Variant report

Variant	nsv832202
Chromosome Location	chr11:71088949-71131368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:212)
CpG islands
(count:305)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:212 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:71103739-71103878	K562	blood:	n/a	n/a
2	ATF1	chr11:71113918-71114253	K562	blood:	n/a	n/a
3	ATF1	chr11:71121445-71121846	K562	blood:	n/a	n/a
4	ATF3	chr11:71095654-71095897	K562	blood:	n/a	n/a
5	BACH1	chr11:71098597-71099809	K562	blood:	n/a	n/a
6	BACH1	chr11:71098510-71099819	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr11:71091457-71091688	GM12878	blood:	n/a	n/a
8	BCL11A	chr11:71129809-71130088	GM12878	blood:	n/a	n/a
9	BCLAF1	chr11:71094502-71094906	GM12878	blood:	n/a	chr11:71094684-71094693
10	BCLAF1	chr11:71094470-71094945	GM12878	blood:	n/a	chr11:71094684-71094693
11	BHLHE40	chr11:71094591-71094797	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:71129894-71130027	GM12878	blood:	n/a	n/a
13	BRCA1	chr11:71113975-71114145	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr11:71121368-71121550	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:71121577-71121717	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:71113933-71114079	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:71121493-71121718	A549	lung:	n/a	n/a
18	CHD2	chr11:71099059-71099254	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr11:71098703-71099681	K562	blood:	n/a	n/a
20	CHD2	chr11:71094564-71094814	GM12878	blood:	n/a	n/a
21	CHD2	chr11:71098741-71099683	HepG2	liver:	n/a	n/a
22	CHD2	chr11:71129820-71130115	GM12878	blood:	n/a	n/a
23	CREB1	chr11:71121367-71121872	GM12878	blood:	n/a	n/a
24	CREB1	chr11:71113753-71114422	HepG2	liver:	n/a	n/a
25	CREB1	chr11:71121296-71121778	K562	blood:	n/a	n/a
26	CREB1	chr11:71113751-71114384	K562	blood:	n/a	n/a
27	CREB1	chr11:71121322-71121784	HepG2	liver:	n/a	n/a
28	CREB1	chr11:71113709-71114381	A549	lung:	n/a	n/a
29	CREB1	chr11:71113752-71114390	K562	blood:	n/a	n/a
30	CREB1	chr11:71113750-71114352	HepG2	liver:	n/a	n/a
31	CTCF	chr11:71093600-71093750	MCF-7	breast:	n/a	n/a
32	CTCF	chr11:71129960-71130110	GM12872	blood:	n/a	n/a
33	CTCF	chr11:71104502-71104546	NHEK	skin:	n/a	n/a
34	CTCF	chr11:71123280-71123430	GM12865	blood:	n/a	n/a
35	CTCF	chr11:71130612-71130661	GM13976	blood:	n/a	n/a
36	CTCF	chr11:71113978-71114211	GM19239	blood:	n/a	n/a
37	CTCF	chr11:71131351-71131936	HCT-116	colon:	n/a	chr11:71131657-71131675 chr11:71131663-71131672 chr11:71131659-71131672 chr11:71131652-71131673 chr11:71131660-71131670 chr11:71131658-71131674
38	CTCF	chr11:71093660-71093810	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr11:71104526-71104619	GM12892	blood:	n/a	n/a
40	CTCF	chr11:71129980-71130130	GM12868	blood:	n/a	n/a
41	CTCF	chr11:71122685-71122743	GM20000	blood:	n/a	n/a
42	CTCF	chr11:71106680-71106830	NHEK	skin:	n/a	n/a
43	CTCF	chr11:71093722-71093789	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:71104475-71104548	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:71131220-71131370	HL-60	blood:	n/a	n/a
46	CTCF	chr11:71093691-71093770	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:71131324-71132042	SK-N-SH	brain:	n/a	chr11:71131657-71131675 chr11:71131663-71131672 chr11:71131659-71131672 chr11:71131652-71131673 chr11:71131660-71131670 chr11:71131658-71131674
48	CTCF	chr11:71130903-71132080	A549	lung:	n/a	chr11:71131657-71131675 chr11:71131663-71131672 chr11:71131659-71131672 chr11:71131652-71131673 chr11:71131660-71131670 chr11:71131658-71131674
49	CTCF	chr11:71131361-71131957	MCF-7	breast:	n/a	chr11:71131657-71131675 chr11:71131663-71131672 chr11:71131659-71131672 chr11:71131652-71131673 chr11:71131660-71131670 chr11:71131658-71131674
50	CTCF	chr11:71130000-71130150	GM12871	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71117840-71117890	NB4	blood:	n/a
2	chr11:71117753-71117803	HMEC	breast:	n/a
3	chr11:71117753-71117803	HEEpiC	esophagus:	n/a
4	chr11:71101631-71101681	HL-60	blood:	n/a
5	chr11:71117679-71117729	Jurkat	blood:	n/a
