Variant report

Variant	nsv885809
Chromosome Location	chr6:36687518-36719079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:667)
CpG islands
(count:122)
Chromatin interactive
region (count:96)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:36694186-36694726	GM12878	blood:	n/a	n/a
2	ATF2	chr6:36694205-36694712	GM12878	blood:	n/a	n/a
3	BATF	chr6:36716203-36716545	GM12878	blood:	n/a	chr6:36716388-36716399
4	BATF	chr6:36694216-36694609	GM12878	blood:	n/a	n/a
5	BATF	chr6:36694218-36694674	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:36694216-36694660	GM12878	blood:	n/a	n/a
7	BCL3	chr6:36694222-36694643	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:36694181-36694671	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:36688203-36688371	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:36692452-36692632	K562	blood:	n/a	n/a
11	BHLHE40	chr6:36708312-36708547	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:36710914-36711102	HepG2	liver:	n/a	n/a
13	BHLHE40	chr6:36694258-36694566	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:36708380-36708460	K562	blood:	n/a	n/a
15	BHLHE40	chr6:36708418-36708433	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:36692402-36692663	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr6:36716462-36716724	K562	blood:	n/a	n/a
18	CEBPB	chr6:36692384-36692679	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:36694380-36694582	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:36692448-36692674	K562	blood:	n/a	n/a
21	CEBPB	chr6:36702907-36703264	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:36692383-36692645	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:36701325-36701540	A549	lung:	n/a	chr6:36701405-36701416
24	CEBPB	chr6:36701348-36701475	HepG2	liver:	n/a	chr6:36701405-36701416
25	CEBPB	chr6:36694132-36694783	GM12878	blood:	n/a	n/a
26	CHD1	chr6:36692276-36693016	IMR90	lung:	n/a	n/a
27	CHD2	chr6:36694362-36694552	GM12878	blood:	n/a	n/a
28	CREB1	chr6:36713614-36713996	K562	blood:	n/a	chr6:36713808-36713821
29	CTCF	chr6:36702920-36703070	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr6:36702897-36703051	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr6:36699740-36699890	HCT-116	colon:	n/a	n/a
32	CTCF	chr6:36692500-36692650	AoAF	blood vessel:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
33	CTCF	chr6:36699760-36699910	HEK293	kidney:	n/a	n/a
34	CTCF	chr6:36692466-36692641	H1-hESC	embryonic stem cell:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
35	CTCF	chr6:36692480-36692630	NHEK	skin:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
36	CTCF	chr6:36692440-36692590	GM12870	blood:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
37	CTCF	chr6:36702820-36702970	HAc	cerebellar:	n/a	n/a
38	CTCF	chr6:36692440-36692590	GM12869	blood:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
39	CTCF	chr6:36699739-36699946	GM12891	blood:	n/a	n/a
40	CTCF	chr6:36702971-36703033	ProgFib	skin:	n/a	n/a
41	CTCF	chr6:36692500-36692650	NHDF-neo	bronchial:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
42	CTCF	chr6:36702940-36703090	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr6:36702887-36703028	GM12891	blood:	n/a	n/a
44	CTCF	chr6:36692480-36692630	HPF	lung:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
45	CTCF	chr6:36702904-36703009	GM12878	blood:	n/a	n/a
46	CTCF	chr6:36692480-36692630	HRPEpiC	eye:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578
47	CTCF	chr6:36692368-36692769	GM12878	blood:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578 chr6:36692644-36692651
48	CTCF	chr6:36692520-36692670	HEEpiC	esophagus:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578 chr6:36692644-36692651
49	CTCF	chr6:36692520-36692670	NHDF-neo	bronchial:	n/a	chr6:36692558-36692579 chr6:36692563-36692581 chr6:36692565-36692578 chr6:36692569-36692578 chr6:36692644-36692651
50	CTCF	chr6:36699738-36699943	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:36703127-36703177	HEK293	kidney:	embryo
2	chr6:36703127-36703177	HRCEpiC	kidney:	n/a
3	chr6:36709214-36709264	U87	brain:	n/a
4	chr6:36709214-36709264	HIPEpiC	eye:	n/a
5	chr6:36703127-36703177	MCF-7	breast:	n/a
6	chr6:36709214-36709264	AG04449	skin:	fetal
7	chr6:36709214-36709264	IMR90	lung:	fetal
8	chr6:36703127-36703177	CMK	blood:	n/a
9	chr6:36709214-36709264	AG09309	skin:	n/a
10	chr6:36703127-36703177	IMR90	lung:	fetal
11	chr6:36709214-36709264	LNCaP	prostate:	n/a
12	chr6:36709214-36709264	MCF-7	breast:	n/a
