Variant report

Variant	nsv1034184
Chromosome Location	chr8:112171949-112274721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:112248761-112248765	HepG2	liver:	n/a	n/a
2	ATF1	chr8:112198523-112198679	K562	blood:	n/a	n/a
3	ATF3	chr8:112248536-112248872	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:112212038-112212250	H1-hESC	embryonic stem cell:	n/a	chr8:112212195-112212209
5	CEBPB	chr8:112258723-112258923	HepG2	liver:	n/a	chr8:112258822-112258833
6	CEBPB	chr8:112181017-112181272	HepG2	liver:	n/a	chr8:112181166-112181177
7	CEBPB	chr8:112199716-112199940	A549	lung:	n/a	n/a
8	CEBPB	chr8:112199683-112200014	HepG2	liver:	n/a	n/a
9	CHD1	chr8:112261182-112261249	GM12878	blood:	n/a	n/a
10	CREB1	chr8:112248270-112248900	H1-hESC	embryonic stem cell:	n/a	n/a
11	CREB1	chr8:112248335-112248802	GM12878	blood:	n/a	n/a
12	CREB1	chr8:112248357-112248847	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:112248644-112248833	GM19239	blood:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
14	CTCF	chr8:112265460-112265610	HepG2	liver:	n/a	n/a
15	CTCF	chr8:112248613-112248863	A549	lung:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
16	CTCF	chr8:112265420-112265570	GM12867	blood:	n/a	n/a
17	CTCF	chr8:112265480-112265630	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr8:112265460-112265610	GM12872	blood:	n/a	n/a
19	CTCF	chr8:112248645-112248844	A549	lung:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
20	CTCF	chr8:112265414-112265418	A549	lung:	n/a	n/a
21	CTCF	chr8:112248680-112248830	HUVEC	blood vessel:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
22	CTCF	chr8:112265483-112265629	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr8:112248660-112248810	GM12868	blood:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
24	CTCF	chr8:112248700-112248850	GM06990	blood:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
25	CTCF	chr8:112248680-112248830	GM06990	blood:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
26	CTCF	chr8:112248640-112248790	BE2_C	brain:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
27	CTCF	chr8:112265521-112265631	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr8:112265200-112265350	GM12878	blood:	n/a	n/a
29	CTCF	chr8:112248640-112248790	GM12867	blood:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
30	CTCF	chr8:112248760-112248910	HAc	cerebellar:	n/a	n/a
31	CTCF	chr8:112248660-112248810	SAEC	small airway:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
32	CTCF	chr8:112265433-112265676	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr8:112248640-112248790	SK-N-SH_RA	brain:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
34	CTCF	chr8:112248593-112248892	MCF-7	breast:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
35	CTCF	chr8:112202100-112202250	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr8:112265361-112265712	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:112265501-112265623	ProgFib	skin:	n/a	n/a
38	CTCF	chr8:112265480-112265630	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr8:112248609-112248841	A549	lung:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
40	CTCF	chr8:112265500-112265650	HMEC	breast:	n/a	n/a
41	CTCF	chr8:112248640-112248790	K562	blood:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
42	CTCF	chr8:112265520-112265670	GM12866	blood:	n/a	n/a
43	CTCF	chr8:112265520-112265670	HepG2	liver:	n/a	n/a
44	CTCF	chr8:112248454-112249079	MCF-7	breast:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
45	CTCF	chr8:112265500-112265650	HAc	cerebellar:	n/a	n/a
46	CTCF	chr8:112248700-112248850	GM12871	blood:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
47	CTCF	chr8:112248500-112248979	A549	lung:	n/a	chr8:112248720-112248738 chr8:112248721-112248737 chr8:112248715-112248736
48	CTCF	chr8:112265500-112265650	HPF	lung:	n/a	n/a
49	CTCF	chr8:112265440-112265590	BE2_C	brain:	n/a	n/a
50	CTCF	chr8:112265419-112265660	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112241152-112241202	PrEC	prostate:	n/a
2	chr8:112241152-112241202	BE2_C	brain:	n/a
3	chr8:112241152-112241202	GM12878	blood:	n/a
4	chr8:112241152-112241202	HCT-116	colon:	n/a
5	chr8:112241152-112241202	HEEpiC	esophagus:	n/a
6	chr8:112241152-112241202	U87	brain:	n/a
7	chr8:112241152-112241202	CMK	blood:	n/a
