Variant report

Variant	nsv1036041
Chromosome Location	chr11:10131018-10212202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:392)
CpG islands
(count:245)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:10203415-10203703	K562	blood:	n/a	n/a
2	ARID3A	chr11:10203333-10203847	HepG2	liver:	n/a	n/a
3	ATF1	chr11:10182066-10182228	K562	blood:	n/a	n/a
4	ATF1	chr11:10186277-10186339	K562	blood:	n/a	n/a
5	BACH1	chr11:10177754-10177829	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:10207839-10207853	K562	blood:	n/a	n/a
7	BHLHE40	chr11:10176193-10176271	GM12878	blood:	n/a	n/a
8	CBX3	chr11:10144271-10144854	HCT-116	colon:	n/a	n/a
9	CEBPB	chr11:10143960-10144805	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:10135431-10135757	HepG2	liver:	n/a	chr11:10135580-10135591
11	CEBPB	chr11:10147371-10147680	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:10166519-10166863	HepG2	liver:	n/a	chr11:10166695-10166706
13	CEBPB	chr11:10141474-10141706	IMR90	lung:	n/a	chr11:10141564-10141575
14	CEBPB	chr11:10141415-10141659	A549	lung:	n/a	chr11:10141564-10141575
15	CEBPB	chr11:10166528-10166850	K562	blood:	n/a	chr11:10166695-10166706
16	CEBPB	chr11:10141255-10141743	Hela-S3	cervix:	n/a	chr11:10141564-10141575
17	CEBPB	chr11:10166575-10166867	A549	lung:	n/a	chr11:10166695-10166706
18	CEBPB	chr11:10166583-10166853	H1-hESC	embryonic stem cell:	n/a	chr11:10166695-10166706
19	CEBPB	chr11:10147381-10147667	A549	lung:	n/a	n/a
20	CEBPB	chr11:10147449-10147593	K562	blood:	n/a	n/a
21	CEBPB	chr11:10204058-10204245	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:10135417-10135774	K562	blood:	n/a	chr11:10135580-10135591
23	CEBPB	chr11:10166536-10166870	Hela-S3	cervix:	n/a	chr11:10166695-10166706
24	CEBPB	chr11:10135435-10135750	IMR90	lung:	n/a	chr11:10135580-10135591
25	CEBPB	chr11:10139197-10139756	Hela-S3	cervix:	n/a	chr11:10139340-10139353 chr11:10139340-10139351 chr11:10139340-10139353
26	CEBPB	chr11:10148634-10148759	K562	blood:	n/a	chr11:10148667-10148678
27	CEBPB	chr11:10147351-10147700	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:10206080-10206154	K562	blood:	n/a	n/a
29	CEBPB	chr11:10184864-10184871	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:10131374-10131662	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:10161150-10161470	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:10166514-10166854	IMR90	lung:	n/a	chr11:10166695-10166706
33	CEBPB	chr11:10206098-10206168	A549	lung:	n/a	n/a
34	CEBPB	chr11:10135476-10135725	H1-hESC	embryonic stem cell:	n/a	chr11:10135580-10135591
35	CEBPB	chr11:10135437-10135736	A549	lung:	n/a	chr11:10135580-10135591
36	CEBPB	chr11:10171181-10171452	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:10147397-10147582	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:10141450-10141735	HepG2	liver:	n/a	chr11:10141564-10141575
39	CEBPB	chr11:10171231-10171437	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:10148529-10148805	HepG2	liver:	n/a	chr11:10148667-10148678
41	CEBPB	chr11:10135438-10135764	Hela-S3	cervix:	n/a	chr11:10135580-10135591
42	CEBPB	chr11:10148534-10148812	IMR90	lung:	n/a	chr11:10148667-10148678
43	CTCF	chr11:10203440-10203590	AG04449	skin:	n/a	chr11:10203529-10203550 chr11:10203527-10203545
44	CTCF	chr11:10203520-10203670	HCM	heart:	n/a	chr11:10203529-10203550 chr11:10203527-10203545
45	CTCF	chr11:10203361-10203722	IMR90	lung:	n/a	chr11:10203529-10203550 chr11:10203527-10203545
46	CTCF	chr11:10203460-10203610	BJ	skin:	n/a	chr11:10203529-10203550 chr11:10203527-10203545
47	CTCF	chr11:10203520-10203670	RPTEC	kidney:	n/a	chr11:10203529-10203550 chr11:10203527-10203545
48	CTCF	chr11:10203480-10203630	HMF	breast:	n/a	chr11:10203529-10203550 chr11:10203527-10203545
49	CTCF	chr11:10203480-10203630	AG04449	skin:	n/a	chr11:10203529-10203550 chr11:10203527-10203545
50	CTCF	chr11:10203420-10203570	Hela-S3	cervix:	n/a	chr11:10203529-10203550 chr11:10203527-10203545

