Variant report

Variant	nsv1030007
Chromosome Location	chr7:33132814-33185470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1789)
CpG islands
(count:1649)
Chromatin interactive
region (count:55)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1789 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:33149133-33149348	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:33148209-33148551	K562	blood:	n/a	n/a
3	ARID3A	chr7:33168603-33169370	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:33168628-33169291	K562	blood:	n/a	n/a
5	ATF1	chr7:33168586-33169396	K562	blood:	n/a	n/a
6	ATF2	chr7:33149076-33149378	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr7:33168994-33169232	K562	blood:	n/a	n/a
8	ATF3	chr7:33168750-33169268	K562	blood:	n/a	chr7:33168833-33168847 chr7:33168839-33168848 chr7:33168875-33168895
9	BACH1	chr7:33168580-33169170	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr7:33183918-33184232	GM12878	blood:	n/a	n/a
11	BCLAF1	chr7:33168858-33169388	GM12878	blood:	n/a	chr7:33168910-33168923 chr7:33169127-33169140
12	BCLAF1	chr7:33148813-33149340	K562	blood:	n/a	chr7:33149104-33149117 chr7:33149110-33149119 chr7:33149113-33149122 chr7:33149107-33149120 chr7:33149111-33149124
13	BCLAF1	chr7:33148767-33149366	GM12878	blood:	n/a	chr7:33149104-33149117 chr7:33149110-33149119 chr7:33149113-33149122 chr7:33149107-33149120 chr7:33149111-33149124
14	BHLHE40	chr7:33183980-33184223	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:33148589-33149273	K562	blood:	n/a	chr7:33148807-33148823 chr7:33149226-33149242
16	BHLHE40	chr7:33148785-33149341	GM12878	blood:	n/a	chr7:33148807-33148823 chr7:33149226-33149242
17	BHLHE40	chr7:33168715-33169284	HepG2	liver:	n/a	n/a
18	BHLHE40	chr7:33143015-33143167	K562	blood:	n/a	n/a
19	BHLHE40	chr7:33183680-33184321	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:33168695-33169412	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:33168366-33169659	K562	blood:	n/a	n/a
22	BRCA1	chr7:33168905-33169244	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr7:33149137-33149301	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr7:33147313-33147583	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:33169012-33169207	GM12878	blood:	n/a	n/a
26	BRCA1	chr7:33149079-33149281	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr7:33149590-33149838	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:33149136-33149233	HepG2	liver:	n/a	n/a
29	CBX3	chr7:33168574-33169350	K562	blood:	n/a	n/a
30	CBX3	chr7:33157896-33158457	K562	blood:	n/a	n/a
31	CBX3	chr7:33157981-33158348	K562	blood:	n/a	n/a
32	CCNT2	chr7:33148596-33149412	K562	blood:	n/a	n/a
33	CCNT2	chr7:33168561-33169258	K562	blood:	n/a	chr7:33168839-33168848
34	CEBPB	chr7:33154924-33155144	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:33153361-33153566	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:33169010-33169210	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:33149972-33150285	K562	blood:	n/a	chr7:33150161-33150172
38	CEBPB	chr7:33182001-33182288	K562	blood:	n/a	chr7:33182139-33182150
39	CEBPB	chr7:33184795-33185097	K562	blood:	n/a	n/a
40	CEBPB	chr7:33168622-33169404	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:33149167-33149447	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:33149792-33150266	HepG2	liver:	n/a	chr7:33150161-33150172
43	CEBPB	chr7:33150081-33150179	A549	lung:	n/a	chr7:33150161-33150172
44	CEBPB	chr7:33182019-33182327	IMR90	lung:	n/a	chr7:33182139-33182150
45	CEBPB	chr7:33141587-33141864	A549	lung:	n/a	chr7:33141691-33141702
46	CEBPB	chr7:33141627-33141798	HepG2	liver:	n/a	chr7:33141691-33141702
47	CEBPB	chr7:33168823-33169163	K562	blood:	n/a	n/a
48	CEBPB	chr7:33176676-33176923	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr7:33181993-33182305	HepG2	liver:	n/a	chr7:33182139-33182150
50	CEBPB	chr7:33149609-33150258	Hela-S3	cervix:	n/a	chr7:33150161-33150172

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:33151206-33151256	HUVEC	blood vessel:	n/a
2	chr7:33146808-33146858	NHDF-neo	bronchial:	n/a
3	chr7:33151206-33151256	HUVEC	blood vessel:	n/a
4	chr7:33146808-33146858	NHDF-neo	bronchial:	n/a
5	chr7:33168625-33168675	GM12878	blood:	n/a
6	chr7:33150037-33150087	Hela-S3	cervix:	n/a
7	chr7:33168802-33168852	GM06990	blood:	n/a
8	chr7:33151206-33151256	HCT-116	colon:	n/a
9	chr7:33169033-33169083	BE2_C	brain:	n/a
10	chr7:33168904-33168954	ECC-1	luminal epithelium:	n/a
11	chr7:33150037-33150087	Jurkat	blood:	n/a
12	chr7:33172994-33173044	H1-hESC	embryonic stem cell:	embryo
13	chr7:33151206-33151256	NT2-D1	testis:	n/a
14	chr7:33172994-33173044	Hela-S3	cervix:	n/a
