Variant report

Variant	nsv1049835
Chromosome Location	chr11:47837089-47928822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1749)
CpG islands
(count:1282)
Chromatin interactive
region (count:61)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1749 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:47874901-47875245	K562	blood:	n/a	chr11:47875162-47875178
2	ARID3A	chr11:47884868-47885261	K562	blood:	n/a	n/a
3	ARID3A	chr11:47874892-47875252	HepG2	liver:	n/a	chr11:47875162-47875178
4	ARID3A	chr11:47877829-47878081	K562	blood:	n/a	n/a
5	ARID3A	chr11:47886206-47886780	K562	blood:	n/a	n/a
6	ATF1	chr11:47869646-47870758	K562	blood:	n/a	n/a
7	ATF1	chr11:47927335-47927555	K562	blood:	n/a	n/a
8	ATF1	chr11:47885031-47885231	K562	blood:	n/a	n/a
9	ATF2	chr11:47886436-47886910	GM12878	blood:	n/a	n/a
10	ATF2	chr11:47876143-47876691	GM12878	blood:	n/a	n/a
11	ATF2	chr11:47865691-47866101	GM12878	blood:	n/a	n/a
12	ATF2	chr11:47869612-47870352	GM12878	blood:	n/a	n/a
13	ATF2	chr11:47884638-47885294	GM12878	blood:	n/a	n/a
14	ATF2	chr11:47921290-47921801	GM12878	blood:	n/a	n/a
15	ATF2	chr11:47874864-47875375	GM12878	blood:	n/a	n/a
16	ATF2	chr11:47921207-47921888	GM12878	blood:	n/a	n/a
17	ATF2	chr11:47871838-47872340	GM12878	blood:	n/a	n/a
18	ATF2	chr11:47876240-47876657	GM12878	blood:	n/a	n/a
19	ATF2	chr11:47869521-47869955	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr11:47869719-47870016	K562	blood:	n/a	n/a
21	ATF3	chr11:47879392-47880138	A549	lung:	n/a	n/a
22	BACH1	chr11:47881557-47881791	K562	blood:	n/a	n/a
23	BACH1	chr11:47870434-47870634	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr11:47865717-47865993	GM12878	blood:	n/a	n/a
25	BATF	chr11:47876204-47876565	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:47876230-47876605	GM12878	blood:	n/a	n/a
27	BCL11A	chr11:47876406-47876599	GM12878	blood:	n/a	n/a
28	BCL11A	chr11:47921445-47921696	GM12878	blood:	n/a	chr11:47921570-47921579 chr11:47921524-47921533
29	BCL11A	chr11:47921347-47921719	GM12878	blood:	n/a	chr11:47921570-47921579 chr11:47921524-47921533
30	BCL3	chr11:47879076-47880150	A549	lung:	n/a	n/a
31	BCL3	chr11:47879225-47880239	A549	lung:	n/a	n/a
32	BCL3	chr11:47876269-47876630	GM12878	blood:	n/a	n/a
33	BCL3	chr11:47869343-47870088	A549	lung:	n/a	n/a
34	BCLAF1	chr11:47901336-47901794	GM12878	blood:	n/a	chr11:47901673-47901682
35	BCLAF1	chr11:47876203-47876723	GM12878	blood:	n/a	n/a
36	BCLAF1	chr11:47871788-47872355	GM12878	blood:	n/a	n/a
37	BCLAF1	chr11:47921248-47921874	GM12878	blood:	n/a	chr11:47921570-47921579 chr11:47921524-47921533
38	BCLAF1	chr11:47869315-47870473	GM12878	blood:	n/a	chr11:47870141-47870154
39	BHLHE40	chr11:47869726-47870358	K562	blood:	n/a	chr11:47870152-47870168
40	BHLHE40	chr11:47896459-47896678	HepG2	liver:	n/a	n/a
41	BHLHE40	chr11:47907718-47907940	K562	blood:	n/a	n/a
42	BHLHE40	chr11:47877909-47878109	K562	blood:	n/a	n/a
43	BHLHE40	chr11:47879343-47879704	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:47896523-47896594	K562	blood:	n/a	n/a
45	BHLHE40	chr11:47883355-47883697	K562	blood:	n/a	n/a
46	BHLHE40	chr11:47921307-47921770	GM12878	blood:	n/a	n/a
47	BHLHE40	chr11:47876271-47876561	GM12878	blood:	n/a	n/a
48	BHLHE40	chr11:47881882-47881942	K562	blood:	n/a	n/a
49	BRCA1	chr11:47869820-47869980	HepG2	liver:	n/a	n/a
50	BRCA1	chr11:47869894-47870336	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:47870340-47870390	SAEC	small airway:	n/a
2	chr11:47870340-47870390	SAEC	small airway:	n/a
3	chr11:47870217-47870267	ovcar-3	ovarian:	n/a
4	chr11:47927148-47927198	LNCaP	prostate:	n/a
5	chr11:47870622-47870672	LNCaP	prostate:	n/a
6	chr11:47870114-47870164	SK-N-MC	brain:	n/a
7	chr11:47927148-47927198	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:47870217-47870267	BJ	skin:	n/a
9	chr11:47870447-47870497	GM12892	blood:	n/a
10	chr11:47861790-47861840	HEEpiC	esophagus:	n/a
11	chr11:47870447-47870497	ECC-1	luminal epithelium:	n/a
12	chr11:47927148-47927198	HRCEpiC	kidney:	n/a
13	chr11:47870622-47870672	NHDF-neo	bronchial:	n/a
14	chr11:47927509-47927559	Hepatocyte	liver:	n/a
15	chr11:47870224-47870274	HRCEpiC	kidney:	n/a
16	chr11:47870340-47870390	CMK	blood:	n/a
17	chr11:47867032-47867082	AoSMC	blood vessel:	n/a
18	chr11:47867032-47867082	HCF	heart:	n/a
19	chr11:47927019-47927069	HUVEC	blood vessel:	n/a
20	chr11:47870217-47870267	AG09319	gingival:	n/a
21	chr11:47927226-47927276	Hela-S3	cervix:	n/a
22	chr11:47869805-47869855	HIPEpiC	eye:	n/a
23	chr11:47927509-47927559	H1-hESC	embryonic stem cell:	embryo
24	chr11:47869805-47869855	AG04449	skin:	fetal
25	chr11:47870622-47870672	HCPEpiC	choroid plexus:	n/a
26	chr11:47870191-47870241	GM12878	blood:	n/a
27	chr11:47870622-47870672	AG10803	skin:	n/a
28	chr11:47861790-47861840	GM12892	blood:	n/a
