Variant report

Variant	nsv1041957
Chromosome Location	chr11:4213658-4470615
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:1220)
Chromatin interactive
region (count:22)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4414807-4414899	K562	blood:	n/a	n/a
2	ARID3A	chr11:4216109-4216597	K562	blood:	n/a	n/a
3	ATF1	chr11:4216207-4216475	K562	blood:	n/a	n/a
4	ATF1	chr11:4390381-4390439	K562	blood:	n/a	n/a
5	ATF1	chr11:4218126-4218315	K562	blood:	n/a	n/a
6	BACH1	chr11:4414833-4414853	K562	blood:	n/a	n/a
7	BACH1	chr11:4224962-4225178	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:4233294-4233648	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
10	BHLHE40	chr11:4414481-4415312	K562	blood:	n/a	n/a
11	BHLHE40	chr11:4414521-4415025	GM12878	blood:	n/a	n/a
12	BRCA1	chr11:4414033-4414430	GM12878	blood:	n/a	n/a
13	CBX3	chr11:4414728-4415145	K562	blood:	n/a	n/a
14	CCNT2	chr11:4414788-4415241	K562	blood:	n/a	n/a
15	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
16	CEBPB	chr11:4257965-4258134	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
17	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
18	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
19	CEBPB	chr11:4216252-4216447	K562	blood:	n/a	n/a
20	CEBPB	chr11:4455134-4455441	HepG2	liver:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
21	CEBPB	chr11:4389257-4389322	K562	blood:	n/a	n/a
22	CEBPB	chr11:4257961-4258189	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
23	CEBPB	chr11:4464273-4464473	HepG2	liver:	n/a	chr11:4464335-4464348 chr11:4464336-4464347
24	CEBPB	chr11:4412752-4412927	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:4228834-4228864	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:4232604-4232820	IMR90	lung:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
27	CEBPB	chr11:4364891-4364954	IMR90	lung:	n/a	n/a
28	CEBPB	chr11:4389067-4389386	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:4257958-4258231	HepG2	liver:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
30	CEBPB	chr11:4455124-4455430	A549	lung:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
31	CEBPB	chr11:4439846-4440117	Hela-S3	cervix:	n/a	chr11:4439975-4439986
32	CEBPB	chr11:4232611-4232857	HepG2	liver:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
33	CEBPB	chr11:4455143-4455440	IMR90	lung:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
34	CEBPB	chr11:4347779-4347817	A549	lung:	n/a	n/a
35	CEBPB	chr11:4435904-4436216	HepG2	liver:	n/a	chr11:4436054-4436063 chr11:4436052-4436063
36	CEBPB	chr11:4233297-4233351	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:4439808-4440108	HepG2	liver:	n/a	chr11:4439975-4439986
38	CEBPB	chr11:4397733-4397989	A549	lung:	n/a	chr11:4397814-4397825 chr11:4397815-4397826 chr11:4397814-4397827
39	CEBPB	chr11:4455223-4455382	K562	blood:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
40	CEBPB	chr11:4232578-4232904	K562	blood:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
41	CEBPB	chr11:4397725-4397972	K562	blood:	n/a	chr11:4397814-4397825 chr11:4397815-4397826 chr11:4397814-4397827
42	CEBPB	chr11:4364746-4365100	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:4414706-4415174	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:4397708-4397983	HepG2	liver:	n/a	chr11:4397814-4397825 chr11:4397815-4397826 chr11:4397814-4397827
45	CEBPD	chr11:4216067-4216617	K562	blood:	n/a	n/a
46	CEBPD	chr11:4353152-4353568	K562	blood:	n/a	n/a
47	CEBPD	chr11:4216035-4216623	K562	blood:	n/a	n/a
48	CHD2	chr11:4414392-4415091	GM12878	blood:	n/a	n/a
49	CHD2	chr11:4414519-4415147	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr11:4414585-4415124	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4469604-4469654	PANC-1	pancreas:	n/a
2	chr11:4469604-4469654	HRE	kidney:	n/a
3	chr11:4407026-4407076	Caco-2	colon:	n/a
4	chr11:4233502-4233552	MCF10A-Er-Src	breast:	n/a
5	chr11:4469073-4469123	PFSK-1	brain:	n/a
6	chr11:4259129-4259179	SK-N-SH	brain:	n/a
7	chr11:4415245-4415295	GM06990	blood:	n/a
8	chr11:4390195-4390245	HCT-116	colon:	n/a
