Variant report

Variant	nsv889716
Chromosome Location	chr8:1632525-1685064
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	chr8:1644107-1644129	K562	blood:	n/a	n/a
2	ARID3A	chr8:1683588-1683957	HepG2	liver:	n/a	n/a
3	BACH1	chr8:1649454-1650069	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:1650236-1650243	K562	blood:	n/a	n/a
5	BATF	chr8:1684612-1684879	GM12878	blood:	n/a	chr8:1684797-1684808
6	BATF	chr8:1684606-1684963	GM12878	blood:	n/a	chr8:1684797-1684808
7	BHLHE40	chr8:1683587-1683959	K562	blood:	n/a	n/a
8	BHLHE40	chr8:1644069-1644250	K562	blood:	n/a	chr8:1644168-1644184 chr8:1644160-1644176
9	BHLHE40	chr8:1650131-1650342	K562	blood:	n/a	n/a
10	BHLHE40	chr8:1684761-1684921	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:1649469-1649782	K562	blood:	n/a	n/a
12	BRCA1	chr8:1649391-1649753	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr8:1649363-1649896	K562	blood:	n/a	n/a
14	CCNT2	chr8:1643955-1644221	K562	blood:	n/a	n/a
15	CCNT2	chr8:1649151-1649813	K562	blood:	n/a	n/a
16	CEBPB	chr8:1648609-1648806	HepG2	liver:	n/a	chr8:1648683-1648694 chr8:1648683-1648696
17	CEBPB	chr8:1644002-1644239	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:1648538-1648896	K562	blood:	n/a	chr8:1648683-1648694 chr8:1648683-1648696
19	CEBPB	chr8:1652172-1652395	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:1649373-1649573	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:1652131-1652460	A549	lung:	n/a	n/a
22	CHD1	chr8:1649259-1649708	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr8:1643837-1644366	IMR90	lung:	n/a	n/a
24	CHD1	chr8:1683623-1683842	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr8:1683561-1684044	GM12878	blood:	n/a	n/a
26	CHD2	chr8:1649068-1649818	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr8:1649444-1649821	A549	lung:	n/a	n/a
28	CREB1	chr8:1649384-1649893	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr8:1649147-1650283	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:1643992-1644278	MCF-7	breast:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
31	CTCF	chr8:1649469-1649759	K562	blood:	n/a	n/a
32	CTCF	chr8:1643999-1644266	GM19238	blood:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
33	CTCF	chr8:1644080-1644230	HEK293	kidney:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
34	CTCF	chr8:1649529-1649783	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr8:1683700-1683850	HPAF	blood vessel:	n/a	chr8:1683787-1683800 chr8:1683784-1683802 chr8:1683741-1683749 chr8:1683786-1683807
36	CTCF	chr8:1683682-1683909	A549	lung:	n/a	chr8:1683787-1683800 chr8:1683784-1683802 chr8:1683741-1683749 chr8:1683786-1683807
37	CTCF	chr8:1683550-1684030	K562	blood:	n/a	chr8:1683787-1683800 chr8:1683784-1683802 chr8:1683741-1683749 chr8:1683786-1683807
38	CTCF	chr8:1644011-1644249	GM12891	blood:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
39	CTCF	chr8:1644000-1644150	BE2_C	brain:	n/a	chr8:1644116-1644137 chr8:1644121-1644139
40	CTCF	chr8:1644100-1644250	AG04450	lung:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
41	CTCF	chr8:1678901-1678965	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:1643980-1644130	GM12866	blood:	n/a	n/a
43	CTCF	chr8:1644025-1644255	ProgFib	skin:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
44	CTCF	chr8:1683524-1684163	GM12878	blood:	n/a	chr8:1683787-1683800 chr8:1683784-1683802 chr8:1683741-1683749 chr8:1683786-1683807
45	CTCF	chr8:1649560-1649710	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr8:1683608-1683990	Spleen_OC	spleen:	n/a	chr8:1683787-1683800 chr8:1683784-1683802 chr8:1683741-1683749 chr8:1683786-1683807
47	CTCF	chr8:1644060-1644210	BJ	skin:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
48	CTCF	chr8:1649560-1649710	GM12868	blood:	n/a	n/a
49	CTCF	chr8:1644060-1644210	HFF-Myc	foreskin:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183
50	CTCF	chr8:1644060-1644210	GM12864	blood:	n/a	chr8:1644116-1644137 chr8:1644121-1644139 chr8:1644170-1644183

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1651197-1651247	ECC-1	luminal epithelium:	n/a
2	chr8:1650035-1650085	SAEC	small airway:	n/a
3	chr8:1653179-1653229	HUVEC	blood vessel:	n/a
4	chr8:1640712-1640762	AG04449	skin:	fetal
