Variant report

Variant	nsv429839
Chromosome Location	chr8:2796813-3024143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:595)
CpG islands
(count:1038)
Chromatin interactive
region (count:45)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2965096-2966032	K562	blood:	n/a	n/a
2	ATF1	chr8:2965509-2965847	K562	blood:	n/a	n/a
3	ATF1	chr8:2856155-2856419	K562	blood:	n/a	n/a
4	ATF2	chr8:2916177-2916545	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr8:2842826-2843057	K562	blood:	n/a	n/a
6	ATF3	chr8:2965422-2965838	K562	blood:	n/a	n/a
7	BACH1	chr8:2916230-2916576	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:2922469-2922529	K562	blood:	n/a	n/a
9	BACH1	chr8:2918202-2918564	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:3000086-3000145	K562	blood:	n/a	n/a
11	BACH1	chr8:2937618-2937797	K562	blood:	n/a	n/a
12	BACH1	chr8:2843082-2843370	H1-hESC	embryonic stem cell:	n/a	chr8:2843219-2843233
13	BATF	chr8:2964313-2964509	GM12878	blood:	n/a	n/a
14	BATF	chr8:2882522-2882786	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:2851732-2852076	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:2882534-2882878	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:2996065-2996299	K562	blood:	n/a	n/a
18	BHLHE40	chr8:2851861-2852089	GM12878	blood:	n/a	chr8:2852033-2852046 chr8:2852034-2852043
19	BHLHE40	chr8:3009535-3009884	K562	blood:	n/a	n/a
20	BHLHE40	chr8:2965476-2965859	K562	blood:	n/a	n/a
21	BHLHE40	chr8:3000304-3000431	K562	blood:	n/a	n/a
22	BHLHE40	chr8:2842702-2843334	K562	blood:	n/a	n/a
23	BHLHE40	chr8:3016188-3016208	K562	blood:	n/a	n/a
24	BHLHE40	chr8:3021027-3021615	K562	blood:	n/a	n/a
25	BHLHE40	chr8:2842852-2842945	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:3005906-3006185	K562	blood:	n/a	n/a
27	CBX3	chr8:3009569-3009811	K562	blood:	n/a	n/a
28	CBX3	chr8:2956908-2957301	K562	blood:	n/a	n/a
29	CBX3	chr8:2842691-2843075	K562	blood:	n/a	n/a
30	CCNT2	chr8:2965497-2965876	K562	blood:	n/a	chr8:2965696-2965716
31	CCNT2	chr8:3009480-3009871	K562	blood:	n/a	chr8:3009721-3009741
32	CEBPB	chr8:2954721-2955095	HepG2	liver:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
33	CEBPB	chr8:2865627-2865770	K562	blood:	n/a	n/a
34	CEBPB	chr8:2951403-2951452	A549	lung:	n/a	chr8:2951435-2951446
35	CEBPB	chr8:2954868-2954947	H1-hESC	embryonic stem cell:	n/a	chr8:2954924-2954937 chr8:2954924-2954935 chr8:2954925-2954936
36	CEBPB	chr8:2954719-2955032	A549	lung:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
37	CEBPB	chr8:2954748-2955039	IMR90	lung:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
38	CEBPB	chr8:2954734-2954993	Hela-S3	cervix:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
39	CEBPB	chr8:3009267-3010011	K562	blood:	n/a	chr8:3009954-3009967
40	CEBPB	chr8:2811413-2811664	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:3003941-3004174	HepG2	liver:	n/a	chr8:3004049-3004060
42	CEBPB	chr8:2865620-2865694	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:2842695-2843052	K562	blood:	n/a	n/a
44	CEBPB	chr8:2886397-2886623	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:2931331-2931584	A549	lung:	n/a	n/a
46	CEBPB	chr8:2952827-2952942	K562	blood:	n/a	n/a
47	CEBPB	chr8:2916260-2916546	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr8:2926963-2927222	K562	blood:	n/a	n/a
49	CEBPB	chr8:2965332-2965758	K562	blood:	n/a	n/a
50	CEBPB	chr8:2849688-2849954	A549	lung:	n/a	chr8:2849859-2849870

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2798026-2798076	RPTEC	kidney:	n/a
2	chr8:2798026-2798076	RPTEC	kidney:	n/a
3	chr8:2997052-2997102	CMK	blood:	n/a
4	chr8:2885516-2885566	AG04449	skin:	fetal
5	chr8:3016640-3016690	HCT-116	colon:	n/a
6	chr8:2997052-2997102	A549	lung:	n/a
7	chr8:2960317-2960367	HRE	kidney:	n/a
8	chr8:2997052-2997102	HCM	heart:	n/a
9	chr8:2990464-2990514	SKMC	muscle:	n/a
10	chr8:2997052-2997102	H1-hESC	embryonic stem cell:	embryo
11	chr8:2820857-2820907	SK-N-SH	brain:	n/a
12	chr8:2879687-2879737	ovcar-3	ovarian:	n/a
13	chr8:2960317-2960367	NT2-D1	testis:	n/a
14	chr8:2885537-2885587	ProgFib	skin:	n/a
15	chr8:2883914-2883964	ProgFib	skin:	n/a