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10209919-10209969	HCT-116	colon:	n/a
2	chr11:10209919-10209969	HCT-116	colon:	n/a
3	chr11:10194996-10195046	AG04449	skin:	fetal
4	chr11:10154929-10154979	HCPEpiC	choroid plexus:	n/a
5	chr11:10154929-10154979	AoSMC	blood vessel:	n/a
6	chr11:10209919-10209969	HCF	heart:	n/a
7	chr11:10161484-10161534	HL-60	blood:	n/a
8	chr11:10194996-10195046	HL-60	blood:	n/a
9	chr11:10154929-10154979	ProgFib	skin:	n/a
10	chr11:10209919-10209969	RPTEC	kidney:	n/a
11	chr11:10161484-10161534	HAEpiC	amniotic membrane:	n/a
12	chr11:10209919-10209969	HepG2	liver:	n/a
13	chr11:10154929-10154979	A549	lung:	n/a
14	chr11:10194996-10195046	SKMC	muscle:	n/a
15	chr11:10209919-10209969	SAEC	small airway:	n/a
16	chr11:10154929-10154979	AG04450	lung:	fetal
17	chr11:10209919-10209969	U87	brain:	n/a
18	chr11:10161484-10161534	AG04450	lung:	fetal
19	chr11:10154929-10154979	HMEC	breast:	n/a
20	chr11:10209919-10209969	ovcar-3	ovarian:	n/a
21	chr11:10154929-10154979	HAEpiC	amniotic membrane:	n/a
22	chr11:10154929-10154979	HEEpiC	esophagus:	n/a
23	chr11:10194996-10195046	HEK293	kidney:	embryo
24	chr11:10154929-10154979	SKMC	muscle:	n/a
25	chr11:10194996-10195046	A549	lung:	n/a
26	chr11:10209919-10209969	Caco-2	colon:	n/a
27	chr11:10161484-10161534	HepG2	liver:	n/a
28	chr11:10194996-10195046	HMEC	breast:	n/a
29	chr11:10194996-10195046	ECC-1	luminal epithelium:	n/a
30	chr11:10209919-10209969	MCF-7	breast:	n/a
31	chr11:10194996-10195046	NB4	blood:	n/a
32	chr11:10161484-10161534	AG09319	gingival:	n/a
33	chr11:10154929-10154979	HUVEC	blood vessel:	n/a
34	chr11:10194996-10195046	Caco-2	colon:	n/a
35	chr11:10209919-10209969	CMK	blood:	n/a
36	chr11:10154929-10154979	NH-A	brain:	n/a
37	chr11:10194996-10195046	HCT-116	colon:	n/a
38	chr11:10194996-10195046	U87	brain:	n/a
39	chr11:10161484-10161534	NHBE	bronchial:	n/a
40	chr11:10194996-10195046	AG10803	skin:	n/a
41	chr11:10209919-10209969	HRE	kidney:	n/a
42	chr11:10161484-10161534	HNPCEpiC	eye:	n/a
43	chr11:10209919-10209969	SKMC	muscle:	n/a
44	chr11:10209919-10209969	H1-hESC	embryonic stem cell:	embryo
45	chr11:10209919-10209969	AG09309	skin:	n/a
46	chr11:10154929-10154979	GM12892	blood:	n/a
47	chr11:10194996-10195046	HEEpiC	esophagus:	n/a
48	chr11:10194996-10195046	AG09309	skin:	n/a
49	chr11:10209919-10209969	GM12892	blood:	n/a
50	chr11:10194996-10195046	HRPEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:10129087..10131222-chr11:10133484..10136579,3	MCF-7	breast:
2	chr11:10136561..10138179-chr11:10323345..10325457,2	MCF-7	breast:
3	chr11:10207800..10209876-chr11:10313858..10315934,3	MCF-7	breast:
4	chr11:10205279..10207435-chr11:10325755..10328065,2	MCF-7	breast:
5	chr11:10203406..10203971-chr11:10344330..10345190,2	K562	blood:
6	chr11:10129087..10131222-chr11:10133484..10136579,3	MCF-7	breast:
7	chr11:10203351..10204041-chr11:10328716..10329800,3	MCF-7	breast:
8	chr11:10201975..10204462-chr11:10314656..10317038,3	MCF-7	breast:
9	chr11:10142764..10144683-chr11:10146496..10148132,2	MCF-7	breast:
10	chr11:10208315..10210271-chr11:10216958..10218674,2	K562	blood:
11	chr11:10186305..10188747-chr11:10324257..10326433,2	MCF-7	breast:
12	chr11:10200393..10205018-chr11:10324375..10327775,4	MCF-7	breast:
13	chr11:10142764..10144683-chr11:10146496..10148132,2	MCF-7	breast:
14	chr11:10207701..10209202-chr11:10322854..10324747,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADM-2	chr11:10170739-10171109	ENSG00000254865.1
2	lnc-ADM-2	chr11:10186506-10186656	ENSG00000254865.1

