Variant report

Variant	nsv1024534
Chromosome Location	chr8:1532291-1583640
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	chr8:1535079-1535122	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr8:1583024-1583221	GM12878	blood:	n/a	chr8:1583128-1583139
3	BHLHE40	chr8:1536031-1536338	K562	blood:	n/a	chr8:1536182-1536203 chr8:1536188-1536197 chr8:1536189-1536198 chr8:1536186-1536199 chr8:1536188-1536197
4	BHLHE40	chr8:1563001-1563164	K562	blood:	n/a	n/a
5	CEBPB	chr8:1580668-1580977	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr8:1577269-1577487	HepG2	liver:	n/a	chr8:1577393-1577404 chr8:1577393-1577406 chr8:1577395-1577406 chr8:1577393-1577406 chr8:1577395-1577404
7	CEBPB	chr8:1532612-1532812	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:1580676-1580906	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:1532711-1532758	K562	blood:	n/a	n/a
10	CHD1	chr8:1535585-1535659	GM12878	blood:	n/a	n/a
11	CTCF	chr8:1540240-1540390	WERI-Rb-1	eye:	n/a	chr8:1540328-1540346
12	CTCF	chr8:1540280-1540430	GM12865	blood:	n/a	chr8:1540328-1540346
13	CTCF	chr8:1540220-1540370	GM12864	blood:	n/a	chr8:1540328-1540346
14	CTCF	chr8:1571562-1571637	Fibrobl	skin:	n/a	n/a
15	CTCF	chr8:1540262-1540391	MCF-7	breast:	n/a	chr8:1540328-1540346
16	CTCF	chr8:1540280-1540430	WERI-Rb-1	eye:	n/a	chr8:1540328-1540346
17	CTCF	chr8:1574740-1574920	K562	blood:	n/a	n/a
18	CTCF	chr8:1540097-1540441	H1-hESC	embryonic stem cell:	n/a	chr8:1540328-1540346
19	CTCF	chr8:1540331-1540377	GM10248	blood:	n/a	n/a
20	CTCF	chr8:1564045-1564082	GM13977	blood:	n/a	n/a
21	CTCF	chr8:1540277-1540386	MCF-7	breast:	n/a	chr8:1540328-1540346
22	CTCF	chr8:1540314-1540372	Pancreas_OC	pancreas:	n/a	chr8:1540328-1540346
23	CTCF	chr8:1574798-1574892	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:1540315-1540373	Gliobla	brain:	n/a	chr8:1540328-1540346
25	CTCF	chr8:1540236-1540435	H1-hESC	embryonic stem cell:	n/a	chr8:1540328-1540346
26	CTCF	chr8:1571043-1571139	H1-hESC	embryonic stem cell:	n/a	chr8:1571110-1571123
27	CTCF	chr8:1540180-1540330	NB4	blood:	n/a	n/a
28	CTCF	chr8:1540240-1540390	HepG2	liver:	n/a	chr8:1540328-1540346
29	CTCF	chr8:1540132-1540435	H1-hESC	embryonic stem cell:	n/a	chr8:1540328-1540346
30	CTCF	chr8:1574369-1574425	H1-hESC	embryonic stem cell:	n/a	n/a
31	ELF1	chr8:1534176-1534413	K562	blood:	n/a	n/a
32	ELK1	chr8:1582547-1582567	Hela-S3	cervix:	n/a	n/a
33	EP300	chr8:1577960-1577963	GM12878	blood:	n/a	n/a
34	ESR1	chr8:1571311-1571914	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
35	ESR1	chr8:1571384-1572033	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
36	ESR1	chr8:1571462-1571868	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
37	ESR1	chr8:1571268-1572042	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
38	FOS	chr8:1536152-1536404	MCF10A-Er-Src	breast:	n/a	chr8:1536283-1536293 chr8:1536283-1536293 chr8:1536284-1536293
39	FOS	chr8:1536099-1536351	MCF10A-Er-Src	breast:	n/a	chr8:1536283-1536293 chr8:1536283-1536293 chr8:1536284-1536293
40	FOS	chr8:1536162-1536430	MCF10A-Er-Src	breast:	n/a	chr8:1536283-1536293 chr8:1536283-1536293 chr8:1536284-1536293
41	FOS	chr8:1536101-1536402	MCF10A-Er-Src	breast:	n/a	chr8:1536283-1536293 chr8:1536283-1536293 chr8:1536284-1536293
42	FOXA1	chr8:1581553-1581686	T-47D	breast:	n/a	n/a
43	FOXA1	chr8:1579869-1580116	HepG2	liver:	n/a	chr8:1580014-1580029
44	FOXA1	chr8:1579862-1580193	HepG2	liver:	n/a	chr8:1580014-1580029
45	FOXA1	chr8:1579905-1580112	HepG2	liver:	n/a	chr8:1580014-1580029
46	FOXA1	chr8:1579880-1580100	T-47D	breast:	n/a	chr8:1580014-1580029
47	FOXA1	chr8:1579783-1580115	HepG2	liver:	n/a	chr8:1580014-1580029
48	FOXA2	chr8:1555779-1556525	A549	lung:	n/a	n/a
49	FOXA2	chr8:1556030-1556410	A549	lung:	n/a	n/a
50	FOXA2	chr8:1579857-1580107	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1570635-1570685	MCF-7	breast:	n/a
2	chr8:1570635-1570685	MCF-7	breast:	n/a
3	chr8:1570715-1570765	AG09319	gingival:	n/a
4	chr8:1563040-1563090	AG09319	gingival:	n/a
5	chr8:1534658-1534708	BE2_C	brain:	n/a
6	chr8:1553395-1553445	IMR90	lung:	fetal
7	chr8:1553261-1553311	GM06990	blood:	n/a
8	chr8:1570715-1570765	ovcar-3	ovarian:	n/a
9	chr8:1580998-1581048	HepG2	liver:	n/a
10	chr8:1581598-1581648	ProgFib	skin:	n/a
11	chr8:1579180-1579230	ProgFib	skin:	n/a
12	chr8:1571105-1571155	BJ	skin:	n/a
13	chr8:1553879-1553929	LNCaP	prostate:	n/a
14	chr8:1570956-1571006	HEK293	kidney:	embryo
15	chr8:1570715-1570765	SKMC	muscle:	n/a
16	chr8:1553879-1553929	HL-60	blood:	n/a
17	chr8:1579240-1579290	AG09309	skin:	n/a
18	chr8:1575750-1575800	GM06990	blood:	n/a
19	chr8:1570956-1571006	AG09319	gingival:	n/a
20	chr8:1579240-1579290	Hela-S3	cervix:	n/a
21	chr8:1581647-1581697	AoSMC	blood vessel:	n/a
22	chr8:1570956-1571006	HRE	kidney:	n/a
23	chr8:1571105-1571155	AG09319	gingival:	n/a
