Variant report

Variant	esv1791777
Chromosome Location	chr8:7790091-8096350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2763)
CpG islands
(count:2933)
Chromatin interactive
region (count:12)
LncRNA
region (count:28)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2763 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8092931-8093297	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8091892-8091896	HepG2	liver:	n/a	n/a
3	ATF2	chr8:8096080-8096557	GM12878	blood:	n/a	n/a
4	ATF3	chr8:8096172-8096477	K562	blood:	n/a	n/a
5	BATF	chr8:8005100-8005302	GM12878	blood:	n/a	n/a
6	BATF	chr8:8025297-8025584	GM12878	blood:	n/a	n/a
7	BATF	chr8:8091245-8091594	GM12878	blood:	n/a	n/a
8	BATF	chr8:7812383-7812672	GM12878	blood:	n/a	n/a
9	BATF	chr8:8025286-8025491	GM12878	blood:	n/a	n/a
10	BATF	chr8:8005702-8005954	GM12878	blood:	n/a	n/a
11	BATF	chr8:7809497-7809672	GM12878	blood:	n/a	chr8:7809580-7809591
12	BATF	chr8:7949085-7949285	GM12878	blood:	n/a	n/a
13	BATF	chr8:7922797-7923045	GM12878	blood:	n/a	n/a
14	BATF	chr8:8029997-8030427	GM12878	blood:	n/a	n/a
15	BATF	chr8:7896260-7896568	GM12878	blood:	n/a	n/a
16	BATF	chr8:8043601-8043892	GM12878	blood:	n/a	n/a
17	BATF	chr8:8000576-8001188	GM12878	blood:	n/a	n/a
18	BATF	chr8:8007429-8007921	GM12878	blood:	n/a	chr8:8007742-8007750
19	BATF	chr8:8004195-8004622	GM12878	blood:	n/a	n/a
20	BATF	chr8:7804596-7805021	GM12878	blood:	n/a	n/a
21	BATF	chr8:7994136-7994338	GM12878	blood:	n/a	n/a
22	BATF	chr8:8004193-8004724	GM12878	blood:	n/a	n/a
23	BATF	chr8:8086606-8086880	GM12878	blood:	n/a	chr8:8086859-8086869
24	BATF	chr8:8030089-8030387	GM12878	blood:	n/a	n/a
25	BATF	chr8:8086957-8087326	GM12878	blood:	n/a	n/a
26	BATF	chr8:8000698-8001151	GM12878	blood:	n/a	n/a
27	BATF	chr8:8007454-8008025	GM12878	blood:	n/a	chr8:8007742-8007750
28	BATF	chr8:8086029-8086344	GM12878	blood:	n/a	n/a
29	BATF	chr8:8056483-8056771	GM12878	blood:	n/a	n/a
30	BATF	chr8:8085189-8085406	GM12878	blood:	n/a	n/a
31	BATF	chr8:8000024-8000529	GM12878	blood:	n/a	n/a
32	BATF	chr8:7936786-7937116	GM12878	blood:	n/a	chr8:7936968-7936979
33	BATF	chr8:8096176-8096555	GM12878	blood:	n/a	n/a
34	BATF	chr8:7936788-7937244	GM12878	blood:	n/a	chr8:7936968-7936979
35	BATF	chr8:8056440-8056802	GM12878	blood:	n/a	n/a
36	BATF	chr8:8035087-8035263	GM12878	blood:	n/a	n/a
37	BATF	chr8:8086780-8087231	GM12878	blood:	n/a	chr8:8086859-8086869
38	BATF	chr8:7994763-7995094	GM12878	blood:	n/a	n/a
39	BATF	chr8:7896196-7896603	GM12878	blood:	n/a	n/a
40	BATF	chr8:8095764-8096661	GM12878	blood:	n/a	n/a
41	BATF	chr8:8005726-8005964	GM12878	blood:	n/a	n/a
42	BATF	chr8:7809440-7809731	GM12878	blood:	n/a	chr8:7809580-7809591
43	BCL11A	chr8:8085568-8085885	GM12878	blood:	n/a	chr8:8085759-8085772
44	BCL11A	chr8:8085174-8085434	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:8025306-8025567	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:8086100-8086324	GM12878	blood:	n/a	n/a
47	BCL11A	chr8:7936461-7937264	GM12878	blood:	n/a	n/a
48	BCL11A	chr8:8003820-8004169	GM12878	blood:	n/a	n/a
49	BCL11A	chr8:8070740-8071105	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:7931536-7931773	GM12878	blood:	n/a	chr8:7931699-7931708

(count:2933 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8085973-8086023	MCF10A-Er-Src	breast:	n/a
2	chr8:8085503-8085553	T-47D	breast:	n/a
3	chr8:8085844-8085894	AoSMC	blood vessel:	n/a
4	chr8:7882393-7882443	CMK	blood:	n/a
5	chr8:7886076-7886126	GM12892	blood:	n/a
6	chr8:8085973-8086023	MCF10A-Er-Src	breast:	n/a
7	chr8:8085503-8085553	T-47D	breast:	n/a
8	chr8:8085844-8085894	AoSMC	blood vessel:	n/a
9	chr8:7882393-7882443	CMK	blood:	n/a
10	chr8:7886076-7886126	GM12892	blood:	n/a
11	chr8:8086686-8086736	NHBE	bronchial:	n/a
12	chr8:7885901-7885951	HNPCEpiC	eye:	n/a
13	chr8:8085946-8085996	GM19239	blood:	n/a
14	chr8:7947282-7947332	BE2_C	brain:	n/a
15	chr8:8034763-8034813	Hela-S3	cervix:	n/a
16	chr8:8086146-8086196	Hepatocyte	liver:	n/a
17	chr8:7891603-7891653	GM12891	blood:	n/a
18	chr8:8086146-8086196	MCF10A-Er-Src	breast:	n/a
19	chr8:7882393-7882443	BJ	skin:	n/a
20	chr8:7871865-7871915	U87	brain:	n/a
21	chr8:8085503-8085553	ProgFib	skin:	n/a
22	chr8:8085946-8085996	AoSMC	blood vessel:	n/a
23	chr8:8034602-8034652	HCF	heart:	n/a
24	chr8:7886357-7886407	ECC-1	luminal epithelium:	n/a
25	chr8:7883822-7883872	AoSMC	blood vessel:	n/a
