Variant report

Variant	esv1800947
Chromosome Location	chr7:97857675-97889672
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1063)
CpG islands
(count:1405)
Chromatin interactive
region (count:25)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1063 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97884715-97884806	K562	blood:	n/a	n/a
2	ARID3A	chr7:97881427-97882096	HepG2	liver:	n/a	n/a
3	ATF1	chr7:97881467-97881729	K562	blood:	n/a	n/a
4	ATF1	chr7:97884669-97884833	K562	blood:	n/a	n/a
5	BACH1	chr7:97881659-97881997	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:97870682-97870974	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr7:97881249-97881690	A549	lung:	n/a	chr7:97881653-97881662 chr7:97881401-97881414 chr7:97881533-97881542
8	BHLHE40	chr7:97889451-97889702	K562	blood:	n/a	n/a
9	BHLHE40	chr7:97881249-97882029	GM12878	blood:	n/a	chr7:97881401-97881417 chr7:97881395-97881411
10	BHLHE40	chr7:97870759-97871026	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:97881121-97881911	HepG2	liver:	n/a	chr7:97881401-97881417 chr7:97881395-97881411
12	BHLHE40	chr7:97870789-97870925	K562	blood:	n/a	n/a
13	BHLHE40	chr7:97881504-97881683	K562	blood:	n/a	n/a
14	BHLHE40	chr7:97880302-97880362	K562	blood:	n/a	n/a
15	BRCA1	chr7:97880965-97881312	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:97882061-97882219	HepG2	liver:	n/a	n/a
17	BRCA1	chr7:97878687-97878761	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:97881691-97881752	HepG2	liver:	n/a	n/a
19	BRCA1	chr7:97880996-97881452	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr7:97881020-97881382	HepG2	liver:	n/a	n/a
21	BRCA1	chr7:97880989-97881824	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr7:97881397-97881851	K562	blood:	n/a	n/a
23	CCNT2	chr7:97857856-97857921	K562	blood:	n/a	n/a
24	CCNT2	chr7:97889528-97889728	K562	blood:	n/a	n/a
25	CCNT2	chr7:97881265-97881918	K562	blood:	n/a	n/a
26	CEBPB	chr7:97857481-97857783	IMR90	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
27	CEBPB	chr7:97857460-97857814	HepG2	liver:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
28	CEBPB	chr7:97881878-97882244	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:97857410-97857839	MCF-7	breast:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
30	CEBPB	chr7:97857468-97857829	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
31	CEBPB	chr7:97881448-97882197	Hela-S3	cervix:	n/a	chr7:97881600-97881608
32	CEBPB	chr7:97870771-97870946	GM12878	blood:	n/a	n/a
33	CEBPB	chr7:97857541-97857759	H1-hESC	embryonic stem cell:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
34	CEBPB	chr7:97869258-97869545	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:97881789-97882137	A549	lung:	n/a	n/a
36	CEBPB	chr7:97881907-97882107	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:97881961-97882161	K562	blood:	n/a	n/a
38	CEBPB	chr7:97857556-97857798	Hela-S3	cervix:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
39	CEBPB	chr7:97857468-97857755	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
40	CEBPB	chr7:97857558-97857722	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
41	CEBPB	chr7:97867006-97867254	MCF-7	breast:	n/a	n/a
42	CEBPB	chr7:97857458-97857785	A549	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
43	CEBPB	chr7:97869322-97869457	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:97869264-97869458	IMR90	lung:	n/a	n/a
45	CEBPD	chr7:97881311-97881818	HepG2	liver:	n/a	n/a
46	CHD1	chr7:97880950-97881228	GM12878	blood:	n/a	n/a
47	CHD2	chr7:97880915-97882206	HepG2	liver:	n/a	n/a
48	CHD2	chr7:97870697-97870975	GM12878	blood:	n/a	n/a
49	CHD2	chr7:97880973-97881770	K562	blood:	n/a	n/a
50	CHD2	chr7:97870894-97870902	HepG2	liver:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97857647-97857697	NB4	blood:	n/a
2	chr7:97882260-97882310	Hela-S3	cervix:	n/a
3	chr7:97857647-97857697	NB4	blood:	n/a
4	chr7:97882260-97882310	Hela-S3	cervix:	n/a
5	chr7:97881167-97881217	SK-N-SH	brain:	n/a
6	chr7:97857938-97857988	GM12878	blood:	n/a