5	chr8:1651197-1651247	ECC-1	luminal epithelium:	n/a
6	chr8:1650035-1650085	SAEC	small airway:	n/a
7	chr8:1653179-1653229	HUVEC	blood vessel:	n/a
8	chr8:1640712-1640762	AG04449	skin:	fetal
9	chr8:1643697-1643747	GM19239	blood:	n/a
10	chr8:1636262-1636312	GM12892	blood:	n/a
11	chr8:1642625-1642675	GM12892	blood:	n/a
12	chr8:1650172-1650222	BJ	skin:	n/a
13	chr8:1654843-1654893	ovcar-3	ovarian:	n/a
14	chr8:1636262-1636312	NT2-D1	testis:	n/a
15	chr8:1681408-1681458	ProgFib	skin:	n/a
16	chr8:1640712-1640762	AG04450	lung:	fetal
17	chr8:1650172-1650222	A549	lung:	n/a
18	chr8:1639573-1639623	BE2_C	brain:	n/a
19	chr8:1636262-1636312	GM12891	blood:	n/a
20	chr8:1642380-1642430	MCF-7	breast:	n/a
21	chr8:1636504-1636554	GM12891	blood:	n/a
22	chr8:1640712-1640762	ECC-1	luminal epithelium:	n/a
23	chr8:1681514-1681564	T-47D	breast:	n/a
24	chr8:1650035-1650085	HL-60	blood:	n/a
25	chr8:1649758-1649808	GM12892	blood:	n/a
26	chr8:1636504-1636554	LNCaP	prostate:	n/a
27	chr8:1639563-1639613	CMK	blood:	n/a
28	chr8:1639563-1639613	Caco-2	colon:	n/a
29	chr8:1651101-1651151	H1-hESC	embryonic stem cell:	embryo
30	chr8:1653566-1653616	HMEC	breast:	n/a
31	chr8:1653215-1653265	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:1650309-1650359	RPTEC	kidney:	n/a
33	chr8:1642380-1642430	CMK	blood:	n/a
34	chr8:1642577-1642627	AG04449	skin:	fetal
35	chr8:1650035-1650085	NT2-D1	testis:	n/a
36	chr8:1636262-1636312	SKMC	muscle:	n/a
37	chr8:1640712-1640762	A549	lung:	n/a
38	chr8:1638304-1638354	HMEC	breast:	n/a
39	chr8:1655752-1655802	HNPCEpiC	eye:	n/a
40	chr8:1643697-1643747	NH-A	brain:	n/a
41	chr8:1649522-1649572	HIPEpiC	eye:	n/a
42	chr8:1681408-1681458	Jurkat	blood:	n/a
43	chr8:1644982-1645032	NHDF-neo	bronchial:	n/a
44	chr8:1648314-1648364	A549	lung:	n/a
45	chr8:1654216-1654266	ProgFib	skin:	n/a
46	chr8:1642498-1642548	HCM	heart:	n/a
47	chr8:1642498-1642548	HCT-116	colon:	n/a
48	chr8:1650035-1650085	A549	lung:	n/a
49	chr8:1638304-1638354	AG10803	skin:	n/a
50	chr8:1649522-1649572	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1681316..1685438-chr8:1724958..1729595,5	K562	blood:
2	chr8:1651243..1653137-chr8:1654644..1656282,2	MCF-7	breast:
3	chr8:1644165..1646557-chr8:1648161..1651623,3	K562	blood:
4	chr8:1649287..1651045-chr8:1651779..1654462,2	K562	blood:
5	chr8:1682026..1683754-chr8:1708602..1710119,2	MCF-7	breast:
6	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
7	chr8:1684265..1686317-chr8:1693828..1695451,2	K562	blood:
8	chr8:1676916..1679793-chr8:1711386..1713857,2	K562	blood:
9	chr8:1644923..1646471-chr8:1647780..1649578,2	MCF-7	breast:
10	chr8:1683326..1684222-chr8:1978338..1978975,3	K562	blood:
11	chr6:86095690..86096566-chr8:1651602..1652159,2	MCF-7	breast:
12	chr8:1683723..1685599-chr8:1688819..1690722,2	K562	blood:
13	chr8:1683449..1684285-chr8:1729073..1729982,8	K562	blood:
14	chr8:1678487..1679403-chr8:1728856..1729643,2	K562	blood:
15	chr8:1681796..1686732-chr8:1704250..1709938,6	K562	blood:
16	chr8:1644165..1646557-chr8:1648161..1651623,3	K562	blood:
17	chr8:1683298..1683841-chr8:1971940..1972481,2	K562	blood:
18	chr8:1683647..1684368-chr8:1711990..1712621,2	MCF-7	breast:
19	chr8:1647929..1650394-chr8:1651041..1654216,3	MCF-7	breast:
20	chr8:1683305..1684236-chr8:1728901..1729771,3	MCF-7	breast:
21	chr8:1682754..1684809-chr8:1691291..1693773,2	MCF-7	breast:
22	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
23	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
24	chr8:1683298..1684246-chr8:1728731..1730059,4	MCF-7	breast:
25	chr8:1684038..1686561-chr8:1711084..1712733,2	MCF-7	breast:
26	chr8:1644923..1646471-chr8:1647780..1649578,2	MCF-7	breast:
27	chr8:1647929..1650394-chr8:1651041..1654216,3	MCF-7	breast:
28	chr8:1648393..1649994-chr8:1655851..1658728,2	MCF-7	breast:
29	chr8:1683387..1685289-chr8:1686133..1688410,3	K562	blood:
30	chr8:1651243..1653137-chr8:1654644..1656282,2	MCF-7	breast:
31	chr8:1648393..1649994-chr8:1655851..1658728,2	MCF-7	breast:
32	chr8:1683243..1684210-chr8:1693916..1694440,2	K562	blood:
33	chr8:1684817..1688387-chr8:1693951..1696420,3	K562	blood:
34	chr8:1656737..1659589-chr8:1707662..1709873,2	K562	blood:
35	chr8:1671883..1674158-chr8:1677266..1679497,2	K562	blood:
