr8:6424019-6424025	GM19239	blood:	n/a	n/a
8	CTCF	chr8:6424377-6424518	GM19239	blood:	n/a	n/a
9	CTCF	chr8:6424143-6424201	GM12891	blood:	n/a	n/a
10	CTCF	chr8:6426300-6426450	GM12866	blood:	n/a	chr8:6426335-6426348
11	CTCF	chr8:6424009-6424086	ProgFib	skin:	n/a	n/a
12	EP300	chr8:6426968-6428377	SK-N-SH	brain:	n/a	chr8:6427744-6427753 chr8:6427065-6427079
13	FOXA1	chr8:6421588-6422368	HepG2	liver:	n/a	n/a
14	FOXA1	chr8:6421799-6422232	HepG2	liver:	n/a	n/a
15	FOXA1	chr8:6421771-6422306	HepG2	liver:	n/a	n/a
16	FOXA1	chr8:6421860-6422364	HepG2	liver:	n/a	n/a
17	FOXA2	chr8:6421637-6422493	HepG2	liver:	n/a	n/a
18	FOXA2	chr8:6421910-6422210	HepG2	liver:	n/a	n/a
19	HNF4A	chr8:6421984-6422252	HepG2	liver:	n/a	n/a
20	KAP1	chr8:6421877-6422238	U2OS	brain:	n/a	n/a
21	MAFF	chr8:6421740-6422188	HepG2	liver:	n/a	chr8:6422049-6422063 chr8:6421828-6421846
22	MAFF	chr8:6425793-6426057	K562	blood:	n/a	chr8:6425926-6425944 chr8:6425925-6425939
23	MAFF	chr8:6425755-6426110	HepG2	liver:	n/a	chr8:6425926-6425944 chr8:6425925-6425939
24	MAFK	chr8:6425960-6425983	Hela-S3	cervix:	n/a	n/a
25	MAFK	chr8:6421802-6422158	HepG2	liver:	n/a	chr8:6421833-6421844 chr8:6421834-6421845 chr8:6421834-6421845 chr8:6421833-6421844
26	MAFK	chr8:6425754-6426104	IMR90	lung:	n/a	chr8:6425922-6425942 chr8:6426023-6426034 chr8:6425927-6425943 chr8:6426024-6426035 chr8:6425924-6425940 chr8:6426024-6426035 chr8:6425927-6425942 chr8:6425925-6425939
27	MAFK	chr8:6425751-6426118	HepG2	liver:	n/a	chr8:6425922-6425942 chr8:6426023-6426034 chr8:6425927-6425943 chr8:6426024-6426035 chr8:6425924-6425940 chr8:6426024-6426035 chr8:6425927-6425942 chr8:6425925-6425939
28	MAFK	chr8:6421808-6422295	HepG2	liver:	n/a	chr8:6421833-6421844 chr8:6421834-6421845 chr8:6421834-6421845 chr8:6421833-6421844
29	MAFK	chr8:6425759-6426131	HepG2	liver:	n/a	chr8:6425922-6425942 chr8:6426023-6426034 chr8:6425927-6425943 chr8:6426024-6426035 chr8:6425924-6425940 chr8:6426024-6426035 chr8:6425927-6425942 chr8:6425925-6425939
30	MAFK	chr8:6425802-6426070	K562	blood:	n/a	chr8:6425922-6425942 chr8:6426023-6426034 chr8:6425927-6425943 chr8:6426024-6426035 chr8:6425924-6425940 chr8:6426024-6426035 chr8:6425927-6425942 chr8:6425925-6425939
31	MXI1	chr8:6426723-6428522	SK-N-SH	brain:	n/a	n/a
32	MYC	chr8:6424885-6424899	MCF-7	breast:	n/a	n/a
33	MYC	chr8:6423814-6424927	MCF-7	breast:	n/a	chr8:6423843-6423850
34	MYC	chr8:6424736-6424848	MCF-7	breast:	n/a	n/a
35	MYC	chr8:6424076-6424106	MCF-7	breast:	n/a	n/a
36	MYC	chr8:6423811-6423952	MCF-7	breast:	n/a	chr8:6423843-6423850
37	MYC	chr8:6424028-6424310	MCF-7	breast:	n/a	n/a
38	MYC	chr8:6424173-6424846	MCF-7	breast:	n/a	n/a
39	MYC	chr8:6424041-6424070	MCF-7	breast:	n/a	n/a
40	NR2C2	chr8:6423914-6424901	GM12878	blood:	n/a	n/a
41	POLR2A	chr8:6423765-6424947	MCF-7	breast:	n/a	n/a
42	POLR2A	chr8:6425710-6425766	MCF-7	breast:	n/a	n/a
43	POLR2A	chr8:6423804-6424956	MCF-7	breast:	n/a	n/a
44	POLR2A	chr8:6424373-6424483	Gliobla	brain:	n/a	n/a
45	POLR2A	chr8:6424515-6424580	Gliobla	brain:	n/a	n/a
46	POLR2A	chr8:6424542-6424786	A549	lung:	n/a	n/a
47	POLR2A	chr8:6426417-6426470	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr8:6423289-6423308	K562	blood:	n/a	n/a
49	REST	chr8:6424472-6424614	PANC-1	pancreas:	n/a	n/a
50	TCF3	chr8:6424197-6424845	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6423908-6423958	AG09319	gingival:	n/a
2	chr8:6424636-6424686	AoSMC	blood vessel:	n/a
3	chr8:6423908-6423958	AG09319	gingival:	n/a
4	chr8:6424636-6424686	AoSMC	blood vessel:	n/a
5	chr8:6424636-6424686	HRPEpiC	eye:	n/a
6	chr8:6424726-6424776	PrEC	prostate:	n/a
7	chr8:6423908-6423958	HMEC	breast:	n/a
8	chr8:6424636-6424686	AG04450	lung:	fetal
9	chr8:6424269-6424319	PANC-1	pancreas:	n/a
10	chr8:6424269-6424319	HCT-116	colon:	n/a
11	chr8:6424726-6424776	ovcar-3	ovarian:	n/a
12	chr8:6424726-6424776	T-47D	breast:	n/a
13	chr8:6424636-6424686	HCT-116	colon:	n/a
14	chr8:6424726-6424776	SK-N-SH_RA	brain:	n/a
15	chr8:6424636-6424686	HEK293	kidney:	embryo
16	chr8:6423908-6423958	U87	brain:	n/a
17	chr8:6424269-6424319	PFSK-1	brain:	n/a
18	chr8:6424726-6424776	HRE	kidney:	n/a
19	chr8:6423908-6423958	AoSMC	blood vessel:	n/a
20	chr8:6424726-6424776	GM12892	blood:	n/a
21	chr8:6424636-6424686	MCF10A-Er-Src	breast:	n/a
22	chr8:6423908-6423958	RPTEC	kidney:	n/a
23	chr8:6424636-6424686	ProgFib	skin:	n/a
24	chr8:6424726-6424776	HAEpiC	amniotic membrane:	n/a
25	chr8:6423908-6423958	GM12878	blood:	n/a
26	chr8:6424269-6424319	NB4	blood:	n/a
27	chr8:6424726-6424776	NHBE	bronchial:	n/a
28	chr8:6423908-6423958	SAEC	small airway:	n/a
29	chr8:6424269-6424319	HCF	heart:	n/a