8	chr8:112241152-112241202	SK-N-SH_RA	brain:	n/a
9	chr8:112241152-112241202	SK-N-MC	brain:	n/a
10	chr8:112241152-112241202	SK-N-SH	brain:	n/a
11	chr8:112241152-112241202	HRPEpiC	eye:	n/a
12	chr8:112241152-112241202	HCF	heart:	n/a
13	chr8:112241152-112241202	HCM	heart:	n/a
14	chr8:112241152-112241202	Jurkat	blood:	n/a
15	chr8:112241152-112241202	HEK293	kidney:	embryo
16	chr8:112241152-112241202	NH-A	brain:	n/a
17	chr8:112241152-112241202	A549	lung:	n/a
18	chr8:112241152-112241202	BJ	skin:	n/a
19	chr8:112241152-112241202	HRCEpiC	kidney:	n/a
20	chr8:112241152-112241202	MCF10A-Er-Src	breast:	n/a
21	chr8:112241152-112241202	SKMC	muscle:	n/a
22	chr8:112241152-112241202	GM12891	blood:	n/a
23	chr8:112241152-112241202	NHBE	bronchial:	n/a
24	chr8:112241152-112241202	ECC-1	luminal epithelium:	n/a
25	chr8:112241152-112241202	H1-hESC	embryonic stem cell:	embryo
26	chr8:112241152-112241202	NHDF-neo	bronchial:	n/a
27	chr8:112241152-112241202	HUVEC	blood vessel:	n/a
28	chr8:112241152-112241202	AG10803	skin:	n/a
29	chr8:112241152-112241202	HCPEpiC	choroid plexus:	n/a
30	chr8:112241152-112241202	HIPEpiC	eye:	n/a
31	chr8:112241152-112241202	HNPCEpiC	eye:	n/a
32	chr8:112241152-112241202	Caco-2	colon:	n/a
33	chr8:112241152-112241202	AG04450	lung:	fetal
34	chr8:112241152-112241202	LNCaP	prostate:	n/a
35	chr8:112241152-112241202	NB4	blood:	n/a
36	chr8:112241152-112241202	HAEpiC	amniotic membrane:	n/a
37	chr8:112241152-112241202	MCF-7	breast:	n/a
38	chr8:112241152-112241202	AG09309	skin:	n/a
39	chr8:112241152-112241202	PFSK-1	brain:	n/a
40	chr8:112241152-112241202	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:112241152-112241202	ProgFib	skin:	n/a
42	chr8:112241152-112241202	IMR90	lung:	fetal
43	chr8:112241152-112241202	GM06990	blood:	n/a
44	chr8:112241152-112241202	Hepatocyte	liver:	n/a
45	chr8:112241152-112241202	RPTEC	kidney:	n/a
46	chr8:112241152-112241202	HRE	kidney:	n/a
47	chr8:112241152-112241202	PANC-1	pancreas:	n/a
48	chr8:112241152-112241202	T-47D	breast:	n/a
49	chr8:112241152-112241202	AG09319	gingival:	n/a
50	chr8:112241152-112241202	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:112210861..112213766-chr8:112215369..112218286,2	K562	blood:
2	chr8:112248673..112250469-chr8:112250523..112252555,2	MCF-7	breast:
3	chr10:29693543..29694543-chr8:112266333..112267300,2	MCF-7	breast:
4	chr8:112259923..112262323-chr8:112263015..112264906,2	MCF-7	breast:
5	chr8:112151809..112153959-chr8:112263594..112266459,2	MCF-7	breast:
6	chr8:112152351..112153276-chr8:112265083..112266006,7	MCF-7	breast:
7	chr8:112248686..112249491-chr8:121617700..121618578,2	MCF-7	breast:
8	chr8:112188112..112190074-chr8:112196600..112198573,2	MCF-7	breast:
9	chr8:112248482..112249338-chr8:112258709..112259294,2	MCF-7	breast:
10	chr18:8609099..8610030-chr8:112248746..112249278,2	MCF-7	breast:
11	chr8:112259923..112262323-chr8:112263015..112264906,2	MCF-7	breast:
12	chr8:112166075..112166697-chr8:112248498..112249074,2	MCF-7	breast:
13	chr8:112236646..112239477-chr8:112249908..112252085,2	MCF-7	breast:
14	chr8:112210861..112213766-chr8:112215369..112218286,2	K562	blood:
15	chr8:112248673..112250469-chr8:112250523..112252555,2	MCF-7	breast:
16	chr8:112272027..112273897-chr8:112273989..112275604,2	MCF-7	breast:
17	chr8:112112298..112113981-chr8:112264995..112266040,10	MCF-7	breast:
18	chr8:112248330..112249162-chr8:112265189..112266065,4	MCF-7	breast:
19	chr8:112248126..112249546-chr8:112265121..112265983,10	MCF-7	breast:
20	chr8:112188112..112190074-chr8:112196600..112198573,2	MCF-7	breast:
21	chr8:112272027..112273897-chr8:112273989..112275604,2	MCF-7	breast:
22	chr8:111846862..111847654-chr8:112265014..112265719,2	MCF-7	breast:
23	chr8:111993072..111993615-chr8:112265097..112265675,2	MCF-7	breast:
24	chr8:112164287..112166378-chr8:112180703..112183075,2	MCF-7	breast:
25	chr8:112248509..112249151-chr8:121951139..121951901,3	MCF-7	breast:
26	chr8:112152279..112153172-chr8:112264812..112266234,7	MCF-7	breast:
27	chr8:112270984..112273845-chr8:112278205..112279805,2	MCF-7	breast:
28	chr8:112248482..112249338-chr8:112258709..112259294,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-8	chr8:112237814-112238443	NONHSAT128324
2	lnc-CSMD3-3	chr8:112248311-112248432	ENSG00000253103
3	lnc-CSMD3-3	chr8:112195521-112195964	ENSG00000253103
4	lnc-CSMD3-3	chr8:112248311-112248400	ENSG00000253103
