Variant report

Variant	nsv889696
Chromosome Location	chr8:1220581-1261114
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:153)
CpG islands
(count:2080)
Chromatin interactive
region (count:2)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:153 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr8:1236888-1237016	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr8:1246225-1246500	K562	blood:	n/a	n/a
3	CBX3	chr8:1232370-1232608	K562	blood:	n/a	n/a
4	CEBPB	chr8:1231221-1231278	K562	blood:	n/a	n/a
5	CEBPB	chr8:1231199-1231377	H1-hESC	embryonic stem cell:	n/a	chr8:1231211-1231224 chr8:1231211-1231222
6	CEBPB	chr8:1231139-1231350	HepG2	liver:	n/a	chr8:1231211-1231224 chr8:1231211-1231222
7	CEBPB	chr8:1260701-1260704	A549	lung:	n/a	n/a
8	CHD2	chr8:1252357-1252367	HepG2	liver:	n/a	n/a
9	CTCF	chr8:1231386-1231480	MCF-7	breast:	n/a	n/a
10	CTCF	chr8:1220925-1220984	Lung_OC	lung:	n/a	n/a
11	CTCF	chr8:1231212-1231548	K562	blood:	n/a	n/a
12	CTCF	chr8:1231340-1231490	K562	blood:	n/a	n/a
13	CTCF	chr8:1231335-1231471	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:1232237-1232335	GM20000	blood:	n/a	n/a
15	CTCF	chr8:1231403-1231418	Gliobla	brain:	n/a	n/a
16	CTCF	chr8:1231288-1231516	K562	blood:	n/a	n/a
17	CTCF	chr8:1232537-1232590	LNCaP	prostate:	n/a	n/a
18	CTCF	chr8:1231320-1231470	K562	blood:	n/a	n/a
19	CTCF	chr8:1236715-1236789	GM10248	blood:	n/a	n/a
20	CTCF	chr8:1243540-1243690	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr8:1231260-1231410	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr8:1231174-1231517	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr8:1231362-1231432	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:1245817-1245837	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr8:1231332-1231436	K562	blood:	n/a	n/a
26	CTCF	chr8:1259097-1259178	K562	blood:	n/a	n/a
27	CTCF	chr8:1231320-1231470	HepG2	liver:	n/a	n/a
28	CTCF	chr8:1231271-1231490	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:1231321-1231473	HepG2	liver:	n/a	n/a
30	CTCF	chr8:1253080-1253230	HepG2	liver:	n/a	n/a
31	CTCF	chr8:1231374-1231443	HepG2	liver:	n/a	n/a
32	CTCF	chr8:1231300-1231450	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr8:1231311-1231507	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:1231314-1231512	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr8:1231222-1231520	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:1231286-1231501	K562	blood:	n/a	n/a
37	CTCF	chr8:1231360-1231510	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:1231219-1231513	K562	blood:	n/a	n/a
39	CTCF	chr8:1231320-1231470	HEK293	kidney:	n/a	n/a
40	CTCF	chr8:1232448-1232500	GM10266	blood:	n/a	n/a
41	CTCF	chr8:1232142-1232192	Kidney_OC	kidney:	n/a	n/a
42	E2F6	chr8:1246193-1246572	K562	blood:	n/a	n/a
43	E2F6	chr8:1246304-1246498	K562	blood:	n/a	n/a
44	EGR1	chr8:1246266-1246599	H1-hESC	embryonic stem cell:	n/a	n/a
45	EGR1	chr8:1245888-1246118	H1-hESC	embryonic stem cell:	n/a	n/a
46	EGR1	chr8:1246258-1246554	H1-hESC	embryonic stem cell:	n/a	n/a
47	EGR1	chr8:1245715-1246467	GM12878	blood:	n/a	n/a
48	EP300	chr8:1232034-1232695	GM12878	blood:	n/a	n/a
49	FOSL2	chr8:1238280-1238591	HepG2	liver:	n/a	chr8:1238419-1238426 chr8:1238418-1238427 chr8:1238417-1238427 chr8:1238418-1238426 chr8:1238416-1238428
50	GABPA	chr8:1246069-1246266	GM12878	blood:	n/a	n/a

