Variant report

Variant	nsv1032697
Chromosome Location	chr8:1564933-1613464
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	ATF1	chr8:1612841-1613066	K562	blood:	n/a	n/a
2	ATF2	chr8:1606188-1606635	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:1600054-1600554	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:1583024-1583221	GM12878	blood:	n/a	chr8:1583128-1583139
5	BCL3	chr8:1613411-1613643	GM12878	blood:	n/a	chr8:1613634-1613643
6	BHLHE40	chr8:1610754-1610850	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:1589261-1589514	K562	blood:	n/a	chr8:1589361-1589370 chr8:1589362-1589371 chr8:1589355-1589376 chr8:1589361-1589370
8	BHLHE40	chr8:1598474-1598541	GM12878	blood:	n/a	n/a
9	CEBPB	chr8:1580668-1580977	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr8:1601039-1601179	IMR90	lung:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
11	CEBPB	chr8:1600968-1601172	MCF-7	breast:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
12	CEBPB	chr8:1600966-1601219	HepG2	liver:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
13	CEBPB	chr8:1598267-1598411	HepG2	liver:	n/a	chr8:1598339-1598350 chr8:1598339-1598348
14	CEBPB	chr8:1601046-1601180	K562	blood:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
15	CEBPB	chr8:1577269-1577487	HepG2	liver:	n/a	chr8:1577393-1577404 chr8:1577393-1577406 chr8:1577395-1577406 chr8:1577393-1577406 chr8:1577395-1577404
16	CEBPB	chr8:1580676-1580906	HepG2	liver:	n/a	n/a
17	CHD2	chr8:1606162-1606617	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:1591277-1591285	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:1571043-1571139	H1-hESC	embryonic stem cell:	n/a	chr8:1571110-1571123
20	CTCF	chr8:1595860-1596010	A549	lung:	n/a	n/a
21	CTCF	chr8:1571562-1571637	Fibrobl	skin:	n/a	n/a
22	CTCF	chr8:1574369-1574425	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr8:1574740-1574920	K562	blood:	n/a	n/a
24	CTCF	chr8:1574798-1574892	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:1590436-1590447	MCF-7	breast:	n/a	n/a
26	CTCF	chr8:1595780-1595930	HepG2	liver:	n/a	n/a
27	CTCF	chr8:1611313-1611348	GM19239	blood:	n/a	n/a
28	CTCF	chr8:1595864-1595915	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:1610925-1611115	GM19239	blood:	n/a	n/a
30	CTCF	chr8:1591266-1591306	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:1609079-1609141	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr8:1607807-1607898	Lung_OC	lung:	n/a	n/a
33	ELK1	chr8:1589785-1589810	K562	blood:	n/a	n/a
34	ELK1	chr8:1582547-1582567	Hela-S3	cervix:	n/a	n/a
35	EP300	chr8:1606113-1606596	H1-hESC	embryonic stem cell:	n/a	n/a
36	EP300	chr8:1577960-1577963	GM12878	blood:	n/a	n/a
37	ESR1	chr8:1571268-1572042	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
38	ESR1	chr8:1571462-1571868	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
39	ESR1	chr8:1571384-1572033	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
40	ESR1	chr8:1571311-1571914	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
41	FOSL2	chr8:1600917-1601193	MCF-7	breast:	n/a	chr8:1601075-1601086 chr8:1601073-1601082 chr8:1601074-1601081 chr8:1601072-1601084 chr8:1601073-1601083 chr8:1601074-1601082
42	FOXA1	chr8:1579905-1580112	HepG2	liver:	n/a	chr8:1580014-1580029
43	FOXA1	chr8:1579869-1580116	HepG2	liver:	n/a	chr8:1580014-1580029
44	FOXA1	chr8:1581553-1581686	T-47D	breast:	n/a	n/a
45	FOXA1	chr8:1579880-1580100	T-47D	breast:	n/a	chr8:1580014-1580029
46	FOXA1	chr8:1579862-1580193	HepG2	liver:	n/a	chr8:1580014-1580029
47	FOXA1	chr8:1579783-1580115	HepG2	liver:	n/a	chr8:1580014-1580029
48	FOXA2	chr8:1579857-1580107	HepG2	liver:	n/a	n/a
49	GATA2	chr8:1566862-1567163	SH-SY5Y	brain:	n/a	n/a
50	GTF2F1	chr8:1606306-1606531	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1575750-1575800	AoSMC	blood vessel:	n/a
2	chr8:1588403-1588453	HRPEpiC	eye:	n/a
3	chr8:1601314-1601364	AG04449	skin:	fetal
4	chr8:1575750-1575800	AoSMC	blood vessel:	n/a
5	chr8:1588403-1588453	HRPEpiC	eye:	n/a
6	chr8:1601314-1601364	AG04449	skin:	fetal
7	chr8:1570956-1571006	Caco-2	colon:	n/a
8	chr8:1581647-1581697	AG09309	skin:	n/a
9	chr8:1592451-1592501	Hela-S3	cervix:	n/a
10	chr8:1585146-1585196	BJ	skin:	n/a
11	chr8:1592281-1592331	H1-hESC	embryonic stem cell:	embryo
12	chr8:1585260-1585310	HAEpiC	amniotic membrane:	n/a
13	chr8:1592736-1592786	NHDF-neo	bronchial:	n/a
14	chr8:1592736-1592786	GM06990	blood:	n/a
15	chr8:1581568-1581618	HCF	heart:	n/a
16	chr8:1601314-1601364	HCM	heart:	n/a
17	chr8:1591382-1591432	ovcar-3	ovarian:	n/a
18	chr8:1579039-1579089	RPTEC	kidney:	n/a
19	chr8:1585146-1585196	HEK293	kidney:	embryo
20	chr8:1605546-1605596	K562	blood:	n/a
21	chr8:1588403-1588453	MCF-7	breast:	n/a
22	chr8:1579039-1579089	AG09319	gingival:	n/a
23	chr8:1585929-1585979	LNCaP	prostate:	n/a
24	chr8:1581568-1581618	IMR90	lung:	fetal
25	chr8:1605546-1605596	AoSMC	blood vessel:	n/a
