Variant report

Variant	nsv917802
Chromosome Location	chr8:7268818-8079920
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4242)
CpG islands
(count:7021)
Chromatin interactive
region (count:2)
LncRNA
region (count:19)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4242 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:7277768-7278018	K562	blood:	n/a	n/a
2	ATF1	chr8:7771027-7771432	K562	blood:	n/a	n/a
3	ATF1	chr8:7694221-7694565	K562	blood:	n/a	n/a
4	BACH1	chr8:7771106-7771311	K562	blood:	n/a	n/a
5	BATF	chr8:7809497-7809672	GM12878	blood:	n/a	chr8:7809580-7809591
6	BATF	chr8:7448204-7448611	GM12878	blood:	n/a	n/a
7	BATF	chr8:8029997-8030427	GM12878	blood:	n/a	n/a
8	BATF	chr8:7809440-7809731	GM12878	blood:	n/a	chr8:7809580-7809591
9	BATF	chr8:7994136-7994338	GM12878	blood:	n/a	n/a
10	BATF	chr8:7922797-7923045	GM12878	blood:	n/a	n/a
11	BATF	chr8:7564517-7564858	GM12878	blood:	n/a	n/a
12	BATF	chr8:7564552-7564860	GM12878	blood:	n/a	n/a
13	BATF	chr8:8030089-8030387	GM12878	blood:	n/a	n/a
14	BATF	chr8:8004193-8004724	GM12878	blood:	n/a	n/a
15	BATF	chr8:8004195-8004622	GM12878	blood:	n/a	n/a
16	BATF	chr8:7994763-7995094	GM12878	blood:	n/a	n/a
17	BATF	chr8:8000698-8001151	GM12878	blood:	n/a	n/a
18	BATF	chr8:7936786-7937116	GM12878	blood:	n/a	chr8:7936968-7936979
19	BATF	chr8:8007429-8007921	GM12878	blood:	n/a	chr8:8007742-8007750
20	BATF	chr8:8005100-8005302	GM12878	blood:	n/a	n/a
21	BATF	chr8:7812383-7812672	GM12878	blood:	n/a	n/a
22	BATF	chr8:7949085-7949285	GM12878	blood:	n/a	n/a
23	BATF	chr8:8056483-8056771	GM12878	blood:	n/a	n/a
24	BATF	chr8:8005702-8005954	GM12878	blood:	n/a	n/a
25	BATF	chr8:7896260-7896568	GM12878	blood:	n/a	n/a
26	BATF	chr8:8000576-8001188	GM12878	blood:	n/a	n/a
27	BATF	chr8:7281851-7282075	GM12878	blood:	n/a	n/a
28	BATF	chr8:7804596-7805021	GM12878	blood:	n/a	n/a
29	BATF	chr8:8025297-8025584	GM12878	blood:	n/a	n/a
30	BATF	chr8:8025286-8025491	GM12878	blood:	n/a	n/a
31	BATF	chr8:7936788-7937244	GM12878	blood:	n/a	chr8:7936968-7936979
32	BATF	chr8:8007454-8008025	GM12878	blood:	n/a	chr8:8007742-8007750
33	BATF	chr8:8035087-8035263	GM12878	blood:	n/a	n/a
34	BATF	chr8:8043601-8043892	GM12878	blood:	n/a	n/a
35	BATF	chr8:7448268-7448576	GM12878	blood:	n/a	n/a
36	BATF	chr8:8005726-8005964	GM12878	blood:	n/a	n/a
37	BATF	chr8:8000024-8000529	GM12878	blood:	n/a	n/a
38	BATF	chr8:8056440-8056802	GM12878	blood:	n/a	n/a
39	BATF	chr8:7744485-7744737	GM12878	blood:	n/a	n/a
40	BATF	chr8:7896196-7896603	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:8023049-8023416	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:8070740-8071105	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:7994053-7994305	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:7468589-7468841	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:8056321-8056608	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:8007410-8007710	GM12878	blood:	n/a	chr8:8007656-8007665
47	BCL11A	chr8:8000199-8000561	GM12878	blood:	n/a	n/a
48	BCL11A	chr8:7936856-7937268	GM12878	blood:	n/a	n/a
49	BCL11A	chr8:8004170-8004760	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:8007408-8007936	GM12878	blood:	n/a	chr8:8007656-8007665

(count:7021 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7434722-7434772	HUVEC	blood vessel:	n/a
2	chr8:7882393-7882443	CMK	blood:	n/a
3	chr8:7631923-7631973	AG09319	gingival:	n/a
4	chr8:7394657-7394707	SK-N-MC	brain:	n/a
5	chr8:7671497-7671547	GM06990	blood:	n/a
6	chr8:7585573-7585623	RPTEC	kidney:	n/a
7	chr8:7434722-7434772	HUVEC	blood vessel:	n/a
8	chr8:7882393-7882443	CMK	blood:	n/a
9	chr8:7631923-7631973	AG09319	gingival:	n/a
10	chr8:7394657-7394707	SK-N-MC	brain:	n/a
11	chr8:7671497-7671547	GM06990	blood:	n/a
12	chr8:7585573-7585623	RPTEC	kidney:	n/a
13	chr8:7625446-7625496	NT2-D1	testis:	n/a
14	chr8:7599376-7599426	A549	lung:	n/a
15	chr8:7305465-7305515	AG10803	skin:	n/a
16	chr8:8032031-8032081	HepG2	liver:	n/a
17	chr8:7599371-7599421	SK-N-MC	brain:	n/a
18	chr8:7833268-7833318	LNCaP	prostate:	n/a
19	chr8:7872389-7872439	HCPEpiC	choroid plexus:	n/a
20	chr8:7833268-7833318	AG09309	skin:	n/a
21	chr8:7694339-7694389	AG10803	skin:	n/a
22	chr8:7651924-7651974	AG10803	skin:	n/a
23	chr8:7651924-7651974	PANC-1	pancreas:	n/a
24	chr8:7918813-7918863	MCF10A-Er-Src	breast:	n/a
25	chr8:7631923-7631973	ProgFib	skin:	n/a
26	chr8:8034763-8034813	U87	brain:	n/a
27	chr8:7539931-7539981	HRPEpiC	eye:	n/a
