Variant report

Variant	nsv889701
Chromosome Location	chr8:1440839-1475823
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	BACH1	chr8:1456764-1456944	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr8:1449883-1450156	GM12878	blood:	n/a	n/a
3	BCL3	chr8:1463690-1465073	GM12878	blood:	n/a	n/a
4	BCL3	chr8:1464008-1465001	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:1451931-1451947	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:1450121-1450295	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:1462786-1462853	K562	blood:	n/a	n/a
8	CHD2	chr8:1456740-1456982	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:1462533-1462907	HepG2	liver:	n/a	chr8:1462756-1462769
10	CTCF	chr8:1464737-1464823	LNCaP	prostate:	n/a	n/a
11	CTCF	chr8:1443208-1443244	LNCaP	prostate:	n/a	n/a
12	CTCF	chr8:1462680-1462830	K562	blood:	n/a	chr8:1462756-1462769
13	CTCF	chr8:1462635-1462855	HepG2	liver:	n/a	chr8:1462756-1462769
14	CTCF	chr8:1462620-1462770	HepG2	liver:	n/a	chr8:1462756-1462769
15	CTCF	chr8:1462720-1462870	MCF-7	breast:	n/a	chr8:1462756-1462769
16	CTCF	chr8:1443219-1443277	H1-hESC	embryonic stem cell:	n/a	chr8:1443235-1443256 chr8:1443238-1443248 chr8:1443233-1443251 chr8:1443255-1443264 chr8:1443236-1443249 chr8:1443231-1443249
17	CTCF	chr8:1459747-1459751	LNCaP	prostate:	n/a	n/a
18	CTCF	chr8:1462653-1462878	LNCaP	prostate:	n/a	chr8:1462756-1462769
19	CTCF	chr8:1462762-1462768	MCF-7	breast:	n/a	n/a
20	CTCF	chr8:1462646-1462870	LNCaP	prostate:	n/a	chr8:1462756-1462769
21	CTCF	chr8:1459401-1459433	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr8:1447352-1447402	GM13976	blood:	n/a	n/a
23	CTCF	chr8:1442460-1442610	GM12864	blood:	n/a	n/a
24	CTCF	chr8:1462658-1462875	H1-hESC	embryonic stem cell:	n/a	chr8:1462756-1462769
25	CTCF	chr8:1443186-1443291	Gliobla	brain:	n/a	chr8:1443235-1443256 chr8:1443238-1443248 chr8:1443233-1443251 chr8:1443255-1443264 chr8:1443236-1443249 chr8:1443231-1443249
26	CTCF	chr8:1443160-1443310	Hela-S3	cervix:	n/a	chr8:1443235-1443256 chr8:1443238-1443248 chr8:1443233-1443251 chr8:1443255-1443264 chr8:1443236-1443249 chr8:1443231-1443249
27	CTCF	chr8:1456825-1456985	K562	blood:	n/a	chr8:1456903-1456916
28	CTCF	chr8:1459400-1459549	GM10248	blood:	n/a	n/a
29	CTCF	chr8:1462660-1462810	WERI-Rb-1	eye:	n/a	chr8:1462756-1462769
30	CTCF	chr8:1454917-1454965	LNCaP	prostate:	n/a	n/a
31	CTCF	chr8:1443218-1443257	MCF-7	breast:	n/a	chr8:1443235-1443256 chr8:1443238-1443248 chr8:1443233-1443251 chr8:1443236-1443249 chr8:1443231-1443249
32	CTCF	chr8:1462716-1462833	MCF-7	breast:	n/a	chr8:1462756-1462769
33	CTCF	chr8:1443205-1443271	LNCaP	prostate:	n/a	chr8:1443235-1443256 chr8:1443238-1443248 chr8:1443233-1443251 chr8:1443255-1443264 chr8:1443236-1443249 chr8:1443231-1443249
34	CTCF	chr8:1462974-1463010	LNCaP	prostate:	n/a	chr8:1462985-1462998
35	CTCF	chr8:1462740-1462890	HCT-116	colon:	n/a	chr8:1462756-1462769
36	CTCF	chr8:1456780-1457043	K562	blood:	n/a	chr8:1456903-1456916
37	CTCF	chr8:1443191-1443375	MCF-7	breast:	n/a	chr8:1443235-1443256 chr8:1443238-1443248 chr8:1443233-1443251 chr8:1443255-1443264 chr8:1443236-1443249 chr8:1443231-1443249
38	CTCF	chr8:1462670-1462838	K562	blood:	n/a	chr8:1462756-1462769
39	CTCF	chr8:1462740-1462890	MCF-7	breast:	n/a	chr8:1462756-1462769
40	CTCF	chr8:1459529-1459564	GM13976	blood:	n/a	n/a
41	CTCF	chr8:1462660-1462810	Caco-2	colon:	n/a	chr8:1462756-1462769
42	CTCF	chr8:1456784-1456997	H1-hESC	embryonic stem cell:	n/a	chr8:1456903-1456916
43	CTCF	chr8:1456691-1457024	H1-hESC	embryonic stem cell:	n/a	chr8:1456903-1456916
44	CTCF	chr8:1459314-1459379	GM13976	blood:	n/a	n/a
45	CTCF	chr8:1463660-1463810	GM12871	blood:	n/a	n/a
46	CTCF	chr8:1443210-1443278	MCF-7	breast:	n/a	chr8:1443235-1443256 chr8:1443238-1443248 chr8:1443233-1443251 chr8:1443255-1443264 chr8:1443236-1443249 chr8:1443231-1443249
47	CTCF	chr8:1459772-1459828	Medullo	brain:	n/a	n/a
48	CTCF	chr8:1462668-1462841	HepG2	liver:	n/a	chr8:1462756-1462769
49	CTCF	chr8:1462608-1462878	K562	blood:	n/a	chr8:1462756-1462769
50	CUX1	chr8:1453971-1453981	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1471679-1471729	AG04450	lung:	fetal
2	chr8:1475228-1475278	Caco-2	colon:	n/a
3	chr8:1444021-1444071	GM06990	blood:	n/a
4	chr8:1445449-1445499	AG10803	skin:	n/a
5	chr8:1471679-1471729	AG04450	lung:	fetal
6	chr8:1475228-1475278	Caco-2	colon:	n/a
7	chr8:1444021-1444071	GM06990	blood:	n/a
8	chr8:1445449-1445499	AG10803	skin:	n/a
9	chr8:1455764-1455814	ECC-1	luminal epithelium:	n/a
10	chr8:1446276-1446326	Jurkat	blood:	n/a
11	chr8:1448361-1448411	GM12878	blood:	n/a
12	chr8:1449497-1449547	HEEpiC	esophagus:	n/a
13	chr8:1458508-1458558	PrEC	prostate:	n/a
14	chr8:1475145-1475195	K562	blood:	n/a
15	chr8:1460268-1460318	BJ	skin:	n/a
16	chr8:1460718-1460768	HAEpiC	amniotic membrane:	n/a
