Variant report

Variant	esv2761646
Chromosome Location	chr11:5406123-5454241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:488)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:5410351-5410419	K562	blood:	n/a	n/a
2	CTCF	chr11:5411480-5411630	GM12870	blood:	n/a	n/a
3	CTCF	chr11:5411620-5411770	HCT-116	colon:	n/a	n/a
4	CTCF	chr11:5442260-5442410	Caco-2	colon:	n/a	n/a
5	CTCF	chr11:5411576-5411704	HUVEC	blood vessel:	n/a	n/a
6	CTCF	chr11:5411500-5411650	GM12864	blood:	n/a	n/a
7	CTCF	chr11:5411540-5411690	GM12869	blood:	n/a	n/a
8	CTCF	chr11:5411580-5411730	AG10803	skin:	n/a	n/a
9	CTCF	chr11:5411540-5411690	HUVEC	blood vessel:	n/a	n/a
10	CTCF	chr11:5411560-5411710	HPF	lung:	n/a	n/a
11	CTCF	chr11:5411560-5411707	K562	blood:	n/a	n/a
12	CTCF	chr11:5411600-5411750	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr11:5411500-5411650	AG04450	lung:	n/a	n/a
14	CTCF	chr11:5411620-5411770	HVMF	connective:	n/a	n/a
15	CTCF	chr11:5411520-5411670	AG09309	skin:	n/a	n/a
16	CTCF	chr11:5411540-5411690	HEK293	kidney:	n/a	n/a
17	CTCF	chr11:5411540-5411690	HMF	breast:	n/a	n/a
18	CTCF	chr11:5411580-5411730	HCT-116	colon:	n/a	n/a
19	CTCF	chr11:5411520-5411670	GM12878	blood:	n/a	n/a
20	CTCF	chr11:5411520-5411670	GM12872	blood:	n/a	n/a
21	CTCF	chr11:5411420-5411670	HFF	foreskin:	n/a	n/a
22	CTCF	chr11:5411460-5411610	NHEK	skin:	n/a	n/a
23	CTCF	chr11:5411580-5411730	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr11:5411600-5411750	NHLF	lung:	n/a	n/a
25	CTCF	chr11:5411520-5411670	AG04449	skin:	n/a	n/a
26	CTCF	chr11:5411460-5411610	RPTEC	kidney:	n/a	n/a
27	CTCF	chr11:5411460-5411610	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr11:5411680-5411830	A549	lung:	n/a	n/a
29	CTCF	chr11:5411520-5411670	HRE	kidney:	n/a	n/a
30	CTCF	chr11:5432429-5432471	Medullo	brain:	n/a	n/a
31	CTCF	chr11:5411500-5411650	K562	blood:	n/a	n/a
32	CTCF	chr11:5411540-5411690	GM12878	blood:	n/a	n/a
33	CTCF	chr11:5411580-5411730	GM12868	blood:	n/a	n/a
34	CTCF	chr11:5411480-5411630	A549	lung:	n/a	n/a
35	CTCF	chr11:5411600-5411750	BJ	skin:	n/a	n/a
36	CTCF	chr11:5411340-5411490	GM12871	blood:	n/a	n/a
37	CTCF	chr11:5411500-5411650	GM12871	blood:	n/a	n/a
38	CTCF	chr11:5411520-5411670	K562	blood:	n/a	n/a
39	CTCF	chr11:5411598-5411668	LNCaP	prostate:	n/a	n/a
40	CTCF	chr11:5411580-5411730	HPF	lung:	n/a	n/a
41	CTCF	chr11:5442220-5442370	GM12864	blood:	n/a	n/a
42	CTCF	chr11:5442187-5442520	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:5411520-5411670	HEK293	kidney:	n/a	n/a
44	CTCF	chr11:5411520-5411670	GM12874	blood:	n/a	n/a
45	CTCF	chr11:5411572-5411676	ProgFib	skin:	n/a	n/a
46	CTCF	chr11:5411480-5411630	RPTEC	kidney:	n/a	n/a
47	CTCF	chr11:5411540-5411690	AG04450	lung:	n/a	n/a
48	CTCF	chr11:5411500-5411650	HCFaa	heart:	n/a	n/a
49	CTCF	chr11:5411532-5411722	HepG2	liver:	n/a	n/a
50	CTCF	chr11:5443640-5443790	GM12871	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5433817-5433867	NH-A	brain:	n/a
2	chr11:5444223-5444273	HCT-116	colon:	n/a
3	chr11:5408788-5408838	SK-N-SH	brain:	n/a
4	chr11:5408788-5408838	T-47D	breast:	n/a
5	chr11:5410452-5410502	Caco-2	colon:	n/a
6	chr11:5410452-5410502	HL-60	blood:	n/a
7	chr11:5433817-5433867	SKMC	muscle:	n/a
8	chr11:5433817-5433867	K562	blood:	n/a
9	chr11:5442434-5442484	A549	lung:	n/a
10	chr11:5442434-5442484	GM12891	blood:	n/a
11	chr11:5410452-5410502	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:5433817-5433867	GM19239	blood:	n/a
13	chr11:5442443-5442493	GM12892	blood:	n/a
14	chr11:5442443-5442493	AG04450	lung:	fetal
15	chr11:5433817-5433867	BJ	skin:	n/a
16	chr11:5410452-5410502	NHBE	bronchial:	n/a
17	chr11:5433817-5433867	HIPEpiC	eye:	n/a
18	chr11:5444223-5444273	NB4	blood:	n/a
19	chr11:5408788-5408838	AG09319	gingival:	n/a
20	chr11:5444223-5444273	IMR90	lung:	fetal
21	chr11:5442443-5442493	ProgFib	skin:	n/a
22	chr11:5442443-5442493	NHBE	bronchial:	n/a
23	chr11:5442434-5442484	HRCEpiC	kidney:	n/a
24	chr11:5410053-5410103	PFSK-1	brain:	n/a
25	chr11:5410053-5410103	CMK	blood:	n/a
26	chr11:5442434-5442484	NT2-D1	testis:	n/a
27	chr11:5433817-5433867	ProgFib	skin:	n/a
28	chr11:5433817-5433867	HL-60	blood:	n/a
29	chr11:5442443-5442493	AG10803	skin:	n/a
30	chr11:5410053-5410103	GM12892	blood:	n/a
31	chr11:5442434-5442484	SK-N-SH_RA	brain:	n/a
32	chr11:5410053-5410103	AG09309	skin:	n/a
33	chr11:5444223-5444273	AoSMC	blood vessel:	n/a
34	chr11:5410053-5410103	PANC-1	pancreas:	n/a
35	chr11:5408788-5408838	HAEpiC	amniotic membrane:	n/a
36	chr11:5433817-5433867	NB4	blood:	n/a
37	chr11:5444223-5444273	PrEC	prostate:	n/a
38	chr11:5442443-5442493	HAEpiC	amniotic membrane:	n/a
39	chr11:5444223-5444273	MCF10A-Er-Src	breast:	n/a
40	chr11:5408788-5408838	GM12892	blood:	n/a
41	chr11:5442511-5442561	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:5442443-5442493	PFSK-1	brain:	n/a
43	chr11:5408788-5408838	HL-60	blood:	n/a
44	chr11:5433817-5433867	HRE	kidney:	n/a
45	chr11:5442511-5442561	A549	lung:	n/a
46	chr11:5410053-5410103	HIPEpiC	eye:	n/a
47	chr11:5433817-5433867	GM12891	blood:	n/a
48	chr11:5442434-5442484	PrEC	prostate:	n/a