24	chr8:1581122-1581172	HIPEpiC	eye:	n/a
25	chr8:1581568-1581618	HEK293	kidney:	embryo
26	chr8:1534376-1534426	Hepatocyte	liver:	n/a
27	chr8:1575750-1575800	Hela-S3	cervix:	n/a
28	chr8:1581647-1581697	GM06990	blood:	n/a
29	chr8:1553698-1553748	HEK293	kidney:	embryo
30	chr8:1534838-1534888	GM12891	blood:	n/a
31	chr8:1570715-1570765	NH-A	brain:	n/a
32	chr8:1571105-1571155	AG10803	skin:	n/a
33	chr8:1563113-1563163	HEEpiC	esophagus:	n/a
34	chr8:1580998-1581048	T-47D	breast:	n/a
35	chr8:1553879-1553929	NHDF-neo	bronchial:	n/a
36	chr8:1553698-1553748	NHDF-neo	bronchial:	n/a
37	chr8:1553698-1553748	HRCEpiC	kidney:	n/a
38	chr8:1534838-1534888	AG04449	skin:	fetal
39	chr8:1581647-1581697	GM12892	blood:	n/a
40	chr8:1581568-1581618	SK-N-MC	brain:	n/a
41	chr8:1581647-1581697	HRCEpiC	kidney:	n/a
42	chr8:1534376-1534426	SAEC	small airway:	n/a
43	chr8:1553879-1553929	H1-hESC	embryonic stem cell:	embryo
44	chr8:1580998-1581048	NB4	blood:	n/a
45	chr8:1534658-1534708	GM12878	blood:	n/a
46	chr8:1579180-1579230	HMEC	breast:	n/a
47	chr8:1581598-1581648	BE2_C	brain:	n/a
48	chr8:1563040-1563090	GM12891	blood:	n/a
49	chr8:1563040-1563090	SKMC	muscle:	n/a
50	chr8:1579108-1579158	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
2	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
3	chr8:1569188..1570751-chr8:1570808..1572953,2	MCF-7	breast:
4	chr1:154989909..154990782-chr8:1569714..1570480,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERICH1-6	chr8:1552718-1552910	ENSG00000253267.1
2	lnc-ERICH1-6	chr8:1568540-1568679	ENSG00000253267.1
3	lnc-ERICH1-6	chr8:1567865-1568059	ENSG00000253267.1
4	lnc-ERICH1-6	chr8:1569302-1570583	ENSG00000253267.1

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

Extended variants
information (count: 2406 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:2406 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567850494	chr8:1532605-1532606	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537129850	chr8:1532614-1532615	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190145820	chr8:1532619-1532620	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556924936	chr8:1532627-1532628	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144247143	chr8:1532642-1532643	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543161676	chr8:1532664-1532665	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553275624	chr8:1532669-1532670	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572488126	chr8:1532689-1532690	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550357199	chr8:1532749-1532750	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148368486	chr8:1532751-1532752	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561244308	chr8:1532753-1532754	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577621491	chr8:1532789-1532790	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73671236	chr8:1532802-1532803	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs117007204	chr8:1532803-1532804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563737283	chr8:1532819-1532820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532690198	chr8:1532847-1532848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142232390	chr8:1532851-1532852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4876095	chr8:1532857-1532858	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs528747774	chr8:1532872-1532873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547400654	chr8:1532881-1532882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547812254	chr8:1532885-1532886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182247612	chr8:1532925-1532926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369507411	chr8:1532940-1532941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536787961	chr8:1532962-1532963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550610924	chr8:1532964-1532965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146402450	chr8:1532980-1532981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373016791	chr8:1532992-1532993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539902567	chr8:1536010-1536011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560319930	chr8:1536011-1536012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547525152	chr8:1536051-1536052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs118163326	chr8:1536104-1536105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75179161	chr8:1536105-1536106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546049535	chr8:1536106-1536107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558928287	chr8:1536112-1536113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139563470	