Variant report

Variant	nsv6073
Chromosome Location	chr8:9189800-9234741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:710)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:9195780-9196096	K562	blood:	n/a	n/a
2	ARID3A	chr8:9195766-9196168	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:9221142-9221337	K562	blood:	n/a	n/a
4	ARID3A	chr8:9226585-9226862	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:9208477-9208661	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:9211751-9212510	HepG2	liver:	n/a	n/a
7	ATF1	chr8:9221037-9221355	K562	blood:	n/a	n/a
8	BACH1	chr8:9226532-9226872	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:9220327-9220372	K562	blood:	n/a	n/a
10	BACH1	chr8:9221030-9221358	K562	blood:	n/a	n/a
11	BATF	chr8:9226494-9226823	GM12878	blood:	n/a	n/a
12	BCLAF1	chr8:9226485-9226841	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:9226526-9226876	K562	blood:	n/a	n/a
14	BHLHE40	chr8:9221180-9221258	K562	blood:	n/a	n/a
15	BRCA1	chr8:9226519-9226761	HepG2	liver:	n/a	n/a
16	BRCA1	chr8:9226534-9226825	Hela-S3	cervix:	n/a	chr8:9226776-9226785
17	CBX3	chr8:9226391-9227032	HCT-116	colon:	n/a	n/a
18	CBX3	chr8:9230323-9230652	K562	blood:	n/a	n/a
19	CBX3	chr8:9226579-9226779	K562	blood:	n/a	n/a
20	CEBPB	chr8:9211560-9211815	HepG2	liver:	n/a	chr8:9211652-9211663
21	CEBPB	chr8:9221242-9221420	K562	blood:	n/a	n/a
22	CEBPB	chr8:9208036-9208060	HepG2	liver:	n/a	chr8:9208041-9208052
23	CEBPB	chr8:9197431-9197553	HepG2	liver:	n/a	chr8:9197505-9197518 chr8:9197505-9197518 chr8:9197506-9197517
24	CEBPB	chr8:9224811-9225019	HepG2	liver:	n/a	chr8:9224894-9224907 chr8:9224894-9224907
25	CEBPB	chr8:9212143-9212444	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:9224773-9224910	A549	lung:	n/a	chr8:9224894-9224907 chr8:9224894-9224907
27	CEBPD	chr8:9221043-9221416	K562	blood:	n/a	n/a
28	CHD2	chr8:9226512-9226789	GM12878	blood:	n/a	chr8:9226776-9226785
29	CHD2	chr8:9226538-9226936	H1-hESC	embryonic stem cell:	n/a	chr8:9226776-9226785
30	CHD2	chr8:9226616-9226878	HepG2	liver:	n/a	chr8:9226776-9226785
31	CHD2	chr8:9221138-9221183	K562	blood:	n/a	n/a
32	CHD2	chr8:9226536-9226967	K562	blood:	n/a	chr8:9226776-9226785
33	CTCF	chr8:9196720-9196870	SAEC	small airway:	n/a	n/a
34	CTCF	chr8:9196600-9196750	NHEK	skin:	n/a	n/a
35	CTCF	chr8:9195860-9196010	AG09309	skin:	n/a	n/a
36	CTCF	chr8:9195900-9196050	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr8:9226980-9227130	GM12870	blood:	n/a	n/a
38	CTCF	chr8:9195809-9195992	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:9195820-9195970	BE2_C	brain:	n/a	n/a
40	CTCF	chr8:9226600-9226750	GM12870	blood:	n/a	chr8:9226673-9226694 chr8:9226674-9226683 chr8:9226672-9226688 chr8:9226674-9226687 chr8:9226671-9226689
41	CTCF	chr8:9226620-9226770	Hela-S3	cervix:	n/a	chr8:9226673-9226694 chr8:9226674-9226683 chr8:9226672-9226688 chr8:9226674-9226687 chr8:9226671-9226689
42	CTCF	chr8:9195880-9196030	GM12872	blood:	n/a	n/a
43	CTCF	chr8:9195816-9195979	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:9195860-9196010	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr8:9226600-9226750	A549	lung:	n/a	chr8:9226673-9226694 chr8:9226674-9226683 chr8:9226672-9226688 chr8:9226674-9226687 chr8:9226671-9226689
46	CTCF	chr8:9226517-9226824	K562	blood:	n/a	chr8:9226673-9226694 chr8:9226674-9226683 chr8:9226672-9226688 chr8:9226674-9226687 chr8:9226671-9226689
47	CTCF	chr8:9195804-9196112	LNCaP	prostate:	n/a	n/a
48	CTCF	chr8:9226600-9226750	WERI-Rb-1	eye:	n/a	chr8:9226673-9226694 chr8:9226674-9226683 chr8:9226672-9226688 chr8:9226674-9226687 chr8:9226671-9226689
49	CTCF	chr8:9196686-9196788	LNCaP	prostate:	n/a	n/a
50	CTCF	chr8:9226591-9226793	SK-N-SH_RA	brain:	n/a	chr8:9226673-9226694 chr8:9226674-9226683 chr8:9226672-9226688 chr8:9226674-9226687 chr8:9226671-9226689