13	chr6:36703127-36703177	NT2-D1	testis:	n/a
14	chr6:36703127-36703177	Hepatocyte	liver:	n/a
15	chr6:36703127-36703177	HepG2	liver:	n/a
16	chr6:36703127-36703177	HEEpiC	esophagus:	n/a
17	chr6:36703127-36703177	NH-A	brain:	n/a
18	chr6:36709214-36709264	Hela-S3	cervix:	n/a
19	chr6:36703127-36703177	ProgFib	skin:	n/a
20	chr6:36703127-36703177	SAEC	small airway:	n/a
21	chr6:36709214-36709264	BE2_C	brain:	n/a
22	chr6:36703127-36703177	H1-hESC	embryonic stem cell:	embryo
23	chr6:36709214-36709264	HCPEpiC	choroid plexus:	n/a
24	chr6:36703127-36703177	BE2_C	brain:	n/a
25	chr6:36709214-36709264	Caco-2	colon:	n/a
26	chr6:36703127-36703177	HIPEpiC	eye:	n/a
27	chr6:36703127-36703177	HUVEC	blood vessel:	n/a
28	chr6:36703127-36703177	RPTEC	kidney:	n/a
29	chr6:36703127-36703177	HMEC	breast:	n/a
30	chr6:36703127-36703177	SK-N-MC	brain:	n/a
31	chr6:36709214-36709264	GM12891	blood:	n/a
32	chr6:36703127-36703177	K562	blood:	n/a
33	chr6:36703127-36703177	NHDF-neo	bronchial:	n/a
34	chr6:36709214-36709264	ovcar-3	ovarian:	n/a
35	chr6:36709214-36709264	HRCEpiC	kidney:	n/a
36	chr6:36709214-36709264	GM06990	blood:	n/a
37	chr6:36709214-36709264	PANC-1	pancreas:	n/a
38	chr6:36709214-36709264	NH-A	brain:	n/a
39	chr6:36703127-36703177	HCF	heart:	n/a
40	chr6:36709214-36709264	HepG2	liver:	n/a
41	chr6:36709214-36709264	HAEpiC	amniotic membrane:	n/a
42	chr6:36703127-36703177	AG10803	skin:	n/a
43	chr6:36709214-36709264	AG10803	skin:	n/a
44	chr6:36709214-36709264	NB4	blood:	n/a
45	chr6:36703127-36703177	MCF10A-Er-Src	breast:	n/a
46	chr6:36703127-36703177	AoSMC	blood vessel:	n/a
47	chr6:36709214-36709264	T-47D	breast:	n/a
48	chr6:36703127-36703177	ovcar-3	ovarian:	n/a
49	chr6:36703127-36703177	NB4	blood:	n/a
50	chr6:36709214-36709264	NT2-D1	testis:	n/a

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:36717988..36719917-chr6:36723476..36726910,3	MCF-7	breast:
2	chr6:36626473..36628728-chr6:36691772..36694267,2	MCF-7	breast:
3	chr6:36696414..36698487-chr6:36724998..36726714,2	MCF-7	breast:
4	chr6:36603987..36606106-chr6:36685798..36688439,2	K562	blood:
5	chr6:36714240..36716919-chr6:36719945..36722727,5	MCF-7	breast:
6	chr6:36706145..36708888-chr6:36709331..36711123,2	MCF-7	breast:
7	chr6:36710588..36713306-chr6:36722738..36724865,2	MCF-7	breast:
8	chr6:36645437..36647373-chr6:36685650..36687672,2	MCF-7	breast:
9	chr6:36684189..36687540-chr6:36688167..36692245,5	MCF-7	breast:
10	chr6:36705988..36708979-chr6:36709402..36712073,2	K562	blood:
11	chr6:36575353..36578968-chr6:36688808..36692284,3	MCF-7	breast:
12	chr6:36561849..36563615-chr6:36700031..36702846,2	K562	blood:
13	chr6:36633980..36636533-chr6:36690989..36693316,2	MCF-7	breast:
14	chr6:36644838..36653438-chr6:36718524..36730954,23	MCF-7	breast:
15	chr6:36695657..36698030-chr6:36700581..36702478,2	K562	blood:
16	chr6:36689656..36693910-chr6:36696758..36700115,6	K562	blood:
17	chr6:36704975..36706910-chr6:36710272..36712382,2	MCF-7	breast:
18	chr6:36692374..36694188-chr6:36726056..36729043,2	MCF-7	breast:
19	chr6:36710180..36712510-chr6:36716987..36718768,2	K562	blood:
20	chr6:36560896..36563675-chr6:36695597..36697920,2	MCF-7	breast:
21	chr6:36645227..36647717-chr6:36711034..36713028,2	K562	blood:
22	chr6:36693621..36695483-chr6:36698291..36701067,2	MCF-7	breast:
23	chr6:36706791..36710785-chr6:36712838..36716064,4	MCF-7	breast:
24	chr6:36693621..36695483-chr6:36698291..36701067,2	MCF-7	breast:
25	chr6:36711266..36713245-chr6:36715954..36717794,2	MCF-7	breast:
26	chr6:36705103..36707775-chr6:36711430..36713266,2	MCF-7	breast:
27	chr6:36589424..36591252-chr6:36691223..36692725,2	MCF-7	breast:
28	chr6:36577343..36580259-chr6:36718203..36721182,2	MCF-7	breast:
29	chr6:36658059..36660618-chr6:36709664..36711830,2	MCF-7	breast:
30	chr6:36583432..36585248-chr6:36700120..36704013,3	MCF-7	breast:
31	chr6:36563235..36565666-chr6:36712198..36714107,2	K562	blood:
32	chr6:36713858..36716285-chr6:36724983..36726678,2	MCF-7	breast:
33	chr6:36717692..36718483-chr6:36726667..36727520,2	K562	blood:
34	chr6:36703852..36706817-chr6:36717625..36719969,2	K562	blood:
35	chr6:36582828..36583431-chr6:36692525..36693052,2	MCF-7	breast:
36	chr6:36655048..36657495-chr6:36690151..36694122,3	MCF-7	breast:
37	chr6:36711266..36713245-chr6:36715954..36717794,2	MCF-7	breast:
38	chr6:36708918..36710565-chr6:36712727..36715586,2	K562	blood:
39	chr6:36708918..36710565-chr6:36712727..36715586,2	K562	blood:
40	chr6:36572662..36574979-chr6:36718444..36721087,2	K562	blood:
41	chr6:36645600..36648162-chr6:36684674..36687564,2	K562	blood:
42	chr6:36591305..36591878-chr6:36692059..36693073,8	K562	blood:
43	chr6:36635018..36637044-chr6:36710933..36713268,2	K562	blood:
44	chr6:36645102..36656546-chr6:36717974..36730993,29	MCF-7	breast:
45	chr6:36684189..36687540-chr6:36688167..36692245,5	MCF-7	breast:
46	chr6:36575316..36577688-chr6:36710838..36712742,2	K562	blood:
47	chr6:36692637..36694151-chr6:36698641..36700541,2	MCF-7	breast:
48	chr6:36648503..36650842-chr6:36690770..36692686,2	MCF-7	breast:
49	chr6:36586905..36589063-chr6:36691247..36692772,2	MCF-7	breast:
50	chr6:36671517..36673727-chr6:36709746..36712131,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000220349	TF binding region
ENSG00000220349	CpG island
ENSG00000263894	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000124772	chromatin interactions
ENSG00000255587	chromatin interactions
ENSG00000220349	chromatin interactions
ENSG00000124762	chromatin interactions

Extended variants
information (count: 1380 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1380 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs236483	chr6:36687518-36687519	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368845972	chr6:36687555-36687556	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7756867	chr6:36687568-36687569	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs181718728	chr6:36687569-36687570	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555512362	chr6:36687579-36687580	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs236482	chr6:36687592-36687593	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs527715550	chr6:36687659-36687660	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77248774	chr6:36687702-36687703	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144095328	chr6:36687737-36687738	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530020501	chr6:36687745-36687746	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11963372	chr6:36687748-36687749	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs78311895	chr6:36687774-36687775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187654109	chr6:36687794-36687795	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs236481	chr6:36687809-36687810	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs191967073	chr6:36687832-36687833	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561093030	chr6:36687950-36687951	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148726784	chr6:36687960-36687961	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373549554	chr6:36687976-36687977	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531518971	chr6:36687987-36687988	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183930610	chr6:36687999-36688000	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs236480	chr6:36688006-36688007	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs144413295	chr6:36688044-36688045	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373464240	chr6:36688091-36688092	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547335203	chr6:36688096-36688097	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566846367	chr6:36688168-36688169	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534250346	chr6:36688209-36688210	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555627089	chr6:36688230-36688231	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547868327	chr6:36688254-36688255	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573939095	chr6:36688283-36688284	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566251860	chr6:36688284-36688285	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564198222	chr6:36688286-36688287	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556387219	chr6:36688297-36688298	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535037648	chr6:36688323-36688324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148667112	chr6:36688338-36688339	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555230227	chr6:36688343-36688344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560482917	chr6:36688382-36688383	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572447599	chr6:36688401-36688402	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540538761	chr6:36688411-36688412	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5875554	chr6:36688425-36688426	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542976419	