17	chr8:1449634-1449684	HepG2	liver:	n/a
18	chr8:1442292-1442342	HCT-116	colon:	n/a
19	chr8:1475257-1475307	SK-N-MC	brain:	n/a
20	chr8:1460216-1460266	U87	brain:	n/a
21	chr8:1441386-1441436	GM12892	blood:	n/a
22	chr8:1448707-1448757	HCT-116	colon:	n/a
23	chr8:1460569-1460619	HCT-116	colon:	n/a
24	chr8:1471564-1471614	GM12892	blood:	n/a
25	chr8:1448707-1448757	SK-N-SH	brain:	n/a
26	chr8:1468625-1468675	HUVEC	blood vessel:	n/a
27	chr8:1449313-1449363	NH-A	brain:	n/a
28	chr8:1470122-1470172	CMK	blood:	n/a
29	chr8:1455354-1455404	NT2-D1	testis:	n/a
30	chr8:1475257-1475307	Jurkat	blood:	n/a
31	chr8:1463125-1463175	MCF-7	breast:	n/a
32	chr8:1442292-1442342	MCF10A-Er-Src	breast:	n/a
33	chr8:1450031-1450081	MCF10A-Er-Src	breast:	n/a
34	chr8:1471679-1471729	SKMC	muscle:	n/a
35	chr8:1448361-1448411	GM06990	blood:	n/a
36	chr8:1460569-1460619	MCF-7	breast:	n/a
37	chr8:1441386-1441436	IMR90	lung:	fetal
38	chr8:1444085-1444135	HCT-116	colon:	n/a
39	chr8:1441539-1441589	K562	blood:	n/a
40	chr8:1475228-1475278	HEK293	kidney:	embryo
41	chr8:1462903-1462953	HEK293	kidney:	embryo
42	chr8:1448998-1449048	NB4	blood:	n/a
43	chr8:1471446-1471496	GM19239	blood:	n/a
44	chr8:1460718-1460768	IMR90	lung:	fetal
45	chr8:1460569-1460619	Caco-2	colon:	n/a
46	chr8:1470122-1470172	MCF-7	breast:	n/a
47	chr8:1475145-1475195	AG04450	lung:	fetal
48	chr8:1445449-1445499	HepG2	liver:	n/a
49	chr8:1460633-1460683	AG04449	skin:	fetal
50	chr8:1441403-1441453	LNCaP	prostate:	n/a

Variant related genes	Relation type
DLGAP2	TF binding region
DLGAP2	CpG island

Extended variants
information (count: 2521 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2521 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7845120	chr8:1440839-1440840	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368344107	chr8:1440840-1440841	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs552723350	chr8:1440857-1440858	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs542715762	chr8:1440886-1440887	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs568483519	chr8:1440889-1440890	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs374446599	chr8:1440890-1440891	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs78330066	chr8:1440900-1440901	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs544950379	chr8:1440940-1440941	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs75311646	chr8:1440943-1440944	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs148608095	chr8:1440945-1440946	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs546970889	chr8:1440972-1440973	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs191402172	chr8:1440977-1440978	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs529372909	chr8:1440986-1440987	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs112860651	chr8:1440987-1440988	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs569332792	chr8:1441077-1441078	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs73172573	chr8:1441078-1441079	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184303006	chr8:1441119-1441120	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs571653108	chr8:1441176-1441177	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs534222843	chr8:1441179-1441180	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs142076734	chr8:1441191-1441192	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs114050100	chr8:1441195-1441196	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs543183150	chr8:1441202-1441203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187089599	chr8:1441233-1441234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556251644	chr8:1441276-1441277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146755651	chr8:1441282-1441283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545227767	chr8:1441287-1441288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192930903	chr8:1441314-1441315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572329363	chr8:1441329-1441330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75904916	chr8:1441334-1441335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560483462	chr8:1441340-1441341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558248489	chr8:1441352-1441353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140448497	chr8:1441353-1441354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17063983	chr8:1441355-1441356	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12543165	chr8:1441363-1441364	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs146487901	chr8:1441365-1441366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73672732	chr8:1441384-1441385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs527942537	