Variant report

Variant	esv1792231
Chromosome Location	chr8:11278307-11289053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:11282883-11283890	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr8:11279080-11280560	GM12878	blood:	n/a	n/a
3	ATF2	chr8:11279079-11280817	GM12878	blood:	n/a	n/a
4	BACH1	chr8:11281249-11281559	K562	blood:	n/a	n/a
5	BACH1	chr8:11281229-11281554	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:11279101-11279992	GM12878	blood:	n/a	n/a
7	BATF	chr8:11279150-11279899	GM12878	blood:	n/a	n/a
8	BATF	chr8:11280097-11280511	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:11279119-11279958	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:11280048-11280701	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:11279109-11279944	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:11280161-11280728	GM12878	blood:	n/a	n/a
13	BCL3	chr8:11280032-11280582	GM12878	blood:	n/a	n/a
14	BCLAF1	chr8:11279615-11280536	GM12878	blood:	n/a	n/a
15	BCLAF1	chr8:11279067-11279641	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:11279822-11280598	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:11287799-11288033	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:11279178-11280689	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:11281273-11281628	K562	blood:	n/a	n/a
20	BHLHE40	chr8:11286896-11287078	K562	blood:	n/a	chr8:11286996-11287012
21	BHLHE40	chr8:11281293-11281538	GM12878	blood:	n/a	n/a
22	CEBPB	chr8:11287865-11288155	IMR90	lung:	n/a	chr8:11287992-11288003
23	CEBPB	chr8:11279034-11280613	GM12878	blood:	n/a	chr8:11279092-11279103
24	CEBPB	chr8:11284263-11284540	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:11286825-11287230	MCF-7	breast:	n/a	n/a
26	CEBPB	chr8:11287864-11288143	A549	lung:	n/a	chr8:11287992-11288003
27	CEBPB	chr8:11287895-11288143	K562	blood:	n/a	chr8:11287992-11288003
28	CEBPB	chr8:11287821-11288135	HepG2	liver:	n/a	chr8:11287992-11288003
29	CEBPB	chr8:11286850-11287152	HepG2	liver:	n/a	n/a
30	CEBPB	chr8:11279064-11279464	IMR90	lung:	n/a	chr8:11279092-11279103
31	CEBPB	chr8:11279065-11279237	HepG2	liver:	n/a	chr8:11279092-11279103
32	CEBPB	chr8:11282717-11283251	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr8:11286925-11287140	K562	blood:	n/a	n/a
34	CEBPB	chr8:11286897-11287122	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr8:11279768-11280377	GM12878	blood:	n/a	n/a
36	CHD1	chr8:11279137-11279566	GM12878	blood:	n/a	n/a
37	CHD1	chr8:11286431-11286565	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr8:11283943-11284143	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr8:11287781-11287943	GM12878	blood:	n/a	n/a
40	CHD2	chr8:11282936-11283379	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr8:11279153-11280751	GM12878	blood:	n/a	n/a
42	CTCF	chr8:11286840-11286990	HMF	breast:	n/a	chr8:11286974-11286983 chr8:11286968-11286986 chr8:11286970-11286983 chr8:11286973-11286986
43	CTCF	chr8:11286916-11287068	HepG2	liver:	n/a	chr8:11286974-11286983 chr8:11286968-11286986 chr8:11286970-11286983 chr8:11286973-11286986
44	CTCF	chr8:11280920-11281070	K562	blood:	n/a	n/a
45	CTCF	chr8:11287480-11287630	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr8:11286900-11287050	SK-N-SH_RA	brain:	n/a	chr8:11286974-11286983 chr8:11286968-11286986 chr8:11286970-11286983 chr8:11286973-11286986
47	CTCF	chr8:11280940-11281090	BJ	skin:	n/a	n/a
48	CTCF	chr8:11286851-11287133	MCF-7	breast:	n/a	chr8:11286974-11286983 chr8:11286968-11286986 chr8:11286970-11286983 chr8:11286973-11286986
49	CTCF	chr8:11286880-11287030	HEEpiC	esophagus:	n/a	chr8:11286974-11286983 chr8:11286968-11286986 chr8:11286970-11286983 chr8:11286973-11286986
50	CTCF	chr8:11286785-11287187	HepG2	liver:	n/a	chr8:11286974-11286983 chr8:11286968-11286986 chr8:11286970-11286983 chr8:11286973-11286986

