Variant report

Variant	nsv522024
Chromosome Location	chr8:95199215-95232449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:693)
CpG islands
(count:611)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:95231164-95231381	K562	blood:	n/a	n/a
2	ATF1	chr8:95218407-95218446	K562	blood:	n/a	n/a
3	ATF2	chr8:95230950-95231630	GM12878	blood:	n/a	n/a
4	ATF2	chr8:95230930-95231587	GM12878	blood:	n/a	n/a
5	ATF2	chr8:95229597-95230197	GM12878	blood:	n/a	n/a
6	BACH1	chr8:95231967-95232122	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr8:95230966-95231514	GM12878	blood:	n/a	n/a
8	BATF	chr8:95231134-95231401	GM12878	blood:	n/a	n/a
9	BATF	chr8:95229668-95229959	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:95231167-95231430	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:95231060-95231542	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:95221856-95222050	GM12878	blood:	n/a	chr8:95222039-95222048
13	BCL3	chr8:95231078-95231513	GM12878	blood:	n/a	n/a
14	BCLAF1	chr8:95229554-95230109	GM12878	blood:	n/a	n/a
15	BCLAF1	chr8:95231000-95231623	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:95221813-95222111	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:95231021-95231589	GM12878	blood:	n/a	n/a
18	BRCA1	chr8:95231883-95232347	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr8:95231655-95232418	HCT-116	colon:	n/a	n/a
20	CBX3	chr8:95210615-95211285	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:95231641-95232411	HCT-116	colon:	n/a	n/a
22	CEBPB	chr8:95231749-95232216	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:95231780-95232174	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:95218254-95218537	A549	lung:	n/a	n/a
25	CEBPB	chr8:95219338-95219696	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:95217372-95217655	IMR90	lung:	n/a	chr8:95217525-95217536 chr8:95217522-95217539
27	CEBPB	chr8:95231651-95232357	HCT-116	colon:	n/a	n/a
28	CEBPB	chr8:95211554-95211626	K562	blood:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
29	CEBPB	chr8:95218105-95219430	HCT-116	colon:	n/a	chr8:95218564-95218576
30	CEBPB	chr8:95218147-95219200	HCT-116	colon:	n/a	chr8:95218564-95218576
31	CEBPB	chr8:95218255-95218560	K562	blood:	n/a	n/a
32	CEBPB	chr8:95210377-95211262	A549	lung:	n/a	n/a
33	CEBPB	chr8:95231146-95231457	GM12878	blood:	n/a	n/a
34	CEBPB	chr8:95217366-95217645	HepG2	liver:	n/a	chr8:95217525-95217536 chr8:95217522-95217539
35	CEBPB	chr8:95231664-95232216	A549	lung:	n/a	n/a
36	CEBPB	chr8:95219343-95219704	A549	lung:	n/a	n/a
37	CEBPB	chr8:95218272-95218526	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:95211452-95211703	IMR90	lung:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
39	CEBPB	chr8:95215789-95215920	K562	blood:	n/a	chr8:95215842-95215853
40	CEBPB	chr8:95231751-95232213	A549	lung:	n/a	n/a
41	CEBPB	chr8:95209598-95209888	HepG2	liver:	n/a	chr8:95209752-95209763 chr8:95209750-95209761
42	CEBPB	chr8:95218787-95219031	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr8:95230947-95231600	GM12878	blood:	n/a	n/a
44	CEBPB	chr8:95210794-95211093	A549	lung:	n/a	n/a
45	CEBPB	chr8:95225938-95226254	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:95231784-95232155	A549	lung:	n/a	n/a
47	CEBPB	chr8:95209585-95209785	IMR90	lung:	n/a	chr8:95209752-95209763 chr8:95209750-95209761
48	CEBPB	chr8:95215809-95216001	HepG2	liver:	n/a	chr8:95215842-95215853
49	CEBPB	chr8:95215723-95215969	Hela-S3	cervix:	n/a	chr8:95215842-95215853
50	CEBPB	chr8:95211432-95211741	HepG2	liver:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95222020-95222070	K562	blood:	n/a
2	chr8:95222020-95222070	K562	blood:	n/a
3	chr8:95220583-95220633	IMR90	lung:	fetal
4	chr8:95230984-95231034	T-47D	breast:	n/a
5	chr8:95222020-95222070	SK-N-SH_RA	brain:	n/a
6	chr8:95220779-95220829	U87	brain:	n/a
7	chr8:95229872-95229922	GM12891	blood:	n/a
8	chr8:95229872-95229922	NHBE	bronchial:	n/a
9	chr8:95220583-95220633	T-47D	breast:	n/a
10	chr8:95229525-95229575	AG04449	skin:	fetal
11	chr8:95221342-95221392	ProgFib	skin:	n/a
12	chr8:95222020-95222070	Hela-S3	cervix:	n/a
13	chr8:95229754-95229804	PrEC	prostate:	n/a
14	chr8:95229664-95229714	GM06990	blood:	n/a
15	chr8:95230984-95231034	HCT-116	colon:	n/a
16	chr8:95221342-95221392	HCT-116	colon:	n/a
17	chr8:95229754-95229804	HL-60	blood:	n/a
18	chr8:95229754-95229804	GM06990	blood:	n/a
19	chr8:95229754-95229804	ProgFib	skin:	n/a
20	chr8:95221197-95221247	CMK	blood:	n/a
21	chr8:95222020-95222070	GM12891	blood:	n/a
22	chr8:95229525-95229575	Jurkat	blood:	n/a
23	chr8:95220779-95220829	NHDF-neo	bronchial:	n/a
24	chr8:95220779-95220829	AG04450	lung:	fetal
25	chr8:95229754-95229804	LNCaP	prostate:	n/a
26	chr8:95220583-95220633	HAEpiC	amniotic membrane:	n/a
27	chr8:95220583-95220633	H1-hESC	embryonic stem cell:	embryo
28	chr8:95230984-95231034	CMK	blood:	n/a
29	chr8:95229525-95229575	NT2-D1	testis:	n/a
30	chr8:95229872-95229922	Hepatocyte	liver:	n/a
31	chr8:95220779-95220829	NB4	blood:	n/a
32	chr8:95220779-95220829	CMK	blood:	n/a
33	chr8:95221342-95221392	SK-N-SH	brain:	n/a
34	chr8:95222020-95222070	GM12892	blood:	n/a
35	chr8:95229525-95229575	ProgFib	skin:	n/a
36	chr8:95229525-95229575	Caco-2	colon:	n/a
37	chr8:95221197-95221247	ECC-1	luminal epithelium:	n/a
38	chr8:95229754-95229804	MCF-7	breast:	n/a
39	chr8:95222020-95222070	PFSK-1	brain:	n/a
