Variant report

Variant	nsv525355
Chromosome Location	chr11:58553771-58632368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:629)
CpG islands
(count:673)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	ATF1	chr11:58555827-58556233	K562	blood:	n/a	n/a
3	ATF3	chr11:58555887-58556150	K562	blood:	n/a	n/a
4	ATF3	chr11:58555952-58556165	K562	blood:	n/a	n/a
5	BACH1	chr11:58554173-58554519	K562	blood:	n/a	n/a
6	BATF	chr11:58618422-58618712	GM12878	blood:	n/a	n/a
7	BATF	chr11:58618228-58618642	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:58618487-58618534	HepG2	liver:	n/a	n/a
9	BHLHE40	chr11:58555518-58556410	K562	blood:	n/a	n/a
10	BHLHE40	chr11:58618380-58618658	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:58618456-58618676	K562	blood:	n/a	n/a
12	CBX3	chr11:58560283-58560581	K562	blood:	n/a	n/a
13	CBX3	chr11:58560325-58560549	K562	blood:	n/a	n/a
14	CEBPB	chr11:58607949-58608053	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:58599213-58599517	IMR90	lung:	n/a	chr11:58599353-58599366 chr11:58599353-58599364 chr11:58599353-58599366
16	CEBPB	chr11:58563807-58564052	A549	lung:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
17	CEBPB	chr11:58563717-58564177	IMR90	lung:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
18	CEBPB	chr11:58579016-58579320	HepG2	liver:	n/a	chr11:58579153-58579164
19	CEBPB	chr11:58579016-58579252	Hela-S3	cervix:	n/a	chr11:58579153-58579164
20	CEBPB	chr11:58604616-58604686	A549	lung:	n/a	n/a
21	CEBPB	chr11:58627346-58627618	HepG2	liver:	n/a	chr11:58627487-58627498
22	CEBPB	chr11:58599314-58599468	K562	blood:	n/a	chr11:58599353-58599366 chr11:58599353-58599364 chr11:58599353-58599366
23	CEBPB	chr11:58563948-58564057	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:58579002-58579335	K562	blood:	n/a	chr11:58579153-58579164
25	CEBPB	chr11:58579001-58579335	IMR90	lung:	n/a	chr11:58579153-58579164
26	CEBPB	chr11:58563679-58564216	Hela-S3	cervix:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
27	CEBPB	chr11:58612869-58613254	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:58627355-58627619	A549	lung:	n/a	chr11:58627487-58627498
29	CEBPB	chr11:58563706-58564156	K562	blood:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
30	CEBPB	chr11:58578999-58579307	A549	lung:	n/a	chr11:58579153-58579164
31	CEBPB	chr11:58613026-58613041	K562	blood:	n/a	n/a
32	CEBPB	chr11:58563733-58564197	HepG2	liver:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
33	CEBPB	chr11:58599210-58599480	Hela-S3	cervix:	n/a	chr11:58599353-58599366 chr11:58599353-58599364 chr11:58599353-58599366
34	CEBPB	chr11:58563735-58564201	H1-hESC	embryonic stem cell:	n/a	chr11:58563817-58563830 chr11:58563852-58563863
35	CEBPB	chr11:58599321-58599449	A549	lung:	n/a	chr11:58599353-58599366 chr11:58599353-58599364 chr11:58599353-58599366
36	CEBPZ	chr11:58581275-58581440	HepG2	liver:	n/a	n/a
37	CTCF	chr11:58556371-58556419	GM12892	blood:	n/a	n/a
38	CTCF	chr11:58555770-58555817	GM10266	blood:	n/a	n/a
39	CTCF	chr11:58618040-58618190	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr11:58618040-58618190	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:58629197-58629233	GM20000	blood:	n/a	n/a
42	CTCF	chr11:58556011-58556172	GM13976	blood:	n/a	n/a
43	CTCF	chr11:58618060-58618210	GM12873	blood:	n/a	n/a
44	CTCF	chr11:58555995-58556147	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:58556000-58556150	WI-38	lung:	n/a	n/a
46	CTCF	chr11:58556020-58556170	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr11:58556020-58556170	Caco-2	colon:	n/a	n/a
