Variant report

Variant	nsv334
Chromosome Location	chr11:59663800-59709104
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59688346-59688393	K562	blood:	n/a	n/a
2	ARID3A	chr11:59686510-59686786	K562	blood:	n/a	n/a
3	ATF1	chr11:59666312-59666437	K562	blood:	n/a	n/a
4	ATF1	chr11:59668904-59669024	K562	blood:	n/a	n/a
5	BHLHE40	chr11:59666212-59666338	K562	blood:	n/a	n/a
6	CBX3	chr11:59699128-59699456	K562	blood:	n/a	n/a
7	CBX3	chr11:59686479-59686948	HCT-116	colon:	n/a	n/a
8	CBX3	chr11:59691328-59691760	K562	blood:	n/a	n/a
9	CBX3	chr11:59691304-59691756	K562	blood:	n/a	n/a
10	CBX3	chr11:59685256-59685778	K562	blood:	n/a	n/a
11	CBX3	chr11:59699006-59699568	K562	blood:	n/a	n/a
12	CEBPB	chr11:59686099-59686353	K562	blood:	n/a	chr11:59686187-59686198
13	CEBPB	chr11:59686030-59686364	IMR90	lung:	n/a	chr11:59686187-59686198
14	CEBPB	chr11:59685882-59687053	Hela-S3	cervix:	n/a	chr11:59686187-59686198
15	CEBPB	chr11:59686126-59686245	H1-hESC	embryonic stem cell:	n/a	chr11:59686187-59686198
16	CEBPB	chr11:59686030-59686341	A549	lung:	n/a	chr11:59686187-59686198
17	CEBPB	chr11:59666059-59666473	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:59667137-59667190	K562	blood:	n/a	n/a
19	CEBPB	chr11:59686022-59686362	HepG2	liver:	n/a	chr11:59686187-59686198
20	CEBPB	chr11:59686543-59686860	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr11:59686540-59686835	HUVEC	blood vessel:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
22	CTCF	chr11:59686587-59686759	GM20000	blood:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
23	CTCF	chr11:59686640-59686790	AG09319	gingival:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
24	CTCF	chr11:59686540-59686690	GM12871	blood:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
25	CTCF	chr11:59686536-59686775	ECC-1	luminal epithelium:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
26	CTCF	chr11:59686600-59686750	HUVEC	blood vessel:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
27	CTCF	chr11:59686575-59686773	Pancreas_OC	pancreas:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
28	CTCF	chr11:59686503-59686873	A549	lung:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
29	CTCF	chr11:59686620-59686770	HRE	kidney:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
30	CTCF	chr11:59686560-59686710	HMF	breast:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
31	CTCF	chr11:59686580-59686730	RPTEC	kidney:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
32	CTCF	chr11:59708294-59708386	GM20000	blood:	n/a	n/a
33	CTCF	chr11:59686407-59687296	SK-N-SH	brain:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
34	CTCF	chr11:59686565-59686756	Lung_OC	lung:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
35	CTCF	chr11:59686580-59686730	WERI-Rb-1	eye:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
36	CTCF	chr11:59686600-59686750	HCPEpiC	choroid plexus:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
37	CTCF	chr11:59686580-59686730	Caco-2	colon:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
38	CTCF	chr11:59686620-59686770	GM12870	blood:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
39	CTCF	chr11:59686560-59686710	AG09309	skin:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
40	CTCF	chr11:59686560-59686710	GM12869	blood:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
41	CTCF	chr11:59686600-59686750	HRPEpiC	eye:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
42	CTCF	chr11:59686487-59686846	IMR90	lung:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
43	CTCF	chr11:59686556-59686750	A549	lung:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
44	CTCF	chr11:59701036-59701136	K562	blood:	n/a	n/a
45	CTCF	chr11:59686600-59686750	RPTEC	kidney:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
46	CTCF	chr11:59686620-59686770	GM12864	blood:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
47	CTCF	chr11:59686640-59686790	GM12865	blood:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
48	CTCF	chr11:59686680-59686830	HCM	heart:	n/a	n/a
49	CTCF	chr11:59686429-59686977	HCT-116	colon:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677
50	CTCF	chr11:59686600-59686750	Caco-2	colon:	n/a	chr11:59686657-59686678 chr11:59686662-59686680 chr11:59686664-59686677

