Variant report

Variant	esv18828
Chromosome Location	chr11:71551614-71592576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:363)
CpG islands
(count:124)
Chromatin interactive
region (count:0)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:71575242-71575395	K562	blood:	n/a	n/a
2	ATF3	chr11:71575077-71575386	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr11:71575100-71575329	K562	blood:	n/a	n/a
4	BATF	chr11:71574985-71575313	GM12878	blood:	n/a	n/a
5	BATF	chr11:71575058-71575377	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:71575170-71575171	K562	blood:	n/a	n/a
7	BHLHE40	chr11:71575106-71575202	HepG2	liver:	n/a	n/a
8	CBX3	chr11:71561434-71561699	K562	blood:	n/a	n/a
9	CBX3	chr11:71561489-71561676	K562	blood:	n/a	n/a
10	CBX3	chr11:71575017-71575414	K562	blood:	n/a	n/a
11	CEBPB	chr11:71587443-71587637	Hela-S3	cervix:	n/a	chr11:71587538-71587547
12	CEBPB	chr11:71587446-71587649	IMR90	lung:	n/a	chr11:71587538-71587547
13	CEBPB	chr11:71573854-71573989	IMR90	lung:	n/a	chr11:71573950-71573963
14	CTCF	chr11:71575460-71575610	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr11:71578471-71578576	GM10266	blood:	n/a	n/a
16	CTCF	chr11:71575160-71575310	GM12866	blood:	n/a	n/a
17	CTCF	chr11:71574840-71574990	AG10803	skin:	n/a	n/a
18	CTCF	chr11:71574840-71574990	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr11:71575079-71575411	GM13977	blood:	n/a	n/a
20	CTCF	chr11:71575160-71575310	RPTEC	kidney:	n/a	n/a
21	CTCF	chr11:71575094-71575424	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr11:71575013-71575407	A549	lung:	n/a	n/a
23	CTCF	chr11:71575077-71575440	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr11:71578450-71578565	ProgFib	skin:	n/a	n/a
25	CTCF	chr11:71575092-71575334	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr11:71575084-71575392	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:71575111-71575405	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr11:71578380-71578530	GM06990	blood:	n/a	n/a
29	CTCF	chr11:71578340-71578490	GM12872	blood:	n/a	n/a
30	CTCF	chr11:71575180-71575330	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr11:71575005-71575477	K562	blood:	n/a	n/a
32	CTCF	chr11:71575160-71575310	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr11:71578491-71578580	GM12878	blood:	n/a	n/a
34	CTCF	chr11:71575082-71575360	Fibrobl	skin:	n/a	n/a
35	CTCF	chr11:71575126-71575380	GM10248	blood:	n/a	n/a
36	CTCF	chr11:71575060-71575439	T-47D	breast:	n/a	n/a
37	CTCF	chr11:71575144-71575326	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr11:71563376-71563427	GM10266	blood:	n/a	n/a
39	CTCF	chr11:71578380-71578530	HEK293	kidney:	n/a	n/a
40	CTCF	chr11:71578360-71578510	Caco-2	colon:	n/a	n/a
41	CTCF	chr11:71578340-71578490	GM12864	blood:	n/a	n/a
42	CTCF	chr11:71578429-71578619	MCF-7	breast:	n/a	n/a