28	chr8:7680853-7680903	HNPCEpiC	eye:	n/a
29	chr8:7585573-7585623	GM19239	blood:	n/a
30	chr8:7572749-7572799	HUVEC	blood vessel:	n/a
31	chr8:7886076-7886126	Jurkat	blood:	n/a
32	chr8:7923629-7923679	Hela-S3	cervix:	n/a
33	chr8:7812741-7812791	HCM	heart:	n/a
34	chr8:7332846-7332896	SK-N-SH	brain:	n/a
35	chr8:7538130-7538180	GM12891	blood:	n/a
36	chr8:7332846-7332896	LNCaP	prostate:	n/a
37	chr8:7885901-7885951	Caco-2	colon:	n/a
38	chr8:7436707-7436757	SKMC	muscle:	n/a
39	chr8:7431189-7431239	PrEC	prostate:	n/a
40	chr8:7275380-7275430	HAEpiC	amniotic membrane:	n/a
41	chr8:7569353-7569403	LNCaP	prostate:	n/a
42	chr8:7686204-7686254	PANC-1	pancreas:	n/a
43	chr8:7871865-7871915	ECC-1	luminal epithelium:	n/a
44	chr8:7431189-7431239	HCT-116	colon:	n/a
45	chr8:7543899-7543949	PANC-1	pancreas:	n/a
46	chr8:7598581-7598631	HNPCEpiC	eye:	n/a
47	chr8:7834142-7834192	HL-60	blood:	n/a
48	chr8:7871865-7871915	AG04449	skin:	fetal
49	chr8:7631469-7631519	HRCEpiC	kidney:	n/a
50	chr8:7868012-7868062	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:7079344..7079857-chr8:7537961..7538472,3	MCF-7	breast:
2	chr8:7255181..7256067-chr8:7770740..7771265,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB104B-1	chr8:7333626-7334120	XLOC_006991
2	lnc-PRAGMIN.1-10	chr8:7974267-7974471	NONHSAT124849
3	lnc-DEFB105A-4	chr8:7854986-7855043	NONHSAT124844
4	lnc-DEFB105A-1	chr8:7748525-7750077	NONHSAT124838
5	lnc-PRAGMIN.1-3	chr8:8042248-8042354	ENSG00000253893.2
6	lnc-DEFB104B-1	chr8:7334999-7335170	XLOC_006991
7	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.1
8	lnc-PRAGMIN.1-3	chr8:8042248-8042354	ENSG00000253893.1
9	lnc-PRAGMIN.1-11	chr8:7943544-7944287	NONHSAT124847
10	lnc-AC068020.1-2	chr8:7996388-7996558	NONHSAT124852
11	lnc-AC068020.1-2	chr8:7997454-7997523	NONHSAT124852
12	lnc-DEFB104B-1	chr8:7337502-7337622	XLOC_006991
13	lnc-PRAGMIN.1-3	chr8:8025341-8025605	ENSG00000253893.2
14	lnc-PRAGMIN.1-3	chr8:8025339-8025605	ENSG00000253893.1
15	lnc-DEFB104B-1	chr8:7334988-7335170	XLOC_006991
16	lnc-DEFB105A-4	chr8:7847937-7848142	NONHSAT124844
17	lnc-PRAGMIN.1-3	chr8:7992174-7992262	ENSG00000253893.1
18	lnc-PRAGMIN.1-3	chr8:8077586-8077704	XLOC_006993
19	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr8:7946552-7946573	MIMAT0005935_2

No data

Variant related genes	Relation type
OR7E96P	TF binding region
FAM90A12P	TF binding region
DEFB107A	TF binding region
FAM90A11P	TF binding region
SPAG11B	TF binding region
FAM90A7P	TF binding region
OR7E157P	TF binding region
ENSG00000253881	TF binding region
FAM90A14P	TF binding region
FAM90A24P	TF binding region
ENSG00000268955	TF binding region
FAM90A19P	TF binding region
FAM66E	TF binding region
ENSG00000244427	TF binding region
ENSG00000221027	TF binding region
DEFB103A	TF binding region
ENSG00000254311	TF binding region
DEFB104A	TF binding region
OR7E154P	TF binding region
FAM90A9P	TF binding region
ENSG00000254889	TF binding region
ENSG00000254776	TF binding region
FAM90A23P	TF binding region
DEFB4B	TF binding region
ENSG00000254796	TF binding region
FAM90A22P	TF binding region
DEFB105A	TF binding region
DEFB106B	TF binding region
ENPP7P1	TF binding region
MIR548I3	TF binding region
DEFB104B	TF binding region
FAM90A6P	TF binding region
ENSG00000216194	TF binding region
HSPD1P2	TF binding region
ZNF705B	TF binding region
PRR23D2	TF binding region
FAM90A21P	TF binding region
FAM90A10P	TF binding region
ENSG00000215977	TF binding region
ENSG00000255459	TF binding region
PRR23D1	TF binding region
DEFB4A	TF binding region
FAM90A18P	TF binding region
FAM90A16P	TF binding region
FAM90A8P	TF binding region
DEFB105B	TF binding region
DEFB108P1	TF binding region
ENSG00000255211	TF binding region
USP17L8	TF binding region
DEFB107B	TF binding region
HSPD1P3	TF binding region
ENSG00000205989	TF binding region
DEFB106A	TF binding region
SPAG11A	TF binding region
DEFB103B	TF binding region
USP17L3	TF binding region
FAM90A17P	TF binding region
OR7E96P	CpG island
FAM90A12P	CpG island
DEFB107A	CpG island
FAM90A11P	CpG island
SPAG11B	CpG island
FAM90A7P	CpG island
OR7E157P	CpG island
ENSG00000253881	CpG island
FAM90A14P	CpG island
FAM90A24P	CpG island
ENSG00000268955	CpG island
FAM90A19P	CpG island
FAM66E	CpG island
ENSG00000244427	CpG island
ENSG00000221027	CpG island
DEFB103A	CpG island
ENSG00000254311	CpG island
DEFB104A	CpG island
OR7E154P	CpG island
FAM90A9P	CpG island
