Variant report

Variant	esv34012
Chromosome Location	chr11:24831174-25090774
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:183)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:25081871-25082042	K562	blood:	n/a	n/a
2	ATF1	chr11:25009070-25009258	K562	blood:	n/a	n/a
3	CBX3	chr11:25021767-25022037	K562	blood:	n/a	n/a
4	CEBPB	chr11:25039134-25039334	HepG2	liver:	n/a	chr11:25039206-25039217
5	CEBPB	chr11:24956664-24957013	HepG2	liver:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
6	CEBPB	chr11:25059803-25060143	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr11:25086865-25087560	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:24989156-24989385	HepG2	liver:	n/a	chr11:24989268-24989279
9	CEBPB	chr11:24956631-24956949	A549	lung:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
10	CEBPB	chr11:24858166-24858525	Hela-S3	cervix:	n/a	chr11:24858338-24858349
11	CEBPB	chr11:24891643-24891951	Hela-S3	cervix:	n/a	chr11:24891795-24891806 chr11:24891793-24891804
12	CEBPB	chr11:24842125-24842480	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:24858194-24858509	A549	lung:	n/a	chr11:24858338-24858349
14	CEBPB	chr11:24842090-24842551	IMR90	lung:	n/a	n/a
15	CEBPB	chr11:24842234-24842452	A549	lung:	n/a	n/a
16	CEBPB	chr11:24858200-24858510	HepG2	liver:	n/a	chr11:24858338-24858349
17	CEBPB	chr11:24956653-24956941	Hela-S3	cervix:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
18	CEBPB	chr11:24985312-24985746	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:25087024-25087563	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:25039084-25039295	Hela-S3	cervix:	n/a	chr11:25039206-25039217
21	CEBPB	chr11:24987290-24987705	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:24956512-24957036	IMR90	lung:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
23	CEBPB	chr11:24999430-24999689	HepG2	liver:	n/a	chr11:24999574-24999585 chr11:24999555-24999566 chr11:24999597-24999610
24	CEBPB	chr11:24956492-24956973	H1-hESC	embryonic stem cell:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
25	CEBPB	chr11:24891615-24891858	HepG2	liver:	n/a	chr11:24891795-24891806 chr11:24891793-24891804
26	CEBPB	chr11:24858210-24858508	IMR90	lung:	n/a	chr11:24858338-24858349
27	CEBPB	chr11:24863857-24864208	HepG2	liver:	n/a	chr11:24864031-24864042 chr11:24864031-24864040 chr11:24864029-24864040
28	CEBPZ	chr11:24883085-24883227	HepG2	liver:	n/a	n/a
29	CTCF	chr11:25026600-25026750	HCFaa	heart:	n/a	n/a
30	CTCF	chr11:24866464-24866705	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:24866560-24866710	SAEC	small airway:	n/a	n/a
32	CTCF	chr11:24866580-24866730	NHEK	skin:	n/a	n/a
33	CTCF	chr11:24866540-24866690	HEK293	kidney:	n/a	n/a
34	CTCF	chr11:24866498-24866673	GM12891	blood:	n/a	n/a
35	CTCF	chr11:24913602-24913652	GM10266	blood:	n/a	n/a
36	CTCF	chr11:24866500-24866650	HL-60	blood:	n/a	n/a
37	CTCF	chr11:24922120-24922270	HAc	cerebellar:	n/a	n/a
38	CTCF	chr11:24866420-24866570	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr11:24866500-24866650	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr11:24866540-24866690	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr11:25077081-25077165	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr11:24866500-24866650	HepG2	liver:	n/a	n/a
43	CTCF	chr11:24866520-24866670	GM12873	blood:	n/a	n/a
44	CTCF	chr11:24866520-24866670	GM12867	blood:	n/a	n/a
45	CTCF	chr11:24866500-24866650	GM12871	blood:	n/a	n/a
46	CTCF	chr11:25005560-25005710	HPF	lung:	n/a	n/a
47	CTCF	chr11:24866512-24866650	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr11:24866478-24866688	GM19238	blood:	n/a	n/a
49	CTCF	chr11:24866440-24866590	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr11:25050560-25050577	LNCaP	prostate:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:25070714-25070764	K562	blood:	n/a
2	chr11:25001602-25001652	AG09319	gingival:	n/a
3	chr11:25001602-25001652	NB4	blood:	n/a
4	chr11:25070714-25070764	AG10803	skin:	n/a
5	chr11:25001602-25001652	ECC-1	luminal epithelium:	n/a
6	chr11:25001602-25001652	HEK293	kidney:	embryo
7	chr11:25001602-25001652	BJ	skin:	n/a
8	chr11:25070714-25070764	HL-60	blood:	n/a
9	chr11:25001602-25001652	PFSK-1	brain:	n/a
10	chr11:24849257-24849307	SK-N-SH_RA	brain:	n/a
11	chr11:25001602-25001652	ProgFib	skin:	n/a
12	chr11:24849257-24849307	HCM	heart:	n/a
13	chr11:25001602-25001652	H1-hESC	embryonic stem cell:	embryo
14	chr11:25001602-25001652	SK-N-SH_RA	brain:	n/a
15	chr11:25070714-25070764	Caco-2	colon:	n/a
16	chr11:24849257-24849307	MCF10A-Er-Src	breast:	n/a
17	chr11:25001602-25001652	MCF-7	breast:	n/a
18	chr11:25001602-25001652	K562	blood:	n/a
19	chr11:25001602-25001652	RPTEC	kidney:	n/a
20	chr11:25070714-25070764	GM12891	blood:	n/a
21	chr11:25070714-25070764	CMK	blood:	n/a
22	chr11:25001602-25001652	HL-60	blood:	n/a
23	chr11:25070714-25070764	BJ	skin:	n/a
24	chr11:25001602-25001652	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:25070714-25070764	RPTEC	kidney:	n/a
26	chr11:24849257-24849307	LNCaP	prostate:	n/a
27	chr11:24849257-24849307	PANC-1	pancreas:	n/a
28	chr11:24849257-24849307	HCPEpiC	choroid plexus:	n/a
