Variant report

Variant	esv2761318
Chromosome Location	chr7:33130687-33185482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1876)
CpG islands
(count:1712)
Chromatin interactive
region (count:56)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1876 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

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	chr7:33148767-33149366	GM12878	blood:	n/a	chr7:33149104-33149117 chr7:33149110-33149119 chr7:33149113-33149122 chr7:33149107-33149120 chr7:33149111-33149124
12	BCLAF1	chr7:33168858-33169388	GM12878	blood:	n/a	chr7:33168910-33168923 chr7:33169127-33169140
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	chr7:33148785-33149341	GM12878	blood:	n/a	chr7:33148807-33148823 chr7:33149226-33149242
15	BHLHE40	chr7:33168366-33169659	K562	blood:	n/a	n/a
16	BHLHE40	chr7:33168695-33169412	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:33143015-33143167	K562	blood:	n/a	n/a
18	BHLHE40	chr7:33183680-33184321	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:33168715-33169284	HepG2	liver:	n/a	n/a
20	BHLHE40	chr7:33148589-33149273	K562	blood:	n/a	chr7:33148807-33148823 chr7:33149226-33149242
21	BHLHE40	chr7:33183980-33184223	HepG2	liver:	n/a	n/a
22	BRCA1	chr7:33149137-33149301	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr7:33169012-33169207	GM12878	blood:	n/a	n/a
24	BRCA1	chr7:33168905-33169244	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:33149590-33149838	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr7:33149136-33149233	HepG2	liver:	n/a	n/a
27	BRCA1	chr7:33147313-33147583	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:33149079-33149281	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr7:33157896-33158457	K562	blood:	n/a	n/a
30	CBX3	chr7:33168574-33169350	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	chr7:33149590-33149867	A549	lung:	n/a	n/a
36	CEBPB	chr7:33141627-33141798	HepG2	liver:	n/a	chr7:33141691-33141702
37	CEBPB	chr7:33150081-33150179	A549	lung:	n/a	chr7:33150161-33150172
38	CEBPB	chr7:33130666-33131011	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:33141605-33141842	IMR90	lung:	n/a	chr7:33141691-33141702
40	CEBPB	chr7:33168622-33169404	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:33149972-33150285	K562	blood:	n/a	chr7:33150161-33150172
42	CEBPB	chr7:33168952-33169151	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:33182001-33182288	K562	blood:	n/a	chr7:33182139-33182150
44	CEBPB	chr7:33184795-33185097	K562	blood:	n/a	n/a
45	CEBPB	chr7:33149167-33149447	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:33153361-33153566	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:33164060-33164160	H1-hESC	embryonic stem cell:	n/a	chr7:33164123-33164134
48	CEBPB	chr7:33148983-33149294	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:33169010-33169210	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:33182019-33182327	IMR90	lung:	n/a	chr7:33182139-33182150

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:33169321-33169371	AG09319	gingival:	n/a
2	chr7:33146067-33146117	GM12891	blood:	n/a
3	chr7:33165554-33165604	HRE	kidney:	n/a
4	chr7:33148942-33148992	AG04449	skin:	fetal
5	chr7:33169321-33169371	AG09319	gingival:	n/a
6	chr7:33146067-33146117	GM12891	blood:	n/a
7	chr7:33165554-33165604	HRE	kidney:	n/a
8	chr7:33148942-33148992	AG04449	skin:	fetal
9	chr7:33149114-33149164	AG04450	lung:	fetal
10	chr7:33169033-33169083	NHBE	bronchial:	n/a
11	chr7:33149117-33149167	HCM	heart:	n/a
12	chr7:33153274-33153324	NB4	blood:	n/a
13	chr7:33169470-33169520	HEEpiC	esophagus:	n/a
14	chr7:33168904-33168954	Hela-S3	cervix:	n/a
15	chr7:33169033-33169083	HMEC	breast:	n/a
16	chr7:33150037-33150087	AG10803	skin:	n/a
17	chr7:33149137-33149187	HepG2	liver:	n/a
18	chr7:33169015-33169065	AG04449	skin:	fetal
19	chr7:33168625-33168675	GM06990	blood:	n/a
20	chr7:33149114-33149164	AG04449	skin:	fetal
21	chr7:33148815-33148865	HCM	heart:	n/a
22	chr7:33149143-33149193	AG04449	skin:	fetal
23	chr7:33148815-33148865	RPTEC	kidney:	n/a
24	chr7:33148868-33148918	AG09319	gingival:	n/a
25	chr7:33169470-33169520	PrEC	prostate:	n/a
26	chr7:33149316-33149366	HL-60	blood:	n/a
27	chr7:33169470-33169520	AoSMC	blood vessel:	n/a
28	chr7:33146067-33146117	HMEC	breast:	n/a
29	chr7:33169033-33169083	GM19239	blood:	n/a
30	chr7:33149137-33149187	HMEC	breast:	n/a
31	chr7:33168802-33168852	K562	blood:	n/a
32	chr7:33151206-33151256	HRE	kidney:	n/a
33	chr7:33168625-33168675	AG04449	skin:	fetal
34	chr7:33169015-33169065	ProgFib	skin:	n/a
35	chr7:33169186-33169236	LNCaP	prostate:	n/a
36	chr7:33130973-33131023	PANC-1	pancreas:	n/a
37	chr7:33148868-33148918	HRE	kidney:	n/a
38	chr7:33165554-33165604	NT2-D1	testis:	n/a
39	chr7:33169321-33169371	PANC-1	pancreas:	n/a
40	chr7:33149316-33149366	ECC-1	luminal epithelium:	n/a
41	chr7:33149255-33149305	PrEC	prostate:	n/a
42	chr7:33169321-33169371	HCM	heart:	n/a
43	chr7:33149277-33149327	LNCaP	prostate:	n/a
44	chr7:33165554-33165604	SKMC	muscle:	n/a
45	chr7:33149114-33149164	PFSK-1	brain:	n/a
46	chr7:33148815-33148865	HepG2	liver:	n/a
47	chr7:33168625-33168675	SK-N-SH	brain:	n/a
48	chr7:33168802-33168852	HIPEpiC	eye:	n/a
49	chr7:33169033-33169083	BE2_C	brain:	n/a
50	chr7:33169186-33169236	U87	brain:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:33147545..33149151-chr7:33167596..33169294,2	K562	blood:
2	chr7:33168152..33172039-chr7:33180833..33185691,4	K562	blood:
3	chr7:33149256..33151960-chr7:33155226..33157184,2	MCF-7	breast:
4	chr7:33173373..33176159-chr7:33177718..33179831,2	K562	blood:
5	chr7:33120839..33123579-chr7:33147074..33148845,2	MCF-7	breast:
6	chr7:33147545..33149151-chr7:33167596..33169294,2	K562	blood:
7	chr7:33131304..33133377-chr7:33140115..33142043,2	K562	blood:
8	chr7:32766854..32769389-chr7:33145298..33147835,2	K562	blood:
9	chr7:33130730..33133581-chr7:33134790..33136889,2	K562	blood:
10	chr7:33147764..33149683-chr7:33167457..33170052,3	MCF-7	breast:
11	chr7:33122616..33124229-chr7:33135048..33136719,2	K562	blood:
12	chr7:33167291..33169895-chr7:33178548..33180361,2	K562	blood:
13	chr7:32930971..32934181-chr7:33147634..33150487,3	MCF-7	breast:
14	chr20:49347482..49349251-chr7:33147388..33148972,2	MCF-7	breast:
15	chr7:33130730..33133581-chr7:33134790..33136889,2	K562	blood:
16	chr7:33101689..33103789-chr7:33147448..33149100,2	MCF-7	breast:
17	chr7:33142504..33144709-chr7:33147297..33150287,2	K562	blood:
18	chr7:33169914..33172476-chr7:33187197..33189119,2	MCF-7	breast:
19	chr7:33151434..33153023-chr7:33155282..33157530,2	K562	blood:
20	chr7:33173373..33176159-chr7:33177718..33179831,2	K562	blood:
21	chr7:33148601..33150604-chr7:33153806..33156546,2	K562	blood:
22	chr7:33179137..33181368-chr7:33185643..33187342,2	MCF-7	breast:
23	chr7:33100859..33104943-chr7:33146945..33149986,6	MCF-7	breast:
24	chr7:33144651..33147364-chr7:33168487..33170158,2	MCF-7	breast:
25	chr7:33179229..33183198-chr7:33185335..33188130,3	K562	blood:
26	chr7:33101592..33103439-chr7:33148174..33150339,2	K562	blood:
27	chr7:32929842..32933813-chr7:33147048..33149516,4	K562	blood:
28	chr7:32981289..32983857-chr7:33147743..33149971,3	K562	blood:
29	chr7:33101766..33103971-chr7:33147720..33150417,2	K562	blood:
30	chr7:33183803..33185518-chr7:33185914..33189355,3	MCF-7	breast:
31	chr7:33148471..33149111-chr8:37962511..37963365,2	HCT-116	colon:
32	chr7:33127364..33129190-chr7:33131831..33134427,2	K562	blood:
33	chr7:33101504..33102499-chr7:33146693..33147349,2	K562	blood:
34	chr7:33094100..33095889-chr7:33158898..33161804,2	K562	blood:
35	chr7:32996816..32997512-chr7:33148545..33149076,2	Hela-S3	cervix:
36	chr7:33137473..33139190-chr7:33143121..33146806,3	K562	blood:
37	chr7:33132440..33134212-chr7:33136928..33139732,2	K562	blood:
38	chr7:33179229..33183198-chr7:33185335..33188130,3	K562	blood:
39	chr7:33098744..33100464-chr7:33145455..33148099,2	K562	blood:
40	chr7:33147514..33149972-chr7:33151690..33154422,2	MCF-7	breast:
41	chr7:33174121..33176456-chr7:33182217..33185074,2	K562	blood:
42	chr7:33145176..33146680-chr7:33147425..33148975,2	K562	blood:
43	chr7:32929813..32931362-chr7:33146969..33149896,3	K562	blood:
44	chr7:33174121..33176456-chr7:33182217..33185074,2	K562	blood:
45	chr19:47730376..47730970-chr7:33148568..33149081,2	Hela-S3	cervix:
46	chr7:33147764..33149683-chr7:33167457..33170052,3	MCF-7	breast:
47	chr7:33151434..33153023-chr7:33155282..33157530,2	K562	blood:
48	chr7:32995811..32998630-chr7:33147873..33150650,5	MCF-7	breast:
49	chr7:33168317..33169892-chr7:33174441..33176886,2	MCF-7	breast:
50	chr7:33137473..33139190-chr7:33143121..33146806,3	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
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
ENSG00000122643	chromatin interactions
ENSG00000228015	chromatin interactions
ENSG00000122507	chromatin interactions
ENSG00000170852	chromatin interactions
ENSG00000105327	chromatin interactions
ENSG00000252706	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000122642	chromatin interactions
ENSG00000164610	chromatin interactions
ENSG00000237004	chromatin interactions
ENSG00000129691	chromatin interactions
ENSG00000205763	chromatin interactions

Extended variants
information (count: 1881 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1881 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112665831	chr7:33130713-33130714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554684162	chr7:33130727-33130728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573008890	chr7:33130760-33130761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540202437	chr7:33130824-33130825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79205787	chr7:33130904-33130905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149943619	chr7:33130916-33130917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs80076114	chr7:33131026-33131027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs564053148	chr7:33131054-33131055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189338793	chr7:33131076-33131077	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs542837879	chr7:33131102-33131103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs561029288	chr7:33131114-33131115	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs528576518	chr7:33131159-33131160	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181142811	chr7:33131173-33131174	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs565137265	chr7:33131314-33131315	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185590239	chr7:33131344-33131345	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532395825	chr7:33131357-33131358	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs17472290	chr7:33131424-33131425	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs549475290	chr7:33131482-33131483	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12667849	