chr8:1441393-1441394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547703919	chr8:1441396-1441397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566900369	chr8:1441403-1441404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372926421	chr8:1441418-1441419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112837741	chr8:1441448-1441449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200855591	chr8:1441451-1441452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528029110	chr8:1441468-1441469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549049524	chr8:1441515-1441516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75161259	chr8:1441533-1441534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561559619	chr8:1441543-1441544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558752676	chr8:1441567-1441568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531964889	chr8:1441568-1441569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554408713	chr8:1441572-1441573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550356598	chr8:1441611-1441612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
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
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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	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
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1435200-1447000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:1438600-1447200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:1439400-1441000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:1439400-1441200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr8:1440600-1441000	Bivalent Enhancer	Fetal Stomach	stomach
6	chr8:1440600-1443200	Enhancers	Brain Germinal Matrix	brain
7	chr8:1440800-1441000	Enhancers	Fetal Brain Male	brain
8	chr8:1441000-1442000	Weak transcription	Fetal Brain Male	brain
9	chr8:1441000-1442200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:1442000-1442400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr8:1442000-1443600	Enhancers	Fetal Brain Male	brain
12	chr8:1442200-1443200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:1443200-1443800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:1443200-1444000	Weak transcription	Brain Germinal Matrix	brain
15	chr8:1443400-1443600	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr8:1443400-1444000	ZNF genes & repeats	Spleen	Spleen
17	chr8:1443600-1448800	Weak transcription	Fetal Brain Male	brain
18	chr8:1443800-1449800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:1444000-1444200	Enhancers	Brain Germinal Matrix	brain
20	chr8:1444000-1444600	Weak transcription	Spleen	Spleen
21	chr8:1444200-1450000	Weak transcription	Brain Germinal Matrix	brain
22	chr8:1444400-1447000	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr8:1445200-1447000	Weak transcription	Pancreas	Pancrea
24	chr8:1445800-1446000	Weak transcription	Spleen	Spleen
25	chr8:1446600-1447200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:1446600-1449200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:1446800-1447400	Enhancers	Fetal Kidney	kidney
28	chr8:1446800-1447600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr8:1446800-1452400	Enhancers	Fetal Stomach	stomach
30	chr8:1447000-1447200	Enhancers	Pancreas	Pancrea
31	chr8:1447000-1447400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:1447000-1447800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:1447000-1447800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr8:1447200-1447600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:1447200-1447600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr8:1447200-1447600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:1447200-1447600	Enhancers	Fetal Muscle Leg	muscle
38	chr8:1447200-1448000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:1447400-1447600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:1447400-1447600	Flanking Active TSS	Fetal Kidney	kidney
41	chr8:1447400-1447600	Enhancers	Fetal Muscle Trunk	muscle
42	chr8:1447600-1448000	Enhancers	Fetal Kidney	kidney
43	chr8:1447600-1449000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr8:1447600-1449200	Weak transcription	Fetal Muscle Leg	muscle
45	chr8:1447600-1449800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr8:1447600-1449800	Weak transcription	Fetal Muscle Trunk	muscle
47	chr8:1447600-1450800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:1447800-1448000	Enhancers	Fetal Brain Female	brain
49	chr8:1447800-1448800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:1448000-1448400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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