29	chr11:47869488-47869538	HIPEpiC	eye:	n/a
30	chr11:47927226-47927276	HEEpiC	esophagus:	n/a
31	chr11:47927019-47927069	HCPEpiC	choroid plexus:	n/a
32	chr11:47867032-47867082	ovcar-3	ovarian:	n/a
33	chr11:47927509-47927559	GM12891	blood:	n/a
34	chr11:47914359-47914409	HCF	heart:	n/a
35	chr11:47869488-47869538	ECC-1	luminal epithelium:	n/a
36	chr11:47867032-47867082	NHBE	bronchial:	n/a
37	chr11:47862559-47862609	HMEC	breast:	n/a
38	chr11:47869488-47869538	CMK	blood:	n/a
39	chr11:47927509-47927559	NHDF-neo	bronchial:	n/a
40	chr11:47914359-47914409	HIPEpiC	eye:	n/a
41	chr11:47870340-47870390	PFSK-1	brain:	n/a
42	chr11:47870447-47870497	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:47927509-47927559	SK-N-SH	brain:	n/a
44	chr11:47870114-47870164	HEK293	kidney:	embryo
45	chr11:47870447-47870497	ovcar-3	ovarian:	n/a
46	chr11:47927019-47927069	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:47869975-47870025	GM12878	blood:	n/a
48	chr11:47870191-47870241	MCF10A-Er-Src	breast:	n/a
49	chr11:47927226-47927276	K562	blood:	n/a
50	chr11:47861790-47861840	PrEC	prostate:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:47869821..47870379-chr7:5569438..5570409,2	Hela-S3	cervix:
2	chr11:47869483..47870186-chr3:150125929..150126438,2	HCT-116	colon:
3	chr11:47787149..47790720-chr11:47868235..47871590,6	MCF-7	breast:
4	chr11:47751522..47753583-chr11:47842006..47843911,2	K562	blood:
5	chr11:47869561..47870247-chr16:88636617..88637521,2	Hela-S3	cervix:
6	chr11:47875918..47878911-chr11:47889352..47891666,2	MCF-7	breast:
7	chr11:47735300..47737622-chr11:47868024..47869979,2	MCF-7	breast:
8	chr11:47869589..47870448-chr3:128206698..128207411,2	Hela-S3	cervix:
9	chr11:47597915..47601799-chr11:47868286..47871887,4	K562	blood:
10	chr11:47599594..47601938-chr11:47869864..47871887,2	K562	blood:
11	chr11:47853054..47855600-chr11:47864603..47866811,2	MCF-7	breast:
12	chr11:47882484..47885060-chr11:47964831..47967242,2	K562	blood:
13	chr11:47870211..47871042-chr3:180319722..180320451,2	Hela-S3	cervix:
14	chr11:47855476..47858340-chr11:47867980..47871002,5	MCF-7	breast:
15	chr11:47788106..47790225-chr11:47868385..47869954,2	K562	blood:
16	chr11:47869220..47869835-chr19:15947124..15948001,2	Hela-S3	cervix:
17	chr11:47631158..47632846-chr11:47873541..47876421,2	MCF-7	breast:
18	chr11:47847046..47849483-chr11:47857033..47859770,3	MCF-7	breast:
19	chr11:47839601..47841333-chr11:48132077..48133886,2	K562	blood:
20	chr11:47839951..47841938-chr11:47841996..47843561,3	MCF-7	breast:
21	chr11:47663732..47665818-chr11:47865617..47868186,2	K562	blood:
22	chr11:47880257..47883214-chr11:47889467..47892420,2	K562	blood:
23	chr11:47734421..47738084-chr11:47868728..47871724,4	K562	blood:
24	chr11:47863437..47865733-chr11:47933034..47935744,2	K562	blood:
25	chr11:47788593..47790214-chr11:47879044..47881112,2	MCF-7	breast:
26	chr11:47531412..47534315-chr11:47879046..47881492,2	K562	blood:
27	chr1:28832502..28833185-chr11:47869116..47869923,2	Hela-S3	cervix:
28	chr11:47875918..47878911-chr11:47889352..47891666,2	MCF-7	breast:
29	chr11:47869106..47869844-chr15:41165965..41166904,2	Hela-S3	cervix:
30	chr11:47870685..47873439-chr11:47876355..47879304,2	MCF-7	breast:
31	chr11:47916274..47916775-chr6:113873100..113873600,2	NB4	blood:
32	chr11:47847488..47849168-chr11:47854049..47856558,2	K562	blood:
33	chr11:47879130..47879931-chr11:48131064..48131706,2	MCF-7	breast:
34	chr11:47869535..47870067-chr12:29533757..29534605,2	HCT-116	colon:
35	chr11:47880257..47883214-chr11:47889467..47892420,2	K562	blood:
36	chr11:47857004..47860326-chr11:47862675..47865645,4	MCF-7	breast:
37	chr11:47869337..47872493-chr11:47872959..47875710,4	MCF-7	breast:
38	chr11:47792091..47794821-chr11:47867403..47869086,2	K562	blood:
39	chr11:47837659..47841122-chr11:47868262..47870678,3	MCF-7	breast:
40	chr11:47858317..47861141-chr11:47883215..47886072,2	K562	blood:
41	chr11:47873347..47874902-chr11:47878009..47880856,2	MCF-7	breast:
42	chr11:47788029..47790788-chr11:47839875..47842622,2	MCF-7	breast:
43	chr11:47787394..47789838-chr11:47868299..47871448,5	MCF-7	breast:
44	chr11:47868432..47872224-chr11:47874279..47876068,4	MCF-7	breast:
45	chr11:47857319..47859657-chr11:48158646..48160993,2	K562	blood:
46	chr11:47873347..47874902-chr11:47878009..47880856,2	MCF-7	breast:
47	chr11:47869135..47869925-chr17:6917768..6918393,2	Hela-S3	cervix:
48	chr11:47858317..47861141-chr11:47883215..47886072,2	K562	blood:
49	chr11:47866017..47867576-chr11:47868325..47870238,2	MCF-7	breast:
50	chr11:47847488..47849168-chr11:47854049..47856558,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP160-3	chr11:47926875-47927159	NONHSAT021289

No data

Variant related genes	Relation type
ENSG00000271557	TF binding region