(count:2080 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1245672-1245722	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:1232045-1232095	BE2_C	brain:	n/a
3	chr8:1238566-1238616	SK-N-SH	brain:	n/a
4	chr8:1244335-1244385	Hepatocyte	liver:	n/a
5	chr8:1253043-1253093	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:1246607-1246657	AG10803	skin:	n/a
7	chr8:1245672-1245722	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:1232045-1232095	BE2_C	brain:	n/a
9	chr8:1238566-1238616	SK-N-SH	brain:	n/a
10	chr8:1244335-1244385	Hepatocyte	liver:	n/a
11	chr8:1253043-1253093	HPAEpiC	pulmonary alveolar:	n/a
12	chr8:1246607-1246657	AG10803	skin:	n/a
13	chr8:1253043-1253093	AoSMC	blood vessel:	n/a
14	chr8:1244286-1244336	RPTEC	kidney:	n/a
15	chr8:1232122-1232172	GM12892	blood:	n/a
16	chr8:1244335-1244385	GM12878	blood:	n/a
17	chr8:1248957-1249007	LNCaP	prostate:	n/a
18	chr8:1249007-1249057	Hela-S3	cervix:	n/a
19	chr8:1249158-1249208	HCPEpiC	choroid plexus:	n/a
20	chr8:1226465-1226515	HUVEC	blood vessel:	n/a
21	chr8:1238522-1238572	HCF	heart:	n/a
22	chr8:1245703-1245753	H1-hESC	embryonic stem cell:	embryo
23	chr8:1232122-1232172	BJ	skin:	n/a
24	chr8:1251106-1251156	HRPEpiC	eye:	n/a
25	chr8:1244286-1244336	GM12891	blood:	n/a
26	chr8:1244286-1244336	HRPEpiC	eye:	n/a
27	chr8:1245943-1245993	SKMC	muscle:	n/a
28	chr8:1245943-1245993	MCF10A-Er-Src	breast:	n/a
29	chr8:1245943-1245993	MCF-7	breast:	n/a
30	chr8:1244039-1244089	SK-N-MC	brain:	n/a
31	chr8:1242282-1242332	AG09319	gingival:	n/a
32	chr8:1238536-1238586	BE2_C	brain:	n/a
33	chr8:1245342-1245392	HUVEC	blood vessel:	n/a
34	chr8:1226405-1226455	ECC-1	luminal epithelium:	n/a
35	chr8:1245703-1245753	HNPCEpiC	eye:	n/a
36	chr8:1246922-1246972	MCF-7	breast:	n/a
37	chr8:1245143-1245193	BE2_C	brain:	n/a
38	chr8:1245672-1245722	HRCEpiC	kidney:	n/a
39	chr8:1245672-1245722	AG09319	gingival:	n/a
40	chr8:1246442-1246492	AG04449	skin:	fetal
41	chr8:1246922-1246972	LNCaP	prostate:	n/a
42	chr8:1244039-1244089	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:1226405-1226455	HAEpiC	amniotic membrane:	n/a
44	chr8:1245698-1245748	U87	brain:	n/a
45	chr8:1245943-1245993	A549	lung:	n/a
46	chr8:1226405-1226455	HEK293	kidney:	embryo
47	chr8:1249215-1249265	GM19239	blood:	n/a
48	chr8:1248957-1249007	NB4	blood:	n/a
49	chr8:1250751-1250801	H1-hESC	embryonic stem cell:	embryo
50	chr8:1245342-1245392	MCF-7	breast:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:1218264..1220141-chr8:1221111..1222674,2	K562	blood:
2	chr8:1218051..1219861-chr8:1223791..1226453,2	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERICH1-2	chr8:1236927-1237155	XLOC_006972
2	lnc-ERICH1-2	chr8:1236775-1236876	XLOC_006972
3	lnc-ERICH1-3	chr8:1244295-1244463	XLOC_006971
4	lnc-ERICH1-2	chr8:1232700-1232895	refGeneNc_4249_NR_033895
5	lnc-ERICH1-3	chr8:1244294-1244463	NR_033895
6	lnc-ERICH1-3	chr8:1245293-1245488	NONHSAT124652
7	lnc-ERICH1-3	chr8:1244294-1244463	NONHSAT124652
8	lnc-ERICH1-3	chr8:1248184-1250827	NR_033895
9	lnc-ERICH1-2	chr8:1231702-1231870	refGeneNc_4249_NR_033895
10	lnc-ERICH1-2	chr8:1236982-1237155	XLOC_006972
11	lnc-ERICH1-2	chr8:1235591-1238234	refGeneNc_4249_NR_033895
12	lnc-ERICH1-3	chr8:1244292-1244463	ENSG00000253640
13	lnc-ERICH1-2	chr8:1236982-1237178	XLOC_006972
14	lnc-ERICH1-2	chr8:1236982-1237014	NONHSAT124646
15	lnc-ERICH1-3	chr8:1245293-1245488	XLOC_006971
16	lnc-ERICH1-3	chr8:1245293-1245488	ENSG00000253640
17	lnc-ERICH1-3	chr8:1248184-1250690	NONHSAT124652
18	lnc-ERICH1-3	chr8:1248184-1250827	XLOC_006971
19	lnc-ERICH1-3	chr8:1245293-1245488	NR_033895
20	lnc-ERICH1-3	chr8:1250717-1250823	NONHSAT124652
21	lnc-ERICH1-2	chr8:1236888-1236922	XLOC_006972
22	lnc-ERICH1-2	chr8:1236927-1237971	XLOC_006972
23	lnc-ERICH1-2	chr8:1236613-1236870	XLOC_006972
24	lnc-ERICH1-2	chr8:1236704-1236876	XLOC_006972
25	lnc-ERICH1-2	chr8:1236982-1237027	XLOC_006972
26	lnc-ERICH1-2	chr8:1236383-1236876	NONHSAT124646
27	lnc-ERICH1-2	chr8:1236403-1236612	XLOC_006972
28	lnc-ERICH1-2	chr8:1236494-1236531	XLOC_006972
29	lnc-ERICH1-3	chr8:1250394-1250862	XLOC_006971
30	lnc-ERICH1-3	chr8:1248184-1250829	ENSG00000253640
31	lnc-ERICH1-3	chr8:1231015-1231036	XLOC_006971