7	chr7:97857647-97857697	HNPCEpiC	eye:	n/a
8	chr7:97881894-97881944	PrEC	prostate:	n/a
9	chr7:97875293-97875343	PrEC	prostate:	n/a
10	chr7:97882212-97882262	HRE	kidney:	n/a
11	chr7:97882260-97882310	MCF10A-Er-Src	breast:	n/a
12	chr7:97881541-97881591	HAEpiC	amniotic membrane:	n/a
13	chr7:97881894-97881944	NHDF-neo	bronchial:	n/a
14	chr7:97877765-97877815	RPTEC	kidney:	n/a
15	chr7:97877765-97877815	GM12891	blood:	n/a
16	chr7:97857989-97858039	GM06990	blood:	n/a
17	chr7:97857971-97858021	HEK293	kidney:	embryo
18	chr7:97880848-97880898	AG09309	skin:	n/a
19	chr7:97868061-97868111	HCT-116	colon:	n/a
20	chr7:97881894-97881944	AG04450	lung:	fetal
21	chr7:97881167-97881217	HMEC	breast:	n/a
22	chr7:97881541-97881591	U87	brain:	n/a
23	chr7:97857647-97857697	Caco-2	colon:	n/a
24	chr7:97868061-97868111	CMK	blood:	n/a
25	chr7:97857938-97857988	PrEC	prostate:	n/a
26	chr7:97857938-97857988	MCF10A-Er-Src	breast:	n/a
27	chr7:97881541-97881591	RPTEC	kidney:	n/a
28	chr7:97868061-97868111	GM12878	blood:	n/a
29	chr7:97857971-97858021	HRPEpiC	eye:	n/a
30	chr7:97880848-97880898	HCT-116	colon:	n/a
31	chr7:97881894-97881944	Hela-S3	cervix:	n/a
32	chr7:97877765-97877815	HRE	kidney:	n/a
33	chr7:97857971-97858021	SKMC	muscle:	n/a
34	chr7:97881541-97881591	HEK293	kidney:	embryo
35	chr7:97880848-97880898	HEEpiC	esophagus:	n/a
36	chr7:97857647-97857697	GM12891	blood:	n/a
37	chr7:97857971-97858021	BJ	skin:	n/a
38	chr7:97881167-97881217	IMR90	lung:	fetal
39	chr7:97857971-97858021	SK-N-MC	brain:	n/a
40	chr7:97884367-97884417	CMK	blood:	n/a
41	chr7:97877765-97877815	HUVEC	blood vessel:	n/a
42	chr7:97880563-97880613	IMR90	lung:	fetal
43	chr7:97877765-97877815	NHBE	bronchial:	n/a
44	chr7:97882137-97882187	U87	brain:	n/a
45	chr7:97875293-97875343	GM19239	blood:	n/a
46	chr7:97882137-97882187	HRPEpiC	eye:	n/a
47	chr7:97881894-97881944	GM12891	blood:	n/a
48	chr7:97882137-97882187	HEEpiC	esophagus:	n/a
49	chr7:97882212-97882262	U87	brain:	n/a
50	chr7:97881541-97881591	SAEC	small airway:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97839660..97842920-chr7:97872632..97874833,3	K562	blood:
2	chr7:97881770..97884305-chr7:97885648..97888001,2	K562	blood:
3	chr7:97860162..97861679-chr7:97865709..97867211,2	K562	blood:
4	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
5	chr7:97844457..97846470-chr7:97865336..97867376,2	MCF-7	breast:
6	chr7:97736018..97736542-chr7:97859141..97859647,2	K562	blood:
7	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
8	chr7:97856853..97859971-chr7:97865587..97869015,3	MCF-7	breast:
9	chr7:97881770..97884305-chr7:97885648..97888001,2	K562	blood:
10	chr7:97880638..97884180-chr7:98029742..98031678,3	MCF-7	breast:
11	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
12	chr7:97880609..97882891-chr7:97909884..97913133,3	MCF-7	breast:
13	chr7:97735682..97736214-chr7:97870411..97871232,2	K562	blood:
14	chr7:97859339..97861738-chr7:97869663..97872291,2	MCF-7	breast:
15	chr7:97650843..97651448-chr7:97870469..97871701,3	MCF-7	breast:
16	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
17	chr7:97797557..97798288-chr7:97870683..97871212,2	MCF-7	breast:
18	chr19:1268870..1269699-chr7:97881275..97881816,2	Hela-S3	cervix:
19	chr7:97847018..97848537-chr7:97878984..97881844,2	K562	blood:
20	chr7:97863932..97867672-chr7:97911936..97914933,4	K562	blood:
21	chr7:97859627..97861679-chr7:97864267..97867211,3	K562	blood:
22	chr7:97864661..97867509-chr7:97913185..97914838,2	K562	blood:
23	chr7:97842812..97845120-chr7:97865672..97868033,2	K562	blood:
24	chr7:97813734..97816516-chr7:97889057..97891236,2	MCF-7	breast:
25	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRI3-2	chr7:97881470-97887682	NONHSAT122186
2	lnc-BAIAP2L1.1-1	chr7:97880226-97880860	NONHSAT122185
3	lnc-BAIAP2L1.1-1	chr7:97880731-97880860	NONHSAT122183
4	lnc-BAIAP2L1.1-1	chr7:97881438-97881468	NONHSAT122183
5	lnc-BRI3-2	chr7:97882196-97882353	NONHSAT122187
6	lnc-BRI3-2	chr7:97881586-97882094	NONHSAT122187
7	lnc-BAIAP2L1.1-1	chr7:97881438-97881487	NONHSAT122185

