Variant report

Variant	nsv555275
Chromosome Location	chr11:67501626-67606530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1632)
CpG islands
(count:732)
Chromatin interactive
region (count:9)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1632 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:67546855-67547018	K562	blood:	n/a	n/a
2	ATF1	chr11:67525774-67525796	K562	blood:	n/a	n/a
3	ATF1	chr11:67572955-67573090	K562	blood:	n/a	n/a
4	ATF3	chr11:67593917-67594176	K562	blood:	n/a	n/a
5	BATF	chr11:67571990-67572187	GM12878	blood:	n/a	chr11:67572041-67572051
6	BATF	chr11:67574662-67574949	GM12878	blood:	n/a	n/a
7	BATF	chr11:67572577-67572827	GM12878	blood:	n/a	n/a
8	BATF	chr11:67559731-67559980	GM12878	blood:	n/a	n/a
9	BATF	chr11:67556628-67556900	GM12878	blood:	n/a	n/a
10	BATF	chr11:67571884-67572418	GM12878	blood:	n/a	chr11:67572041-67572051
11	BATF	chr11:67555087-67555437	GM12878	blood:	n/a	n/a
12	BATF	chr11:67555151-67555449	GM12878	blood:	n/a	n/a
13	BATF	chr11:67548940-67549181	GM12878	blood:	n/a	chr11:67549020-67549031
14	BATF	chr11:67567330-67567611	GM12878	blood:	n/a	n/a
15	BATF	chr11:67548820-67549170	GM12878	blood:	n/a	chr11:67549020-67549031
16	BCL11A	chr11:67556040-67556201	GM12878	blood:	n/a	n/a
17	BCL11A	chr11:67559808-67560040	GM12878	blood:	n/a	n/a
18	BCL11A	chr11:67555126-67555504	GM12878	blood:	n/a	chr11:67555323-67555332
19	BCL11A	chr11:67557563-67557812	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:67571942-67572288	GM12878	blood:	n/a	chr11:67572039-67572048
21	BCL11A	chr11:67571899-67572434	GM12878	blood:	n/a	chr11:67572039-67572048
22	BCL11A	chr11:67559730-67560046	GM12878	blood:	n/a	n/a
23	BCL11A	chr11:67601358-67601522	GM12878	blood:	n/a	n/a
24	BCL11A	chr11:67555194-67555488	GM12878	blood:	n/a	chr11:67555323-67555332
25	BCL11A	chr11:67551659-67551843	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:67572576-67572779	GM12878	blood:	n/a	n/a
27	BCL3	chr11:67512345-67513204	GM12878	blood:	n/a	n/a
28	BCL3	chr11:67512545-67513208	GM12878	blood:	n/a	n/a
29	BCL3	chr11:67502361-67502545	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:67572443-67572791	K562	blood:	n/a	n/a
31	BHLHE40	chr11:67573319-67573396	HepG2	liver:	n/a	n/a
32	BHLHE40	chr11:67572571-67572810	GM12878	blood:	n/a	n/a
33	BHLHE40	chr11:67572527-67572744	HepG2	liver:	n/a	n/a
34	BHLHE40	chr11:67573246-67573456	K562	blood:	n/a	n/a
35	BHLHE40	chr11:67572550-67572923	HepG2	liver:	n/a	n/a
36	BHLHE40	chr11:67588064-67588278	HepG2	liver:	n/a	n/a
37	BHLHE40	chr11:67573136-67573469	HepG2	liver:	n/a	n/a
38	BHLHE40	chr11:67573211-67573403	GM12878	blood:	n/a	n/a
39	BRCA1	chr11:67572702-67572758	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr11:67594403-67594717	K562	blood:	n/a	n/a
41	CBX3	chr11:67571962-67572455	K562	blood:	n/a	n/a
42	CBX3	chr11:67572540-67573426	K562	blood:	n/a	n/a
43	CBX3	chr11:67555125-67555481	K562	blood:	n/a	n/a
44	CCNT2	chr11:67593931-67594123	K562	blood:	n/a	n/a
45	CEBPB	chr11:67571798-67572171	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:67571888-67572154	A549	lung:	n/a	n/a
47	CEBPB	chr11:67544472-67544565	K562	blood:	n/a	chr11:67544532-67544543
48	CEBPB	chr11:67547514-67547884	K562	blood:	n/a	chr11:67547692-67547703
49	CEBPB	chr11:67547525-67547882	A549	lung:	n/a	chr11:67547692-67547703
