Variant report

Variant	nsv1045858
Chromosome Location	chr11:58547772-58674568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1414)
CpG islands
(count:1711)
Chromatin interactive
region (count:24)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1414 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58555898-58556206	K562	blood:	n/a	n/a
2	ARID3A	chr11:58648155-58648546	HepG2	liver:	n/a	n/a
3	ATF1	chr11:58555827-58556233	K562	blood:	n/a	n/a
4	ATF3	chr11:58555952-58556165	K562	blood:	n/a	n/a
5	ATF3	chr11:58555887-58556150	K562	blood:	n/a	n/a
6	BACH1	chr11:58554173-58554519	K562	blood:	n/a	n/a
7	BACH1	chr11:58672951-58673767	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr11:58618228-58618642	GM12878	blood:	n/a	n/a
9	BATF	chr11:58634982-58635318	GM12878	blood:	n/a	n/a
10	BATF	chr11:58552466-58552804	GM12878	blood:	n/a	n/a
11	BATF	chr11:58552489-58552838	GM12878	blood:	n/a	n/a
12	BATF	chr11:58618422-58618712	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:58618380-58618658	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:58673515-58673655	K562	blood:	n/a	n/a
15	BHLHE40	chr11:58668343-58668597	K562	blood:	n/a	n/a
16	BHLHE40	chr11:58618456-58618676	K562	blood:	n/a	n/a
17	BHLHE40	chr11:58668390-58668584	HepG2	liver:	n/a	n/a
18	BHLHE40	chr11:58618487-58618534	HepG2	liver:	n/a	n/a
19	BHLHE40	chr11:58555518-58556410	K562	blood:	n/a	n/a
20	BRCA1	chr11:58673350-58673665	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr11:58560325-58560549	K562	blood:	n/a	n/a
22	CBX3	chr11:58547847-58548419	K562	blood:	n/a	n/a
23	CBX3	chr11:58548048-58548359	K562	blood:	n/a	n/a
24	CBX3	chr11:58560283-58560581	K562	blood:	n/a	n/a
25	CEBPB	chr11:58599321-58599449	A549	lung:	n/a	chr11:58599353-58599366 chr11:58599353-58599364 chr11:58599353-58599366
26	CEBPB	chr11:58579002-58579335	K562	blood:	n/a	chr11:58579153-58579164
27	CEBPB	chr11:58656085-58656389	Hela-S3	cervix:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
28	CEBPB	chr11:58563717-58564177	IMR90	lung:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
29	CEBPB	chr11:58656078-58656414	A549	lung:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
30	CEBPB	chr11:58579001-58579335	IMR90	lung:	n/a	chr11:58579153-58579164
31	CEBPB	chr11:58648024-58648392	HepG2	liver:	n/a	chr11:58648287-58648300
32	CEBPB	chr11:58599210-58599480	Hela-S3	cervix:	n/a	chr11:58599353-58599366 chr11:58599353-58599364 chr11:58599353-58599366
33	CEBPB	chr11:58579016-58579320	HepG2	liver:	n/a	chr11:58579153-58579164
34	CEBPB	chr11:58656131-58656456	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
35	CEBPB	chr11:58613026-58613041	K562	blood:	n/a	n/a
36	CEBPB	chr11:58578999-58579307	A549	lung:	n/a	chr11:58579153-58579164
37	CEBPB	chr11:58599213-58599517	IMR90	lung:	n/a	chr11:58599353-58599366 chr11:58599353-58599364 chr11:58599353-58599366
38	CEBPB	chr11:58648183-58648434	A549	lung:	n/a	chr11:58648287-58648300
39	CEBPB	chr11:58627355-58627619	A549	lung:	n/a	chr11:58627487-58627498
40	CEBPB	chr11:58604616-58604686	A549	lung:	n/a	n/a
41	CEBPB	chr11:58656689-58656951	HepG2	liver:	n/a	n/a
42	CEBPB	chr11:58656150-58656434	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
43	CEBPB	chr11:58612869-58613254	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:58656053-58656436	HepG2	liver:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
45	CEBPB	chr11:58563706-58564156	K562	blood:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
46	CEBPB	chr11:58579016-58579252	Hela-S3	cervix:	n/a	chr11:58579153-58579164
47	CEBPB	chr11:58648118-58648482	HepG2	liver:	n/a	chr11:58648287-58648300
48	CEBPB	chr11:58656127-58656438	K562	blood:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
49	CEBPB	chr11:58648074-58648804	HepG2	liver:	n/a	chr11:58648287-58648300
50	CEBPB	chr11:58656076-58656380	IMR90	lung:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58598338-58598388	NHDF-neo	bronchial:	n/a
2	chr11:58668488-58668538	Caco-2	colon:	n/a
3	chr11:58668068-58668118	HEK293	kidney:	embryo
4	chr11:58598338-58598388	NHDF-neo	bronchial:	n/a
5	chr11:58668488-58668538	Caco-2	colon:	n/a
6	chr11:58668068-58668118	HEK293	kidney:	embryo
7	chr11:58672702-58672752	HL-60	blood:	n/a
8	chr11:58668634-58668684	MCF10A-Er-Src	breast:	n/a