9	chr11:4415245-4415295	HNPCEpiC	eye:	n/a
10	chr11:4390195-4390245	Jurkat	blood:	n/a
11	chr11:4390240-4390290	Hepatocyte	liver:	n/a
12	chr11:4407026-4407076	LNCaP	prostate:	n/a
13	chr11:4390263-4390313	HCT-116	colon:	n/a
14	chr11:4389638-4389688	SK-N-SH_RA	brain:	n/a
15	chr11:4390240-4390290	NH-A	brain:	n/a
16	chr11:4469604-4469654	HEK293	kidney:	embryo
17	chr11:4469604-4469654	HCT-116	colon:	n/a
18	chr11:4389408-4389458	IMR90	lung:	fetal
19	chr11:4469604-4469654	SK-N-SH	brain:	n/a
20	chr11:4389638-4389688	Caco-2	colon:	n/a
21	chr11:4407026-4407076	PrEC	prostate:	n/a
22	chr11:4389408-4389458	HUVEC	blood vessel:	n/a
23	chr11:4414916-4414966	A549	lung:	n/a
24	chr11:4389856-4389906	HL-60	blood:	n/a
25	chr11:4258933-4258983	BE2_C	brain:	n/a
26	chr11:4469894-4469944	AoSMC	blood vessel:	n/a
27	chr11:4389856-4389906	IMR90	lung:	fetal
28	chr11:4407026-4407076	SK-N-MC	brain:	n/a
29	chr11:4469894-4469944	U87	brain:	n/a
30	chr11:4389638-4389688	NHDF-neo	bronchial:	n/a
31	chr11:4469604-4469654	HCF	heart:	n/a
32	chr11:4415245-4415295	HRE	kidney:	n/a
33	chr11:4389638-4389688	HUVEC	blood vessel:	n/a
34	chr11:4233502-4233552	NB4	blood:	n/a
35	chr11:4469604-4469654	AG10803	skin:	n/a
36	chr11:4259129-4259179	Caco-2	colon:	n/a
37	chr11:4456403-4456453	NT2-D1	testis:	n/a
38	chr11:4407026-4407076	A549	lung:	n/a
39	chr11:4469073-4469123	A549	lung:	n/a
40	chr11:4390195-4390245	AG09309	skin:	n/a
41	chr11:4388493-4388543	MCF10A-Er-Src	breast:	n/a
42	chr11:4389856-4389906	HEEpiC	esophagus:	n/a
43	chr11:4415203-4415253	AG09319	gingival:	n/a
44	chr11:4415245-4415295	PrEC	prostate:	n/a
45	chr11:4407026-4407076	GM12891	blood:	n/a
46	chr11:4407026-4407076	HCPEpiC	choroid plexus:	n/a
47	chr11:4388493-4388543	HRCEpiC	kidney:	n/a
48	chr11:4414916-4414966	HepG2	liver:	n/a
49	chr11:4415203-4415253	AG09309	skin:	n/a
50	chr11:4259129-4259179	AG04450	lung:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4453118..4455290-chr11:4455987..4457955,2	MCF-7	breast:
2	chr11:4441835..4444233-chr11:4445411..4447480,2	K562	blood:
3	chr11:4397541..4399241-chr11:4403401..4406097,2	K562	blood:
4	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
5	chr11:4441835..4444233-chr11:4445411..4447480,2	K562	blood:
6	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
7	chr11:4414486..4415099-chr9:33264253..33265106,2	HCT-116	colon:
8	chr11:4402110..4404126-chr11:4484207..4486605,2	K562	blood:
9	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
10	chr11:4403224..4406199-chr11:4413436..4415508,2	K562	blood:
11	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
12	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
13	chr11:4408168..4410098-chr11:4413197..4414944,2	K562	blood:
14	chr11:4451655..4453436-chr11:4454768..4456529,2	K562	blood:
15	chr11:4228086..4230506-chr11:4230807..4233604,2	K562	blood:
16	chr11:4406758..4409112-chr11:4414514..4416251,2	K562	blood:
17	chr11:4406758..4409112-chr11:4414514..4416251,2	K562	blood:
18	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
19	chr11:4451655..4453436-chr11:4454768..4456529,2	K562	blood:
20	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
21	chr11:4397541..4399241-chr11:4403401..4406097,2	K562	blood:
22	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR52K2-2	chr11:4406237-4407172	NONHSAT017647
2	lnc-OR52K2-1	chr11:4431629-4432109	XLOC_009037
3	lnc-RRM1-2	chr11:4223489-4223883	NR_047550
4	lnc-RRM1-2	chr11:4223489-4223881	NONHSAT017642
5	lnc-RRM1-2	chr11:4223489-4223875	NONHSAT017640
6	lnc-OR52B4-3	chr11:4223487-4223875	NONHSAT017641
7	lnc-RRM1-2	chr11:4223489-4223885	ENSG00000254480.1
8	lnc-OR52K2-2	chr11:4407312-4407485	NONHSAT017647
9	lnc-OR52K2-1	chr11:4415042-4415395	XLOC_009037

No data

Variant related genes	Relation type
ENSG00000255387	TF binding region
SSU72P3	TF binding region
SSU72P5	TF binding region
OR52P2P	TF binding region
TRIM21	TF binding region
SSU72P4	TF binding region
OR52B4	TF binding region
ENSG00000221030	TF binding region
SSU72P7	TF binding region
OR52K2	TF binding region
SSU72P2	TF binding region
