Variant report

Variant	nsv524137
Chromosome Location	chr11:59936979-59947252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:59943277-59943643	GM12878	blood:	n/a	n/a
2	BATF	chr11:59943289-59943622	GM12878	blood:	n/a	n/a
3	BCL11A	chr11:59943260-59943782	GM12878	blood:	n/a	n/a
4	BCL11A	chr11:59943312-59943754	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:59943291-59943766	GM12878	blood:	n/a	n/a
6	BRCA1	chr11:59936747-59937294	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr11:59936709-59937256	HCT-116	colon:	n/a	n/a
8	CBX3	chr11:59936750-59937326	K562	blood:	n/a	n/a
9	CBX3	chr11:59936668-59937147	HCT-116	colon:	n/a	n/a
10	CBX3	chr11:59936531-59937429	K562	blood:	n/a	n/a
11	CEBPB	chr11:59936786-59937096	K562	blood:	n/a	n/a
12	CEBPB	chr11:59940902-59940936	K562	blood:	n/a	n/a
13	CEBPB	chr11:59936903-59937114	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:59936727-59937366	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:59943241-59943836	GM12878	blood:	n/a	chr11:59943749-59943762
16	CEBPB	chr11:59943009-59943267	Hela-S3	cervix:	n/a	n/a
17	CHD1	chr11:59936960-59937014	GM12878	blood:	n/a	n/a
18	CHD2	chr11:59936702-59937270	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr11:59937098-59937342	Hela-S3	cervix:	n/a	chr11:59937221-59937242
20	CTCF	chr11:59937115-59937280	A549	lung:	n/a	chr11:59937221-59937242
21	CTCF	chr11:59937081-59937397	GM12878	blood:	n/a	chr11:59937221-59937242
22	CTCF	chr11:59937080-59937230	HCM	heart:	n/a	n/a
23	CTCF	chr11:59937120-59937270	HUVEC	blood vessel:	n/a	chr11:59937221-59937242
24	CTCF	chr11:59937175-59937269	Medullo	brain:	n/a	chr11:59937221-59937242
25	CTCF	chr11:59937120-59937270	GM12864	blood:	n/a	chr11:59937221-59937242
26	CTCF	chr11:59936921-59936990	Gliobla	brain:	n/a	n/a
27	CTCF	chr11:59936840-59936990	GM12865	blood:	n/a	n/a
28	CTCF	chr11:59937080-59937230	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr11:59937180-59937330	HCPEpiC	choroid plexus:	n/a	chr11:59937221-59937242
30	CTCF	chr11:59937120-59937270	GM12873	blood:	n/a	chr11:59937221-59937242
31	CTCF	chr11:59937220-59937370	HMF	breast:	n/a	chr11:59937221-59937242
32	CTCF	chr11:59937160-59937310	HCT-116	colon:	n/a	chr11:59937221-59937242
33	CTCF	chr11:59937120-59937270	BE2_C	brain:	n/a	chr11:59937221-59937242
34	CTCF	chr11:59936960-59937110	A549	lung:	n/a	n/a
35	CTCF	chr11:59937160-59937310	GM06990	blood:	n/a	chr11:59937221-59937242
36	CTCF	chr11:59937120-59937270	GM12868	blood:	n/a	chr11:59937221-59937242
37	CTCF	chr11:59937120-59937270	Caco-2	colon:	n/a	chr11:59937221-59937242
38	CTCF	chr11:59937134-59937142	HepG2	liver:	n/a	n/a
39	CTCF	chr11:59937160-59937310	HPAF	blood vessel:	n/a	chr11:59937221-59937242
40	CTCF	chr11:59937180-59937330	HEEpiC	esophagus:	n/a	chr11:59937221-59937242
41	CTCF	chr11:59937140-59937290	NHEK	skin:	n/a	chr11:59937221-59937242
42	CTCF	chr11:59937156-59937305	LNCaP	prostate:	n/a	chr11:59937221-59937242
43	CTCF	chr11:59937140-59937290	GM12867	blood:	n/a	chr11:59937221-59937242
44	CTCF	chr11:59937240-59937390	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr11:59937100-59937250	HL-60	blood:	n/a	chr11:59937221-59937242
