Variant report

Variant	esv2756883
Chromosome Location	chr1:210579523-210620779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:210580626-210580893	HepG2	liver:	n/a	n/a
2	ATF1	chr1:210591909-210591993	K562	blood:	n/a	n/a
3	ATF3	chr1:210612457-210612901	A549	lung:	n/a	n/a
4	ATF3	chr1:210612405-210612891	A549	lung:	n/a	n/a
5	BATF	chr1:210619807-210620273	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:210580537-210580923	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:210619822-210620085	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:210580601-210580904	K562	blood:	n/a	n/a
9	BHLHE40	chr1:210580581-210580980	GM12878	blood:	n/a	n/a
10	CEBPB	chr1:210618825-210619192	MCF-7	breast:	n/a	n/a
11	CEBPB	chr1:210612131-210613087	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:210618865-210619155	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:210612073-210612902	A549	lung:	n/a	n/a
14	CREB1	chr1:210612249-210612449	A549	lung:	n/a	n/a
15	CREB1	chr1:210580673-210580821	A549	lung:	n/a	n/a
16	CREB1	chr1:210612246-210612516	A549	lung:	n/a	n/a
17	CREB1	chr1:210580499-210580973	K562	blood:	n/a	n/a
18	CREB1	chr1:210580614-210580827	A549	lung:	n/a	n/a
19	CTCF	chr1:210580720-210580870	GM06990	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
20	CTCF	chr1:210580680-210580830	GM12866	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
21	CTCF	chr1:210580680-210580830	HA-sp	spinal cord:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
22	CTCF	chr1:210589420-210589570	AG04450	lung:	n/a	chr1:210589527-210589540
23	CTCF	chr1:210580640-210580790	GM12864	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
24	CTCF	chr1:210580680-210580830	GM12875	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
25	CTCF	chr1:210580700-210580850	WI-38	lung:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
26	CTCF	chr1:210580605-210580853	A549	lung:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
27	CTCF	chr1:210580640-210580790	GM12871	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
28	CTCF	chr1:210589360-210589510	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr1:210580612-210580880	Fibrobl	skin:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
30	CTCF	chr1:210580541-210580928	ECC-1	luminal epithelium:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
31	CTCF	chr1:210580700-210580850	HepG2	liver:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
32	CTCF	chr1:210580720-210580870	GM12872	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
33	CTCF	chr1:210580680-210580830	HRE	kidney:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
34	CTCF	chr1:210589440-210589590	GM06990	blood:	n/a	chr1:210589527-210589540
35	CTCF	chr1:210580700-210580850	NHLF	lung:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
36	CTCF	chr1:210614344-210614499	GM12878	blood:	n/a	n/a
37	CTCF	chr1:210580700-210580850	GM12865	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
38	CTCF	chr1:210580646-210581005	MCF-7	breast:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
39	CTCF	chr1:210580583-210580916	Spleen_OC	spleen:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
40	CTCF	chr1:210580523-210580962	GM12878	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
41	CTCF	chr1:210580680-210580830	GM12873	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
42	CTCF	chr1:210580527-210580854	SK-N-SH_RA	brain:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
43	CTCF	chr1:210580720-210580870	GM12869	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
44	CTCF	chr1:210580571-210580944	HepG2	liver:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
45	CTCF	chr1:210580621-210580886	GM12891	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
46	CTCF	chr1:210580471-210580977	HCT-116	colon:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
47	CTCF	chr1:210580640-210580790	GM12867	blood:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
48	CTCF	chr1:210580597-210580894	Medullo	brain:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
49	CTCF	chr1:210580720-210580870	WI-38	lung:	n/a	chr1:210580738-210580756 chr1:210580743-210580753 chr1:210580741-210580750 chr1:210580741-210580754 chr1:210580739-210580755 chr1:210580740-210580761
50	CTCF	chr1:210614405-210614497	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:210613691-210613741	T-47D	breast:	n/a
2	chr1:210607796-210607846	AG10803	skin:	n/a
3	chr1:210613691-210613741	BE2_C	brain:	n/a
4	chr1:210613691-210613741	LNCaP	prostate:	n/a
5	chr1:210612391-210612441	IMR90	lung:	fetal
6	chr1:210580909-210580959	PANC-1	pancreas:	n/a
7	chr1:210612391-210612441	A549	lung:	n/a
8	chr1:210607796-210607846	GM19239	blood:	n/a
9	chr1:210589683-210589733	NH-A	brain:	n/a
10	chr1:210612391-210612441	SKMC	muscle:	n/a
11	chr1:210607796-210607846	SK-N-SH	brain:	n/a
12	chr1:210580909-210580959	CMK	blood:	n/a
13	chr1:210607796-210607846	NHDF-neo	bronchial:	n/a
14	chr1:210607796-210607846	PFSK-1	brain:	n/a
15	chr1:210612391-210612441	CMK	blood:	n/a
16	chr1:210580909-210580959	HEK293	kidney:	embryo
17	chr1:210589683-210589733	HUVEC	blood vessel:	n/a
18	chr1:210607796-210607846	K562	blood:	n/a
19	chr1:210589683-210589733	BJ	skin:	n/a
20	chr1:210607796-210607846	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:210580909-210580959	T-47D	breast:	n/a
22	chr1:210589683-210589733	HAEpiC	amniotic membrane:	n/a
23	chr1:210607796-210607846	CMK	blood:	n/a
24	chr1:210613691-210613741	PANC-1	pancreas:	n/a
25	chr1:210580909-210580959	BE2_C	brain:	n/a
26	chr1:210580909-210580959	NHDF-neo	bronchial:	n/a
27	chr1:210612391-210612441	GM12878	blood:	n/a
28	chr1:210607796-210607846	PANC-1	pancreas:	n/a
29	chr1:210612391-210612441	AG04449	skin:	fetal
30	chr1:210607796-210607846	HUVEC	blood vessel:	n/a
31	chr1:210612391-210612441	AG10803	skin:	n/a