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59666274-59666324	GM12878	blood:	n/a
2	chr11:59665786-59665836	HPAEpiC	pulmonary alveolar:	n/a
3	chr11:59666274-59666324	GM12878	blood:	n/a
4	chr11:59665786-59665836	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:59665786-59665836	SK-N-SH_RA	brain:	n/a
6	chr11:59665648-59665698	LNCaP	prostate:	n/a
7	chr11:59666274-59666324	ovcar-3	ovarian:	n/a
8	chr11:59664229-59664279	CMK	blood:	n/a
9	chr11:59665648-59665698	AG09309	skin:	n/a
10	chr11:59666274-59666324	PFSK-1	brain:	n/a
11	chr11:59666274-59666324	SK-N-SH_RA	brain:	n/a
12	chr11:59665648-59665698	NT2-D1	testis:	n/a
13	chr11:59665786-59665836	A549	lung:	n/a
14	chr11:59665786-59665836	GM12892	blood:	n/a
15	chr11:59666274-59666324	LNCaP	prostate:	n/a
16	chr11:59666274-59666324	HIPEpiC	eye:	n/a
17	chr11:59664229-59664279	HUVEC	blood vessel:	n/a
18	chr11:59664229-59664279	HepG2	liver:	n/a
19	chr11:59665648-59665698	Caco-2	colon:	n/a
20	chr11:59665786-59665836	HCM	heart:	n/a
21	chr11:59665698-59665748	NT2-D1	testis:	n/a
22	chr11:59666274-59666324	HRE	kidney:	n/a
23	chr11:59666274-59666324	GM06990	blood:	n/a
24	chr11:59664229-59664279	GM19239	blood:	n/a
25	chr11:59665786-59665836	CMK	blood:	n/a
26	chr11:59664229-59664279	AG09319	gingival:	n/a
27	chr11:59665648-59665698	AG10803	skin:	n/a
28	chr11:59665648-59665698	BJ	skin:	n/a
29	chr11:59664229-59664279	HCT-116	colon:	n/a
30	chr11:59665698-59665748	BE2_C	brain:	n/a
31	chr11:59665786-59665836	HL-60	blood:	n/a
32	chr11:59665786-59665836	HEK293	kidney:	embryo
33	chr11:59664229-59664279	HCF	heart:	n/a
34	chr11:59666274-59666324	SK-N-MC	brain:	n/a
35	chr11:59666274-59666324	HCPEpiC	choroid plexus:	n/a
36	chr11:59665786-59665836	T-47D	breast:	n/a
37	chr11:59668329-59668379	A549	lung:	n/a
38	chr11:59668329-59668379	PANC-1	pancreas:	n/a
39	chr11:59665698-59665748	NB4	blood:	n/a
40	chr11:59664229-59664279	HCPEpiC	choroid plexus:	n/a
41	chr11:59664229-59664279	T-47D	breast:	n/a
42	chr11:59665698-59665748	MCF-7	breast:	n/a
43	chr11:59665648-59665698	NB4	blood:	n/a
44	chr11:59664229-59664279	GM12892	blood:	n/a
45	chr11:59668329-59668379	NHBE	bronchial:	n/a
46	chr11:59665648-59665698	PANC-1	pancreas:	n/a
47	chr11:59668329-59668379	HCPEpiC	choroid plexus:	n/a
48	chr11:59665648-59665698	H1-hESC	embryonic stem cell:	embryo
49	chr11:59665648-59665698	HAEpiC	amniotic membrane:	n/a
50	chr11:59665786-59665836	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:59694266..59696253-chr11:59696278..59698008,2	K562	blood:
2	chr11:59664471..59667398-chr11:59667570..59669763,2	K562	blood:
3	chr11:59676104..59678991-chr11:59688257..59690026,2	K562	blood:
4	chr11:59661730..59664350-chr11:59667223..59669290,2	K562	blood:
5	chr11:59667916..59670616-chr11:59674911..59677255,2	K562	blood:
6	chr11:59702370..59703893-chr11:59706554..59708573,2	K562	blood:
7	chr11:59569788..59570640-chr11:59686271..59687396,4	K562	blood:
8	chr11:59702370..59703893-chr11:59706554..59708573,2	K562	blood:
9	chr11:59667916..59670616-chr11:59674911..59677255,2	K562	blood:
10	chr11:59699928..59702632-chr11:59711240..59714047,2	K562	blood:
11	chr11:59683097..59687852-chr11:59717114..59720144,4	K562	blood:
12	chr11:59590172..59590989-chr11:59686223..59687124,2	K562	blood:
13	chr11:59705992..59709228-chr11:59710363..59713651,4	K562	blood:
14	chr11:59572980..59575934-chr11:59668133..59670505,2	K562	blood:
15	chr11:59590046..59591697-chr11:59685948..59687158,11	MCF-7	breast:
16	chr11:59664471..59666030-chr11:59668263..59670929,2	K562	blood:
17	chr11:59587343..59588855-chr11:59684384..59686840,2	K562	blood:
18	chr11:59694266..59696253-chr11:59696278..59698008,2	K562	blood:
19	chr11:59676104..59678991-chr11:59688257..59690026,2	K562	blood:
20	chr11:59661730..59664350-chr11:59667223..59669290,2	K562	blood:
21	chr11:59590157..59591079-chr11:59686234..59686794,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000790.1-3	chr11:59686674-59686726	NONHSAT021551
2	lnc-AP000790.1-3	chr11:59695602-59696128	NONHSAT021551

Variant related genes	Relation type
OOSP1	TF binding region
SRD5A3P1	TF binding region
OOSP1	CpG island
SRD5A3P1	CpG island
ENSG00000270929	chromatin interactions