36	chr8:1649287..1651045-chr8:1651779..1654462,2	K562	blood:
37	chr8:1683414..1685975-chr8:1702028..1704859,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254265	TF binding region
ENSG00000254265	CpG island
ENSG00000182372	chromatin interactions
ENSG00000254265	chromatin interactions
ENSG00000253982	chromatin interactions

Extended variants
information (count: 2395 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2395 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4507794	chr8:1632525-1632526	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555805728	chr8:1632561-1632562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575696382	chr8:1632571-1632572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544762085	chr8:1632624-1632625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558260098	chr8:1632628-1632629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35170474	chr8:1632673-1632674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs578151624	chr8:1632679-1632680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540488116	chr8:1632680-1632681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377125819	chr8:1632693-1632694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149862224	chr8:1632740-1632741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182294518	chr8:1632748-1632749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185024537	chr8:1632759-1632760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs80262204	chr8:1632765-1632766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560247009	chr8:1632773-1632774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551094583	chr8:1632788-1632789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147929011	chr8:1632809-1632810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373496883	chr8:1632817-1632818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572700682	chr8:1632851-1632852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141762139	chr8:1632858-1632859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547276546	chr8:1632865-1632866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4602919	chr8:1632867-1632868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs537319996	chr8:1632874-1632875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190186253	chr8:1632876-1632877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4520189	chr8:1632880-1632881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs182783790	chr8:1632885-1632886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200710302	chr8:1632899-1632900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10691322	chr8:1632900-1632901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs67342881	chr8:1632901-1632902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397791334	chr8:1632904-1632905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541176698	chr8:1632949-1632950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569300713	chr8:1632976-1632977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145096994	chr8:1632998-1632999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147594466	chr8:1633011-1633012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370260124	chr8:1633033-1633034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578051791	chr8:1633038-1633039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374033793	chr8:1633043-1633044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554081541	chr8:1633053-1633054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116748791	chr8:1633072-1633073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542924784	chr8:1633079-1633080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562821117	chr8:1633087-1633088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576292713	chr8:1633104-1633105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544624893	chr8:1633118-1633119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188694631	chr8:1633125-1633126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527404027	chr8:1633131-1633132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191749758	chr8:1633137-1633138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561547282	chr8:1633138-1633139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183649739	chr8:1633199-1633200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149066914	chr8:1633202-1633203	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs4521789	chr8:1633229-1633230	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs187995121	chr8:1633244-1633245	Weak transcription ZNF genes & repeats	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
