Variant report

Variant	nsv889705
Chromosome Location	chr8:1581839-1676147
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	ATF1	chr8:1631106-1631363	K562	blood:	n/a	n/a
3	ATF1	chr8:1612841-1613066	K562	blood:	n/a	n/a
4	ATF2	chr8:1606188-1606635	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr8:1631111-1631356	K562	blood:	n/a	n/a
6	BACH1	chr8:1649454-1650069	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:1650236-1650243	K562	blood:	n/a	n/a
8	BACH1	chr8:1600054-1600554	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:1583024-1583221	GM12878	blood:	n/a	chr8:1583128-1583139
10	BCL3	chr8:1613411-1613643	GM12878	blood:	n/a	chr8:1613634-1613643
11	BHLHE40	chr8:1589261-1589514	K562	blood:	n/a	chr8:1589361-1589370 chr8:1589362-1589371 chr8:1589355-1589376 chr8:1589361-1589370
12	BHLHE40	chr8:1649469-1649782	K562	blood:	n/a	n/a
13	BHLHE40	chr8:1650131-1650342	K562	blood:	n/a	n/a
14	BHLHE40	chr8:1610754-1610850	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:1598474-1598541	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:1644069-1644250	K562	blood:	n/a	chr8:1644168-1644184 chr8:1644160-1644176
17	BRCA1	chr8:1649391-1649753	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr8:1649363-1649896	K562	blood:	n/a	n/a
19	CCNT2	chr8:1643955-1644221	K562	blood:	n/a	n/a
20	CCNT2	chr8:1649151-1649813	K562	blood:	n/a	n/a
21	CEBPB	chr8:1631129-1631386	IMR90	lung:	n/a	chr8:1631220-1631231
22	CEBPB	chr8:1652172-1652395	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:1628117-1628387	Hela-S3	cervix:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
24	CEBPB	chr8:1648609-1648806	HepG2	liver:	n/a	chr8:1648683-1648694 chr8:1648683-1648696
25	CEBPB	chr8:1628240-1628361	H1-hESC	embryonic stem cell:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
26	CEBPB	chr8:1631113-1631408	A549	lung:	n/a	chr8:1631220-1631231
27	CEBPB	chr8:1648538-1648896	K562	blood:	n/a	chr8:1648683-1648694 chr8:1648683-1648696
28	CEBPB	chr8:1652131-1652460	A549	lung:	n/a	n/a
29	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
30	CEBPB	chr8:1631046-1631432	Hela-S3	cervix:	n/a	chr8:1631220-1631231
31	CEBPB	chr8:1631054-1631361	K562	blood:	n/a	chr8:1631220-1631231
32	CEBPB	chr8:1628133-1628450	K562	blood:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
33	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
34	CEBPB	chr8:1644002-1644239	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:1631004-1631475	HCT-116	colon:	n/a	chr8:1631220-1631231
36	CEBPB	chr8:1631078-1631329	K562	blood:	n/a	chr8:1631220-1631231
37	CEBPB	chr8:1598267-1598411	HepG2	liver:	n/a	chr8:1598339-1598350 chr8:1598339-1598348
38	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
39	CEBPB	chr8:1628099-1628437	HepG2	liver:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
40	CEBPB	chr8:1628160-1628398	A549	lung:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
41	CEBPB	chr8:1649373-1649573	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:1631051-1631490	K562	blood:	n/a	chr8:1631220-1631231
43	CEBPB	chr8:1630919-1631593	HCT-116	colon:	n/a	chr8:1631220-1631231
44	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
45	CEBPB	chr8:1631047-1631403	HepG2	liver:	n/a	chr8:1631220-1631231
46	CEBPB	chr8:1628110-1628439	IMR90	lung:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
47	CHD1	chr8:1649259-1649708	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr8:1643837-1644366	IMR90	lung:	n/a	n/a
49	CHD2	chr8:1649068-1649818	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr8:1606162-1606617	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1616925-1616975	RPTEC	kidney:	n/a
2	chr8:1650172-1650222	GM12892	blood:	n/a
3	chr8:1618151-1618201	HEEpiC	esophagus:	n/a
4	chr8:1585929-1585979	HAEpiC	amniotic membrane:	n/a
5	chr8:1645455-1645505	SK-N-SH	brain:	n/a
6	chr8:1596244-1596294	GM12878	blood:	n/a
7	chr8:1616767-1616817	NHBE	bronchial:	n/a
8	chr8:1653566-1653616	GM19239	blood:	n/a
9	chr8:1590039-1590089	BJ	skin:	n/a
10	chr8:1649143-1649193	HCT-116	colon:	n/a
11	chr8:1651197-1651247	HCF	heart:	n/a
12	chr8:1605546-1605596	PrEC	prostate:	n/a
13	chr8:1650035-1650085	K562	blood:	n/a
14	chr8:1616925-1616975	RPTEC	kidney:	n/a
15	chr8:1650172-1650222	GM12892	blood:	n/a
16	chr8:1618151-1618201	HEEpiC	esophagus:	n/a
17	chr8:1585929-1585979	HAEpiC	amniotic membrane:	n/a
18	chr8:1645455-1645505	SK-N-SH	brain:	n/a
19	chr8:1596244-1596294	GM12878	blood:	n/a
20	chr8:1616767-1616817	NHBE	bronchial:	n/a
21	chr8:1653566-1653616	GM19239	blood:	n/a
22	chr8:1590039-1590089	BJ	skin:	n/a
23	chr8:1649143-1649193	HCT-116	colon:	n/a
24	chr8:1651197-1651247	HCF	heart:	n/a
25	chr8:1605546-1605596	PrEC	prostate:	n/a
26	chr8:1650035-1650085	K562	blood:	n/a
27	chr8:1624818-1624868	GM19239	blood:	n/a
28	chr8:1645108-1645158	PrEC	prostate:	n/a
29	chr8:1639536-1639586	CMK	blood:	n/a
30	chr8:1626697-1626747	A549	lung:	n/a
31	chr8:1640712-1640762	HCM	heart:	n/a
32	chr8:1636504-1636554	AG04449	skin:	fetal
33	chr8:1638304-1638354	PFSK-1	brain:	n/a
34	chr8:1590916-1590966	HCM	heart:	n/a
35	chr8:1623303-1623353	PrEC	prostate:	n/a
36	chr8:1616622-1616672	AG04449	skin:	fetal
37	chr8:1644982-1645032	BE2_C	brain:	n/a