6	chr11:71101631-71101681	SK-N-MC	brain:	n/a
7	chr11:71117753-71117803	HNPCEpiC	eye:	n/a
8	chr11:71117753-71117803	SK-N-SH	brain:	n/a
9	chr11:71117679-71117729	NB4	blood:	n/a
10	chr11:71117840-71117890	HL-60	blood:	n/a
11	chr11:71117753-71117803	HUVEC	blood vessel:	n/a
12	chr11:71101880-71101930	Hela-S3	cervix:	n/a
13	chr11:71117840-71117890	HMEC	breast:	n/a
14	chr11:71101880-71101930	HCT-116	colon:	n/a
15	chr11:71101631-71101681	HUVEC	blood vessel:	n/a
16	chr11:71117840-71117890	ovcar-3	ovarian:	n/a
17	chr11:71117753-71117803	HCT-116	colon:	n/a
18	chr11:71101631-71101681	HMEC	breast:	n/a
19	chr11:71117753-71117803	ECC-1	luminal epithelium:	n/a
20	chr11:71101631-71101681	AG04450	lung:	fetal
21	chr11:71117753-71117803	Jurkat	blood:	n/a
22	chr11:71117840-71117890	Hepatocyte	liver:	n/a
23	chr11:71101631-71101681	MCF-7	breast:	n/a
24	chr11:71117840-71117890	GM12891	blood:	n/a
25	chr11:71117840-71117890	NT2-D1	testis:	n/a
26	chr11:71117679-71117729	Hepatocyte	liver:	n/a
27	chr11:71117840-71117890	Hela-S3	cervix:	n/a
28	chr11:71101631-71101681	Caco-2	colon:	n/a
29	chr11:71101631-71101681	Hela-S3	cervix:	n/a
30	chr11:71101880-71101930	SK-N-MC	brain:	n/a
31	chr11:71117679-71117729	SK-N-SH	brain:	n/a
32	chr11:71117679-71117729	HMEC	breast:	n/a
33	chr11:71117679-71117729	HRPEpiC	eye:	n/a
34	chr11:71117679-71117729	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:71101880-71101930	SKMC	muscle:	n/a
36	chr11:71117840-71117890	PFSK-1	brain:	n/a
37	chr11:71117753-71117803	Hela-S3	cervix:	n/a
38	chr11:71117753-71117803	SK-N-SH_RA	brain:	n/a
39	chr11:71101880-71101930	HL-60	blood:	n/a
40	chr11:71101631-71101681	HCT-116	colon:	n/a
41	chr11:71117753-71117803	AG10803	skin:	n/a
42	chr11:71117840-71117890	HUVEC	blood vessel:	n/a
43	chr11:71101631-71101681	HCM	heart:	n/a
44	chr11:71101631-71101681	GM06990	blood:	n/a
45	chr11:71101880-71101930	HCPEpiC	choroid plexus:	n/a
46	chr11:71117753-71117803	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:71101880-71101930	HUVEC	blood vessel:	n/a
48	chr11:71117753-71117803	MCF10A-Er-Src	breast:	n/a
49	chr11:71117840-71117890	SK-N-SH_RA	brain:	n/a
50	chr11:71117753-71117803	AG04450	lung:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71093138..71095670-chr11:71100121..71102374,2	K562	blood:
2	chr11:71124869..71127186-chr11:71130587..71132175,2	K562	blood:
3	chr11:71091514..71093926-chr11:71098118..71101181,3	MCF-7	breast:
4	chr11:70831355..70832593-chr11:71131146..71132091,4	MCF-7	breast:
5	chr11:71083987..71085496-chr11:71108216..71110305,2	MCF-7	breast:
6	chr11:71113585..71115621-chr11:71119782..71121639,2	K562	blood:
7	chr11:71093138..71095670-chr11:71100121..71102374,2	K562	blood:
8	chr11:71113585..71115621-chr11:71119782..71121639,2	K562	blood:
9	chr11:71101438..71103370-chr11:71105330..71106999,2	MCF-7	breast:
10	chr11:71124869..71127186-chr11:71130587..71132175,2	K562	blood:
11	chr11:71118859..71120385-chr11:71125434..71128124,2	MCF-7	breast:
12	chr11:71118859..71120385-chr11:71125434..71128124,2	MCF-7	breast:
13	chr11:71122603..71125509-chr11:71135103..71137138,2	K562	blood:
14	chr11:71131198..71133245-chr11:71150610..71153048,2	MCF-7	breast:
15	chr11:71091514..71093926-chr11:71098118..71101181,3	MCF-7	breast:
16	chr11:71124009..71126373-chr11:71135133..71137138,2	K562	blood:
17	chr11:71111891..71114927-chr11:71116804..71119287,3	K562	blood:
18	chr11:71083691..71084429-chr11:71131113..71131671,2	MCF-7	breast:
19	chr11:71101438..71103370-chr11:71105330..71106999,2	MCF-7	breast:
20	chr11:71100930..71102789-chr11:71115222..71118166,2	MCF-7	breast:
21	chr11:71087162..71090123-chr11:71091485..71095220,3	MCF-7	breast:
22	chr11:71087162..71090123-chr11:71091485..71095220,3	MCF-7	breast:
23	chr11:71100930..71102789-chr11:71115222..71118166,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DHCR7-3	chr11:71125206-71125471	NONHSAT022677

No data

Variant related genes	Relation type
ENSG00000172900	TF binding region
ENSG00000172900	CpG island
ENSG00000172900	chromatin interactions
