Variant report

Variant	nsv464422
Chromosome Location	chr7:33131729-33187279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1807)
CpG islands
(count:1651)
Chromatin interactive
region (count:58)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1807 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:33168628-33169291	K562	blood:	n/a	n/a
2	ARID3A	chr7:33148209-33148551	K562	blood:	n/a	n/a
3	ARID3A	chr7:33149133-33149348	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:33168603-33169370	HepG2	liver:	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	chr7:33168750-33169268	K562	blood:	n/a	chr7:33168833-33168847 chr7:33168839-33168848 chr7:33168875-33168895
8	ATF3	chr7:33168994-33169232	K562	blood:	n/a	n/a
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	chr7:33148767-33149366	GM12878	blood:	n/a	chr7:33149104-33149117 chr7:33149110-33149119 chr7:33149113-33149122 chr7:33149107-33149120 chr7:33149111-33149124
13	BCLAF1	chr7:33148813-33149340	K562	blood:	n/a	chr7:33149104-33149117 chr7:33149110-33149119 chr7:33149113-33149122 chr7:33149107-33149120 chr7:33149111-33149124
14	BHLHE40	chr7:33183680-33184321	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:33168366-33169659	K562	blood:	n/a	n/a
16	BHLHE40	chr7:33168695-33169412	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:33168715-33169284	HepG2	liver:	n/a	n/a
18	BHLHE40	chr7:33148785-33149341	GM12878	blood:	n/a	chr7:33148807-33148823 chr7:33149226-33149242
19	BHLHE40	chr7:33148589-33149273	K562	blood:	n/a	chr7:33148807-33148823 chr7:33149226-33149242
20	BHLHE40	chr7:33183980-33184223	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:33143015-33143167	K562	blood:	n/a	n/a
22	BRCA1	chr7:33149079-33149281	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr7:33149590-33149838	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr7:33169012-33169207	GM12878	blood:	n/a	n/a
25	BRCA1	chr7:33149136-33149233	HepG2	liver:	n/a	n/a
26	BRCA1	chr7:33149137-33149301	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr7:33147313-33147583	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:33168905-33169244	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr7:33157981-33158348	K562	blood:	n/a	n/a
30	CBX3	chr7:33157896-33158457	K562	blood:	n/a	n/a
31	CBX3	chr7:33168574-33169350	K562	blood:	n/a	n/a
32	CCNT2	chr7:33168561-33169258	K562	blood:	n/a	chr7:33168839-33168848
33	CCNT2	chr7:33148596-33149412	K562	blood:	n/a	n/a
34	CEBPB	chr7:33153361-33153566	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:33181993-33182305	HepG2	liver:	n/a	chr7:33182139-33182150
36	CEBPB	chr7:33154924-33155144	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:33168823-33169163	K562	blood:	n/a	n/a
38	CEBPB	chr7:33168622-33169404	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr7:33184795-33185097	K562	blood:	n/a	n/a
40	CEBPB	chr7:33182019-33182327	IMR90	lung:	n/a	chr7:33182139-33182150
41	CEBPB	chr7:33149167-33149447	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:33149972-33150285	K562	blood:	n/a	chr7:33150161-33150172
