Variant report

Variant	nsv553477
Chromosome Location	chr11:10403539-10429998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:721)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:10416170-10416381	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:10427690-10428034	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:10427623-10427993	K562	blood:	n/a	n/a
4	ATF1	chr11:10427721-10428057	K562	blood:	n/a	n/a
5	ATF1	chr11:10428531-10428836	K562	blood:	n/a	n/a
6	ATF2	chr11:10427476-10428112	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:10427584-10428087	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:10427678-10428055	K562	blood:	n/a	n/a
9	ATF3	chr11:10415795-10416789	A549	lung:	n/a	n/a
10	ATF3	chr11:10415972-10416702	A549	lung:	n/a	n/a
11	BACH1	chr11:10427668-10428146	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:10427632-10428122	K562	blood:	n/a	n/a
13	BATF	chr11:10427779-10428076	GM12878	blood:	n/a	n/a
14	BCL3	chr11:10415827-10416866	A549	lung:	n/a	n/a
15	BCL3	chr11:10416011-10416772	A549	lung:	n/a	n/a
16	BHLHE40	chr11:10409105-10409183	K562	blood:	n/a	n/a
17	BHLHE40	chr11:10427709-10428016	GM12878	blood:	n/a	n/a
18	BHLHE40	chr11:10415949-10416571	A549	lung:	n/a	n/a
19	BHLHE40	chr11:10420060-10420390	K562	blood:	n/a	n/a
20	BHLHE40	chr11:10427800-10428059	K562	blood:	n/a	n/a
21	BHLHE40	chr11:10428563-10429003	K562	blood:	n/a	n/a
22	BHLHE40	chr11:10416071-10416459	HepG2	liver:	n/a	n/a
23	BHLHE40	chr11:10414416-10414595	K562	blood:	n/a	chr11:10414507-10414520 chr11:10414509-10414518 chr11:10414509-10414518
24	BRCA1	chr11:10427709-10428064	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr11:10428716-10428744	GM12878	blood:	n/a	n/a
26	BRCA1	chr11:10428471-10428867	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr11:10420917-10421015	HepG2	liver:	n/a	n/a
28	CBX3	chr11:10427633-10428124	K562	blood:	n/a	n/a
29	CCNT2	chr11:10428561-10428785	K562	blood:	n/a	n/a
30	CEBPB	chr11:10416408-10416536	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:10428595-10428790	A549	lung:	n/a	n/a
32	CEBPB	chr11:10416164-10416668	A549	lung:	n/a	n/a
33	CEBPB	chr11:10427718-10428048	A549	lung:	n/a	chr11:10427770-10427781
34	CEBPB	chr11:10427736-10428035	K562	blood:	n/a	chr11:10427770-10427781
35	CEBPB	chr11:10427706-10427973	HepG2	liver:	n/a	chr11:10427770-10427781
36	CEBPB	chr11:10427678-10428003	A549	lung:	n/a	chr11:10427770-10427781
37	CEBPB	chr11:10408724-10408875	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:10427674-10427989	H1-hESC	embryonic stem cell:	n/a	chr11:10427770-10427781
39	CEBPB	chr11:10416143-10416656	A549	lung:	n/a	n/a
40	CEBPB	chr11:10427680-10428054	Hela-S3	cervix:	n/a	chr11:10427770-10427781
41	CEBPB	chr11:10428481-10428944	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:10427647-10428045	K562	blood:	n/a	chr11:10427770-10427781
43	CEBPB	chr11:10415975-10416827	A549	lung:	n/a	n/a
44	CEBPB	chr11:10416211-10416638	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:10427629-10428001	IMR90	lung:	n/a	chr11:10427770-10427781
46	CEBPB	chr11:10408558-10409277	IMR90	lung:	n/a	n/a
47	CEBPD	chr11:10428491-10428859	K562	blood:	n/a	n/a
48	CEBPD	chr11:10428407-10428939	K562	blood:	n/a	n/a
49	CHD1	chr11:10427699-10427740	GM12878	blood:	n/a	n/a
50	CHD2	chr11:10428579-10428899	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10408528-10408578	HCM	heart:	n/a
2	chr11:10429980-10430030	GM06990	blood:	n/a
3	chr11:10408528-10408578	HAEpiC	amniotic membrane:	n/a
4	chr11:10427964-10428014	NHDF-neo	bronchial:	n/a
5	chr11:10408528-10408578	SK-N-SH_RA	brain:	n/a
6	chr11:10408528-10408578	HCF	heart:	n/a
7	chr11:10427964-10428014	Hela-S3	cervix:	n/a
8	chr11:10416227-10416277	NHBE	bronchial:	n/a
9	chr11:10408528-10408578	SAEC	small airway:	n/a
10	chr11:10427964-10428014	HMEC	breast:	n/a
11	chr11:10429980-10430030	SK-N-MC	brain:	n/a
12	chr11:10429980-10430030	T-47D	breast:	n/a
13	chr11:10427964-10428014	AG09319	gingival:	n/a
14	chr11:10427964-10428014	Hepatocyte	liver:	n/a
15	chr11:10416227-10416277	SKMC	muscle:	n/a
16	chr11:10408528-10408578	Jurkat	blood:	n/a
17	chr11:10416227-10416277	GM12891	blood:	n/a
18	chr11:10427964-10428014	SK-N-MC	brain:	n/a
19	chr11:10427964-10428014	HRCEpiC	kidney:	n/a
20	chr11:10408528-10408578	RPTEC	kidney:	n/a
21	chr11:10408528-10408578	GM12878	blood:	n/a
22	chr11:10429980-10430030	AG10803	skin:	n/a
23	chr11:10416227-10416277	AG10803	skin:	n/a
24	chr11:10416227-10416277	PrEC	prostate:	n/a
25	chr11:10416227-10416277	HCT-116	colon:	n/a
26	chr11:10408528-10408578	ProgFib	skin:	n/a
27	chr11:10408528-10408578	HRPEpiC	eye:	n/a
28	chr11:10429980-10430030	BE2_C	brain:	n/a
29	chr11:10408528-10408578	HRE	kidney:	n/a
30	chr11:10416227-10416277	SK-N-SH	brain:	n/a
31	chr11:10416227-10416277	PFSK-1	brain:	n/a
32	chr11:10408528-10408578	HNPCEpiC	eye:	n/a
33	chr11:10429980-10430030	HRE	kidney:	n/a
34	chr11:10408528-10408578	HL-60	blood:	n/a
35	chr11:10408528-10408578	LNCaP	prostate:	n/a
36	chr11:10416227-10416277	HRE	kidney:	n/a
37	chr11:10429980-10430030	BJ	skin:	n/a
38	chr11:10416227-10416277	Hepatocyte	liver:	n/a
39	chr11:10416227-10416277	HNPCEpiC	eye:	n/a
40	chr11:10427964-10428014	CMK	blood:	n/a