40	chr8:95229872-95229922	HEEpiC	esophagus:	n/a
41	chr8:95221197-95221247	ProgFib	skin:	n/a
42	chr8:95221197-95221247	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:95230984-95231034	HCM	heart:	n/a
44	chr8:95221342-95221392	IMR90	lung:	fetal
45	chr8:95229525-95229575	AG10803	skin:	n/a
46	chr8:95229664-95229714	PANC-1	pancreas:	n/a
47	chr8:95220779-95220829	GM12891	blood:	n/a
48	chr8:95230984-95231034	HUVEC	blood vessel:	n/a
49	chr8:95230984-95231034	BJ	skin:	n/a
50	chr8:95229525-95229575	NB4	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95217922..95218880-chr8:95369574..95370256,2	MCF-7	breast:
2	chr8:95092028..95092964-chr8:95199448..95200050,4	MCF-7	breast:
3	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:
4	chr8:95091661..95092727-chr8:95199725..95200487,4	MCF-7	breast:
5	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
6	chr8:95104717..95105462-chr8:95199836..95200440,2	MCF-7	breast:
7	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
8	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
9	chr8:95200777..95202734-chr8:95202948..95204607,2	K562	blood:
10	chr8:95199696..95200396-chr8:95284281..95284998,2	MCF-7	breast:
11	chr8:95201827..95203670-chr8:95208153..95211021,2	MCF-7	breast:
12	chr8:95200777..95202734-chr8:95202948..95204607,2	K562	blood:
13	chr21:41711010..41712741-chr8:95200062..95201579,2	MCF-7	breast:
14	chr8:95218436..95218963-chr8:95284617..95285220,2	MCF-7	breast:
15	chr8:95215544..95217656-chr8:95220305..95222366,3	MCF-7	breast:
16	chr8:95201827..95203670-chr8:95208153..95211021,2	MCF-7	breast:
17	chr8:95091864..95092388-chr8:95200565..95201228,2	MCF-7	breast:
18	chr8:95200401..95202545-chr8:95205826..95207380,2	K562	blood:
19	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
20	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:
21	chr8:95006687..95007623-chr8:95199581..95200583,4	MCF-7	breast:
22	chr8:95176962..95177482-chr8:95225796..95226601,2	MCF-7	breast:
23	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
24	chr8:95219101..95220726-chr8:95272538..95274563,2	MCF-7	breast:
25	chr8:94751681..94753437-chr8:95200264..95202250,2	MCF-7	breast:
26	chr8:95216472..95218639-chr8:95229347..95231439,2	MCF-7	breast:
27	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
28	chr8:95200401..95202545-chr8:95205826..95207380,2	K562	blood:
29	chr8:95224589..95225412-chr8:95369113..95370095,2	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
ENSG00000164949	chromatin interactions
ENSG00000079112	chromatin interactions
ENSG00000253848	chromatin interactions
ENSG00000212998	chromatin interactions
ENSG00000183808	chromatin interactions

Extended variants
information (count: 1302 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1302 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2613217	chr8:95199215-95199216	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62526264	chr8:95199227-95199228	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs113434588	chr8:95199242-95199243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574634243	chr8:95199257-95199258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2158	chr8:95199264-95199265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2157	chr8:95199302-95199303	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs565721548	chr8:95199326-95199327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571641546	chr8:95199359-95199360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116846272	chr8:95199377-95199378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532224123	chr8:95199385-95199386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191592725	chr8:95199386-95199387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559423115	chr8:95199426-95199427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561865266	chr8:95199442-95199443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183109653	chr8:95199444-95199445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186513161	chr8:95199476-95199477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548223376	chr8:95199480-95199481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373824927	chr8:95199497-95199498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530770772	chr8:95199528-95199529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575567336	chr8:95199553-95199554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550673472	chr8:95199563-95199564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189838060	chr8:95199564-95199565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544219405	chr8:95199599-95199600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539675799	chr8:95199617-95199618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564504244	chr8:95199628-95199629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533201065	chr8:95199629-95199630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553519106	chr8:95199631-95199632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182403725	chr8:95199736-95199737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564535711	chr8:95199808-95199809	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536154074	chr8:95199816-95199817	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114743207	