Variant report

Variant	nsv517878
Chromosome Location	chr11:59441271-59480969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:661)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:661 , 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	ARID3A	chr11:59478145-59478159	K562	blood:	n/a	n/a
2	ARID3A	chr11:59443733-59443859	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:59474183-59474710	K562	blood:	n/a	n/a
4	ATF1	chr11:59478022-59478291	K562	blood:	n/a	n/a
5	ATF1	chr11:59448694-59449064	K562	blood:	n/a	n/a
6	ATF1	chr11:59474303-59474883	K562	blood:	n/a	n/a
7	BACH1	chr11:59448049-59448307	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:59448156-59448317	K562	blood:	n/a	n/a
9	BHLHE40	chr11:59474318-59474701	K562	blood:	n/a	n/a
10	BHLHE40	chr11:59448047-59448372	K562	blood:	n/a	n/a
11	BHLHE40	chr11:59473840-59473935	K562	blood:	n/a	n/a
12	BHLHE40	chr11:59441723-59441934	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:59441701-59441811	K562	blood:	n/a	n/a
14	CBX3	chr11:59448619-59449321	K562	blood:	n/a	n/a
15	CBX3	chr11:59474376-59474749	K562	blood:	n/a	n/a
16	CBX3	chr11:59474334-59474819	HCT-116	colon:	n/a	n/a
17	CBX3	chr11:59474310-59474749	K562	blood:	n/a	n/a
18	CBX3	chr11:59460402-59460693	K562	blood:	n/a	n/a
19	CBX3	chr11:59460387-59460873	HCT-116	colon:	n/a	n/a
20	CBX3	chr11:59460459-59460781	K562	blood:	n/a	n/a
21	CBX3	chr11:59459964-59460276	K562	blood:	n/a	n/a
22	CBX3	chr11:59460492-59460788	HCT-116	colon:	n/a	n/a
23	CCNT2	chr11:59448700-59449217	K562	blood:	n/a	n/a
24	CCNT2	chr11:59474319-59474675	K562	blood:	n/a	n/a
25	CEBPB	chr11:59448030-59448366	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:59474329-59474752	K562	blood:	n/a	n/a
27	CEBPB	chr11:59474341-59474673	K562	blood:	n/a	n/a
28	CEBPB	chr11:59466071-59466278	A549	lung:	n/a	n/a
29	CEBPB	chr11:59474432-59474693	A549	lung:	n/a	n/a
30	CEBPB	chr11:59448056-59448366	A549	lung:	n/a	n/a
31	CEBPB	chr11:59448015-59448369	K562	blood:	n/a	n/a
32	CEBPB	chr11:59448036-59448373	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:59474375-59474667	K562	blood:	n/a	n/a
34	CEBPB	chr11:59448043-59448363	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:59447972-59448399	K562	blood:	n/a	n/a
36	CEBPB	chr11:59447998-59448383	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:59466141-59466280	K562	blood:	n/a	n/a
38	CEBPB	chr11:59474344-59474695	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:59474344-59474731	IMR90	lung:	n/a	n/a
40	CEBPD	chr11:59448584-59449053	K562	blood:	n/a	n/a
41	CEBPD	chr11:59477913-59478341	K562	blood:	n/a	n/a
42	CEBPD	chr11:59474163-59474895	K562	blood:	n/a	n/a
43	CEBPD	chr11:59448627-59449283	K562	blood:	n/a	n/a
44	CEBPD	chr11:59474185-59474834	K562	blood:	n/a	n/a
45	CHD1	chr11:59447890-59448596	IMR90	lung:	n/a	n/a
46	CHD2	chr11:59473833-59473981	K562	blood:	n/a	n/a
47	CHD2	chr11:59448083-59448374	HepG2	liver:	n/a	n/a
48	CHD2	chr11:59448084-59448355	K562	blood:	n/a	n/a
49	CREB1	chr11:59474131-59474818	K562	blood:	n/a	n/a
50	CREB1	chr11:59474363-59474693	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59480501-59480551	ProgFib	skin:	n/a
2	chr11:59480501-59480551	MCF10A-Er-Src	breast:	n/a
3	chr11:59480501-59480551	NB4	blood:	n/a
4	chr11:59480501-59480551	H1-hESC	embryonic stem cell:	embryo
5	chr11:59480501-59480551	SAEC	small airway:	n/a
6	chr11:59480501-59480551	Hepatocyte	liver:	n/a
7	chr11:59480501-59480551	HIPEpiC	eye:	n/a
8	chr11:59480501-59480551	CMK	blood:	n/a
9	chr11:59480501-59480551	SKMC	muscle:	n/a
10	chr11:59480501-59480551	Jurkat	blood:	n/a
