Variant report

Variant	nsv889038
Chromosome Location	chr7:111137752-111329082
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1965)
CpG islands
(count:916)
Chromatin interactive
region (count:142)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1965 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111290526-111290531	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:111290764-111291175	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
4	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
5	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
10	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
12	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
13	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
14	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
15	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
16	ATF1	chr7:111319096-111319299	K562	blood:	n/a	n/a
17	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
18	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
19	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
21	ATF3	chr7:111156586-111157138	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
22	ATF3	chr7:111201918-111202678	K562	blood:	n/a	n/a
23	ATF3	chr7:111290708-111291147	A549	lung:	n/a	n/a
24	ATF3	chr7:111156585-111157142	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
25	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a
26	BACH1	chr7:111160755-111160869	K562	blood:	n/a	n/a
27	BACH1	chr7:111188905-111189076	K562	blood:	n/a	n/a
28	BACH1	chr7:111202015-111202410	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr7:111172186-111172416	K562	blood:	n/a	n/a
30	BACH1	chr7:111169257-111169277	K562	blood:	n/a	n/a
31	BACH1	chr7:111201779-111202839	K562	blood:	n/a	n/a
32	BACH1	chr7:111312247-111312255	K562	blood:	n/a	n/a
33	BATF	chr7:111228155-111228552	GM12878	blood:	n/a	chr7:111228280-111228290 chr7:111228384-111228394 chr7:111228383-111228394
34	BCL11A	chr7:111168484-111168730	GM12878	blood:	n/a	n/a
35	BCL3	chr7:111156597-111157052	A549	lung:	n/a	n/a
36	BCL3	chr7:111156319-111157358	A549	lung:	n/a	n/a
37	BCL3	chr7:111138913-111139703	A549	lung:	n/a	chr7:111138981-111138990
38	BCL3	chr7:111139024-111139659	A549	lung:	n/a	n/a
39	BCL3	chr7:111201738-111202909	A549	lung:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549
40	BCLAF1	chr7:111201762-111202357	GM12878	blood:	n/a	n/a
41	BCLAF1	chr7:111168247-111168782	GM12878	blood:	n/a	n/a
42	BCLAF1	chr7:111202426-111202931	GM12878	blood:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549
43	BHLHE40	chr7:111201889-111202773	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:111167550-111167999	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:111201850-111202859	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:111168429-111168772	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:111198942-111199292	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:111202134-111202334	A549	lung:	n/a	n/a
49	BHLHE40	chr7:111200634-111202933	K562	blood:	n/a	n/a
50	BHLHE40	chr7:111161346-111161405	K562	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111202395-111202445	HepG2	liver:	n/a
2	chr7:111202395-111202445	HepG2	liver:	n/a
3	chr7:111200944-111200994	HRE	kidney:	n/a
4	chr7:111202682-111202732	SK-N-MC	brain:	n/a
5	chr7:111249924-111249974	HEK293	kidney:	embryo
6	chr7:111202755-111202805	HIPEpiC	eye:	n/a
7	chr7:111203008-111203058	AG09319	gingival:	n/a
8	chr7:111202682-111202732	NH-A	brain:	n/a
9	chr7:111202457-111202507	HRCEpiC	kidney:	n/a
10	chr7:111202666-111202716	SKMC	muscle:	n/a
11	chr7:111202666-111202716	SK-N-SH	brain:	n/a
12	chr7:111204826-111204876	HIPEpiC	eye:	n/a
13	chr7:111202389-111202439	NHDF-neo	bronchial:	n/a
14	chr7:111202389-111202439	SKMC	muscle:	n/a
15	chr7:111202682-111202732	GM12892	blood:	n/a
16	chr7:111203008-111203058	PFSK-1	brain:	n/a
17	chr7:111202450-111202500	K562	blood:	n/a
18	chr7:111202222-111202272	Caco-2	colon:	n/a
19	chr7:111202395-111202445	GM06990	blood:	n/a
20	chr7:111204826-111204876	MCF10A-Er-Src	breast:	n/a
21	chr7:111249576-111249626	SK-N-SH_RA	brain:	n/a
22	chr7:111202222-111202272	HCT-116	colon:	n/a
23	chr7:111202679-111202729	HUVEC	blood vessel:	n/a
24	chr7:111202222-111202272	PANC-1	pancreas:	n/a
25	chr7:111202222-111202272	NT2-D1	testis:	n/a
26	chr7:111202450-111202500	AG09309	skin:	n/a
27	chr7:111203008-111203058	AG04450	lung:	fetal
28	chr7:111202457-111202507	PANC-1	pancreas:	n/a
29	chr7:111204826-111204876	K562	blood:	n/a
30	chr7:111198163-111198213	HIPEpiC	eye:	n/a
31	chr7:111202395-111202445	Caco-2	colon:	n/a
32	chr7:111202222-111202272	T-47D	breast:	n/a
33	chr7:111200944-111200994	HCPEpiC	choroid plexus:	n/a
34	chr7:111202395-111202445	HEEpiC	esophagus:	n/a
35	chr7:111202682-111202732	U87	brain:	n/a
36	chr7:111202222-111202272	NHDF-neo	bronchial:	n/a
37	chr7:111202679-111202729	HRCEpiC	kidney:	n/a
38	chr7:111202679-111202729	A549	lung:	n/a
39	chr7:111202755-111202805	GM12891	blood:	n/a
40	chr7:111249576-111249626	AoSMC	blood vessel:	n/a
41	chr7:111202457-111202507	Hepatocyte	liver:	n/a
42	chr7:111249576-111249626	GM06990	blood:	n/a
43	chr7:111202395-111202445	A549	lung:	n/a
44	chr7:111204826-111204876	AG09319	gingival:	n/a
45	chr7:111249924-111249974	H1-hESC	embryonic stem cell:	embryo
46	chr7:111202679-111202729	HEEpiC	esophagus:	n/a
47	chr7:111249924-111249974	HAEpiC	amniotic membrane:	n/a
48	chr7:111203008-111203058	HRPEpiC	eye:	n/a
49	chr7:111202389-111202439	HRPEpiC	eye:	n/a
50	chr7:111202450-111202500	NHBE	bronchial:	n/a