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9194889-9194939	NHDF-neo	bronchial:	n/a
2	chr8:9194889-9194939	RPTEC	kidney:	n/a
3	chr8:9194889-9194939	LNCaP	prostate:	n/a
4	chr8:9194889-9194939	PANC-1	pancreas:	n/a
5	chr8:9194889-9194939	AG09319	gingival:	n/a
6	chr8:9194889-9194939	T-47D	breast:	n/a
7	chr8:9194889-9194939	SK-N-MC	brain:	n/a
8	chr8:9194889-9194939	SKMC	muscle:	n/a
9	chr8:9194889-9194939	HRPEpiC	eye:	n/a
10	chr8:9194889-9194939	AoSMC	blood vessel:	n/a
11	chr8:9194889-9194939	NH-A	brain:	n/a
12	chr8:9194889-9194939	HCF	heart:	n/a
13	chr8:9194889-9194939	NHBE	bronchial:	n/a
14	chr8:9194889-9194939	ProgFib	skin:	n/a
15	chr8:9194889-9194939	HepG2	liver:	n/a
16	chr8:9194889-9194939	AG10803	skin:	n/a
17	chr8:9194889-9194939	GM06990	blood:	n/a
18	chr8:9194889-9194939	HCPEpiC	choroid plexus:	n/a
19	chr8:9194889-9194939	AG04450	lung:	fetal
20	chr8:9194889-9194939	HEEpiC	esophagus:	n/a
21	chr8:9194889-9194939	Caco-2	colon:	n/a
22	chr8:9194889-9194939	GM12878	blood:	n/a
23	chr8:9194889-9194939	GM12892	blood:	n/a
24	chr8:9194889-9194939	MCF10A-Er-Src	breast:	n/a
25	chr8:9194889-9194939	HRCEpiC	kidney:	n/a
26	chr8:9194889-9194939	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:9194889-9194939	Hepatocyte	liver:	n/a
28	chr8:9194889-9194939	SK-N-SH_RA	brain:	n/a
29	chr8:9194889-9194939	MCF-7	breast:	n/a
30	chr8:9194889-9194939	HMEC	breast:	n/a
31	chr8:9194889-9194939	HRE	kidney:	n/a
32	chr8:9194889-9194939	HIPEpiC	eye:	n/a
33	chr8:9194889-9194939	AG09309	skin:	n/a
34	chr8:9194889-9194939	BE2_C	brain:	n/a
35	chr8:9194889-9194939	HCM	heart:	n/a
36	chr8:9194889-9194939	HCT-116	colon:	n/a
37	chr8:9194889-9194939	SK-N-SH	brain:	n/a
38	chr8:9194889-9194939	H1-hESC	embryonic stem cell:	embryo
39	chr8:9194889-9194939	HAEpiC	amniotic membrane:	n/a
40	chr8:9194889-9194939	BJ	skin:	n/a
41	chr8:9194889-9194939	HNPCEpiC	eye:	n/a
42	chr8:9194889-9194939	SAEC	small airway:	n/a
43	chr8:9194889-9194939	HUVEC	blood vessel:	n/a
44	chr8:9194889-9194939	U87	brain:	n/a
45	chr8:9194889-9194939	AG04449	skin:	fetal
46	chr8:9194889-9194939	Hela-S3	cervix:	n/a
47	chr8:9194889-9194939	NB4	blood:	n/a
48	chr8:9194889-9194939	HL-60	blood:	n/a
49	chr8:9194889-9194939	CMK	blood:	n/a
50	chr8:9194889-9194939	HEK293	kidney:	embryo