50	CEBPB	chr11:67571891-67572059	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67573741-67573791	T-47D	breast:	n/a
2	chr11:67571294-67571344	AG09309	skin:	n/a
3	chr11:67572999-67573049	IMR90	lung:	fetal
4	chr11:67573741-67573791	AG10803	skin:	n/a
5	chr11:67572714-67572764	NHBE	bronchial:	n/a
6	chr11:67577512-67577562	GM06990	blood:	n/a
7	chr11:67571294-67571344	ECC-1	luminal epithelium:	n/a
8	chr11:67573741-67573791	Hepatocyte	liver:	n/a
9	chr11:67572999-67573049	GM19239	blood:	n/a
10	chr11:67568593-67568643	Hepatocyte	liver:	n/a
11	chr11:67572988-67573038	GM19239	blood:	n/a
12	chr11:67572988-67573038	NT2-D1	testis:	n/a
13	chr11:67573741-67573791	BE2_C	brain:	n/a
14	chr11:67559939-67559989	ovcar-3	ovarian:	n/a
15	chr11:67572716-67572766	AG09309	skin:	n/a
16	chr11:67571294-67571344	LNCaP	prostate:	n/a
17	chr11:67572988-67573038	AG04449	skin:	fetal
18	chr11:67574013-67574063	H1-hESC	embryonic stem cell:	embryo
19	chr11:67572716-67572766	AG04450	lung:	fetal
20	chr11:67577512-67577562	HNPCEpiC	eye:	n/a
21	chr11:67572716-67572766	HRPEpiC	eye:	n/a
22	chr11:67573741-67573791	PANC-1	pancreas:	n/a
23	chr11:67572988-67573038	MCF10A-Er-Src	breast:	n/a
24	chr11:67573103-67573153	SK-N-MC	brain:	n/a
25	chr11:67577512-67577562	SAEC	small airway:	n/a
26	chr11:67559939-67559989	PANC-1	pancreas:	n/a
27	chr11:67572729-67572779	HIPEpiC	eye:	n/a
28	chr11:67572714-67572764	ovcar-3	ovarian:	n/a
29	chr11:67572988-67573038	IMR90	lung:	fetal
30	chr11:67573103-67573153	HCPEpiC	choroid plexus:	n/a
31	chr11:67572988-67573038	HNPCEpiC	eye:	n/a
32	chr11:67571294-67571344	A549	lung:	n/a
33	chr11:67577512-67577562	LNCaP	prostate:	n/a
34	chr11:67573741-67573791	HAEpiC	amniotic membrane:	n/a
35	chr11:67572999-67573049	T-47D	breast:	n/a
36	chr11:67573741-67573791	HUVEC	blood vessel:	n/a
37	chr11:67572988-67573038	AoSMC	blood vessel:	n/a
38	chr11:67572988-67573038	SAEC	small airway:	n/a
39	chr11:67568593-67568643	HL-60	blood:	n/a
40	chr11:67573103-67573153	HIPEpiC	eye:	n/a
41	chr11:67559939-67559989	HUVEC	blood vessel:	n/a
42	chr11:67573741-67573791	K562	blood:	n/a
43	chr11:67573741-67573791	HEEpiC	esophagus:	n/a
44	chr11:67573741-67573791	HCPEpiC	choroid plexus:	n/a
45	chr11:67559939-67559989	HNPCEpiC	eye:	n/a
46	chr11:67574013-67574063	SK-N-SH_RA	brain:	n/a
47	chr11:67572999-67573049	SAEC	small airway:	n/a
48	chr11:67574013-67574063	SKMC	muscle:	n/a
49	chr11:67571294-67571344	HepG2	liver:	n/a
50	chr11:67572988-67573038	NHDF-neo	bronchial:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67396168..67397948-chr11:67571471..67573438,2	K562	blood:
2	chr11:67572608..67573347-chr4:3956745..3957344,2	Hela-S3	cervix:
3	chr11:67395020..67397974-chr11:67571574..67573157,2	MCF-7	breast:
4	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
5	chr11:67407400..67409857-chr11:67556404..67559360,2	MCF-7	breast:
6	chr11:67349032..67351635-chr11:67571367..67573562,2	K562	blood:
7	chr1:8938391..8938936-chr11:67572724..67573509,2	Hela-S3	cervix:
8	chr1:150551803..150552520-chr11:67572791..67573460,2	Hela-S3	cervix:
9	chr11:67571227..67572733-chr3:125634522..125636253,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFV1-7	chr11:67511793-67512116	NONHSAT022465
2	lnc-NDUFV1-2	chr11:67547802-67550430	ENSG00000248509
3	lnc-NDUFV1-2	chr11:67544666-67545111	ENSG00000248509