48	CTCF	chr11:58618020-58618170	GM12872	blood:	n/a	n/a
49	CTCF	chr11:58618040-58618190	HMEC	breast:	n/a	n/a
50	CTCF	chr11:58556021-58556120	H1-hESC	embryonic stem cell:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58612853-58612903	HCM	heart:	n/a
2	chr11:58605845-58605895	GM12892	blood:	n/a
3	chr11:58612853-58612903	HCM	heart:	n/a
4	chr11:58605845-58605895	GM12892	blood:	n/a
5	chr11:58605845-58605895	AG10803	skin:	n/a
6	chr11:58605845-58605895	GM19239	blood:	n/a
7	chr11:58601627-58601677	MCF-7	breast:	n/a
8	chr11:58598444-58598494	HRCEpiC	kidney:	n/a
9	chr11:58605832-58605882	RPTEC	kidney:	n/a
10	chr11:58598444-58598494	AG04449	skin:	fetal
11	chr11:58612087-58612137	MCF10A-Er-Src	breast:	n/a
12	chr11:58612027-58612077	H1-hESC	embryonic stem cell:	embryo
13	chr11:58598444-58598494	Jurkat	blood:	n/a
14	chr11:58598444-58598494	CMK	blood:	n/a
15	chr11:58598338-58598388	BE2_C	brain:	n/a
16	chr11:58598239-58598289	HCF	heart:	n/a
17	chr11:58612814-58612864	SAEC	small airway:	n/a
18	chr11:58612087-58612137	IMR90	lung:	fetal
19	chr11:58601627-58601677	ovcar-3	ovarian:	n/a
20	chr11:58612853-58612903	CMK	blood:	n/a
21	chr11:58605832-58605882	CMK	blood:	n/a
22	chr11:58598239-58598289	ECC-1	luminal epithelium:	n/a
23	chr11:58605845-58605895	A549	lung:	n/a
24	chr11:58612027-58612077	ovcar-3	ovarian:	n/a
25	chr11:58612814-58612864	HCF	heart:	n/a
26	chr11:58612087-58612137	NHDF-neo	bronchial:	n/a
27	chr11:58605845-58605895	HNPCEpiC	eye:	n/a
28	chr11:58598444-58598494	AG04450	lung:	fetal
29	chr11:58612027-58612077	Hepatocyte	liver:	n/a
30	chr11:58612027-58612077	T-47D	breast:	n/a
31	chr11:58610406-58610456	Hela-S3	cervix:	n/a
32	chr11:58612087-58612137	SK-N-MC	brain:	n/a
33	chr11:58605832-58605882	ovcar-3	ovarian:	n/a
34	chr11:58610406-58610456	AG10803	skin:	n/a
35	chr11:58612814-58612864	HIPEpiC	eye:	n/a
36	chr11:58598239-58598289	GM12878	blood:	n/a
37	chr11:58610406-58610456	GM12892	blood:	n/a
38	chr11:58612087-58612137	RPTEC	kidney:	n/a
39	chr11:58612087-58612137	GM19239	blood:	n/a
40	chr11:58610406-58610456	HL-60	blood:	n/a
41	chr11:58598444-58598494	SK-N-MC	brain:	n/a
42	chr11:58612087-58612137	HEEpiC	esophagus:	n/a
43	chr11:58598239-58598289	T-47D	breast:	n/a
44	chr11:58610406-58610456	H1-hESC	embryonic stem cell:	embryo
45	chr11:58598239-58598289	Hepatocyte	liver:	n/a
46	chr11:58612853-58612903	GM12892	blood:	n/a
47	chr11:58612027-58612077	A549	lung:	n/a
48	chr11:58598338-58598388	SKMC	muscle:	n/a
49	chr11:58612853-58612903	HAEpiC	amniotic membrane:	n/a
50	chr11:58605832-58605882	AG09309	skin:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58397577..58400348-chr11:58551728..58554179,2	K562	blood:
2	chr11:58539643..58542298-chr11:58554397..58556445,2	K562	blood:
3	chr11:58567691..58569634-chr11:58571935..58573618,2	K562	blood:
4	chr11:58551491..58553930-chr11:58557459..58559749,2	K562	blood:
5	chr11:58335090..58336072-chr11:58555654..58556534,3	K562	blood:
6	chr11:58420893..58422551-chr11:58555581..58556580,16	K562	blood:
7	chr11:58599747..58602498-chr11:58604323..58607050,2	K562	blood:
8	chr11:58344188..58345053-chr11:58555383..58556475,3	MCF-7	breast:
9	chr11:58442750..58443528-chr11:58555605..58556306,2	K562	blood:
10	chr11:58344812..58347551-chr11:58552824..58556823,4	K562	blood:
11	chr11:58567691..58569634-chr11:58571935..58573618,2	K562	blood:
12	chr11:58551491..58553930-chr11:58557459..58559749,2	K562	blood:
13	chr11:58599747..58602498-chr11:58604323..58607050,2	K562	blood:
14	chr11:58421175..58421959-chr11:58555571..58556541,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-3	chr11:58563710-58564327	NONHSAT021482