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:9226234..9227282-chr8:9688101..9689055,3	K562	blood:
2	chr8:9007894..9008784-chr8:9195169..9196375,4	MCF-7	breast:
3	chr8:9195933..9196478-chr8:9688212..9689059,2	MCF-7	breast:
4	chr8:9226621..9227308-chr8:9534051..9534690,2	MCF-7	breast:
5	chr8:8922930..8923887-chr8:9195546..9196445,3	K562	blood:
6	chr8:9178254..9179002-chr8:9195700..9196483,2	K562	blood:
7	chr8:9177828..9179105-chr8:9195409..9196219,4	MCF-7	breast:
8	chr8:9195700..9196570-chr8:9534210..9534969,2	MCF-7	breast:
9	chr8:9225162..9228698-chr8:9411632..9414803,4	MCF-7	breast:
10	chr8:9224923..9225494-chr8:9688129..9688755,2	MCF-7	breast:
11	chr8:8608326..8608981-chr8:9195964..9196742,2	MCF-7	breast:
12	chr8:9185407..9187173-chr8:9188435..9190916,2	MCF-7	breast:
13	chr8:9195714..9196690-chr8:9534240..9534889,2	MCF-7	breast:
14	chr8:8887023..8887982-chr8:9195505..9196570,5	K562	blood:
15	chr8:8886723..8887985-chr8:9195522..9196377,3	MCF-7	breast:
16	chr8:9210981..9212635-chr8:9215863..9218673,2	K562	blood:
17	chr8:9177871..9178799-chr8:9195168..9196018,3	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R3B-3	chr8:9215112-9215261	ENSG00000253735
2	lnc-RP11-10A14.4.1-4	chr8:9220772-9220892	ENSG00000254235
3	lnc-TNKS-6	chr8:9233409-9235120	NONHSAT124952
4	lnc-RP11-10A14.4.1-4	chr8:9218876-9218933	ENSG00000254235
5	lnc-RP11-10A14.4.1-4	chr8:9189914-9190023	NONHSAT124941
6	lnc-RP11-10A14.4.1-4	chr8:9190349-9190370	NONHSAT124941
7	lnc-PPP1R3B-3	chr8:9215851-9215951	ENSG00000253735
8	lnc-RP11-10A14.4.1-4	chr8:9220768-9220892	NONHSAT124947
9	lnc-RP11-10A14.4.1-4	chr8:9189914-9192590	ENSG00000254235
10	lnc-PPP1R3B-3	chr8:9215851-9215948	XLOC_007000
11	lnc-PPP1R3B-4	chr8:9229480-9229649	ENSG00000254237
12	lnc-RP11-10A14.4.1-4	chr8:9220768-9220892	NONHSAT124948
13	lnc-PPP1R3B-3	chr8:9217110-9217269	XLOC_007000
14	lnc-RP11-10A14.4.1-4	chr8:9219971-9220333	ucscGeneNc_uc003wsq_1
15	lnc-RP11-10A14.4.1-4	chr8:9224971-9225402	ENSG00000254235
16	lnc-RP11-10A14.4.1-4	chr8:9227324-9230000	ucscGeneNc_uc003wsq_1
17	lnc-PPP1R3B-3	chr8:9208767-9209059	XLOC_007000
18	lnc-PPP1R3B-4	chr8:9232444-9232475	ENSG00000254237
19	lnc-PPP1R3B-4	chr8:9230365-9230616	ENSG00000254237
20	lnc-RP11-10A14.4.1-4	chr8:9220822-9221223	ucscGeneNc_uc003wsq_1
21	lnc-PPP1R3B-4	chr8:9232408-9232649	ENSG00000254237
22	lnc-RP11-10A14.4.1-4	chr8:9218876-9218896	NONHSAT124940
23	lnc-PPP1R3B-3	chr8:9208748-9209059	ENSG00000253735

No data

Variant related genes	Relation type
ENSG00000254237	TF binding region
RNU6-526P	TF binding region
ENSG00000253735	TF binding region
ENSG00000254237	CpG island
RNU6-526P	CpG island
ENSG00000253735	CpG island
ENSG00000253735	chromatin interactions
ENSG00000173281	chromatin interactions
ENSG00000272267	chromatin interactions
ENSG00000173273	chromatin interactions