(count:142 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:111150255..111152424-chr7:111159146..111160781,2	K562	blood:
2	chr7:111226016..111229076-chr7:111232229..111235664,3	K562	blood:
3	chr7:111227327..111229119-chr7:111232502..111234968,2	K562	blood:
4	chr7:111199186..111200731-chr7:111244724..111246694,2	K562	blood:
5	chr7:111198400..111201071-chr7:111297443..111299093,2	K562	blood:
6	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
7	chr7:111138086..111139591-chr7:111219192..111221961,2	MCF-7	breast:
8	chr7:111165046..111167501-chr7:111171827..111173680,2	K562	blood:
9	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
10	chr7:111320859..111323048-chr7:111329201..111331055,2	K562	blood:
11	chr17:39844599..39845278-chr7:111202262..111202763,2	Hela-S3	cervix:
12	chr7:111172655..111174823-chr7:111200872..111202478,2	MCF-7	breast:
13	chr7:111164149..111167742-chr7:111173784..111176807,4	K562	blood:
14	chr7:111186407..111189009-chr7:111189104..111191721,2	K562	blood:
15	chr19:4065266..4065879-chr7:111202106..111203058,2	HCT-116	colon:
16	chr7:111160191..111162473-chr7:111166967..111168569,3	K562	blood:
17	chr7:111252721..111255749-chr7:111259045..111261451,3	K562	blood:
18	chr7:111149997..111152577-chr7:111162240..111165050,2	K562	blood:
19	chr7:111176200..111178839-chr7:111180322..111182875,3	K562	blood:
20	chr7:111201205..111204064-chr7:111204287..111207408,3	K562	blood:
21	chr7:111293955..111295853-chr7:111296098..111298925,2	K562	blood:
22	chr7:111164432..111166766-chr7:111167043..111169484,2	MCF-7	breast:
23	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
24	chr7:111180162..111182327-chr7:111200913..111202538,2	MCF-7	breast:
25	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
26	chr7:111150770..111153588-chr7:111154725..111157322,3	K562	blood:
27	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
28	chr7:111179597..111181133-chr7:111200922..111203708,2	K562	blood:
29	chr7:111226200..111228452-chr7:111228554..111231372,2	K562	blood:
30	chr7:111299093..111300961-chr7:111312313..111315147,2	K562	blood:
31	chr7:111238331..111240393-chr7:111247235..111250162,2	K562	blood:
32	chr7:111166819..111169168-chr7:111191445..111193799,2	K562	blood:
33	chr7:111167719..111169526-chr7:111174940..111178460,3	K562	blood:
34	chr7:111198013..111199792-chr7:111239009..111241221,2	K562	blood:
35	chr7:111296753..111298671-chr7:111300525..111303326,2	K562	blood:
36	chr7:111154605..111156613-chr7:111179034..111181673,2	K562	blood:
37	chr7:111164149..111167742-chr7:111173784..111176807,4	K562	blood:
38	chr7:111149997..111152577-chr7:111162240..111165050,2	K562	blood:
39	chr7:111257306..111261237-chr7:111261907..111264448,3	K562	blood:
40	chr7:111222849..111225723-chr7:111230601..111232352,2	K562	blood:
41	chr19:16738439..16739222-chr7:111202426..111202989,2	HCT-116	colon:
42	chr7:111226016..111229076-chr7:111232229..111235664,3	K562	blood:
43	chr7:111159302..111161681-chr7:111166227..111168647,2	MCF-7	breast:
44	chr7:111164134..111166601-chr7:111201959..111203789,2	MCF-7	breast:
45	chr7:111164432..111166766-chr7:111167043..111169484,2	MCF-7	breast:
46	chr7:111299147..111302092-chr7:111316986..111318533,2	K562	blood:
47	chr1:11967838..11968645-chr7:111201747..111202647,2	Hela-S3	cervix:
48	chr7:111199186..111200731-chr7:111244724..111246694,2	K562	blood:
49	chr7:111257306..111261237-chr7:111261907..111264448,3	K562	blood:
50	chr7:111181285..111183708-chr7:111185192..111188559,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRN3-2	chr7:111246670-111249064	ucscGeneNc_uc003vfz_2
2	lnc-LRRN3-2	chr7:111235830-111235905	ucscGeneNc_uc003vfz_2