29	chr11:24849257-24849307	SK-N-SH	brain:	n/a
30	chr11:25001602-25001652	HCT-116	colon:	n/a
31	chr11:24849257-24849307	NH-A	brain:	n/a
32	chr11:24849257-24849307	Jurkat	blood:	n/a
33	chr11:24849257-24849307	BJ	skin:	n/a
34	chr11:24849257-24849307	GM12878	blood:	n/a
35	chr11:25001602-25001652	HNPCEpiC	eye:	n/a
36	chr11:25070714-25070764	MCF-7	breast:	n/a
37	chr11:25070714-25070764	HCF	heart:	n/a
38	chr11:25001602-25001652	HCM	heart:	n/a
39	chr11:25070714-25070764	SK-N-MC	brain:	n/a
40	chr11:24849257-24849307	HepG2	liver:	n/a
41	chr11:24849257-24849307	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:25001602-25001652	HCF	heart:	n/a
43	chr11:24849257-24849307	HIPEpiC	eye:	n/a
44	chr11:24849257-24849307	GM19239	blood:	n/a
45	chr11:24849257-24849307	AG09309	skin:	n/a
46	chr11:24849257-24849307	T-47D	breast:	n/a
47	chr11:25001602-25001652	SK-N-SH	brain:	n/a
48	chr11:25001602-25001652	SAEC	small airway:	n/a
49	chr11:24849257-24849307	AG04450	lung:	fetal
50	chr11:25001602-25001652	GM12892	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:24884268..24885897-chr11:24886910..24889026,2	K562	blood:
2	chr11:24963255..24966039-chr11:24972736..24975455,2	MCF-7	breast:
3	chr11:24946469..24947067-chr5:172264421..172265010,2	MCF-7	breast:
4	chr11:24963255..24966039-chr11:24972736..24975455,2	MCF-7	breast:
5	chr11:24849820..24852040-chr11:24856564..24859378,2	MCF-7	breast:
6	chr11:24996714..24999047-chr11:25009138..25011539,2	K562	blood:
7	chr11:24903396..24905343-chr11:24907051..24909322,2	MCF-7	breast:
8	chr11:24903396..24905343-chr11:24907051..24909322,2	MCF-7	breast:
9	chr11:24849820..24852040-chr11:24856564..24859378,2	MCF-7	breast:
10	chr11:25033492..25034324-chr14:24994179..24994819,2	MCF-7	breast:
11	chr11:22849480..22851377-chr11:25062549..25065391,2	K562	blood:
12	chr11:24884268..24885897-chr11:24886910..24889026,2	K562	blood:
13	chr11:24996714..24999047-chr11:25009138..25011539,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANO3-5	chr11:24913311-24913474	NONHSAT018440
2	lnc-ANO3-5	chr11:24913775-24914067	NONHSAT018440

No data

Variant related genes	Relation type
LUZP2	TF binding region
LUZP2	CpG island
ENSG00000246225	chromatin interactions
ENSG00000198168	chromatin interactions

Extended variants
information (count: 4043 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4043 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149835764	chr11:24832000-24832001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2716474	chr11:24832009-24832010	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs77417860	chr11:24832014-24832015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529231863	chr11:24832050-24832051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113040631	chr11:24832072-24832073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76481711	chr11:24832076-24832077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10631751	chr11:24832092-24832093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528371633	chr11:24832120-24832121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73426036	chr11:24832145-24832146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571344489	chr11:24832174-24832175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80222151	chr11:24832246-24832247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550383571	chr11:24832256-24832257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79079324	chr11:24832283-24832284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575756591	chr11:24832285-24832286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574964492	chr11:24832347-24832348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530769189	chr11:24832401-24832402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553027924	chr11:24832402-24832403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72886133	chr11:24832443-24832444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs542103795	chr11:24832447-24832448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs578109880	chr11:24832458-24832459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544027176	chr11:24832461-24832462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563404239	chr11:24832507-24832508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573816346	chr11:24832509-24832510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147670831	chr11:24832538-24832539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149130096	chr11:24832633-24832634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2716475	chr11:24832707-24832708	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs12294826	chr11:24832715-24832716	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs184570036	chr11:24832745-24832746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72886135	chr11:24832854-24832855	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550768134	chr11:24832855-24832856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145878168	chr11:24832890-24832891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368444926	