Variant report

Variant	nsv1043197
Chromosome Location	chr11:71423465-71527699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2518)
CpG islands
(count:1403)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2518 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
2	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
3	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
4	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
5	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
7	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
8	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
9	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
10	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
11	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
12	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
13	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
15	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
16	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
17	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
18	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
19	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
20	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
21	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
22	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
23	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
24	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
25	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
26	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
27	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
28	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
29	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
30	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
31	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:71428570-71428787	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:71497628-71497822	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:71498840-71499221	GM12878	blood:	n/a	chr11:71498863-71498876
35	BCL11A	chr11:71473978-71474126	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:71428574-71429024	GM12878	blood:	n/a	chr11:71428833-71428842
37	BCL11A	chr11:71425402-71425946	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:71457382-71457727	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:71425028-71425302	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:71498971-71499169	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:71445521-71445844	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:71511419-71511802	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:71426893-71427066	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:71503781-71503969	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:71499963-71500296	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:71425414-71425925	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:71511333-71511561	GM12878	blood:	n/a	n/a
48	BHLHE40	chr11:71511560-71511619	K562	blood:	n/a	n/a
49	BHLHE40	chr11:71498674-71498871	K562	blood:	n/a	n/a
50	BHLHE40	chr11:71497885-71498210	K562	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71524971-71525021	HAEpiC	amniotic membrane:	n/a
2	chr11:71499006-71499056	AG09309	skin:	n/a
3	chr11:71499117-71499167	NT2-D1	testis:	n/a
4	chr11:71524852-71524902	SK-N-SH	brain:	n/a
5	chr11:71498202-71498252	Caco-2	colon:	n/a
6	chr11:71524500-71524550	SK-N-SH_RA	brain:	n/a
7	chr11:71524734-71524784	HMEC	breast:	n/a
8	chr11:71499117-71499167	LNCaP	prostate:	n/a
9	chr11:71462149-71462199	NHDF-neo	bronchial:	n/a
10	chr11:71524971-71525021	AG09309	skin:	n/a
11	chr11:71456947-71456997	NB4	blood:	n/a
12	chr11:71498715-71498765	HNPCEpiC	eye:	n/a
13	chr11:71524500-71524550	HRCEpiC	kidney:	n/a
14	chr11:71497688-71497738	HCT-116	colon:	n/a
15	chr11:71497552-71497602	HCF	heart:	n/a
16	chr11:71485830-71485880	T-47D	breast:	n/a
17	chr11:71497575-71497625	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:71498715-71498765	HRPEpiC	eye:	n/a
19	chr11:71497575-71497625	AG04450	lung:	fetal
20	chr11:71524971-71525021	GM12892	blood:	n/a
21	chr11:71498202-71498252	HRPEpiC	eye:	n/a
22	chr11:71493933-71493983	HCM	heart:	n/a
23	chr11:71499006-71499056	PFSK-1	brain:	n/a
24	chr11:71497552-71497602	HNPCEpiC	eye:	n/a
25	chr11:71524971-71525021	NB4	blood:	n/a
26	chr11:71524540-71524590	A549	lung:	n/a
27	chr11:71497688-71497738	ProgFib	skin:	n/a
28	chr11:71498202-71498252	HEK293	kidney:	embryo
29	chr11:71502816-71502866	HRCEpiC	kidney:	n/a
30	chr11:71493933-71493983	ProgFib	skin:	n/a
31	chr11:71497575-71497625	GM19239	blood:	n/a
32	chr11:71498202-71498252	AG04450	lung:	fetal
33	chr11:71462582-71462632	HIPEpiC	eye:	n/a
34	chr11:71462582-71462632	NHBE	bronchial:	n/a
35	chr11:71456947-71456997	AG04449	skin:	fetal
36	chr11:71524540-71524590	NH-A	brain:	n/a
37	chr11:71524971-71525021	NHDF-neo	bronchial:	n/a
38	chr11:71462582-71462632	A549	lung:	n/a
39	chr11:71457160-71457210	AG04450	lung:	fetal
40	chr11:71498202-71498252	A549	lung:	n/a
41	chr11:71498715-71498765	HRE	kidney:	n/a
42	chr11:71499117-71499167	HL-60	blood:	n/a
43	chr11:71524852-71524902	GM12891	blood:	n/a
44	chr11:71497688-71497738	HCF	heart:	n/a
45	chr11:71524540-71524590	T-47D	breast:	n/a
46	chr11:71498609-71498659	Hela-S3	cervix:	n/a
47	chr11:71499006-71499056	BJ	skin:	n/a
48	chr11:71499117-71499167	BE2_C	brain:	n/a
49	chr11:71524540-71524590	LNCaP	prostate:	n/a
50	chr11:71456947-71456997	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:71489714..71493464-chr11:71497648..71499552,3	MCF-7	breast:
2	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
3	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
4	chr11:3442224..3443750-chr11:71497854..71499382,2	MCF-7	breast:
5	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
6	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
7	chr11:71502585..71504558-chr11:71523085..71525009,2	MCF-7	breast:
8	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
9	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
10	chr11:71498143..71498944-chr16:5147397..5148064,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
2	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
3	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
4	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
5	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713

