Variant report

Variant	nsv1018531
Chromosome Location	chr8:9093176-9135199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:247)
Chromatin interactive
region (count:17)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:9106581-9106674	K562	blood:	n/a	n/a
2	ATF1	chr8:9106470-9106696	K562	blood:	n/a	n/a
3	ATF1	chr8:9112997-9113254	K562	blood:	n/a	n/a
4	ATF1	chr8:9117581-9118000	K562	blood:	n/a	n/a
5	ATF2	chr8:9127281-9127808	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:9106362-9106824	GM12878	blood:	n/a	n/a
7	ATF2	chr8:9126603-9127053	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:9121573-9122206	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr8:9127354-9127820	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr8:9106397-9106813	GM12878	blood:	n/a	n/a
11	ATF2	chr8:9121581-9122231	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:9128854-9129049	K562	blood:	n/a	n/a
13	BACH1	chr8:9126989-9127668	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr8:9106372-9106826	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
15	BATF	chr8:9106307-9106946	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
16	BCL11A	chr8:9121767-9122132	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr8:9106380-9106943	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
18	BCL11A	chr8:9127376-9127725	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr8:9106430-9106921	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
20	BCL11A	chr8:9127365-9127744	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCLAF1	chr8:9106457-9106732	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
22	BHLHE40	chr8:9110246-9110274	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:9106199-9106847	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:9112909-9113255	K562	blood:	n/a	n/a
25	BHLHE40	chr8:9128671-9129189	K562	blood:	n/a	n/a
26	BHLHE40	chr8:9110612-9110648	K562	blood:	n/a	n/a
27	BHLHE40	chr8:9117711-9118064	K562	blood:	n/a	n/a
28	BHLHE40	chr8:9110181-9110378	K562	blood:	n/a	n/a
29	BHLHE40	chr8:9095362-9095700	K562	blood:	n/a	n/a
30	BHLHE40	chr8:9123990-9124058	K562	blood:	n/a	n/a
31	BRCA1	chr8:9121619-9122124	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr8:9100534-9100869	HepG2	liver:	n/a	chr8:9100620-9100631
33	CEBPB	chr8:9117691-9118023	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:9100492-9100818	K562	blood:	n/a	chr8:9100620-9100631
35	CEBPB	chr8:9100618-9100654	H1-hESC	embryonic stem cell:	n/a	chr8:9100620-9100631
36	CEBPB	chr8:9117674-9117963	K562	blood:	n/a	n/a
37	CEBPB	chr8:9127384-9127821	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:9121074-9121429	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:9132288-9132590	HepG2	liver:	n/a	chr8:9132455-9132466
40	CEBPB	chr8:9100544-9100750	IMR90	lung:	n/a	chr8:9100620-9100631
41	CEBPB	chr8:9117816-9117945	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:9100552-9100824	A549	lung:	n/a	chr8:9100620-9100631
43	CEBPB	chr8:9132288-9132592	A549	lung:	n/a	chr8:9132455-9132466
44	CEBPB	chr8:9132328-9132571	Hela-S3	cervix:	n/a	chr8:9132455-9132466
45	CHD1	chr8:9120610-9120786	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr8:9126810-9127176	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr8:9127378-9127760	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr8:9106307-9106725	GM12878	blood:	n/a	n/a
49	CHD2	chr8:9121198-9122494	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr8:9095412-9095533	H1-hESC	embryonic stem cell:	n/a	n/a