32	chr1:210580909-210580959	AoSMC	blood vessel:	n/a
33	chr1:210607796-210607846	LNCaP	prostate:	n/a
34	chr1:210613691-210613741	GM06990	blood:	n/a
35	chr1:210607796-210607846	AG09309	skin:	n/a
36	chr1:210613691-210613741	SAEC	small airway:	n/a
37	chr1:210589683-210589733	PFSK-1	brain:	n/a
38	chr1:210613691-210613741	H1-hESC	embryonic stem cell:	embryo
39	chr1:210607796-210607846	HNPCEpiC	eye:	n/a
40	chr1:210580909-210580959	HCM	heart:	n/a
41	chr1:210580909-210580959	Jurkat	blood:	n/a
42	chr1:210589683-210589733	NB4	blood:	n/a
43	chr1:210613691-210613741	SK-N-MC	brain:	n/a
44	chr1:210613691-210613741	PFSK-1	brain:	n/a
45	chr1:210580909-210580959	NT2-D1	testis:	n/a
46	chr1:210607796-210607846	AG04449	skin:	fetal
47	chr1:210612391-210612441	MCF10A-Er-Src	breast:	n/a
48	chr1:210580909-210580959	MCF10A-Er-Src	breast:	n/a
49	chr1:210589683-210589733	Jurkat	blood:	n/a
50	chr1:210612391-210612441	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:210580344..210581229-chr1:211307198..211308039,4	MCF-7	breast:
2	chr1:210580352..210581221-chr1:211308252..211309278,4	MCF-7	breast:
3	chr1:210545312..210548912-chr1:210591590..210593685,3	MCF-7	breast:
4	chr1:210565840..210568269-chr1:210585284..210587364,2	K562	blood:
5	chr1:210580289..210581488-chr1:211307440..211308125,4	K562	blood:
6	chr1:210542938..210544518-chr1:210591171..210592878,2	MCF-7	breast:
7	chr1:210590026..210592841-chr1:211432035..211434761,3	MCF-7	breast:
8	chr1:210544698..210555948-chr1:210566953..210584306,65	MCF-7	breast:
9	chr1:210545710..210547947-chr1:210586975..210589311,2	MCF-7	breast:
10	chr1:210580604..210582108-chr1:210584910..210587345,2	MCF-7	breast:
11	chr1:210546163..210547950-chr1:210586402..210589713,3	K562	blood:
12	chr1:210603462..210605610-chr1:210606812..210609556,2	MCF-7	breast:
13	chr1:210580317..210581126-chr1:211307369..211308490,3	MCF-7	breast:
14	chr1:210545093..210547950-chr1:210587294..210588958,2	K562	blood:
15	chr1:210573314..210577563-chr1:210578533..210582759,4	K562	blood:
16	chr1:210612929..210615850-chr1:210617890..210620157,2	K562	blood:
17	chr1:210545855..210547911-chr1:210612937..210615260,3	K562	blood:
18	chr1:210572425..210575594-chr1:210579116..210581300,3	K562	blood:
19	chr1:210580467..210581234-chr1:211308480..211309338,4	K562	blood:
20	chr1:210583255..210586128-chr1:210592478..210594714,2	MCF-7	breast:
21	chr1:210612929..210615850-chr1:210617890..210620157,2	K562	blood:
22	chr1:210546209..210547906-chr1:210583781..210585817,2	K562	blood:
23	chr1:210545308..210548162-chr1:210603373..210605975,2	MCF-7	breast:
24	chr1:210546219..210548484-chr1:210580147..210582038,2	K562	blood:
25	chr1:210544032..210549009-chr1:210579509..210584636,8	MCF-7	breast:
26	chr1:210545823..210547818-chr1:210606420..210608728,2	K562	blood:
27	chr1:210545794..210547749-chr1:210620055..210622714,2	MCF-7	breast:
28	chr1:210583255..210586128-chr1:210592478..210594714,2	MCF-7	breast:
29	chr1:210618870..210621785-chr1:211306135..211307908,2	MCF-7	breast:
30	chr1:210580604..210582108-chr1:210584910..210587345,2	MCF-7	breast:
31	chr1:210545786..210547818-chr1:210606420..210608180,2	K562	blood:
32	chr1:210545333..210549114-chr1:210576030..210582834,11	K562	blood:
33	chr1:210617470..210620137-chr1:211308701..211310289,2	MCF-7	breast:
34	chr1:210603462..210605610-chr1:210606812..210609556,2	MCF-7	breast:

Variant related genes	Relation type
HHAT	TF binding region
HHAT	CpG island
ENSG00000200972	chromatin interactions
ENSG00000234233	chromatin interactions
ENSG00000143473	chromatin interactions
ENSG00000117625	chromatin interactions

Extended variants
information (count: 1689 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1689 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10489383	chr1:210579523-210579524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12085633	chr1:210579649-210579650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs12085635	chr1:210579657-210579658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs12070523	chr1:210579666-210579667	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12071616	chr1:210579717-210579718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs11462087	chr1:210579744-210579745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs398103650	chr1:210579755-210579756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs151304228	chr1:210579801-210579802	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200224275	chr1:210579816-210579817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112241948	chr1:210579819-210579820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574307065	chr1:210579821-210579822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185538669	chr1:210579822-210579823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200381407	chr1:210579824-210579825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543437009	chr1:210579845-210579846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562232586	chr1:210579848-210579849	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190778053	chr1:210579878-210579879	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574037133	chr1:210579890-210579891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541225385	chr1:210579909-210579910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575290370	chr1:210579928-210579929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs115280401	chr1:210579938-210579939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148486201	chr1:210579950-210579951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535014407	chr1:210579953-210579954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6684845	chr1:210580017-210580018	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142664467	chr1:210580028-210580029	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs182187518	