Extended variants
information (count: 2518 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:2518 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192708796	chr8:9189800-9189801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554952468	chr8:9189808-9189809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369724307	chr8:9189810-9189811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370658377	chr8:9189816-9189817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144860201	chr8:9189817-9189818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs59772956	chr8:9189819-9189820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112890367	chr8:9189830-9189831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184363605	chr8:9189862-9189863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543626244	chr8:9189866-9189867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148168749	chr8:9189904-9189905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531854044	chr8:9189911-9189912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190472222	chr8:9189915-9189916	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs562057146	chr8:9189962-9189963	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs17149797	chr8:9189971-9189972	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs548092761	chr8:9189991-9189992	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs141976157	chr8:9189995-9189996	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs150673446	chr8:9190013-9190014	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs550351558	chr8:9190022-9190023	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs569609508	chr8:9190029-9190030	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs140112949	chr8:9190114-9190115	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs555071586	chr8:9190128-9190129	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs543145154	chr8:9190132-9190133	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs181967627	chr8:9190164-9190165	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs534332897	chr8:9190165-9190166	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs184422994	chr8:9190170-9190171	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs577873591	chr8:9190178-9190179	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs188980166	chr8:9190237-9190238	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs557113059	chr8:9190249-9190250	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs181701660	chr8:9190275-9190276	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs542319455	chr8:9190282-9190283	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs562195679	chr8:9190294-9190295	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs201236110	chr8:9190295-9190296	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs542232387	chr8:9190327-9190328	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs185658178	chr8:9190335-9190336	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs541435758	chr8:9190372-9190373	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs564577052	chr8:9190403-9190404	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs17660164	chr8:9190427-9190428	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143734866	chr8:9190433-9190434	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs35570911	chr8:9190434-9190435	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs191359318	chr8:9190453-9190454	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs6984133	chr8:9190468-9190469	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs373812703	chr8:9190489-9190490	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs115471556	chr8:9190497-9190498	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs114272836	chr8:9190510-9190511	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs564974522	chr8:9190512-9190513	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs139566467	chr8:9190520-9190521	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs571198610	chr8:9190521-9190522	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs537351384	chr8:9190550-9190551	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs76453951	chr8:9190564-9190565	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs7003905	chr8:9190573-9190574	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:137)

Disease	PMID	Source
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
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
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9178600-9193600	Weak transcription	Left Ventricle	heart
2	chr8:9178600-9194000	Weak transcription	Right Atrium	heart
3	chr8:9186800-9190000	Weak transcription	Liver	Liver
4	chr8:9187000-9195400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:9189400-9190600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr8:9189400-9192800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:9189400-9199800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:9190000-9190800	Enhancers	Liver	Liver
9	chr8:9190400-9190800	Enhancers	Fetal Intestine Large	intestine
10	chr8:9190800-9193600	Weak transcription	Liver	Liver
11	chr8:9190800-9195400	Weak transcription	Fetal Intestine Large	intestine
12	chr8:9192000-9193800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr8:9192000-9194200	Enhancers	Brain Anterior Caudate	brain
14	chr8:9192200-9192400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:9192200-9193800	Enhancers	Brain Angular Gyrus	brain
16	chr8:9192200-9194200	Enhancers	Brain Cingulate Gyrus	brain
17	chr8:9192200-9194400	Enhancers	Brain Substantia Nigra	brain
18	chr8:9192200-9196200	Enhancers	Brain Hippocampus Middle	brain
19	chr8:9192400-9193400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:9192400-9193800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:9192400-9193800	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr8:9192400-9195400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr8:9192600-9193200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr8:9192800-9193800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:9193000-9196400	Enhancers	Fetal Heart	heart
26	chr8:9193200-9193600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr8:9193400-9194600	Enhancers	Fetal Lung	lung
28	chr8:9193400-9195200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:9193600-9193800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:9193600-9194400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:9193600-9196000	Enhancers	Left Ventricle	heart
32	chr8:9193600-9197000	Enhancers	Liver	Liver
33	chr8:9193800-9194200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr8:9193800-9195400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr8:9193800-9195600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:9193800-9195600	Weak transcription	Brain Angular Gyrus	brain
37	chr8:9193800-9195600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr8:9194000-9194200	Enhancers	Right Atrium	heart
39	chr8:9194000-9194800	Enhancers	Placenta	Placenta
40	chr8:9194200-9194800	Weak transcription	Right Atrium	heart
41	chr8:9194200-9195400	Weak transcription	Brain Anterior Caudate	brain
42	chr8:9194200-9195400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr8:9194400-9195400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr8:9194400-9195400	Weak transcription	Brain Substantia Nigra	brain
45	chr8:9194400-9196200	Enhancers	Fetal Stomach	stomach
46	chr8:9194600-9195000	Flanking Active TSS	Fetal Lung	lung
47	chr8:9194600-9196000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr8:9194600-9196000	Enhancers	Right Ventricle	heart
49	chr8:9194800-9195800	Weak transcription	Placenta	Placenta
50	chr8:9194800-9195800	Enhancers	Right Atrium	heart

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