No data

Variant related genes	Relation type
ENSG00000254865	TF binding region
ENSG00000254865	CpG island
ENSG00000148926	chromatin interactions
ENSG00000254554	chromatin interactions
ENSG00000133812	chromatin interactions

Extended variants
information (count: 3192 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3192 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562069733	chr11:10131030-10131031	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs34799966	chr11:10131048-10131049	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs143006560	chr11:10131055-10131056	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs76527160	chr11:10131090-10131091	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs541680665	chr11:10131123-10131124	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs561508246	chr11:10131169-10131170	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs530600997	chr11:10131189-10131190	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs530716622	chr11:10131214-10131215	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs544125659	chr11:10131215-10131216	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs148171560	chr11:10131218-10131219	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs16907460	chr11:10131270-10131271	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs12799068	chr11:10131342-10131343	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569045395	chr11:10131345-10131346	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs570721835	chr11:10131358-10131359	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs2044146	chr11:10131411-10131412	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs539353866	chr11:10131446-10131447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181444811	chr11:10131492-10131493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528553520	chr11:10131494-10131495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185051903	chr11:10131511-10131512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568699460	chr11:10131592-10131593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537639481	chr11:10131619-10131620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557728328	chr11:10131633-10131634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571115163	chr11:10131634-10131635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534138761	chr11:10131669-10131670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141085706	chr11:10131723-10131724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552904210	chr11:10131725-10131726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145127107	chr11:10131762-10131763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189093744	chr11:10131796-10131797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376066657	chr11:10131817-10131818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541939581	chr11:10131877-10131878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555019729	chr11:10131895-10131896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181804944	chr11:10131898-10131899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369135481	chr11:10131911-10131912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186576257	chr11:10131943-10131944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567275973	chr11:10131973-10131974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189844551	chr11:10132006-10132007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs180986087	chr11:10132047-10132048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1822290	chr11:10132077-10132078	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528455009	chr11:10132107-10132108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12786436	chr11:10132137-10132138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568558708	chr11:10132179-10132180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200532784	chr11:10132180-10132181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186448796	chr11:10132186-10132187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551147962	chr11:10132229-10132230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191048786	chr11:10132257-10132258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76405787	chr11:10132272-10132273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183360325	chr11:10132305-10132306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540090800	chr11:10132353-10132354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558364680	chr11:10132386-10132387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142089190	chr11:10132451-10132452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10120400-10142800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:10121400-10131200	Weak transcription	Liver	Liver
3	chr11:10122200-10144200	Weak transcription	Left Ventricle	heart
4	chr11:10122200-10156400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:10122400-10131200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:10122400-10138600	Weak transcription	Esophagus	oesophagus
7	chr11:10122800-10132800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:10122800-10141200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr11:10122800-10142600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:10123200-10156400	Weak transcription	Fetal Intestine Small	intestine
11	chr11:10126200-10143000	Weak transcription	Ovary	ovary
12	chr11:10128800-10132200	Enhancers	Colon Smooth Muscle	Colon
13	chr11:10128800-10132200	Enhancers	Fetal Heart	heart
14	chr11:10129000-10131400	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr11:10129000-10131800	Enhancers	Adipose Nuclei	Adipose
16	chr11:10129000-10131800	Enhancers	Rectal Smooth Muscle	rectum
17	chr11:10129000-10132400	Enhancers	Osteobl	bone
18	chr11:10130200-10131200	Enhancers	Fetal Muscle Leg	muscle
19	chr11:10130400-10131200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr11:10130400-10131400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:10130400-10131400	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr11:10130400-10131800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:10130400-10132000	Enhancers	Muscle Satellite Cultured Cells	--
24	chr11:10130400-10132200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:10130400-10133000	Enhancers	NHLF	lung
26	chr11:10130600-10131400	Enhancers	Stomach Smooth Muscle	stomach
27	chr11:10130600-10131800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr11:10130800-10131600	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr11:10130800-10131800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr11:10130800-10131800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:10130800-10131800	Enhancers	Fetal Lung	lung
32	chr11:10130800-10131800	Enhancers	HSMM	muscle
33	chr11:10130800-10132000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:10130800-10132200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr11:10130800-10132600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:10130800-10132600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:10131000-10131200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr11:10131000-10131200	Enhancers	Aorta	Aorta
39	chr11:10131000-10131200	Enhancers	Gastric	stomach
40	chr11:10131000-10131200	Enhancers	Psoas Muscle	Psoas
41	chr11:10131000-10131400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr11:10131000-10131400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:10131000-10131400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:10131000-10131400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr11:10131000-10131400	Flanking Active TSS	HSMMtube	muscle
46	chr11:10131000-10131400	Flanking Active TSS	NHDF-Ad	bronchial
47	chr11:10131000-10131600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr11:10131000-10131600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr11:10131000-10131600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr11:10131000-10131600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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