No data

Variant related genes	Relation type
OR7E11P	TF binding region
ENSG00000255147	TF binding region
ALG1L8P	TF binding region
FAM86C2P	TF binding region
ENSG00000266451	TF binding region
ENSG00000254792	TF binding region
ENSG00000254883	TF binding region
OR7E11P	CpG island
ENSG00000255147	CpG island
ALG1L8P	CpG island
FAM86C2P	CpG island
ENSG00000266451	CpG island
ENSG00000254792	CpG island
ENSG00000254883	CpG island
ENSG00000084207	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000171084	chromatin interactions
ENSG00000167799	chromatin interactions
TMC7	miRNA target sites
VOPP1	miRNA target sites

Extended variants
information (count: 5823 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:5823 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10791923	chr11:67501626-67501627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200626954	chr11:67501651-67501652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373150414	chr11:67501660-67501661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372503205	chr11:67501672-67501673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560645522	chr11:67501676-67501677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140380549	chr11:67501701-67501702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189389579	chr11:67501713-67501714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200037266	chr11:67501754-67501755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528003435	chr11:67501761-67501762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200974055	chr11:67501778-67501779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570614468	chr11:67501812-67501813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528054709	chr11:67501813-67501814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34483968	chr11:67501831-67501832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs568148901	chr11:67501832-67501833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535469817	chr11:67501836-67501837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201696638	chr11:67501856-67501857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554105030	chr11:67501872-67501873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7104939	chr11:67501910-67501911	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs10750803	chr11:67501915-67501916	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368063408	chr11:67501934-67501935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558111910	chr11:67501965-67501966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202162148	chr11:67501973-67501974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576708987	chr11:67501981-67501982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374402432	chr11:67502007-67502008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10736661	chr11:67502021-67502022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568747697	chr11:67502031-67502032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574354319	chr11:67502032-67502033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372860262	chr11:67502039-67502040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541868522	chr11:67502102-67502103	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs193140024	chr11:67502116-67502117	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs527406022	chr11:67502120-67502121	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs552245787	chr11:67502130-67502131	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs368167786	chr11:67502162-67502163	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs185674286	chr11:67502179-67502180	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs56759932	chr11:67502180-67502181	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs189082687	chr11:67502181-67502182	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181460698	chr11:67502183-67502184	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs371409230	chr11:67502187-67502188	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs7121571	chr11:67502208-67502209	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs547482100	chr11:67502211-67502212	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs566058129	chr11:67502231-67502232	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs368714973	chr11:67502260-67502261	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539596371	chr11:67502261-67502262	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs558212831	chr11:67502266-67502267	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs576747575	chr11:67502276-67502277	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs202013338	chr11:67502302-67502303	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs185751459	chr11:67502303-67502304	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs555969390	chr11:67502309-67502310	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200337319	chr11:67502310-67502311	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs113050039	chr11:67502322-67502323	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD

Chromatin state (count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67499800-67504800	Weak transcription	Placenta	Placenta
2	chr11:67499800-67512800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:67499800-67515200	Weak transcription	Right Atrium	heart
4	chr11:67500000-67521400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr11:67504800-67505000	Enhancers	Placenta	Placenta
6	chr11:67505000-67505800	Weak transcription	Placenta	Placenta
7	chr11:67505200-67505400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:67505200-67506000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:67505800-67506400	Enhancers	Placenta	Placenta
10	chr11:67506000-67512600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:67506400-67511600	Weak transcription	Placenta	Placenta
12	chr11:67511000-67513000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr11:67511200-67512200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:67511200-67513000	Enhancers	Fetal Heart	heart
15	chr11:67511400-67512000	Enhancers	Fetal Muscle Trunk	muscle
16	chr11:67511600-67511800	Enhancers	Left Ventricle	heart
17	chr11:67511600-67512000	Enhancers	Fetal Muscle Leg	muscle
18	chr11:67511600-67512200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:67511600-67512400	Enhancers	Placenta	Placenta
20	chr11:67512000-67512600	Weak transcription	Gastric	stomach
21	chr11:67512400-67512600	Active TSS	Fetal Lung	lung
22	chr11:67512400-67521000	Weak transcription	Placenta	Placenta
23	chr11:67512600-67512800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:67512600-67512800	Enhancers	Left Ventricle	heart
25	chr11:67512600-67513000	Flanking Active TSS	Fetal Lung	lung
26	chr11:67512600-67513000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
27	chr11:67512600-67513200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:67512600-67513200	Enhancers	Esophagus	oesophagus
29	chr11:67512600-67513200	ZNF genes & repeats	Fetal Kidney	kidney
30	chr11:67512600-67513200	ZNF genes & repeats	Gastric	stomach
31	chr11:67512600-67513200	Active TSS	Pancreas	Pancrea
32	chr11:67512600-67513200	Enhancers	Spleen	Spleen
33	chr11:67512800-67513000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:67512800-67513200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr11:67512800-67513200	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr11:67512800-67513200	Bivalent/Poised TSS	NHDF-Ad	bronchial
37	chr11:67513000-67513200	Active TSS	Fetal Lung	lung
38	chr11:67513000-67515600	Weak transcription	Fetal Heart	heart
39	chr11:67513000-67519000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr11:67513200-67514000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr11:67513200-67521400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:67513200-67525400	Weak transcription	Fetal Kidney	kidney
43	chr11:67514400-67515400	Enhancers	Primary B cells from peripheral blood	blood
44	chr11:67514600-67515000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:67514800-67515200	Enhancers	Fetal Stomach	stomach
46	chr11:67515200-67515400	Weak transcription	Fetal Stomach	stomach
47	chr11:67515400-67515800	Enhancers	Fetal Stomach	stomach
48	chr11:67515600-67516200	Enhancers	Fetal Heart	heart
49	chr11:67515600-67516600	Enhancers	Colon Smooth Muscle	Colon
50	chr11:67515800-67521200	Weak transcription	Fetal Stomach	stomach

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