Extended variants
information (count: 1004 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186556182	chr11:59663845-59663846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116523392	chr11:59663850-59663851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561867203	chr11:59663866-59663867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115962920	chr11:59663883-59663884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550786946	chr11:59663901-59663902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79201580	chr11:59663910-59663911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533037889	chr11:59663913-59663914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148517973	chr11:59663920-59663921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566432474	chr11:59663938-59663939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535019583	chr11:59663939-59663940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370035580	chr11:59663977-59663978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372721716	chr11:59664018-59664019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191333018	chr11:59664028-59664029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111516375	chr11:59664112-59664113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575351957	chr11:59664155-59664156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531435400	chr11:59664162-59664163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs517997	chr11:59664187-59664188	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs184709870	chr11:59664212-59664213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189571656	chr11:59664230-59664231	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs142971918	chr11:59664249-59664250	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs75308205	chr11:59664288-59664289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73490973	chr11:59664340-59664341	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs544448458	chr11:59664356-59664357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562644738	chr11:59664411-59664412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372854458	chr11:59664472-59664473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs193144673	chr11:59664488-59664489	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs551417691	chr11:59664527-59664528	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs554129299	chr11:59664549-59664550	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs527329166	chr11:59664583-59664584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146636808	chr11:59664591-59664592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568440512	chr11:59664649-59664650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185326293	chr11:59664656-59664657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12274522	chr11:59664663-59664664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs75913697	chr11:59664673-59664674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189400921	chr11:59664781-59664782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376429457	chr11:59664787-59664788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182002841	chr11:59664870-59664871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186490568	chr11:59664878-59664879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530366310	chr11:59664952-59664953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61903594	chr11:59665038-59665039	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs572362164	chr11:59665062-59665063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555636144	chr11:59665069-59665070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs59287057	chr11:59665072-59665073	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs143812905	chr11:59665104-59665105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188131250	chr11:59665109-59665110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146445058	chr11:59665130-59665131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577721963	chr11:59665141-59665142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180872790	chr11:59665175-59665176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560236728	chr11:59665185-59665186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527372372	chr11:59665200-59665201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Lung adenocarcinoma	17086460	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59660000-59666400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:59660000-59667000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:59660000-59668800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr11:59662800-59668200	Weak transcription	NHEK	skin
5	chr11:59662800-59668400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:59665600-59665800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:59665600-59665800	Enhancers	Fetal Brain Male	brain
8	chr11:59665800-59667200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:59666000-59666200	ZNF genes & repeats	Spleen	Spleen
10	chr11:59666000-59666400	Enhancers	K562	blood
11	chr11:59666000-59667000	Weak transcription	Fetal Brain Male	brain
12	chr11:59666000-59667200	Enhancers	Hela-S3	cervix
13	chr11:59666200-59669800	Weak transcription	Spleen	Spleen
14	chr11:59666400-59668800	Weak transcription	K562	blood
15	chr11:59666800-59667400	Enhancers	Dnd41	blood
16	chr11:59666800-59667600	Enhancers	HUVEC	blood vessel
17	chr11:59667000-59667200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:59667000-59667400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr11:59667000-59667400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr11:59667000-59667400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:59667000-59667400	Enhancers	Fetal Brain Male	brain
22	chr11:59667000-59667400	Enhancers	Pancreas	Pancrea
23	chr11:59667000-59669400	Enhancers	Fetal Brain Female	brain
24	chr11:59667200-59667400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:59667200-59667400	Enhancers	NH-A	brain
26	chr11:59667200-59668400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:59667200-59668400	Weak transcription	Hela-S3	cervix
28	chr11:59667400-59668200	Weak transcription	NH-A	brain
29	chr11:59667400-59669000	Weak transcription	Fetal Brain Male	brain
30	chr11:59667600-59668000	Weak transcription	HUVEC	blood vessel
31	chr11:59667600-59669000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:59668000-59669000	Enhancers	HUVEC	blood vessel
33	chr11:59668200-59669000	Enhancers	NH-A	brain
34	chr11:59668200-59669400	Enhancers	NHEK	skin
35	chr11:59668400-59669200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr11:59668400-59669400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr11:59668400-59669400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:59668400-59669600	Enhancers	Hela-S3	cervix
39	chr11:59668800-59669200	Enhancers	Brain Hippocampus Middle	brain
40	chr11:59668800-59669400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:59668800-59669400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr11:59668800-59669400	Enhancers	HMEC	breast
43	chr11:59668800-59669400	Enhancers	K562	blood
44	chr11:59669000-59669200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr11:59669000-59669200	Enhancers	Dnd41	blood
46	chr11:59669000-59669400	Flanking Active TSS	HUVEC	blood vessel
47	chr11:59669000-59669400	Flanking Active TSS	NH-A	brain
48	chr11:59669000-59669600	Enhancers	Fetal Brain Male	brain
49	chr11:59669000-59669600	Enhancers	Ovary	ovary
50	chr11:59669400-59669800	Enhancers	HUVEC	blood vessel

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