Variant report

Variant	esv3419415
Chromosome Location	chr8:103525141-103575507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1528)
CpG islands
(count:1100)
Chromatin interactive
region (count:69)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:103540422-103540495	K562	blood:	n/a	n/a
2	ARID3A	chr8:103540902-103541163	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:103553642-103554293	K562	blood:	n/a	n/a
4	ATF1	chr8:103540895-103541211	K562	blood:	n/a	n/a
5	ATF1	chr8:103553901-103554231	K562	blood:	n/a	n/a
6	ATF2	chr8:103542406-103542818	GM12878	blood:	n/a	n/a
7	ATF2	chr8:103547869-103548776	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:103546365-103547306	GM12878	blood:	n/a	n/a
9	ATF2	chr8:103546132-103547419	GM12878	blood:	n/a	n/a
10	ATF2	chr8:103547900-103548672	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr8:103547563-103548901	GM12878	blood:	n/a	n/a
12	ATF2	chr8:103540678-103541280	GM12878	blood:	n/a	n/a
13	ATF2	chr8:103567386-103568250	GM12878	blood:	n/a	n/a
14	ATF2	chr8:103567472-103568289	GM12878	blood:	n/a	n/a
15	ATF2	chr8:103569010-103570182	GM12878	blood:	n/a	n/a
16	ATF2	chr8:103540805-103541279	GM12878	blood:	n/a	n/a
17	ATF2	chr8:103542850-103543411	GM12878	blood:	n/a	n/a
18	ATF2	chr8:103547816-103548791	GM12878	blood:	n/a	n/a
19	ATF2	chr8:103568983-103569885	GM12878	blood:	n/a	n/a
20	ATF2	chr8:103542777-103543425	GM12878	blood:	n/a	n/a
21	BACH1	chr8:103553989-103554295	K562	blood:	n/a	n/a
22	BACH1	chr8:103549087-103549536	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr8:103548009-103548877	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr8:103567669-103567677	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:103556365-103556558	K562	blood:	n/a	n/a
26	BATF	chr8:103542519-103542832	GM12878	blood:	n/a	n/a
27	BATF	chr8:103542497-103542796	GM12878	blood:	n/a	n/a
28	BATF	chr8:103567478-103567932	GM12878	blood:	n/a	n/a
29	BATF	chr8:103546533-103547273	GM12878	blood:	n/a	n/a
30	BATF	chr8:103540852-103541211	GM12878	blood:	n/a	n/a
31	BATF	chr8:103544091-103544388	GM12878	blood:	n/a	n/a
32	BATF	chr8:103546865-103547208	GM12878	blood:	n/a	n/a
33	BATF	chr8:103569172-103569766	GM12878	blood:	n/a	n/a
34	BATF	chr8:103569289-103569755	GM12878	blood:	n/a	n/a
35	BATF	chr8:103547888-103548710	GM12878	blood:	n/a	chr8:103548046-103548056
36	BATF	chr8:103543019-103543298	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:103546700-103547273	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:103546539-103547304	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:103569336-103569623	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:103569270-103569779	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:103548037-103548629	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:103548111-103548617	H1-hESC	embryonic stem cell:	n/a	n/a
43	BCL11A	chr8:103567452-103567911	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:103567561-103567909	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:103547879-103548475	GM12878	blood:	n/a	n/a
46	BCL3	chr8:103563509-103563875	GM12878	blood:	n/a	n/a
47	BCL3	chr8:103540607-103541569	A549	lung:	n/a	n/a
48	BCL3	chr8:103567498-103567955	GM12878	blood:	n/a	n/a
49	BCL3	chr8:103548955-103549576	A549	lung:	n/a	n/a
50	BCL3	chr8:103547923-103548688	GM12878	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103563653-103563703	U87	brain:	n/a
2	chr8:103556749-103556799	U87	brain:	n/a
3	chr8:103563653-103563703	U87	brain:	n/a
4	chr8:103556749-103556799	U87	brain:	n/a
5	chr8:103563653-103563703	GM12891	blood:	n/a
6	chr8:103563653-103563703	H1-hESC	embryonic stem cell:	embryo
7	chr8:103551067-103551117	HUVEC	blood vessel:	n/a
8	chr8:103549622-103549672	BE2_C	brain:	n/a
9	chr8:103564136-103564186	HMEC	breast:	n/a
10	chr8:103551067-103551117	Hela-S3	cervix:	n/a
11	chr8:103550807-103550857	NHDF-neo	bronchial:	n/a
12	chr8:103556749-103556799	PrEC	prostate:	n/a
13	chr8:103573117-103573167	ECC-1	luminal epithelium:	n/a
14	chr8:103568792-103568842	MCF10A-Er-Src	breast:	n/a
15	chr8:103563698-103563748	PANC-1	pancreas:	n/a
16	chr8:103549622-103549672	T-47D	breast:	n/a
17	chr8:103540783-103540833	GM06990	blood:	n/a
18	chr8:103564136-103564186	HIPEpiC	eye:	n/a
19	chr8:103573117-103573167	A549	lung:	n/a
20	chr8:103551067-103551117	AG10803	skin:	n/a
21	chr8:103541014-103541064	PANC-1	pancreas:	n/a
22	chr8:103568792-103568842	SK-N-MC	brain:	n/a
23	chr8:103548145-103548195	H1-hESC	embryonic stem cell:	embryo
24	chr8:103549622-103549672	AG04450	lung:	fetal
25	chr8:103564136-103564186	HCT-116	colon:	n/a
26	chr8:103563327-103563377	HRPEpiC	eye:	n/a
27	chr8:103556749-103556799	LNCaP	prostate:	n/a