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9107382-9107432	AG04450	lung:	fetal
2	chr8:9095150-9095200	H1-hESC	embryonic stem cell:	embryo
3	chr8:9123484-9123534	K562	blood:	n/a
4	chr8:9107382-9107432	AG04450	lung:	fetal
5	chr8:9095150-9095200	H1-hESC	embryonic stem cell:	embryo
6	chr8:9123484-9123534	K562	blood:	n/a
7	chr8:9095150-9095200	HEK293	kidney:	embryo
8	chr8:9095150-9095200	Jurkat	blood:	n/a
9	chr8:9123484-9123534	HNPCEpiC	eye:	n/a
10	chr8:9095150-9095200	HCPEpiC	choroid plexus:	n/a
11	chr8:9107382-9107432	SK-N-SH	brain:	n/a
12	chr8:9106953-9107003	NHDF-neo	bronchial:	n/a
13	chr8:9107382-9107432	AoSMC	blood vessel:	n/a
14	chr8:9107382-9107432	HEEpiC	esophagus:	n/a
15	chr8:9123484-9123534	PrEC	prostate:	n/a
16	chr8:9095150-9095200	SK-N-MC	brain:	n/a
17	chr8:9106953-9107003	HRE	kidney:	n/a
18	chr8:9107382-9107432	NH-A	brain:	n/a
19	chr8:9107382-9107432	GM12891	blood:	n/a
20	chr8:9106953-9107003	NH-A	brain:	n/a
21	chr8:9095150-9095200	GM19239	blood:	n/a
22	chr8:9107382-9107432	A549	lung:	n/a
23	chr8:9095150-9095200	AG10803	skin:	n/a
24	chr8:9095150-9095200	AG04449	skin:	fetal
25	chr8:9123484-9123534	RPTEC	kidney:	n/a
26	chr8:9106953-9107003	HCF	heart:	n/a
27	chr8:9123484-9123534	HIPEpiC	eye:	n/a
28	chr8:9106953-9107003	Hela-S3	cervix:	n/a
29	chr8:9107382-9107432	NHDF-neo	bronchial:	n/a
30	chr8:9123484-9123534	GM12892	blood:	n/a
31	chr8:9106953-9107003	HAEpiC	amniotic membrane:	n/a
32	chr8:9106953-9107003	CMK	blood:	n/a
33	chr8:9123484-9123534	AG10803	skin:	n/a
34	chr8:9107382-9107432	K562	blood:	n/a
35	chr8:9106953-9107003	Caco-2	colon:	n/a
36	chr8:9107382-9107432	U87	brain:	n/a
37	chr8:9095150-9095200	HCM	heart:	n/a
38	chr8:9095150-9095200	BJ	skin:	n/a
39	chr8:9106953-9107003	ProgFib	skin:	n/a
40	chr8:9106953-9107003	GM19239	blood:	n/a
41	chr8:9123484-9123534	Jurkat	blood:	n/a
42	chr8:9106953-9107003	HUVEC	blood vessel:	n/a
43	chr8:9123484-9123534	CMK	blood:	n/a
44	chr8:9107382-9107432	AG09309	skin:	n/a
45	chr8:9107382-9107432	SK-N-MC	brain:	n/a
46	chr8:9106953-9107003	ovcar-3	ovarian:	n/a
47	chr8:9123484-9123534	HEK293	kidney:	embryo
48	chr8:9107382-9107432	BJ	skin:	n/a
49	chr8:9095150-9095200	HRPEpiC	eye:	n/a
50	chr8:9123484-9123534	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
2	chr8:9090534..9092903-chr8:9095758..9098005,2	MCF-7	breast:
3	chr8:9094088..9097084-chr8:9119791..9121846,2	K562	blood:
4	chr8:9121493..9123437-chr8:9133381..9135913,2	K562	blood:
5	chr8:9121493..9123437-chr8:9133381..9135913,2	K562	blood:
6	chr8:9098947..9101284-chr8:9104230..9106988,2	K562	blood:
7	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:
8	chr8:9130214..9132621-chr8:9133703..9136409,3	K562	blood:
9	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
10	chr8:9095921..9098459-chr8:9104554..9106558,2	K562	blood:
11	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:
12	chr8:8922824..8923700-chr8:9130087..9130667,2	MCF-7	breast:
13	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
14	chr8:9095921..9098459-chr8:9104554..9106558,2	K562	blood:
15	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
16	chr8:9094088..9097084-chr8:9119791..9121846,2	K562	blood:
17	chr8:9130214..9132621-chr8:9133703..9136409,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-10A14.4.1-6	chr8:9097312-9097798	l_3543_chr8:9084119-9097777_placenta
2	lnc-PPP1R3B-2	chr8:9112859-9113012	ENSG00000253887
3	lnc-PPP1R3B-2	chr8:9112315-9112398	XLOC_006999
4	lnc-PPP1R3B-2	chr8:9115957-9116369	XLOC_006999
5	lnc-RP11-10A14.4.1-6	chr8:9093844-9093911	l_3543_chr8:9084119-9097777_placenta
6	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999
7	lnc-PPP1R3B-2	chr8:9117538-9117788	XLOC_006999
8	lnc-PPP1R3B-2	chr8:9112893-9113012	XLOC_006999
9	lnc-PPP1R3B-2	chr8:9117538-9117805	ENSG00000253887
10	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999