26	chr8:7871865-7871915	HAEpiC	amniotic membrane:	n/a
27	chr8:7870244-7870294	AG04449	skin:	fetal
28	chr8:7882393-7882443	HUVEC	blood vessel:	n/a
29	chr8:8085503-8085553	AG04450	lung:	fetal
30	chr8:7882393-7882443	AG10803	skin:	n/a
31	chr8:7886357-7886407	ProgFib	skin:	n/a
32	chr8:7812741-7812791	LNCaP	prostate:	n/a
33	chr8:8084610-8084660	SK-N-SH	brain:	n/a
34	chr8:7871865-7871915	HEEpiC	esophagus:	n/a
35	chr8:8086686-8086736	BJ	skin:	n/a
36	chr8:7881548-7881598	HCM	heart:	n/a
37	chr8:7868012-7868062	SK-N-SH_RA	brain:	n/a
38	chr8:8084610-8084660	HepG2	liver:	n/a
39	chr8:7872389-7872439	A549	lung:	n/a
40	chr8:7886357-7886407	AG10803	skin:	n/a
41	chr8:7873837-7873887	GM06990	blood:	n/a
42	chr8:7882164-7882214	HMEC	breast:	n/a
43	chr8:7884052-7884102	HL-60	blood:	n/a
44	chr8:8032031-8032081	HCT-116	colon:	n/a
45	chr8:8085496-8085546	AG04450	lung:	fetal
46	chr8:7947282-7947332	MCF10A-Er-Src	breast:	n/a
47	chr8:8086144-8086194	CMK	blood:	n/a
48	chr8:7884052-7884102	PFSK-1	brain:	n/a
49	chr8:8082819-8082869	A549	lung:	n/a
50	chr8:7926131-7926181	U87	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
2	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
3	chr11:3443497..3444149-chr8:8085706..8086350,2	HCT-116	colon:
4	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
5	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:
6	chr8:8094096..8094629-chr8:8147947..8148540,2	MCF-7	breast:
7	chr15:59062813..59063449-chr8:8085838..8086625,2	Hela-S3	cervix:
8	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
9	chr3:129829770..129830533-chr8:8085798..8086673,3	Hela-S3	cervix:
10	chr8:8086683..8088508-chr8:8193858..8196209,2	MCF-7	breast:
11	chr6:26031709..26032614-chr8:8085130..8085961,2	Hela-S3	cervix:
12	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-3	chr8:8025339-8025605	ENSG00000253893.1
2	lnc-PRAGMIN.1-3	chr8:7992174-7992262	ENSG00000253893.1
3	lnc-PRAGMIN.1-3	chr8:8081348-8081432	XLOC_006993
4	lnc-AC068020.1-2	chr8:7996388-7996558	NONHSAT124852
5	lnc-PRAGMIN.1-10	chr8:7974267-7974471	NONHSAT124849
6	lnc-PRAGMIN.1-7	chr8:8093525-8093885	NONHSAT124858
7	lnc-PRAGMIN.1-7	chr8:8094648-8095823	NONHSAT124860
8	lnc-PRAGMIN.1-3	chr8:8084256-8084265	XLOC_006994
9	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.2
10	lnc-PRAGMIN.1-3	chr8:8084842-8085129	XLOC_006994
11	lnc-DEFB105A-4	chr8:7854986-7855043	NONHSAT124844
12	lnc-AC068020.1-2	chr8:7997454-7997523	NONHSAT124852
13	lnc-PRAGMIN.1-7	chr8:8095713-8095872	NONHSAT124858
14	lnc-PRAGMIN.1-7	chr8:8095696-8095860	NONHSAT124863
15	lnc-AC068020.1-1	chr8:8094730-8094797	NONHSAT124861
16	lnc-PRAGMIN.1-3	chr8:8083918-8084265	ENSG00000253893.1
17	lnc-PRAGMIN.1-3	chr8:8042248-8042354	ENSG00000253893.2
18	lnc-AC068020.1-1	chr8:8095815-8096448	NONHSAT124861
19	lnc-PRAGMIN.1-3	chr8:8042248-8042354	ENSG00000253893.1
20	lnc-PRAGMIN.1-3	chr8:8081348-8081409	ENSG00000253893.2
21	lnc-PRAGMIN.1-3	chr8:8081348-8081409	ENSG00000253893.1
22	lnc-PRAGMIN.1-3	chr8:8084720-8085385	ENSG00000253893.1
23	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.1
24	lnc-PRAGMIN.1-3	chr8:8025341-8025605	ENSG00000253893.2
25	lnc-PRAGMIN.1-11	chr8:7943544-7944287	NONHSAT124847
26	lnc-DEFB105A-4	chr8:7847937-7848142	NONHSAT124844
27	lnc-PRAGMIN.1-3	chr8:8083918-8084136	ENSG00000253893.2
28	lnc-PRAGMIN.1-3	chr8:8077586-8077704	XLOC_006993

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
FAM90A11P	TF binding region
ENSG00000253881	TF binding region
FAM90A24P	TF binding region
FAM66E	TF binding region
FAM86B3P	TF binding region
FAM85B	TF binding region
ENPP7P1	TF binding region
MIR548I3	TF binding region
ZNF705B	TF binding region
ENSG00000255459	TF binding region
USP17L8	TF binding region
USP17L3	TF binding region
ENSG00000268955	TF binding region
ENSG00000244427	TF binding region
ENSG00000221027	TF binding region
ENSG00000254311	TF binding region
DEFB108P1	TF binding region
ENSG00000255211	TF binding region
ALG1L13P	TF binding region
ENSG00000205989	TF binding region
OR7E96P	CpG island
FAM90A12P	CpG island
FAM90A11P	CpG island
ENSG00000253881	CpG island
FAM90A24P	CpG island
FAM66E	CpG island
FAM86B3P	CpG island
FAM85B	CpG island
ENPP7P1	CpG island
MIR548I3	CpG island
ZNF705B	CpG island
ENSG00000255459	CpG island
USP17L8	CpG island
USP17L3	CpG island
ENSG00000268955	CpG island
ENSG00000244427	CpG island