chr1:210580079-210580080	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185205422	chr1:210580088-210580089	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549392718	chr1:210580106-210580107	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568254781	chr1:210580107-210580108	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs556583939	chr1:210580181-210580182	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188299875	chr1:210580182-210580183	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535794555	chr1:210580197-210580198	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547575354	chr1:210580224-210580225	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368944725	chr1:210580238-210580239	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539512685	chr1:210580261-210580262	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181126515	chr1:210580288-210580289	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557547773	chr1:210580301-210580302	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs576123471	chr1:210580348-210580349	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs1033491	chr1:210580381-210580382	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs555389572	chr1:210580483-210580484	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs1033490	chr1:210580487-210580488	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs78485988	chr1:210580560-210580561	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs185869306	chr1:210580569-210580570	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs577175494	chr1:210580573-210580574	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190633656	chr1:210580582-210580583	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559484204	chr1:210580636-210580637	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs114023038	chr1:210580670-210580671	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376108481	chr1:210580680-210580681	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563615182	chr1:210580688-210580689	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371046993	chr1:210580699-210580700	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs374462046	chr1:210580717-210580718	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210529600-210586000	Weak transcription	Pancreas	Pancrea
2	chr1:210551400-210586000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:210559000-210584400	Weak transcription	Fetal Stomach	stomach
4	chr1:210566800-210586200	Weak transcription	Lung	lung
5	chr1:210567400-210617200	Weak transcription	Left Ventricle	heart
6	chr1:210570200-210594000	Weak transcription	Fetal Lung	lung
7	chr1:210571200-210586200	Weak transcription	Colonic Mucosa	Colon
8	chr1:210571200-210592400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:210571400-210591400	Weak transcription	Ovary	ovary
10	chr1:210571400-210641000	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr1:210573600-210592400	Weak transcription	Fetal Intestine Small	intestine
12	chr1:210573800-210592200	Weak transcription	Primary T cells from cord blood	blood
13	chr1:210573800-210594400	Weak transcription	Spleen	Spleen
14	chr1:210574000-210586600	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr1:210574200-210581000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:210574400-210580600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:210574400-210587400	Weak transcription	Colon Smooth Muscle	Colon
18	chr1:210574400-210592200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:210574400-210594400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr1:210574400-210595200	Weak transcription	Right Ventricle	heart
21	chr1:210575800-210584600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:210577400-210591600	Weak transcription	Thymus	Thymus
23	chr1:210578200-210581000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:210578400-210580800	Enhancers	HMEC	breast
25	chr1:210578400-210581000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:210578400-210581000	Enhancers	NHEK	skin
27	chr1:210578800-210581400	Enhancers	HSMMtube	muscle
28	chr1:210578800-210584400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr1:210579000-210580400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:210579400-210580000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr1:210579400-210581200	Enhancers	HSMM	muscle
32	chr1:210580000-210581200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:210580000-210581200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr1:210580200-210581000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:210580200-210581000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:210580400-210581200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr1:210580400-210581200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr1:210580600-210581000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr1:210580800-210581000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr1:210580800-210581200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr1:210580800-210581200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:210580800-210581200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:210580800-210581200	Enhancers	Brain Angular Gyrus	brain
44	chr1:210580800-210581200	Enhancers	HepG2	liver
45	chr1:210581000-210581200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:210581000-210581200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr1:210581000-210581400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr1:210581000-210581400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:210581000-210581400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:210581000-210584800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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