5	lnc-CSMD3-2	chr8:112191422-112191587	ENSG00000253489
6	lnc-RP11-422N16.3.1-7	chr8:112174769-112174905	l_3668_chr8:112174768-112194925_testes
7	lnc-CSMD3-2	chr8:112192077-112192101	ENSG00000253489
8	lnc-RP11-422N16.3.1-8	chr8:112239194-112239278	NONHSAT128324
9	lnc-RP11-422N16.3.1-7	chr8:112194839-112194925	l_3668_chr8:112174768-112194925_testes

No data

Variant related genes	Relation type
ENSG00000253489	TF binding region
ENSG00000253103	TF binding region
EEF1A1P37	TF binding region
ENSG00000253489	CpG island
ENSG00000253103	CpG island
EEF1A1P37	CpG island
ENSG00000253103	chromatin interactions
ENSG00000254124	chromatin interactions
ENSG00000206418	chromatin interactions

Extended variants
information (count: 1361 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2433665	chr8:112174819-112174820	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550484616	chr8:112174854-112174855	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs549553006	chr8:112174855-112174856	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs574900258	chr8:112179010-112179011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146930605	chr8:112179020-112179021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560743637	chr8:112179035-112179036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185189057	chr8:112179046-112179047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545809612	chr8:112179081-112179082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189106949	chr8:112179089-112179090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7006174	chr8:112179121-112179122	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs547938236	chr8:112179126-112179127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6986008	chr8:112179161-112179162	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138587625	chr8:112179196-112179197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142624211	chr8:112179270-112179271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368313984	chr8:112179329-112179330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143356497	chr8:112179365-112179366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558026839	chr8:112179432-112179433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181564382	chr8:112179452-112179453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117829630	chr8:112179507-112179508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569115954	chr8:112179609-112179610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148356463	chr8:112179617-112179618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141502613	chr8:112179619-112179620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186337204	chr8:112179641-112179642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191884559	chr8:112179671-112179672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554450593	chr8:112179678-112179679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577611223	chr8:112179705-112179706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532868820	chr8:112179726-112179727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35150764	chr8:112179807-112179808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563206424	chr8:112179813-112179814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531174913	chr8:112179835-112179836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182877459	chr8:112179836-112179837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186479728	chr8:112179866-112179867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527423736	chr8:112179900-112179901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374691679	chr8:112179937-112179938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112681277	chr8:112179944-112179945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547185979	chr8:112179954-112179955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190911678	chr8:112179991-112179992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532969225	chr8:112180045-112180046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183323017	chr8:112180099-112180100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569953215	chr8:112180119-112180120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537826494	