30	chr8:6424636-6424686	Caco-2	colon:	n/a
31	chr8:6424726-6424776	HNPCEpiC	eye:	n/a
32	chr8:6423908-6423958	HCT-116	colon:	n/a
33	chr8:6424269-6424319	HCM	heart:	n/a
34	chr8:6424636-6424686	GM12892	blood:	n/a
35	chr8:6424269-6424319	SK-N-MC	brain:	n/a
36	chr8:6423908-6423958	MCF10A-Er-Src	breast:	n/a
37	chr8:6424726-6424776	LNCaP	prostate:	n/a
38	chr8:6424636-6424686	HRE	kidney:	n/a
39	chr8:6424636-6424686	Hela-S3	cervix:	n/a
40	chr8:6423908-6423958	H1-hESC	embryonic stem cell:	embryo
41	chr8:6424636-6424686	Hepatocyte	liver:	n/a
42	chr8:6423908-6423958	BJ	skin:	n/a
43	chr8:6424636-6424686	NH-A	brain:	n/a
44	chr8:6424269-6424319	AG09319	gingival:	n/a
45	chr8:6424726-6424776	SK-N-MC	brain:	n/a
46	chr8:6423908-6423958	PrEC	prostate:	n/a
47	chr8:6424636-6424686	GM12878	blood:	n/a
48	chr8:6424636-6424686	HAEpiC	amniotic membrane:	n/a
49	chr8:6423908-6423958	Hepatocyte	liver:	n/a
50	chr8:6424269-6424319	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:6426332..6429176-chr8:6564535..6567216,2	MCF-7	breast:
2	chr8:6280960..6282945-chr8:6426818..6429637,2	K562	blood:

Variant related genes	Relation type
ANGPT2	TF binding region
ANGPT2	CpG island
ENSG00000249898	chromatin interactions
ENSG00000155189	chromatin interactions

Extended variants
information (count: 328 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:328 , 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	rs78088481	chr8:6421950-6421951	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs560417161	chr8:6421970-6421971	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs532636617	chr8:6421974-6421975	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs548010920	chr8:6421984-6421985	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs2515508	chr8:6421998-6421999	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs562738034	chr8:6422008-6422009	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10108504	chr8:6422030-6422031	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73201304	chr8:6422057-6422058	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs73661405	chr8:6422064-6422065	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs76053320	chr8:6422069-6422070	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs10646441	chr8:6422104-6422105	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs66508730	chr8:6422105-6422106	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs397825958	chr8:6422108-6422109	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs559138370	chr8:6422124-6422125	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs140986495	chr8:6422130-6422131	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs2515509	chr8:6422141-6422142	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs570748659	chr8:6422145-6422146	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs113779460	chr8:6422146-6422147	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112654618	chr8:6422155-6422156	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558621018	chr8:6422172-6422173	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs192782374	chr8:6422197-6422198	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs561683598	chr8:6422201-6422202	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs530463082	chr8:6422221-6422222	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs554539162	chr8:6422222-6422223	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs183259591	chr8:6422232-6422233	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs540568258	chr8:6422245-6422246	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs149353728	chr8:6422257-6422258	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs147001212	chr8:6422258-6422259	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs374717987	chr8:6422304-6422305	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs118100309	chr8:6422317-6422318	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs564795462	chr8:6422330-6422331	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs369975394	chr8:6422337-6422338	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs531575287	chr8:6422342-6422343	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs138217937	chr8:6422352-6422353	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs10090540	chr8:6422373-6422374	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143761408	chr8:6422395-6422396	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527966665	chr8:6422508-6422509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188485803	chr8:6422546-6422547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564291214	