Variant report

Variant	nsv1048605
Chromosome Location	chr11:58534660-58672438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1421)
CpG islands
(count:1161)
Chromatin interactive
region (count:33)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1421 , 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	chr11:58648155-58648546	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:58539357-58539557	K562	blood:	n/a	n/a
3	ARID3A	chr11:58555898-58556206	K562	blood:	n/a	n/a
4	ARID3A	chr11:58544320-58544736	K562	blood:	n/a	n/a
5	ARID3A	chr11:58537620-58537935	K562	blood:	n/a	n/a
6	ARID3A	chr11:58541793-58542131	K562	blood:	n/a	n/a
7	ARID3A	chr11:58538249-58538649	K562	blood:	n/a	n/a
8	ATF1	chr11:58538250-58538779	K562	blood:	n/a	n/a
9	ATF1	chr11:58541771-58542006	K562	blood:	n/a	n/a
10	ATF1	chr11:58544343-58544716	K562	blood:	n/a	n/a
11	ATF1	chr11:58537653-58537949	K562	blood:	n/a	n/a
12	ATF1	chr11:58555827-58556233	K562	blood:	n/a	n/a
13	ATF2	chr11:58542649-58543207	GM12878	blood:	n/a	n/a
14	ATF3	chr11:58555952-58556165	K562	blood:	n/a	n/a
15	ATF3	chr11:58538300-58538666	K562	blood:	n/a	n/a
16	ATF3	chr11:58555887-58556150	K562	blood:	n/a	n/a
17	BACH1	chr11:58544587-58544608	K562	blood:	n/a	n/a
18	BACH1	chr11:58541528-58542135	K562	blood:	n/a	n/a
19	BACH1	chr11:58545467-58545513	K562	blood:	n/a	n/a
20	BACH1	chr11:58554173-58554519	K562	blood:	n/a	n/a
21	BATF	chr11:58542744-58543140	GM12878	blood:	n/a	n/a
22	BATF	chr11:58634982-58635318	GM12878	blood:	n/a	n/a
23	BATF	chr11:58552466-58552804	GM12878	blood:	n/a	n/a
24	BATF	chr11:58618422-58618712	GM12878	blood:	n/a	n/a
25	BATF	chr11:58618228-58618642	GM12878	blood:	n/a	n/a
26	BATF	chr11:58552489-58552838	GM12878	blood:	n/a	n/a
27	BATF	chr11:58542759-58543208	GM12878	blood:	n/a	n/a
28	BCL11A	chr11:58542801-58543149	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:58668390-58668584	HepG2	liver:	n/a	n/a
30	BHLHE40	chr11:58542502-58542698	K562	blood:	n/a	n/a
31	BHLHE40	chr11:58668343-58668597	K562	blood:	n/a	n/a
32	BHLHE40	chr11:58541711-58542162	K562	blood:	n/a	n/a
33	BHLHE40	chr11:58555518-58556410	K562	blood:	n/a	n/a
34	BHLHE40	chr11:58618380-58618658	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:58544109-58544807	K562	blood:	n/a	n/a
36	BHLHE40	chr11:58618456-58618676	K562	blood:	n/a	n/a
37	BHLHE40	chr11:58537633-58539308	K562	blood:	n/a	n/a
38	BHLHE40	chr11:58618487-58618534	HepG2	liver:	n/a	n/a
39	BHLHE40	chr11:58536883-58537112	K562	blood:	n/a	n/a
40	BRCA1	chr11:58538759-58538766	GM12878	blood:	n/a	n/a
41	CBX3	chr11:58560283-58560581	K562	blood:	n/a	n/a
42	CBX3	chr11:58537598-58538050	K562	blood:	n/a	n/a
43	CBX3	chr11:58538169-58538871	K562	blood:	n/a	n/a
44	CBX3	chr11:58544332-58544741	K562	blood:	n/a	n/a
45	CBX3	chr11:58548048-58548359	K562	blood:	n/a	n/a
46	CBX3	chr11:58541653-58542083	K562	blood:	n/a	n/a
47	CBX3	chr11:58538125-58538670	HCT-116	colon:	n/a	n/a
48	CBX3	chr11:58547847-58548419	K562	blood:	n/a	n/a
49	CBX3	chr11:58544256-58544777	K562	blood:	n/a	n/a
50	CBX3	chr11:58560325-58560549	K562	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58605845-58605895	AG09309	skin:	n/a
2	chr11:58612027-58612077	AG04449	skin:	fetal
3	chr11:58605845-58605895	AG09309	skin:	n/a
4	chr11:58612027-58612077	AG04449	skin:	fetal
5	chr11:58612853-58612903	BE2_C	brain:	n/a
6	chr11:58612027-58612077	BE2_C	brain:	n/a
7	chr11:58612087-58612137	AG04450	lung:	fetal
8	chr11:58610406-58610456	AG04449	skin:	fetal
9	chr11:58612814-58612864	ECC-1	luminal epithelium:	n/a
10	chr11:58605845-58605895	Jurkat	blood:	n/a
11	chr11:58651984-58652034	HIPEpiC	eye:	n/a
12	chr11:58598239-58598289	GM19239	blood:	n/a
13	chr11:58605832-58605882	PANC-1	pancreas:	n/a
14	chr11:58598239-58598289	AoSMC	blood vessel:	n/a
15	chr11:58668634-58668684	Caco-2	colon:	n/a
16	chr11:58667960-58668010	IMR90	lung:	fetal
17	chr11:58605832-58605882	MCF10A-Er-Src	breast:	n/a
18	chr11:58605845-58605895	MCF-7	breast:	n/a
19	chr11:58610406-58610456	Caco-2	colon:	n/a
20	chr11:58668977-58669027	K562	blood:	n/a
