Variant report

Variant	esv11824
Chromosome Location	chr11:71515433-71603968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71599388-71599657	HepG2	liver:	n/a	n/a
2	ATF1	chr11:71575242-71575395	K562	blood:	n/a	n/a
3	ATF2	chr11:71540829-71541073	GM12878	blood:	n/a	n/a
4	ATF3	chr11:71575100-71575329	K562	blood:	n/a	n/a
5	ATF3	chr11:71575077-71575386	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:71574985-71575313	GM12878	blood:	n/a	n/a
7	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
8	BATF	chr11:71575058-71575377	GM12878	blood:	n/a	n/a
9	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
10	BATF	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
11	BCL11A	chr11:71532424-71532928	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:71532549-71532834	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:71540694-71541007	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:71524868-71525086	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:71532638-71532832	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:71541854-71542142	K562	blood:	n/a	n/a
17	BHLHE40	chr11:71575170-71575171	K562	blood:	n/a	n/a
18	BHLHE40	chr11:71541847-71542211	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:71540852-71541062	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:71575106-71575202	HepG2	liver:	n/a	n/a
21	CBX3	chr11:71575017-71575414	K562	blood:	n/a	n/a
22	CBX3	chr11:71561434-71561699	K562	blood:	n/a	n/a
23	CBX3	chr11:71561489-71561676	K562	blood:	n/a	n/a
24	CEBPB	chr11:71549235-71549396	K562	blood:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
25	CEBPB	chr11:71597024-71597114	K562	blood:	n/a	n/a
26	CEBPB	chr11:71549224-71549424	A549	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
27	CEBPB	chr11:71549258-71549410	HepG2	liver:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
28	CEBPB	chr11:71587446-71587649	IMR90	lung:	n/a	chr11:71587538-71587547
29	CEBPB	chr11:71587443-71587637	Hela-S3	cervix:	n/a	chr11:71587538-71587547
30	CEBPB	chr11:71549344-71549406	Hela-S3	cervix:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
31	CEBPB	chr11:71549210-71549469	IMR90	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
32	CEBPB	chr11:71573854-71573989	IMR90	lung:	n/a	chr11:71573950-71573963
33	CEBPB	chr11:71599387-71599581	HepG2	liver:	n/a	n/a
34	CHD1	chr11:71524751-71525147	IMR90	lung:	n/a	n/a
35	CTCF	chr11:71575160-71575310	GM12872	blood:	n/a	n/a
36	CTCF	chr11:71524880-71525030	GM06990	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
37	CTCF	chr11:71524672-71525123	H1-hESC	embryonic stem cell:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
38	CTCF	chr11:71578380-71578530	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr11:71524832-71525109	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
40	CTCF	chr11:71575180-71575330	GM12871	blood:	n/a	n/a
41	CTCF	chr11:71575160-71575310	GM12801	blood:	n/a	n/a
42	CTCF	chr11:71575400-71575550	AG04450	lung:	n/a	n/a
43	CTCF	chr11:71524827-71525096	GM12891	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
44	CTCF	chr11:71524824-71525112	LNCaP	prostate:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
45	CTCF	chr11:71518191-71518249	GM10266	blood:	n/a	n/a
46	CTCF	chr11:71575019-71575480	GM12878	blood:	n/a	n/a
47	CTCF	chr11:71575160-71575310	HCT-116	colon:	n/a	n/a
48	CTCF	chr11:71524900-71525050	GM12871	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
49	CTCF	chr11:71524780-71524930	HCM	heart:	n/a	n/a
50	CTCF	chr11:71575046-71575368	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71527895-71527945	SK-N-SH	brain:	n/a
2	chr11:71543471-71543521	SAEC	small airway:	n/a
3	chr11:71527895-71527945	K562	blood:	n/a
4	chr11:71524852-71524902	NB4	blood:	n/a
5	chr11:71524500-71524550	SKMC	muscle:	n/a
6	chr11:71527895-71527945	GM19239	blood:	n/a
7	chr11:71527895-71527945	BJ	skin:	n/a
8	chr11:71522461-71522511	SK-N-SH_RA	brain:	n/a
9	chr11:71597171-71597221	AG04449	skin:	fetal
10	chr11:71524500-71524550	NHDF-neo	bronchial:	n/a
11	chr11:71524500-71524550	NH-A	brain:	n/a
12	chr11:71524852-71524902	HEEpiC	esophagus:	n/a
13	chr11:71601069-71601119	HCF	heart:	n/a
14	chr11:71543583-71543633	U87	brain:	n/a
15	chr11:71524852-71524902	GM12892	blood:	n/a
16	chr11:71524971-71525021	AG04450	lung:	fetal
17	chr11:71601069-71601119	HRE	kidney:	n/a
18	chr11:71543583-71543633	A549	lung:	n/a
19	chr11:71601069-71601119	NH-A	brain:	n/a
20	chr11:71524852-71524902	MCF-7	breast:	n/a
21	chr11:71601069-71601119	K562	blood:	n/a
22	chr11:71524852-71524902	Hepatocyte	liver:	n/a
23	chr11:71597171-71597221	Hepatocyte	liver:	n/a
24	chr11:71524852-71524902	AG09319	gingival:	n/a
25	chr11:71524500-71524550	AG04450	lung:	fetal
26	chr11:71524971-71525021	SK-N-SH_RA	brain:	n/a
27	chr11:71543583-71543633	BE2_C	brain:	n/a
28	chr11:71597184-71597234	SAEC	small airway:	n/a
29	chr11:71601069-71601119	HUVEC	blood vessel:	n/a
30	chr11:71597171-71597221	RPTEC	kidney:	n/a
31	chr11:71597171-71597221	MCF-7	breast:	n/a
32	chr11:71567175-71567225	HL-60	blood:	n/a
33	chr11:71600961-71601011	ECC-1	luminal epithelium:	n/a
34	chr11:71524540-71524590	AG10803	skin:	n/a
