Variant report

Variant	nsv1021180
Chromosome Location	chr7:39424988-39642261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2713)
CpG islands
(count:2016)
Chromatin interactive
region (count:88)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2713 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39528586-39528662	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:39559568-39560308	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:39629196-39629849	K562	blood:	n/a	n/a
4	ARID3A	chr7:39605696-39606077	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:39504617-39504923	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:39619920-39620322	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:39559554-39559774	K562	blood:	n/a	n/a
8	ATF1	chr7:39629296-39629800	K562	blood:	n/a	n/a
9	ATF1	chr7:39620042-39620358	K562	blood:	n/a	n/a
10	ATF1	chr7:39544575-39544759	K562	blood:	n/a	n/a
11	ATF2	chr7:39620059-39620415	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:39605695-39606255	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:39629214-39629775	GM12878	blood:	n/a	n/a
14	ATF2	chr7:39629257-39629794	GM12878	blood:	n/a	n/a
15	ATF3	chr7:39629296-39629758	K562	blood:	n/a	n/a
16	ATF3	chr7:39629324-39629589	K562	blood:	n/a	n/a
17	BACH1	chr7:39504575-39505029	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:39460082-39460104	K562	blood:	n/a	n/a
19	BACH1	chr7:39605642-39605702	K562	blood:	n/a	n/a
20	BACH1	chr7:39623626-39623709	K562	blood:	n/a	n/a
21	BACH1	chr7:39504641-39505056	K562	blood:	n/a	n/a
22	BACH1	chr7:39431848-39432018	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:39453441-39454296	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:39605695-39606256	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr7:39629280-39629727	GM12878	blood:	n/a	chr7:39629520-39629531
26	BATF	chr7:39431880-39432090	GM12878	blood:	n/a	n/a
27	BATF	chr7:39629347-39629718	GM12878	blood:	n/a	chr7:39629520-39629531
28	BATF	chr7:39504666-39504886	GM12878	blood:	n/a	n/a
29	BATF	chr7:39504633-39504960	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:39629238-39629667	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:39629312-39629663	GM12878	blood:	n/a	n/a
32	BCL3	chr7:39629295-39629695	GM12878	blood:	n/a	n/a
33	BCL3	chr7:39605532-39606336	A549	lung:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
34	BCL3	chr7:39556282-39556573	GM12878	blood:	n/a	n/a
35	BCLAF1	chr7:39605736-39606198	K562	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
36	BCLAF1	chr7:39605624-39606257	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
37	BCLAF1	chr7:39605565-39606356	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
38	BHLHE40	chr7:39629250-39629748	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:39453754-39454208	GM12878	blood:	n/a	chr7:39454190-39454206
40	BHLHE40	chr7:39555294-39555818	K562	blood:	n/a	n/a
41	BHLHE40	chr7:39605211-39606254	K562	blood:	n/a	n/a
42	BHLHE40	chr7:39629275-39629703	K562	blood:	n/a	n/a
43	BHLHE40	chr7:39559598-39559764	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:39619986-39620611	K562	blood:	n/a	n/a
45	BHLHE40	chr7:39620025-39620654	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:39559617-39559759	K562	blood:	n/a	n/a
47	BHLHE40	chr7:39446015-39446266	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:39605270-39606262	GM12878	blood:	n/a	n/a
49	BHLHE40	chr7:39556351-39556520	K562	blood:	n/a	n/a
50	BHLHE40	chr7:39620025-39620413	HepG2	liver:	n/a	n/a

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39453532-39453582	GM12892	blood:	n/a
2	chr7:39451576-39451626	NH-A	brain:	n/a
3	chr7:39472716-39472766	PrEC	prostate:	n/a
4	chr7:39453532-39453582	GM12892	blood:	n/a
5	chr7:39451576-39451626	NH-A	brain:	n/a
6	chr7:39472716-39472766	PrEC	prostate:	n/a
7	chr7:39500223-39500273	Caco-2	colon:	n/a
8	chr7:39569916-39569966	GM06990	blood:	n/a
9	chr7:39453855-39453905	HRE	kidney:	n/a
10	chr7:39606280-39606330	SK-N-SH	brain:	n/a
11	chr7:39606013-39606063	PrEC	prostate:	n/a
12	chr7:39606071-39606121	AG10803	skin:	n/a
13	chr7:39605861-39605911	HRE	kidney:	n/a
14	chr7:39457814-39457864	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:39446909-39446959	AG09309	skin:	n/a
16	chr7:39606280-39606330	H1-hESC	embryonic stem cell:	embryo
17	chr7:39629290-39629340	SK-N-SH_RA	brain:	n/a
18	chr7:39606002-39606052	HCM	heart:	n/a
19	chr7:39606071-39606121	AG04450	lung:	fetal
20	chr7:39451576-39451626	HRE	kidney:	n/a
21	chr7:39454310-39454360	ovcar-3	ovarian:	n/a
22	chr7:39605996-39606046	IMR90	lung:	fetal
23	chr7:39605883-39605933	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:39450193-39450243	AoSMC	blood vessel:	n/a
25	chr7:39457814-39457864	CMK	blood:	n/a
26	chr7:39569916-39569966	PFSK-1	brain:	n/a
27	chr7:39472716-39472766	GM12892	blood:	n/a