No data

Variant related genes	Relation type
ENSG00000254235	TF binding region
ENSG00000253887	TF binding region
ENSG00000254235	CpG island
ENSG00000253887	CpG island
ENSG00000254235	chromatin interactions

Extended variants
information (count: 2543 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:2543 , 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	rs570660179	chr8:9093192-9093193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185223035	chr8:9093193-9093194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535738598	chr8:9093199-9093200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143595731	chr8:9093200-9093201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551762167	chr8:9093227-9093228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549344620	chr8:9093239-9093240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568398102	chr8:9093285-9093286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374155	chr8:9093286-9093287	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567248176	chr8:9093295-9093296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554913703	chr8:9093309-9093310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200616241	chr8:9093310-9093311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374843384	chr8:9093313-9093314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540306461	chr8:9093327-9093328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560361407	chr8:9093340-9093341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112702108	chr8:9093369-9093370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557394938	chr8:9093370-9093371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577290486	chr8:9093400-9093401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190725757	chr8:9093401-9093402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377691401	chr8:9093409-9093410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12549645	chr8:9093413-9093414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs531999415	chr8:9093428-9093429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs56285715	chr8:9093453-9093454	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs184053820	chr8:9093461-9093462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199941803	chr8:9093502-9093503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147176130	chr8:9093523-9093524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188253358	chr8:9093549-9093550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11249909	chr8:9093558-9093559	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12547962	chr8:9093575-9093576	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs419192	chr8:9093584-9093585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114693195	chr8:9093586-9093587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73531363	chr8:9093602-9093603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535722695	chr8:9093609-9093610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138711660	chr8:9093614-9093615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574771919	chr8:9093672-9093673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193173179	chr8:9093674-9093675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563788955	chr8:9093684-9093685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528168044	chr8:9093694-9093695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs55880004	chr8:9093744-9093745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12547961	chr8:9093767-9093768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs149257760	chr8:9093783-9093784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113073723	chr8:9093784-9093785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13277288	chr8:9093802-9093803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183587079	chr8:9093813-9093814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545650822	chr8:9093848-9093849	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs542508647	chr8:9093850-9093851	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs13276525	chr8:9093851-9093852	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs561572468	chr8:9093875-9093876	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs138271967	chr8:9093887-9093888	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs138545633	chr8:9093890-9093891	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs569112958	chr8:9093903-9093904	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

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

Chromatin state (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9089200-9094600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:9089200-9094600	Weak transcription	Brain Substantia Nigra	brain
3	chr8:9089200-9096800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:9092000-9093200	Enhancers	HMEC	breast
5	chr8:9092200-9093200	Enhancers	NHEK	skin
6	chr8:9092200-9093600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:9092400-9093200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:9092800-9093200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr8:9092800-9093200	Enhancers	Osteobl	bone
10	chr8:9092800-9093400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:9093000-9093200	Enhancers	Right Atrium	heart
12	chr8:9093000-9094600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:9093000-9095000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:9093200-9095600	Weak transcription	Right Atrium	heart
15	chr8:9093400-9093600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:9093600-9094600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:9094000-9098200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:9094200-9095200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr8:9094400-9094800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:9094400-9095600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr8:9094400-9096200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr8:9094400-9096400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr8:9094600-9095000	Enhancers	Brain Substantia Nigra	brain
24	chr8:9094600-9095200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:9094600-9095200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:9094600-9095200	Bivalent Enhancer	Brain Angular Gyrus	brain
27	chr8:9094600-9095600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr8:9094600-9095600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr8:9094600-9098200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr8:9094800-9095000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
31	chr8:9094800-9095200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr8:9094800-9095600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr8:9095000-9095600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr8:9095000-9099200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr8:9095200-9095800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr8:9095200-9097000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:9095200-9114400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:9095600-9096000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr8:9095600-9097200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr8:9095600-9101800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr8:9095600-9102400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:9095800-9102200	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr8:9096000-9096200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr8:9096200-9097200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr8:9096200-9097200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr8:9096400-9097200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr8:9096800-9097600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr8:9097000-9097600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:9097000-9098000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr8:9097200-9097400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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