chr8:1536161-1536162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542392147	chr8:1536206-1536207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547998488	chr8:1536208-1536209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186771402	chr8:1536220-1536221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190892518	chr8:1536238-1536239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550800554	chr8:1536249-1536250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563016057	chr8:1536250-1536251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530065142	chr8:1536276-1536277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143390248	chr8:1536294-1536295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78365263	chr8:1536341-1536342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532001594	chr8:1536343-1536344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116837767	chr8:1536346-1536347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566095247	chr8:1536371-1536372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367820606	chr8:1536384-1536385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569922952	chr8:1536401-1536402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140334621	chr8:1536407-1536408	Enhancers	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:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1532600-1532800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
2	chr8:1532600-1533000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
3	chr8:1536000-1536600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:1536400-1536800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr8:1536600-1538200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:1538200-1539000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:1540000-1540400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:1550400-1550800	Enhancers	Fetal Brain Female	brain
9	chr8:1550600-1550800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:1550800-1553400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:1551000-1551200	Enhancers	Esophagus	oesophagus
12	chr8:1553400-1553600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:1553600-1562200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:1555200-1555400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr8:1555400-1555600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
16	chr8:1555400-1555600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
17	chr8:1555400-1555600	Bivalent/Poised TSS	A549	lung
18	chr8:1555400-1555600	Enhancers	NHEK	skin
19	chr8:1555400-1555800	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr8:1555400-1555800	Active TSS	H1 Cell Line	embryonic stem cell
21	chr8:1555400-1555800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr8:1555400-1556000	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr8:1555400-1556000	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr8:1555400-1556000	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr8:1555400-1556000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:1555600-1555800	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr8:1555600-1556000	Active TSS	H9 Cell Line	embryonic stem cell
28	chr8:1555600-1556000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:1555600-1556000	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr8:1555800-1556000	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr8:1562200-1562600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:1562400-1562600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:1562400-1562600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:1562600-1564800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:1562600-1569400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:1562800-1572600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:1567800-1570200	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr8:1568000-1568400	Enhancers	Fetal Muscle Leg	muscle
39	chr8:1569400-1570000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr8:1569800-1570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:1569800-1570400	Active TSS	Spleen	Spleen
42	chr8:1570000-1570400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr8:1570000-1571400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:1570200-1570800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:1570200-1571000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr8:1570400-1571600	Weak transcription	Spleen	Spleen
47	chr8:1570400-1579800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr8:1571400-1571800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:1571600-1571800	ZNF genes & repeats	Pancreas	Pancrea
50	chr8:1571600-1571800	Enhancers	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links