Variant report

Variant	nsv469932
Chromosome Location	chr11:4200169-4272343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1131)
CpG islands
(count:736)
Chromatin interactive
region (count:21)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4205750-4205950	K562	blood:	n/a	n/a
2	ARID3A	chr11:4208203-4208403	K562	blood:	n/a	n/a
3	ARID3A	chr11:4216109-4216597	K562	blood:	n/a	n/a
4	ARID3A	chr11:4203458-4203639	HepG2	liver:	n/a	n/a
5	ATF1	chr11:4216207-4216475	K562	blood:	n/a	n/a
6	ATF1	chr11:4218126-4218315	K562	blood:	n/a	n/a
7	ATF3	chr11:4208748-4209028	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:4208789-4209061	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:4224962-4225178	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:4233294-4233648	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:4209051-4209129	K562	blood:	n/a	n/a
12	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
13	BHLHE40	chr11:4208122-4208459	K562	blood:	n/a	n/a
14	BHLHE40	chr11:4208769-4209074	GM12878	blood:	n/a	chr11:4208989-4209005
15	BHLHE40	chr11:4202929-4203828	K562	blood:	n/a	n/a
16	BHLHE40	chr11:4208773-4209110	K562	blood:	n/a	chr11:4208989-4209005
17	BRCA1	chr11:4208855-4208989	HepG2	liver:	n/a	n/a
18	BRCA1	chr11:4208834-4209055	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr11:4208772-4209129	K562	blood:	n/a	n/a
20	CBX3	chr11:4208019-4208474	K562	blood:	n/a	n/a
21	CBX3	chr11:4203292-4203924	K562	blood:	n/a	n/a
22	CBX3	chr11:4207969-4208291	K562	blood:	n/a	n/a
23	CCNT2	chr11:4208203-4209367	K562	blood:	n/a	chr11:4209066-4209075 chr11:4208444-4208453
24	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
25	CCNT2	chr11:4205703-4206232	K562	blood:	n/a	n/a
26	CEBPB	chr11:4232611-4232857	HepG2	liver:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
27	CEBPB	chr11:4257958-4258231	HepG2	liver:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
28	CEBPB	chr11:4205574-4205936	A549	lung:	n/a	chr11:4205745-4205756
29	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
30	CEBPB	chr11:4216252-4216447	K562	blood:	n/a	n/a
31	CEBPB	chr11:4228834-4228864	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr11:4208794-4209159	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:4205560-4205942	IMR90	lung:	n/a	chr11:4205745-4205756
34	CEBPB	chr11:4208020-4208479	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
36	CEBPB	chr11:4205574-4206017	K562	blood:	n/a	chr11:4205745-4205756
37	CEBPB	chr11:4233297-4233351	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:4232604-4232820	IMR90	lung:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
39	CEBPB	chr11:4205566-4205944	HepG2	liver:	n/a	chr11:4205745-4205756
40	CEBPB	chr11:4205568-4205916	Hela-S3	cervix:	n/a	chr11:4205745-4205756
41	CEBPB	chr11:4205634-4205851	K562	blood:	n/a	chr11:4205745-4205756
42	CEBPB	chr11:4208893-4208908	K562	blood:	n/a	n/a
43	CEBPB	chr11:4208855-4209254	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr11:4205582-4205901	H1-hESC	embryonic stem cell:	n/a	chr11:4205745-4205756
45	CEBPB	chr11:4208295-4208391	K562	blood:	n/a	n/a
46	CEBPB	chr11:4257965-4258134	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
47	CEBPB	chr11:4232578-4232904	K562	blood:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
48	CEBPB	chr11:4257961-4258189	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
49	CEBPD	chr11:4216035-4216623	K562	blood:	n/a	n/a
50	CEBPD	chr11:4216067-4216617	K562	blood:	n/a	n/a