ENSG00000172893	chromatin interactions

Extended variants
information (count: 1979 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1979 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563852097	chr11:71088968-71088969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559415016	chr11:71088973-71088974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533239781	chr11:71089030-71089031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs80013972	chr11:71089045-71089046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569860460	chr11:71089074-71089075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111740150	chr11:71089082-71089083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1660892	chr11:71089147-71089148	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs189727131	chr11:71089150-71089151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540229972	chr11:71089154-71089155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1620013	chr11:71089210-71089211	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs118060803	chr11:71089227-71089228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181275015	chr11:71089261-71089262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1790338	chr11:71089270-71089271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185797563	chr11:71089274-71089275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113154796	chr11:71089282-71089283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115541675	chr11:71089310-71089311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76592064	chr11:71089403-71089404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573378352	chr11:71089407-71089408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539731948	chr11:71089426-71089427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569113359	chr11:71089449-71089450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540704078	chr11:71089463-71089464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533185386	chr11:71089484-71089485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148176886	chr11:71089489-71089490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181863409	chr11:71089490-71089491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563481631	chr11:71089502-71089503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556528373	chr11:71089587-71089588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143080585	chr11:71089598-71089599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550321908	chr11:71089666-71089667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12292350	chr11:71089699-71089700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs368106485	chr11:71089706-71089707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534337223	chr11:71089727-71089728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112786280	chr11:71089736-71089737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61385087	chr11:71089737-71089738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115615441	chr11:71089747-71089748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397786697	chr11:71089749-71089750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547517564	chr11:71089773-71089774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146114007	chr11:71089793-71089794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61885881	chr11:71089880-71089881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79955390	chr11:71089896-71089897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186068794	chr11:71089920-71089921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569932482	chr11:71089958-71089959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140132338	chr11:71090015-71090016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555524741	chr11:71090049-71090050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573441828	chr11:71090050-71090051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111737500	chr11:71090051-71090052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184741445	chr11:71090054-71090055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527635349	chr11:71090062-71090063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534712364	chr11:71090072-71090073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201779758	chr11:71090076-71090077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141998424	chr11:71090100-71090101	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