46	CTCF	chr11:59937160-59937310	GM12864	blood:	n/a	chr11:59937221-59937242
47	CTCF	chr11:59937090-59937336	SK-N-SH_RA	brain:	n/a	chr11:59937221-59937242
48	CTCF	chr11:59937200-59937350	HCT-116	colon:	n/a	chr11:59937221-59937242
49	CTCF	chr11:59937240-59937390	HCM	heart:	n/a	n/a
50	CTCF	chr11:59936940-59936982	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59940485-59940535	PFSK-1	brain:	n/a
2	chr11:59940485-59940535	HMEC	breast:	n/a
3	chr11:59940485-59940535	HepG2	liver:	n/a
4	chr11:59940485-59940535	GM12891	blood:	n/a
5	chr11:59942032-59942082	ProgFib	skin:	n/a
6	chr11:59942032-59942082	GM19239	blood:	n/a
7	chr11:59942032-59942082	SAEC	small airway:	n/a
8	chr11:59942032-59942082	K562	blood:	n/a
9	chr11:59940485-59940535	AoSMC	blood vessel:	n/a
10	chr11:59940485-59940535	Jurkat	blood:	n/a
11	chr11:59942032-59942082	MCF10A-Er-Src	breast:	n/a
12	chr11:59942032-59942082	PANC-1	pancreas:	n/a
13	chr11:59942032-59942082	U87	brain:	n/a
14	chr11:59940485-59940535	ECC-1	luminal epithelium:	n/a
15	chr11:59940485-59940535	Hepatocyte	liver:	n/a
16	chr11:59940485-59940535	Caco-2	colon:	n/a
17	chr11:59942032-59942082	HNPCEpiC	eye:	n/a
18	chr11:59940485-59940535	HPAEpiC	pulmonary alveolar:	n/a
19	chr11:59942032-59942082	HCM	heart:	n/a
20	chr11:59940485-59940535	K562	blood:	n/a
21	chr11:59942032-59942082	SK-N-SH_RA	brain:	n/a
22	chr11:59942032-59942082	MCF-7	breast:	n/a
23	chr11:59942032-59942082	AG04450	lung:	fetal
24	chr11:59942032-59942082	AG04449	skin:	fetal
25	chr11:59942032-59942082	H1-hESC	embryonic stem cell:	embryo
26	chr11:59940485-59940535	GM12878	blood:	n/a
27	chr11:59942032-59942082	GM12892	blood:	n/a
28	chr11:59940485-59940535	HL-60	blood:	n/a
29	chr11:59940485-59940535	IMR90	lung:	fetal
30	chr11:59940485-59940535	AG09309	skin:	n/a
31	chr11:59942032-59942082	Caco-2	colon:	n/a
32	chr11:59942032-59942082	HCPEpiC	choroid plexus:	n/a
33	chr11:59940485-59940535	MCF10A-Er-Src	breast:	n/a
34	chr11:59942032-59942082	GM12891	blood:	n/a
35	chr11:59942032-59942082	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:59940485-59940535	SAEC	small airway:	n/a
37	chr11:59940485-59940535	HRPEpiC	eye:	n/a
38	chr11:59940485-59940535	NT2-D1	testis:	n/a
39	chr11:59940485-59940535	H1-hESC	embryonic stem cell:	embryo
40	chr11:59942032-59942082	PrEC	prostate:	n/a
41	chr11:59940485-59940535	HCT-116	colon:	n/a
42	chr11:59940485-59940535	HEEpiC	esophagus:	n/a
43	chr11:59940485-59940535	AG04450	lung:	fetal
44	chr11:59942032-59942082	PFSK-1	brain:	n/a
45	chr11:59942032-59942082	SK-N-MC	brain:	n/a
46	chr11:59940485-59940535	SK-N-SH	brain:	n/a
47	chr11:59942032-59942082	HEEpiC	esophagus:	n/a
48	chr11:59942032-59942082	HEK293	kidney:	embryo
49	chr11:59940485-59940535	HAEpiC	amniotic membrane:	n/a
50	chr11:59940485-59940535	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:59936023..59937006-chr11:59960779..59961684,2	MCF-7	breast:
2	chr11:59929729..59931318-chr11:59936371..59938548,3	K562	blood:
3	chr11:59926779..59928855-chr11:59938111..59940679,2	K562	blood:
4	chr11:59926973..59929170-chr11:59934444..59937067,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MS4A4E-1	chr11:59946964-59949214	NONHSAT021562
2	lnc-MS4A4E-1	chr11:59945644-59945789	NONHSAT021561