9	chr11:58667960-58668010	MCF-7	breast:	n/a
10	chr11:58668345-58668395	HCM	heart:	n/a
11	chr11:58612814-58612864	HUVEC	blood vessel:	n/a
12	chr11:58673167-58673217	GM19239	blood:	n/a
13	chr11:58598444-58598494	Jurkat	blood:	n/a
14	chr11:58612853-58612903	HUVEC	blood vessel:	n/a
15	chr11:58668345-58668395	H1-hESC	embryonic stem cell:	embryo
16	chr11:58672768-58672818	HUVEC	blood vessel:	n/a
17	chr11:58668634-58668684	HNPCEpiC	eye:	n/a
18	chr11:58673087-58673137	HepG2	liver:	n/a
19	chr11:58605832-58605882	HUVEC	blood vessel:	n/a
20	chr11:58610406-58610456	T-47D	breast:	n/a
21	chr11:58672768-58672818	HIPEpiC	eye:	n/a
22	chr11:58605832-58605882	GM12892	blood:	n/a
23	chr11:58667964-58668014	PFSK-1	brain:	n/a
24	chr11:58651984-58652034	AG09319	gingival:	n/a
25	chr11:58667964-58668014	AoSMC	blood vessel:	n/a
26	chr11:58672702-58672752	AoSMC	blood vessel:	n/a
27	chr11:58601627-58601677	BE2_C	brain:	n/a
28	chr11:58668634-58668684	HMEC	breast:	n/a
29	chr11:58612027-58612077	HCF	heart:	n/a
30	chr11:58673615-58673665	HNPCEpiC	eye:	n/a
31	chr11:58667960-58668010	CMK	blood:	n/a
32	chr11:58605845-58605895	HNPCEpiC	eye:	n/a
33	chr11:58667960-58668010	Caco-2	colon:	n/a
34	chr11:58673453-58673503	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:58601627-58601677	HRE	kidney:	n/a
36	chr11:58668068-58668118	HRCEpiC	kidney:	n/a
37	chr11:58673453-58673503	HCM	heart:	n/a
38	chr11:58598444-58598494	ProgFib	skin:	n/a
39	chr11:58668488-58668538	Hepatocyte	liver:	n/a
40	chr11:58668634-58668684	PANC-1	pancreas:	n/a
41	chr11:58612853-58612903	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:58668488-58668538	HepG2	liver:	n/a
43	chr11:58673477-58673527	Hela-S3	cervix:	n/a
44	chr11:58673477-58673527	SKMC	muscle:	n/a
45	chr11:58612814-58612864	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:58598338-58598388	HCF	heart:	n/a
47	chr11:58672702-58672752	AG09309	skin:	n/a
48	chr11:58673577-58673627	HUVEC	blood vessel:	n/a
49	chr11:58605845-58605895	IMR90	lung:	fetal
50	chr11:58672888-58672938	HAEpiC	amniotic membrane:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58344188..58345053-chr11:58555383..58556475,3	MCF-7	breast:
2	chr11:58599747..58602498-chr11:58604323..58607050,2	K562	blood:
3	chr11:58335090..58336072-chr11:58555654..58556534,3	K562	blood:
4	chr11:58546256..58548670-chr11:58549514..58551227,2	K562	blood:
5	chr11:58539643..58542298-chr11:58554397..58556445,2	K562	blood:
6	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
7	chr11:58547170..58548940-chr11:58549727..58551973,2	K562	blood:
8	chr11:58546256..58548670-chr11:58549514..58551227,2	K562	blood:
9	chr11:58599747..58602498-chr11:58604323..58607050,2	K562	blood:
10	chr11:58421175..58421959-chr11:58555571..58556541,3	MCF-7	breast:
11	chr11:58344812..58347551-chr11:58552824..58556823,4	K562	blood:
12	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
13	chr11:58567691..58569634-chr11:58571935..58573618,2	K562	blood:
14	chr11:58420893..58422551-chr11:58555581..58556580,16	K562	blood:
15	chr11:58551491..58553930-chr11:58557459..58559749,2	K562	blood:
16	chr11:58567691..58569634-chr11:58571935..58573618,2	K562	blood:
17	chr11:58551491..58553930-chr11:58557459..58559749,2	K562	blood:
18	chr11:58668032..58668917-chr11:58825619..58826508,3	K562	blood:
19	chr11:58345930..58347450-chr11:58657978..58660327,2	K562	blood:
20	chr11:58667985..58668808-chr11:58825960..58826578,4	MCF-7	breast:
21	chr11:58547170..58548940-chr11:58549727..58551973,2	K562	blood:
22	chr11:58397577..58400348-chr11:58551728..58554179,2	K562	blood:
23	chr11:58346639..58348965-chr11:58654113..58656554,2	K562	blood:
24	chr11:58442750..58443528-chr11:58555605..58556306,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYAT-1	chr11:58657761-58659741	l_477_chr11:58656260-58660325_ovary
2	lnc-GLYAT-1	chr11:58656394-58657698	l_477_chr11:58656260-58660325_ovary
3	lnc-GLYAT-1	chr11:58659760-58660337	l_477_chr11:58656260-58660325_ovary
4	lnc-GLYATL1-1	chr11:58645775-58645854	ENSG00000254717
5	lnc-GLYATL1-1	chr11:58660135-58660266	NONHSAT021485
6	lnc-GLYAT-1	chr11:58664013-58664214	l_477_chr11:58656260-58660325_ovary
7	lnc-GLYATL2-3	chr11:58563710-58564327	NONHSAT021482
8	lnc-GLYAT-1	chr11:58656261-58656370	l_477_chr11:58656260-58660325_ovary