38	chr8:1645108-1645158	ovcar-3	ovarian:	n/a
39	chr8:1642577-1642627	HAEpiC	amniotic membrane:	n/a
40	chr8:1626555-1626605	U87	brain:	n/a
41	chr8:1644982-1645032	HepG2	liver:	n/a
42	chr8:1618151-1618201	GM12891	blood:	n/a
43	chr8:1645455-1645505	AG04450	lung:	fetal
44	chr8:1586825-1586875	ovcar-3	ovarian:	n/a
45	chr8:1639563-1639613	HCF	heart:	n/a
46	chr8:1616925-1616975	A549	lung:	n/a
47	chr8:1615950-1616000	PANC-1	pancreas:	n/a
48	chr8:1591382-1591432	GM12878	blood:	n/a
49	chr8:1619861-1619911	GM12878	blood:	n/a
50	chr8:1643697-1643747	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1656737..1659589-chr8:1707662..1709873,2	K562	blood:
2	chr8:1647929..1650394-chr8:1651041..1654216,3	MCF-7	breast:
3	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
4	chr8:1649287..1651045-chr8:1651779..1654462,2	K562	blood:
5	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
6	chr8:1648393..1649994-chr8:1655851..1658728,2	MCF-7	breast:
7	chr8:1644165..1646557-chr8:1648161..1651623,3	K562	blood:
8	chr8:1671883..1674158-chr8:1677266..1679497,2	K562	blood:
9	chr8:1593850..1596302-chr8:1622198..1625044,2	K562	blood:
10	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
11	chr8:1644923..1646471-chr8:1647780..1649578,2	MCF-7	breast:
12	chr8:1648393..1649994-chr8:1655851..1658728,2	MCF-7	breast:
13	chr8:1647929..1650394-chr8:1651041..1654216,3	MCF-7	breast:
14	chr6:86095690..86096566-chr8:1651602..1652159,2	MCF-7	breast:
15	chr8:1651243..1653137-chr8:1654644..1656282,2	MCF-7	breast:
16	chr8:1644165..1646557-chr8:1648161..1651623,3	K562	blood:
17	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
18	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
19	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
20	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
21	chr8:1651243..1653137-chr8:1654644..1656282,2	MCF-7	breast:
22	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
23	chr8:1615891..1617815-chr8:1624787..1626742,2	K562	blood:
24	chr8:1649287..1651045-chr8:1651779..1654462,2	K562	blood:
25	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
26	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
27	chr8:1621344..1623146-chr8:1688699..1690451,2	K562	blood:
28	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
29	chr8:1644923..1646471-chr8:1647780..1649578,2	MCF-7	breast:

Variant related genes	Relation type
DLGAP2	TF binding region
ENSG00000254265	TF binding region
DLGAP2	CpG island
ENSG00000254265	CpG island
ENSG00000254265	chromatin interactions
ENSG00000198010	chromatin interactions

Extended variants
information (count: 4999 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:4999 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6980953	chr8:1581839-1581840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532661714	chr8:1581886-1581887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546272151	chr8:1581887-1581888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7017831	chr8:1581891-1581892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs76435909	chr8:1581894-1581895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192689840	chr8:1581908-1581909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568712258	chr8:1581914-1581915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531081567	chr8:1581934-1581935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550562553	chr8:1581943-1581944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371868002	chr8:1581957-1581958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116562125	chr8:1581963-1581964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376209677	chr8:1581977-1581978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558949449	chr8:1581987-1581988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544879316	chr8:1581993-1581994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369134547	chr8:1582004-1582005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs151089631	chr8:1582012-1582013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572344038	chr8:1582013-1582014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372799379	chr8:1582034-1582035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575511562	chr8:1582043-1582044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544136445	chr8:1582060-1582061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557394412	chr8:1582073-1582074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142542850	chr8:1582093-1582094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185386577	chr8:1582113-1582114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6981355	chr8:1582119-1582120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs368905781	chr8:1582146-1582147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188305946	chr8:1582149-1582150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542427212	chr8:1582155-1582156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562104278	chr8:1582166-1582167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192562748	chr8:1582170-1582171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550861694	chr8:1582270-1582271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184799954	