ENSG00000254889	CpG island
ENSG00000254776	CpG island
FAM90A23P	CpG island
DEFB4B	CpG island
ENSG00000254796	CpG island
FAM90A22P	CpG island
DEFB105A	CpG island
DEFB106B	CpG island
ENPP7P1	CpG island
MIR548I3	CpG island
DEFB104B	CpG island
FAM90A6P	CpG island
ENSG00000216194	CpG island
HSPD1P2	CpG island
ZNF705B	CpG island
PRR23D2	CpG island
FAM90A21P	CpG island
FAM90A10P	CpG island
ENSG00000215977	CpG island
ENSG00000255459	CpG island
PRR23D1	CpG island
DEFB4A	CpG island
FAM90A18P	CpG island
FAM90A16P	CpG island
FAM90A8P	CpG island
DEFB105B	CpG island
DEFB108P1	CpG island
ENSG00000255211	CpG island
USP17L8	CpG island
DEFB107B	CpG island
HSPD1P3	CpG island
ENSG00000205989	CpG island
DEFB106A	CpG island
SPAG11A	CpG island
DEFB103B	CpG island
USP17L3	CpG island
FAM90A17P	CpG island
JARID2	miRNA target sites

Extended variants
information (count: 5538 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:5538 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201249504	chr8:7272043-7272044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567392681	chr8:7272063-7272064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529902233	chr8:7272071-7272072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546946128	chr8:7272114-7272115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566795613	chr8:7272116-7272117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199647374	chr8:7272153-7272154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538901702	chr8:7272176-7272177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568789239	chr8:7272221-7272222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537589571	chr8:7272234-7272235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554638551	chr8:7272309-7272310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574966145	chr8:7272312-7272313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540404731	chr8:7272313-7272314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2737531	chr8:7272329-7272330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553918256	chr8:7272332-7272333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577133930	chr8:7272339-7272340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546045283	chr8:7272340-7272341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562740170	chr8:7272350-7272351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531725130	chr8:7272353-7272354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541995568	chr8:7272355-7272356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2737913	chr8:7272356-7272357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140131735	chr8:7272379-7272380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562192342	chr8:7272397-7272398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546833734	chr8:7272398-7272399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566630844	chr8:7272423-7272424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200803965	chr8:7272439-7272440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532450891	chr8:7272488-7272489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201554444	chr8:7272559-7272560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552443505	chr8:7272578-7272579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568800099	chr8:7272584-7272585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201824968	chr8:7272594-7272595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537831527	chr8:7272617-7272618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544469266	chr8:7272628-7272629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554394157	chr8:7272634-7272635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567835709	chr8:7272643-7272644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533606534	chr8:7272654-7272655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553951761	chr8:7272697-7272698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576974127	chr8:7272868-7272869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370160959	chr8:7272879-7272880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546221869	chr8:7272884-7272885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190146745	chr8:7272899-7272900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576388646	chr8:7272901-7272902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372504789	