11	chr11:59480501-59480551	HAEpiC	amniotic membrane:	n/a
12	chr11:59480501-59480551	HMEC	breast:	n/a
13	chr11:59480501-59480551	HRE	kidney:	n/a
14	chr11:59480501-59480551	AG09309	skin:	n/a
15	chr11:59480501-59480551	GM12878	blood:	n/a
16	chr11:59480501-59480551	BJ	skin:	n/a
17	chr11:59480501-59480551	NT2-D1	testis:	n/a
18	chr11:59480501-59480551	IMR90	lung:	fetal
19	chr11:59480501-59480551	AoSMC	blood vessel:	n/a
20	chr11:59480501-59480551	ECC-1	luminal epithelium:	n/a
21	chr11:59480501-59480551	SK-N-MC	brain:	n/a
22	chr11:59480501-59480551	A549	lung:	n/a
23	chr11:59480501-59480551	MCF-7	breast:	n/a
24	chr11:59480501-59480551	HRPEpiC	eye:	n/a
25	chr11:59480501-59480551	SK-N-SH_RA	brain:	n/a
26	chr11:59480501-59480551	GM19239	blood:	n/a
27	chr11:59480501-59480551	Caco-2	colon:	n/a
28	chr11:59480501-59480551	AG04449	skin:	fetal
29	chr11:59480501-59480551	GM12891	blood:	n/a
30	chr11:59480501-59480551	ovcar-3	ovarian:	n/a
31	chr11:59480501-59480551	HEK293	kidney:	embryo
32	chr11:59480501-59480551	Hela-S3	cervix:	n/a
33	chr11:59480501-59480551	HCF	heart:	n/a
34	chr11:59480501-59480551	HepG2	liver:	n/a
35	chr11:59480501-59480551	HEEpiC	esophagus:	n/a
36	chr11:59480501-59480551	PrEC	prostate:	n/a
37	chr11:59480501-59480551	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:59480501-59480551	PANC-1	pancreas:	n/a
39	chr11:59480501-59480551	HCT-116	colon:	n/a
40	chr11:59480501-59480551	HCPEpiC	choroid plexus:	n/a
41	chr11:59480501-59480551	AG09319	gingival:	n/a
42	chr11:59480501-59480551	HRCEpiC	kidney:	n/a
43	chr11:59480501-59480551	BE2_C	brain:	n/a
44	chr11:59480501-59480551	U87	brain:	n/a
45	chr11:59480501-59480551	HL-60	blood:	n/a
46	chr11:59480501-59480551	SK-N-SH	brain:	n/a
47	chr11:59480501-59480551	NHBE	bronchial:	n/a
48	chr11:59480501-59480551	LNCaP	prostate:	n/a
49	chr11:59480501-59480551	GM12892	blood:	n/a
50	chr11:59480501-59480551	AG10803	skin:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59451000..59453627-chr11:59521681..59524289,3	MCF-7	breast:
2	chr11:59446578..59448587-chr11:59521403..59523165,2	K562	blood:
3	chr11:59459291..59461515-chr11:59463513..59466171,3	K562	blood:
4	chr11:59303328..59305254-chr11:59447598..59450069,2	K562	blood:
5	chr11:59304452..59305342-chr11:59447720..59448612,3	K562	blood:
6	chr11:59382734..59385576-chr11:59440781..59442919,2	K562	blood:
7	chr11:59453648..59457625-chr11:59458136..59461041,3	K562	blood:
8	chr11:59459291..59461515-chr11:59463513..59466171,3	K562	blood:
9	chr11:58938973..58939965-chr11:59447518..59448398,3	K562	blood:
10	chr11:59435145..59438848-chr11:59444207..59446941,3	MCF-7	breast:
11	chr11:59197459..59198444-chr11:59447527..59448507,2	K562	blood:
12	chr11:59456082..59458840-chr11:59461567..59463981,3	K562	blood:
13	chr11:59453648..59457625-chr11:59458136..59461041,3	K562	blood:
14	chr11:59476148..59479085-chr11:59479730..59481553,2	K562	blood:
15	chr11:59435458..59437530-chr11:59446685..59449413,3	K562	blood:
16	chr11:59479954..59482315-chr11:59521677..59523287,2	K562	blood:
17	chr1:114226647..114228206-chr11:59448085..59449746,2	MCF-7	breast:
18	chr11:59480505..59482058-chr11:59521372..59523220,2	MCF-7	breast:
19	chr11:59380994..59383091-chr11:59446545..59448432,2	K562	blood:
20	chr11:59447806..59448672-chr11:59569775..59570386,2	MCF-7	breast:
21	chr11:59456082..59458840-chr11:59461567..59463981,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX3-1	chr11:59442409-59442446	ENSG00000255355.1
2	lnc-STX3-1	chr11:59442870-59443514	ENSG00000255355.1
3	lnc-OR10V1-2	chr11:59473530-59473856	NONHSAT021539
4	lnc-STX3-1	chr11:59442870-59443268	ENSG00000255355.1