28	chr8:103564136-103564186	T-47D	breast:	n/a
29	chr8:103530461-103530511	HRCEpiC	kidney:	n/a
30	chr8:103548145-103548195	RPTEC	kidney:	n/a
31	chr8:103572833-103572883	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:103563327-103563377	PANC-1	pancreas:	n/a
33	chr8:103540783-103540833	PFSK-1	brain:	n/a
34	chr8:103549622-103549672	MCF-7	breast:	n/a
35	chr8:103540783-103540833	HL-60	blood:	n/a
36	chr8:103550807-103550857	HCM	heart:	n/a
37	chr8:103549622-103549672	HCPEpiC	choroid plexus:	n/a
38	chr8:103563029-103563079	GM12891	blood:	n/a
39	chr8:103563653-103563703	MCF-7	breast:	n/a
40	chr8:103530461-103530511	AG04450	lung:	fetal
41	chr8:103562972-103563022	H1-hESC	embryonic stem cell:	embryo
42	chr8:103551067-103551117	HRE	kidney:	n/a
43	chr8:103572833-103572883	NHDF-neo	bronchial:	n/a
44	chr8:103563029-103563079	HUVEC	blood vessel:	n/a
45	chr8:103551067-103551117	SK-N-SH_RA	brain:	n/a
46	chr8:103564136-103564186	SKMC	muscle:	n/a
47	chr8:103572833-103572883	U87	brain:	n/a
48	chr8:103556749-103556799	AG09309	skin:	n/a
49	chr8:103563327-103563377	HCM	heart:	n/a
50	chr8:103549622-103549672	GM12878	blood:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:103537823..103539914-chr8:103541615..103544140,2	K562	blood:
2	chr8:103255266..103257268-chr8:103548486..103550242,2	MCF-7	breast:
3	chr8:103528321..103530383-chr8:103533029..103535139,2	K562	blood:
4	chr8:103545241..103546971-chr8:103549394..103552114,2	MCF-7	breast:
5	chr8:103559929..103561966-chr8:103584130..103585766,2	MCF-7	breast:
6	chr8:103552930..103556301-chr8:103557588..103560805,4	K562	blood:
7	chr8:103525311..103527226-chr8:103533440..103535357,2	K562	blood:
8	chr8:103563316..103565121-chr8:103568233..103570660,2	K562	blood:
9	chr8:103556702..103559349-chr8:103559916..103561821,3	MCF-7	breast:
10	chr8:103561720..103564415-chr8:103565108..103567782,4	K562	blood:
11	chr8:103515933..103517750-chr8:103525696..103527762,2	MCF-7	breast:
12	chr8:103540947..103542816-chr8:103666262..103668771,2	K562	blood:
13	chr8:103561576..103563655-chr8:103568323..103570576,2	MCF-7	breast:
14	chr8:103525032..103526811-chr8:103533837..103535357,2	K562	blood:
15	chr8:103540698..103544207-chr8:103546696..103550142,4	MCF-7	breast:
16	chr8:103566130..103569047-chr8:103588313..103590545,3	MCF-7	breast:
17	chr8:103552849..103555582-chr8:103602690..103604723,2	K562	blood:
18	chr8:103547915..103550298-chr8:103554370..103557167,3	K562	blood:
19	chr8:103548290..103549858-chr8:103666660..103669466,2	K562	blood:
20	chr8:103566007..103567719-chr8:103573163..103576041,2	K562	blood:
21	chr8:103553403..103555856-chr8:103556123..103559694,3	MCF-7	breast:
22	chr8:103554141..103557178-chr8:103560582..103564192,4	K562	blood:
23	chr8:103537823..103539914-chr8:103541615..103544140,2	K562	blood:
24	chr8:103552930..103556301-chr8:103557588..103560805,4	K562	blood:
25	chr8:103541502..103544412-chr8:103664265..103666950,2	MCF-7	breast:
26	chr8:103571721..103574356-chr8:103574864..103576859,2	MCF-7	breast:
27	chr8:103561576..103563655-chr8:103568323..103570576,2	MCF-7	breast:
28	chr8:103525032..103526811-chr8:103533837..103535357,2	K562	blood:
29	chr8:103564890..103567326-chr8:103568575..103570813,2	MCF-7	breast:
30	chr8:103568483..103570807-chr8:103581196..103582779,2	MCF-7	breast:
31	chr8:103553403..103555856-chr8:103556123..103559694,3	MCF-7	breast:
32	chr8:103547915..103550298-chr8:103554370..103557167,3	K562	blood:
33	chr8:103523909..103525501-chr8:103526582..103528205,2	MCF-7	breast:
34	chr8:103561236..103562878-chr8:103564860..103566759,2	MCF-7	breast:
35	chr8:103567304..103569694-chr8:103578366..103580055,2	MCF-7	breast:
36	chr8:103422775..103425553-chr8:103523894..103525443,2	MCF-7	breast:
37	chr8:103561837..103564044-chr8:103571936..103573800,2	MCF-7	breast:
38	chr8:103561236..103562878-chr8:103564860..103566759,2	MCF-7	breast:
39	chr8:103423608..103426588-chr8:103558212..103561124,2	K562	blood:
40	chr8:103422537..103425322-chr8:103540234..103542841,3	K562	blood:
41	chr8:103523909..103525501-chr8:103526582..103528205,2	MCF-7	breast:
42	chr8:103575313..103581780-chr8:103582663..103591933,12	MCF-7	breast:
43	chr8:103525311..103527226-chr8:103533440..103535357,2	K562	blood:
44	chr8:103540102..103543996-chr8:103574718..103578411,4	MCF-7	breast:
45	chr8:103423160..103425899-chr8:103539167..103542509,5	MCF-7	breast:
46	chr8:103549075..103551753-chr8:103552917..103555861,3	MCF-7	breast:
47	chr8:103564890..103567326-chr8:103568575..103570813,2	MCF-7	breast:
48	chr8:103549075..103551753-chr8:103552917..103555861,3	MCF-7	breast:
49	chr8:103422090..103425844-chr8:103540841..103544782,4	MCF-7	breast:
50	chr8:103423156..103426710-chr8:103547734..103551186,4	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF10-5	chr8:103553392-103553821	NONHSAT128100
2	lnc-ODF1-1	chr8:103540968-103541083	NONHSAT128098
3	lnc-ODF1-1	chr8:103550612-103550896	NONHSAT128098
4	lnc-ODF1-2	chr8:103561889-103562037	NONHSAT128101
5	lnc-ODF1-1	chr8:103547961-103548188	NONHSAT128098
6	lnc-ODF1-1	chr8:103541539-103541931	XLOC_006892
7	lnc-ODF1-2	chr8:103562735-103563312	NONHSAT128101
8	lnc-KLF10-5	chr8:103562771-103563312	NONHSAT128100
9	lnc-ODF1-1	chr8:103545983-103546093	NONHSAT128098
10	lnc-ODF1-1	chr8:103541045-103541083	XLOC_006892

No data

Variant related genes	Relation type
ENSG00000253633	TF binding region
ODF1	TF binding region
RNU6-1224P	TF binding region
ENSG00000253633	CpG island
ODF1	CpG island
RNU6-1224P	CpG island
ENSG00000155087	chromatin interactions
ENSG00000253633	chromatin interactions
ENSG00000252593	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000240724	chromatin interactions
ENSG00000104517	chromatin interactions
ENSG00000246263	chromatin interactions

Extended variants
information (count: 2063 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2063 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4734630	chr8:103525177-103525178	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559063968	chr8:103525197-103525198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs62524821	chr8:103525217-103525218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs2511756	chr8:103525237-103525238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79633329	chr8:103525268-103525269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537314427	chr8:103525276-103525277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184064816	chr8:103525333-103525334	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567527815	chr8:103525351-103525352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111841720	chr8:103525399-103525400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs62524822	chr8:103525404-103525405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181667953	chr8:103525430-103525431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs578176423	chr8:103525548-103525549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569825952	chr8:103525567-103525568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538664105	chr8:103525590-103525591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539137513	chr8:103525600-103525601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557626951	chr8:103525796-103525797	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs36028318	chr8:103525813-103525814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs4734631	chr8:103525841-103525842	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs553036493	chr8:103525871-103525872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543323381	chr8:103525926-103525927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150594307	chr8:103525936-103525937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs4734632	chr8:103525975-103525976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs367990865	chr8:103525978-103525979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs187632969	chr8:103526012-103526013	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370495468	chr8:103526051-103526052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558928271	chr8:103526063-103526064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115852740	chr8:103526070-103526071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs551472637	chr8:103526095-103526096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79658122	chr8:103526123-103526124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34663930	chr8:103526138-103526139	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531159939	chr8:103526206-103526207	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139644008	chr8:103526304-103526305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs567987352	chr8:103526306-103526307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574737666	chr8:103526317-103526318	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112827284	chr8:103526399-103526400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112221758	chr8:103526404-103526405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535771597	chr8:103526425-103526426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571676324	chr8:103526469-103526470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113147639	chr8:103526473-103526474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74843732	chr8:103526490-103526491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191948724	