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
Glioma	20126413	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1620000-1643800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1621200-1633400	Weak transcription	Brain Germinal Matrix	brain
3	chr8:1621400-1646200	Weak transcription	Brain Angular Gyrus	brain
4	chr8:1626200-1633200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr8:1633200-1633400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
6	chr8:1634000-1634200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:1637600-1638200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr8:1637800-1638000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:1637800-1638000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:1638000-1643800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:1640200-1649000	Weak transcription	Pancreas	Pancrea
12	chr8:1641800-1644800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr8:1643600-1644600	Bivalent Enhancer	Fetal Stomach	stomach
14	chr8:1643800-1644000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:1643800-1644000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:1643800-1644000	Enhancers	Brain Germinal Matrix	brain
17	chr8:1643800-1644000	Flanking Active TSS	Colon Smooth Muscle	Colon
18	chr8:1643800-1644200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr8:1643800-1644200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:1643800-1644200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:1643800-1644200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:1643800-1644200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:1643800-1644200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr8:1643800-1644200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr8:1643800-1644200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
26	chr8:1643800-1644400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:1643800-1644400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr8:1643800-1644400	Enhancers	Brain Anterior Caudate	brain
29	chr8:1643800-1644400	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr8:1643800-1644400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
31	chr8:1643800-1644400	Enhancers	Fetal Brain Male	brain
32	chr8:1643800-1644400	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr8:1643800-1644400	Enhancers	Rectal Smooth Muscle	rectum
34	chr8:1643800-1644800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:1643800-1644800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr8:1644000-1644400	Enhancers	Colon Smooth Muscle	Colon
37	chr8:1644000-1644400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
38	chr8:1644000-1646600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:1644000-1648800	Weak transcription	Brain Germinal Matrix	brain
40	chr8:1644200-1645400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr8:1644200-1646200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:1644200-1646400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:1644200-1648200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr8:1644200-1649200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr8:1644400-1648400	Weak transcription	Colon Smooth Muscle	Colon
46	chr8:1645000-1645400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr8:1645400-1645600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr8:1646200-1647400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr8:1646200-1647400	Strong transcription	Brain Angular Gyrus	brain
50	chr8:1646400-1647200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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