43	CTCF	chr11:71578451-71578587	GM12892	blood:	n/a	n/a
44	CTCF	chr11:71574700-71574850	GM12873	blood:	n/a	chr11:71574830-71574843
45	CTCF	chr11:71575160-71575310	HCFaa	heart:	n/a	n/a
46	CTCF	chr11:71575140-71575290	HVMF	connective:	n/a	n/a
47	CTCF	chr11:71575160-71575310	HAc	cerebellar:	n/a	n/a
48	CTCF	chr11:71575160-71575310	GM12873	blood:	n/a	n/a
49	CTCF	chr11:71575160-71575310	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr11:71578340-71578490	MCF-7	breast:	n/a	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71567175-71567225	HMEC	breast:	n/a
2	chr11:71554504-71554554	SAEC	small airway:	n/a
3	chr11:71567175-71567225	HMEC	breast:	n/a
4	chr11:71554504-71554554	SAEC	small airway:	n/a
5	chr11:71554504-71554554	HRPEpiC	eye:	n/a
6	chr11:71554504-71554554	SK-N-MC	brain:	n/a
7	chr11:71567175-71567225	ovcar-3	ovarian:	n/a
8	chr11:71554504-71554554	CMK	blood:	n/a
9	chr11:71567175-71567225	HRCEpiC	kidney:	n/a
10	chr11:71554504-71554554	BJ	skin:	n/a
11	chr11:71567175-71567225	AG09309	skin:	n/a
12	chr11:71567175-71567225	SK-N-SH_RA	brain:	n/a
13	chr11:71554504-71554554	MCF10A-Er-Src	breast:	n/a
14	chr11:71554504-71554554	Jurkat	blood:	n/a
15	chr11:71567175-71567225	HNPCEpiC	eye:	n/a
16	chr11:71567175-71567225	Hepatocyte	liver:	n/a
17	chr11:71554504-71554554	HEEpiC	esophagus:	n/a
18	chr11:71554504-71554554	NHBE	bronchial:	n/a
19	chr11:71567175-71567225	AG04449	skin:	fetal
20	chr11:71567175-71567225	HUVEC	blood vessel:	n/a
21	chr11:71567175-71567225	NHDF-neo	bronchial:	n/a
22	chr11:71567175-71567225	HEEpiC	esophagus:	n/a
23	chr11:71554504-71554554	SK-N-SH	brain:	n/a
24	chr11:71567175-71567225	T-47D	breast:	n/a
25	chr11:71567175-71567225	PrEC	prostate:	n/a
26	chr11:71567175-71567225	A549	lung:	n/a
27	chr11:71554504-71554554	GM12878	blood:	n/a
28	chr11:71567175-71567225	GM06990	blood:	n/a
29	chr11:71554504-71554554	U87	brain:	n/a
30	chr11:71567175-71567225	NB4	blood:	n/a
31	chr11:71554504-71554554	HMEC	breast:	n/a
32	chr11:71567175-71567225	AG10803	skin:	n/a
33	chr11:71567175-71567225	PANC-1	pancreas:	n/a
34	chr11:71567175-71567225	HepG2	liver:	n/a
35	chr11:71554504-71554554	PANC-1	pancreas:	n/a
36	chr11:71567175-71567225	HEK293	kidney:	embryo
37	chr11:71567175-71567225	BJ	skin:	n/a
38	chr11:71567175-71567225	HCM	heart:	n/a
39	chr11:71567175-71567225	CMK	blood:	n/a
40	chr11:71567175-71567225	HIPEpiC	eye:	n/a
41	chr11:71567175-71567225	HL-60	blood:	n/a
42	chr11:71567175-71567225	GM19239	blood:	n/a
43	chr11:71554504-71554554	ProgFib	skin:	n/a
44	chr11:71567175-71567225	H1-hESC	embryonic stem cell:	embryo
45	chr11:71554504-71554554	T-47D	breast:	n/a
46	chr11:71567175-71567225	MCF-7	breast:	n/a
47	chr11:71567175-71567225	HCPEpiC	choroid plexus:	n/a
48	chr11:71567175-71567225	MCF10A-Er-Src	breast:	n/a
49	chr11:71554504-71554554	BE2_C	brain:	n/a
50	chr11:71554504-71554554	LNCaP	prostate:	n/a

