Variant report

Variant	nsv539678
Chromosome Location	chr8:95197036-95225644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:306)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 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	ATF1	chr8:95218407-95218446	K562	blood:	n/a	n/a
2	BCL11A	chr8:95221856-95222050	GM12878	blood:	n/a	chr8:95222039-95222048
3	BHLHE40	chr8:95221813-95222111	GM12878	blood:	n/a	n/a
4	CBX3	chr8:95210615-95211285	HCT-116	colon:	n/a	n/a
5	CEBPB	chr8:95211432-95211741	HepG2	liver:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
6	CEBPB	chr8:95218255-95218560	K562	blood:	n/a	n/a
7	CEBPB	chr8:95210377-95211262	A549	lung:	n/a	n/a
8	CEBPB	chr8:95218105-95219430	HCT-116	colon:	n/a	chr8:95218564-95218576
9	CEBPB	chr8:95215789-95215920	K562	blood:	n/a	chr8:95215842-95215853
10	CEBPB	chr8:95218787-95219031	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:95218254-95218537	A549	lung:	n/a	n/a
12	CEBPB	chr8:95211452-95211703	IMR90	lung:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
13	CEBPB	chr8:95219343-95219704	A549	lung:	n/a	n/a
14	CEBPB	chr8:95217372-95217655	IMR90	lung:	n/a	chr8:95217525-95217536 chr8:95217522-95217539
15	CEBPB	chr8:95209598-95209888	HepG2	liver:	n/a	chr8:95209752-95209763 chr8:95209750-95209761
16	CEBPB	chr8:95215809-95216001	HepG2	liver:	n/a	chr8:95215842-95215853
17	CEBPB	chr8:95209585-95209785	IMR90	lung:	n/a	chr8:95209752-95209763 chr8:95209750-95209761
18	CEBPB	chr8:95210794-95211093	A549	lung:	n/a	n/a
19	CEBPB	chr8:95217366-95217645	HepG2	liver:	n/a	chr8:95217525-95217536 chr8:95217522-95217539
20	CEBPB	chr8:95219338-95219696	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:95218147-95219200	HCT-116	colon:	n/a	chr8:95218564-95218576
22	CEBPB	chr8:95211554-95211626	K562	blood:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
23	CEBPB	chr8:95215723-95215969	Hela-S3	cervix:	n/a	chr8:95215842-95215853
24	CEBPB	chr8:95218272-95218526	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr8:95221848-95222048	GM12878	blood:	n/a	n/a
26	CTCF	chr8:95218420-95218570	HPAF	blood vessel:	n/a	chr8:95218433-95218442
27	CTCF	chr8:95218360-95218510	GM12875	blood:	n/a	chr8:95218433-95218442
28	CTCF	chr8:95218460-95218610	GM12871	blood:	n/a	n/a
29	CTCF	chr8:95218320-95218470	K562	blood:	n/a	chr8:95218433-95218442
30	CTCF	chr8:95199879-95200081	A549	lung:	n/a	n/a
31	CTCF	chr8:95199908-95200056	NHEK	skin:	n/a	n/a
32	CTCF	chr8:95218020-95218170	GM06990	blood:	n/a	n/a
33	CTCF	chr8:95218180-95218330	AG09309	skin:	n/a	n/a
34	CTCF	chr8:95218360-95218510	AG09309	skin:	n/a	chr8:95218433-95218442
35	CTCF	chr8:95218671-95218757	K562	blood:	n/a	n/a
36	CTCF	chr8:95218520-95218670	HAc	cerebellar:	n/a	n/a
37	CTCF	chr8:95218696-95218729	GM12892	blood:	n/a	n/a
38	CTCF	chr8:95218640-95218790	K562	blood:	n/a	n/a
39	CTCF	chr8:95218322-95218541	K562	blood:	n/a	chr8:95218433-95218442
40	CTCF	chr8:95218340-95218490	GM12878	blood:	n/a	chr8:95218433-95218442
41	CTCF	chr8:95218220-95218370	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr8:95218980-95219130	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr8:95218280-95218430	HAc	cerebellar:	n/a	n/a
44	CTCF	chr8:95218380-95218530	HBMEC	blood vessel:	n/a	chr8:95218433-95218442
45	CTCF	chr8:95200080-95200230	A549	lung:	n/a	n/a
46	CTCF	chr8:95218600-95218750	AG09309	skin:	n/a	n/a
47	CTCF	chr8:95199860-95200010	A549	lung:	n/a	n/a
48	CTCF	chr8:95218380-95218530	SAEC	small airway:	n/a	chr8:95218433-95218442
49	CTCF	chr8:95218720-95218870	A549	lung:	n/a	n/a
50	CTCF	chr8:95199900-95200050	GM12875	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95221197-95221247	RPTEC	kidney:	n/a
2	chr8:95221197-95221247	RPTEC	kidney:	n/a
3	chr8:95221342-95221392	PrEC	prostate:	n/a
4	chr8:95221342-95221392	GM06990	blood:	n/a
5	chr8:95221197-95221247	NH-A	brain:	n/a
6	chr8:95221342-95221392	CMK	blood:	n/a
7	chr8:95220779-95220829	HRCEpiC	kidney:	n/a
8	chr8:95221342-95221392	HAEpiC	amniotic membrane:	n/a
9	chr8:95221197-95221247	HAEpiC	amniotic membrane:	n/a