chr8:6422576-6422577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533580400	chr8:6422590-6422591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551950384	chr8:6422602-6422603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147188977	chr8:6422614-6422615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373440810	chr8:6422647-6422648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537571006	chr8:6422648-6422649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549762395	chr8:6422707-6422708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548192901	chr8:6422716-6422717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17624399	chr8:6422753-6422754	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs556785062	chr8:6422798-6422799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534077776	chr8:6422803-6422804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576572705	chr8:6422856-6422857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	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
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	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
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6364200-6478200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:6407800-6423800	Weak transcription	Spleen	Spleen
3	chr8:6415200-6424000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:6416400-6422200	Enhancers	Primary B cells from peripheral blood	blood
5	chr8:6416800-6442400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr8:6417600-6424000	Weak transcription	NHEK	skin
7	chr8:6417600-6442800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:6418600-6422600	Enhancers	HepG2	liver
9	chr8:6419000-6462400	Weak transcription	GM12878-XiMat	blood
10	chr8:6419600-6423400	Weak transcription	Primary T cells from cord blood	blood
11	chr8:6419600-6423800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:6419800-6423600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:6420000-6427400	Weak transcription	Thymus	Thymus
14	chr8:6420600-6423800	Weak transcription	Pancreas	Pancrea
15	chr8:6420800-6423800	Weak transcription	Gastric	stomach
16	chr8:6420800-6424000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr8:6420800-6424200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:6420800-6424400	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr8:6420800-6427600	Weak transcription	NHDF-Ad	bronchial
20	chr8:6420800-6429800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:6420800-6433200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:6421000-6422000	Weak transcription	Placenta	Placenta
23	chr8:6421000-6422200	Weak transcription	Fetal Intestine Small	intestine
24	chr8:6421000-6423000	Weak transcription	Brain Hippocampus Middle	brain
25	chr8:6421000-6423800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:6421000-6423800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:6421000-6423800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr8:6421000-6423800	Weak transcription	Esophagus	oesophagus
29	chr8:6421000-6423800	Weak transcription	Lung	lung
30	chr8:6421000-6423800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr8:6421000-6424600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:6421000-6424800	Weak transcription	Fetal Thymus	thymus
33	chr8:6421000-6425200	Weak transcription	Fetal Muscle Leg	muscle
34	chr8:6421000-6425400	Weak transcription	Fetal Stomach	stomach
35	chr8:6421000-6425800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:6421000-6426000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr8:6421000-6427400	Weak transcription	Left Ventricle	heart
38	chr8:6421000-6427400	Weak transcription	Ovary	ovary
39	chr8:6421000-6427800	Weak transcription	Aorta	Aorta
40	chr8:6421000-6427800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr8:6421000-6435400	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr8:6421200-6422000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr8:6421200-6422000	Weak transcription	Dnd41	blood
44	chr8:6421200-6424000	Weak transcription	Adipose Nuclei	Adipose
45	chr8:6421200-6424800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:6421200-6425200	Weak transcription	Primary hematopoietic stem cells	blood
47	chr8:6421200-6425600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr8:6421200-6436200	Weak transcription	Right Atrium	heart
49	chr8:6421400-6427400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:6421400-6433200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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