Variant report

Variant	nsv889888
Chromosome Location	chr8:2749829-2954915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:1222)
Chromatin interactive
region (count:50)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:2856155-2856419	K562	blood:	n/a	n/a
2	ATF2	chr8:2916177-2916545	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr8:2842826-2843057	K562	blood:	n/a	n/a
4	BACH1	chr8:2918202-2918564	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:2843082-2843370	H1-hESC	embryonic stem cell:	n/a	chr8:2843219-2843233
6	BACH1	chr8:2916230-2916576	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:2922469-2922529	K562	blood:	n/a	n/a
8	BACH1	chr8:2937618-2937797	K562	blood:	n/a	n/a
9	BATF	chr8:2882522-2882786	GM12878	blood:	n/a	n/a
10	BATF	chr8:2780025-2780346	GM12878	blood:	n/a	chr8:2780214-2780225
11	BCL11A	chr8:2882534-2882878	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:2851732-2852076	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:2851861-2852089	GM12878	blood:	n/a	chr8:2852033-2852046 chr8:2852034-2852043
14	BHLHE40	chr8:2842852-2842945	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:2842702-2843334	K562	blood:	n/a	n/a
16	CBX3	chr8:2842691-2843075	K562	blood:	n/a	n/a
17	CEBPB	chr8:2916260-2916546	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:2865620-2865694	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:2954868-2954947	H1-hESC	embryonic stem cell:	n/a	chr8:2954924-2954937 chr8:2954924-2954935 chr8:2954925-2954936
20	CEBPB	chr8:2954748-2955039	IMR90	lung:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
21	CEBPB	chr8:2849686-2850016	HepG2	liver:	n/a	chr8:2849859-2849870
22	CEBPB	chr8:2774780-2775333	IMR90	lung:	n/a	chr8:2775148-2775156
23	CEBPB	chr8:2849688-2849954	A549	lung:	n/a	chr8:2849859-2849870
24	CEBPB	chr8:2954719-2955032	A549	lung:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
25	CEBPB	chr8:2811413-2811664	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:2952827-2952942	K562	blood:	n/a	n/a
27	CEBPB	chr8:2926963-2927222	K562	blood:	n/a	n/a
28	CEBPB	chr8:2954721-2955095	HepG2	liver:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
29	CEBPB	chr8:2849698-2849994	K562	blood:	n/a	chr8:2849859-2849870
30	CEBPB	chr8:2915827-2915913	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:2951403-2951452	A549	lung:	n/a	chr8:2951435-2951446
32	CEBPB	chr8:2886397-2886623	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:2954734-2954993	Hela-S3	cervix:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
34	CEBPB	chr8:2951365-2951579	HepG2	liver:	n/a	chr8:2951435-2951446 chr8:2951460-2951472 chr8:2951554-2951567
35	CEBPB	chr8:2842695-2843052	K562	blood:	n/a	n/a
36	CEBPB	chr8:2931331-2931584	A549	lung:	n/a	n/a
37	CEBPB	chr8:2865627-2865770	K562	blood:	n/a	n/a
38	CREB1	chr8:2797721-2798156	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:2898217-2898301	Fibrobl	skin:	n/a	n/a
40	CTCF	chr8:2877460-2877610	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr8:2884055-2884129	Fibrobl	skin:	n/a	n/a
42	CTCF	chr8:2842820-2842970	K562	blood:	n/a	n/a
43	CTCF	chr8:2870524-2870610	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr8:2842876-2842956	ProgFib	skin:	n/a	n/a
45	CTCF	chr8:2877504-2877636	LNCaP	prostate:	n/a	n/a
46	CTCF	chr8:2816040-2816190	GM12866	blood:	n/a	n/a
47	CTCF	chr8:2842803-2843017	K562	blood:	n/a	n/a
48	CTCF	chr8:2877460-2877610	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr8:2877498-2877624	Medullo	brain:	n/a	n/a
50	CTCF	chr8:2842862-2842986	A549	lung:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2879917-2879967	A549	lung:	n/a
2	chr8:2774531-2774581	HRCEpiC	kidney:	n/a
3	chr8:2879917-2879967	A549	lung:	n/a
4	chr8:2774531-2774581	HRCEpiC	kidney:	n/a
5	chr8:2877217-2877267	PrEC	prostate:	n/a
6	chr8:2798026-2798076	HEEpiC	esophagus:	n/a
7	chr8:2883914-2883964	HCM	heart:	n/a
8	chr8:2752736-2752786	HepG2	liver:	n/a
9	chr8:2774531-2774581	NHDF-neo	bronchial:	n/a
10	chr8:2752759-2752809	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:2877217-2877267	BE2_C	brain:	n/a
12	chr8:2877217-2877267	HepG2	liver:	n/a
13	chr8:2793467-2793517	SK-N-MC	brain:	n/a
14	chr8:2752782-2752832	HRPEpiC	eye:	n/a
15	chr8:2879917-2879967	HCM	heart:	n/a
16	chr8:2774531-2774581	HIPEpiC	eye:	n/a
17	chr8:2793577-2793627	HRCEpiC	kidney:	n/a
18	chr8:2774531-2774581	A549	lung:	n/a
19	chr8:2795929-2795979	AG04449	skin:	fetal
20	chr8:2885537-2885587	HCM	heart:	n/a
21	chr8:2885537-2885587	CMK	blood:	n/a
22	chr8:2793577-2793627	HL-60	blood:	n/a