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4212446-4212496	T-47D	breast:	n/a
2	chr11:4212471-4212521	A549	lung:	n/a
3	chr11:4209120-4209170	HNPCEpiC	eye:	n/a
4	chr11:4209397-4209447	HIPEpiC	eye:	n/a
5	chr11:4212446-4212496	T-47D	breast:	n/a
6	chr11:4212471-4212521	A549	lung:	n/a
7	chr11:4209120-4209170	HNPCEpiC	eye:	n/a
8	chr11:4209397-4209447	HIPEpiC	eye:	n/a
9	chr11:4206098-4206148	HEK293	kidney:	embryo
10	chr11:4208278-4208328	SK-N-SH_RA	brain:	n/a
11	chr11:4209120-4209170	GM06990	blood:	n/a
12	chr11:4208449-4208499	BE2_C	brain:	n/a
13	chr11:4208905-4208955	SK-N-MC	brain:	n/a
14	chr11:4208449-4208499	GM19239	blood:	n/a
15	chr11:4208449-4208499	GM12878	blood:	n/a
16	chr11:4208905-4208955	LNCaP	prostate:	n/a
17	chr11:4208905-4208955	HRE	kidney:	n/a
18	chr11:4208449-4208499	AG04449	skin:	fetal
19	chr11:4212471-4212521	HNPCEpiC	eye:	n/a
20	chr11:4212471-4212521	SK-N-SH_RA	brain:	n/a
21	chr11:4259129-4259179	HCM	heart:	n/a
22	chr11:4259129-4259179	RPTEC	kidney:	n/a
23	chr11:4212471-4212521	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:4258933-4258983	NT2-D1	testis:	n/a
25	chr11:4212471-4212521	HCF	heart:	n/a
26	chr11:4209397-4209447	PFSK-1	brain:	n/a
27	chr11:4209120-4209170	MCF10A-Er-Src	breast:	n/a
28	chr11:4259129-4259179	HNPCEpiC	eye:	n/a
29	chr11:4208278-4208328	HUVEC	blood vessel:	n/a
30	chr11:4206098-4206148	NHBE	bronchial:	n/a
31	chr11:4212471-4212521	SAEC	small airway:	n/a
32	chr11:4208278-4208328	NHBE	bronchial:	n/a
33	chr11:4209120-4209170	AoSMC	blood vessel:	n/a
34	chr11:4208449-4208499	NB4	blood:	n/a
35	chr11:4212446-4212496	PFSK-1	brain:	n/a
36	chr11:4233502-4233552	HCT-116	colon:	n/a
37	chr11:4233502-4233552	AG04449	skin:	fetal
38	chr11:4212471-4212521	GM19239	blood:	n/a
39	chr11:4209120-4209170	GM19239	blood:	n/a
40	chr11:4212446-4212496	HAEpiC	amniotic membrane:	n/a
41	chr11:4206098-4206148	BJ	skin:	n/a
42	chr11:4233502-4233552	HAEpiC	amniotic membrane:	n/a
43	chr11:4209120-4209170	HepG2	liver:	n/a
44	chr11:4206098-4206148	CMK	blood:	n/a
45	chr11:4209397-4209447	HRPEpiC	eye:	n/a
46	chr11:4233502-4233552	AG04450	lung:	fetal
47	chr11:4233502-4233552	Caco-2	colon:	n/a
48	chr11:4206098-4206148	T-47D	breast:	n/a
49	chr11:4233502-4233552	HepG2	liver:	n/a
50	chr11:4209397-4209447	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
2	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
3	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
4	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
5	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:
6	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
7	chr11:4202964..4204119-chr11:4560777..4561880,3	MCF-7	breast:
8	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
9	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:
10	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
11	chr11:4228086..4230506-chr11:4230807..4233604,2	K562	blood:
12	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
13	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
14	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
15	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
16	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
17	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
18	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
19	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
20	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
21	chr11:4201110..4205265-chr11:4206798..4209054,5	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRM1-2	chr11:4208370-4208434	ENSG00000254480.1
2	lnc-RRM1-2	chr11:4208382-4208434	NR_047550
3	lnc-RRM1-2	chr11:4223489-4223883	NR_047550
4	lnc-RRM1-2	chr11:4201859-4201941	NONHSAT017642
5	lnc-RRM1-2	chr11:4200829-4201124	NONHSAT017640
6	lnc-OR52B4-3	chr11:4223487-4223875	NONHSAT017641
7	lnc-RRM1-2	chr11:4223489-4223885	ENSG00000254480.1
8	lnc-RRM1-2	chr11:4223489-4223881	NONHSAT017642
9	lnc-OR52B4-3	chr11:4201787-4201939	NONHSAT017641
10	lnc-RRM1-2	chr11:4201862-4201941	NONHSAT017640
11	lnc-RRM1-2	chr11:4223489-4223875	NONHSAT017640

No data

Variant related genes	Relation type
SSU72P2	TF binding region
ENSG00000255387	TF binding region
SSU72P5	TF binding region
ENSG00000254480	TF binding region
SSU72P2	CpG island
ENSG00000255387	CpG island
SSU72P5	CpG island
ENSG00000254480	CpG island
ENSG00000254480	chromatin interactions
ENSG00000255387	chromatin interactions

