Variant report

Variant	nsv1020212
Chromosome Location	chr7:111944370-112032596
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:489)
Chromatin interactive
region (count:75)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111976293-111976878	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:111997931-111998361	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111997222-111997393	K562	blood:	n/a	n/a
4	ATF2	chr7:112032057-112032458	GM12878	blood:	n/a	n/a
5	BATF	chr7:112031356-112031934	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:112031297-112032222	HepG2	liver:	n/a	n/a
7	BHLHE40	chr7:112031178-112031614	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:112032006-112032350	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:112031074-112032310	HepG2	liver:	n/a	n/a
10	BHLHE40	chr7:112031339-112031608	A549	lung:	n/a	n/a
11	BRCA1	chr7:111978124-111978188	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr7:112032142-112032399	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr7:111983248-111983388	K562	blood:	n/a	n/a
14	CEBPB	chr7:112012311-112012572	A549	lung:	n/a	n/a
15	CEBPB	chr7:112012263-112012591	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:112012335-112012535	K562	blood:	n/a	n/a
17	CEBPB	chr7:111995232-111995338	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:112001445-112001698	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:112004522-112004811	HepG2	liver:	n/a	n/a
20	CHD2	chr7:112032113-112032242	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr7:112002373-112002523	MCF-7	breast:	n/a	chr7:112002438-112002447
22	CTCF	chr7:112023740-112023890	HL-60	blood:	n/a	chr7:112023806-112023822
23	CTCF	chr7:112023797-112023882	ProgFib	skin:	n/a	chr7:112023806-112023822
24	CTCF	chr7:111997320-111997470	BE2_C	brain:	n/a	n/a
25	CTCF	chr7:112002320-112002470	AG04449	skin:	n/a	chr7:112002438-112002447
26	CTCF	chr7:111997340-111997490	BE2_C	brain:	n/a	n/a
27	CTCF	chr7:112002300-112002450	HPAF	blood vessel:	n/a	chr7:112002438-112002447
28	CTCF	chr7:112032045-112032125	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr7:112023720-112023870	Hela-S3	cervix:	n/a	chr7:112023806-112023822
30	CTCF	chr7:112002423-112002496	HepG2	liver:	n/a	chr7:112002438-112002447
31	CTCF	chr7:111993840-111993916	GM20000	blood:	n/a	n/a
32	CTCF	chr7:111997333-111997450	HepG2	liver:	n/a	n/a
33	CTCF	chr7:112023740-112023890	NB4	blood:	n/a	chr7:112023806-112023822
34	CTCF	chr7:112031444-112031581	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr7:112023780-112023930	HBMEC	blood vessel:	n/a	chr7:112023806-112023822
36	CTCF	chr7:112023920-112024070	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr7:112031957-112031999	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr7:111997312-111997502	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:112023700-112023850	HEK293	kidney:	n/a	chr7:112023806-112023822
40	CTCF	chr7:112023700-112023850	AG10803	skin:	n/a	chr7:112023806-112023822
41	CTCF	chr7:112002420-112002570	HRE	kidney:	n/a	chr7:112002438-112002447
42	CTCF	chr7:112002300-112002450	HAc	cerebellar:	n/a	chr7:112002438-112002447
43	CTCF	chr7:112023640-112023790	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:112023760-112023910	MCF-7	breast:	n/a	chr7:112023806-112023822
45	CTCF	chr7:112023780-112023930	HRE	kidney:	n/a	chr7:112023806-112023822
46	CTCF	chr7:112002380-112002530	HEK293	kidney:	n/a	chr7:112002438-112002447
47	CTCF	chr7:112002340-112002490	HA-sp	spinal cord:	n/a	chr7:112002438-112002447
48	CTCF	chr7:112002300-112002450	HRE	kidney:	n/a	chr7:112002438-112002447
49	CTCF	chr7:112023660-112023810	HPF	lung:	n/a	n/a
50	CTCF	chr7:112023693-112023870	IMR90	lung:	n/a	chr7:112023806-112023822

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112030679-112030729	GM19239	blood:	n/a
2	chr7:112030679-112030729	GM19239	blood:	n/a
3	chr7:112031660-112031710	HUVEC	blood vessel:	n/a
4	chr7:112001736-112001786	SK-N-SH_RA	brain:	n/a
5	chr7:112031374-112031424	AG09309	skin:	n/a
6	chr7:112027731-112027781	AG09309	skin:	n/a
7	chr7:112031374-112031424	HCPEpiC	choroid plexus:	n/a
8	chr7:111977542-111977592	SK-N-SH_RA	brain:	n/a
9	chr7:112031660-112031710	HCPEpiC	choroid plexus:	n/a
10	chr7:112030679-112030729	HUVEC	blood vessel:	n/a
11	chr7:112002922-112002972	H1-hESC	embryonic stem cell:	embryo
12	chr7:112031660-112031710	Hela-S3	cervix:	n/a
13	chr7:112032146-112032196	PrEC	prostate:	n/a
14	chr7:112031374-112031424	Hela-S3	cervix:	n/a
15	chr7:112027731-112027781	HNPCEpiC	eye:	n/a
16	chr7:111977542-111977592	GM06990	blood:	n/a
17	chr7:112032146-112032196	AG09319	gingival:	n/a
18	chr7:112001736-112001786	HAEpiC	amniotic membrane:	n/a
19	chr7:112027731-112027781	SK-N-SH	brain:	n/a
20	chr7:112031374-112031424	LNCaP	prostate:	n/a