chr7:33131607-33131608	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs115525158	chr7:33131614-33131615	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548421944	chr7:33131638-33131639	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs372713656	chr7:33131660-33131661	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533878182	chr7:33131701-33131702	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12667900	chr7:33131729-33131730	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs12672159	chr7:33131745-33131746	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571169360	chr7:33131808-33131809	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145043047	chr7:33131819-33131820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537896745	chr7:33131841-33131842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557346236	chr7:33131883-33131884	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575564311	chr7:33131930-33131931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542776566	chr7:33131940-33131941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181574345	chr7:33131974-33131975	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76533910	chr7:33132063-33132064	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs71738128	chr7:33132073-33132074	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372322449	chr7:33132077-33132078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199897531	chr7:33132078-33132079	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370380128	chr7:33132168-33132169	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77349727	chr7:33132181-33132182	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs565417623	chr7:33132183-33132184	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143637072	chr7:33132193-33132194	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550987442	chr7:33132258-33132259	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138237301	chr7:33132318-33132319	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530039914	chr7:33132336-33132337	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548358782	chr7:33132360-33132361	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563740453	chr7:33132390-33132391	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377294720	chr7:33132441-33132442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141246257	chr7:33132479-33132480	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186988452	chr7:33132490-33132491	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551985442	chr7:33132509-33132510	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs570558014	chr7:33132531-33132532	Weak transcription Strong transcription	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:1720 , 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	chr7:33128200-33131600	Weak transcription	Left Ventricle	heart
16	chr7:33128200-33135400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:33128800-33132600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:33129000-33132800	Weak transcription	Spleen	Spleen
19	chr7:33129200-33132000	Weak transcription	Primary T cells from cord blood	blood
20	chr7:33129400-33132000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr7:33129400-33132400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:33129400-33132800	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr7:33129400-33135200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:33129600-33132200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr7:33129600-33132400	Weak transcription	Primary B cells from cord blood	blood
26	chr7:33129600-33132600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr7:33129600-33135800	Weak transcription	K562	blood
28	chr7:33129800-33131400	Weak transcription	Fetal Brain Female	brain
29	chr7:33130000-33131800	Weak transcription	Fetal Muscle Leg	muscle
30	chr7:33130000-33132000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr7:33130000-33132800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:33130000-33132800	Weak transcription	Brain Hippocampus Middle	brain
33	chr7:33130000-33133800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:33130200-33132600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:33130200-33132800	Weak transcription	A549	lung
36	chr7:33130200-33133400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:33130200-33135200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:33130400-33132000	Weak transcription	Brain Angular Gyrus	brain
39	chr7:33130400-33132400	Weak transcription	Fetal Intestine Large	intestine
40	chr7:33130400-33132400	Weak transcription	Dnd41	blood
41	chr7:33130400-33132600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr7:33130400-33132800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr7:33130400-33132800	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr7:33130400-33132800	Weak transcription	Thymus	Thymus
45	chr7:33130600-33131000	Enhancers	NH-A	brain
46	chr7:33130600-33131600	Enhancers	Osteobl	bone
47	chr7:33130600-33132400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr7:33130600-33132400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr7:33130600-33132600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:33130600-33132600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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