No data

Variant related genes	Relation type
FAM86C1	TF binding region
ENSG00000248671	TF binding region
ENSG00000264091	TF binding region
ALG1L9P	TF binding region
ENPP7P8	TF binding region
FAM86C1	CpG island
ENSG00000248671	CpG island
ENSG00000264091	CpG island
ALG1L9P	CpG island
ENPP7P8	CpG island
ENSG00000158483	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000160172	chromatin interactions

Extended variants
information (count: 5522 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:5522 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11234609	chr11:71423465-71423466	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572004418	chr11:71423488-71423489	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200879326	chr11:71423496-71423497	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184493087	chr11:71423501-71423502	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113749324	chr11:71423523-71423524	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557451748	chr11:71423587-71423588	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531433031	chr11:71423588-71423589	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11825370	chr11:71423633-71423634	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs142987826	chr11:71423652-71423653	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61633748	chr11:71423653-71423654	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188026440	chr11:71423679-71423680	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527975260	chr11:71423703-71423704	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111617640	chr11:71423732-71423733	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373483316	chr11:71423740-71423741	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571081398	chr11:71423749-71423750	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531699388	chr11:71423782-71423783	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192456411	chr11:71423788-71423789	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61414067	chr11:71423791-71423792	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568403439	chr11:71423792-71423793	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368127877	chr11:71423794-71423795	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59178663	chr11:71423813-71423814	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs189321877	chr11:71423843-71423844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4945171	chr11:71423869-71423870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs60714232	chr11:71423875-71423876	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs149740951	chr11:71423887-71423888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576273169	chr11:71423917-71423918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9667085	chr11:71423947-71423948	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs9667218	chr11:71423953-71423954	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573771677	chr11:71424110-71424111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541163534	chr11:71424143-71424144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188157418	chr11:71424172-71424173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369479545	chr11:71424178-71424179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527860891	chr11:71424186-71424187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546097728	chr11:71424193-71424194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540232226	chr11:71424197-71424198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145653906	chr11:71424199-71424200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531917803	chr11:71424204-71424205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377583198	chr11:71424213-71424214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550142202	chr11:71424221-71424222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs56144326	chr11:71424257-71424258	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs139659749	chr11:71424261-71424262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537675987	chr11:71424265-71424266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565856849	chr11:71424270-71424271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181314658	chr11:71424275-71424276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145267191	chr11:71424281-71424282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112919069	chr11:71424283-71424284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201115544	chr11:71424311-71424312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs57535030	chr11:71424316-71424317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577857753	chr11:71424331-71424332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184705868	chr11:71424356-71424357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71420600-71424800	Enhancers	K562	blood
2	chr11:71422200-71424800	Enhancers	Fetal Intestine Large	intestine
3	chr11:71422200-71424800	Enhancers	Fetal Intestine Small	intestine
4	chr11:71422400-71423800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:71422400-71424000	Weak transcription	Fetal Lung	lung
6	chr11:71423800-71425600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:71424000-71424600	Enhancers	Fetal Lung	lung
8	chr11:71424800-71425600	Weak transcription	Fetal Intestine Small	intestine
9	chr11:71424800-71430200	Weak transcription	K562	blood
10	chr11:71424800-71435800	Weak transcription	Fetal Intestine Large	intestine
11	chr11:71425600-71426200	Strong transcription	Fetal Intestine Small	intestine
12	chr11:71425600-71430600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:71426200-71433600	Weak transcription	Fetal Intestine Small	intestine
14	chr11:71430200-71430600	Enhancers	K562	blood
15	chr11:71430600-71433600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:71433600-71434800	Strong transcription	Fetal Intestine Small	intestine
17	chr11:71433600-71436200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:71433800-71434600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:71434400-71434600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:71434400-71434600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr11:71434600-71435000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:71434600-71435400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:71434800-71449000	Weak transcription	Fetal Intestine Small	intestine
24	chr11:71435000-71435600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr11:71435400-71435600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr11:71442600-71446000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:71445800-71446400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr11:71445800-71446600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr11:71445800-71446600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr11:71446000-71446800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr11:71446000-71447200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:71446400-71447600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr11:71447200-71447600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:71447600-71447800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:71447600-71447800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr11:71447600-71449800	Enhancers	K562	blood
37	chr11:71449000-71449600	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr11:71449600-71459400	Weak transcription	Fetal Intestine Small	intestine
39	chr11:71449800-71451000	Weak transcription	K562	blood
40	chr11:71451000-71455000	Enhancers	K562	blood
41	chr11:71451000-71464200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:71451600-71454000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:71451800-71456000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:71453400-71453800	Enhancers	Primary hematopoietic stem cells	blood
45	chr11:71454000-71454800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:71454400-71454600	Enhancers	Fetal Lung	lung
47	chr11:71454400-71456800	Enhancers	Stomach Mucosa	stomach
48	chr11:71454800-71455400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:71455000-71455600	Flanking Active TSS	K562	blood
50	chr11:71455600-71456400	Active TSS	K562	blood

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