Variant report

Variant	nsv1053145
Chromosome Location	chr11:47967902-48086950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3134)
CpG islands
(count:1711)
Chromatin interactive
region (count:134)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3134 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48007735-48008092	K562	blood:	n/a	n/a
2	ARID3A	chr11:48020351-48020690	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48014991-48015408	K562	blood:	n/a	n/a
4	ARID3A	chr11:48034789-48035164	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:47976936-47977170	K562	blood:	n/a	n/a
6	ARID3A	chr11:48028182-48028572	K562	blood:	n/a	n/a
7	ARID3A	chr11:48012687-48013089	K562	blood:	n/a	n/a
8	ARID3A	chr11:47969693-47969977	K562	blood:	n/a	n/a
9	ARID3A	chr11:48082899-48083240	K562	blood:	n/a	n/a
10	ARID3A	chr11:48011206-48011933	K562	blood:	n/a	n/a
11	ATF1	chr11:48007751-48008118	K562	blood:	n/a	n/a
12	ATF1	chr11:48014956-48015365	K562	blood:	n/a	n/a
13	ATF1	chr11:48077433-48077920	K562	blood:	n/a	n/a
14	ATF1	chr11:48005044-48005362	K562	blood:	n/a	n/a
15	ATF1	chr11:47968512-47968837	K562	blood:	n/a	n/a
16	ATF1	chr11:47969704-47970008	K562	blood:	n/a	n/a
17	ATF1	chr11:48028142-48028476	K562	blood:	n/a	n/a
18	ATF1	chr11:48082834-48083315	K562	blood:	n/a	n/a
19	ATF2	chr11:48027746-48028715	GM12878	blood:	n/a	n/a
20	ATF2	chr11:48028018-48028663	GM12878	blood:	n/a	n/a
21	ATF2	chr11:47995884-47996433	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr11:48085000-48085533	GM12878	blood:	n/a	n/a
23	ATF2	chr11:48030290-48030856	GM12878	blood:	n/a	n/a
24	ATF2	chr11:48040721-48041289	GM12878	blood:	n/a	n/a
25	ATF2	chr11:48040883-48041370	GM12878	blood:	n/a	n/a
26	ATF2	chr11:48030273-48030957	GM12878	blood:	n/a	n/a
27	ATF2	chr11:48034745-48035476	GM12878	blood:	n/a	n/a
28	ATF2	chr11:48041464-48042090	GM12878	blood:	n/a	n/a
29	ATF2	chr11:48009223-48009665	GM12878	blood:	n/a	n/a
30	ATF2	chr11:48077237-48077812	GM12878	blood:	n/a	n/a
31	ATF2	chr11:48073780-48074198	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr11:48053178-48054057	GM12878	blood:	n/a	n/a
33	ATF2	chr11:48041357-48042266	GM12878	blood:	n/a	n/a
34	ATF2	chr11:48009201-48009809	GM12878	blood:	n/a	n/a
35	ATF2	chr11:47995987-47996296	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr11:48040073-48040556	GM12878	blood:	n/a	n/a
37	ATF3	chr11:48014919-48015447	A549	lung:	n/a	n/a
38	ATF3	chr11:48015032-48015330	K562	blood:	n/a	n/a
39	ATF3	chr11:48014906-48015366	K562	blood:	n/a	n/a
40	ATF3	chr11:48014919-48015429	A549	lung:	n/a	n/a
41	ATF3	chr11:48082760-48083237	K562	blood:	n/a	n/a
42	ATF3	chr11:48082790-48083256	K562	blood:	n/a	n/a
43	ATF3	chr11:47968298-47968882	K562	blood:	n/a	n/a
44	ATF3	chr11:47968206-47969232	A549	lung:	n/a	n/a
45	ATF3	chr11:48008321-48008661	K562	blood:	n/a	n/a
46	BACH1	chr11:48001120-48001869	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr11:47968277-47969060	K562	blood:	n/a	n/a
48	BACH1	chr11:48005088-48005498	K562	blood:	n/a	n/a
49	BACH1	chr11:48082870-48083255	K562	blood:	n/a	n/a
50	BACH1	chr11:47968440-47968897	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48001669-48001719	SK-N-MC	brain:	n/a
2	chr11:48001761-48001811	HL-60	blood:	n/a
3	chr11:48003169-48003219	Hela-S3	cervix:	n/a
4	chr11:48001669-48001719	SK-N-MC	brain:	n/a
5	chr11:48001761-48001811	HL-60	blood:	n/a
6	chr11:48003169-48003219	Hela-S3	cervix:	n/a
7	chr11:48083100-48083150	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:48065851-48065901	AG04449	skin:	fetal
9	chr11:48085137-48085187	MCF-7	breast:	n/a
10	chr11:48069893-48069943	T-47D	breast:	n/a
11	chr11:48001940-48001990	HCF	heart:	n/a
12	chr11:48019123-48019173	Jurkat	blood:	n/a
13	chr11:48001835-48001885	CMK	blood:	n/a
14	chr11:48006811-48006861	PFSK-1	brain:	n/a
15	chr11:48057861-48057911	Jurkat	blood:	n/a
16	chr11:48040772-48040822	GM12892	blood:	n/a
17	chr11:48001761-48001811	GM06990	blood:	n/a
18	chr11:48001940-48001990	HMEC	breast:	n/a
19	chr11:48019123-48019173	GM12891	blood:	n/a
20	chr11:48085137-48085187	Caco-2	colon:	n/a
21	chr11:48006811-48006861	HRCEpiC	kidney:	n/a
22	chr11:48065851-48065901	H1-hESC	embryonic stem cell:	embryo
23	chr11:48069893-48069943	PFSK-1	brain:	n/a
24	chr11:48001954-48002004	Caco-2	colon:	n/a
25	chr11:47997690-47997740	HRCEpiC	kidney:	n/a
26	chr11:48036852-48036902	NB4	blood:	n/a
27	chr11:48040772-48040822	HIPEpiC	eye:	n/a
28	chr11:48026889-48026939	Hela-S3	cervix:	n/a