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11279352-11279402	ProgFib	skin:	n/a
2	chr8:11279352-11279402	GM12892	blood:	n/a
3	chr8:11279352-11279402	AG04449	skin:	fetal
4	chr8:11284912-11284962	Caco-2	colon:	n/a
5	chr8:11287657-11287707	NH-A	brain:	n/a
6	chr8:11283299-11283349	ovcar-3	ovarian:	n/a
7	chr8:11279352-11279402	LNCaP	prostate:	n/a
8	chr8:11284912-11284962	HCM	heart:	n/a
9	chr8:11283299-11283349	HepG2	liver:	n/a
10	chr8:11284912-11284962	HUVEC	blood vessel:	n/a
11	chr8:11279352-11279402	HL-60	blood:	n/a
12	chr8:11283299-11283349	PrEC	prostate:	n/a
13	chr8:11287657-11287707	HCF	heart:	n/a
14	chr8:11283299-11283349	HNPCEpiC	eye:	n/a
15	chr8:11283299-11283349	SK-N-SH_RA	brain:	n/a
16	chr8:11287657-11287707	HNPCEpiC	eye:	n/a
17	chr8:11287657-11287707	AG04449	skin:	fetal
18	chr8:11284912-11284962	GM12892	blood:	n/a
19	chr8:11283299-11283349	HEK293	kidney:	embryo
20	chr8:11287657-11287707	MCF-7	breast:	n/a
21	chr8:11283299-11283349	HRPEpiC	eye:	n/a
22	chr8:11283299-11283349	Hepatocyte	liver:	n/a
23	chr8:11287657-11287707	PrEC	prostate:	n/a
24	chr8:11283299-11283349	Caco-2	colon:	n/a
25	chr8:11283299-11283349	IMR90	lung:	fetal
26	chr8:11284912-11284962	SK-N-SH	brain:	n/a
27	chr8:11283299-11283349	HRE	kidney:	n/a
28	chr8:11279352-11279402	GM19239	blood:	n/a
29	chr8:11283299-11283349	MCF-7	breast:	n/a
30	chr8:11284912-11284962	Hela-S3	cervix:	n/a
31	chr8:11283299-11283349	HEEpiC	esophagus:	n/a
32	chr8:11284912-11284962	ECC-1	luminal epithelium:	n/a
33	chr8:11287657-11287707	U87	brain:	n/a
34	chr8:11283299-11283349	AG09309	skin:	n/a
35	chr8:11279352-11279402	AG09309	skin:	n/a
36	chr8:11287657-11287707	SK-N-SH_RA	brain:	n/a
37	chr8:11283299-11283349	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:11279352-11279402	NT2-D1	testis:	n/a
39	chr8:11279352-11279402	HAEpiC	amniotic membrane:	n/a
40	chr8:11284912-11284962	SKMC	muscle:	n/a
41	chr8:11287657-11287707	AG10803	skin:	n/a
42	chr8:11283299-11283349	HRCEpiC	kidney:	n/a
43	chr8:11283299-11283349	H1-hESC	embryonic stem cell:	embryo
44	chr8:11284912-11284962	GM12878	blood:	n/a
45	chr8:11283299-11283349	RPTEC	kidney:	n/a
46	chr8:11284912-11284962	CMK	blood:	n/a
47	chr8:11279352-11279402	Jurkat	blood:	n/a
48	chr8:11284912-11284962	SAEC	small airway:	n/a
49	chr8:11279352-11279402	RPTEC	kidney:	n/a
50	chr8:11284912-11284962	GM12891	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11271338..11271849-chr8:11286552..11287065,2	MCF-7	breast:
2	chr8:11278797..11280380-chr8:11316966..11319071,2	K562	blood:
3	chr8:11280386..11282841-chr8:11298445..11301046,2	MCF-7	breast:
4	chr8:11277465..11279000-chr8:11280296..11282136,2	K562	blood:
5	chr8:11286965..11287640-chr8:11410754..11411417,2	MCF-7	breast:
6	chr8:11204194..11206548-chr8:11284736..11287319,2	K562	blood:
7	chr8:11269226..11269868-chr8:11286430..11287417,2	K562	blood:
8	chr8:11277465..11279000-chr8:11280296..11282136,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLK-2	chr8:11279007-11280419	NONHSAT125057
2	lnc-BLK-2	chr8:11280428-11280443	NONHSAT125057
3	lnc-C8orf12-1	chr8:11278732-11278920	ucscGeneNc_uc003wtu_2

No data

Variant related genes	Relation type
C8orf12	TF binding region
C8orf12	CpG island
ENSG00000154316	chromatin interactions
ENSG00000255020	chromatin interactions