chr8:7272909-7272910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144804940	chr8:7272911-7272912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181166357	chr8:7272926-7272927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527797152	chr8:7272929-7272930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541491764	chr8:7272933-7272934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560435697	chr8:7272945-7272946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532335988	chr8:7272999-7273000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552222389	chr8:7273032-7273033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2737532	chr8:7273050-7273051	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	20369283	CNVD
Urothelial carcinoma	21177765	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	23813976	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21364760	CNVD
Developmental disorder	20461109	CNVD
Crohn''s disease	17953491	CNVD
Immune disease	21076436	CNVD
Crohn''s disease	21956041	CNVD
Autism	21865298	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	22302058	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:7272000-7281800	Enhancers	Dnd41	blood
2	chr8:7272200-7272400	Enhancers	Fetal Thymus	thymus
3	chr8:7273800-7279200	Weak transcription	Fetal Thymus	thymus
4	chr8:7275800-7276600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr8:7275800-7276600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr8:7275800-7276600	Enhancers	Osteobl	bone
7	chr8:7276000-7276200	Enhancers	HSMM	muscle
8	chr8:7276000-7276600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:7276000-7277800	Enhancers	HSMMtube	muscle
10	chr8:7276200-7278800	Weak transcription	HSMM	muscle
11	chr8:7276400-7277400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:7277800-7279800	Weak transcription	HSMMtube	muscle
13	chr8:7278800-7279400	Enhancers	HSMM	muscle
14	chr8:7279200-7280400	Enhancers	Fetal Thymus	thymus
15	chr8:7279400-7280000	Weak transcription	HSMM	muscle
16	chr8:7279800-7280200	Enhancers	Fetal Muscle Trunk	muscle
17	chr8:7279800-7280200	Enhancers	HSMMtube	muscle
18	chr8:7279800-7280400	Enhancers	Fetal Muscle Leg	muscle
19	chr8:7280000-7280200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:7280000-7280200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:7280000-7280200	Enhancers	HSMM	muscle
22	chr8:7281400-7281800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:7299400-7299600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:7299600-7302200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr8:7302200-7302400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr8:7302400-7303000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:7303000-7303200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:7303200-7322200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr8:7304400-7306200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr8:7305200-7305600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:7308400-7308800	Enhancers	Duodenum Mucosa	Duodenum
32	chr8:7329400-7329800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:7331800-7332200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:7338600-7339000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr8:7369600-7369800	Enhancers	Fetal Brain Male	brain
36	chr8:7378600-7379000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr8:7461200-7461400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:7469000-7469400	Active TSS	H1 Cell Line	embryonic stem cell
39	chr8:7469000-7469400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:7469000-7469400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:7537200-7538200	Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr8:7537400-7537600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
43	chr8:7537400-7537600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr8:7537400-7538200	Active TSS	Stomach Smooth Muscle	stomach
45	chr8:7537400-7538200	Active TSS	Dnd41	blood
46	chr8:7537400-7538600	Enhancers	Primary B cells from peripheral blood	blood
47	chr8:7537600-7538200	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr8:7537600-7538200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr8:7537800-7538200	Active TSS	Brain Germinal Matrix	brain
50	chr8:7537800-7538200	Active TSS	Fetal Brain Female	brain

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