Variant report

Variant	esv2762763
Chromosome Location	chr8:105943295-106218634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1610)
CpG islands
(count:244)
Chromatin interactive
region (count:103)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:106136243-106136505	K562	blood:	n/a	n/a
2	ARID3A	chr8:106113101-106113326	K562	blood:	n/a	n/a
3	ARID3A	chr8:106214260-106214501	K562	blood:	n/a	n/a
4	ARID3A	chr8:106002548-106002659	K562	blood:	n/a	n/a
5	ARID3A	chr8:106110265-106110589	K562	blood:	n/a	n/a
6	ARID3A	chr8:106104585-106104933	K562	blood:	n/a	n/a
7	ATF1	chr8:106190453-106190599	K562	blood:	n/a	n/a
8	ATF1	chr8:106214244-106214490	K562	blood:	n/a	n/a
9	ATF1	chr8:105997863-105997972	K562	blood:	n/a	n/a
10	ATF1	chr8:106110238-106110657	K562	blood:	n/a	n/a
11	ATF1	chr8:106113059-106113259	K562	blood:	n/a	n/a
12	ATF3	chr8:106104600-106104925	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr8:106104625-106104863	K562	blood:	n/a	n/a
14	ATF3	chr8:106131917-106132151	K562	blood:	n/a	n/a
15	BATF	chr8:106110262-106110621	GM12878	blood:	n/a	n/a
16	BATF	chr8:106012935-106013138	GM12878	blood:	n/a	n/a
17	BCL3	chr8:106146358-106146559	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:106110252-106110554	K562	blood:	n/a	n/a
19	BHLHE40	chr8:105987708-105987926	K562	blood:	n/a	n/a
20	BHLHE40	chr8:106157194-106157286	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:106034536-106034696	K562	blood:	n/a	n/a
22	BHLHE40	chr8:106104689-106104910	K562	blood:	n/a	n/a
23	BRCA1	chr8:106081962-106082383	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr8:106131863-106132252	K562	blood:	n/a	n/a
25	CBX3	chr8:106056189-106056567	K562	blood:	n/a	n/a
26	CBX3	chr8:106110192-106110722	K562	blood:	n/a	n/a
27	CBX3	chr8:106210730-106210956	K562	blood:	n/a	n/a
28	CBX3	chr8:106025954-106026212	K562	blood:	n/a	n/a
29	CBX3	chr8:106056254-106056495	K562	blood:	n/a	n/a
30	CBX3	chr8:106210582-106211052	K562	blood:	n/a	n/a
31	CCNT2	chr8:106110247-106110598	K562	blood:	n/a	n/a
32	CCNT2	chr8:106214286-106214435	K562	blood:	n/a	n/a
33	CCNT2	chr8:106104643-106104836	K562	blood:	n/a	n/a
34	CCNT2	chr8:106081681-106081766	K562	blood:	n/a	n/a
35	CEBPB	chr8:106185278-106185580	K562	blood:	n/a	chr8:106185419-106185432
36	CEBPB	chr8:106185230-106185657	IMR90	lung:	n/a	chr8:106185419-106185432
37	CEBPB	chr8:106165964-106166170	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:105963574-105963865	A549	lung:	n/a	chr8:105963582-105963594 chr8:105963697-105963708 chr8:105963699-105963708 chr8:105963739-105963752 chr8:105963699-105963710
39	CEBPB	chr8:106123568-106123669	K562	blood:	n/a	n/a
40	CEBPB	chr8:106003753-106004166	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:106165853-106166149	K562	blood:	n/a	n/a
42	CEBPB	chr8:106152057-106152064	K562	blood:	n/a	n/a
43	CEBPB	chr8:106200245-106200607	K562	blood:	n/a	chr8:106200421-106200432
44	CEBPB	chr8:106081714-106082511	IMR90	lung:	n/a	chr8:106082344-106082353
45	CEBPB	chr8:106017721-106018007	A549	lung:	n/a	chr8:106017853-106017866 chr8:106017853-106017864
46	CEBPB	chr8:106081725-106082543	Hela-S3	cervix:	n/a	chr8:106082344-106082353
47	CEBPB	chr8:106170979-106171011	K562	blood:	n/a	n/a
48	CEBPB	chr8:106038045-106038146	K562	blood:	n/a	chr8:106038094-106038105
49	CEBPB	chr8:106003781-106004145	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:106102307-106102998	Hela-S3	cervix:	n/a	chr8:106102526-106102537 chr8:106102527-106102539

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:105962177-105962227	LNCaP	prostate:	n/a
2	chr8:105962177-105962227	HRCEpiC	kidney:	n/a
3	chr8:105995203-105995253	SKMC	muscle:	n/a
4	chr8:106185570-106185620	Caco-2	colon:	n/a
5	chr8:105962177-105962227	HEEpiC	esophagus:	n/a
6	chr8:106185570-106185620	HEEpiC	esophagus:	n/a
7	chr8:105962177-105962227	GM19239	blood:	n/a
8	chr8:105962177-105962227	Hela-S3	cervix:	n/a
9	chr8:105962177-105962227	AG09319	gingival:	n/a
10	chr8:105988283-105988333	RPTEC	kidney:	n/a
11	chr8:105962177-105962227	MCF-7	breast:	n/a
12	chr8:105995203-105995253	ProgFib	skin:	n/a
13	chr8:106185570-106185620	GM12878	blood:	n/a
14	chr8:105988283-105988333	GM12891	blood:	n/a
15	chr8:105988283-105988333	HepG2	liver:	n/a
16	chr8:105962177-105962227	Hepatocyte	liver:	n/a
17	chr8:105995203-105995253	Jurkat	blood:	n/a
18	chr8:105988283-105988333	NHBE	bronchial:	n/a
19	chr8:106185570-106185620	SK-N-MC	brain:	n/a
20	chr8:106185570-106185620	T-47D	breast:	n/a
21	chr8:105988283-105988333	HCM	heart:	n/a
22	chr8:106185570-106185620	IMR90	lung:	fetal
23	chr8:105962177-105962227	HL-60	blood:	n/a
24	chr8:105962177-105962227	AG04449	skin:	fetal