35	chr11:71567175-71567225	T-47D	breast:	n/a
36	chr11:71600961-71601011	AG09309	skin:	n/a
37	chr11:71524734-71524784	NB4	blood:	n/a
38	chr11:71522461-71522511	AG09309	skin:	n/a
39	chr11:71543583-71543633	ProgFib	skin:	n/a
40	chr11:71524734-71524784	MCF10A-Er-Src	breast:	n/a
41	chr11:71524734-71524784	AG04450	lung:	fetal
42	chr11:71567175-71567225	PrEC	prostate:	n/a
43	chr11:71597104-71597154	ovcar-3	ovarian:	n/a
44	chr11:71567175-71567225	AG10803	skin:	n/a
45	chr11:71545243-71545293	HRE	kidney:	n/a
46	chr11:71524500-71524550	Hela-S3	cervix:	n/a
47	chr11:71522461-71522511	HCPEpiC	choroid plexus:	n/a
48	chr11:71597184-71597234	HL-60	blood:	n/a
49	chr11:71527895-71527945	HIPEpiC	eye:	n/a
50	chr11:71524852-71524902	AoSMC	blood vessel:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB108B-1	chr11:71578414-71578614	XLOC_009200
2	lnc-DEFB108B-2	chr11:71545758-71545904	NONHSAT022717
3	lnc-DEFB108B-2	chr11:71548445-71548756	NONHSAT022717
4	lnc-RP11-849H4.2.1-1	chr11:71527956-71528142	ENSG00000248671.3
5	lnc-DEFB108B-1	chr11:71595455-71595604	NONHSAT022724
6	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
7	lnc-DEFB108B-1	chr11:71589499-71589564	NONHSAT022724
8	lnc-DEFB108B-2	chr11:71548070-71548218	NONHSAT022717
9	lnc-DEFB108B-1	chr11:71595453-71596531	XLOC_009200
10	lnc-DEFB108B-1	chr11:71580800-71580844	XLOC_009200
11	lnc-NUMA1-1	chr11:71589418-71589551	XLOC_009494
12	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
13	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
14	lnc-NUMA1-1	chr11:71581076-71581470	XLOC_009494
15	lnc-RP11-849H4.2.1-1	chr11:71529199-71529284	ENSG00000248671.3

Variant related genes	Relation type
DEFB108B	TF binding region
OR7E128P	TF binding region
ENSG00000225805	TF binding region
ENSG00000248671	TF binding region
ZNF705E	TF binding region
ENSG00000255157	TF binding region
ENSG00000264091	TF binding region
ALG1L9P	TF binding region
RNA5SP342	TF binding region
DEFB108B	CpG island
OR7E128P	CpG island
ENSG00000225805	CpG island
ENSG00000248671	CpG island
ZNF705E	CpG island
ENSG00000255157	CpG island
ENSG00000264091	CpG island
ALG1L9P	CpG island
RNA5SP342	CpG island
OR11A1	miRNA target sites
KIAA1217	miRNA target sites

Extended variants
information (count: 3829 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3829 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556225389	chr11:71515434-71515435	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs574368872	chr11:71515440-71515441	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541413624	chr11:71515455-71515456	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs143053721	chr11:71515458-71515459	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572135138	chr11:71515466-71515467	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs545944157	chr11:71515467-71515468	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs565463904	chr11:71515477-71515478	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs532637244	chr11:71515499-71515500	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544886762	chr11:71515519-71515520	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs577212837	chr11:71515555-71515556	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs150805406	chr11:71515582-71515583	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs530434345	chr11:71515584-71515585	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs548146489	chr11:71515588-71515589	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs10898623	chr11:71515610-71515611	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs113779704	chr11:71515656-71515657	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs146188555	chr11:71515657-71515658	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs61301176	chr11:71515687-71515688	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs143094826	chr11:71515701-71515702	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs556326957	chr11:71515707-71515708	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs634230	chr11:71515721-71515722	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs568222437	chr11:71515734-71515735	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs535763392	chr11:71515737-71515738	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs553782826	chr11:71515742-71515743	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs56891431	chr11:71515759-71515760	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs539530797	chr11:71515764-71515765	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs377631536	chr11:71515766-71515767	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs557932615	chr11:71515779-71515780	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs537671417	chr11:71515782-71515783	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs115579865	chr11:71515816-71515817	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs150665239	chr11:71515850-71515851	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs139934401	chr11:71515854-71515855	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs371769960	chr11:71515904-71515905	