Variant report

Variant	nsv563099
Chromosome Location	chr13:110749252-110778894
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1157)
CpG islands
(count:489)
Chromatin interactive
region (count:23)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:110773872-110774337	GM12878	blood:	n/a	n/a
2	ATF2	chr13:110773850-110774299	GM12878	blood:	n/a	n/a
3	BACH1	chr13:110768376-110768694	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:110762205-110762495	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr13:110776482-110776695	GM12878	blood:	n/a	n/a
6	BATF	chr13:110773722-110774295	GM12878	blood:	n/a	n/a
7	BATF	chr13:110776459-110776715	GM12878	blood:	n/a	n/a
8	BATF	chr13:110773902-110774287	GM12878	blood:	n/a	n/a
9	BCL11A	chr13:110773949-110774178	GM12878	blood:	n/a	n/a
10	BCL11A	chr13:110773865-110774246	GM12878	blood:	n/a	n/a
11	BCL3	chr13:110760593-110761387	GM12878	blood:	n/a	n/a
12	BCL3	chr13:110760679-110761348	GM12878	blood:	n/a	n/a
13	BCLAF1	chr13:110768371-110768728	GM12878	blood:	n/a	n/a
14	BHLHE40	chr13:110761395-110761569	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:110768430-110768710	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:110773698-110774578	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:110761462-110761478	HepG2	liver:	n/a	n/a
18	BRCA1	chr13:110767973-110768019	GM12878	blood:	n/a	n/a
19	BRCA1	chr13:110768422-110768622	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr13:110774664-110774710	GM12878	blood:	n/a	n/a
21	CEBPB	chr13:110768499-110768879	IMR90	lung:	n/a	chr13:110768797-110768808
22	CEBPB	chr13:110768360-110768884	A549	lung:	n/a	chr13:110768797-110768808
23	CEBPB	chr13:110768505-110768753	MCF-7	breast:	n/a	n/a
24	CEBPB	chr13:110768519-110768835	Hela-S3	cervix:	n/a	chr13:110768797-110768808
25	CEBPB	chr13:110778743-110779016	Hela-S3	cervix:	n/a	chr13:110778845-110778858
26	CEBPB	chr13:110768517-110768880	K562	blood:	n/a	chr13:110768797-110768808
27	CEBPB	chr13:110768390-110768877	H1-hESC	embryonic stem cell:	n/a	chr13:110768797-110768808
28	CEBPB	chr13:110765671-110765881	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr13:110755830-110756439	HCT-116	colon:	n/a	chr13:110755918-110755926
30	CEBPB	chr13:110768072-110768887	A549	lung:	n/a	chr13:110768178-110768195 chr13:110768797-110768808
31	CEBPB	chr13:110778724-110778924	A549	lung:	n/a	chr13:110778845-110778858
32	CEBPB	chr13:110778666-110779083	IMR90	lung:	n/a	chr13:110778845-110778858
33	CEBPB	chr13:110756097-110756102	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr13:110768512-110768858	HepG2	liver:	n/a	chr13:110768797-110768808
35	CEBPB	chr13:110753343-110753483	HepG2	liver:	n/a	n/a
36	CEBPB	chr13:110765589-110765960	IMR90	lung:	n/a	n/a
37	CEBPB	chr13:110756017-110756125	HepG2	liver:	n/a	n/a
38	CHD1	chr13:110773902-110774938	GM12878	blood:	n/a	n/a
39	CHD1	chr13:110760988-110761761	IMR90	lung:	n/a	n/a
40	CHD1	chr13:110768494-110768623	GM12878	blood:	n/a	n/a
41	CHD2	chr13:110761306-110761693	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr13:110773741-110774638	GM12878	blood:	n/a	n/a
43	CHD2	chr13:110768387-110768672	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr13:110761077-110761512	GM12878	blood:	n/a	n/a
45	CREB1	chr13:110772597-110773362	A549	lung:	n/a	n/a
46	CREB1	chr13:110772702-110773254	A549	lung:	n/a	n/a
47	CREB1	chr13:110768406-110768631	A549	lung:	n/a	n/a
48	CTCF	chr13:110768480-110768630	NHEK	skin:	n/a	n/a
49	CTCF	chr13:110760520-110760670	GM12871	blood:	n/a	n/a
50	CTCF	chr13:110764880-110765030	NHEK	skin:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110768683-110768733	HAEpiC	amniotic membrane:	n/a
2	chr13:110768683-110768733	HAEpiC	amniotic membrane:	n/a
3	chr13:110768683-110768733	HCM	heart:	n/a
4	chr13:110759424-110759474	HPAEpiC	pulmonary alveolar:	n/a
5	chr13:110768551-110768601	HepG2	liver:	n/a
6	chr13:110763402-110763452	Jurkat	blood:	n/a
7	chr13:110768493-110768543	HRCEpiC	kidney:	n/a
8	chr13:110768493-110768543	GM19239	blood:	n/a
9	chr13:110763342-110763392	AG04449	skin:	fetal
10	chr13:110763402-110763452	SK-N-SH_RA	brain:	n/a
11	chr13:110759424-110759474	GM12891	blood:	n/a
12	chr13:110768551-110768601	HCPEpiC	choroid plexus:	n/a
13	chr13:110768683-110768733	HPAEpiC	pulmonary alveolar:	n/a
14	chr13:110768493-110768543	SK-N-SH	brain:	n/a
15	chr13:110759424-110759474	HEK293	kidney:	embryo
16	chr13:110768683-110768733	GM12892	blood:	n/a
17	chr13:110768683-110768733	ovcar-3	ovarian:	n/a
18	chr13:110768683-110768733	AG04450	lung:	fetal
19	chr13:110768493-110768543	SKMC	muscle:	n/a
20	chr13:110768683-110768733	Jurkat	blood:	n/a
21	chr13:110763402-110763452	HCF	heart:	n/a
22	chr13:110768493-110768543	GM12891	blood:	n/a
23	chr13:110768683-110768733	SAEC	small airway:	n/a
24	chr13:110763342-110763392	HRCEpiC	kidney:	n/a
25	chr13:110759424-110759474	AG04450	lung:	fetal
26	chr13:110763402-110763452	CMK	blood:	n/a
27	chr13:110768683-110768733	HNPCEpiC	eye:	n/a
28	chr13:110759424-110759474	GM19239	blood:	n/a
29	chr13:110763402-110763452	BJ	skin:	n/a
30	chr13:110763342-110763392	HPAEpiC	pulmonary alveolar:	n/a
31	chr13:110763342-110763392	MCF-7	breast:	n/a
32	chr13:110761577-110761627	HNPCEpiC	eye:	n/a
33	chr13:110763342-110763392	GM12891	blood:	n/a
34	chr13:110763402-110763452	Caco-2	colon:	n/a
35	chr13:110759424-110759474	CMK	blood:	n/a
36	chr13:110777186-110777236	A549	lung:	n/a
37	chr13:110777186-110777236	PrEC	prostate:	n/a
38	chr13:110777186-110777236	HL-60	blood:	n/a