15	chr7:33153274-33153324	SK-N-MC	brain:	n/a
16	chr7:33169015-33169065	BE2_C	brain:	n/a
17	chr7:33169015-33169065	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:33149316-33149366	HCM	heart:	n/a
19	chr7:33148815-33148865	AG04449	skin:	fetal
20	chr7:33149137-33149187	AG04449	skin:	fetal
21	chr7:33165554-33165604	GM19239	blood:	n/a
22	chr7:33149316-33149366	AG10803	skin:	n/a
23	chr7:33151206-33151256	HEEpiC	esophagus:	n/a
24	chr7:33168802-33168852	NH-A	brain:	n/a
25	chr7:33146808-33146858	SKMC	muscle:	n/a
26	chr7:33148942-33148992	RPTEC	kidney:	n/a
27	chr7:33150037-33150087	HIPEpiC	eye:	n/a
28	chr7:33150037-33150087	SK-N-SH	brain:	n/a
29	chr7:33149277-33149327	HEEpiC	esophagus:	n/a
30	chr7:33168904-33168954	HUVEC	blood vessel:	n/a
31	chr7:33149137-33149187	CMK	blood:	n/a
32	chr7:33148815-33148865	NH-A	brain:	n/a
33	chr7:33149255-33149305	H1-hESC	embryonic stem cell:	embryo
34	chr7:33151206-33151256	GM06990	blood:	n/a
35	chr7:33149117-33149167	BE2_C	brain:	n/a
36	chr7:33148868-33148918	PrEC	prostate:	n/a
37	chr7:33169026-33169076	AoSMC	blood vessel:	n/a
38	chr7:33149122-33149172	HCPEpiC	choroid plexus:	n/a
39	chr7:33168904-33168954	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:33149277-33149327	HCF	heart:	n/a
41	chr7:33149255-33149305	CMK	blood:	n/a
42	chr7:33169015-33169065	AG10803	skin:	n/a
43	chr7:33168625-33168675	LNCaP	prostate:	n/a
44	chr7:33146808-33146858	AG09309	skin:	n/a
45	chr7:33169470-33169520	HCT-116	colon:	n/a
46	chr7:33169026-33169076	GM06990	blood:	n/a
47	chr7:33149137-33149187	MCF10A-Er-Src	breast:	n/a
48	chr7:33172994-33173044	AG10803	skin:	n/a
49	chr7:33149117-33149167	Jurkat	blood:	n/a
50	chr7:33169026-33169076	ECC-1	luminal epithelium:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:33160632..33164590-chr7:33165983..33168897,4	K562	blood:
2	chr7:33094100..33095889-chr7:33158898..33161804,2	K562	blood:
3	chr7:33131500..33135891-chr7:33143738..33147461,3	K562	blood:
4	chr7:33167291..33169895-chr7:33178548..33180361,2	K562	blood:
5	chr7:33101766..33103971-chr7:33147720..33150417,2	K562	blood:
6	chr7:33101689..33103789-chr7:33147448..33149100,2	MCF-7	breast:
7	chr7:32929813..32931362-chr7:33146969..33149896,3	K562	blood:
8	chr7:33179229..33183198-chr7:33185335..33188130,3	K562	blood:
9	chr7:33101592..33103439-chr7:33148174..33150339,2	K562	blood:
10	chr7:33132440..33134212-chr7:33136928..33139732,2	K562	blood:
11	chr7:33122616..33124229-chr7:33135048..33136719,2	K562	blood:
12	chr7:33098744..33100464-chr7:33145455..33148099,2	K562	blood:
13	chr7:33147514..33149972-chr7:33151690..33154422,2	MCF-7	breast:
14	chr7:33144651..33147364-chr7:33168487..33170158,2	MCF-7	breast:
15	chr7:33147764..33149683-chr7:33167457..33170052,3	MCF-7	breast:
16	chr7:33151434..33153023-chr7:33155282..33157530,2	K562	blood:
17	chr7:32930971..32934181-chr7:33147634..33150487,3	MCF-7	breast:
18	chr7:33179229..33183198-chr7:33185335..33188130,3	K562	blood:
19	chr7:33169914..33172476-chr7:33187197..33189119,2	MCF-7	breast:
20	chr7:33101504..33102499-chr7:33146693..33147349,2	K562	blood:
21	chr7:33149256..33151960-chr7:33155226..33157184,2	MCF-7	breast:
22	chr7:33137473..33139190-chr7:33143121..33146806,3	K562	blood:
23	chr7:32981289..32983857-chr7:33147743..33149971,3	K562	blood:
24	chr7:33173373..33176159-chr7:33177718..33179831,2	K562	blood:
25	chr7:33168317..33169892-chr7:33174441..33176886,2	MCF-7	breast:
26	chr7:33174121..33176456-chr7:33182217..33185074,2	K562	blood:
27	chr7:33148601..33150604-chr7:33153806..33156546,2	K562	blood:
28	chr7:33151434..33153023-chr7:33155282..33157530,2	K562	blood:
29	chr7:33130730..33133581-chr7:33134790..33136889,2	K562	blood:
30	chr7:33179137..33181368-chr7:33185643..33187342,2	MCF-7	breast:
31	chr7:32995811..32998630-chr7:33147873..33150650,5	MCF-7	breast:
32	chr7:32996816..32997512-chr7:33148545..33149076,2	Hela-S3	cervix:
33	chr7:33130730..33133581-chr7:33134790..33136889,2	K562	blood:
34	chr7:33147545..33149151-chr7:33167596..33169294,2	K562	blood:
35	chr7:33142504..33144709-chr7:33147297..33150287,2	K562	blood:
36	chr7:33131304..33133377-chr7:33140115..33142043,2	K562	blood:
37	chr7:33127364..33129190-chr7:33131831..33134427,2	K562	blood:
38	chr7:33137473..33139190-chr7:33143121..33146806,3	K562	blood:
39	chr7:33148601..33150604-chr7:33153806..33156546,2	K562	blood:
40	chr7:33173373..33176159-chr7:33177718..33179831,2	K562	blood:
41	chr7:33183803..33185518-chr7:33185914..33189355,3	MCF-7	breast:
42	chr7:33100859..33104943-chr7:33146945..33149986,6	MCF-7	breast:
43	chr7:33148471..33149111-chr8:37962511..37963365,2	HCT-116	colon:
44	chr7:33131500..33135891-chr7:33143738..33147461,3	K562	blood:
45	chr7:33132440..33134212-chr7:33136928..33139732,2	K562	blood:
46	chr20:49347482..49349251-chr7:33147388..33148972,2	MCF-7	breast:
47	chr7:33168152..33172039-chr7:33180833..33185691,4	K562	blood:
48	chr7:33120839..33123579-chr7:33147074..33148845,2	MCF-7	breast:
49	chr7:33145176..33146680-chr7:33147425..33148975,2	K562	blood:
50	chr19:47730376..47730970-chr7:33148568..33149081,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AVL9-2	chr7:33134451-33135216	NONHSAT120017
2	lnc-AVL9-2	chr7:33134451-33135216	NONHSAT120016

No data

Variant related genes	Relation type
RP9	TF binding region
BBS9	TF binding region
ENSG00000252706	TF binding region
ENSG00000228015	TF binding region
RP9	CpG island
BBS9	CpG island
ENSG00000252706	CpG island
ENSG00000228015	CpG island
ENSG00000170852	chromatin interactions
ENSG00000122642	chromatin interactions
ENSG00000228015	chromatin interactions
ENSG00000129691	chromatin interactions
ENSG00000122507	chromatin interactions
ENSG00000205763	chromatin interactions
ENSG00000122643	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000105327	chromatin interactions
ENSG00000237004	chromatin interactions
ENSG00000252706	chromatin interactions
ENSG00000164610	chromatin interactions

Extended variants
information (count: 1822 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1822 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9942687	chr7:33132814-33132815	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141518973	chr7:33132862-33132863	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150456394	chr7:33132894-33132895	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs542138232	chr7:33132923-33132924	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560477863	chr7:33132931-33132932	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138310301	chr7:33132980-33132981	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112297996	chr7:33133031-33133032	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537201733	chr7:33133037-33133038	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528718005	chr7:33133049-33133050	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184063269	chr7:33133085-33133086	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs558467089	chr7:33133112-33133113	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149646760	chr7:33133117-33133118	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187795519	chr7:33133155-33133156	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567725250	chr7:33133166-33133167	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs577105688	chr7:33133173-33133174	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114915555	chr7:33133197-33133198	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs11981778	chr7:33133207-33133208	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs566852093	chr7:33133234-33133235	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534098705	chr7:33133236-33133237	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559809569	chr7:33133242-33133243	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150360218	chr7:33133283-33133284	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189949244	chr7:33133310-33133311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs77041459	chr7:33133346-33133347	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs144407510	chr7:33133351-33133352	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73687323	chr7:33133374-33133375	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs13238052	chr7:33133384-33133385	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs74500532	chr7:33133393-33133394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77034624	chr7:33133414-33133415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530906773	chr7:33133433-33133434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542274589	chr7:33133513-33133514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552777818	chr7:33133535-33133536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527595429	chr7:33133538-33133539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545649271	chr7:33133539-33133540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375900286	chr7:33133540-33133541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143082421	chr7:33133545-33133546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564506992	chr7:33133560-33133561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367735162	chr7:33133561-33133562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs36044675	chr7:33133568-33133569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564307854	