chr11:24832892-24832893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546588107	chr11:24832896-24832897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567342855	chr11:24832909-24832910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536358276	chr11:24832955-24832956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546581044	chr11:24832979-24832980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369870712	chr11:24833003-24833004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566468975	chr11:24833005-24833006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538677715	chr11:24833050-24833051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560585853	chr11:24833056-24833057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560495552	chr11:24833084-24833085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs578206128	chr11:24833121-24833122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372252924	chr11:24833134-24833135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143228102	chr11:24833140-24833141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189810279	chr11:24833141-24833142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573755379	chr11:24833162-24833163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12277087	chr11:24833171-24833172	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559467584	chr11:24833182-24833183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148334567	chr11:24833237-24833238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573133563	chr11:24833261-24833262	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24832000-24832600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:24832600-24834600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr11:24832800-24833200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:24832800-24833200	Enhancers	Adipose Nuclei	Adipose
5	chr11:24832800-24833400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:24841600-24842400	Enhancers	Stomach Mucosa	stomach
7	chr11:24843800-24844800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr11:24844800-24850000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr11:24848000-24848200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:24848200-24849400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:24849400-24850000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:24850000-24850800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr11:24850000-24851000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr11:24850000-24851000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:24850000-24851600	Enhancers	Fetal Heart	heart
16	chr11:24850000-24851600	Enhancers	HUVEC	blood vessel
17	chr11:24850200-24850400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr11:24850200-24850600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr11:24850200-24850600	Enhancers	Pancreas	Pancrea
20	chr11:24850200-24850600	Enhancers	Stomach Mucosa	stomach
21	chr11:24850200-24850800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:24850200-24851000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr11:24850200-24851000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr11:24850200-24851000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr11:24850200-24851000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr11:24850200-24851200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:24850200-24851400	Enhancers	Fetal Lung	lung
28	chr11:24850400-24851000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr11:24850400-24851200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:24850400-24851400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr11:24850400-24851400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr11:24851000-24851200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr11:24851000-24851400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:24851000-24858000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr11:24851200-24854400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr11:24851400-24854400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:24851400-24855000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr11:24851600-24853000	Weak transcription	Fetal Heart	heart
39	chr11:24851600-24854400	Weak transcription	HUVEC	blood vessel
40	chr11:24853000-24853200	Enhancers	Fetal Heart	heart
41	chr11:24854200-24855400	Enhancers	Primary hematopoietic stem cells	blood
42	chr11:24854400-24854800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:24854400-24855000	Enhancers	HUVEC	blood vessel
44	chr11:24854400-24855600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr11:24854800-24855600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:24855000-24855400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:24855000-24855600	Flanking Active TSS	HUVEC	blood vessel
48	chr11:24855600-24855800	Enhancers	HUVEC	blood vessel
49	chr11:24858000-24858800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr11:24862800-24863400	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links