28	chr7:39453855-39453905	AG04449	skin:	fetal
29	chr7:39605536-39605586	NHDF-neo	bronchial:	n/a
30	chr7:39606013-39606063	AoSMC	blood vessel:	n/a
31	chr7:39457814-39457864	NT2-D1	testis:	n/a
32	chr7:39500288-39500338	HRPEpiC	eye:	n/a
33	chr7:39605683-39605733	HMEC	breast:	n/a
34	chr7:39605883-39605933	PANC-1	pancreas:	n/a
35	chr7:39606071-39606121	GM06990	blood:	n/a
36	chr7:39605536-39605586	NHBE	bronchial:	n/a
37	chr7:39605790-39605840	HCF	heart:	n/a
38	chr7:39569916-39569966	Caco-2	colon:	n/a
39	chr7:39454310-39454360	GM06990	blood:	n/a
40	chr7:39605883-39605933	NHBE	bronchial:	n/a
41	chr7:39629290-39629340	PANC-1	pancreas:	n/a
42	chr7:39569916-39569966	T-47D	breast:	n/a
43	chr7:39453784-39453834	U87	brain:	n/a
44	chr7:39453704-39453754	HRPEpiC	eye:	n/a
45	chr7:39454310-39454360	BJ	skin:	n/a
46	chr7:39453855-39453905	SK-N-MC	brain:	n/a
47	chr7:39454090-39454140	Hepatocyte	liver:	n/a
48	chr7:39605683-39605733	SAEC	small airway:	n/a
49	chr7:39454310-39454360	HCM	heart:	n/a
50	chr7:39453625-39453675	PFSK-1	brain:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:39424668..39427286-chr7:39432218..39433755,2	MCF-7	breast:
2	chr7:39606078..39608053-chr7:39609216..39613025,4	MCF-7	breast:
3	chr7:39613001..39614812-chr7:39768164..39770870,2	K562	blood:
4	chr7:39559251..39560178-chr7:39581010..39581845,2	K562	blood:
5	chr7:39623431..39626186-chr7:39627006..39629338,2	MCF-7	breast:
6	chr7:39493099..39494043-chr7:39559206..39560190,4	MCF-7	breast:
7	chr7:39621618..39625232-chr7:39625771..39627613,3	K562	blood:
8	chr7:39597430..39600567-chr7:39603197..39606224,3	MCF-7	breast:
9	chr7:39629985..39632213-chr7:39633896..39637546,5	K562	blood:
10	chr7:39538609..39540979-chr7:39546036..39547767,2	K562	blood:
11	chr7:39630501..39633434-chr7:39759020..39762831,5	K562	blood:
12	chr7:39619917..39620450-chr7:39831240..39831746,2	K562	blood:
13	chr7:38836232..38836866-chr7:39504695..39505205,2	MCF-7	breast:
14	chr7:39638958..39641769-chr7:39651985..39654836,2	K562	blood:
15	chr7:39567068..39569157-chr7:39570895..39573557,2	K562	blood:
16	chr7:39440359..39443090-chr7:39454354..39455934,2	K562	blood:
17	chr7:39610504..39612853-chr7:39613535..39615540,2	K562	blood:
18	chr7:39604710..39608797-chr7:39663149..39665225,4	K562	blood:
19	chr7:39493293..39495900-chr7:39499088..39502872,3	K562	blood:
20	chr7:39635799..39637643-chr7:39637768..39639590,2	MCF-7	breast:
21	chr7:39435823..39437973-chr7:39441882..39444304,3	K562	blood:
22	chr7:39575609..39577326-chr7:39580919..39582737,2	MCF-7	breast:
23	chr7:39435823..39437973-chr7:39441882..39444304,3	K562	blood:
24	chr7:39617765..39620727-chr7:39709688..39712417,2	K562	blood:
25	chr7:39493116..39494045-chr7:39504502..39505143,2	K562	blood:
26	chr7:39597542..39600192-chr7:39605435..39607184,2	MCF-7	breast:
27	chr7:39620191..39622665-chr7:39628141..39629776,2	K562	blood:
28	chr7:39620205..39622227-chr7:39661483..39663721,3	K562	blood:
29	chr7:39604590..39607851-chr7:39609967..39614867,7	K562	blood:
30	chr7:39453463..39455969-chr7:39846035..39848815,2	K562	blood:
31	chr7:38944229..38945857-chr7:39522828..39525500,2	K562	blood:
32	chr7:39493099..39494043-chr7:39559206..39560190,4	MCF-7	breast:
33	chr7:39640592..39642673-chr7:39644409..39647009,2	K562	blood:
34	chr7:39605618..39607861-chr7:39772706..39774759,2	K562	blood:
35	chr7:39605012..39607338-chr7:39986740..39989686,2	K562	blood:
36	chr7:39634741..39636459-chr7:39661820..39664615,2	K562	blood:
37	chr7:39606078..39608053-chr7:39609216..39613025,4	MCF-7	breast:
38	chr7:39619647..39620204-chr7:40092201..40092766,2	K562	blood:
39	chr7:39424668..39427286-chr7:39432218..39433755,2	MCF-7	breast:
40	chr7:39432032..39434536-chr7:39435628..39438240,2	K562	blood:
41	chr7:39621618..39625232-chr7:39625771..39627613,3	K562	blood:
42	chr7:39595139..39597686-chr7:39605135..39607425,2	K562	blood:
43	chr7:39616830..39619300-chr7:39660316..39662885,2	K562	blood:
44	chr7:39619358..39620673-chr7:39785487..39786442,10	K562	blood:
45	chr7:39620146..39620721-chr7:39781543..39782233,2	MCF-7	breast:
46	chr7:39638996..39641307-chr7:39643111..39644755,2	K562	blood:
47	chr7:39575609..39577326-chr7:39580919..39582737,2	MCF-7	breast:
48	chr7:39619664..39620687-chr7:39782996..39783915,3	K562	blood:
49	chr7:39581559..39584136-chr7:39585096..39587437,2	K562	blood:
50	chr7:39635799..39637643-chr7:39637768..39639590,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf11-7	chr7:39593475-39593543	ENSG00000227172.2
2	lnc-C7orf11-7	chr7:39605742-39605838	XLOC_006414
3	lnc-RALA-3	chr7:39622404-39622930	NONHSAT120209
4	lnc-VPS41-2	chr7:39444343-39444382	NONHSAT120202
5	lnc-C7orf11-7	chr7:39593475-39593543	XLOC_006414
6	lnc-C7orf11-7	chr7:39605742-39605943	XLOC_006414
7	lnc-POU6F2-1	chr7:39504691-39504775	NONHSAT120203
8	lnc-VPS41-2	chr7:39444526-39444604	NONHSAT120202
9	lnc-C7orf11-14	chr7:39608975-39609797	NONHSAT120207