ENSG00000221027	CpG island
ENSG00000254311	CpG island
DEFB108P1	CpG island
ENSG00000255211	CpG island
ALG1L13P	CpG island
ENSG00000205989	CpG island
ENSG00000166492	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000173295	chromatin interactions
ENSG00000253540	chromatin interactions
ENSG00000253981	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000128923	chromatin interactions
UBQLN1	miRNA target sites

Extended variants
information (count: 4226 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:4226 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531909927	chr8:7797976-7797977	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs548943924	chr8:7797986-7797987	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs568760077	chr8:7797989-7797990	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs539150284	chr8:7797999-7798000	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs116547710	chr8:7798008-7798009	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs200578962	chr8:7798012-7798013	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs554211409	chr8:7798051-7798052	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs570795896	chr8:7798074-7798075	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs539565014	chr8:7798097-7798098	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs556605237	chr8:7798112-7798113	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs575378577	chr8:7798113-7798114	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs9773388	chr8:7798126-7798127	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs2739919	chr8:7798129-7798130	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544000325	chr8:7798131-7798132	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs2740655	chr8:7798133-7798134	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs373851906	chr8:7798145-7798146	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs2739920	chr8:7798176-7798177	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs9773402	chr8:7798192-7798193	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs9774079	chr8:7798204-7798205	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs554484747	chr8:7798208-7798209	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs574404167	chr8:7798212-7798213	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs540093125	chr8:7798213-7798214	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs559917529	chr8:7798217-7798218	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs532114209	chr8:7798218-7798219	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs545606306	chr8:7798222-7798223	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs562598555	chr8:7798227-7798228	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs377626282	chr8:7798231-7798232	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs548809147	chr8:7798289-7798290	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs568622293	chr8:7798293-7798294	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs147984521	chr8:7798294-7798295	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs76988260	chr8:7798303-7798304	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs56093011	chr8:7798306-7798307	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs548074700	chr8:7798313-7798314	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs570790761	chr8:7798386-7798387	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs2739921	chr8:7798387-7798388	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs539799913	chr8:7798390-7798391	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs377050539	chr8:7798442-7798443	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs370379824	chr8:7798458-7798459	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs550054688	chr8:7798468-7798469	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs528531969	chr8:7807574-7807575	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs547580406	chr8:7807577-7807578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570521654	chr8:7807679-7807680	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539743288	chr8:7807682-7807683	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs2740676	chr8:7808219-7808220	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs564730869	chr8:7812530-7812531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs558344192	chr8:7812754-7812755	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs578088188	chr8:7812770-7812771	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs200631611	chr8:7826071-7826072	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs367569527	chr8:7826122-7826123	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs536577087	chr8:7826124-7826125	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:151)