25	chr8:105995203-105995253	GM12892	blood:	n/a
26	chr8:105962177-105962227	GM06990	blood:	n/a
27	chr8:105988283-105988333	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:105962177-105962227	A549	lung:	n/a
29	chr8:106185570-106185620	HCM	heart:	n/a
30	chr8:105988283-105988333	AG09309	skin:	n/a
31	chr8:105988283-105988333	Jurkat	blood:	n/a
32	chr8:105988283-105988333	GM12878	blood:	n/a
33	chr8:105962177-105962227	GM12892	blood:	n/a
34	chr8:105962177-105962227	HCF	heart:	n/a
35	chr8:106185570-106185620	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:106185570-106185620	AG04449	skin:	fetal
37	chr8:105995203-105995253	PrEC	prostate:	n/a
38	chr8:106185570-106185620	HepG2	liver:	n/a
39	chr8:106185570-106185620	HMEC	breast:	n/a
40	chr8:105988283-105988333	H1-hESC	embryonic stem cell:	embryo
41	chr8:105962177-105962227	HepG2	liver:	n/a
42	chr8:105962177-105962227	HUVEC	blood vessel:	n/a
43	chr8:105995203-105995253	HAEpiC	amniotic membrane:	n/a
44	chr8:106185570-106185620	SK-N-SH	brain:	n/a
45	chr8:105962177-105962227	T-47D	breast:	n/a
46	chr8:105988283-105988333	NB4	blood:	n/a
47	chr8:105962177-105962227	MCF10A-Er-Src	breast:	n/a
48	chr8:105988283-105988333	AG10803	skin:	n/a
49	chr8:106185570-106185620	NH-A	brain:	n/a
50	chr8:105995203-105995253	HEK293	kidney:	embryo

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:106128189..106130965-chr8:106133459..106136157,2	K562	blood:
2	chr8:106128119..106129741-chr8:106131952..106134022,2	K562	blood:
3	chr8:106019214..106021005-chr8:106023119..106025146,2	K562	blood:
4	chr8:105800104..105800636-chr8:106104255..106105140,2	MCF-7	breast:
5	chr8:105986775..105989189-chr8:105989318..105991553,2	MCF-7	breast:
6	chr8:106102068..106103875-chr8:106586214..106588552,2	K562	blood:
7	chr8:106165403..106167393-chr8:106167637..106170274,2	K562	blood:
8	chr8:106131031..106133323-chr8:106139720..106141521,2	K562	blood:
9	chr8:106115361..106119364-chr8:106123346..106125677,3	K562	blood:
10	chr8:106104770..106105296-chr8:106154309..106154928,2	MCF-7	breast:
11	chr8:106003697..106006144-chr8:106007178..106008786,2	K562	blood:
12	chr8:106057531..106060306-chr8:106071260..106074898,3	K562	blood:
13	chr8:105990352..105992630-chr8:105993447..105995544,2	K562	blood:
14	chr8:106115361..106119364-chr8:106123346..106125677,3	K562	blood:
15	chr8:106124060..106126969-chr8:106126998..106128732,2	K562	blood:
16	chr8:106171531..106173617-chr9:130211990..130214005,2	MCF-7	breast:
17	chr8:106075494..106077166-chr8:106081357..106083896,2	MCF-7	breast:
18	chr8:106138231..106139133-chr8:106146754..106147617,2	MCF-7	breast:
19	chr8:106136690..106139159-chr8:106144055..106146884,2	MCF-7	breast:
20	chr8:106185670..106187920-chr8:106191413..106194105,2	K562	blood:
21	chr8:106124290..106126979-chr8:106301850..106304617,2	K562	blood:
22	chr8:106082783..106085372-chr8:106087525..106090132,2	K562	blood:
23	chr8:106163120..106165061-chr8:106166603..106168874,2	K562	blood:
24	chr8:106122701..106124864-chr8:106382103..106383677,2	K562	blood:
25	chr8:106075494..106077166-chr8:106081357..106083896,2	MCF-7	breast:
26	chr8:106110267..106112599-chr8:106425928..106428860,2	K562	blood:
27	chr8:106110955..106112913-chr8:106113488..106116192,2	K562	blood:
28	chr8:106082822..106084651-chr8:106097372..106099591,2	K562	blood:
29	chr8:106128189..106130965-chr8:106133459..106136157,2	K562	blood:
30	chr8:106087603..106090110-chr8:106101395..106103199,2	K562	blood:
31	chr8:105985920..105987592-chr8:105991269..105993272,2	K562	blood:
32	chr8:106102491..106104440-chr8:106106753..106108347,2	MCF-7	breast:
33	chr8:106184974..106187423-chr8:106194828..106198492,3	K562	blood:
34	chr8:106082783..106085372-chr8:106087525..106090132,2	K562	blood:
35	chr8:106003697..106006144-chr8:106007178..106008786,2	K562	blood:
36	chr8:106084503..106086972-chr8:106332274..106334398,2	K562	blood:
37	chr8:106098062..106099625-chr8:106102482..106104994,2	MCF-7	breast:
38	chr8:106145928..106149549-chr8:106151108..106155039,3	K562	blood:
39	chr8:106034177..106035101-chr8:106784875..106785931,5	K562	blood:
40	chr8:106104141..106105251-chr8:106729947..106730923,5	MCF-7	breast:
41	chr8:105958122..105961194-chr8:105964039..105966907,3	K562	blood:
42	chr8:106128119..106129741-chr8:106131952..106134022,2	K562	blood:
43	chr8:106098685..106100875-chr8:106101996..106103590,2	K562	blood:
44	chr8:105985920..105987592-chr8:105991269..105993272,2	K562	blood:
45	chr8:106065191..106067685-chr8:106074185..106076444,2	K562	blood:
46	chr8:106108103..106110619-chr8:106122748..106124588,2	MCF-7	breast:
47	chr8:105892551..105895193-chr8:105962901..105965815,2	MCF-7	breast:
48	chr8:106059067..106061144-chr8:106430161..106432374,2	K562	blood:
49	chr8:106094210..106096629-chr8:106098616..106100274,3	K562	blood:
50	chr8:106104219..106105278-chr8:106672513..106673764,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFPM2-5	chr8:106023335-106023796	NONHSAT128224
2	lnc-ZFPM2-4	chr8:106031525-106031845	uc_244_+
3	lnc-LRP12-7	chr8:106031525-106031845	uc_244_-
4	lnc-LRP12-1	chr8:106200764-106200834	ENSG00000254041.1
5	lnc-LRP12-6	chr8:106002536-106002920	NONHSAT128223
6	lnc-LRP12-1	chr8:106155088-106155975	ENSG00000254041.1
7	lnc-LRP12-1	chr8:106179646-106179717	ENSG00000254041.1
8	lnc-LRP12-5	chr8:105993392-105993807	NONHSAT128222

No data

Variant related genes	Relation type
ENSG00000254041	TF binding region
ENSG00000240271	TF binding region
ENSG00000243939	TF binding region
TMCC1P1	TF binding region
ENSG00000253997	TF binding region
ENSG00000254041	CpG island
ENSG00000240271	CpG island
ENSG00000243939	CpG island
TMCC1P1	CpG island
ENSG00000253997	CpG island
ENSG00000197958	chromatin interactions
ENSG00000243939	chromatin interactions
ENSG00000148356	chromatin interactions
ENSG00000169946	chromatin interactions
ENSG00000240271	chromatin interactions

Extended variants
information (count: 4819 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4819 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181701031	chr8:105959224-105959225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186894755	chr8:105959226-105959227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532036393	chr8:105959229-105959230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141146800	chr8:105959242-105959243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370521419	chr8:105959250-105959251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35196569	chr8:105959254-105959255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569022139	chr8:105959278-105959279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536569166	chr8:105959312-105959313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554757716	chr8:105959350-105959351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111310373	chr8:105959366-105959367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144882733	chr8:105959379-105959380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs284492	chr8:105959600-105959601	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs185299190	chr8:105959607-105959608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561135046	chr8:105959657-105959658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531653826	chr8:105959698-105959699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34240589	chr8:105959712-105959713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189651332	chr8:105959728-105959729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564257493	chr8:105959730-105959731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539916742	chr8:105959731-105959732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77454886	chr8:105959732-105959733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138549382	chr8:105959780-105959781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550278122	chr8:105959806-105959807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182325066	chr8:105959811-105959812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188910090	chr8:105959824-105959825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372190507	chr8:105959826-105959827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529905026	chr8:105959865-105959866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566284688	chr8:105959872-105959873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566651005	chr8:105959880-105959881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563996933	chr8:105959881-105959882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376837881	chr8:105959905-105959906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193119500	chr8:105959919-105959920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552417945	chr8:105959928-105959929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571625326	chr8:105959932-105959933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539128274	chr8:105959933-105959934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535185497	chr8:105959935-105959936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376249380	chr8:105959950-105959951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62509466	chr8:105959962-105959963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs3107534	