chr8:112180136-112180137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188034428	chr8:112180204-112180205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568560516	chr8:112180240-112180241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534339230	chr8:112180247-112180248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554313815	chr8:112180286-112180287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577475103	chr8:112180330-112180331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540039688	chr8:112180352-112180353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556551570	chr8:112180433-112180434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73703807	chr8:112180535-112180536	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs541446316	chr8:112180592-112180593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112179000-112179600	Enhancers	Fetal Brain Male	brain
2	chr8:112179400-112179800	Enhancers	Fetal Brain Female	brain
3	chr8:112179600-112181200	Weak transcription	Fetal Brain Male	brain
4	chr8:112179800-112180200	Weak transcription	Fetal Brain Female	brain
5	chr8:112180000-112180400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:112180200-112180800	Enhancers	Fetal Brain Female	brain
7	chr8:112180400-112183400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:112181200-112181600	Enhancers	Fetal Brain Male	brain
9	chr8:112183200-112183600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:112183400-112183800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:112200000-112201000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:112200600-112200800	Enhancers	HSMM	muscle
13	chr8:112200600-112201200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr8:112200600-112201400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:112200600-112201600	Enhancers	NH-A	brain
16	chr8:112200600-112201800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr8:112200600-112202000	Enhancers	HMEC	breast
18	chr8:112200600-112202000	Enhancers	HSMMtube	muscle
19	chr8:112200600-112202200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr8:112200800-112201800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:112201000-112201400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:112201200-112201400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:112201200-112201600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr8:112201200-112202000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr8:112201400-112201600	Enhancers	HSMM	muscle
26	chr8:112201400-112206400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:112202000-112202200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:112202000-112202800	Weak transcription	HSMMtube	muscle
29	chr8:112202800-112203000	Enhancers	HSMMtube	muscle
30	chr8:112206400-112206800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:112207400-112208200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:112210800-112211000	Enhancers	Fetal Brain Male	brain
33	chr8:112211800-112212400	Enhancers	Muscle Satellite Cultured Cells	--
34	chr8:112212000-112213400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr8:112212200-112212800	Enhancers	HMEC	breast
36	chr8:112212600-112213000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:112212600-112213000	Enhancers	Fetal Brain Male	brain
38	chr8:112223000-112224400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:112223800-112224000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:112223800-112224200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:112223800-112224400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr8:112223800-112224600	Enhancers	HMEC	breast
43	chr8:112224000-112225200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr8:112224400-112224800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr8:112224600-112224800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:112224800-112225400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:112230800-112231400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:112230800-112231600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:112231200-112231600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:112231200-112231600	Enhancers	HUES48 Cell Line	embryonic stem cell

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