No data

Variant related genes	Relation type
RN7SKP192	TF binding region
STX3	TF binding region
ENSG00000255355	TF binding region
PATL1	TF binding region
RN7SKP192	CpG island
STX3	CpG island
ENSG00000255355	CpG island
PATL1	CpG island
ENSG00000172289	chromatin interactions
ENSG00000110048	chromatin interactions
ENSG00000255355	chromatin interactions
ENSG00000255139	chromatin interactions
ENSG00000254477	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000166900	chromatin interactions

Extended variants
information (count: 1393 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1393 , 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	rs7117032	chr11:59441271-59441272	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117978904	chr11:59441300-59441301	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs578258013	chr11:59441474-59441475	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs74445403	chr11:59441502-59441503	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560637983	chr11:59441513-59441514	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188239583	chr11:59441516-59441517	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs144744875	chr11:59441518-59441519	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs116240500	chr11:59441533-59441534	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs574900791	chr11:59441542-59441543	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138684733	chr11:59441555-59441556	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531535685	chr11:59441585-59441586	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs564823548	chr11:59441600-59441601	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572690990	chr11:59441613-59441614	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs532302035	chr11:59441729-59441730	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs373603068	chr11:59441745-59441746	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs547310724	chr11:59441764-59441765	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs115539900	chr11:59441772-59441773	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs139451344	chr11:59441789-59441790	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs192188449	chr11:59441868-59441869	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs536054635	chr11:59441930-59441931	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs184458230	chr11:59441964-59441965	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs569699345	chr11:59442007-59442008	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs189287336	chr11:59442054-59442055	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs77831261	chr11:59442087-59442088	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs576932909	chr11:59442097-59442098	Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs539302544	chr11:59442108-59442109	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs35637829	chr11:59442119-59442120	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182027317	chr11:59442139-59442140	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs572625396	chr11:59442170-59442171	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184119766	chr11:59442229-59442230	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs370375319	chr11:59442252-59442253	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374446020	chr11:59442291-59442292	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532113	chr11:59442374-59442375	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145456830	chr11:59442386-59442387	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12293459	chr11:59442417-59442418	Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs189485298	chr11:59442437-59442438	Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs576935554	chr11:59442455-59442456	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs576496733	chr11:59442457-59442458	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs543778737	chr11:59442504-59442505	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs568254101	chr11:59442551-59442552	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564908835	chr11:59442564-59442565	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs181144994	chr11:59442571-59442572	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547251205	chr11:59442574-59442575	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs141785752	chr11:59442582-59442583	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150845803	chr11:59442608-59442609	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186644111	chr11:59442610-59442611	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs569710093	chr11:59442654-59442655	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536715769	chr11:59442703-59442704	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs552262310	chr11:59442709-59442710	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375344881	chr11:59442725-59442726	Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59438600-59441600	Weak transcription	Fetal Intestine Small	intestine
2	chr11:59440000-59442000	Enhancers	Liver	Liver
3	chr11:59440800-59441800	Weak transcription	HepG2	liver
4	chr11:59441600-59444200	Enhancers	Fetal Intestine Small	intestine
5	chr11:59441800-59444600	Enhancers	HepG2	liver
6	chr11:59442000-59443200	Flanking Active TSS	Liver	Liver
7	chr11:59443200-59444000	Enhancers	Liver	Liver
8	chr11:59443400-59443600	Weak transcription	Fetal Intestine Large	intestine
9	chr11:59443600-59444000	Enhancers	Fetal Intestine Large	intestine
10	chr11:59444000-59447400	Weak transcription	Fetal Intestine Large	intestine
11	chr11:59444000-59447800	Weak transcription	Liver	Liver
12	chr11:59444200-59446800	Weak transcription	Fetal Intestine Small	intestine
13	chr11:59445200-59446200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:59445600-59446600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr11:59446000-59447000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr11:59446000-59447000	Enhancers	HMEC	breast
17	chr11:59446200-59446600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr11:59446400-59447000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:59446800-59449600	Enhancers	Fetal Intestine Small	intestine
20	chr11:59447000-59447200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr11:59447200-59448000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr11:59447400-59448800	Enhancers	Fetal Intestine Large	intestine
23	chr11:59447600-59447800	Enhancers	K562	blood
24	chr11:59447600-59448000	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr11:59447600-59449000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:59447800-59448000	Flanking Active TSS	K562	blood
27	chr11:59447800-59448200	Enhancers	Liver	Liver
28	chr11:59447800-59448200	Enhancers	Fetal Muscle Trunk	muscle
29	chr11:59447800-59448800	Enhancers	Stomach Mucosa	stomach
30	chr11:59447800-59448800	Enhancers	HepG2	liver
31	chr11:59447800-59450600	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr11:59448000-59448200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr11:59448000-59448200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:59448000-59448400	Enhancers	K562	blood
35	chr11:59448000-59448800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr11:59448200-59448800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:59448400-59448800	Flanking Active TSS	K562	blood
38	chr11:59448600-59449400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:59448800-59449000	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr11:59448800-59449200	Weak transcription	Fetal Intestine Large	intestine
41	chr11:59448800-59449600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:59448800-59450000	Enhancers	K562	blood
43	chr11:59448800-59459600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:59449000-59455600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr11:59449200-59450200	Enhancers	Fetal Intestine Large	intestine
46	chr11:59449600-59449800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:59449600-59455200	Weak transcription	Fetal Intestine Small	intestine
48	chr11:59449800-59450000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:59450600-59455000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr11:59455000-59457000	Enhancers	Primary neutrophils fromperipheralblood	blood

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