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
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
Cognitive impairment	21505072	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
Urothelial carcinoma	21177765	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	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
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:7812600-7813000	Active TSS	H1 Cell Line	embryonic stem cell
2	chr8:7812600-7813000	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr8:7812600-7813000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:7812600-7813000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:7812600-7813000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:7812600-7813000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:7812600-7813000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:7812600-7813000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:7812600-7813000	Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr8:7812600-7813000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:7812600-7813000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr8:7812600-7813000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:7812600-7813000	Active TSS	Muscle Satellite Cultured Cells	--
14	chr8:7812600-7813000	Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr8:7812600-7813000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:7812600-7813000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:7812600-7813000	Active TSS	Brain Germinal Matrix	brain
18	chr8:7812600-7813000	Active TSS	Fetal Muscle Leg	muscle
19	chr8:7812600-7813000	Active TSS	Left Ventricle	heart
20	chr8:7812600-7813000	Active TSS	Psoas Muscle	Psoas
21	chr8:7812600-7813000	Active TSS	Right Atrium	heart
22	chr8:7812600-7813000	Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr8:7812600-7813000	Active TSS	Stomach Smooth Muscle	stomach
24	chr8:7812600-7813000	Active TSS	A549	lung
25	chr8:7812600-7813000	Active TSS	Osteobl	bone
26	chr8:7877400-7877800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:7877800-7882800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:7882800-7883000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:7883000-7885600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr8:7885400-7885800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:7885600-7886600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:7885800-7886000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:7885800-7886000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:7885800-7886200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:7885800-7886200	ZNF genes & repeats	Fetal Brain Female	brain
36	chr8:7886000-7889000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:7886600-7889200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:7887000-7887400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:7888200-7888600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:7889000-7889400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:7889200-7889400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:7889400-7896400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:7889400-7903200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr8:7903200-7903400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr8:7903200-7903400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:7911600-7912400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr8:7916800-7917200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr8:7917000-7917200	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
49	chr8:7917000-7917200	Enhancers	Placenta	Placenta
50	chr8:7917000-7917400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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