No data

Variant related genes	Relation type
ENSG00000253640	TF binding region
ENSG00000253640	CpG island
SUN2	miRNA target sites
SUMF1	miRNA target sites
IL13	miRNA target sites
SUFU	miRNA target sites
IL17RD	miRNA target sites

Extended variants
information (count: 2390 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2390 , 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	rs4495453	chr8:1220581-1220582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555861592	chr8:1220591-1220592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576838681	chr8:1220594-1220595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10101171	chr8:1220595-1220596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546620717	chr8:1220596-1220597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530800572	chr8:1220604-1220605	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs561440703	chr8:1220611-1220612	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs530104113	chr8:1220622-1220623	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs149138252	chr8:1220623-1220624	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs184242344	chr8:1220624-1220625	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs532402570	chr8:1220632-1220633	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs531533139	chr8:1220635-1220636	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs551260512	chr8:1220638-1220639	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs571163462	chr8:1220639-1220640	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs527492599	chr8:1220640-1220641	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs567707289	chr8:1220641-1220642	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs567379128	chr8:1220647-1220648	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs368265809	chr8:1220662-1220663	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs386720597	chr8:1220682-1220683	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs187428576	chr8:1220688-1220689	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs13249062	chr8:1220694-1220695	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs569662197	chr8:1220700-1220701	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs377121564	chr8:1220702-1220703	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs10576506	chr8:1220705-1220706	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs75287307	chr8:1220706-1220707	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs200614508	chr8:1220720-1220721	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs201654991	chr8:1220723-1220724	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs372651704	chr8:1220734-1220735	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs142296251	chr8:1220742-1220743	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs151322149	chr8:1220772-1220773	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs552513984	chr8:1220774-1220775	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs74468979	chr8:1220782-1220783	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140631144	chr8:1220788-1220789	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs550985265	chr8:1220791-1220792	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs145285119	chr8:1220805-1220806	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs566054911	chr8:1220814-1220815	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs541627878	chr8:1220828-1220829	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs554836931	chr8:1220837-1220838	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs10087758	chr8:1220864-1220865	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs543535326	chr8:1220866-1220867	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs563389850	chr8:1220867-1220868	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532375295	chr8:1220868-1220869	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs4445249	chr8:1220894-1220895	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs564851783	chr8:1220896-1220897	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs7823900	chr8:1220902-1220903	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs185501614	chr8:1220905-1220906	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528618703	chr8:1220917-1220918	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs138429216	chr8:1220926-1220927	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs117251615	chr8:1220932-1220933	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs569830010	chr8:1220950-1220951	Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Congenital diaphragmatic hernia	21064195	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1217400-1229600	Weak transcription	Gastric	stomach
2	chr8:1219200-1223000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:1219400-1220600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:1219400-1223000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr8:1219600-1223200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr8:1220600-1221000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:1220600-1221000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
8	chr8:1221000-1223200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:1222600-1223800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:1223000-1223600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr8:1223000-1223600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr8:1223000-1223600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:1223200-1223600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:1223200-1223600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr8:1223200-1223600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:1223200-1223600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr8:1223200-1223600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:1223200-1223600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr8:1223600-1224800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:1223600-1224800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:1223600-1225200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr8:1223600-1231800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:1223800-1242200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:1224800-1225000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:1225000-1225200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr8:1225000-1225200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:1225200-1225600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr8:1225200-1232000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:1227600-1227800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:1229600-1230000	Active TSS	Gastric	stomach
31	chr8:1230000-1232400	Weak transcription	Gastric	stomach
32	chr8:1230800-1231000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
33	chr8:1231400-1232600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr8:1231800-1232800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:1232000-1232800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:1232200-1232800	ZNF genes & repeats	Spleen	Spleen
37	chr8:1232400-1232600	ZNF genes & repeats	Gastric	stomach
38	chr8:1232400-1233800	Enhancers	Fetal Brain Male	brain
39	chr8:1232600-1236800	Weak transcription	Gastric	stomach
40	chr8:1232800-1234000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr8:1232800-1234000	Enhancers	Fetal Brain Female	brain
42	chr8:1232800-1234600	Weak transcription	Spleen	Spleen
43	chr8:1232800-1240400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:1233800-1236400	Weak transcription	Fetal Brain Male	brain
45	chr8:1234000-1234200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:1234200-1234800	Enhancers	Colon Smooth Muscle	Colon
47	chr8:1236400-1237600	Enhancers	Fetal Brain Male	brain
48	chr8:1236600-1236800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr8:1236600-1236800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:1236800-1237000	Flanking Active TSS	Gastric	stomach

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