41	chr11:10408528-10408578	HUVEC	blood vessel:	n/a
42	chr11:10408528-10408578	GM06990	blood:	n/a
43	chr11:10429980-10430030	HEK293	kidney:	embryo
44	chr11:10427964-10428014	HCT-116	colon:	n/a
45	chr11:10427964-10428014	Caco-2	colon:	n/a
46	chr11:10408528-10408578	NB4	blood:	n/a
47	chr11:10429980-10430030	CMK	blood:	n/a
48	chr11:10416227-10416277	HEK293	kidney:	embryo
49	chr11:10408528-10408578	GM12891	blood:	n/a
50	chr11:10427964-10428014	MCF-7	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:10410521..10412872-chr11:10414972..10416524,2	K562	blood:
2	chr11:10410521..10412872-chr11:10414972..10416524,2	K562	blood:
3	chr11:10325849..10328171-chr11:10416407..10418101,2	MCF-7	breast:
4	chr11:10427272..10428747-chr11:10756868..10757977,15	K562	blood:
5	chr11:10408455..10411116-chr11:10414237..10415892,3	MCF-7	breast:
6	chr11:10427758..10428669-chr11:10756932..10757785,3	MCF-7	breast:
7	chr11:10322917..10326761-chr11:10411066..10413981,3	MCF-7	breast:
8	chr11:10419157..10420679-chr11:10421309..10424308,2	MCF-7	breast:
9	chr11:10388047..10388889-chr11:10408886..10409883,3	MCF-7	breast:
10	chr11:10423702..10425304-chr11:10426286..10427844,2	MCF-7	breast:
11	chr11:10408455..10411116-chr11:10414237..10415892,3	MCF-7	breast:
12	chr11:10427811..10428324-chr11:10675560..10676361,2	MCF-7	breast:
13	chr11:10427762..10428619-chr11:10675503..10676394,3	K562	blood:
14	chr11:10427450..10428226-chr11:10535022..10536041,3	MCF-7	breast:
15	chr11:10423702..10425304-chr11:10426286..10427844,2	MCF-7	breast:
16	chr11:10427808..10432250-chr11:10475440..10478017,5	K562	blood:
17	chr11:10387938..10388816-chr11:10427798..10428324,2	MCF-7	breast:
18	chr11:10419157..10420679-chr11:10421309..10424308,2	MCF-7	breast:
19	chr11:10427821..10428361-chr11:10562807..10563319,2	K562	blood:
20	chr11:10414737..10416495-chr11:10419246..10421042,2	MCF-7	breast:
21	chr11:10428535..10430173-chr11:10471249..10473167,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPD3-2	chr11:10413829-10413952	NONHSAT017963
2	lnc-AMPD3-2	chr11:10413830-10413952	NONHSAT017964
3	lnc-AMPD3-2	chr11:10429915-10430052	NONHSAT017967

No data

Variant related genes	Relation type
AMPD3	TF binding region
RNU6ATAC33P	TF binding region
AMPD3	CpG island
RNU6ATAC33P	CpG island
ENSG00000254554	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000148926	chromatin interactions
ENSG00000221574	chromatin interactions
ENSG00000177112	chromatin interactions

Extended variants
information (count: 1164 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1164 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2198010	chr11:10403539-10403540	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192104122	chr11:10403548-10403549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2198009	chr11:10403577-10403578	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs536838233	chr11:10403588-10403589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184592199	chr11:10403613-10403614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576685113	chr11:10403666-10403667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368178293	chr11:10403692-10403693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2198008	chr11:10403725-10403726	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs16907739	chr11:10403757-10403758	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571686052	chr11:10403834-10403835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189378383	chr11:10403836-10403837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533518495	chr11:10403877-10403878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2957667	chr11:10403930-10403931	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574147827	chr11:10403973-10403974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201437969	chr11:10403977-10403978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573612435	chr11:10404091-10404092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543222108	chr11:10404096-10404097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs16907747	chr11:10404111-10404112	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs180774333	chr11:10404133-10404134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547293877	chr11:10404149-10404150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552163233	chr11:10404172-10404173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12792137	chr11:10404203-10404204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12786336	chr11:10404204-10404205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565313427	chr11:10404209-10404210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12792165	chr11:10404241-10404242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12787104	chr11:10404245-10404246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs66553261	chr11:10404253-10404254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373987167	chr11:10404254-10404255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs386750604	chr11:10404255-10404256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71204279	chr11:10404256-10404257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374543929	