10	chr8:95220779-95220829	HRE	kidney:	n/a
11	chr8:95220583-95220633	CMK	blood:	n/a
12	chr8:95220583-95220633	U87	brain:	n/a
13	chr8:95222020-95222070	HCT-116	colon:	n/a
14	chr8:95221197-95221247	Hela-S3	cervix:	n/a
15	chr8:95220583-95220633	T-47D	breast:	n/a
16	chr8:95220583-95220633	H1-hESC	embryonic stem cell:	embryo
17	chr8:95221197-95221247	HRPEpiC	eye:	n/a
18	chr8:95220583-95220633	HRCEpiC	kidney:	n/a
19	chr8:95222020-95222070	MCF10A-Er-Src	breast:	n/a
20	chr8:95220583-95220633	HEK293	kidney:	embryo
21	chr8:95222020-95222070	AG09309	skin:	n/a
22	chr8:95220583-95220633	BE2_C	brain:	n/a
23	chr8:95221197-95221247	HRCEpiC	kidney:	n/a
24	chr8:95221197-95221247	SK-N-SH	brain:	n/a
25	chr8:95220779-95220829	SKMC	muscle:	n/a
26	chr8:95220583-95220633	SK-N-SH_RA	brain:	n/a
27	chr8:95221342-95221392	HMEC	breast:	n/a
28	chr8:95222020-95222070	IMR90	lung:	fetal
29	chr8:95220583-95220633	Hela-S3	cervix:	n/a
30	chr8:95222020-95222070	GM12891	blood:	n/a
31	chr8:95222020-95222070	AG09319	gingival:	n/a
32	chr8:95221342-95221392	K562	blood:	n/a
33	chr8:95220779-95220829	BE2_C	brain:	n/a
34	chr8:95220779-95220829	PFSK-1	brain:	n/a
35	chr8:95221342-95221392	MCF-7	breast:	n/a
36	chr8:95221342-95221392	GM19239	blood:	n/a
37	chr8:95221197-95221247	AG09309	skin:	n/a
38	chr8:95221197-95221247	PANC-1	pancreas:	n/a
39	chr8:95221342-95221392	NB4	blood:	n/a
40	chr8:95221197-95221247	AoSMC	blood vessel:	n/a
41	chr8:95222020-95222070	MCF-7	breast:	n/a
42	chr8:95221197-95221247	AG04450	lung:	fetal
43	chr8:95222020-95222070	CMK	blood:	n/a
44	chr8:95220779-95220829	U87	brain:	n/a
45	chr8:95221197-95221247	NHDF-neo	bronchial:	n/a
46	chr8:95220779-95220829	HNPCEpiC	eye:	n/a
47	chr8:95221197-95221247	GM06990	blood:	n/a
48	chr8:95222020-95222070	HIPEpiC	eye:	n/a
49	chr8:95220583-95220633	PFSK-1	brain:	n/a
50	chr8:95221342-95221392	BE2_C	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95091864..95092388-chr8:95200565..95201228,2	MCF-7	breast:
2	chr8:95181437..95183595-chr8:95195671..95197695,2	MCF-7	breast:
3	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
4	chr8:95201827..95203670-chr8:95208153..95211021,2	MCF-7	breast:
5	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
6	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:
7	chr8:95200777..95202734-chr8:95202948..95204607,2	K562	blood:
8	chr8:95091661..95092727-chr8:95199725..95200487,4	MCF-7	breast:
9	chr8:95217922..95218880-chr8:95369574..95370256,2	MCF-7	breast:
10	chr8:95201827..95203670-chr8:95208153..95211021,2	MCF-7	breast:
11	chr8:95199696..95200396-chr8:95284281..95284998,2	MCF-7	breast:
12	chr8:95006687..95007623-chr8:95199581..95200583,4	MCF-7	breast:
13	chr8:95200401..95202545-chr8:95205826..95207380,2	K562	blood:
14	chr8:95218436..95218963-chr8:95284617..95285220,2	MCF-7	breast:
15	chr8:95104717..95105462-chr8:95199836..95200440,2	MCF-7	breast:
16	chr21:41711010..41712741-chr8:95200062..95201579,2	MCF-7	breast:
17	chr8:94751681..94753437-chr8:95200264..95202250,2	MCF-7	breast:
18	chr8:95200777..95202734-chr8:95202948..95204607,2	K562	blood:
19	chr8:95092028..95092964-chr8:95199448..95200050,4	MCF-7	breast:
20	chr8:95219101..95220726-chr8:95272538..95274563,2	MCF-7	breast:
21	chr8:95200401..95202545-chr8:95205826..95207380,2	K562	blood:
22	chr8:95215544..95217656-chr8:95220305..95222366,3	MCF-7	breast:
23	chr8:95224589..95225412-chr8:95369113..95370095,2	MCF-7	breast:
24	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
25	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
26	chr8:95216472..95218639-chr8:95229347..95231439,2	MCF-7	breast:
27	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GEM-1	chr8:95214141-95214393	NONHSAT127766
2	lnc-GEM-1	chr8:95214701-95215280	NONHSAT127766

No data

Variant related genes	Relation type
CDH17	TF binding region
ENSG00000249510	TF binding region
CDH17	CpG island
ENSG00000249510	CpG island
ENSG00000183808	chromatin interactions
ENSG00000253848	chromatin interactions
ENSG00000079112	chromatin interactions