21	chr7:112030679-112030729	U87	brain:	n/a
22	chr7:112001736-112001786	Hepatocyte	liver:	n/a
23	chr7:112032146-112032196	HCPEpiC	choroid plexus:	n/a
24	chr7:112030679-112030729	HCF	heart:	n/a
25	chr7:112031660-112031710	SKMC	muscle:	n/a
26	chr7:112031374-112031424	BJ	skin:	n/a
27	chr7:112027731-112027781	MCF10A-Er-Src	breast:	n/a
28	chr7:112031660-112031710	NH-A	brain:	n/a
29	chr7:112027731-112027781	ovcar-3	ovarian:	n/a
30	chr7:111977542-111977592	BE2_C	brain:	n/a
31	chr7:112002922-112002972	HEK293	kidney:	embryo
32	chr7:112030679-112030729	AoSMC	blood vessel:	n/a
33	chr7:112001736-112001786	AG09309	skin:	n/a
34	chr7:112032146-112032196	ProgFib	skin:	n/a
35	chr7:112027731-112027781	HCF	heart:	n/a
36	chr7:112030679-112030729	Jurkat	blood:	n/a
37	chr7:112001736-112001786	T-47D	breast:	n/a
38	chr7:112031374-112031424	SAEC	small airway:	n/a
39	chr7:112030679-112030729	AG09309	skin:	n/a
40	chr7:112001736-112001786	HCM	heart:	n/a
41	chr7:112027731-112027781	GM12892	blood:	n/a
42	chr7:111977542-111977592	HRCEpiC	kidney:	n/a
43	chr7:112001736-112001786	ovcar-3	ovarian:	n/a
44	chr7:112027731-112027781	HRE	kidney:	n/a
45	chr7:112032146-112032196	U87	brain:	n/a
46	chr7:112002922-112002972	SK-N-SH	brain:	n/a
47	chr7:112027731-112027781	NT2-D1	testis:	n/a
48	chr7:112002922-112002972	GM19239	blood:	n/a
49	chr7:111977542-111977592	BJ	skin:	n/a
50	chr7:111977542-111977592	AG09319	gingival:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:111977500..111980295-chr7:111984843..111986520,2	K562	blood:
2	chr7:111972425..111975420-chr7:111977051..111978873,2	MCF-7	breast:
3	chr7:111970934..111972982-chr7:111975133..111976694,2	K562	blood:
4	chr7:111979755..111984894-chr7:111986750..111988962,5	K562	blood:
5	chr7:111965666..111967562-chr7:111973508..111976479,2	MCF-7	breast:
6	chr7:112031184..112032769-chr7:112035283..112037253,2	MCF-7	breast:
7	chr7:111979755..111984894-chr7:111986750..111988962,5	K562	blood:
8	chr7:112032001..112033811-chr7:112035670..112039221,3	MCF-7	breast:
9	chr7:111957865..111960569-chr7:111963076..111967286,5	K562	blood:
10	chr7:112005791..112008546-chr7:112090128..112092085,3	K562	blood:
11	chr7:111844854..111847845-chr7:112004638..112006881,2	MCF-7	breast:
12	chr7:111935052..111937949-chr7:111944380..111946424,2	K562	blood:
13	chr7:111808781..111810939-chr7:112023038..112025421,2	K562	blood:
14	chr7:111965666..111967562-chr7:111973508..111976479,2	MCF-7	breast:
15	chr7:111982916..111985880-chr7:111989635..111992335,2	K562	blood:
16	chr7:111929064..111930733-chr7:111964333..111965879,2	K562	blood:
17	chr7:111963557..111967020-chr7:111968697..111972390,4	K562	blood:
18	chr7:111897853..111899387-chr7:112024609..112027579,2	K562	blood:
19	chr7:112029526..112032512-chr7:112089416..112091655,2	K562	blood:
20	chr7:111963557..111967020-chr7:111968697..111972390,4	K562	blood:
21	chr7:111850231..111853782-chr7:112032412..112034689,3	MCF-7	breast:
22	chr7:112005791..112008546-chr7:112090128..112092085,2	K562	blood:
23	chr7:112013395..112014930-chr7:112015433..112017395,2	MCF-7	breast:
24	chr7:111960085..111962357-chr7:111965697..111968570,2	K562	blood:
25	chr7:111975441..111977682-chr7:111980035..111981752,2	MCF-7	breast:
26	chr7:111995574..111997351-chr7:111999443..112001258,2	K562	blood:
27	chr7:111955858..111957422-chr7:111959374..111961415,2	MCF-7	breast:
28	chr7:111947172..111951025-chr7:111951049..111954206,4	K562	blood:
29	chr7:111857821..111859574-chr7:112030551..112032739,2	MCF-7	breast:
30	chr7:111975573..111978614-chr7:111997499..112000995,3	K562	blood:
31	chr15:65588341..65590081-chr7:112023852..112026562,2	MCF-7	breast:
32	chr7:111953427..111955871-chr7:111961966..111964536,3	K562	blood:
33	chr7:111953427..111955871-chr7:111961966..111964536,3	K562	blood:
34	chr7:111957865..111959684-chr7:111963076..111965574,2	K562	blood:
35	chr13:65064336..65064836-chr7:112019541..112020159,2	MCF-7	breast:
36	chr7:111966020..111968583-chr7:111970529..111973341,2	MCF-7	breast:
37	chr7:111970934..111972982-chr7:111975133..111976694,2	K562	blood:
38	chr7:111981020..111983369-chr7:111995911..111998371,2	MCF-7	breast:
39	chr7:111995574..111997351-chr7:111999443..112001258,2	K562	blood:
40	chr7:111957865..111959684-chr7:111963076..111965574,2	K562	blood:
41	chr7:111981020..111983369-chr7:111995911..111998371,2	MCF-7	breast:
42	chr7:111996890..111999706-chr7:112089816..112092344,3	K562	blood:
43	chr7:112010041..112012440-chr7:112089229..112091559,2	MCF-7	breast:
44	chr7:111930275..111932583-chr7:111961875..111964299,2	K562	blood:
45	chr7:111989108..111993301-chr7:111995018..111998714,4	K562	blood:
46	chr7:111990563..111992725-chr7:111998722..112000873,2	MCF-7	breast:
47	chr7:111955858..111957422-chr7:111959374..111961415,2	MCF-7	breast:
48	chr7:112023824..112026066-chr7:112090573..112093193,2	MCF-7	breast:
49	chr7:112026430..112029317-chr7:112088905..112090838,2	K562	blood:
50	chr7:112029372..112031621-chr7:112036798..112039526,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-1	chr7:111968312-111968453	ENSG00000226851.1
2	lnc-DOCK4-1	chr7:111990519-111990596	ENSG00000226851.1
3	lnc-DOCK4-1	chr7:111968244-111968453	ENSG00000226851.1
4	lnc-DOCK4-3	chr7:112013788-112014305	NONHSAT122783
5	lnc-DOCK4-1	chr7:112024994-112025159	ENSG00000226851.1
6	lnc-ZNF277-3	chr7:112014379-112015484	NONHSAT122784
7	lnc-DOCK4-1	chr7:111981110-111981177	ENSG00000226851.1

No data

Variant related genes	Relation type
ZNF277	TF binding region
MTND5P8	TF binding region
ENSG00000236232	TF binding region
ENSG00000226851	TF binding region
ENSG00000232922	TF binding region
ZNF277	CpG island
MTND5P8	CpG island
ENSG00000236232	CpG island
ENSG00000226851	CpG island
ENSG00000232922	CpG island
ENSG00000006652	chromatin interactions
ENSG00000128512	chromatin interactions
ENSG00000198839	chromatin interactions
ENSG00000236232	chromatin interactions
ENSG00000232922	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000226851	chromatin interactions
ENSG00000230999	chromatin interactions

Extended variants
information (count: 2943 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2943 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73424457	chr7:111944455-111944456	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141688900	chr7:111944607-111944608	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192360833	chr7:111944691-111944692	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565422998	chr7:111944716-111944717	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs542505641	chr7:111944766-111944767	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10268520	chr7:111944767-111944768	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560645545	chr7:111944803-111944804	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs182268592	chr7:111944807-111944808	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs546066649	chr7:111944818-111944819	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs150497708	chr7:111944899-111944900	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532077366	chr7:111944907-111944908	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187689431	chr7:111944935-111944936	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376192444	chr7:111944944-111944945	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556240849	chr7:111944994-111944995	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs117450857	chr7:111945014-111945015	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138415688	chr7:111945067-111945068	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114319659	chr7:111945087-111945088	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10269057	chr7:111945093-111945094	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534134384	chr7:111945112-111945113	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144226341	chr7:111945115-111945116	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534790110	chr7:111945117-111945118	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552081191	chr7:111945132-111945133	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs10269074	chr7:111945133-111945134	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs538301409	chr7:111945214-111945215	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs149427897	chr7:111945216-111945217	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs373480125	chr7:111945250-111945251	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553080116	chr7:111945260-111945261	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554172316	chr7:111945266-111945267	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144857693	chr7:111945282-111945283	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62473139	chr7:111945287-111945288	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568301347	chr7:111945292-111945293	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557886419	chr7:111945332-111945333	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576240032	chr7:111945511-111945512	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543872002	chr7:111945554-111945555	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370835897	chr7:111945590-111945591	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562221333	chr7:111945628-111945629	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540488079	chr7:111945652-111945653	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143876399	chr7:111945674-111945675	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529771588	