Variant report

Variant	nsv465342
Chromosome Location	chr8:2730069-3032861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:805)
CpG islands
(count:1587)
Chromatin interactive
region (count:71)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	ARID3A	chr8:2743138-2743788	K562	blood:	n/a	n/a
3	ARID3A	chr8:2736432-2736497	K562	blood:	n/a	n/a
4	ATF1	chr8:2965509-2965847	K562	blood:	n/a	n/a
5	ATF1	chr8:2856155-2856419	K562	blood:	n/a	n/a
6	ATF1	chr8:2743389-2743805	K562	blood:	n/a	n/a
7	ATF2	chr8:2916177-2916545	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr8:2842826-2843057	K562	blood:	n/a	n/a
9	ATF3	chr8:2743392-2743791	K562	blood:	n/a	n/a
10	ATF3	chr8:2965422-2965838	K562	blood:	n/a	n/a
11	BACH1	chr8:2743312-2743830	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:2937618-2937797	K562	blood:	n/a	n/a
13	BACH1	chr8:3000086-3000145	K562	blood:	n/a	n/a
14	BACH1	chr8:2922469-2922529	K562	blood:	n/a	n/a
15	BACH1	chr8:2916230-2916576	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:3029134-3029226	K562	blood:	n/a	n/a
17	BACH1	chr8:2743400-2743878	K562	blood:	n/a	n/a
18	BACH1	chr8:2918202-2918564	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:2843082-2843370	H1-hESC	embryonic stem cell:	n/a	chr8:2843219-2843233
20	BATF	chr8:2780025-2780346	GM12878	blood:	n/a	chr8:2780214-2780225
21	BATF	chr8:2882522-2882786	GM12878	blood:	n/a	n/a
22	BATF	chr8:2964313-2964509	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:2882534-2882878	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:2851732-2852076	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:2743404-2743839	K562	blood:	n/a	n/a
26	BHLHE40	chr8:3021027-3021615	K562	blood:	n/a	n/a
27	BHLHE40	chr8:3016188-3016208	K562	blood:	n/a	n/a
28	BHLHE40	chr8:2965476-2965859	K562	blood:	n/a	n/a
29	BHLHE40	chr8:3009535-3009884	K562	blood:	n/a	n/a
30	BHLHE40	chr8:2851861-2852089	GM12878	blood:	n/a	chr8:2852033-2852046 chr8:2852034-2852043
31	BHLHE40	chr8:3005906-3006185	K562	blood:	n/a	n/a
32	BHLHE40	chr8:3000304-3000431	K562	blood:	n/a	n/a
33	BHLHE40	chr8:2842852-2842945	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:2996065-2996299	K562	blood:	n/a	n/a
35	BHLHE40	chr8:2842702-2843334	K562	blood:	n/a	n/a
36	CBX3	chr8:2842691-2843075	K562	blood:	n/a	n/a
37	CBX3	chr8:3009569-3009811	K562	blood:	n/a	n/a
38	CBX3	chr8:2743353-2743846	K562	blood:	n/a	n/a
39	CBX3	chr8:2956908-2957301	K562	blood:	n/a	n/a
40	CCNT2	chr8:2965497-2965876	K562	blood:	n/a	chr8:2965696-2965716
41	CCNT2	chr8:3009480-3009871	K562	blood:	n/a	chr8:3009721-3009741
42	CCNT2	chr8:2743309-2743731	K562	blood:	n/a	chr8:2743335-2743355
43	CEBPB	chr8:3030493-3030781	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr8:3003941-3004174	HepG2	liver:	n/a	chr8:3004049-3004060
45	CEBPB	chr8:3009267-3010011	K562	blood:	n/a	chr8:3009954-3009967
46	CEBPB	chr8:2732713-2733057	HepG2	liver:	n/a	chr8:2732962-2732973
47	CEBPB	chr8:2954719-2955032	A549	lung:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
48	CEBPB	chr8:2926963-2927222	K562	blood:	n/a	n/a
49	CEBPB	chr8:2743404-2743829	K562	blood:	n/a	n/a
50	CEBPB	chr8:2951365-2951579	HepG2	liver:	n/a	chr8:2951435-2951446 chr8:2951460-2951472 chr8:2951554-2951567