Breast cancer	21785460	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71085600-71092000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr11:71088800-71091800	Weak transcription	GM12878-XiMat	blood
3	chr11:71090400-71096000	Enhancers	Primary B cells from peripheral blood	blood
4	chr11:71090800-71091200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr11:71091200-71095800	Enhancers	Primary B cells from cord blood	blood
6	chr11:71091800-71093000	Enhancers	GM12878-XiMat	blood
7	chr11:71092000-71092200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:71092000-71092200	Enhancers	Spleen	Spleen
9	chr11:71092200-71093000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:71092200-71093000	Weak transcription	Spleen	Spleen
11	chr11:71093000-71093200	Flanking Active TSS	GM12878-XiMat	blood
12	chr11:71093000-71093400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:71093000-71093600	Enhancers	Spleen	Spleen
14	chr11:71093000-71093800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:71093200-71093400	Enhancers	GM12878-XiMat	blood
16	chr11:71093400-71093600	Flanking Active TSS	GM12878-XiMat	blood
17	chr11:71093600-71094200	Enhancers	GM12878-XiMat	blood
18	chr11:71094200-71094800	Flanking Active TSS	GM12878-XiMat	blood
19	chr11:71094800-71095600	Enhancers	GM12878-XiMat	blood
20	chr11:71095600-71097800	Enhancers	Brain Cingulate Gyrus	brain
21	chr11:71095600-71098000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr11:71095800-71096200	Weak transcription	Primary B cells from cord blood	blood
23	chr11:71095800-71097000	Enhancers	Brain Hippocampus Middle	brain
24	chr11:71095800-71097800	Enhancers	Brain Angular Gyrus	brain
25	chr11:71095800-71098000	Enhancers	Brain Substantia Nigra	brain
26	chr11:71096000-71096400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr11:71096200-71098400	Enhancers	Primary B cells from cord blood	blood
28	chr11:71096400-71099000	Enhancers	Primary B cells from peripheral blood	blood
29	chr11:71096600-71097000	Enhancers	Brain Anterior Caudate	brain
30	chr11:71097000-71097400	Weak transcription	Brain Hippocampus Middle	brain
31	chr11:71097400-71097800	Enhancers	Brain Hippocampus Middle	brain
32	chr11:71100000-71100200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:71100000-71101000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr11:71100200-71100400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr11:71100200-71101400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr11:71100400-71100600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:71100400-71100800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr11:71100400-71100800	Enhancers	Esophagus	oesophagus
39	chr11:71100400-71100800	Bivalent Enhancer	NHEK	skin
40	chr11:71100400-71102400	Enhancers	Fetal Muscle Leg	muscle
41	chr11:71100600-71100800	Bivalent Enhancer	Fetal Stomach	stomach
42	chr11:71100600-71101000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:71101000-71101400	Enhancers	Esophagus	oesophagus
44	chr11:71101400-71102000	Enhancers	Primary B cells from peripheral blood	blood
45	chr11:71101600-71101800	Bivalent Enhancer	Primary B cells from cord blood	blood
46	chr11:71102400-71102600	Bivalent Enhancer	Placenta	Placenta
47	chr11:71102400-71102800	Enhancers	Pancreas	Pancrea
48	chr11:71102400-71102800	Enhancers	Small Intestine	intestine
49	chr11:71102400-71103000	Enhancers	HSMM	muscle
50	chr11:71102400-71103000	Enhancers	HSMMtube	muscle

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