ENSG00000212998	chromatin interactions
ENSG00000164949	chromatin interactions

Extended variants
information (count: 1130 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543710514	chr8:95197061-95197062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75759452	chr8:95197068-95197069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62526263	chr8:95197126-95197127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531227456	chr8:95197156-95197157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551067452	chr8:95197177-95197178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530844859	chr8:95197189-95197190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369290448	chr8:95197229-95197230	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35670873	chr8:95197246-95197247	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547615486	chr8:95197253-95197254	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34429581	chr8:95197263-95197264	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2514819	chr8:95197291-95197292	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191467431	chr8:95197323-95197324	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183339985	chr8:95197372-95197373	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564330943	chr8:95197469-95197470	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145701627	chr8:95197472-95197473	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199680821	chr8:95197502-95197503	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556516192	chr8:95197505-95197506	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71277462	chr8:95197539-95197540	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533455693	chr8:95197543-95197544	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188082857	chr8:95197586-95197587	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546828494	chr8:95197613-95197614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2623170	chr8:95197655-95197656	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs149599646	chr8:95197686-95197687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192077993	chr8:95197690-95197691	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549185215	chr8:95197705-95197706	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534805555	chr8:95197707-95197708	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184675492	chr8:95197750-95197751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73695143	chr8:95197760-95197761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543581420	chr8:95197800-95197801	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375469432	chr8:95197822-95197823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138513390	chr8:95197927-95197928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190060201	chr8:95197954-95197955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577104995	chr8:95197996-95197997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545027850	chr8:95198007-95198008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564722223	chr8:95198015-95198016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527236385	chr8:95198025-95198026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547182361	chr8:95198041-95198042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192863105	chr8:95198042-95198043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560653948	chr8:95198051-95198052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529939183	chr8:95198125-95198126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549982176	chr8:95198155-95198156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570002919	chr8:95198188-95198189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184795251	chr8:95198205-95198206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150635684	chr8:95198218-95198219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200616746	chr8:95198231-95198232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73695144	chr8:95198265-95198266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189409034	chr8:95198267-95198268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534976804	chr8:95198269-95198270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554660105	chr8:95198297-95198298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79627393	chr8:95198329-95198330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95189600-95200600	Weak transcription	Colonic Mucosa	Colon