chr8:95199846-95199847	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187839978	chr8:95199861-95199862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547058130	chr8:95199865-95199866	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556802369	chr8:95199916-95199917	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368025645	chr8:95199970-95199971	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545720674	chr8:95199988-95199989	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370575907	chr8:95200014-95200015	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571688604	chr8:95200064-95200065	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559495660	chr8:95200093-95200094	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140088466	chr8:95200156-95200157	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532428563	chr8:95200157-95200158	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561613382	chr8:95200197-95200198	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530832729	chr8:95200261-95200262	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550928024	chr8:95200271-95200272	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs62526265	chr8:95200306-95200307	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs150324135	chr8:95200309-95200310	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs146442397	chr8:95200339-95200340	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs567060083	chr8:95200343-95200344	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs573829584	chr8:95200359-95200360	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs536016669	chr8:95200403-95200404	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs141027486	chr8:95200410-95200411	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	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:392 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr8:95196600-95202600	Weak transcription	Small Intestine	intestine
4	chr8:95196800-95200600	Strong transcription	Fetal Intestine Large	intestine
5	chr8:95197000-95200200	Strong transcription	Rectal Mucosa Donor 31	rectum
6	chr8:95197200-95200000	Strong transcription	Duodenum Mucosa	Duodenum
7	chr8:95198200-95200000	Strong transcription	Rectal Mucosa Donor 29	rectum
8	chr8:95198600-95200000	Strong transcription	Fetal Intestine Small	intestine
9	chr8:95199200-95200000	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr8:95199800-95200800	Enhancers	Stomach Mucosa	stomach
11	chr8:95200000-95201400	Genic enhancers	Rectal Mucosa Donor 29	rectum
12	chr8:95200000-95201600	Genic enhancers	Sigmoid Colon	Sigmoid Colon
13	chr8:95200000-95202800	Genic enhancers	Duodenum Mucosa	Duodenum
14	chr8:95200000-95210200	Genic enhancers	Fetal Intestine Small	intestine
15	chr8:95200200-95201400	Genic enhancers	Rectal Mucosa Donor 31	rectum
16	chr8:95200600-95201600	Enhancers	Colonic Mucosa	Colon
17	chr8:95200600-95207400	Genic enhancers	Fetal Intestine Large	intestine
18	chr8:95200800-95201200	Flanking Active TSS	Stomach Mucosa	stomach
19	chr8:95201000-95201200	Enhancers	Pancreas	Pancrea
20	chr8:95201200-95201600	Enhancers	Stomach Mucosa	stomach
21	chr8:95201200-95210800	Weak transcription	Pancreas	Pancrea
22	chr8:95201400-95201800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr8:95201400-95202400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr8:95201600-95202000	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr8:95201600-95202600	Weak transcription	Colonic Mucosa	Colon
26	chr8:95201600-95203000	Weak transcription	Stomach Mucosa	stomach
27	chr8:95201800-95202200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr8:95202000-95203400	Genic enhancers	Sigmoid Colon	Sigmoid Colon
29	chr8:95202200-95202800	Genic enhancers	Rectal Mucosa Donor 31	rectum
30	chr8:95202400-95204600	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr8:95202600-95203400	Genic enhancers	Colonic Mucosa	Colon
32	chr8:95202600-95203600	Enhancers	Small Intestine	intestine
33	chr8:95202800-95204800	Enhancers	Duodenum Mucosa	Duodenum
34	chr8:95202800-95204800	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr8:95203000-95206600	Enhancers	Stomach Mucosa	stomach
36	chr8:95203400-95203800	Enhancers	Colonic Mucosa	Colon
37	chr8:95203400-95204800	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr8:95203600-95204600	Weak transcription	Small Intestine	intestine
39	chr8:95203800-95204600	Weak transcription	Colonic Mucosa	Colon
40	chr8:95204000-95204400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:95204200-95204400	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr8:95204400-95205400	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr8:95204600-95205000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
44	chr8:95204600-95205200	Enhancers	Colonic Mucosa	Colon
45	chr8:95204600-95206400	Enhancers	Small Intestine	intestine
46	chr8:95204800-95205000	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr8:95204800-95205400	Genic enhancers	Rectal Mucosa Donor 31	rectum
48	chr8:95204800-95206000	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr8:95205000-95205400	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr8:95205000-95209200	Enhancers	Duodenum Mucosa	Duodenum

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