No data

Variant related genes	Relation type
MS4A6A	TF binding region
MS4A6A	CpG island
ENSG00000254952	chromatin interactions

Extended variants
information (count: 464 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs667897	chr11:59936979-59936980	ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534811354	chr11:59936987-59936988	ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535109802	chr11:59936989-59936990	ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575201929	chr11:59937015-59937016	ZNF genes & repeats Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557494081	chr11:59937029-59937030	ZNF genes & repeats Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs142173091	chr11:59937030-59937031	ZNF genes & repeats Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570055119	chr11:59937046-59937047	ZNF genes & repeats Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537758085	chr11:59937070-59937071	ZNF genes & repeats Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577398969	chr11:59937086-59937087	ZNF genes & repeats Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558938710	chr11:59937112-59937113	ZNF genes & repeats Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs646227	chr11:59937261-59937262	ZNF genes & repeats Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577389182	chr11:59937352-59937353	ZNF genes & repeats Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543280403	chr11:59937368-59937369	ZNF genes & repeats Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557217370	chr11:59937392-59937393	ZNF genes & repeats Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553536564	chr11:59937396-59937397	ZNF genes & repeats Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574963223	chr11:59937406-59937407	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112082661	chr11:59937439-59937440	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557379958	chr11:59937447-59937448	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575665439	chr11:59937466-59937467	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372693257	chr11:59937546-59937547	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77285389	chr11:59937547-59937548	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397725961	chr11:59937564-59937565	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140519704	chr11:59937588-59937589	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546103912	chr11:59937611-59937612	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145876608	chr11:59937625-59937626	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528324705	chr11:59937630-59937631	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540032969	chr11:59937640-59937641	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561494200	chr11:59937643-59937644	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528948074	chr11:59937653-59937654	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375434483	chr11:59937719-59937720	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191572001	chr11:59937721-59937722	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568516418	chr11:59937822-59937823	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs532761649	chr11:59937848-59937849	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs552849373	chr11:59937855-59937856	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs571039259	chr11:59937860-59937861	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs79365052	chr11:59937881-59937882	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs553598021	chr11:59937905-59937906	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs373985816	chr11:59937922-59937923	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs114864648	chr11:59937926-59937927	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs12289592	chr11:59937927-59937928	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs368678741	chr11:59937940-59937941	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs372012472	chr11:59937991-59937992	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs182634254	chr11:59938038-59938039	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs188152758	chr11:59938072-59938073	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs575611911	chr11:59938106-59938107	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs545864073	chr11:59938200-59938201	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558061548	chr11:59938235-59938236	Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs376961184	chr11:59938241-59938242	Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs683892	chr11:59938266-59938267	Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192717060	chr11:59938339-59938340	Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
Splenic marginal zone lymphoma	21957467	CNVD
Lung adenocarcinoma	17086460	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59935600-59937200	Strong transcription	Primary monocytes fromperipheralblood	blood
2	chr11:59935600-59937400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:59935600-59940400	Enhancers	HUVEC	blood vessel
4	chr11:59935800-59937000	ZNF genes & repeats	Spleen	Spleen
5	chr11:59935800-59947200	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr11:59936200-59937800	Genic enhancers	Monocytes-CD14+_RO01746	blood
7	chr11:59936200-59938200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:59936400-59937000	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr11:59936400-59937000	ZNF genes & repeats	Dnd41	blood
10	chr11:59936400-59938600	Enhancers	Hela-S3	cervix
11	chr11:59936600-59937000	Enhancers	Adipose Nuclei	Adipose
12	chr11:59936600-59937200	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:59937000-59943000	Weak transcription	Adipose Nuclei	Adipose
14	chr11:59937000-59943400	Weak transcription	Spleen	Spleen
15	chr11:59937200-59941800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr11:59937200-59946600	Genic enhancers	Primary monocytes fromperipheralblood	blood
17	chr11:59937200-59949800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr11:59937800-59938200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr11:59937800-59938400	ZNF genes & repeats	Primary B cells from cord blood	blood
20	chr11:59937800-59938600	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
21	chr11:59938400-59946600	Weak transcription	Primary B cells from cord blood	blood
22	chr11:59938600-59943400	Genic enhancers	Monocytes-CD14+_RO01746	blood
23	chr11:59940200-59940600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:59940200-59940600	Enhancers	K562	blood
25	chr11:59940400-59940600	Enhancers	Esophagus	oesophagus
26	chr11:59941400-59941600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:59941400-59941800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr11:59941400-59942000	Enhancers	Fetal Intestine Large	intestine
29	chr11:59941800-59942200	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:59942200-59947000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr11:59942600-59949200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr11:59942800-59943200	Enhancers	GM12878-XiMat	blood
33	chr11:59942800-59943800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:59942800-59944600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:59943000-59943400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:59943000-59943600	Enhancers	Hela-S3	cervix
37	chr11:59943000-59943800	Enhancers	Adipose Nuclei	Adipose
38	chr11:59943000-59944600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr11:59943200-59943400	Flanking Active TSS	GM12878-XiMat	blood
40	chr11:59943200-59943600	Enhancers	Liver	Liver
41	chr11:59943200-59943600	Enhancers	HMEC	breast
42	chr11:59943200-59943800	Enhancers	Primary B cells from peripheral blood	blood
43	chr11:59943400-59943600	Enhancers	GM12878-XiMat	blood
44	chr11:59943400-59943800	Enhancers	Lung	lung
45	chr11:59943400-59943800	Enhancers	Spleen	Spleen
46	chr11:59943400-59943800	Enhancers	Dnd41	blood
47	chr11:59943400-59943800	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
48	chr11:59943600-59943800	Flanking Active TSS	GM12878-XiMat	blood
49	chr11:59943600-59948600	Weak transcription	Liver	Liver
50	chr11:59943800-59944000	Enhancers	GM12878-XiMat	blood

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