2	chr8:95189800-95205800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr8:95192000-95198600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr8:95193200-95197200	Weak transcription	Fetal Intestine Small	intestine
5	chr8:95196400-95197200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr8:95196600-95202600	Weak transcription	Small Intestine	intestine
7	chr8:95196800-95197600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr8:95196800-95200600	Strong transcription	Fetal Intestine Large	intestine
9	chr8:95197000-95200200	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr8:95197200-95197400	Strong transcription	Fetal Intestine Small	intestine
11	chr8:95197200-95197600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:95197200-95197800	Enhancers	NHDF-Ad	bronchial
13	chr8:95197200-95200000	Strong transcription	Duodenum Mucosa	Duodenum
14	chr8:95197400-95197800	Enhancers	Osteobl	bone
15	chr8:95197400-95198600	Weak transcription	Fetal Intestine Small	intestine
16	chr8:95197600-95198000	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr8:95198000-95198200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr8:95198200-95200000	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr8:95198600-95199000	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr8:95198600-95200000	Strong transcription	Fetal Intestine Small	intestine
21	chr8:95199000-95199200	Genic enhancers	Sigmoid Colon	Sigmoid Colon
22	chr8:95199200-95200000	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr8:95199800-95200800	Enhancers	Stomach Mucosa	stomach
24	chr8:95200000-95201400	Genic enhancers	Rectal Mucosa Donor 29	rectum
25	chr8:95200000-95201600	Genic enhancers	Sigmoid Colon	Sigmoid Colon
26	chr8:95200000-95202800	Genic enhancers	Duodenum Mucosa	Duodenum
27	chr8:95200000-95210200	Genic enhancers	Fetal Intestine Small	intestine
28	chr8:95200200-95201400	Genic enhancers	Rectal Mucosa Donor 31	rectum
29	chr8:95200600-95201600	Enhancers	Colonic Mucosa	Colon
30	chr8:95200600-95207400	Genic enhancers	Fetal Intestine Large	intestine
31	chr8:95200800-95201200	Flanking Active TSS	Stomach Mucosa	stomach
32	chr8:95201000-95201200	Enhancers	Pancreas	Pancrea
33	chr8:95201200-95201600	Enhancers	Stomach Mucosa	stomach
34	chr8:95201200-95210800	Weak transcription	Pancreas	Pancrea
35	chr8:95201400-95201800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr8:95201400-95202400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
37	chr8:95201600-95202000	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr8:95201600-95202600	Weak transcription	Colonic Mucosa	Colon
39	chr8:95201600-95203000	Weak transcription	Stomach Mucosa	stomach
40	chr8:95201800-95202200	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr8:95202000-95203400	Genic enhancers	Sigmoid Colon	Sigmoid Colon
42	chr8:95202200-95202800	Genic enhancers	Rectal Mucosa Donor 31	rectum
43	chr8:95202400-95204600	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr8:95202600-95203400	Genic enhancers	Colonic Mucosa	Colon
45	chr8:95202600-95203600	Enhancers	Small Intestine	intestine
46	chr8:95202800-95204800	Enhancers	Duodenum Mucosa	Duodenum
47	chr8:95202800-95204800	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr8:95203000-95206600	Enhancers	Stomach Mucosa	stomach
49	chr8:95203400-95203800	Enhancers	Colonic Mucosa	Colon
50	chr8:95203400-95204800	Weak transcription	Sigmoid Colon	Sigmoid Colon

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