chr8:103526520-103526521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537293340	chr8:103526560-103526561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555372103	chr8:103526612-103526613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs16869483	chr8:103526633-103526634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs540938428	chr8:103526687-103526688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs117275961	chr8:103526712-103526713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577243780	chr8:103526723-103526724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182201527	chr8:103526763-103526764	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34756019	chr8:103526774-103526775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563429055	chr8:103526779-103526780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
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
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	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
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103502800-103529800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:103518200-103529600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:103518200-103529600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr8:103518400-103529600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr8:103518400-103529600	Weak transcription	Right Atrium	heart
6	chr8:103524200-103529600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr8:103524400-103529600	Weak transcription	Fetal Brain Male	brain
8	chr8:103524400-103529800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr8:103524600-103526600	Weak transcription	Esophagus	oesophagus
10	chr8:103524600-103529400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr8:103524600-103529600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:103524600-103529600	Weak transcription	Fetal Intestine Large	intestine
13	chr8:103524600-103529600	Weak transcription	Fetal Intestine Small	intestine
14	chr8:103524600-103529800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr8:103524800-103525200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr8:103524800-103529600	Weak transcription	HepG2	liver
17	chr8:103525200-103527400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr8:103526600-103526800	Enhancers	Esophagus	oesophagus
19	chr8:103529000-103529600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr8:103529400-103529600	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr8:103529400-103530800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr8:103529600-103529800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:103529600-103529800	Enhancers	Right Atrium	heart
24	chr8:103529600-103530000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:103529600-103530000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:103529600-103530000	Enhancers	Fetal Brain Male	brain
27	chr8:103529600-103530000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
28	chr8:103529600-103530200	Enhancers	Stomach Mucosa	stomach
29	chr8:103529600-103530400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr8:103529600-103530400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:103529600-103530400	Enhancers	Colonic Mucosa	Colon
32	chr8:103529600-103530600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:103529600-103530600	Enhancers	Fetal Intestine Large	intestine
34	chr8:103529600-103530600	Enhancers	Fetal Intestine Small	intestine
35	chr8:103529600-103530600	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr8:103529600-103530800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr8:103529600-103530800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr8:103529600-103530800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr8:103529600-103531600	Enhancers	Duodenum Mucosa	Duodenum
40	chr8:103529600-103531600	Enhancers	HepG2	liver
41	chr8:103529800-103530200	Enhancers	Fetal Brain Female	brain
42	chr8:103529800-103530600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:103529800-103530600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:103529800-103530600	Enhancers	K562	blood
45	chr8:103529800-103530800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr8:103529800-103531000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:103530000-103530400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:103530000-103530600	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr8:103530000-103530800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr8:103530000-103540400	Weak transcription	Fetal Brain Male	brain

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