Extended variants
information (count: 689 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60580857	chr8:11278319-11278320	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567393373	chr8:11278320-11278321	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs537538932	chr8:11278350-11278351	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs545111935	chr8:11278360-11278361	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs549975259	chr8:11278368-11278369	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs571338119	chr8:11278383-11278384	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs538412302	chr8:11278391-11278392	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs74604441	chr8:11278392-11278393	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs571963705	chr8:11278397-11278398	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs536256800	chr8:11278421-11278422	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34392268	chr8:11278430-11278431	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139319143	chr8:11278431-11278432	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150030551	chr8:11278455-11278456	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185702163	chr8:11278456-11278457	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565511068	chr8:11278460-11278461	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147729469	chr8:11278478-11278479	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558093251	chr8:11278487-11278488	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541589706	chr8:11278528-11278529	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34906655	chr8:11278541-11278542	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs141016229	chr8:11278542-11278543	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190377217	chr8:11278608-11278609	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560699142	chr8:11278609-11278610	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117197686	chr8:11278639-11278640	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561462228	chr8:11278709-11278710	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549625092	chr8:11278714-11278715	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144875891	chr8:11278735-11278736	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs538449450	chr8:11278738-11278739	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs547149343	chr8:11278804-11278805	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs76880474	chr8:11278866-11278867	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs377301879	chr8:11278896-11278897	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs144383592	chr8:11278898-11278899	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs139632135	chr8:11278899-11278900	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs111590610	chr8:11278907-11278908	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs564367536	chr8:11278927-11278928	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs200997640	chr8:11278934-11278935	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs550081018	chr8:11278940-11278941	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs151294142	chr8:11278984-11278985	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs192267276	chr8:11278998-11278999	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs536140043	chr8:11279017-11279018	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs554978519	chr8:11279030-11279031	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs570280545	chr8:11279084-11279085	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs184286437	chr8:11279088-11279089	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs537421526	chr8:11279125-11279126	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs79575216	chr8:11279164-11279165	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs73663131	chr8:11279221-11279222	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs541684321	chr8:11279237-11279238	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs199711571	chr8:11279239-11279240	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs553599764	chr8:11279241-11279242	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs201709124	chr8:11279242-11279243	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs188664822	chr8:11279255-11279256	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

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
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
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
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11269400-11287400	Weak transcription	Right Atrium	heart
2	chr8:11269800-11279800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr8:11270000-11279200	Weak transcription	Brain Anterior Caudate	brain
4	chr8:11271600-11291000	Weak transcription	Pancreas	Pancrea
5	chr8:11273000-11286800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:11273000-11287000	Weak transcription	NHEK	skin
7	chr8:11273200-11279200	Weak transcription	HSMM	muscle
8	chr8:11274000-11281600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr8:11274600-11279800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:11274600-11281600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:11275600-11282200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:11275800-11280400	Weak transcription	Brain Hippocampus Middle	brain
13	chr8:11275800-11280600	Enhancers	Primary B cells from cord blood	blood
14	chr8:11275800-11281400	Enhancers	Primary B cells from peripheral blood	blood
15	chr8:11276200-11279000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr8:11276200-11279000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:11276200-11279000	Weak transcription	Osteobl	bone
18	chr8:11276200-11279200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr8:11276200-11279400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr8:11276200-11279400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr8:11276200-11279400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr8:11276200-11280200	Weak transcription	Spleen	Spleen
23	chr8:11276200-11280600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:11276200-11280600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr8:11276400-11279000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr8:11276400-11279200	Weak transcription	Thymus	Thymus
27	chr8:11276400-11280000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr8:11276600-11280200	Weak transcription	Brain Substantia Nigra	brain
29	chr8:11276600-11280600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr8:11276600-11281200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr8:11276600-11291200	Weak transcription	Gastric	stomach
32	chr8:11276800-11279200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr8:11277400-11279000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:11277600-11278400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:11277600-11287000	Enhancers	Fetal Thymus	thymus
36	chr8:11278000-11278400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:11278200-11278400	Flanking Active TSS	GM12878-XiMat	blood
38	chr8:11278200-11280000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:11278400-11278800	Enhancers	GM12878-XiMat	blood
40	chr8:11278400-11279200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:11278400-11280200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr8:11278600-11278800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr8:11278800-11280600	Flanking Active TSS	GM12878-XiMat	blood
44	chr8:11279000-11280400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr8:11279000-11280600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:11279000-11280600	Enhancers	Osteobl	bone
47	chr8:11279000-11280800	Enhancers	Primary T cells fromperipheralblood	blood
48	chr8:11279000-11281000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr8:11279000-11281400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr8:11279000-11281600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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