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2831994-2832044	HepG2	liver:	n/a
2	chr8:2831994-2832044	HepG2	liver:	n/a
3	chr8:2752759-2752809	SK-N-SH	brain:	n/a
4	chr8:2798026-2798076	HCPEpiC	choroid plexus:	n/a
5	chr8:2883914-2883964	PFSK-1	brain:	n/a
6	chr8:2832048-2832098	HL-60	blood:	n/a
7	chr8:2997052-2997102	AG04450	lung:	fetal
8	chr8:2885627-2885677	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:2752736-2752786	HRCEpiC	kidney:	n/a
10	chr8:2883914-2883964	SK-N-SH	brain:	n/a
11	chr8:2879917-2879967	HMEC	breast:	n/a
12	chr8:2877217-2877267	AG04449	skin:	fetal
13	chr8:2877217-2877267	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:3016640-3016690	PFSK-1	brain:	n/a
15	chr8:2752736-2752786	SAEC	small airway:	n/a
16	chr8:2879917-2879967	LNCaP	prostate:	n/a
17	chr8:2820857-2820907	NHBE	bronchial:	n/a
18	chr8:2883914-2883964	HCF	heart:	n/a
19	chr8:2885537-2885587	HCPEpiC	choroid plexus:	n/a
20	chr8:2752736-2752786	NH-A	brain:	n/a
21	chr8:2877217-2877267	A549	lung:	n/a
22	chr8:2916814-2916864	PFSK-1	brain:	n/a
23	chr8:2885516-2885566	NT2-D1	testis:	n/a
24	chr8:2960317-2960367	SKMC	muscle:	n/a
25	chr8:2820857-2820907	HCF	heart:	n/a
26	chr8:2997052-2997102	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:2798026-2798076	SK-N-MC	brain:	n/a
28	chr8:2798026-2798076	Caco-2	colon:	n/a
29	chr8:2885516-2885566	BE2_C	brain:	n/a
30	chr8:2741025-2741075	GM12892	blood:	n/a
31	chr8:2798026-2798076	GM12878	blood:	n/a
32	chr8:2832048-2832098	MCF-7	breast:	n/a
33	chr8:2741025-2741075	NB4	blood:	n/a
34	chr8:2960317-2960367	GM06990	blood:	n/a
35	chr8:2820857-2820907	AG10803	skin:	n/a
36	chr8:2879687-2879737	MCF10A-Er-Src	breast:	n/a
37	chr8:2831994-2832044	NHBE	bronchial:	n/a
38	chr8:2997052-2997102	HIPEpiC	eye:	n/a
39	chr8:2752782-2752832	BE2_C	brain:	n/a
40	chr8:2997052-2997102	NH-A	brain:	n/a
41	chr8:2752759-2752809	NHDF-neo	bronchial:	n/a
42	chr8:2752782-2752832	CMK	blood:	n/a
43	chr8:2793577-2793627	NH-A	brain:	n/a
44	chr8:2885516-2885566	HEK293	kidney:	embryo
45	chr8:2831994-2832044	SAEC	small airway:	n/a
46	chr8:2832048-2832098	AG09309	skin:	n/a
47	chr8:2752782-2752832	GM06990	blood:	n/a
48	chr8:2832048-2832098	HRPEpiC	eye:	n/a
49	chr8:2877217-2877267	HUVEC	blood vessel:	n/a
50	chr8:2832078-2832128	GM12878	blood:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
2	chr8:2790313..2793074-chr8:2794638..2796914,2	K562	blood:
3	chr8:2783957..2786248-chr8:2796648..2799482,2	K562	blood:
4	chr8:2735475..2738288-chr8:2740776..2743385,2	K562	blood:
5	chr8:3024715..3026622-chr8:3029423..3032227,2	K562	blood:
6	chr8:3030633..3032243-chr8:3035809..3037381,2	K562	blood:
7	chr8:2832391..2834459-chr8:2835771..2837988,2	K562	blood:
8	chr8:2733961..2735891-chr8:2736089..2737715,2	K562	blood:
9	chr8:2807090..2809618-chr8:2810131..2812538,2	K562	blood:
10	chr8:3028449..3030172-chr8:3031870..3033947,2	K562	blood:
11	chr8:2735475..2738288-chr8:2740776..2743385,2	K562	blood:
12	chr8:2807090..2809618-chr8:2810131..2812538,2	K562	blood:
13	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
14	chr8:2943250..2945425-chr8:2952775..2955064,2	K562	blood:
15	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
16	chr8:2733961..2735891-chr8:2736089..2737715,2	K562	blood:
17	chr8:3004483..3006837-chr8:3020468..3022186,2	K562	blood:
18	chr8:2829379..2830950-chr8:2834355..2837068,2	K562	blood:
19	chr8:2924503..2926165-chr8:2927948..2929693,2	K562	blood:
20	chr8:2784674..2786393-chr8:2792193..2794250,2	K562	blood:
21	chr8:2768643..2771123-chr8:2792166..2794441,2	K562	blood:
22	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
23	chr8:2934204..2935975-chr8:2939449..2941530,2	K562	blood:
24	chr8:2884129..2886374-chr8:2888333..2890117,2	K562	blood:
25	chr8:3012415..3014148-chr8:3015659..3017279,2	K562	blood:
26	chr8:2917024..2919683-chr8:2921100..2923818,2	K562	blood:
27	chr12:56367505..56368235-chr8:2894157..2894798,2	MCF-7	breast:
28	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
29	chr8:3029280..3032071-chr8:3037936..3040025,3	K562	blood:
30	chr8:2956076..2958014-chr8:2965704..2967882,2	K562	blood:
31	chr8:2768643..2771123-chr8:2792166..2794441,2	K562	blood:
32	chr8:3028449..3030172-chr8:3031870..3033947,2	K562	blood:
33	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:
34	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
35	chr8:2822063..2824754-chr8:2827562..2829659,2	K562	blood:
36	chr8:2784674..2786393-chr8:2792193..2794250,2	K562	blood:
37	chr8:2865247..2867969-chr8:2868176..2872126,4	K562	blood:
38	chr8:2949313..2951484-chr8:2956361..2958211,2	K562	blood:
39	chr8:2956076..2958014-chr8:2965704..2967882,2	K562	blood:
40	chr8:2770834..2772446-chr8:2773950..2776616,2	K562	blood:
41	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:
42	chr8:2832391..2834459-chr8:2835771..2837988,2	K562	blood:
43	chr8:2743139..2745505-chr8:2752998..2755650,2	K562	blood:
44	chr8:3024715..3026622-chr8:3029423..3032227,2	K562	blood:
45	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
46	chr16:12825533..12827033-chr8:2762155..2763733,2	K562	blood:
47	chr8:2790313..2793074-chr8:2794638..2796914,2	K562	blood:
48	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
49	chr8:2828762..2830879-chr8:2834821..2837068,2	K562	blood:
50	chr8:2783957..2786248-chr8:2796648..2799482,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOM2-14	chr8:2879062-2880003	NONHSAT124740
2	lnc-MYOM2-13	chr8:2778500-2779629	NONHSAT124739
3	lnc-MYOM2-14	chr8:2877373-2877426	NONHSAT124740