chr8:105960011-105960012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs536540256	chr8:105960014-105960015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554868615	chr8:105960019-105960020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79669191	chr8:105960023-105960024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540392726	chr8:105960048-105960049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188546412	chr8:105960084-105960085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537475206	chr8:105960107-105960108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557721679	chr8:105960146-105960147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576815384	chr8:105960203-105960204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191678199	chr8:105960226-105960227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375556786	chr8:105960232-105960233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75150876	chr8:105960286-105960287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548488468	chr8:105960347-105960348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
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
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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:105959200-105959400	Enhancers	Fetal Lung	lung
2	chr8:105959600-105960600	Weak transcription	Fetal Lung	lung
3	chr8:105960600-105962000	Enhancers	Fetal Lung	lung
4	chr8:105961200-105961600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:105961400-105962000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:105961400-105963000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr8:105961600-105962200	Enhancers	Adipose Nuclei	Adipose
8	chr8:105961600-105962200	Enhancers	HUVEC	blood vessel
9	chr8:105961600-105962800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:105961600-105963000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr8:105961600-105963200	Enhancers	Stomach Mucosa	stomach
12	chr8:105961600-105963600	Enhancers	Brain Germinal Matrix	brain
13	chr8:105961800-105962400	Enhancers	Fetal Brain Male	brain
14	chr8:105962000-105962400	Active TSS	Right Atrium	heart
15	chr8:105962000-105962600	Active TSS	Ovary	ovary
16	chr8:105962000-105962800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:105962000-105962800	Active TSS	Fetal Lung	lung
18	chr8:105962200-105962600	Enhancers	Fetal Heart	heart
19	chr8:105962200-105962600	Flanking Active TSS	HUVEC	blood vessel
20	chr8:105962200-105962800	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr8:105962200-105962800	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr8:105962400-105962800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:105962400-105962800	Flanking Active TSS	Fetal Brain Male	brain
24	chr8:105962400-105962800	Enhancers	Fetal Brain Female	brain
25	chr8:105962400-105963200	Weak transcription	Aorta	Aorta
26	chr8:105962600-105963000	Enhancers	HUVEC	blood vessel
27	chr8:105962600-105963600	Enhancers	Ovary	ovary
28	chr8:105962800-105963000	Weak transcription	Fetal Lung	lung
29	chr8:105962800-105963200	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr8:105962800-105963400	Enhancers	Fetal Brain Male	brain
31	chr8:105962800-105963600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:105962800-105963800	Enhancers	Adipose Nuclei	Adipose
33	chr8:105963000-105963600	Enhancers	Fetal Lung	lung
34	chr8:105963000-105966000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr8:105963200-105963400	Enhancers	Aorta	Aorta
36	chr8:105963200-105966400	Weak transcription	Stomach Mucosa	stomach
37	chr8:105963600-105964600	Weak transcription	Fetal Lung	lung
38	chr8:105963600-105964800	Weak transcription	Brain Germinal Matrix	brain
39	chr8:105964600-105965800	Enhancers	Fetal Lung	lung
40	chr8:105964800-105965000	Enhancers	Brain Germinal Matrix	brain
41	chr8:105966000-105966600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr8:105966400-105967000	Enhancers	Stomach Mucosa	stomach
43	chr8:105967000-105967600	Weak transcription	Stomach Mucosa	stomach
44	chr8:105967600-105968600	Enhancers	Stomach Mucosa	stomach
45	chr8:105967800-105968600	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr8:105967800-105968600	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr8:105968000-105968400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:105968200-105968600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr8:105968200-105968800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:105968400-105968800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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