9	lnc-GLYATL1-3	chr11:58672343-58672709	NONHSAT021486
10	lnc-GLYATL1-1	chr11:58652424-58652497	NONHSAT021485
11	lnc-GLYATL1-1	chr11:58652379-58652497	ENSG00000254717
12	lnc-GLYATL1-1	chr11:58660135-58660445	ENSG00000254717

No data

Variant related genes	Relation type
GLYATL1P2	TF binding region
ENSG00000224130	TF binding region
TMA16P1	TF binding region
GLYATL2	TF binding region
GLYATL1	TF binding region
GLYATL1P2	CpG island
ENSG00000224130	CpG island
TMA16P1	CpG island
GLYATL2	CpG island
GLYATL1	CpG island
ENSG00000110031	chromatin interactions
ENSG00000255073	chromatin interactions
ENSG00000255240	chromatin interactions
ENSG00000186660	chromatin interactions

Extended variants
information (count: 3998 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3998 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548183123	chr11:58551804-58551805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569973338	chr11:58551849-58551850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114456400	chr11:58551856-58551857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551757911	chr11:58551954-58551955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570184200	chr11:58551964-58551965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534426977	chr11:58551987-58551988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186271903	chr11:58552013-58552014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140172063	chr11:58552045-58552046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566120982	chr11:58552050-58552051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191082635	chr11:58552058-58552059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554955906	chr11:58552059-58552060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144530176	chr11:58552069-58552070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534027451	chr11:58552085-58552086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576686768	chr11:58552183-58552184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182179520	chr11:58552195-58552196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553923050	chr11:58552229-58552230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573290368	chr11:58552280-58552281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577341191	chr11:58552297-58552298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541514284	chr11:58552440-58552441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139203637	chr11:58552500-58552501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149917983	chr11:58552520-58552521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35107562	chr11:58552526-58552527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186783639	chr11:58552533-58552534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563389273	chr11:58552553-58552554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192874924	chr11:58552602-58552603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551721165	chr11:58552611-58552612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570099105	chr11:58552625-58552626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549039076	chr11:58552631-58552632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183081742	chr11:58552710-58552711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565204942	chr11:58552713-58552714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568190054	chr11:58552742-58552743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568464601	chr11:58552766-58552767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371761003	chr11:58552851-58552852	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs374591043	chr11:58552858-58552859	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs555150421	chr11:58552870-58552871	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs570216317	chr11:58552871-58552872	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs533027395	chr11:58552899-58552900	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75938743	chr11:58552911-58552912	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs559318654	chr11:58552945-58552946	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs56027401	