ENSG00000252874	TF binding region
ENSG00000254780	TF binding region
NUP160	TF binding region
ENSG00000271557	CpG island
ENSG00000252874	CpG island
ENSG00000254780	CpG island
NUP160	CpG island
ENSG00000109920	chromatin interactions
ENSG00000163728	chromatin interactions
ENSG00000057663	chromatin interactions
ENSG00000158545	chromatin interactions
ENSG00000030066	chromatin interactions
ENSG00000177606	chromatin interactions
ENSG00000123444	chromatin interactions
ENSG00000213619	chromatin interactions
ENSG00000200376	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000168273	chromatin interactions
ENSG00000179348	chromatin interactions
ENSG00000120742	chromatin interactions
ENSG00000231880	chromatin interactions
ENSG00000252874	chromatin interactions
ENSG00000144895	chromatin interactions
ENSG00000239774	chromatin interactions
ENSG00000165923	chromatin interactions
ENSG00000104140	chromatin interactions
ENSG00000258315	chromatin interactions
ENSG00000087502	chromatin interactions
ENSG00000271557	chromatin interactions
ENSG00000109919	chromatin interactions
ENSG00000196428	chromatin interactions
ENSG00000075624	chromatin interactions

Extended variants
information (count: 3100 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3100 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181307097	chr11:47837111-47837112	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs143544149	chr11:47837127-47837128	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557482115	chr11:47837160-47837161	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374050741	chr11:47837204-47837205	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375878829	chr11:47837206-47837207	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs556093706	chr11:47837319-47837320	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555415561	chr11:47837320-47837321	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs17727140	chr11:47837333-47837334	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs6485786	chr11:47837408-47837409	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs564143343	chr11:47837431-47837432	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs578006440	chr11:47837447-47837448	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200741219	chr11:47837451-47837452	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376466356	chr11:47837454-47837455	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs78447172	chr11:47837466-47837467	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370012109	chr11:47837490-47837491	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148068119	chr11:47837546-47837547	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141773064	chr11:47837571-47837572	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150091964	chr11:47837573-47837574	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs76657809	chr11:47837594-47837595	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186503326	chr11:47837610-47837611	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375543143	chr11:47837619-47837620	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs112073362	chr11:47837620-47837621	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs75482404	chr11:47837637-47837638	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs7130715	chr11:47837638-47837639	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs527382626	chr11:47837662-47837663	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141082263	chr11:47837681-47837682	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs150324642	chr11:47837767-47837768	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532981926	chr11:47837839-47837840	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs561993997	chr11:47837852-47837853	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs75322002	chr11:47837873-47837874	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535640919	chr11:47837926-47837927	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567829525	chr11:47837932-47837933	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535122958	chr11:47838032-47838033	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555551620	chr11:47838134-47838135	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572298387	chr11:47838154-47838155	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191709680	chr11:47838184-47838185	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181639388	chr11:47838283-47838284	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557863829	chr11:47838288-47838289	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186299086	chr11:47838291-47838292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543820807	chr11:47838311-47838312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191041302	chr11:47838314-47838315	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs61895764	chr11:47838331-47838332	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