39	chr13:110768493-110768543	HCT-116	colon:	n/a
40	chr13:110761577-110761627	SK-N-SH	brain:	n/a
41	chr13:110777186-110777236	K562	blood:	n/a
42	chr13:110763402-110763452	ProgFib	skin:	n/a
43	chr13:110777186-110777236	HCPEpiC	choroid plexus:	n/a
44	chr13:110768493-110768543	CMK	blood:	n/a
45	chr13:110777186-110777236	T-47D	breast:	n/a
46	chr13:110768683-110768733	ECC-1	luminal epithelium:	n/a
47	chr13:110761577-110761627	HepG2	liver:	n/a
48	chr13:110768551-110768601	NHDF-neo	bronchial:	n/a
49	chr13:110768493-110768543	NH-A	brain:	n/a
50	chr13:110768683-110768733	HIPEpiC	eye:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:
2	chr13:110651999..110652742-chr13:110760981..110761503,2	MCF-7	breast:
3	chr13:110583476..110584263-chr13:110760363..110760981,2	MCF-7	breast:
4	chr13:110436096..110439350-chr13:110760184..110763012,5	MCF-7	breast:
5	chr13:110760613..110762563-chr13:110777021..110779083,2	MCF-7	breast:
6	chr13:110654511..110656415-chr13:110759069..110761693,2	MCF-7	breast:
7	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:
8	chr13:110436205..110441713-chr13:110758837..110762777,7	MCF-7	breast:
9	chr13:110761020..110763183-chr13:110765963..110768234,2	MCF-7	breast:
10	chr13:110761020..110763183-chr13:110765963..110768234,2	MCF-7	breast:
11	chr13:109613700..109614457-chr13:110760895..110761419,2	MCF-7	breast:
12	chr13:110651354..110653633-chr13:110756277..110757904,2	MCF-7	breast:
13	chr13:110768940..110770470-chr13:110777999..110780195,2	K562	blood:
14	chr13:110769994..110772224-chr13:110776399..110779306,2	MCF-7	breast:
15	chr13:110769994..110772224-chr13:110776399..110779306,2	MCF-7	breast:
16	chr13:110417399..110417917-chr13:110760942..110761494,2	MCF-7	breast:
17	chr13:110445785..110447746-chr13:110765342..110767976,2	MCF-7	breast:
18	chr13:110443953..110447179-chr13:110758507..110762069,3	MCF-7	breast:
19	chr13:110768940..110770470-chr13:110777999..110780195,2	K562	blood:
20	chr13:110760613..110762563-chr13:110777021..110779083,2	MCF-7	breast:
21	chr13:110748461..110750541-chr13:110753298..110755107,2	K562	blood:
22	chr13:110717144..110719381-chr13:110752515..110754017,2	K562	blood:
23	chr13:109567424..109568073-chr13:110760960..110761768,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A2-5	chr13:110775555-110777581	NONHSAT035138
2	lnc-COL4A1-3	chr13:110769924-110770858	l_918_chr13:110767285-110770858_testes
3	lnc-COL4A1-4	chr13:110750200-110750498	NONHSAT035136
4	lnc-COL4A2-1	chr13:110774800-110774945	XLOC_010497
5	lnc-COL4A1-3	chr13:110767286-110769562	l_918_chr13:110767285-110770858_testes
6	lnc-COL4A2-1	chr13:110774616-110774690	XLOC_010497

No data

Variant related genes	Relation type
RN7SL783P	TF binding region
RN7SL783P	CpG island
ENSG00000265885	chromatin interactions
ENSG00000185950	chromatin interactions

Extended variants
information (count: 1165 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9588090	chr13:110749252-110749253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567493980	chr13:110749254-110749255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536129711	chr13:110749413-110749414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142251253	chr13:110749449-110749450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs9588091	chr13:110749491-110749492	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538367535	chr13:110749546-110749547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150855317	chr13:110749551-110749552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139591032	chr13:110749568-110749569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535726261	chr13:110749585-110749586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs16975320	chr13:110749653-110749654	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs574426353	chr13:110749655-110749656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543304308	chr13:110749657-110749658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555891503	chr13:110749710-110749711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575712923	chr13:110749735-110749736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560080786	chr13:110749767-110749768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144268140	chr13:110749768-110749769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531915247	chr13:110749810-110749811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545535858	chr13:110749829-110749830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565273598	chr13:110749856-110749857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113253651	chr13:110749864-110749865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146616700	chr13:110749909-110749910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77389315	chr13:110749920-110749921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529940053	chr13:110749933-110749934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549634578	chr13:110749935-110749936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569529049	chr13:110749947-110749948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538479332	chr13:110749970-110749971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558696061	chr13:110749999-110750000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561855643	chr13:110750017-110750018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565684114	chr13:110750063-110750064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534708099	