21	chr11:58667964-58668014	BE2_C	brain:	n/a
22	chr11:58605845-58605895	NHDF-neo	bronchial:	n/a
23	chr11:58668634-58668684	HIPEpiC	eye:	n/a
24	chr11:58612814-58612864	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:58601627-58601677	HL-60	blood:	n/a
26	chr11:58668488-58668538	MCF-7	breast:	n/a
27	chr11:58668977-58669027	HIPEpiC	eye:	n/a
28	chr11:58598444-58598494	SK-N-SH	brain:	n/a
29	chr11:58668345-58668395	NB4	blood:	n/a
30	chr11:58612087-58612137	HRCEpiC	kidney:	n/a
31	chr11:58668634-58668684	HCT-116	colon:	n/a
32	chr11:58668068-58668118	PANC-1	pancreas:	n/a
33	chr11:58612853-58612903	HMEC	breast:	n/a
34	chr11:58612814-58612864	HNPCEpiC	eye:	n/a
35	chr11:58668634-58668684	GM12878	blood:	n/a
36	chr11:58612814-58612864	ovcar-3	ovarian:	n/a
37	chr11:58612027-58612077	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:58668345-58668395	IMR90	lung:	fetal
39	chr11:58668634-58668684	PFSK-1	brain:	n/a
40	chr11:58668634-58668684	LNCaP	prostate:	n/a
41	chr11:58668068-58668118	HL-60	blood:	n/a
42	chr11:58668634-58668684	SK-N-SH_RA	brain:	n/a
43	chr11:58667964-58668014	GM06990	blood:	n/a
44	chr11:58651984-58652034	SK-N-SH	brain:	n/a
45	chr11:58612027-58612077	HRPEpiC	eye:	n/a
46	chr11:58605845-58605895	GM06990	blood:	n/a
47	chr11:58610406-58610456	AG09319	gingival:	n/a
48	chr11:58668488-58668538	HRE	kidney:	n/a
49	chr11:58668634-58668684	HAEpiC	amniotic membrane:	n/a
50	chr11:58598338-58598388	PrEC	prostate:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58420893..58422551-chr11:58555581..58556580,16	K562	blood:
2	chr11:58344188..58345053-chr11:58555383..58556475,3	MCF-7	breast:
3	chr11:58599747..58602498-chr11:58604323..58607050,2	K562	blood:
4	chr11:58335090..58336072-chr11:58555654..58556534,3	K562	blood:
5	chr11:58512569..58514471-chr11:58539113..58540674,2	K562	blood:
6	chr1:149213382..149215537-chr11:58543195..58544714,2	MCF-7	breast:
7	chr11:58346639..58348965-chr11:58654113..58656554,2	K562	blood:
8	chr11:58539643..58542298-chr11:58554397..58556445,2	K562	blood:
9	chr11:58442750..58443528-chr11:58555605..58556306,2	K562	blood:
10	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
11	chr11:58546256..58548670-chr11:58549514..58551227,2	K562	blood:
12	chr11:58567691..58569634-chr11:58571935..58573618,2	K562	blood:
13	chr11:58546256..58548670-chr11:58549514..58551227,2	K562	blood:
14	chr11:58534531..58540413-chr11:58541939..58546893,7	K562	blood:
15	chr11:58537258..58541361-chr11:58541719..58544001,4	K562	blood:
16	chr11:58668032..58668917-chr11:58825619..58826508,3	K562	blood:
17	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
18	chr11:58667985..58668808-chr11:58825960..58826578,4	MCF-7	breast:
19	chr11:58397577..58400348-chr11:58551728..58554179,2	K562	blood:
20	chr11:58537258..58541361-chr11:58541719..58544001,4	K562	blood:
21	chr11:58344812..58347551-chr11:58552824..58556823,4	K562	blood:
22	chr11:58345930..58347450-chr11:58657978..58660327,2	K562	blood:
23	chr11:58551491..58553930-chr11:58557459..58559749,2	K562	blood:
24	chr11:58599747..58602498-chr11:58604323..58607050,2	K562	blood:
25	chr11:58513430..58516648-chr11:58544097..58546491,4	K562	blood:
26	chr11:58530284..58532765-chr11:58534043..58536278,2	K562	blood:
27	chr11:58421175..58421959-chr11:58555571..58556541,3	MCF-7	breast:
28	chr11:58534531..58540413-chr11:58541939..58546893,7	K562	blood:
29	chr11:58547170..58548940-chr11:58549727..58551973,2	K562	blood:
30	chr11:58567691..58569634-chr11:58571935..58573618,2	K562	blood:
31	chr11:58539643..58542298-chr11:58554397..58556445,2	K562	blood:
32	chr11:58547170..58548940-chr11:58549727..58551973,2	K562	blood:
33	chr11:58551491..58553930-chr11:58557459..58559749,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ENSG00000224130	TF binding region
TMA16P1	TF binding region
GLYATL1	TF binding region
GLYATL1P2	TF binding region
GLYATL2	TF binding region
ENSG00000224130	CpG island
TMA16P1	CpG island
GLYATL1	CpG island
GLYATL1P2	CpG island
GLYATL2	CpG island