43	CEBPB	chr7:33169010-33169210	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:33141587-33141864	A549	lung:	n/a	chr7:33141691-33141702
45	CEBPB	chr7:33154759-33155071	K562	blood:	n/a	n/a
46	CEBPB	chr7:33164060-33164160	H1-hESC	embryonic stem cell:	n/a	chr7:33164123-33164134
47	CEBPB	chr7:33141627-33141798	HepG2	liver:	n/a	chr7:33141691-33141702
48	CEBPB	chr7:33150081-33150179	A549	lung:	n/a	chr7:33150161-33150172
49	CEBPB	chr7:33149590-33149867	A549	lung:	n/a	n/a
50	CEBPB	chr7:33168952-33169151	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1651 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:33153274-33153324	T-47D	breast:	n/a
2	chr7:33165554-33165604	HAEpiC	amniotic membrane:	n/a
3	chr7:33172994-33173044	HMEC	breast:	n/a
4	chr7:33169015-33169065	HRCEpiC	kidney:	n/a
5	chr7:33153274-33153324	T-47D	breast:	n/a
6	chr7:33165554-33165604	HAEpiC	amniotic membrane:	n/a
7	chr7:33172994-33173044	HMEC	breast:	n/a
8	chr7:33169015-33169065	HRCEpiC	kidney:	n/a
9	chr7:33153274-33153324	MCF10A-Er-Src	breast:	n/a
10	chr7:33168802-33168852	HMEC	breast:	n/a
11	chr7:33165554-33165604	AG09319	gingival:	n/a
12	chr7:33150037-33150087	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:33146067-33146117	NH-A	brain:	n/a
14	chr7:33149137-33149187	PFSK-1	brain:	n/a
15	chr7:33148942-33148992	HRCEpiC	kidney:	n/a
16	chr7:33148942-33148992	HUVEC	blood vessel:	n/a
17	chr7:33169033-33169083	NT2-D1	testis:	n/a
18	chr7:33169470-33169520	NHBE	bronchial:	n/a
19	chr7:33151206-33151256	PANC-1	pancreas:	n/a
20	chr7:33149122-33149172	HCF	heart:	n/a
21	chr7:33168625-33168675	RPTEC	kidney:	n/a
22	chr7:33169015-33169065	GM19239	blood:	n/a
23	chr7:33169033-33169083	IMR90	lung:	fetal
24	chr7:33150037-33150087	AG10803	skin:	n/a
25	chr7:33149255-33149305	PFSK-1	brain:	n/a
26	chr7:33172994-33173044	SAEC	small airway:	n/a
27	chr7:33169015-33169065	SK-N-SH	brain:	n/a
28	chr7:33168625-33168675	HEK293	kidney:	embryo
29	chr7:33168625-33168675	HRPEpiC	eye:	n/a
30	chr7:33169186-33169236	HRE	kidney:	n/a
31	chr7:33149316-33149366	PANC-1	pancreas:	n/a
32	chr7:33149277-33149327	Hepatocyte	liver:	n/a
33	chr7:33169470-33169520	HIPEpiC	eye:	n/a
34	chr7:33151206-33151256	GM12891	blood:	n/a
35	chr7:33169026-33169076	SKMC	muscle:	n/a
36	chr7:33151206-33151256	HEK293	kidney:	embryo
37	chr7:33169026-33169076	GM06990	blood:	n/a
38	chr7:33148868-33148918	BJ	skin:	n/a
39	chr7:33168904-33168954	GM19239	blood:	n/a
40	chr7:33165554-33165604	Hepatocyte	liver:	n/a
41	chr7:33165554-33165604	Jurkat	blood:	n/a
42	chr7:33149117-33149167	AG09319	gingival:	n/a
43	chr7:33146808-33146858	GM19239	blood:	n/a
44	chr7:33149114-33149164	LNCaP	prostate:	n/a
45	chr7:33169321-33169371	LNCaP	prostate:	n/a
46	chr7:33149122-33149172	HAEpiC	amniotic membrane:	n/a
47	chr7:33149137-33149187	CMK	blood:	n/a
48	chr7:33169470-33169520	AG04449	skin:	fetal
49	chr7:33169015-33169065	AG09319	gingival:	n/a
50	chr7:33149137-33149187	MCF10A-Er-Src	breast:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:33169914..33172476-chr7:33187197..33189119,2	MCF-7	breast:
2	chr7:33179229..33183198-chr7:33185335..33188130,3	K562	blood:
3	chr20:49347482..49349251-chr7:33147388..33148972,2	MCF-7	breast:
4	chr7:33142504..33144709-chr7:33147297..33150287,2	K562	blood:
5	chr7:33131500..33135891-chr7:33143738..33147461,3	K562	blood:
6	chr7:33174121..33176456-chr7:33182217..33185074,2	K562	blood:
7	chr7:33148601..33150604-chr7:33153806..33156546,2	K562	blood:
8	chr7:33167291..33169895-chr7:33178548..33180361,2	K562	blood:
9	chr7:33137473..33139190-chr7:33143121..33146806,3	K562	blood:
10	chr7:33179137..33181368-chr7:33185643..33187342,2	MCF-7	breast:
11	chr7:32981289..32983857-chr7:33147743..33149971,3	K562	blood:
12	chr7:32929842..32933813-chr7:33147048..33149516,4	K562	blood:
13	chr7:33101504..33102499-chr7:33146693..33147349,2	K562	blood:
14	chr7:33149256..33151960-chr7:33155226..33157184,2	MCF-7	breast:
15	chr7:33183803..33185518-chr7:33185914..33189355,3	MCF-7	breast:
16	chr7:33131500..33135891-chr7:33143738..33147461,3	K562	blood:
17	chr7:33145176..33146680-chr7:33147425..33148975,2	K562	blood:
18	chr7:33137473..33139190-chr7:33143121..33146806,3	K562	blood:
19	chr7:33151434..33153023-chr7:33155282..33157530,2	K562	blood:
20	chr7:33131304..33133377-chr7:33140115..33142043,2	K562	blood:
21	chr7:33120839..33123579-chr7:33147074..33148845,2	MCF-7	breast:
22	chr7:33132440..33134212-chr7:33136928..33139732,2	K562	blood:
23	chr19:47730376..47730970-chr7:33148568..33149081,2	Hela-S3	cervix:
24	chr7:33130730..33133581-chr7:33134790..33136889,2	K562	blood:
25	chr7:33101592..33103439-chr7:33148174..33150339,2	K562	blood:
26	chr7:33148601..33150604-chr7:33153806..33156546,2	K562	blood:
27	chr7:33130730..33133581-chr7:33134790..33136889,2	K562	blood:
28	chr7:33147764..33149683-chr7:33167457..33170052,3	MCF-7	breast:
29	chr7:33132440..33134212-chr7:33136928..33139732,2	K562	blood:
30	chr7:33148471..33149111-chr8:37962511..37963365,2	HCT-116	colon:
31	chr7:33173373..33176159-chr7:33177718..33179831,2	K562	blood:
32	chr7:33100859..33104943-chr7:33146945..33149986,6	MCF-7	breast:
33	chr7:33101766..33103971-chr7:33147720..33150417,2	K562	blood:
34	chr7:33168152..33172039-chr7:33180833..33185691,4	K562	blood:
35	chr7:33147545..33149151-chr7:33167596..33169294,2	K562	blood:
36	chr7:32996816..32997512-chr7:33148545..33149076,2	Hela-S3	cervix:
37	chr7:33101689..33103789-chr7:33147448..33149100,2	MCF-7	breast:
38	chr7:33147545..33149151-chr7:33167596..33169294,2	K562	blood:
39	chr7:33094100..33095889-chr7:33158898..33161804,2	K562	blood:
40	chr7:33098744..33100464-chr7:33145455..33148099,2	K562	blood:
41	chr7:33183803..33185518-chr7:33185914..33189355,3	MCF-7	breast:
42	chr7:33169914..33172476-chr7:33187197..33189119,2	MCF-7	breast:
43	chr7:32995811..32998630-chr7:33147873..33150650,5	MCF-7	breast:
44	chr7:32930971..32934181-chr7:33147634..33150487,3	MCF-7	breast:
45	chr7:33144651..33147364-chr7:33168487..33170158,2	MCF-7	breast:
46	chr7:33168317..33169892-chr7:33174441..33176886,2	MCF-7	breast:
47	chr7:33127364..33129190-chr7:33131831..33134427,2	K562	blood:
48	chr7:33151434..33153023-chr7:33155282..33157530,2	K562	blood:
49	chr7:33147514..33149972-chr7:33151690..33154422,2	MCF-7	breast:
50	chr7:32929813..32931362-chr7:33146969..33149896,3	K562	blood:

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

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

No data

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

Extended variants
information (count: 1930 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1930 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12667900	chr7:33131729-33131730	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12672159	chr7:33131745-33131746	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571169360	chr7:33131808-33131809	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs145043047	chr7:33131819-33131820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537896745	chr7:33131841-33131842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557346236	chr7:33131883-33131884	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575564311	chr7:33131930-33131931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542776566	chr7:33131940-33131941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs181574345	chr7:33131974-33131975	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76533910	chr7:33132063-33132064	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs71738128	chr7:33132073-33132074	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372322449	chr7:33132077-33132078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199897531	chr7:33132078-33132079	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370380128	chr7:33132168-33132169	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77349727	chr7:33132181-33132182	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs565417623	chr7:33132183-33132184	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143637072	chr7:33132193-33132194	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550987442	chr7:33132258-33132259	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138237301	chr7:33132318-33132319	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530039914	chr7:33132336-33132337	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548358782	chr7:33132360-33132361	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563740453	chr7:33132390-33132391	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377294720	chr7:33132441-33132442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs141246257	chr7:33132479-33132480	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs186988452	chr7:33132490-33132491	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551985442	chr7:33132509-33132510	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570558014	chr7:33132531-33132532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537424941	chr7:33132532-33132533	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs199667398	chr7:33132538-33132539	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192277910	chr7:33132554-33132555	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112489173	chr7:33132565-33132566	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75007499	chr7:33132598-33132599	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573091284	chr7:33132616-33132617	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs118162746	chr7:33132641-33132642	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558768060	chr7:33132648-33132649	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs77659465	chr7:33132765-33132766	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs9942687	chr7:33132814-33132815	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141518973	chr7:33132862-33132863	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs150456394	chr7:33132894-33132895	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542138232	chr7:33132923-33132924	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560477863	chr7:33132931-33132932	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138310301	chr7:33132980-33132981	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112297996	chr7:33133031-33133032	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537201733	chr7:33133037-33133038	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528718005	chr7:33133049-33133050	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184063269	chr7:33133085-33133086	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558467089	chr7:33133112-33133113	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149646760	chr7:33133117-33133118	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187795519	chr7:33133155-33133156	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567725250	chr7:33133166-33133167	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	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:1713 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33115800-33148000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:33120400-33132800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:33121000-33133000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:33124600-33135800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr7:33126000-33132600	Weak transcription	Fetal Intestine Small	intestine
6	chr7:33126600-33133000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:33127400-33132600	Weak transcription	Adipose Nuclei	Adipose
8	chr7:33127400-33135800	Weak transcription	Fetal Brain Male	brain
9	chr7:33127600-33132200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:33127800-33133000	Weak transcription	Pancreas	Pancrea
11	chr7:33127800-33133000	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr7:33127800-33135200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:33127800-33135400	Weak transcription	Aorta	Aorta
14	chr7:33127800-33147000	Weak transcription	Right Atrium	heart
15	chr7:33128200-33135400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:33128800-33132600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:33129000-33132800	Weak transcription	Spleen	Spleen
18	chr7:33129200-33132000	Weak transcription	Primary T cells from cord blood	blood
19	chr7:33129400-33132000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr7:33129400-33132400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr7:33129400-33132800	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr7:33129400-33135200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr7:33129600-33132200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr7:33129600-33132400	Weak transcription	Primary B cells from cord blood	blood
25	chr7:33129600-33132600	Weak transcription	Primary B cells from peripheral blood	blood
26	chr7:33129600-33135800	Weak transcription	K562	blood
27	chr7:33130000-33131800	Weak transcription	Fetal Muscle Leg	muscle
28	chr7:33130000-33132000	Weak transcription	Fetal Muscle Trunk	muscle
29	chr7:33130000-33132800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:33130000-33132800	Weak transcription	Brain Hippocampus Middle	brain
31	chr7:33130000-33133800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:33130200-33132600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:33130200-33132800	Weak transcription	A549	lung
34	chr7:33130200-33133400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:33130200-33135200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr7:33130400-33132000	Weak transcription	Brain Angular Gyrus	brain
37	chr7:33130400-33132400	Weak transcription	Fetal Intestine Large	intestine
38	chr7:33130400-33132400	Weak transcription	Dnd41	blood
39	chr7:33130400-33132600	Weak transcription	Brain Cingulate Gyrus	brain
40	chr7:33130400-33132800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr7:33130400-33132800	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr7:33130400-33132800	Weak transcription	Thymus	Thymus
43	chr7:33130600-33132400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr7:33130600-33132400	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr7:33130600-33132600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:33130600-33132600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:33130600-33132600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr7:33130600-33132800	Weak transcription	Stomach Smooth Muscle	stomach
49	chr7:33130600-33135400	Weak transcription	Ovary	ovary
50	chr7:33130600-33135600	Weak transcription	NHLF	lung

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