chr11:10404257-10404258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76135819	chr11:10404265-10404266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147573681	chr11:10404266-10404267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79628311	chr11:10404269-10404270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112465964	chr11:10404298-10404299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111316014	chr11:10404301-10404302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111316986	chr11:10404304-10404305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567766172	chr11:10404328-10404329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189841990	chr11:10404331-10404332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2957668	chr11:10404382-10404383	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs80144649	chr11:10404398-10404399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78270217	chr11:10404485-10404486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558971634	chr11:10404525-10404526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549069622	chr11:10404533-10404534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569237715	chr11:10404536-10404537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564734007	chr11:10404548-10404549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181442765	chr11:10404561-10404562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573418400	chr11:10404587-10404588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201239587	chr11:10404588-10404589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75264902	chr11:10404603-10404604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10391800-10403800	Enhancers	Adipose Nuclei	Adipose
2	chr11:10398000-10403800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:10398000-10404000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr11:10398000-10404000	Enhancers	Osteobl	bone
5	chr11:10399400-10403800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr11:10400600-10407200	Weak transcription	Ovary	ovary
7	chr11:10401800-10407200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:10401800-10407200	Weak transcription	Fetal Muscle Leg	muscle
9	chr11:10401800-10407200	Weak transcription	Lung	lung
10	chr11:10401800-10407200	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:10402000-10404600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:10402000-10407200	Weak transcription	Colon Smooth Muscle	Colon
13	chr11:10402000-10407200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr11:10402000-10407200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr11:10402200-10407200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr11:10402200-10407200	Weak transcription	NHDF-Ad	bronchial
17	chr11:10402800-10408400	Weak transcription	Esophagus	oesophagus
18	chr11:10403000-10407200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:10403400-10404000	Enhancers	Muscle Satellite Cultured Cells	--
20	chr11:10403400-10404200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr11:10403400-10408400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:10403800-10404600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr11:10403800-10407200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:10403800-10407200	Weak transcription	Adipose Nuclei	Adipose
25	chr11:10404000-10404600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr11:10404000-10407200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:10404000-10407200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr11:10404000-10407400	Weak transcription	Osteobl	bone
29	chr11:10404400-10404600	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr11:10404600-10407200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:10407200-10407400	Bivalent Enhancer	Fetal Stomach	stomach
32	chr11:10407200-10407600	Enhancers	Lung	lung
33	chr11:10407200-10407600	Enhancers	NHDF-Ad	bronchial
34	chr11:10407200-10407800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:10407200-10407800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr11:10407200-10408200	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr11:10407200-10408200	Enhancers	Stomach Smooth Muscle	stomach
38	chr11:10407200-10408400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr11:10407200-10408400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr11:10407200-10408600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:10407200-10408800	Enhancers	Fetal Muscle Leg	muscle
42	chr11:10407200-10410000	Enhancers	HSMM	muscle
43	chr11:10407200-10410400	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr11:10407200-10410600	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr11:10407200-10410800	Enhancers	Colon Smooth Muscle	Colon
46	chr11:10407200-10411000	Enhancers	Ovary	ovary
47	chr11:10407200-10411000	Enhancers	NHLF	lung
48	chr11:10407200-10412800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:10407200-10412800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:10407200-10412800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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