chr7:33133578-33133579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187239640	chr7:33133582-33133583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140284323	chr7:33133697-33133698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10245553	chr7:33133742-33133743	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs528836040	chr7:33133749-33133750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547005031	chr7:33133750-33133751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567026772	chr7:33133756-33133757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534512443	chr7:33133787-33133788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558844989	chr7:33133788-33133789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544339292	chr7:33133811-33133812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112784578	chr7:33133857-33133858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10275149	chr7:33133879-33133880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Williams-beuren syndrome	18553513	CNVD
Autism	22495309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:1642 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33115800-33148000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:33121000-33133000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr7:33124600-33135800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr7:33126600-33133000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:33127400-33135800	Weak transcription	Fetal Brain Male	brain
6	chr7:33127800-33133000	Weak transcription	Pancreas	Pancrea
7	chr7:33127800-33133000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr7:33127800-33135200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:33127800-33135400	Weak transcription	Aorta	Aorta
10	chr7:33127800-33147000	Weak transcription	Right Atrium	heart
11	chr7:33128200-33135400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:33129400-33135200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:33129600-33135800	Weak transcription	K562	blood
14	chr7:33130000-33133800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:33130200-33133400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:33130200-33135200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr7:33130600-33135400	Weak transcription	Ovary	ovary
18	chr7:33130600-33135600	Weak transcription	NHLF	lung
19	chr7:33130800-33133000	Weak transcription	NHEK	skin
20	chr7:33130800-33133200	Weak transcription	Fetal Kidney	kidney
21	chr7:33130800-33133400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr7:33131000-33135400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr7:33131000-33135600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr7:33131200-33133000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:33131200-33133000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr7:33131200-33133400	Weak transcription	Esophagus	oesophagus
27	chr7:33131200-33133600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr7:33131200-33135000	Weak transcription	NHDF-Ad	bronchial
29	chr7:33131200-33147400	Weak transcription	Small Intestine	intestine
30	chr7:33131400-33133000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr7:33131400-33133000	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr7:33131400-33133200	Weak transcription	GM12878-XiMat	blood
33	chr7:33131400-33133800	Weak transcription	HMEC	breast
34	chr7:33131400-33135200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr7:33131400-33135200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:33131400-33135200	Weak transcription	HUVEC	blood vessel
37	chr7:33131400-33139200	Strong transcription	Fetal Brain Female	brain
38	chr7:33131600-33133000	Weak transcription	Osteobl	bone
39	chr7:33131600-33133200	Weak transcription	Colonic Mucosa	Colon
40	chr7:33131600-33133200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr7:33131600-33133400	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr7:33131600-33133400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr7:33131600-33133400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr7:33131600-33133400	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr7:33131600-33134000	Weak transcription	HSMMtube	muscle
46	chr7:33131600-33135000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr7:33131600-33135400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr7:33131600-33135800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:33131800-33133000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:33131800-33133000	Weak transcription	Gastric	stomach

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