Variant report

Variant	nsv1034464
Chromosome Location	chr8:9082008-9127516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr8:9117581-9118000	K562	blood:	n/a	n/a
3	ATF1	chr8:9112997-9113254	K562	blood:	n/a	n/a
4	ATF1	chr8:9106470-9106696	K562	blood:	n/a	n/a
5	ATF2	chr8:9126603-9127053	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:9127354-9127820	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:9121573-9122206	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:9121581-9122231	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr8:9127281-9127808	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr8:9106397-9106813	GM12878	blood:	n/a	n/a
11	ATF2	chr8:9106362-9106824	GM12878	blood:	n/a	n/a
12	BACH1	chr8:9126989-9127668	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr8:9106307-9106946	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
14	BATF	chr8:9106372-9106826	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
15	BCL11A	chr8:9106380-9106943	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
16	BCL11A	chr8:9121767-9122132	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr8:9127376-9127725	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr8:9127365-9127744	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	BCLAF1	chr8:9106457-9106732	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
21	BHLHE40	chr8:9123990-9124058	K562	blood:	n/a	n/a
22	BHLHE40	chr8:9112909-9113255	K562	blood:	n/a	n/a
23	BHLHE40	chr8:9110181-9110378	K562	blood:	n/a	n/a
24	BHLHE40	chr8:9090326-9090623	K562	blood:	n/a	n/a
25	BHLHE40	chr8:9110246-9110274	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:9106199-9106847	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:9117711-9118064	K562	blood:	n/a	n/a
28	BHLHE40	chr8:9095362-9095700	K562	blood:	n/a	n/a
29	BHLHE40	chr8:9110612-9110648	K562	blood:	n/a	n/a
30	BRCA1	chr8:9121619-9122124	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr8:9082474-9083014	HCT-116	colon:	n/a	n/a
32	CEBPB	chr8:9117691-9118023	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:9083175-9083467	K562	blood:	n/a	chr8:9083307-9083318
34	CEBPB	chr8:9083143-9083447	A549	lung:	n/a	chr8:9083307-9083318
35	CEBPB	chr8:9083140-9083406	HepG2	liver:	n/a	chr8:9083307-9083318
36	CEBPB	chr8:9127384-9127821	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:9121074-9121429	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:9090364-9090709	K562	blood:	n/a	n/a
39	CEBPB	chr8:9100492-9100818	K562	blood:	n/a	chr8:9100620-9100631
40	CEBPB	chr8:9100618-9100654	H1-hESC	embryonic stem cell:	n/a	chr8:9100620-9100631
41	CEBPB	chr8:9100534-9100869	HepG2	liver:	n/a	chr8:9100620-9100631
42	CEBPB	chr8:9100544-9100750	IMR90	lung:	n/a	chr8:9100620-9100631
43	CEBPB	chr8:9083148-9083487	MCF-7	breast:	n/a	chr8:9083307-9083318
44	CEBPB	chr8:9088688-9088983	K562	blood:	n/a	chr8:9088845-9088853 chr8:9088871-9088879
45	CEBPB	chr8:9117674-9117963	K562	blood:	n/a	n/a
46	CEBPB	chr8:9083216-9083416	H1-hESC	embryonic stem cell:	n/a	chr8:9083307-9083318
47	CEBPB	chr8:9100552-9100824	A549	lung:	n/a	chr8:9100620-9100631
48	CEBPB	chr8:9092228-9092358	K562	blood:	n/a	n/a
49	CEBPB	chr8:9117816-9117945	HepG2	liver:	n/a	n/a
50	CHD1	chr8:9120610-9120786	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9106953-9107003	AG10803	skin:	n/a
2	chr8:9107382-9107432	HepG2	liver:	n/a
3	chr8:9123484-9123534	AG09309	skin:	n/a
4	chr8:9095150-9095200	BJ	skin:	n/a
5	chr8:9095150-9095200	HNPCEpiC	eye:	n/a
6	chr8:9107382-9107432	AG10803	skin:	n/a
7	chr8:9095150-9095200	HCPEpiC	choroid plexus:	n/a
8	chr8:9107382-9107432	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:9123484-9123534	Jurkat	blood:	n/a