No data

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

Extended variants
information (count: 2196 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2196 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10896825	chr11:58553771-58553772	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187877198	chr11:58553772-58553773	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs537845129	chr11:58553785-58553786	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192644804	chr11:58553822-58553823	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs112486125	chr11:58553857-58553858	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535894888	chr11:58553876-58553877	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs539821785	chr11:58553924-58553925	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs561706096	chr11:58553946-58553947	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs11229621	chr11:58553950-58553951	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs550645864	chr11:58553982-58553983	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs183724083	chr11:58553993-58553994	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs373552617	chr11:58554027-58554028	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548205459	chr11:58554042-58554043	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs146507101	chr11:58554136-58554137	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs11229622	chr11:58554141-58554142	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs554270744	chr11:58554165-58554166	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs12793741	chr11:58554167-58554168	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370707287	chr11:58554269-58554270	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs571131784	chr11:58554379-58554380	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs535355085	chr11:58554401-58554402	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs547012722	chr11:58554417-58554418	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs572577868	chr11:58554455-58554456	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs113911802	chr11:58554469-58554470	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs188392889	chr11:58554516-58554517	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs557419650	chr11:58554528-58554529	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs112099052	chr11:58554533-58554534	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs77424592	chr11:58554549-58554550	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539619884	chr11:58554580-58554581	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs80269573	chr11:58554582-58554583	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs147909723	chr11:58554660-58554661	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs141510341	chr11:58554688-58554689	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs375376711	chr11:58554703-58554704	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs60595965	chr11:58554730-58554731	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs377437286	chr11:58554752-58554753	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs543872465	chr11:58554756-58554757	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs562519698	chr11:58554761-58554762	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs533081120	chr11:58554770-58554771	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs200313127	chr11:58554787-58554788	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs148154522	chr11:58554803-58554804	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113111050	chr11:58554836-58554837	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs112818230	chr11:58554876-58554877	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs547269732	chr11:58554877-58554878	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs202208826	chr11:58554883-58554884	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs111589881	chr11:58554975-58554976	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568701267	chr11:58554990-58554991	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs529249171	chr11:58554995-58554996	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs74737858	chr11:58554999-58555000	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs201151306	chr11:58555003-58555004	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs7939161	chr11:58555049-58555050	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs117222882	chr11:58555051-58555052	Enhancers 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:159 , 50 per page) page: 1 2 3 4

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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