Variant report

Variant	nsv897832
Chromosome Location	chr11:67491330-67625039
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2103)
CpG islands
(count:1282)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2103 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

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	chr11:67572955-67573090	K562	blood:	n/a	n/a
3	ATF1	chr11:67525774-67525796	K562	blood:	n/a	n/a
4	ATF3	chr11:67593917-67594176	K562	blood:	n/a	n/a
5	BATF	chr11:67571884-67572418	GM12878	blood:	n/a	chr11:67572041-67572051
6	BATF	chr11:67559731-67559980	GM12878	blood:	n/a	n/a
7	BATF	chr11:67572577-67572827	GM12878	blood:	n/a	n/a
8	BATF	chr11:67555151-67555449	GM12878	blood:	n/a	n/a
9	BATF	chr11:67556628-67556900	GM12878	blood:	n/a	n/a
10	BATF	chr11:67615409-67615586	GM12878	blood:	n/a	n/a
11	BATF	chr11:67567330-67567611	GM12878	blood:	n/a	n/a
12	BATF	chr11:67555087-67555437	GM12878	blood:	n/a	n/a
13	BATF	chr11:67548940-67549181	GM12878	blood:	n/a	chr11:67549020-67549031
14	BATF	chr11:67548820-67549170	GM12878	blood:	n/a	chr11:67549020-67549031
15	BATF	chr11:67571990-67572187	GM12878	blood:	n/a	chr11:67572041-67572051
16	BATF	chr11:67574662-67574949	GM12878	blood:	n/a	n/a
17	BATF	chr11:67606914-67607130	GM12878	blood:	n/a	n/a
18	BCL11A	chr11:67556040-67556201	GM12878	blood:	n/a	n/a
19	BCL11A	chr11:67601358-67601522	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:67559730-67560046	GM12878	blood:	n/a	n/a
21	BCL11A	chr11:67559808-67560040	GM12878	blood:	n/a	n/a
22	BCL11A	chr11:67557563-67557812	GM12878	blood:	n/a	n/a
23	BCL11A	chr11:67555126-67555504	GM12878	blood:	n/a	chr11:67555323-67555332
24	BCL11A	chr11:67555194-67555488	GM12878	blood:	n/a	chr11:67555323-67555332
25	BCL11A	chr11:67571942-67572288	GM12878	blood:	n/a	chr11:67572039-67572048
26	BCL11A	chr11:67571899-67572434	GM12878	blood:	n/a	chr11:67572039-67572048
27	BCL11A	chr11:67572576-67572779	GM12878	blood:	n/a	n/a
28	BCL11A	chr11:67551659-67551843	GM12878	blood:	n/a	n/a
29	BCL3	chr11:67512345-67513204	GM12878	blood:	n/a	n/a
30	BCL3	chr11:67512545-67513208	GM12878	blood:	n/a	n/a
31	BCL3	chr11:67502361-67502545	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:67573136-67573469	HepG2	liver:	n/a	n/a
33	BHLHE40	chr11:67572550-67572923	HepG2	liver:	n/a	n/a
34	BHLHE40	chr11:67572443-67572791	K562	blood:	n/a	n/a
35	BHLHE40	chr11:67572527-67572744	HepG2	liver:	n/a	n/a
36	BHLHE40	chr11:67573211-67573403	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:67588064-67588278	HepG2	liver:	n/a	n/a
38	BHLHE40	chr11:67572571-67572810	GM12878	blood:	n/a	n/a
39	BHLHE40	chr11:67573246-67573456	K562	blood:	n/a	n/a
40	BHLHE40	chr11:67573319-67573396	HepG2	liver:	n/a	n/a
41	BRCA1	chr11:67572702-67572758	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr11:67499670-67499817	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr11:67594403-67594717	K562	blood:	n/a	n/a
44	CBX3	chr11:67572540-67573426	K562	blood:	n/a	n/a
45	CBX3	chr11:67606617-67606851	K562	blood:	n/a	n/a
46	CBX3	chr11:67606695-67606870	K562	blood:	n/a	n/a
47	CBX3	chr11:67555125-67555481	K562	blood:	n/a	n/a
48	CBX3	chr11:67618219-67618684	K562	blood:	n/a	n/a
49	CBX3	chr11:67571962-67572455	K562	blood:	n/a	n/a
