Variant report

Variant	nsv1043207
Chromosome Location	chr11:71293875-71442666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1640)
CpG islands
(count:3784)
Chromatin interactive
region (count:2)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
2	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
3	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
4	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
5	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
6	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
7	ATF1	chr11:71328834-71328851	K562	blood:	n/a	n/a
8	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
9	ATF3	chr11:71300244-71300497	K562	blood:	n/a	n/a
10	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
11	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
12	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
14	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
15	BATF	chr11:71300267-71300538	GM12878	blood:	n/a	n/a
16	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
17	BATF	chr11:71325819-71326075	GM12878	blood:	n/a	n/a
18	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
19	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
20	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
21	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
22	BATF	chr11:71325884-71326044	GM12878	blood:	n/a	n/a
23	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
24	BATF	chr11:71315927-71316371	GM12878	blood:	n/a	n/a
25	BATF	chr11:71300267-71300512	GM12878	blood:	n/a	n/a
26	BATF	chr11:71364018-71364247	GM12878	blood:	n/a	chr11:71364110-71364121
27	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
28	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
29	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
30	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
31	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
32	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
33	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:71316096-71316292	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:71363953-71364282	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:71425414-71425925	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:71421456-71421625	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:71398790-71398946	GM12878	blood:	n/a	chr11:71398860-71398869
39	BCL11A	chr11:71428574-71429024	GM12878	blood:	n/a	chr11:71428833-71428842
40	BCL11A	chr11:71363951-71364544	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:71428570-71428787	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:71364327-71364546	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:71407051-71407260	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:71398722-71399032	GM12878	blood:	n/a	chr11:71398860-71398869
45	BCL11A	chr11:71423022-71423248	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:71425028-71425302	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:71422007-71422279	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:71376120-71376905	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:71406992-71407565	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:71369783-71369963	GM12878	blood:	n/a	n/a

(count:3784 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71322873-71322923	LNCaP	prostate:	n/a
2	chr11:71417657-71417707	GM12891	blood:	n/a
3	chr11:71322873-71322923	LNCaP	prostate:	n/a
4	chr11:71417657-71417707	GM12891	blood:	n/a
5	chr11:71418204-71418254	H1-hESC	embryonic stem cell:	embryo
6	chr11:71421279-71421329	MCF-7	breast:	n/a
7	chr11:71324346-71324396	BE2_C	brain:	n/a
8	chr11:71350743-71350793	Hepatocyte	liver:	n/a
9	chr11:71321132-71321182	BE2_C	brain:	n/a
10	chr11:71350346-71350396	AG04449	skin:	fetal
11	chr11:71417657-71417707	HIPEpiC	eye:	n/a
12	chr11:71294605-71294655	GM19239	blood:	n/a
13	chr11:71324028-71324078	CMK	blood:	n/a
14	chr11:71350888-71350938	U87	brain:	n/a
15	chr11:71320766-71320816	GM19239	blood:	n/a
16	chr11:71417713-71417763	GM12892	blood:	n/a
17	chr11:71324525-71324575	MCF10A-Er-Src	breast:	n/a
18	chr11:71418204-71418254	HMEC	breast:	n/a
19	chr11:71294819-71294869	Jurkat	blood:	n/a
20	chr11:71418204-71418254	A549	lung:	n/a
21	chr11:71353991-71354041	HUVEC	blood vessel:	n/a
22	chr11:71340288-71340338	HEK293	kidney:	embryo
23	chr11:71301401-71301451	MCF10A-Er-Src	breast:	n/a
24	chr11:71421380-71421430	HEK293	kidney:	embryo
25	chr11:71350888-71350938	NB4	blood:	n/a
26	chr11:71351271-71351321	H1-hESC	embryonic stem cell:	embryo
27	chr11:71320766-71320816	ovcar-3	ovarian:	n/a
28	chr11:71350346-71350396	H1-hESC	embryonic stem cell:	embryo
29	chr11:71315863-71315913	GM06990	blood:	n/a
30	chr11:71301062-71301112	Caco-2	colon:	n/a
31	chr11:71301401-71301451	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:71324188-71324238	AG09319	gingival:	n/a
33	chr11:71340352-71340402	A549	lung:	n/a
34	chr11:71294819-71294869	T-47D	breast:	n/a
35	chr11:71350975-71351025	T-47D	breast:	n/a
36	chr11:71421279-71421329	U87	brain:	n/a
37	chr11:71346528-71346578	HRPEpiC	eye:	n/a
38	chr11:71311984-71312034	Jurkat	blood:	n/a
39	chr11:71320735-71320785	SAEC	small airway:	n/a
40	chr11:71350975-71351025	NHBE	bronchial:	n/a
41	chr11:71340288-71340338	HCPEpiC	choroid plexus:	n/a
42	chr11:71417713-71417763	HIPEpiC	eye:	n/a
43	chr11:71297203-71297253	IMR90	lung:	fetal
44	chr11:71420947-71420997	A549	lung:	n/a
45	chr11:71297203-71297253	HEEpiC	esophagus:	n/a
46	chr11:71318057-71318107	LNCaP	prostate:	n/a
47	chr11:71324525-71324575	IMR90	lung:	fetal
48	chr11:71320513-71320563	HEEpiC	esophagus:	n/a
49	chr11:71327885-71327935	AG10803	skin:	n/a
50	chr11:71321132-71321182	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:71290639..71292875-chr11:71296370..71298788,2	MCF-7	breast:
2	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-3	chr11:71310043-71310371	NONHSAT022693
2	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
3	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
4	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
5	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
6	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
7	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
8	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
9	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
10	lnc-AP000867.1-3	chr11:71314349-71314399	NONHSAT022693
11	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
12	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
13	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
14	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
15	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697