chr8:1582284-1582285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532752556	chr8:1582298-1582299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6980498	chr8:1582302-1582303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs566251466	chr8:1582309-1582310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572611841	chr8:1582331-1582332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549170076	chr8:1582348-1582349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6980650	chr8:1582363-1582364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs145829621	chr8:1582373-1582374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78604328	chr8:1582382-1582383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138739411	chr8:1582390-1582391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188300277	chr8:1582411-1582412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553372955	chr8:1582413-1582414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111720930	chr8:1582421-1582422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541914043	chr8:1582430-1582431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562356676	chr8:1582431-1582432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575741679	chr8:1582455-1582456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544540880	chr8:1582482-1582483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564418779	chr8:1582506-1582507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533418745	chr8:1582543-1582544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546203477	chr8:1582544-1582545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1575200-1599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1593400-1594600	Weak transcription	Fetal Brain Male	brain
3	chr8:1594200-1594400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:1594400-1595000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:1595000-1595200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:1595800-1596800	Enhancers	Gastric	stomach
7	chr8:1596000-1596200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:1596800-1598000	Weak transcription	Gastric	stomach
9	chr8:1599400-1599600	Bivalent Enhancer	Brain Substantia Nigra	brain
10	chr8:1599400-1600000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr8:1599400-1600200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:1599400-1601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:1599600-1599800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
14	chr8:1599600-1600400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr8:1599600-1600600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr8:1599600-1601000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:1599600-1601600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr8:1599800-1600000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
19	chr8:1599800-1600400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:1599800-1600800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:1599800-1601200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr8:1600000-1601000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr8:1600000-1601200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
24	chr8:1600200-1600400	Enhancers	Fetal Kidney	kidney
25	chr8:1600200-1600800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr8:1600200-1601200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:1600400-1601000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr8:1600400-1601000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr8:1600400-1601000	Bivalent Enhancer	Fetal Kidney	kidney
30	chr8:1600400-1604800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr8:1600800-1604800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr8:1600800-1605000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr8:1601000-1601200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr8:1601000-1603400	Weak transcription	Gastric	stomach
35	chr8:1601000-1604800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr8:1601200-1601800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:1601200-1604600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:1601800-1605600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:1602000-1604800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr8:1604000-1604200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr8:1604000-1604200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:1604000-1604200	Enhancers	Gastric	stomach
43	chr8:1604600-1605400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:1604800-1605000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:1604800-1605000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr8:1604800-1605800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:1604800-1605800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:1604800-1605800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr8:1604800-1605800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:1604800-1605800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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