chr6:36688459-36688460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561156804	chr6:36688480-36688481	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142149000	chr6:36688512-36688513	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549908136	chr6:36688562-36688563	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368043842	chr6:36688602-36688603	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs376854521	chr6:36688654-36688655	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs129546	chr6:36688729-36688730	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556149485	chr6:36688736-36688737	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs147909720	chr6:36688759-36688760	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs547155759	chr6:36688771-36688772	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs565374254	chr6:36688812-36688813	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36661400-36696400	Weak transcription	Right Atrium	heart
2	chr6:36671800-36694000	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr6:36672200-36693600	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:36677000-36694000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr6:36681400-36688800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:36683800-36689400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:36683800-36695200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr6:36685800-36690400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:36686200-36689600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:36686200-36690000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:36686400-36688400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:36686400-36688400	Weak transcription	Esophagus	oesophagus
13	chr6:36686400-36689600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:36686800-36688400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:36686800-36688400	Strong transcription	Spleen	Spleen
16	chr6:36687000-36688600	Enhancers	GM12878-XiMat	blood
17	chr6:36687000-36688800	Enhancers	Primary B cells from peripheral blood	blood
18	chr6:36687400-36688400	Enhancers	Primary B cells from cord blood	blood
19	chr6:36687400-36688800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:36687600-36688200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:36688200-36688400	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr6:36688200-36688800	Enhancers	Fetal Thymus	thymus
23	chr6:36688200-36690600	Enhancers	Fetal Muscle Trunk	muscle
24	chr6:36688200-36692400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:36688400-36688800	Enhancers	Esophagus	oesophagus
26	chr6:36688400-36689200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr6:36688400-36690000	Weak transcription	Spleen	Spleen
28	chr6:36688400-36690400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr6:36688400-36692400	Weak transcription	Primary B cells from cord blood	blood
30	chr6:36688400-36702200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:36688600-36688800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:36688600-36688800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr6:36688600-36692400	Weak transcription	GM12878-XiMat	blood
34	chr6:36688800-36689000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:36688800-36689000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr6:36688800-36689600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:36688800-36690200	Weak transcription	Esophagus	oesophagus
38	chr6:36688800-36692000	Weak transcription	Primary B cells from peripheral blood	blood
39	chr6:36689000-36689800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr6:36689200-36702400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:36689400-36690000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr6:36689400-36690000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr6:36689400-36690000	Enhancers	Fetal Heart	heart
44	chr6:36689400-36690000	Enhancers	Fetal Muscle Leg	muscle
45	chr6:36689600-36689800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:36689600-36690000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:36689600-36691000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr6:36689600-36691200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr6:36689800-36693600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:36689800-36696600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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