No data

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB108B-1	chr11:71580800-71580844	XLOC_009200
2	lnc-NUMA1-1	chr11:71589418-71589551	XLOC_009494
3	lnc-DEFB108B-1	chr11:71589499-71589564	NONHSAT022724
4	lnc-DEFB108B-1	chr11:71578414-71578614	XLOC_009200
5	lnc-NUMA1-1	chr11:71581076-71581470	XLOC_009494

No data

Variant related genes	Relation type
ENSG00000225805	TF binding region
ENSG00000255157	TF binding region
RNA5SP342	TF binding region
ENSG00000225805	CpG island
ENSG00000255157	CpG island
RNA5SP342	CpG island
KIAA1217	miRNA target sites
OR11A1	miRNA target sites

Extended variants
information (count: 1811 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1811 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561252193	chr11:71551640-71551641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528809293	chr11:71551647-71551648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113768098	chr11:71551652-71551653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571650785	chr11:71551740-71551741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532382253	chr11:71551772-71551773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146260690	chr11:71551782-71551783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376314153	chr11:71551800-71551801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569217531	chr11:71551827-71551828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138097835	chr11:71551830-71551831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554755687	chr11:71551881-71551882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs59658697	chr11:71551883-71551884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs190778485	chr11:71551884-71551885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144070794	chr11:71551898-71551899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183387771	chr11:71551899-71551900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554899728	chr11:71551906-71551907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562442929	chr11:71551913-71551914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576799282	chr11:71551924-71551925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186956147	chr11:71551930-71551931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59795410	chr11:71551936-71551937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190566235	chr11:71551943-71551944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112284908	chr11:71551944-71551945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541521047	chr11:71551970-71551971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561190267	chr11:71551973-71551974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573088861	chr11:71552001-71552002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59823976	chr11:71552002-71552003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201874789	chr11:71552003-71552004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144354362	chr11:71552018-71552019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113243357	chr11:71552019-71552020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187769294	chr11:71552022-71552023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368068681	chr11:71552023-71552024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55959754	chr11:71552045-71552046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs193292867	chr11:71552077-71552078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530264226	chr11:71552086-71552087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566705811	chr11:71552088-71552089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139409528	chr11:71552092-71552093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554117112	chr11:71552098-71552099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570614955	chr11:71552107-71552108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185542038	chr11:71552116-71552117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555933174	chr11:71552118-71552119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145041866	chr11:71552120-71552121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535210269	chr11:71552147-71552148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59022517	chr11:71552152-71552153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs201101405	chr11:71552165-71552166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548165047	chr11:71552174-71552175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368190993	chr11:71552180-71552181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187976222	chr11:71552218-71552219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376481043	chr11:71552242-71552243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565579858	chr11:71552279-71552280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141112484	chr11:71552307-71552308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544882887	chr11:71552317-71552318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71542600-71553400	Weak transcription	Fetal Stomach	stomach
2	chr11:71549400-71553200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:71549400-71553400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr11:71551400-71554800	Weak transcription	Spleen	Spleen
5	chr11:71552800-71554000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:71553000-71553800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:71553000-71554000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:71553200-71553600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:71553200-71553800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr11:71553200-71554000	Enhancers	Esophagus	oesophagus
11	chr11:71553200-71554000	Enhancers	HepG2	liver
12	chr11:71553200-71554200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:71553200-71554200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr11:71553200-71554400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:71553200-71554400	Enhancers	NHEK	skin
16	chr11:71553400-71553600	Enhancers	Fetal Stomach	stomach
17	chr11:71553400-71553800	Enhancers	A549	lung
18	chr11:71553400-71554000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr11:71553400-71554000	Enhancers	Primary hematopoietic stem cells	blood
20	chr11:71553400-71554200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:71553400-71555400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr11:71553600-71554000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr11:71553600-71554200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr11:71553600-71555200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:71553800-71554000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr11:71553800-71554200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:71554000-71555000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr11:71554000-71555400	Weak transcription	Esophagus	oesophagus
29	chr11:71554000-71566200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr11:71554200-71554600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr11:71554200-71554600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr11:71554200-71554600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:71554200-71566400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr11:71554600-71554800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr11:71554600-71554800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr11:71554600-71555200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr11:71554600-71555400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr11:71554600-71555400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr11:71554800-71555000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr11:71554800-71555000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr11:71554800-71555200	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr11:71554800-71555200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:71554800-71555200	Enhancers	Spleen	Spleen
44	chr11:71554800-71555400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr11:71555000-71555200	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr11:71555000-71555400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr11:71555000-71555600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr11:71555200-71555600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr11:71555400-71555600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr11:71555400-71555600	Enhancers	HUES64 Cell Line	embryonic stem cell

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