No data

Variant related genes	Relation type
TECPR1	TF binding region
BRI3	TF binding region
TECPR1	CpG island
BRI3	CpG island
ENSG00000099622	chromatin interactions
ENSG00000164713	chromatin interactions
ENSG00000164715	chromatin interactions
ENSG00000006453	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000180535	chromatin interactions

Extended variants
information (count: 1467 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2270604	chr7:97857675-97857676	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116360254	chr7:97857698-97857699	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374763535	chr7:97857795-97857796	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528130735	chr7:97857802-97857803	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546686119	chr7:97857837-97857838	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115793943	chr7:97857888-97857889	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs529109949	chr7:97857956-97857957	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs75234817	chr7:97857966-97857967	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs535495402	chr7:97857971-97857972	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs569209152	chr7:97857989-97857990	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs539834513	chr7:97857990-97857991	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558229531	chr7:97857996-97857997	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566873323	chr7:97858012-97858013	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150624128	chr7:97858027-97858028	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555845637	chr7:97858036-97858037	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs574122065	chr7:97858037-97858038	Strong transcription Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553850292	chr7:97858041-97858042	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544815588	chr7:97858065-97858066	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139675478	chr7:97858091-97858092	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs571996953	chr7:97858132-97858133	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112940485	chr7:97858133-97858134	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370714356	chr7:97858180-97858181	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs569305825	chr7:97858184-97858185	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs118118548	chr7:97858199-97858200	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs539925545	chr7:97858203-97858204	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs117093858	chr7:97858242-97858243	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529063313	chr7:97858295-97858296	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550792761	chr7:97858296-97858297	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374861977	chr7:97858311-97858312	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547871111	chr7:97858326-97858327	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369602942	chr7:97858332-97858333	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75148471	chr7:97858338-97858339	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371067096	chr7:97858342-97858343	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs146318963	chr7:97858360-97858361	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566836665	chr7:97858363-97858364	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534219425	chr7:97858376-97858377	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374428997	chr7:97858394-97858395	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373215203	chr7:97858409-97858410	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs202140896	chr7:97858411-97858412	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112013398	chr7:97858424-97858425	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375317554	chr7:97858428-97858429	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs372982193	chr7:97858448-97858449	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374571399	chr7:97858449-97858450	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370716856	chr7:97858493-97858494	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181351938	chr7:97858496-97858497	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377508826	chr7:97858513-97858514	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs73710400	chr7:97858555-97858556	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs58936900	chr7:97858591-97858592	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs576630323	chr7:97858600-97858601	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554953591	chr7:97858616-97858617	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1582 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97841000-97858600	Weak transcription	Psoas Muscle	Psoas
2	chr7:97841200-97867800	Weak transcription	HUVEC	blood vessel
3	chr7:97841200-97880200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:97841400-97858600	Weak transcription	NH-A	brain
5	chr7:97841400-97866200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:97841400-97879400	Weak transcription	Fetal Brain Male	brain
7	chr7:97841400-97880200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr7:97841800-97867400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr7:97842200-97868400	Weak transcription	Colon Smooth Muscle	Colon
10	chr7:97845200-97877400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr7:97848000-97877600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr7:97848000-97880600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:97848600-97873200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr7:97849000-97864600	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr7:97849200-97857800	Strong transcription	Fetal Muscle Leg	muscle
16	chr7:97849400-97863400	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr7:97849800-97858000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr7:97850000-97871800	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:97850000-97878000	Strong transcription	Fetal Stomach	stomach
20	chr7:97850200-97858200	Strong transcription	Liver	Liver
21	chr7:97850200-97874400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr7:97850200-97875400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr7:97850400-97872800	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr7:97850400-97878600	Weak transcription	GM12878-XiMat	blood
25	chr7:97850600-97864200	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr7:97850600-97872800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr7:97850600-97874400	Strong transcription	Adipose Nuclei	Adipose
28	chr7:97850600-97875600	Strong transcription	Fetal Brain Female	brain
29	chr7:97850800-97858400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:97850800-97860600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr7:97850800-97863000	Strong transcription	Ovary	ovary
32	chr7:97850800-97863600	Strong transcription	Lung	lung
33	chr7:97850800-97864200	Strong transcription	Fetal Intestine Small	intestine
34	chr7:97850800-97875400	Strong transcription	Thymus	Thymus
35	chr7:97850800-97877400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:97851000-97863400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:97851000-97863400	Strong transcription	Right Ventricle	heart
38	chr7:97851000-97863800	Strong transcription	Brain Hippocampus Middle	brain
39	chr7:97851000-97864600	Strong transcription	Brain Inferior Temporal Lobe	brain
40	chr7:97851600-97862800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:97851600-97867600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr7:97851800-97858400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:97851800-97867600	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr7:97852000-97878000	Weak transcription	Small Intestine	intestine
45	chr7:97852400-97859800	Weak transcription	Fetal Thymus	thymus
46	chr7:97852600-97858200	Strong transcription	Spleen	Spleen
47	chr7:97852600-97875600	Strong transcription	Primary T cells from cord blood	blood
48	chr7:97853200-97880000	Weak transcription	A549	lung
49	chr7:97853400-97880200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:97853800-97858200	Strong transcription	Rectal Mucosa Donor 29	rectum

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