26	chr8:1592281-1592331	HL-60	blood:	n/a
27	chr8:1580998-1581048	HAEpiC	amniotic membrane:	n/a
28	chr8:1580998-1581048	AG04449	skin:	fetal
29	chr8:1586825-1586875	HRPEpiC	eye:	n/a
30	chr8:1575750-1575800	NHBE	bronchial:	n/a
31	chr8:1601314-1601364	HEEpiC	esophagus:	n/a
32	chr8:1579240-1579290	HRE	kidney:	n/a
33	chr8:1579108-1579158	BE2_C	brain:	n/a
34	chr8:1589365-1589415	ProgFib	skin:	n/a
35	chr8:1592281-1592331	HRE	kidney:	n/a
36	chr8:1579180-1579230	AG10803	skin:	n/a
37	chr8:1590039-1590089	BJ	skin:	n/a
38	chr8:1585146-1585196	HMEC	breast:	n/a
39	chr8:1588822-1588872	ProgFib	skin:	n/a
40	chr8:1588403-1588453	NH-A	brain:	n/a
41	chr8:1581122-1581172	AG09319	gingival:	n/a
42	chr8:1601372-1601422	PANC-1	pancreas:	n/a
43	chr8:1591382-1591432	HCM	heart:	n/a
44	chr8:1585146-1585196	Jurkat	blood:	n/a
45	chr8:1570956-1571006	T-47D	breast:	n/a
46	chr8:1592736-1592786	GM12891	blood:	n/a
47	chr8:1588403-1588453	PrEC	prostate:	n/a
48	chr8:1579039-1579089	SKMC	muscle:	n/a
49	chr8:1570956-1571006	AG04450	lung:	fetal
50	chr8:1601372-1601422	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
2	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
3	chr8:1593850..1596302-chr8:1622198..1625044,2	K562	blood:
4	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
5	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
6	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
7	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
8	chr1:154989909..154990782-chr8:1569714..1570480,2	MCF-7	breast:
9	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
10	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
11	chr8:1569188..1570751-chr8:1570808..1572953,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERICH1-6	chr8:1569302-1570583	ENSG00000253267.1
2	lnc-ERICH1-6	chr8:1568540-1568679	ENSG00000253267.1
3	lnc-ERICH1-6	chr8:1567865-1568059	ENSG00000253267.1

Variant related genes	Relation type
ENSG00000253267	TF binding region
ENSG00000253267	CpG island
ENSG00000198010	chromatin interactions
ENSG00000253267	chromatin interactions

Extended variants
information (count: 3159 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:3159 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138409916	chr8:1564934-1564935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548728464	chr8:1564964-1564965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201721570	chr8:1564970-1564971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375613675	chr8:1564972-1564973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs398006921	chr8:1564975-1564976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149318961	chr8:1565015-1565016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531607097	chr8:1565021-1565022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146284326	chr8:1565064-1565065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71516201	chr8:1565067-1565068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191531860	chr8:1565071-1565072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555734842	chr8:1565078-1565079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139259090	chr8:1565128-1565129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142563217	chr8:1565142-1565143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536062137	chr8:1565155-1565156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75128922	chr8:1565168-1565169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146323804	chr8:1565188-1565189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575867490	chr8:1565202-1565203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537788226	chr8:1565226-1565227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148537823	chr8:1565232-1565233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182832287	chr8:1565252-1565253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558150922	chr8:1565261-1565262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556036294	chr8:1565262-1565263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116384013	chr8:1565267-1565268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187593642	chr8:1565277-1565278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145801948	chr8:1565283-1565284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57407874	chr8:1565295-1565296	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs142888452	chr8:1565300-1565301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542436667	chr8:1565306-1565307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574876958	chr8:1565320-1565321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553650406	chr8:1565352-1565353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116870314	chr8:1565423-1565424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543508683	chr8:1565431-1565432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111996314	