chr7:111945735-111945736	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192787393	chr7:111945747-111945748	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184873735	chr7:111945796-111945797	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527546413	chr7:111945830-111945831	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17159446	chr7:111945832-111945833	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs570625793	chr7:111945852-111945853	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531558308	chr7:111945873-111945874	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535688676	chr7:111945925-111945926	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568552425	chr7:111945926-111945927	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535985653	chr7:111945959-111945960	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553877461	chr7:111945963-111945964	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190104625	chr7:111945987-111945988	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1576 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111903400-111949200	Weak transcription	Fetal Intestine Small	intestine
2	chr7:111913200-111965200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:111913600-111949600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:111918000-111963000	Weak transcription	Aorta	Aorta
5	chr7:111921400-111961800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr7:111922000-111949800	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:111922400-111949800	Weak transcription	Ovary	ovary
8	chr7:111922800-111945000	Weak transcription	Pancreas	Pancrea
9	chr7:111923600-111964600	Weak transcription	Esophagus	oesophagus
10	chr7:111923600-111964800	Weak transcription	Gastric	stomach
11	chr7:111926200-111948000	Weak transcription	Spleen	Spleen
12	chr7:111926200-111979600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr7:111926600-111982200	Weak transcription	Right Ventricle	heart
14	chr7:111926800-111949000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:111926800-111949800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:111926800-111949800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr7:111926800-111962000	Weak transcription	Fetal Brain Female	brain
18	chr7:111926800-111964800	Weak transcription	Lung	lung
19	chr7:111927200-111965000	Weak transcription	Brain Anterior Caudate	brain
20	chr7:111927400-111945800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr7:111927400-111964800	Weak transcription	Fetal Stomach	stomach
22	chr7:111928600-111947000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:111928600-111978000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr7:111928800-111946600	Weak transcription	Brain Substantia Nigra	brain
25	chr7:111928800-111949800	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:111928800-111949800	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:111928800-111950000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr7:111928800-111961000	Weak transcription	Placenta	Placenta
29	chr7:111929000-111947000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:111929000-111948800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr7:111929000-111949000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr7:111929000-111949600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:111929000-111949800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr7:111929000-111958800	Weak transcription	Fetal Thymus	thymus
35	chr7:111929000-111959000	Weak transcription	Fetal Intestine Large	intestine
36	chr7:111929200-111949000	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr7:111929600-111949000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr7:111930000-111949800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr7:111930200-111961800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:111930600-111959000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:111930800-111947200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:111930800-111949200	Weak transcription	NHEK	skin
43	chr7:111930800-111965200	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr7:111931000-111949200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr7:111931000-111949200	Weak transcription	HMEC	breast
46	chr7:111931000-111949200	Weak transcription	HSMM	muscle
47	chr7:111931000-111949400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:111931000-111949800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:111931000-111981000	Weak transcription	HSMMtube	muscle
50	chr7:111931400-111947400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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