10	chr8:9123484-9123534	SK-N-SH_RA	brain:	n/a
11	chr8:9095150-9095200	SK-N-MC	brain:	n/a
12	chr8:9107382-9107432	GM12891	blood:	n/a
13	chr8:9123484-9123534	AG09319	gingival:	n/a
14	chr8:9106953-9107003	GM12878	blood:	n/a
15	chr8:9107382-9107432	AG09309	skin:	n/a
16	chr8:9106953-9107003	SKMC	muscle:	n/a
17	chr8:9123484-9123534	GM06990	blood:	n/a
18	chr8:9107382-9107432	BJ	skin:	n/a
19	chr8:9106953-9107003	NH-A	brain:	n/a
20	chr8:9107382-9107432	HEEpiC	esophagus:	n/a
21	chr8:9106953-9107003	HAEpiC	amniotic membrane:	n/a
22	chr8:9095150-9095200	SK-N-SH_RA	brain:	n/a
23	chr8:9106953-9107003	PFSK-1	brain:	n/a
24	chr8:9123484-9123534	IMR90	lung:	fetal
25	chr8:9095150-9095200	HRCEpiC	kidney:	n/a
26	chr8:9106953-9107003	HL-60	blood:	n/a
27	chr8:9106953-9107003	Hepatocyte	liver:	n/a
28	chr8:9095150-9095200	MCF10A-Er-Src	breast:	n/a
29	chr8:9123484-9123534	K562	blood:	n/a
30	chr8:9107382-9107432	Hela-S3	cervix:	n/a
31	chr8:9107382-9107432	CMK	blood:	n/a
32	chr8:9123484-9123534	MCF-7	breast:	n/a
33	chr8:9095150-9095200	NHBE	bronchial:	n/a
34	chr8:9106953-9107003	IMR90	lung:	fetal
35	chr8:9095150-9095200	SAEC	small airway:	n/a
36	chr8:9095150-9095200	HL-60	blood:	n/a
37	chr8:9123484-9123534	Caco-2	colon:	n/a
38	chr8:9107382-9107432	A549	lung:	n/a
39	chr8:9107382-9107432	HCF	heart:	n/a
40	chr8:9107382-9107432	GM19239	blood:	n/a
41	chr8:9095150-9095200	IMR90	lung:	fetal
42	chr8:9107382-9107432	AG04449	skin:	fetal
43	chr8:9095150-9095200	HIPEpiC	eye:	n/a
44	chr8:9106953-9107003	HepG2	liver:	n/a
45	chr8:9123484-9123534	AG04450	lung:	fetal
46	chr8:9106953-9107003	Hela-S3	cervix:	n/a
47	chr8:9123484-9123534	GM12891	blood:	n/a
48	chr8:9123484-9123534	NB4	blood:	n/a
49	chr8:9123484-9123534	SAEC	small airway:	n/a
50	chr8:9106953-9107003	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:9090534..9092903-chr8:9095758..9098005,2	MCF-7	breast:
2	chr8:9075405..9078700-chr8:9080220..9082269,4	K562	blood:
3	chr8:9094088..9097084-chr8:9119791..9121846,2	K562	blood:
4	chr8:9094088..9097084-chr8:9119791..9121846,2	K562	blood:
5	chr8:9095921..9098459-chr8:9104554..9106558,2	K562	blood:
6	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
7	chr8:9069999..9071504-chr8:9082002..9084260,2	K562	blood:
8	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:
9	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
10	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
11	chr8:9095921..9098459-chr8:9104554..9106558,2	K562	blood:
12	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:
13	chr8:9090534..9092903-chr8:9095758..9098005,2	MCF-7	breast:
14	chr8:9121493..9123437-chr8:9133381..9135913,2	K562	blood:
15	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
16	chr8:9056772..9059082-chr8:9087003..9089013,2	K562	blood:
17	chr8:9098947..9101284-chr8:9104230..9106988,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999
2	lnc-RP11-10A14.4.1-6	chr8:9093844-9093911	l_3543_chr8:9084119-9097777_placenta
3	lnc-RP11-10A14.4.1-6	chr8:9088317-9088952	l_3543_chr8:9084119-9097777_placenta
4	lnc-PPP1R3B-2	chr8:9112859-9113012	ENSG00000253887
5	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999
6	lnc-PPP1R3B-2	chr8:9112315-9112398	XLOC_006999
7	lnc-PPP1R3B-2	chr8:9117538-9117788	XLOC_006999
8	lnc-RP11-10A14.4.1-6	chr8:9097312-9097798	l_3543_chr8:9084119-9097777_placenta
9	lnc-RP11-10A14.4.1-6	chr8:9084120-9084517	l_3543_chr8:9084119-9097777_placenta
10	lnc-PPP1R3B-2	chr8:9117538-9117805	ENSG00000253887
11	lnc-PPP1R3B-2	chr8:9115957-9116369	XLOC_006999
12	lnc-RP11-10A14.4.1-5	chr8:9090523-9090959	NONHSAT124932
13	lnc-PPP1R3B-2	chr8:9112893-9113012	XLOC_006999