No data

Variant related genes	Relation type
OR7E87P	TF binding region
OR7E4P	TF binding region
ENSG00000255415	TF binding region
ENSG00000223235	TF binding region
ENSG00000254805	TF binding region
ENPP7P8	TF binding region
ENSG00000254972	TF binding region
KRTAP5-14P	TF binding region
ENSG00000187811	TF binding region
ENSG00000221458	TF binding region
KRTAP5-11	TF binding region
UNC93B6	TF binding region
RPS3AP41	TF binding region
OR7E87P	CpG island
OR7E4P	CpG island
ENSG00000255415	CpG island
ENSG00000223235	CpG island
ENSG00000254805	CpG island
ENPP7P8	CpG island
ENSG00000254972	CpG island
KRTAP5-14P	CpG island
ENSG00000187811	CpG island
ENSG00000221458	CpG island
KRTAP5-11	CpG island
UNC93B6	CpG island
RPS3AP41	CpG island
ENSG00000249387	chromatin interactions

Extended variants
information (count: 7598 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:7598 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372189076	chr11:71293879-71293880	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs75907819	chr11:71293892-71293893	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs201546007	chr11:71293893-71293894	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs113127873	chr11:71293902-71293903	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs566368046	chr11:71293914-71293915	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs200426136	chr11:71293925-71293926	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
7	rs533819329	chr11:71293932-71293933	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
8	rs369225975	chr11:71293979-71293980	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs184718035	chr11:71293996-71293997	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
10	rs543817832	chr11:71293997-71293998	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
11	rs373271559	chr11:71294000-71294001	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
12	rs574481350	chr11:71294013-71294014	Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
13	rs541609644	chr11:71294124-71294125	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs561525584	chr11:71294208-71294209	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs188799528	chr11:71294209-71294210	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs540908242	chr11:71294230-71294231	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs565599825	chr11:71294231-71294232	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs532515607	chr11:71294279-71294280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572960607	chr11:71294329-71294330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550954717	chr11:71294338-71294339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569202636	chr11:71294353-71294354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530201096	chr11:71294417-71294418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548427158	chr11:71294427-71294428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566306979	chr11:71294437-71294438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149637492	chr11:71294494-71294495	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs376552287	chr11:71294500-71294501	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs117415704	chr11:71294518-71294519	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs537398948	chr11:71294525-71294526	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs577432002	chr11:71294556-71294557	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs574392445	chr11:71294557-71294558	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs541249100	chr11:71294581-71294582	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs535520425	chr11:71294606-71294607	Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
33	rs553614781	chr11:71294609-71294610	Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
34	rs573448266	chr11:71294610-71294611	Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
35	rs540845004	chr11:71294626-71294627	Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
36	rs113464238	chr11:71294668-71294669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112427871	chr11:71294672-71294673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549601808	chr11:71294673-71294674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373869089	chr11:71294705-71294706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192861314	chr11:71294718-71294719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56371419	chr11:71294745-71294746	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