ENSG00000255073	chromatin interactions
ENSG00000186660	chromatin interactions
ENSG00000255240	chromatin interactions
ENSG00000110031	chromatin interactions
ENSG00000252826	chromatin interactions

Extended variants
information (count: 4401 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4401 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186648435	chr11:58534660-58534661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548336934	chr11:58534666-58534667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570152579	chr11:58534683-58534684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535310086	chr11:58534702-58534703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552356333	chr11:58534745-58534746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570684110	chr11:58534799-58534800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76227395	chr11:58534818-58534819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553218585	chr11:58534825-58534826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568293630	chr11:58534876-58534877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535429658	chr11:58534884-58534885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556579249	chr11:58534900-58534901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568251221	chr11:58534913-58534914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368758052	chr11:58534914-58534915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191956611	chr11:58534928-58534929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183112904	chr11:58535024-58535025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558691226	chr11:58535046-58535047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577352126	chr11:58535066-58535067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78698862	chr11:58535143-58535144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533994067	chr11:58535178-58535179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559990842	chr11:58535201-58535202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572667491	chr11:58535209-58535210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373848621	chr11:58535213-58535214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186295085	chr11:58535215-58535216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563678478	chr11:58535220-58535221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117069767	chr11:58535269-58535270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116131605	chr11:58535312-58535313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546387864	chr11:58535318-58535319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11229615	chr11:58535360-58535361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs367574175	chr11:58535364-58535365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs57483467	chr11:58535376-58535377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189527580	chr11:58535390-58535391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568335110	chr11:58535436-58535437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28431286	chr11:58535458-58535459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138140621	chr11:58535475-58535476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372125387	chr11:58535481-58535482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540850886	chr11:58535489-58535490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373899350	chr11:58535496-58535497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539078600	chr11:58535520-58535521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142635660	chr11:58535554-58535555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182189256	chr11:58535626-58535627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572896822	chr11:58535705-58535706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146068365	chr11:58535728-58535729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553297467	