10	lnc-VPS41-2	chr7:39445933-39445945	ENSG00000224122.1
11	lnc-POU6F2-1	chr7:39510687-39510841	NONHSAT120203
12	lnc-VPS41-2	chr7:39444197-39444382	ENSG00000224122.1
13	lnc-VPS41-2	chr7:39445933-39445945	NR_046711
14	lnc-VPS41-2	chr7:39444198-39444382	NR_046711
15	lnc-VPS41-2	chr7:39445616-39445718	NR_046711
16	lnc-C7orf11-7	chr7:39585245-39585492	ENSG00000227172.2
17	lnc-POU6F2-1	chr7:39529969-39530208	NONHSAT120203
18	lnc-VPS41-2	chr7:39445616-39445718	ENSG00000224122.1
19	lnc-VPS41-2	chr7:39444526-39444604	NR_046711
20	lnc-VPS41-2	chr7:39444526-39444604	ENSG00000224122.1
21	lnc-C7orf11-7	chr7:39593494-39593543	XLOC_006414
22	lnc-POU6F2-1	chr7:39532643-39532694	NONHSAT120203
23	lnc-VPS41-2	chr7:39445616-39445728	NONHSAT120202
24	lnc-C7orf11-7	chr7:39605742-39605838	ENSG00000227172.2
25	lnc-VPS41-2	chr7:39446035-39446111	NONHSAT120202
26	lnc-C7orf11-7	chr7:39585249-39585492	XLOC_006414

No data

Variant related genes	Relation type
ENSG00000236015	TF binding region
YAE1D1	TF binding region
POU6F2-AS1	TF binding region
POU6F2	TF binding region
ENSG00000227172	TF binding region
ENSG00000236015	CpG island
YAE1D1	CpG island
POU6F2-AS1	CpG island
POU6F2	CpG island
ENSG00000227172	CpG island
ENSG00000106536	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000241127	chromatin interactions
ENSG00000227172	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000006451	chromatin interactions
ENSG00000006715	chromatin interactions
ENSG00000236015	chromatin interactions
ENSG00000188185	chromatin interactions
ENSG00000065883	chromatin interactions

Extended variants
information (count: 6998 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6998 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553278490	chr7:39425229-39425230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187774263	chr7:39425274-39425275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs60586729	chr7:39425323-39425324	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs11760438	chr7:39425403-39425404	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs74960466	chr7:39425418-39425419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572135523	chr7:39425549-39425550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544423019	chr7:39425575-39425576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369757254	chr7:39425658-39425659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373547925	chr7:39425663-39425664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569584286	chr7:39425717-39425718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369113750	chr7:39425735-39425736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574576095	chr7:39425750-39425751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540414723	chr7:39425752-39425753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116927651	chr7:39425785-39425786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192469041	chr7:39425801-39425802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370915607	chr7:39425808-39425809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545815859	chr7:39425820-39425821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562302088	chr7:39425832-39425833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561038362	chr7:39425900-39425901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78667160	chr7:39425902-39425903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531326224	chr7:39425947-39425948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535374867	chr7:39425952-39425953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548026881	chr7:39425955-39425956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111974636	chr7:39425988-39425989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185022265	chr7:39425998-39425999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115813752	chr7:39426005-39426006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546763743	chr7:39426026-39426027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71536642	chr7:39426049-39426050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373779222	chr7:39426053-39426054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189545906	chr7:39426074-39426075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538906526	chr7:39426118-39426119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150250697	chr7:39426124-39426125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370119400	chr7:39426146-39426147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571254412	chr7:39426150-39426151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569204329	chr7:39426162-39426163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538219029	chr7:39426203-39426204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112964341	