49	chr11:5433817-5433867	MCF10A-Er-Src	breast:	n/a
50	chr11:5442434-5442484	GM12878	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:5421776-5424121..11:5425882-5426881	GM12878	blood:
2	11:5243048-5250847..11:5425882-5426881	GM12878	blood:
3	11:4778081-4789138..11:5398331-5406514	Hela-S3	cervix:
4	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
5	chr11:5454190..5457946-chr11:5459430..5461152,3	K562	blood:
6	11:4778081-4789138..11:5425882-5426881	H1-hESC	embryonic stem cell:	embryo
7	chr11:5404523..5406570-chr11:5525377..5527235,2	K562	blood:
8	chr11:5442840..5444659-chr11:5449789..5452716,3	K562	blood:
9	chr11:5403316..5405023-chr11:5406492..5408561,2	K562	blood:
10	chr11:5402054..5402614-chr11:5441811..5442439,2	MCF-7	breast:
11	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
12	11:5398331-5406514..11:5707362-5712027	K562	blood:
13	11:5243048-5250847..11:5398331-5406514	H1-hESC	embryonic stem cell:	embryo
14	chr11:5448582..5452295-chr11:5454742..5458081,4	K562	blood:
15	11:5250847-5268367..11:5398331-5406514	Hela-S3	cervix:
16	chr11:5403286..5405023-chr11:5406097..5408561,2	K562	blood:
17	11:5218976-5222789..11:5398331-5406514	GM12878	blood:
18	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:
19	chr11:5405070..5407795-chr11:5524807..5526877,2	K562	blood:
20	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:
21	11:5398331-5406514..11:5700314-5707362	GM12878	blood:
22	11:5018576-5020673..11:5398331-5406514	H1-hESC	embryonic stem cell:	embryo
23	11:5218976-5222789..11:5425882-5426881	GM12878	blood:
24	11:5146608-5154908..11:5398331-5406514	GM12878	blood:
25	chr11:5415584..5416428-chr20:41864268..41865032,2	MCF-7	breast:
26	11:5250847-5268367..11:5406514-5407716	Hela-S3	cervix:
27	11:5398331-5406514..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
OR51M1	TF binding region
OR51K1P	TF binding region
OR51J1	TF binding region
OR51Q1	TF binding region
OR51M1	CpG island
OR51K1P	CpG island
OR51J1	CpG island
OR51Q1	CpG island
ENSG00000175520	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000176798	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000184321	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000167360	chromatin interactions

Extended variants
information (count: 2693 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2693 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4910780	chr11:5406123-5406124	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534250592	chr11:5406131-5406132	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs185882822	chr11:5406135-5406136	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs58465147	chr11:5406137-5406138	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
5	rs367863861	chr11:5406188-5406189	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs563762476	chr11:5406193-5406194	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
7	rs115748935	chr11:5406221-5406222	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
8	rs191019617	chr11:5406295-5406296	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
9	rs11604520	chr11:5406314-5406315	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs149063399	chr11:5406315-5406316	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
11	rs75149603	chr11:5406336-5406337	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs77476241	chr11:5406360-5406361	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
13	rs2647557	chr11:5406383-5406384	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550198783	chr11:5406397-5406398	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
15	rs142038887	chr11:5406412-5406413	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
16	rs576674638	chr11:5406449-5406450	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs539096920	chr11:5406452-5406453	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs372518831	chr11:5406461-5406462	Weak transcription Enhancers	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
19	rs376499491	chr11:5406472-5406473	Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
20	rs147772113	chr11:5406494-5406495	Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
21	rs141172775	chr11:5406503-5406504	Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
22	rs115281094	chr11:5406518-5406519	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs146901104	chr11:5406537-5406538	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs139382870	chr11:5406546-5406547	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs542241867	chr11:5406559-5406560	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs566483559	chr11:5406579-5406580	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs181573702	chr11:5406587-5406588	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs572707739	chr11:5406591-5406592	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs140604442	chr11:5406593-5406594	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs577414560	chr11:5406639-5406640	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs368475048	