29	chr11:48001835-48001885	T-47D	breast:	n/a
30	chr11:48057861-48057911	HCPEpiC	choroid plexus:	n/a
31	chr11:48036852-48036902	AoSMC	blood vessel:	n/a
32	chr11:48003169-48003219	GM12892	blood:	n/a
33	chr11:48026889-48026939	H1-hESC	embryonic stem cell:	embryo
34	chr11:48040772-48040822	HRPEpiC	eye:	n/a
35	chr11:48083100-48083150	IMR90	lung:	fetal
36	chr11:47995865-47995915	ECC-1	luminal epithelium:	n/a
37	chr11:48001761-48001811	HCT-116	colon:	n/a
38	chr11:48001940-48001990	SAEC	small airway:	n/a
39	chr11:48077221-48077271	HRE	kidney:	n/a
40	chr11:48065851-48065901	AG04450	lung:	fetal
41	chr11:48083100-48083150	HMEC	breast:	n/a
42	chr11:48006811-48006861	PrEC	prostate:	n/a
43	chr11:47997690-47997740	Caco-2	colon:	n/a
44	chr11:48000611-48000661	HUVEC	blood vessel:	n/a
45	chr11:48001669-48001719	HUVEC	blood vessel:	n/a
46	chr11:48001761-48001811	AG09309	skin:	n/a
47	chr11:48052092-48052142	HUVEC	blood vessel:	n/a
48	chr11:48003169-48003219	Hepatocyte	liver:	n/a
49	chr11:48001954-48002004	AG04450	lung:	fetal
50	chr11:48040772-48040822	HRE	kidney:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:48023010..48025902-chr11:48026149..48029415,3	K562	blood:
2	chr11:48037574..48039959-chr11:48041081..48044491,3	K562	blood:
3	chr11:48009714..48011875-chr11:48013703..48016314,2	K562	blood:
4	chr11:47974806..47977219-chr11:47979617..47982192,2	K562	blood:
5	chr11:47989706..47992406-chr11:48001068..48002963,2	K562	blood:
6	chr11:47974806..47977219-chr11:47979617..47982192,2	K562	blood:
7	chr11:48011467..48013224-chr11:48076838..48078616,2	K562	blood:
8	chr11:48016915..48018555-chr11:48019817..48022552,2	MCF-7	breast:
9	chr11:47993972..47999221-chr11:48000961..48004940,8	MCF-7	breast:
10	chr11:48001588..48003458-chr11:48072327..48074096,3	MCF-7	breast:
11	chr11:48073485..48075927-chr11:48082055..48084574,2	MCF-7	breast:
12	chr11:48002531..48005255-chr11:48006333..48009338,3	K562	blood:
13	chr11:48072810..48075370-chr11:48080373..48082997,2	K562	blood:
14	chr11:48017179..48020205-chr11:48021877..48026415,4	K562	blood:
15	chr11:48003107..48006285-chr11:48013442..48016525,3	MCF-7	breast:
16	chr11:48072810..48075370-chr11:48080373..48082997,2	K562	blood:
17	chr11:48082980..48084917-chr11:48096551..48099093,2	K562	blood:
18	chr11:47967141..47970110-chr11:47980010..47981597,2	MCF-7	breast:
19	chr11:48071477..48072173-chr11:48130347..48131089,2	MCF-7	breast:
20	chr11:48075993..48078690-chr11:48080770..48083090,2	MCF-7	breast:
21	chr11:48011771..48014595-chr11:48017994..48019667,2	K562	blood:
22	chr11:48024330..48026388-chr11:48082917..48084428,2	K562	blood:
23	chr11:48061733..48064075-chr11:48066877..48069020,2	K562	blood:
24	chr11:47964394..47966332-chr11:47982936..47984660,2	MCF-7	breast:
25	chr11:48042672..48045138-chr11:48049010..48052417,3	MCF-7	breast:
26	chr11:48017179..48020205-chr11:48021877..48026415,4	K562	blood:
27	chr11:48080961..48082777-chr11:48083891..48085697,2	MCF-7	breast:
28	chr11:48069835..48071887-chr11:48083817..48085807,2	MCF-7	breast:
29	chr11:48024330..48026388-chr11:48082917..48084428,2	K562	blood:
30	chr11:48061951..48065074-chr11:48065733..48069871,4	MCF-7	breast:
31	chr11:47987012..47989559-chr11:48000553..48002157,2	MCF-7	breast:
32	chr11:47985562..47986062-chr11:48130641..48131468,2	K562	blood:
33	chr11:47967015..47968589-chr11:48075080..48077424,2	MCF-7	breast:
34	chr11:47985506..47986348-chr11:48130588..48131464,3	MCF-7	breast:
35	chr11:48000322..48003543-chr11:48021769..48024813,4	MCF-7	breast:
36	chr11:48035360..48038062-chr11:48039286..48041376,2	MCF-7	breast:
37	chr11:48081533..48083185-chr11:48091579..48093994,2	MCF-7	breast:
38	chr11:48013018..48014696-chr11:48016577..48019365,2	MCF-7	breast:
39	chr11:47964759..47967260-chr11:47968299..47969907,3	K562	blood:
40	chr11:48016915..48018555-chr11:48019817..48022552,2	MCF-7	breast:
41	chr11:48068334..48069860-chr11:48070016..48072544,2	MCF-7	breast:
42	chr11:48075993..48078690-chr11:48080770..48083090,2	MCF-7	breast:
43	chr11:48002002..48003604-chr11:48052430..48054818,2	MCF-7	breast:
44	chr11:48046572..48047306-chr11:48130972..48131586,2	MCF-7	breast:
45	chr11:48009254..48011214-chr11:48013700..48016314,2	K562	blood:
46	chr11:48000640..48001500-chr11:48131020..48132149,3	MCF-7	breast:
47	chr11:48009714..48011875-chr11:48013703..48016314,2	K562	blood:
48	chr11:48072741..48074310-chr11:48080242..48082997,2	K562	blood:
49	chr11:48002272..48005145-chr11:48021590..48026495,6	K562	blood:
50	chr11:48077645..48080175-chr11:48086953..48089270,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP160-1	chr11:48037379-48037407	ENSG00000254879.1
2	lnc-NUP160-1	chr11:48035958-48036229	ENSG00000254879.1
3	lnc-PTPRJ-1	chr11:47967903-47968054	NONHSAT021290
4	lnc-PTPRJ-1	chr11:47968934-47969181	NONHSAT021290

No data

Variant related genes	Relation type
ENSG00000254879	TF binding region
PTPRJ	TF binding region
ENSG00000254879	CpG island
PTPRJ	CpG island
ENSG00000254879	chromatin interactions
ENSG00000149177	chromatin interactions
ENSG00000030066	chromatin interactions

Extended variants
information (count: 4075 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4075 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570290700	chr11:47967956-47967957	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs572705493	chr11:47967980-47967981	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs568452899	chr11:47967987-47967988	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs547956879	chr11:47968002-47968003	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs564620728	chr11:47968026-47968027	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs75700551	chr11:47968034-47968035	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs530545990	chr11:47968043-47968044	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs185744304	chr11:47968058-47968059	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560978053	chr11:47968067-47968068	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367955293	chr11:47968078-47968079	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530289299	chr11:47968081-47968082	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554401056	chr11:47968090-47968091	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145890850	chr11:47968118-47968119	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs539789569	chr11:47968134-47968135	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567044214	chr11:47968205-47968206	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539252257	chr11:47968256-47968257	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs78853195	chr11:47968263-47968264	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147794392	chr11:47968312-47968313	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576584224	chr11:47968425-47968426	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs77668124	chr11:47968458-47968459	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11039469	chr11:47968480-47968481	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs11039470	chr11:47968506-47968507	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs117506841	chr11:47968558-47968559	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554659434	chr11:47968616-47968617	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574787897	chr11:47968625-47968626	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188991248	chr11:47968626-47968627	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574536422	chr11:47968648-47968649	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs552863415	chr11:47968665-47968666	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572834462	chr11:47968686-47968687	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs111736633	chr11:47968690-47968691	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544780975	chr11:47968725-47968726	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs57639610	chr11:47968743-47968744	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs575240129	chr11:47968764-47968765	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113269712	chr11:47968772-47968773	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544304505	chr11:47968824-47968825	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs72897994	chr11:47968842-47968843	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371599025	chr11:47968844-47968845	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377608049	chr11:47968880-47968881	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546945115	chr11:47968885-47968886	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560753828	chr11:47968993-47968994	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs371023493	chr11:47968996-47968997	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs540177598	chr11:47969087-47969088	