chr11:58553068-58553069	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541477419	chr11:58553072-58553073	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs188513443	chr11:58553088-58553089	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs569626399	chr11:58553101-58553102	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs142205864	chr11:58553169-58553170	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs563514420	chr11:58553229-58553230	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs561247865	chr11:58553234-58553235	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs530323174	chr11:58553244-58553245	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs117163726	chr11:58553281-58553282	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs73475749	chr11:58553282-58553283	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs528069792	chr11:58553340-58553341	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58551800-58555400	Weak transcription	Fetal Intestine Large	intestine
2	chr11:58553600-58554400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:58554000-58554400	Enhancers	NHDF-Ad	bronchial
4	chr11:58554000-58555800	Enhancers	NHEK	skin
5	chr11:58554000-58556400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:58554000-58556800	Enhancers	HMEC	breast
7	chr11:58554200-58554400	Enhancers	K562	blood
8	chr11:58554400-58555400	Weak transcription	K562	blood
9	chr11:58554400-58555400	Weak transcription	NHDF-Ad	bronchial
10	chr11:58554400-58556600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:58554400-58557000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:58554800-58556600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:58554800-58557200	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr11:58555400-58555800	Enhancers	Liver	Liver
15	chr11:58555400-58556000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:58555400-58556000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:58555400-58556000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:58555400-58556000	Enhancers	HepG2	liver
19	chr11:58555400-58556000	Enhancers	NHDF-Ad	bronchial
20	chr11:58555400-58556400	Enhancers	K562	blood
21	chr11:58555400-58559000	Enhancers	Fetal Intestine Large	intestine
22	chr11:58555600-58556000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:58555600-58556000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr11:58555600-58556000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:58555600-58556000	Enhancers	Adipose Nuclei	Adipose
26	chr11:58555800-58556000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr11:58555800-58556000	Flanking Active TSS	NHEK	skin
28	chr11:58555800-58556400	Enhancers	Pancreas	Pancrea
29	chr11:58556000-58556200	Enhancers	NHEK	skin
30	chr11:58556200-58556400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:58556200-58556400	Flanking Active TSS	NHEK	skin
32	chr11:58556400-58557000	Enhancers	NHEK	skin
33	chr11:58556400-58557400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:58556400-58558800	Weak transcription	Pancreas	Pancrea
35	chr11:58556600-58557800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr11:58556600-58561600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr11:58557400-58558400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr11:58558000-58558200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr11:58558000-58558400	Enhancers	Fetal Intestine Small	intestine
40	chr11:58558200-58559000	Enhancers	Gastric	stomach
41	chr11:58558800-58559000	Enhancers	Pancreas	Pancrea
42	chr11:58561600-58562000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:58562000-58572000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:58563600-58564000	Enhancers	Fetal Brain Female	brain
45	chr11:58563800-58564000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:58563800-58564200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:58563800-58564200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr11:58563800-58564200	Active TSS	Brain Anterior Caudate	brain
49	chr11:58563800-58564200	Bivalent/Poised TSS	A549	lung
50	chr11:58563800-58564400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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