chr11:5406651-5406652	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs575720426	chr11:5406675-5406676	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs114148296	chr11:5406688-5406689	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs564447366	chr11:5406724-5406725	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs199761927	chr11:5406727-5406728	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs148030461	chr11:5406733-5406734	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs35403463	chr11:5406734-5406735	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs7108979	chr11:5406735-5406736	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs386372981	chr11:5406743-5406744	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs58690573	chr11:5406744-5406745	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs200720108	chr11:5406745-5406746	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs140538305	chr11:5406773-5406774	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs536246678	chr11:5406775-5406776	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs191148260	chr11:5406776-5406777	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs529195448	chr11:5406786-5406787	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs550462843	chr11:5406824-5406825	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs150462707	chr11:5406866-5406867	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs34713315	chr11:5406901-5406902	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs10837971	chr11:5406902-5406903	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138191777	chr11:5406914-5406915	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	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
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5404400-5407400	Weak transcription	K562	blood
2	chr11:5404600-5406400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:5405400-5406800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:5405400-5408400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr11:5405400-5408600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr11:5405600-5408600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:5405800-5408400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr11:5405800-5408800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:5406000-5408400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr11:5406000-5410200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr11:5406800-5408600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:5407400-5409200	Strong transcription	K562	blood
13	chr11:5408400-5410200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr11:5408400-5410200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr11:5408400-5410400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr11:5408600-5409600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:5408600-5410000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr11:5408600-5410200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr11:5408800-5410600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:5409200-5410600	Weak transcription	K562	blood
21	chr11:5409600-5412200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:5410200-5410400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr11:5410600-5412600	Strong transcription	K562	blood
24	chr11:5411200-5411400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:5412200-5412400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:5412600-5415000	Weak transcription	K562	blood
27	chr11:5415000-5417000	Strong transcription	K562	blood
28	chr11:5415800-5417000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:5417000-5417400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:5417000-5420000	Weak transcription	K562	blood
31	chr11:5417400-5420800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:5420000-5423000	Strong transcription	K562	blood
33	chr11:5420800-5421000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:5422000-5422200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr11:5423000-5424200	Weak transcription	K562	blood
36	chr11:5424200-5425800	Strong transcription	K562	blood
37	chr11:5425800-5432400	Weak transcription	K562	blood
38	chr11:5429600-5430000	Enhancers	Fetal Kidney	kidney
39	chr11:5432400-5433400	Enhancers	K562	blood
40	chr11:5433000-5433400	Enhancers	Hela-S3	cervix
41	chr11:5433200-5433600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr11:5433200-5433800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr11:5433400-5433600	Flanking Active TSS	K562	blood
44	chr11:5433400-5433800	Active TSS	A549	lung
45	chr11:5433600-5433800	Active TSS	K562	blood
46	chr11:5433600-5434000	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr11:5433800-5434400	Enhancers	K562	blood
48	chr11:5434400-5440400	Weak transcription	K562	blood
49	chr11:5440400-5441200	Strong transcription	K562	blood
50	chr11:5441200-5442400	Weak transcription	K562	blood

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