chr7:39426221-39426222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574953352	chr7:39426239-39426240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138424322	chr7:39426240-39426241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149280040	chr7:39426264-39426265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577215968	chr7:39426266-39426267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10258232	chr7:39426359-39426360	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs547112093	chr7:39426399-39426400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185200701	chr7:39426555-39426556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541792490	chr7:39426557-39426558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561651477	chr7:39426584-39426585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527341073	chr7:39426615-39426616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368885557	chr7:39426651-39426652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78554610	chr7:39426705-39426706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566764611	chr7:39426707-39426708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	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
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2249 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39425200-39426000	Enhancers	Fetal Muscle Leg	muscle
2	chr7:39425200-39426800	Enhancers	Fetal Muscle Trunk	muscle
3	chr7:39426000-39432800	Weak transcription	Fetal Muscle Leg	muscle
4	chr7:39431400-39431600	Enhancers	Fetal Muscle Trunk	muscle
5	chr7:39431800-39432200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:39431800-39432200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr7:39431800-39432400	Enhancers	Fetal Stomach	stomach
8	chr7:39431800-39432600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:39431800-39432800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:39432000-39432200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr7:39432000-39432400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr7:39432000-39432400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr7:39432000-39432400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:39432000-39432400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:39432000-39432400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:39432000-39433200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr7:39432400-39434000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:39432400-39434000	Weak transcription	Fetal Stomach	stomach
19	chr7:39432400-39439600	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr7:39432400-39439800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr7:39432800-39433200	Enhancers	Fetal Muscle Leg	muscle
22	chr7:39432800-39433200	Enhancers	HSMMtube	muscle
23	chr7:39433200-39434400	Weak transcription	HSMMtube	muscle
24	chr7:39433200-39439400	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr7:39434000-39434200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:39434000-39434200	Enhancers	Fetal Stomach	stomach
27	chr7:39434000-39438800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr7:39434200-39434400	Enhancers	Fetal Kidney	kidney
29	chr7:39434400-39434600	Enhancers	HSMMtube	muscle
30	chr7:39436200-39436400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:39436200-39436800	Enhancers	HSMMtube	muscle
32	chr7:39436400-39445400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:39437600-39446000	Weak transcription	Pancreas	Pancrea
34	chr7:39438800-39441000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr7:39439400-39441200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:39439600-39440200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:39439600-39440600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:39439600-39440800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr7:39439600-39440800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr7:39439600-39440800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:39439600-39441600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:39439800-39440000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:39439800-39441000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr7:39439800-39441000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr7:39439800-39441400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr7:39440000-39440800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:39440200-39446000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:39440400-39440800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:39440600-39440800	Enhancers	Right Atrium	heart
50	chr7:39440600-39441800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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