chr8:1565473-1565474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565033581	chr8:1565493-1565494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533364985	chr8:1565510-1565511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113547886	chr8:1565519-1565520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183406472	chr8:1565520-1565521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566984946	chr8:1565547-1565548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151030496	chr8:1565580-1565581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549185952	chr8:1565659-1565660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13249878	chr8:1565676-1565677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560949406	chr8:1565682-1565683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139720789	chr8:1565690-1565691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571807876	chr8:1565691-1565692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533559354	chr8:1565702-1565703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553325332	chr8:1565705-1565706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573280752	chr8:1565711-1565712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542350620	chr8:1565734-1565735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531326820	chr8:1565763-1565764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555978233	chr8:1565766-1565767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1562600-1569400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1562800-1572600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:1567800-1570200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr8:1568000-1568400	Enhancers	Fetal Muscle Leg	muscle
5	chr8:1569400-1570000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:1569800-1570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:1569800-1570400	Active TSS	Spleen	Spleen
8	chr8:1570000-1570400	Enhancers	H9 Cell Line	embryonic stem cell
9	chr8:1570000-1571400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:1570200-1570800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr8:1570200-1571000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr8:1570400-1571600	Weak transcription	Spleen	Spleen
13	chr8:1570400-1579800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr8:1571400-1571800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:1571600-1571800	ZNF genes & repeats	Pancreas	Pancrea
16	chr8:1571600-1571800	Enhancers	Spleen	Spleen
17	chr8:1571800-1574800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:1573200-1573400	Enhancers	Colon Smooth Muscle	Colon
19	chr8:1573400-1573800	Enhancers	Adipose Nuclei	Adipose
20	chr8:1573400-1573800	Flanking Active TSS	Colon Smooth Muscle	Colon
21	chr8:1573800-1574200	Enhancers	Colon Smooth Muscle	Colon
22	chr8:1574000-1574200	Enhancers	Fetal Muscle Leg	muscle
23	chr8:1574800-1575200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:1575000-1575200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr8:1575200-1575400	Enhancers	Spleen	Spleen
26	chr8:1575200-1599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:1579800-1580000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr8:1579800-1581200	Enhancers	Fetal Brain Male	brain
29	chr8:1580000-1580800	Enhancers	Fetal Brain Female	brain
30	chr8:1580600-1581000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr8:1580800-1581200	Active TSS	Gastric	stomach
32	chr8:1581400-1581800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr8:1593400-1594600	Weak transcription	Fetal Brain Male	brain
34	chr8:1594200-1594400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:1594400-1595000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:1595000-1595200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:1595800-1596800	Enhancers	Gastric	stomach
38	chr8:1596000-1596200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:1596800-1598000	Weak transcription	Gastric	stomach
40	chr8:1599400-1599600	Bivalent Enhancer	Brain Substantia Nigra	brain
41	chr8:1599400-1600000	Enhancers	H9 Cell Line	embryonic stem cell
42	chr8:1599400-1600200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:1599400-1601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:1599600-1599800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
45	chr8:1599600-1600400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr8:1599600-1600600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
47	chr8:1599600-1601000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr8:1599600-1601600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr8:1599800-1600000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr8:1599800-1600400	Enhancers	HUES48 Cell Line	embryonic stem cell

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