No data

Variant related genes	Relation type
CSMD1	TF binding region
CSMD1	CpG island
ENSG00000111540	chromatin interactions
ENSG00000183117	chromatin interactions

Extended variants
information (count: 16459 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:16459 , 50 per page) page: 1 2 3 4 5 6 7 ... 330

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2924911	chr8:2730069-2730070	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542531440	chr8:2730072-2730073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562108169	chr8:2730099-2730100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531146081	chr8:2730100-2730101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550616049	chr8:2730129-2730130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs60854612	chr8:2730138-2730139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546521010	chr8:2730174-2730175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139306591	chr8:2730236-2730237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182436628	chr8:2730260-2730261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566515378	chr8:2730266-2730267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535498507	chr8:2730305-2730306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549272434	chr8:2730307-2730308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568916681	chr8:2730312-2730313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141571803	chr8:2730329-2730330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558029359	chr8:2730353-2730354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577802468	chr8:2730363-2730364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533907726	chr8:2730365-2730366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553780831	chr8:2730366-2730367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs341691	chr8:2730413-2730414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs542118268	chr8:2730443-2730444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562409609	chr8:2730519-2730520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs61635363	chr8:2730526-2730527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544394754	chr8:2730563-2730564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564376503	chr8:2730566-2730567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2924910	chr8:2730586-2730587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2924909	chr8:2730622-2730623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188404668	chr8:2730643-2730644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546708960	chr8:2730679-2730680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560250684	chr8:2730738-2730739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13249082	chr8:2730749-2730750	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs192640673	chr8:2730783-2730784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113182868	chr8:2730787-2730788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376483105	chr8:2730798-2730799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79497789	chr8:2730811-2730812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551585353	chr8:2730821-2730822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149493534	chr8:2730841-2730842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533837729	chr8:2730865-2730866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547742076	chr8:2730882-2730883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553915592	chr8:2730884-2730885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558038416	chr8:2730889-2730890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2924908	chr8:2730902-2730903	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs341692	chr8:2730906-2730907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536242881	chr8:2730923-2730924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145958468	chr8:2730964-2730965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575880307	chr8:2730970-2730971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138536058	chr8:2731024-2731025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189105846	chr8:2731053-2731054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577828199	chr8:2731060-2731061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141479918	chr8:2731091-2731092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560636817	chr8:2731107-2731108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

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
Breast cancer	20932292	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2730000-2732800	Weak transcription	Fetal Kidney	kidney
2	chr8:2732600-2733200	Enhancers	Fetal Muscle Leg	muscle
3	chr8:2732800-2733400	Enhancers	Fetal Kidney	kidney
4	chr8:2732800-2736600	Enhancers	Fetal Brain Male	brain
5	chr8:2733200-2734200	Weak transcription	Fetal Muscle Leg	muscle
6	chr8:2733400-2734400	Weak transcription	Fetal Kidney	kidney
7	chr8:2733400-2734600	Enhancers	Fetal Brain Female	brain
8	chr8:2734200-2735200	Enhancers	Fetal Muscle Leg	muscle
9	chr8:2734400-2735200	Enhancers	Fetal Kidney	kidney
10	chr8:2735200-2735800	Weak transcription	Fetal Kidney	kidney
11	chr8:2735800-2736000	Enhancers	Fetal Kidney	kidney
12	chr8:2736000-2741400	Weak transcription	Fetal Kidney	kidney
13	chr8:2736400-2736800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:2736600-2737400	Weak transcription	Fetal Brain Male	brain
15	chr8:2737400-2737600	Enhancers	Fetal Brain Male	brain
16	chr8:2737600-2743000	Weak transcription	Fetal Brain Male	brain
17	chr8:2741400-2742200	Enhancers	Fetal Kidney	kidney
18	chr8:2742800-2743000	Enhancers	K562	blood
19	chr8:2743000-2743200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr8:2743000-2743200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr8:2743000-2743600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:2743000-2743600	Enhancers	Fetal Brain Male	brain
23	chr8:2743000-2744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr8:2743000-2744000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:2743000-2744000	Flanking Active TSS	K562	blood
26	chr8:2743000-2744000	Enhancers	NH-A	brain
27	chr8:2743200-2743400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr8:2743200-2743400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr8:2743200-2743600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:2743200-2743600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:2743200-2743600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr8:2743200-2743600	Enhancers	Fetal Brain Female	brain
33	chr8:2743200-2743600	Enhancers	Fetal Lung	lung
34	chr8:2743200-2743600	Active TSS	Osteobl	bone
35	chr8:2743200-2743800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:2743400-2743800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:2743400-2743800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr8:2743400-2743800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr8:2743400-2744000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr8:2743400-2744000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:2743400-2744400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr8:2743600-2744000	Enhancers	Osteobl	bone
43	chr8:2743600-2744200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:2743600-2744200	Enhancers	Muscle Satellite Cultured Cells	--
45	chr8:2743600-2744200	Active TSS	Brain Hippocampus Middle	brain
46	chr8:2743600-2747000	Weak transcription	Fetal Brain Male	brain
47	chr8:2743800-2744200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:2743800-2744200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:2743800-2744200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr8:2744000-2744200	Enhancers	K562	blood

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