23	chr8:2793577-2793627	CMK	blood:	n/a
24	chr8:2916814-2916864	A549	lung:	n/a
25	chr8:2793467-2793517	Hepatocyte	liver:	n/a
26	chr8:2831994-2832044	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:2877217-2877267	NH-A	brain:	n/a
28	chr8:2885516-2885566	HepG2	liver:	n/a
29	chr8:2883914-2883964	NB4	blood:	n/a
30	chr8:2885627-2885677	SAEC	small airway:	n/a
31	chr8:2793577-2793627	HAEpiC	amniotic membrane:	n/a
32	chr8:2774531-2774581	CMK	blood:	n/a
33	chr8:2885516-2885566	HEEpiC	esophagus:	n/a
34	chr8:2798026-2798076	LNCaP	prostate:	n/a
35	chr8:2883914-2883964	H1-hESC	embryonic stem cell:	embryo
36	chr8:2798026-2798076	GM19239	blood:	n/a
37	chr8:2832048-2832098	SKMC	muscle:	n/a
38	chr8:2879687-2879737	GM12878	blood:	n/a
39	chr8:2798026-2798076	PFSK-1	brain:	n/a
40	chr8:2916814-2916864	GM12891	blood:	n/a
41	chr8:2879687-2879737	H1-hESC	embryonic stem cell:	embryo
42	chr8:2752759-2752809	U87	brain:	n/a
43	chr8:2820857-2820907	HMEC	breast:	n/a
44	chr8:2831994-2832044	HMEC	breast:	n/a
45	chr8:2795929-2795979	NHDF-neo	bronchial:	n/a
46	chr8:2774531-2774581	HNPCEpiC	eye:	n/a
47	chr8:2798026-2798076	HIPEpiC	eye:	n/a
48	chr8:2774531-2774581	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:2793577-2793627	AoSMC	blood vessel:	n/a
50	chr8:2798026-2798076	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:2770834..2772446-chr8:2773950..2776616,2	K562	blood:
2	chr8:2934204..2935975-chr8:2939449..2941530,2	K562	blood:
3	chr8:2770834..2772446-chr8:2773950..2776616,2	K562	blood:
4	chr8:2783957..2786248-chr8:2796648..2799482,2	K562	blood:
5	chr8:2768643..2771123-chr8:2792166..2794441,2	K562	blood:
6	chr8:2750431..2753920-chr8:2754914..2757254,3	K562	blood:
7	chr8:2784674..2786393-chr8:2792193..2794250,2	K562	blood:
8	chr8:2753797..2757716-chr8:2758640..2762168,3	K562	blood:
9	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
10	chr8:2750431..2753920-chr8:2754914..2757254,3	K562	blood:
11	chr8:2884129..2886374-chr8:2888333..2890117,2	K562	blood:
12	chr8:2884129..2886374-chr8:2888333..2890117,2	K562	blood:
13	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
14	chr8:2829379..2830950-chr8:2834355..2837068,2	K562	blood:
15	chr8:2865247..2867969-chr8:2868176..2872126,4	K562	blood:
16	chr8:2743139..2745505-chr8:2752998..2755650,2	K562	blood:
17	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:
18	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
19	chr8:2917024..2919683-chr8:2921100..2923818,2	K562	blood:
20	chr8:2822063..2824754-chr8:2827562..2829659,2	K562	blood:
21	chr8:2949313..2951484-chr8:2956361..2958211,2	K562	blood:
22	chr8:2783957..2786248-chr8:2796648..2799482,2	K562	blood:
23	chr8:2917024..2919683-chr8:2921100..2923818,2	K562	blood:
24	chr8:2829379..2830950-chr8:2834355..2837068,2	K562	blood:
25	chr8:2924503..2926165-chr8:2927948..2929693,2	K562	blood:
26	chr8:2768643..2771123-chr8:2792166..2794441,2	K562	blood:
27	chr8:2832391..2834459-chr8:2835771..2837988,2	K562	blood:
28	chr8:2934204..2935975-chr8:2939449..2941530,2	K562	blood:
29	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
30	chr12:56367505..56368235-chr8:2894157..2894798,2	MCF-7	breast:
31	chr8:2822063..2824754-chr8:2827562..2829659,2	K562	blood:
32	chr8:2832391..2834459-chr8:2835771..2837988,2	K562	blood:
33	chr16:12825533..12827033-chr8:2762155..2763733,2	K562	blood:
34	chr8:2828762..2830879-chr8:2834821..2837068,2	K562	blood:
35	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
36	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
37	chr8:2790313..2793074-chr8:2794638..2796914,2	K562	blood:
38	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:
39	chr8:2943250..2945425-chr8:2952775..2955064,2	K562	blood:
40	chr8:2807090..2809618-chr8:2810131..2812538,2	K562	blood:
41	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
42	chr8:2924503..2926165-chr8:2927948..2929693,2	K562	blood:
43	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
44	chr8:2753797..2757716-chr8:2758640..2762168,3	K562	blood:
45	chr8:2807090..2809618-chr8:2810131..2812538,2	K562	blood:
46	chr8:2943250..2945425-chr8:2952775..2955064,2	K562	blood:
47	chr8:2790313..2793074-chr8:2794638..2796914,2	K562	blood:
48	chr8:2784674..2786393-chr8:2792193..2794250,2	K562	blood:
49	chr8:2865247..2867969-chr8:2868176..2872126,4	K562	blood:
50	chr8:2828762..2830879-chr8:2834821..2837068,2	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-MYOM2-14	chr8:2877373-2877426	NONHSAT124740
3	lnc-MYOM2-13	chr8:2778500-2779629	NONHSAT124739