50	CCNT2	chr11:67593931-67594123	K562	blood:	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	chr11:67572729-67572779	HPAEpiC	pulmonary alveolar:	n/a
2	chr11:67572729-67572779	HPAEpiC	pulmonary alveolar:	n/a
3	chr11:67499431-67499481	ECC-1	luminal epithelium:	n/a
4	chr11:67559939-67559989	GM12891	blood:	n/a
5	chr11:67499431-67499481	SAEC	small airway:	n/a
6	chr11:67498995-67499045	MCF-7	breast:	n/a
7	chr11:67577512-67577562	HMEC	breast:	n/a
8	chr11:67499849-67499899	GM06990	blood:	n/a
9	chr11:67571294-67571344	HRPEpiC	eye:	n/a
10	chr11:67572988-67573038	HL-60	blood:	n/a
11	chr11:67559939-67559989	A549	lung:	n/a
12	chr11:67494416-67494466	MCF10A-Er-Src	breast:	n/a
13	chr11:67498316-67498366	BJ	skin:	n/a
14	chr11:67498316-67498366	A549	lung:	n/a
15	chr11:67499849-67499899	AoSMC	blood vessel:	n/a
16	chr11:67572999-67573049	NH-A	brain:	n/a
17	chr11:67572714-67572764	HCPEpiC	choroid plexus:	n/a
18	chr11:67499849-67499899	HEEpiC	esophagus:	n/a
19	chr11:67572999-67573049	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:67574013-67574063	HCF	heart:	n/a
21	chr11:67494416-67494466	RPTEC	kidney:	n/a
22	chr11:67571294-67571344	Hepatocyte	liver:	n/a
23	chr11:67499525-67499575	SK-N-SH	brain:	n/a
24	chr11:67577512-67577562	U87	brain:	n/a
25	chr11:67572988-67573038	SK-N-MC	brain:	n/a
26	chr11:67494327-67494377	Hela-S3	cervix:	n/a
27	chr11:67573741-67573791	PrEC	prostate:	n/a
28	chr11:67499431-67499481	U87	brain:	n/a
29	chr11:67577512-67577562	Caco-2	colon:	n/a
30	chr11:67499525-67499575	HL-60	blood:	n/a
31	chr11:67572729-67572779	ECC-1	luminal epithelium:	n/a
32	chr11:67572988-67573038	GM12892	blood:	n/a
33	chr11:67573103-67573153	HEEpiC	esophagus:	n/a
34	chr11:67574013-67574063	RPTEC	kidney:	n/a
35	chr11:67572999-67573049	SK-N-MC	brain:	n/a
36	chr11:67498995-67499045	HEEpiC	esophagus:	n/a
37	chr11:67494416-67494466	Hepatocyte	liver:	n/a
38	chr11:67499849-67499899	NHDF-neo	bronchial:	n/a
39	chr11:67568593-67568643	AG04449	skin:	fetal
40	chr11:67574013-67574063	NB4	blood:	n/a
41	chr11:67499849-67499899	AG04449	skin:	fetal
42	chr11:67494327-67494377	GM19239	blood:	n/a
43	chr11:67572714-67572764	T-47D	breast:	n/a
44	chr11:67498271-67498321	HUVEC	blood vessel:	n/a
45	chr11:67577512-67577562	GM12891	blood:	n/a
46	chr11:67499849-67499899	K562	blood:	n/a
47	chr11:67572729-67572779	H1-hESC	embryonic stem cell:	embryo
48	chr11:67571294-67571344	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:67499849-67499899	GM12891	blood:	n/a
50	chr11:67573103-67573153	NB4	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150551803..150552520-chr11:67572791..67573460,2	Hela-S3	cervix:
2	chr11:67349032..67351635-chr11:67571367..67573562,2	K562	blood:
3	chr11:67572608..67573347-chr4:3956745..3957344,2	Hela-S3	cervix:
4	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
5	chr11:67615533..67616044-chr11:67722872..67723766,2	K562	blood:
6	chr1:8938391..8938936-chr11:67572724..67573509,2	Hela-S3	cervix:
7	chr11:67407400..67409857-chr11:67556404..67559360,2	MCF-7	breast:
8	chr11:67571227..67572733-chr3:125634522..125636253,2	MCF-7	breast:
9	chr11:67395020..67397974-chr11:67571574..67573157,2	MCF-7	breast:
10	chr11:67396168..67397948-chr11:67571471..67573438,2	K562	blood:

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

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

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
ENSG00000235855	TF binding region
OR7E11P	CpG island
ENSG00000255147	CpG island
ALG1L8P	CpG island
FAM86C2P	CpG island
ENSG00000266451	CpG island
ENSG00000254792	CpG island
ENSG00000254883	CpG island
ENSG00000235855	CpG island
ENSG00000251669	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000171084	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000158483	chromatin interactions
VOPP1	miRNA target sites
TMC7	miRNA target sites

Extended variants
information (count: 7170 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:7170 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112368223	chr11:67491330-67491331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535537969	chr11:67491337-67491338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560654163	chr11:67491343-67491344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190365629	chr11:67491347-67491348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565904087	chr11:67491361-67491362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182625714	chr11:67491380-67491381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7102529	chr11:67491381-67491382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575914923	chr11:67491386-67491387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375252606	chr11:67491404-67491405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551425955	chr11:67491406-67491407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370080567	chr11:67491407-67491408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536911383	chr11:67491432-67491433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555753152	chr11:67491504-67491505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186950198	chr11:67491538-67491539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189840040	chr11:67491586-67491587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373500120	chr11:67491588-67491589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7102585	chr11:67491591-67491592	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs183890757	chr11:67491592-67491593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545605293	chr11:67491599-67491600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188894112	chr11:67491613-67491614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544191408	chr11:67491618-67491619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531255872	chr11:67491641-67491642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562184755	chr11:67491670-67491671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549653927	chr11:67491671-67491672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561730720	chr11:67491677-67491678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192932744	chr11:67491714-67491715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185169453	chr11:67491715-67491716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565615409	chr11:67491721-67491722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532848601	chr11:67491726-67491727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145531976	chr11:67491734-67491735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148845579	chr11:67491748-67491749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551086445	chr11:67491793-67491794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs72936362	chr11:67491806-67491807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs143777434	chr11:67491815-67491816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555365869	chr11:67491850-67491851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567700483	chr11:67491950-67491951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9666749	chr11:67491991-67491992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553466282	chr11:67492019-67492020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578157054	chr11:67492084-67492085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545492812	chr11:67492092-67492093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377493676	chr11:67492136-67492137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370794110	chr11:67492141-67492142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575864426	chr11:67492157-67492158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187292797	chr11:67492168-67492169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561417776	chr11:67492202-67492203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112427355	chr11:67492232-67492233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548916655	chr11:67492244-67492245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191816367	chr11:67492259-67492260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78039001	chr11:67492261-67492262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75570625	chr11:67492262-67492263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Lung cancer	19153074	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
early-passage human iPS cells	21368824	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:1081 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67481200-67499400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:67490000-67495200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:67490200-67494400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr11:67490200-67495000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr11:67494000-67495600	Enhancers	Pancreas	Pancrea
6	chr11:67494400-67495400	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr11:67494400-67495800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr11:67494400-67496400	Enhancers	Placenta	Placenta
9	chr11:67494400-67496800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:67494400-67497000	Enhancers	Stomach Mucosa	stomach
11	chr11:67494400-67499200	Weak transcription	Right Atrium	heart
12	chr11:67494800-67495600	Enhancers	Gastric	stomach
13	chr11:67495000-67495400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr11:67495000-67495400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:67495000-67495400	Enhancers	Duodenum Mucosa	Duodenum
16	chr11:67495000-67495800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr11:67495000-67496800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr11:67495000-67498400	Enhancers	Fetal Intestine Large	intestine
19	chr11:67495000-67498600	Enhancers	Fetal Intestine Small	intestine
20	chr11:67495200-67495400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr11:67495200-67495400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr11:67495200-67495400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr11:67495200-67495400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:67495200-67495600	Enhancers	Esophagus	oesophagus
25	chr11:67495200-67495800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr11:67495200-67496200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr11:67495200-67497000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr11:67495200-67497200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:67495200-67497200	Enhancers	HepG2	liver
30	chr11:67495200-67498200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:67495400-67496200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:67495400-67496400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr11:67495400-67497200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:67495400-67499200	Weak transcription	Duodenum Mucosa	Duodenum
35	chr11:67495400-67499400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr11:67495600-67499600	Weak transcription	Pancreas	Pancrea
37	chr11:67495600-67499800	Weak transcription	Gastric	stomach
38	chr11:67495800-67496200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr11:67495800-67499200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr11:67495800-67499200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr11:67496200-67496400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr11:67496200-67496400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr11:67496200-67496600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:67496200-67499200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr11:67496400-67499200	Weak transcription	Placenta	Placenta
46	chr11:67496400-67499200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr11:67496600-67499200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:67496800-67499200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr11:67497000-67498000	Weak transcription	Stomach Mucosa	stomach
50	chr11:67497000-67499400	Weak transcription	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links