42	rs571817066	chr11:71294746-71294747	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
43	rs61010146	chr11:71294754-71294755	Weak transcription	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs143177253	chr11:71294765-71294766	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
45	rs147519914	chr11:71294766-71294767	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs570363253	chr11:71294790-71294791	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs139954021	chr11:71294791-71294792	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs10898347	chr11:71294802-71294803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs371122018	chr11:71294819-71294820	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
50	rs10751118	chr11:71294826-71294827	Weak transcription	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD

Chromatin state (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71291400-71295200	Weak transcription	Right Atrium	heart
2	chr11:71291800-71297000	Weak transcription	Fetal Intestine Large	intestine
3	chr11:71291800-71299000	Weak transcription	Gastric	stomach
4	chr11:71292400-71294000	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:71293000-71294000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:71293000-71294000	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr11:71293600-71300000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:71293800-71294000	Enhancers	Placenta	Placenta
9	chr11:71297000-71297600	Enhancers	Fetal Intestine Large	intestine
10	chr11:71297000-71301000	Enhancers	Fetal Intestine Small	intestine
11	chr11:71297600-71299000	Weak transcription	Fetal Intestine Large	intestine
12	chr11:71298000-71298800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:71298800-71299000	Weak transcription	Pancreas	Pancrea
14	chr11:71298800-71299800	Enhancers	HepG2	liver
15	chr11:71299000-71299200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:71299000-71299200	Enhancers	Stomach Mucosa	stomach
17	chr11:71299000-71299600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr11:71299000-71299800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr11:71299000-71300200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:71299000-71300200	Enhancers	Fetal Intestine Large	intestine
21	chr11:71299000-71300200	Enhancers	Gastric	stomach
22	chr11:71299000-71300400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr11:71299000-71300800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr11:71299000-71301000	Enhancers	Duodenum Mucosa	Duodenum
25	chr11:71299000-71301000	Enhancers	Placenta	Placenta
26	chr11:71299000-71301000	Enhancers	Pancreas	Pancrea
27	chr11:71299200-71299800	Weak transcription	Stomach Mucosa	stomach
28	chr11:71299200-71300000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr11:71299600-71300200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:71299800-71300000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:71299800-71300600	Enhancers	Stomach Mucosa	stomach
32	chr11:71300000-71300200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:71300000-71300600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr11:71314200-71314600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr11:71314400-71314600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr11:71315200-71316000	Enhancers	Fetal Thymus	thymus
37	chr11:71316400-71316600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr11:71316400-71316600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr11:71317800-71318000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:71317800-71319000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr11:71317800-71319000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:71317800-71319600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr11:71318000-71318200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
44	chr11:71318000-71318200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
45	chr11:71318000-71318200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:71318000-71318200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr11:71318000-71318400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr11:71318000-71318600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
49	chr11:71318000-71318600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
50	chr11:71318000-71318600	Bivalent Enhancer	Placenta	Placenta

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