No data

Variant related genes	Relation type
ENSG00000254091	TF binding region
ENSG00000253887	TF binding region
ENSG00000254235	TF binding region
ENSG00000254091	CpG island
ENSG00000253887	CpG island
ENSG00000254235	CpG island
ENSG00000254235	chromatin interactions

Extended variants
information (count: 2631 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:2631 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187127062	chr8:9082047-9082048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574325472	chr8:9082086-9082087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146905497	chr8:9082097-9082098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553559006	chr8:9082118-9082119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139306638	chr8:9082125-9082126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554553144	chr8:9082141-9082142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1809431	chr8:9082159-9082160	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs564762343	chr8:9082185-9082186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575154949	chr8:9082196-9082197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543947999	chr8:9082201-9082202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542659484	chr8:9082203-9082204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560638315	chr8:9082248-9082249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2929457	chr8:9082249-9082250	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs540061607	chr8:9082263-9082264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375399592	chr8:9082270-9082271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552097934	chr8:9082282-9082283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559882383	chr8:9082283-9082284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532340954	chr8:9082285-9082286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552427806	chr8:9082288-9082289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76964847	chr8:9082329-9082330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192406165	chr8:9082359-9082360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550954226	chr8:9082361-9082362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141797304	chr8:9082376-9082377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536714577	chr8:9082397-9082398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10536977	chr8:9082400-9082401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370079845	chr8:9082402-9082403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553618549	chr8:9082447-9082448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371165891	chr8:9082480-9082481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567037941	chr8:9082531-9082532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538991934	chr8:9082542-9082543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11787450	chr8:9082575-9082576	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs575168966	chr8:9082611-9082612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374962747	chr8:9082623-9082624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543811920	chr8:9082625-9082626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138235710	chr8:9082649-9082650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574210751	chr8:9082671-9082672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539926702	chr8:9082692-9082693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183021170	chr8:9082724-9082725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528107352	chr8:9082750-9082751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187643298	chr8:9082783-9082784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532335197	chr8:9082830-9082831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545819170	chr8:9082840-9082841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562811713	chr8:9082855-9082856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531591078	chr8:9082878-9082879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149585315	chr8:9082880-9082881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567628909	chr8:9082910-9082911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530251670	chr8:9082914-9082915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560859693	chr8:9082964-9082965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553945482	chr8:9082965-9082966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2929312	chr8:9082973-9082974	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9064800-9082400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:9077800-9082200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr8:9078000-9082200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr8:9078000-9082200	Weak transcription	Brain Substantia Nigra	brain
5	chr8:9079200-9088000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr8:9080800-9084000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:9081000-9083200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:9081000-9083400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:9081000-9083600	Enhancers	HMEC	breast
10	chr8:9081000-9085400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:9081200-9084000	Enhancers	Aorta	Aorta
12	chr8:9081200-9084400	Enhancers	Osteobl	bone
13	chr8:9081400-9084200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:9081600-9083000	Enhancers	Brain Angular Gyrus	brain
15	chr8:9081600-9083400	Enhancers	NHEK	skin
16	chr8:9081800-9082200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:9081800-9083400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr8:9082000-9083000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:9082000-9083000	Enhancers	Brain Hippocampus Middle	brain
20	chr8:9082000-9083400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:9082200-9082600	Enhancers	Placenta Amnion	Placenta Amnion
22	chr8:9082200-9082800	Enhancers	Brain Cingulate Gyrus	brain
23	chr8:9082200-9082800	Enhancers	Brain Substantia Nigra	brain
24	chr8:9082200-9083000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:9082200-9083000	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr8:9082400-9083000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr8:9082400-9083200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr8:9082600-9083000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr8:9082600-9083400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:9082800-9088000	Weak transcription	Brain Substantia Nigra	brain
31	chr8:9082800-9088600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr8:9083000-9087800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:9083000-9087800	Weak transcription	Brain Hippocampus Middle	brain
34	chr8:9083000-9087800	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr8:9083200-9087200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:9083200-9090200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:9084000-9084200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:9084000-9084400	Weak transcription	Aorta	Aorta
39	chr8:9084200-9084400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:9084400-9084600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:9084400-9084600	Flanking Active TSS	Osteobl	bone
42	chr8:9084400-9085000	Enhancers	Aorta	Aorta
43	chr8:9084600-9085000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:9085000-9088000	Weak transcription	Aorta	Aorta
45	chr8:9085400-9085600	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr8:9085400-9086200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:9086400-9086600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:9087000-9088000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr8:9087000-9088200	Enhancers	Fetal Brain Male	brain
50	chr8:9087200-9088000	Enhancers	Cortex derived primary cultured neurospheres	brain

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