16	chr8:2960317-2960367	HCF	heart:	n/a
17	chr8:2877217-2877267	T-47D	breast:	n/a
18	chr8:2831994-2832044	PANC-1	pancreas:	n/a
19	chr8:2885537-2885587	HUVEC	blood vessel:	n/a
20	chr8:3016640-3016690	PrEC	prostate:	n/a
21	chr8:2990464-2990514	HAEpiC	amniotic membrane:	n/a
22	chr8:2997052-2997102	PFSK-1	brain:	n/a
23	chr8:2832078-2832128	GM12878	blood:	n/a
24	chr8:2820857-2820907	GM12891	blood:	n/a
25	chr8:2885516-2885566	U87	brain:	n/a
26	chr8:2885537-2885587	MCF10A-Er-Src	breast:	n/a
27	chr8:2831994-2832044	HRCEpiC	kidney:	n/a
28	chr8:2831994-2832044	HRPEpiC	eye:	n/a
29	chr8:3016640-3016690	GM19239	blood:	n/a
30	chr8:2831994-2832044	HCF	heart:	n/a
31	chr8:2832078-2832128	HEEpiC	esophagus:	n/a
32	chr8:2832048-2832098	PFSK-1	brain:	n/a
33	chr8:2879687-2879737	BJ	skin:	n/a
34	chr8:2885627-2885677	AG09309	skin:	n/a
35	chr8:2883914-2883964	SK-N-SH_RA	brain:	n/a
36	chr8:2883914-2883964	MCF-7	breast:	n/a
37	chr8:2885627-2885677	IMR90	lung:	fetal
38	chr8:2885516-2885566	SK-N-SH_RA	brain:	n/a
39	chr8:2798026-2798076	HEK293	kidney:	embryo
40	chr8:2916814-2916864	HIPEpiC	eye:	n/a
41	chr8:2997052-2997102	SK-N-SH	brain:	n/a
42	chr8:2832078-2832128	HNPCEpiC	eye:	n/a
43	chr8:2831994-2832044	BE2_C	brain:	n/a
44	chr8:2885537-2885587	HMEC	breast:	n/a
45	chr8:2885627-2885677	LNCaP	prostate:	n/a
46	chr8:2997052-2997102	AoSMC	blood vessel:	n/a
47	chr8:2879917-2879967	AG10803	skin:	n/a
48	chr8:2798026-2798076	HepG2	liver:	n/a
49	chr8:2831994-2832044	LNCaP	prostate:	n/a
50	chr8:2885516-2885566	SAEC	small airway:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56367505..56368235-chr8:2894157..2894798,2	MCF-7	breast:
2	chr8:2828762..2830879-chr8:2834821..2837068,2	K562	blood:
3	chr8:2884129..2886374-chr8:2888333..2890117,2	K562	blood:
4	chr8:2807090..2809618-chr8:2810131..2812538,2	K562	blood:
5	chr8:2994979..2996724-chr8:3012349..3015232,2	K562	blood:
6	chr8:2884129..2886374-chr8:2888333..2890117,2	K562	blood:
7	chr8:2956076..2958014-chr8:2965704..2967882,2	K562	blood:
8	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
9	chr8:2956076..2958014-chr8:2965704..2967882,2	K562	blood:
10	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
11	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
12	chr8:3012415..3014148-chr8:3015659..3017279,2	K562	blood:
13	chr8:2829379..2830950-chr8:2834355..2837068,2	K562	blood:
14	chr8:2949313..2951484-chr8:2956361..2958211,2	K562	blood:
15	chr8:3004483..3006837-chr8:3020468..3022186,2	K562	blood:
16	chr8:3012415..3014148-chr8:3015659..3017279,2	K562	blood:
17	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
18	chr8:2807090..2809618-chr8:2810131..2812538,2	K562	blood:
19	chr8:2783957..2786248-chr8:2796648..2799482,2	K562	blood:
20	chr8:2832391..2834459-chr8:2835771..2837988,2	K562	blood:
21	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
22	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
23	chr8:2924503..2926165-chr8:2927948..2929693,2	K562	blood:
24	chr8:2865247..2867969-chr8:2868176..2872126,4	K562	blood:
25	chr8:2994979..2996724-chr8:3012349..3015232,2	K562	blood:
26	chr8:2924503..2926165-chr8:2927948..2929693,2	K562	blood:
27	chr8:2934204..2935975-chr8:2939449..2941530,2	K562	blood:
28	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
29	chr8:2934204..2935975-chr8:2939449..2941530,2	K562	blood:
30	chr8:2949313..2951484-chr8:2956361..2958211,2	K562	blood:
31	chr8:2822063..2824754-chr8:2827562..2829659,2	K562	blood:
32	chr8:2832391..2834459-chr8:2835771..2837988,2	K562	blood:
33	chr8:3004483..3006837-chr8:3020468..3022186,2	K562	blood:
34	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:
35	chr8:2943250..2945425-chr8:2952775..2955064,2	K562	blood:
36	chr8:2865247..2867969-chr8:2868176..2872126,4	K562	blood:
37	chr8:2790313..2793074-chr8:2794638..2796914,2	K562	blood:
38	chr8:2822063..2824754-chr8:2827562..2829659,2	K562	blood:
39	chr8:2917024..2919683-chr8:2921100..2923818,2	K562	blood:
40	chr8:2943250..2945425-chr8:2952775..2955064,2	K562	blood:
41	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
42	chr8:2828762..2830879-chr8:2834821..2837068,2	K562	blood:
43	chr8:2917024..2919683-chr8:2921100..2923818,2	K562	blood:
44	chr8:2829379..2830950-chr8:2834355..2837068,2	K562	blood:
45	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOM2-14	chr8:2879062-2880003	NONHSAT124740
2	lnc-MYOM2-14	chr8:2877373-2877426	NONHSAT124740

No data

Variant related genes	Relation type
CSMD1	TF binding region
CSMD1	CpG island
ENSG00000111540	chromatin interactions

Extended variants
information (count: 13079 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:13079 , 50 per page) page: 1 2 3 4 5 6 7 ... 262

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535642508	chr8:2796814-2796815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146589471	chr8:2796832-2796833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186685133	chr8:2796839-2796840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141297133	chr8:2796856-2796857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571146081	chr8:2796874-2796875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557693975	chr8:2796876-2796877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375451406	chr8:2796879-2796880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577957038	chr8:2796886-2796887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372397366	chr8:2796887-2796888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560395598	chr8:2796947-2796948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35744525	chr8:2796949-2796950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191139900	chr8:2796967-2796968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542804643	chr8:2796975-2796976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34574904	chr8:2796977-2796978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76931398	chr8:2796980-2796981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552833871	chr8:2797023-2797024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558557508	chr8:2797045-2797046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs598985	chr8:2797092-2797093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs150200793	chr8:2797109-2797110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184062045	chr8:2797113-2797114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs599016	chr8:2797119-2797120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs568395896	chr8:2797131-2797132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574592168	chr8:2797143-2797144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117580024	chr8:2797167-2797168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs665045	chr8:2797172-2797173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs549136229	chr8:2797188-2797189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370079087	chr8:2797189-2797190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138685672	chr8:2797190-2797191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs599814	chr8:2797246-2797247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs13255958	chr8:2797258-2797259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13264537	chr8:2797259-2797260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534190379	chr8:2797313-2797314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569896681	chr8:2797322-2797323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34436000	chr8:2797327-2797328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553889450	chr8:2797329-2797330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77683819	chr8:2797336-2797337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576703881	chr8:2797350-2797351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545809260	chr8:2797393-2797394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34562041	chr8:2797418-2797419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73179572	chr8:2797428-2797429	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs149012471	chr8:2797431-2797432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545269831	chr8:2797459-2797460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571922915	