No data

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

Extended variants
information (count: 10203 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:10203 , 50 per page) page: 1 2 3 4 5 6 7 ... 205

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561524325	chr8:2756828-2756829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530735181	chr8:2756842-2756843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563961172	chr8:2756893-2756894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs59277313	chr8:2756914-2756915	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs537967794	chr8:2756923-2756924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565931479	chr8:2756941-2756942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528691009	chr8:2756974-2756975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557908273	chr8:2757001-2757002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75999683	chr8:2757020-2757021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151299586	chr8:2757078-2757079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537426025	chr8:2757122-2757123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs57543390	chr8:2757128-2757129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533308861	chr8:2757139-2757140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75677933	chr8:2757150-2757151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190878935	chr8:2757156-2757157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370120650	chr8:2757160-2757161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553348917	chr8:2757237-2757238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369707158	chr8:2757264-2757265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78161352	chr8:2757288-2757289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74956388	chr8:2757318-2757319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555405653	chr8:2757341-2757342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs60360122	chr8:2757342-2757343	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs544154816	chr8:2757355-2757356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77129729	chr8:2757364-2757365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566992776	chr8:2757369-2757370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532810682	chr8:2757371-2757372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12548252	chr8:2757414-2757415	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559656861	chr8:2757422-2757423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140224681	chr8:2757430-2757431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548521101	chr8:2757451-2757452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568496705	chr8:2757452-2757453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530916481	chr8:2757455-2757456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551093364	chr8:2757460-2757461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570752025	chr8:2757474-2757475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367792455	chr8:2757490-2757491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10712718	chr8:2757495-2757496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149895656	chr8:2757511-2757512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539866927	chr8:2757512-2757513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576108601	chr8:2757537-2757538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553287913	chr8:2757606-2757607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566787305	chr8:2757611-2757612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535616623	chr8:2757612-2757613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538550783	chr8:2757624-2757625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369924562	chr8:2757633-2757634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7821995	chr8:2757637-2757638	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543969976	chr8:2757674-2757675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557862418	chr8:2757685-2757686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577204835	chr8:2757728-2757729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117500196	chr8:2757768-2757769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2670064	chr8:2768034-2768035	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2756800-2757200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:2756800-2757400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr8:2756800-2757600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr8:2756800-2757600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr8:2757000-2757600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr8:2757000-2757800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:2757200-2757600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:2757200-2757600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr8:2757200-2757800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:2768000-2768200	Enhancers	Gastric	stomach
11	chr8:2768000-2769200	Enhancers	Brain Germinal Matrix	brain
12	chr8:2768200-2772000	Weak transcription	Gastric	stomach
13	chr8:2769600-2769800	Enhancers	Fetal Intestine Small	intestine
14	chr8:2769800-2773400	Weak transcription	Fetal Intestine Small	intestine
15	chr8:2772000-2772200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:2772000-2772200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr8:2772000-2772200	ZNF genes & repeats	Gastric	stomach
18	chr8:2772200-2772800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:2772200-2777400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr8:2772200-2779600	Weak transcription	Gastric	stomach
21	chr8:2772400-2773800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:2772400-2779800	Weak transcription	Fetal Stomach	stomach
23	chr8:2772600-2772800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:2772800-2773400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr8:2772800-2774400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:2773200-2773400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:2773200-2774200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr8:2773200-2774400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:2773400-2774000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:2773400-2774400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr8:2773400-2774400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr8:2773400-2774600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:2773400-2774600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr8:2773400-2774800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr8:2773400-2775000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:2773400-2775000	Enhancers	Fetal Intestine Small	intestine
37	chr8:2773400-2776000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:2773600-2774400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:2773600-2774800	Enhancers	Fetal Intestine Large	intestine
40	chr8:2773600-2775400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr8:2773600-2775400	Enhancers	Osteobl	bone
42	chr8:2773800-2774200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:2773800-2774600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr8:2773800-2774800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr8:2773800-2775600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:2774000-2774400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:2774000-2774400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:2774000-2774400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:2774200-2776000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr8:2774200-2776800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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