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs148339871	chr11:47969098-47969099	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs552801456	chr11:47969101-47969102	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs180950177	chr11:47969139-47969140	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs1681630	chr11:47969152-47969153	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs12294218	chr11:47969171-47969172	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs1681631	chr11:47969179-47969180	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs141576958	chr11:47969180-47969181	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs553775868	chr11:47969239-47969240	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Glioblastoma multiforme	21390271	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5312 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47950800-47971800	Weak transcription	Fetal Thymus	thymus
2	chr11:47954400-47968200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr11:47956800-47970200	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr11:47959800-47968800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:47960000-47972400	Weak transcription	Lung	lung
6	chr11:47964000-47968400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr11:47964000-47968400	Weak transcription	GM12878-XiMat	blood
8	chr11:47964000-47972200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr11:47964200-47968400	Weak transcription	Placenta	Placenta
10	chr11:47964400-47968800	Weak transcription	Right Atrium	heart
11	chr11:47964600-47968600	Weak transcription	Liver	Liver
12	chr11:47966000-47968200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr11:47966200-47968000	Weak transcription	Stomach Mucosa	stomach
14	chr11:47966200-47968600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:47966200-47968600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr11:47966200-47968600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:47966200-47968600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:47966200-47969800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:47966200-47972200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr11:47966400-47968200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr11:47966400-47968200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr11:47966400-47968200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:47966400-47968200	Weak transcription	NHDF-Ad	bronchial
24	chr11:47966400-47968600	Weak transcription	NHLF	lung
25	chr11:47966400-47969000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr11:47966400-47969200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr11:47966600-47968000	Weak transcription	NH-A	brain
28	chr11:47966600-47968200	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr11:47966600-47968200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr11:47966600-47968200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr11:47966600-47968200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr11:47966600-47968200	Weak transcription	HSMM	muscle
33	chr11:47966600-47968200	Weak transcription	HUVEC	blood vessel
34	chr11:47966600-47968200	Enhancers	K562	blood
35	chr11:47966600-47968200	Weak transcription	Osteobl	bone
36	chr11:47966600-47968400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr11:47966600-47968400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr11:47966600-47968600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr11:47966600-47972000	Weak transcription	Dnd41	blood
40	chr11:47966800-47968600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr11:47966800-47968600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:47966800-47970000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:47967000-47968200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr11:47967200-47968600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:47967200-47971000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:47967400-47968200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr11:47967400-47969400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr11:47967400-47973200	Enhancers	Primary B cells from cord blood	blood
49	chr11:47967400-47974000	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr11:47967600-47968000	Weak transcription	Placenta Amnion	Placenta Amnion

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