43	rs63083461	chr11:47838334-47838335	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570962940	chr11:47838335-47838336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183554164	chr11:47838403-47838404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564629404	chr11:47838443-47838444	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557031993	chr11:47838445-47838446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs371077064	chr11:47838528-47838529	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533649304	chr11:47838581-47838582	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541997296	chr11:47838646-47838647	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	22581003	CNVD

Chromatin state (count:2153 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47790000-47837800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:47790200-47869200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr11:47795200-47845600	Strong transcription	Fetal Muscle Trunk	muscle
4	chr11:47795400-47866600	Strong transcription	Fetal Thymus	thymus
5	chr11:47795400-47868400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:47796200-47837800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr11:47796200-47843600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:47796200-47845200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr11:47796200-47845600	Strong transcription	Placenta	Placenta
10	chr11:47796200-47849400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:47796200-47849800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:47796200-47850200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:47796200-47867400	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr11:47796200-47868200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:47796200-47868200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr11:47796200-47868400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr11:47796200-47868400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
18	chr11:47796200-47868600	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr11:47796400-47844000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr11:47796400-47848800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr11:47796400-47848800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr11:47796400-47850600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr11:47796400-47858800	Strong transcription	Liver	Liver
24	chr11:47796400-47867600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:47796600-47843600	Strong transcription	Brain Germinal Matrix	brain
26	chr11:47796600-47850800	Strong transcription	Hela-S3	cervix
27	chr11:47796600-47868600	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr11:47796800-47837600	Strong transcription	Dnd41	blood
29	chr11:47796800-47843800	Strong transcription	Primary B cells from peripheral blood	blood
30	chr11:47796800-47852000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr11:47798000-47868000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr11:47798400-47837800	Strong transcription	Thymus	Thymus
33	chr11:47798400-47845200	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr11:47798400-47864800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr11:47798600-47851600	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr11:47805200-47846200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:47807000-47865600	Strong transcription	Duodenum Mucosa	Duodenum
38	chr11:47810200-47846000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr11:47812400-47849000	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr11:47814600-47850000	Strong transcription	Fetal Muscle Leg	muscle
41	chr11:47815200-47851800	Strong transcription	Fetal Intestine Large	intestine
42	chr11:47815400-47837600	Strong transcription	Stomach Smooth Muscle	stomach
43	chr11:47815400-47837800	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr11:47817200-47838400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr11:47817600-47851400	Strong transcription	Fetal Brain Female	brain
46	chr11:47817800-47837800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:47818200-47839200	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr11:47819600-47841000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:47819800-47839600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr11:47819800-47840400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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