SSU72P6	TF binding region
OR52B3P	TF binding region
OR51R1P	TF binding region
ENSG00000255387	CpG island
SSU72P3	CpG island
SSU72P5	CpG island
OR52P2P	CpG island
TRIM21	CpG island
SSU72P4	CpG island
OR52B4	CpG island
ENSG00000221030	CpG island
SSU72P7	CpG island
OR52K2	CpG island
SSU72P2	CpG island
SSU72P6	CpG island
OR52B3P	CpG island
OR51R1P	CpG island
ENSG00000132109	chromatin interactions
ENSG00000255387	chromatin interactions
ENSG00000107262	chromatin interactions
ENSG00000171999	chromatin interactions
ENSG00000086065	chromatin interactions

Extended variants
information (count: 4916 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4916 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560126084	chr11:4213672-4213673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373709286	chr11:4213725-4213726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563073556	chr11:4213740-4213741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182017165	chr11:4213757-4213758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563252490	chr11:4213760-4213761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376735777	chr11:4213763-4213764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530414138	chr11:4213772-4213773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs16929571	chr11:4213813-4213814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs894460	chr11:4213853-4213854	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs528304036	chr11:4213865-4213866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546355414	chr11:4213887-4213888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114277117	chr11:4213888-4213889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573458177	chr11:4213890-4213891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545431291	chr11:4213913-4213914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184481796	chr11:4213925-4213926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs55947443	chr11:4213976-4213977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56233409	chr11:4213979-4213980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528100870	chr11:4213982-4213983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539405247	chr11:4213986-4213987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370718591	chr11:4214052-4214053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548302960	chr11:4214067-4214068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113904804	chr11:4214078-4214079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570074621	chr11:4214112-4214113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189140066	chr11:4214151-4214152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559039707	chr11:4214170-4214171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570944916	chr11:4214177-4214178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143958285	chr11:4214185-4214186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553577657	chr11:4214226-4214227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367831736	chr11:4214301-4214302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575217453	chr11:4214303-4214304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148629496	chr11:4214369-4214370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199595940	chr11:4214384-4214385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558930287	chr11:4214421-4214422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528027264	chr11:4214433-4214434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75361291	chr11:4214441-4214442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575222193	chr11:4214444-4214445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376625200	chr11:4214462-4214463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545465775	chr11:4214516-4214517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564221980	chr11:4214517-4214518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528146601	chr11:4214529-4214530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371825302	