chr8:2797479-2797480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528589847	chr8:2797492-2797493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564983378	chr8:2797502-2797503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143792604	chr8:2797601-2797602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540973955	chr8:2797613-2797614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs193186024	chr8:2797636-2797637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534370755	chr8:2797641-2797642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138484077	chr8:2797647-2797648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2792800-2842800	Weak transcription	K562	blood
2	chr8:2797400-2798000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr8:2797400-2798200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr8:2797400-2798400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:2797600-2798000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:2797600-2798000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:2797600-2798400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr8:2797600-2798400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr8:2797600-2798400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:2797800-2798000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr8:2798000-2798400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr8:2800600-2836800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr8:2804200-2812600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr8:2810200-2810600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:2811200-2836800	Weak transcription	Brain Anterior Caudate	brain
16	chr8:2811800-2836800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr8:2812400-2813200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr8:2812400-2853000	Weak transcription	Brain Angular Gyrus	brain
19	chr8:2812600-2813200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr8:2813200-2819600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr8:2815200-2816600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:2815200-2816800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:2815800-2816000	Enhancers	Fetal Muscle Leg	muscle
24	chr8:2816600-2816800	Enhancers	Fetal Muscle Leg	muscle
25	chr8:2819600-2820800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr8:2820400-2824000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr8:2820800-2832600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr8:2823600-2824400	Enhancers	Fetal Muscle Leg	muscle
29	chr8:2824000-2824400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:2824000-2824400	Enhancers	Fetal Muscle Trunk	muscle
31	chr8:2824200-2825600	Enhancers	Brain Germinal Matrix	brain
32	chr8:2824600-2825000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr8:2824800-2825000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr8:2825000-2836600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr8:2833800-2834200	Enhancers	Fetal Muscle Trunk	muscle
36	chr8:2834000-2834200	Enhancers	Fetal Muscle Leg	muscle
37	chr8:2834200-2835600	Weak transcription	Lung	lung
38	chr8:2834200-2836000	Weak transcription	Fetal Muscle Leg	muscle
39	chr8:2834200-2840000	Weak transcription	Fetal Muscle Trunk	muscle
40	chr8:2835600-2836000	ZNF genes & repeats	Lung	lung
41	chr8:2836000-2839000	Enhancers	Fetal Muscle Leg	muscle
42	chr8:2836600-2838000	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr8:2836800-2837400	Enhancers	Brain Cingulate Gyrus	brain
44	chr8:2836800-2837600	Enhancers	Brain Hippocampus Middle	brain
45	chr8:2836800-2837800	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr8:2836800-2837800	Enhancers	Brain Substantia Nigra	brain
47	chr8:2836800-2838000	Enhancers	Brain Anterior Caudate	brain
48	chr8:2837000-2837800	Enhancers	Brain Germinal Matrix	brain
49	chr8:2837000-2837800	Weak transcription	Lung	lung
50	chr8:2837000-2838000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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