No data

Variant related genes	Relation type
IMMP2L	TF binding region
IMMP2L	CpG island
ENSG00000164327	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000178951	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000143643	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000240053	chromatin interactions

Extended variants
information (count: 4975 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4975 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11977096	chr7:111137752-111137753	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531795329	chr7:111137774-111137775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146425867	chr7:111137785-111137786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140842095	chr7:111137824-111137825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529530381	chr7:111137870-111137871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78529918	chr7:111137877-111137878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188547248	chr7:111137904-111137905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11983982	chr7:111137943-111137944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs558095488	chr7:111137948-111137949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570123633	chr7:111137980-111137981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191558288	chr7:111137999-111138000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537499858	chr7:111138031-111138032	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556274047	chr7:111138032-111138033	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145161036	chr7:111138069-111138070	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569099060	chr7:111138128-111138129	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146887132	chr7:111138161-111138162	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554028417	chr7:111138169-111138170	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140543507	chr7:111138207-111138208	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184383328	chr7:111138219-111138220	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs564423884	chr7:111138244-111138245	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531777762	chr7:111138390-111138391	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189068371	chr7:111138400-111138401	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540738272	chr7:111138415-111138416	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78248595	chr7:111138432-111138433	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs76761233	chr7:111138433-111138434	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562242663	chr7:111138452-111138453	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529443456	chr7:111138487-111138488	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372645227	chr7:111138488-111138489	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376146470	chr7:111138494-111138495	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565948853	chr7:111138501-111138502	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370842455	chr7:111138583-111138584	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372779840	chr7:111138590-111138591	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533406745	chr7:111138609-111138610	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs150460742	chr7:111138628-111138629	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs570113337	chr7:111138629-111138630	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553537733	chr7:111138714-111138715	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537888880	chr7:111138717-111138718	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370370555	chr7:111138742-111138743	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532954419	chr7:111138748-111138749	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181720116	chr7:111138769-111138770	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552691954	chr7:111138778-111138779	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535210835	chr7:111138784-111138785	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372158472	chr7:111138803-111138804	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147550815	chr7:111138837-111138838	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553966663	chr7:111138865-111138866	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573231467	chr7:111138914-111138915	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539741960	chr7:111138970-111138971	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187409436	chr7:111139006-111139007	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs74589679	chr7:111139016-111139017	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74476313	chr7:111139025-111139026	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1336 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111111400-111150600	Weak transcription	Pancreas	Pancrea
2	chr7:111123000-111159000	Weak transcription	Aorta	Aorta
3	chr7:111126600-111138000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:111128800-111150600	Weak transcription	Ovary	ovary
5	chr7:111131800-111138600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:111136400-111138000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:111136600-111138600	Enhancers	A549	lung
8	chr7:111137000-111138600	Weak transcription	Stomach Mucosa	stomach
9	chr7:111138000-111138200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:111138000-111139200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:111138200-111138600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:111138200-111139800	Enhancers	NHEK	skin
13	chr7:111138400-111139800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:111138400-111139800	Enhancers	Hela-S3	cervix
15	chr7:111138400-111139800	Enhancers	HMEC	breast
16	chr7:111138600-111138800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:111138600-111139000	Flanking Active TSS	A549	lung
18	chr7:111138600-111139200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:111138600-111139600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:111138600-111139600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:111138600-111139600	Enhancers	Stomach Mucosa	stomach
22	chr7:111138600-111139800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:111138800-111139200	Enhancers	Osteobl	bone
24	chr7:111138800-111139400	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr7:111139000-111139400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:111139000-111139400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:111139000-111139400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr7:111139000-111139400	Active TSS	A549	lung
29	chr7:111139000-111139600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr7:111139000-111139600	ZNF genes & repeats	K562	blood
31	chr7:111139000-111139600	Enhancers	NHLF	lung
32	chr7:111139200-111139400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:111139200-111139400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr7:111139200-111139400	Enhancers	Gastric	stomach
35	chr7:111139200-111139800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:111139200-111140800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr7:111139400-111139800	Flanking Active TSS	A549	lung
38	chr7:111139400-111140800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:111139400-111141600	Weak transcription	Gastric	stomach
40	chr7:111139600-111140600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:111139800-111146600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:111139800-111148800	Weak transcription	A549	lung
43	chr7:111139800-111149200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr7:111139800-111150800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:111140600-111140800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:111140800-111148800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr7:111140800-111150600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:111141000-111141200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:111142000-111142200	Weak transcription	Fetal Intestine Small	intestine
50	chr7:111145200-111146000	Weak transcription	Fetal Intestine Small	intestine

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