Extended variants
information (count: 1739 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11031226	chr11:4200169-4200170	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35431137	chr11:4200187-4200188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs397735036	chr11:4200189-4200190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs398114965	chr11:4200190-4200191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572065154	chr11:4200208-4200209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572703329	chr11:4200228-4200229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541626385	chr11:4200231-4200232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542658272	chr11:4200241-4200242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185202523	chr11:4200296-4200297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138445482	chr11:4200312-4200313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114536971	chr11:4200327-4200328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35984170	chr11:4200349-4200350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs397848176	chr11:4200351-4200352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11827323	chr11:4200391-4200392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575229859	chr11:4200407-4200408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73427003	chr11:4200422-4200423	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551816422	chr11:4200471-4200472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111855816	chr11:4200491-4200492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71459803	chr11:4200501-4200502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527786451	chr11:4200559-4200560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144680903	chr11:4200646-4200647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549496978	chr11:4200652-4200653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11827377	chr11:4200685-4200686	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs118086435	chr11:4200694-4200695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556322038	chr11:4200711-4200712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10835716	chr11:4200715-4200716	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538916717	chr11:4200748-4200749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564055933	chr11:4200778-4200779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571964251	chr11:4200797-4200798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542251595	chr11:4200819-4200820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368593781	chr11:4200849-4200850	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs554699486	chr11:4200874-4200875	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs190129233	chr11:4200875-4200876	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs543678415	chr11:4200885-4200886	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs142953875	chr11:4200887-4200888	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs10500595	chr11:4200916-4200917	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs11826962	chr11:4200923-4200924	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs11826975	chr11:4200961-4200962	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs116198590	chr11:4200976-4200977	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs549085566	chr11:4200981-4200982	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs11031228	chr11:4200982-4200983	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs12786754	chr11:4201004-4201005	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs529525002	chr11:4201019-4201020	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs145164827	chr11:4201020-4201021	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs571457540	chr11:4201022-4201023	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs538954102	chr11:4201143-4201144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138923590	chr11:4201186-4201187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs372365402	chr11:4201200-4201201	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs149355133	chr11:4201220-4201221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536275386	chr11:4201228-4201229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	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
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	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4197600-4208200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:4197600-4208200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:4198000-4203000	Weak transcription	K562	blood
4	chr11:4200000-4208200	Enhancers	Liver	Liver
5	chr11:4200200-4200600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:4200600-4201000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:4201000-4201200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:4201200-4201800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:4201800-4202000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr11:4202200-4205400	Weak transcription	Fetal Heart	heart
11	chr11:4203000-4203400	Enhancers	Fetal Muscle Trunk	muscle
12	chr11:4203000-4203800	Enhancers	K562	blood
13	chr11:4203200-4203600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr11:4203800-4205400	Weak transcription	K562	blood
15	chr11:4205400-4206200	Enhancers	Right Ventricle	heart
16	chr11:4205400-4206400	Enhancers	Colon Smooth Muscle	Colon
17	chr11:4205400-4206400	Enhancers	K562	blood
18	chr11:4205400-4206800	Enhancers	Fetal Heart	heart
19	chr11:4205600-4205800	Enhancers	Fetal Lung	lung
20	chr11:4205600-4208000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:4205800-4206000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr11:4205800-4206200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:4205800-4209000	Weak transcription	Fetal Lung	lung
24	chr11:4206200-4208200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr11:4206200-4208200	Weak transcription	Right Ventricle	heart
26	chr11:4206400-4208000	Weak transcription	Colon Smooth Muscle	Colon
27	chr11:4206400-4208000	Weak transcription	K562	blood
28	chr11:4206400-4208200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:4206800-4207800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr11:4206800-4208200	Enhancers	Primary hematopoietic stem cells	blood
31	chr11:4206800-4209200	Weak transcription	Fetal Heart	heart
32	chr11:4207800-4208000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr11:4208000-4208200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr11:4208000-4208200	Enhancers	Brain Germinal Matrix	brain
35	chr11:4208000-4208200	Enhancers	Colon Smooth Muscle	Colon
36	chr11:4208000-4208200	Enhancers	HUVEC	blood vessel
37	chr11:4208000-4208400	Flanking Active TSS	Hela-S3	cervix
38	chr11:4208000-4208600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr11:4208000-4209000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:4208000-4209200	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr11:4208000-4209200	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr11:4208000-4209200	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr11:4208000-4209200	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr11:4208000-4209200	Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr11:4208000-4209200	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr11:4208000-4209200	Active TSS	K562	blood
47	chr11:4208000-4209400	Active TSS	H1 Cell Line	embryonic stem cell
48	chr11:4208000-4209400	Active TSS	A549	lung
49	chr11:4208000-4209600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr11:4208200-4208400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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