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs59253989	chr11:71515906-71515907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35142804	chr11:71515919-71515920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61248388	chr11:71515943-71515944	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs560096959	chr11:71515954-71515955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182336199	chr11:71515998-71515999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376781475	chr11:71516036-71516037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558911167	chr11:71516081-71516082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577006961	chr11:71516082-71516083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186949216	chr11:71516083-71516084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564377083	chr11:71516093-71516094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531842043	chr11:71516096-71516097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549674171	chr11:71516100-71516101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77432775	chr11:71516118-71516119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183393201	chr11:71516123-71516124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547755986	chr11:71516134-71516135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369483152	chr11:71516144-71516145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187930698	chr11:71516224-71516225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193172127	chr11:71516246-71516247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71499400-71515600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:71500400-71515600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr11:71506000-71515600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr11:71506400-71515600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr11:71506600-71515600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:71508200-71524400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:71508800-71524400	Weak transcription	Fetal Intestine Small	intestine
8	chr11:71511600-71523600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr11:71511600-71524400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:71511600-71524400	Weak transcription	Brain Angular Gyrus	brain
11	chr11:71513600-71515600	Weak transcription	Fetal Muscle Leg	muscle
12	chr11:71515200-71515800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:71515200-71515800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr11:71515200-71515800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:71515200-71515800	Enhancers	Fetal Intestine Large	intestine
16	chr11:71515200-71515800	Enhancers	Lung	lung
17	chr11:71515600-71515800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr11:71515600-71515800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:71515600-71515800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:71515600-71515800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr11:71515600-71515800	Enhancers	Fetal Muscle Leg	muscle
22	chr11:71515800-71517200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr11:71522000-71523600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:71523200-71524000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr11:71523400-71523600	Enhancers	Brain Hippocampus Middle	brain
26	chr11:71523400-71523600	Enhancers	Rectal Smooth Muscle	rectum
27	chr11:71523400-71523800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr11:71523400-71524400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:71523600-71523800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:71523600-71523800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr11:71523600-71523800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr11:71523600-71523800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:71523600-71523800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr11:71523600-71523800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:71523600-71523800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr11:71523600-71523800	Enhancers	Brain Anterior Caudate	brain
37	chr11:71523600-71523800	Enhancers	Brain Cingulate Gyrus	brain
38	chr11:71523600-71523800	Enhancers	Brain Substantia Nigra	brain
39	chr11:71523600-71523800	Enhancers	Fetal Brain Female	brain
40	chr11:71523600-71523800	Enhancers	Fetal Stomach	stomach
41	chr11:71523600-71523800	Enhancers	Left Ventricle	heart
42	chr11:71523600-71523800	Enhancers	Lung	lung
43	chr11:71523600-71523800	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr11:71523600-71523800	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr11:71523600-71523800	Enhancers	HSMMtube	muscle
46	chr11:71523600-71524000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr11:71523600-71524200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:71523600-71524200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:71523600-71524200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr11:71523600-71524200	Enhancers	Osteobl	bone

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