chr11:4214571-4214572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142935259	chr11:4214583-4214584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74355877	chr11:4214593-4214594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529044562	chr11:4214611-4214612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550901175	chr11:4214689-4214690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568625237	chr11:4214756-4214757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531168063	chr11:4214761-4214762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186360790	chr11:4214801-4214802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551172902	chr11:4214805-4214806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530971221	chr11:4214829-4214830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Autism	22495311	CNVD
Lung cancer	18438408	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4209600-4213800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:4209600-4213800	Weak transcription	K562	blood
3	chr11:4212400-4213800	Weak transcription	Esophagus	oesophagus
4	chr11:4212400-4215200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:4212800-4216800	Weak transcription	Liver	Liver
6	chr11:4213000-4217400	Weak transcription	Fetal Heart	heart
7	chr11:4213000-4217800	Weak transcription	Left Ventricle	heart
8	chr11:4213400-4214600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:4213600-4215200	Enhancers	Placenta	Placenta
10	chr11:4213800-4214200	Enhancers	Esophagus	oesophagus
11	chr11:4213800-4214800	Enhancers	Placenta Amnion	Placenta Amnion
12	chr11:4213800-4216000	Enhancers	K562	blood
13	chr11:4215200-4215400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:4215400-4215800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:4215800-4217800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr11:4216000-4216600	Flanking Active TSS	K562	blood
17	chr11:4216600-4218800	Enhancers	K562	blood
18	chr11:4216800-4218600	Enhancers	Liver	Liver
19	chr11:4217400-4218400	Enhancers	Fetal Heart	heart
20	chr11:4217800-4218000	Enhancers	Left Ventricle	heart
21	chr11:4217800-4218400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:4218400-4223200	Weak transcription	Fetal Heart	heart
23	chr11:4218600-4222200	Weak transcription	Liver	Liver
24	chr11:4222200-4222800	Enhancers	Liver	Liver
25	chr11:4222800-4223600	Weak transcription	Liver	Liver
26	chr11:4223200-4224000	Enhancers	Fetal Heart	heart
27	chr11:4223400-4223600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:4223400-4223800	Enhancers	Left Ventricle	heart
29	chr11:4223600-4223800	Enhancers	Liver	Liver
30	chr11:4223600-4224800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:4223800-4225000	Weak transcription	Left Ventricle	heart
32	chr11:4224000-4224400	Flanking Active TSS	Fetal Heart	heart
33	chr11:4224000-4225400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr11:4224400-4225600	Enhancers	Fetal Heart	heart
35	chr11:4224800-4225200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:4224800-4225400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:4224800-4225400	Enhancers	K562	blood
38	chr11:4225000-4225400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr11:4225000-4225600	Enhancers	Left Ventricle	heart
40	chr11:4225200-4227200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:4225400-4225600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:4225400-4225600	Enhancers	Right Atrium	heart
43	chr11:4226000-4228200	Weak transcription	Right Atrium	heart
44	chr11:4227200-4227400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:4227800-4228200	Enhancers	Ovary	ovary
46	chr11:4228000-4228200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
47	chr11:4228200-4233200	Weak transcription	Ovary	ovary
48	chr11:4231400-4231600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:4231600-4231800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
50	chr11:4233000-4233800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links