chr11:58535755-58535756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368537373	chr11:58535776-58535777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115703140	chr11:58535784-58535785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563641566	chr11:58535801-58535802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1938709	chr11:58535831-58535832	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs138804178	chr11:58535844-58535845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564603161	chr11:58535845-58535846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528619695	chr11:58535849-58535850	Enhancers Weak transcription	n/a	n/a	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:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58530600-58536800	Enhancers	Liver	Liver
2	chr11:58531200-58538000	Weak transcription	Fetal Intestine Small	intestine
3	chr11:58532200-58535000	Weak transcription	Fetal Intestine Large	intestine
4	chr11:58532800-58535000	Weak transcription	HepG2	liver
5	chr11:58534400-58535400	Weak transcription	Adipose Nuclei	Adipose
6	chr11:58535000-58536800	Enhancers	HepG2	liver
7	chr11:58535000-58537600	Enhancers	Fetal Intestine Large	intestine
8	chr11:58535400-58536400	Enhancers	Adipose Nuclei	Adipose
9	chr11:58535600-58537600	Enhancers	K562	blood
10	chr11:58536200-58536400	Enhancers	Pancreas	Pancrea
11	chr11:58536400-58537800	Weak transcription	Adipose Nuclei	Adipose
12	chr11:58536800-58538000	Weak transcription	HepG2	liver
13	chr11:58537400-58538800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr11:58537600-58538600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:58537600-58538800	Enhancers	NHDF-Ad	bronchial
16	chr11:58537600-58539200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:58537600-58539200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:58537600-58539600	Flanking Active TSS	Fetal Intestine Large	intestine
19	chr11:58537600-58539600	Enhancers	HMEC	breast
20	chr11:58537600-58539800	Enhancers	NHEK	skin
21	chr11:58537600-58540200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:58537600-58540200	Flanking Active TSS	K562	blood
23	chr11:58537800-58538600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:58537800-58539200	Enhancers	Adipose Nuclei	Adipose
25	chr11:58538000-58538400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:58538000-58538600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:58538000-58538600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:58538000-58538600	Enhancers	Hela-S3	cervix
29	chr11:58538000-58538800	ZNF genes & repeats	Fetal Intestine Small	intestine
30	chr11:58538000-58539000	Enhancers	HepG2	liver
31	chr11:58538000-58539200	Enhancers	Esophagus	oesophagus
32	chr11:58538200-58538600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr11:58538200-58538800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr11:58538400-58538800	Enhancers	HSMM	muscle
35	chr11:58538600-58539000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:58538800-58539000	Weak transcription	Fetal Intestine Small	intestine
37	chr11:58539000-58539400	Weak transcription	HepG2	liver
38	chr11:58539000-58541000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr11:58539000-58542600	Enhancers	Fetal Intestine Small	intestine
40	chr11:58539200-58541200	Weak transcription	Adipose Nuclei	Adipose
41	chr11:58539400-58540000	Enhancers	HepG2	liver
42	chr11:58539600-58543000	Enhancers	Fetal Intestine Large	intestine
43	chr11:58540200-58541200	Enhancers	K562	blood
44	chr11:58541000-58541600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:58541200-58541800	Enhancers	Adipose Nuclei	Adipose
46	chr11:58541200-58542200	Flanking Active TSS	K562	blood
47	chr11:58541600-58541800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:58541800-58542000	Enhancers	HepG2	liver
49	chr11:58542200-58542600	Enhancers	K562	blood
50	chr11:58542600-58543000	Flanking Active TSS	K562	blood

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