chr13:110750086-110750087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111266060	chr13:110750090-110750091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574440606	chr13:110750102-110750103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74124139	chr13:110750137-110750138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190454317	chr13:110750155-110750156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556863408	chr13:110750164-110750165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576796125	chr13:110750180-110750181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571925751	chr13:110750181-110750182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141343524	chr13:110750204-110750205	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs565464369	chr13:110750236-110750237	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs182325453	chr13:110750252-110750253	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs145843026	chr13:110750320-110750321	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs561145021	chr13:110750382-110750383	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs148827229	chr13:110750392-110750393	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs186890597	chr13:110750400-110750401	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs569641957	chr13:110750415-110750416	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs558883379	chr13:110750416-110750417	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs552128285	chr13:110750423-110750424	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs564080706	chr13:110750434-110750435	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs371571823	chr13:110750518-110750519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560152997	chr13:110750546-110750547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110747000-110750200	Enhancers	Colon Smooth Muscle	Colon
2	chr13:110747600-110749600	Weak transcription	Esophagus	oesophagus
3	chr13:110747600-110750000	Enhancers	NHEK	skin
4	chr13:110747600-110758400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr13:110747800-110749400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr13:110747800-110749600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr13:110748400-110749800	Weak transcription	Pancreas	Pancrea
8	chr13:110748400-110758400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr13:110749000-110749400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr13:110749000-110750000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:110749200-110750000	Enhancers	HMEC	breast
12	chr13:110749400-110749800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr13:110749400-110750000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr13:110749600-110749800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr13:110749600-110749800	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr13:110749600-110750600	Enhancers	Esophagus	oesophagus
17	chr13:110749800-110750000	Enhancers	Pancreas	Pancrea
18	chr13:110749800-110750200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr13:110750000-110752000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr13:110752000-110752400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr13:110752400-110755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr13:110752600-110752800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr13:110752800-110753200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr13:110753200-110754000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr13:110755000-110755200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:110755000-110757200	Enhancers	HMEC	breast
27	chr13:110755200-110755800	Enhancers	Adipose Nuclei	Adipose
28	chr13:110755200-110756400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:110755400-110755600	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr13:110755400-110755800	Enhancers	Pancreas	Pancrea
31	chr13:110755400-110756000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr13:110755400-110756600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr13:110755400-110756800	Enhancers	NHEK	skin
34	chr13:110755400-110757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr13:110755400-110760000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr13:110755600-110755800	Enhancers	Brain Substantia Nigra	brain
37	chr13:110755600-110756200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr13:110755600-110756400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr13:110755800-110757000	Weak transcription	Pancreas	Pancrea
40	chr13:110755800-110758600	Weak transcription	Adipose Nuclei	Adipose
41	chr13:110756000-110758400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr13:110756200-110759000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:110756400-110758600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr13:110756400-110761400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr13:110756600-110760800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr13:110756800-110758600	Enhancers	Placenta	Placenta
47	chr13:110756800-110761200	Weak transcription	NHEK	skin
48	chr13:110757000-110757200	Enhancers	Fetal Stomach	stomach
49	chr13:110757000-110759600	Enhancers	Pancreas	Pancrea
50	chr13:110757000-110761400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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