Variant report

Variant	nsv1041994
Chromosome Location	chr13:80123596-80247708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr13:80234775-80235020	GM12878	blood:	n/a	chr13:80234951-80234960
2	BCL11A	chr13:80234549-80234846	GM12878	blood:	n/a	n/a
3	BCL11A	chr13:80234561-80234759	GM12878	blood:	n/a	n/a
4	CBX3	chr13:80205338-80205818	HCT-116	colon:	n/a	n/a
5	CCNT2	chr13:80159175-80159546	K562	blood:	n/a	n/a
6	CEBPB	chr13:80180075-80180350	Hela-S3	cervix:	n/a	chr13:80180255-80180266
7	CEBPB	chr13:80159169-80159538	K562	blood:	n/a	n/a
8	CEBPB	chr13:80180098-80180421	IMR90	lung:	n/a	chr13:80180255-80180266
9	CEBPB	chr13:80178917-80179264	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr13:80180088-80180361	A549	lung:	n/a	chr13:80180255-80180266
11	CEBPB	chr13:80233549-80233618	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:80159186-80159446	K562	blood:	n/a	n/a
13	CEBPB	chr13:80180091-80180401	HepG2	liver:	n/a	chr13:80180255-80180266
14	CEBPD	chr13:80159119-80159586	K562	blood:	n/a	n/a
15	CEBPD	chr13:80159132-80159601	K562	blood:	n/a	n/a
16	CTCF	chr13:80216840-80216990	AG09309	skin:	n/a	n/a
17	CTCF	chr13:80205380-80205530	RPTEC	kidney:	n/a	n/a
18	CTCF	chr13:80205420-80205570	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr13:80205420-80205570	AG09319	gingival:	n/a	n/a
20	CTCF	chr13:80216820-80216970	AG09319	gingival:	n/a	n/a
21	CTCF	chr13:80205392-80205640	Medullo	brain:	n/a	n/a
22	CTCF	chr13:80237120-80237270	SK-N-SH_RA	brain:	n/a	chr13:80237200-80237210 chr13:80237197-80237218 chr13:80237195-80237213
23	CTCF	chr13:80237201-80237227	MCF-7	breast:	n/a	n/a
24	CTCF	chr13:80216860-80217010	AG10803	skin:	n/a	n/a
25	CTCF	chr13:80205480-80205630	NHEK	skin:	n/a	n/a
26	CTCF	chr13:80237162-80237263	Gliobla	brain:	n/a	chr13:80237200-80237210 chr13:80237197-80237218 chr13:80237195-80237213
27	CTCF	chr13:80237080-80237230	WERI-Rb-1	eye:	n/a	chr13:80237200-80237210 chr13:80237197-80237218 chr13:80237195-80237213
28	CTCF	chr13:80205461-80205595	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:80216900-80217050	BJ	skin:	n/a	n/a
30	CTCF	chr13:80216860-80217010	AG04450	lung:	n/a	n/a
31	CTCF	chr13:80178006-80178084	Medullo	brain:	n/a	n/a
32	CTCF	chr13:80205450-80205600	LNCaP	prostate:	n/a	n/a
33	CTCF	chr13:80216819-80217065	GM12878	blood:	n/a	n/a
34	CTCF	chr13:80216840-80216990	HMEC	breast:	n/a	n/a
35	CTCF	chr13:80234280-80234430	BE2_C	brain:	n/a	n/a
36	CTCF	chr13:80205440-80205590	AG09309	skin:	n/a	n/a
37	CTCF	chr13:80205420-80205570	AG04449	skin:	n/a	n/a
38	CTCF	chr13:80205382-80205685	IMR90	lung:	n/a	n/a
39	CTCF	chr13:80205440-80205590	NHEK	skin:	n/a	n/a
40	CTCF	chr13:80205360-80205510	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr13:80216840-80216990	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr13:80237148-80237294	NHEK	skin:	n/a	chr13:80237200-80237210 chr13:80237197-80237218 chr13:80237195-80237213
43	CTCF	chr13:80216840-80216990	AG04449	skin:	n/a	n/a
44	CTCF	chr13:80205320-80205470	HCM	heart:	n/a	n/a
45	CTCF	chr13:80205480-80205630	A549	lung:	n/a	n/a
46	CTCF	chr13:80205452-80205567	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr13:80205340-80205490	SAEC	small airway:	n/a	n/a
48	CTCF	chr13:80237080-80237230	SK-N-SH_RA	brain:	n/a	chr13:80237200-80237210 chr13:80237197-80237218 chr13:80237195-80237213
49	CTCF	chr13:80205175-80205823	A549	lung:	n/a	n/a
50	CTCF	chr13:80205400-80205550	HMF	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:80174349-80174399	AG04449	skin:	fetal
2	chr13:80233183-80233233	SK-N-SH_RA	brain:	n/a
3	chr13:80173719-80173769	NH-A	brain:	n/a
4	chr13:80173719-80173769	IMR90	lung:	fetal
5	chr13:80173719-80173769	HUVEC	blood vessel:	n/a
6	chr13:80174349-80174399	NH-A	brain:	n/a
7	chr13:80173719-80173769	SKMC	muscle:	n/a
8	chr13:80174349-80174399	HL-60	blood:	n/a
9	chr13:80174349-80174399	HIPEpiC	eye:	n/a
10	chr13:80233183-80233233	MCF10A-Er-Src	breast:	n/a
11	chr13:80233183-80233233	PFSK-1	brain:	n/a
12	chr13:80233183-80233233	HCT-116	colon:	n/a
13	chr13:80174349-80174399	HepG2	liver:	n/a
14	chr13:80174349-80174399	GM12878	blood:	n/a
15	chr13:80233183-80233233	CMK	blood:	n/a
16	chr13:80174349-80174399	HRE	kidney:	n/a
17	chr13:80174349-80174399	PrEC	prostate:	n/a
18	chr13:80233183-80233233	HMEC	breast:	n/a
19	chr13:80233183-80233233	T-47D	breast:	n/a
20	chr13:80233183-80233233	HAEpiC	amniotic membrane:	n/a
21	chr13:80173719-80173769	PrEC	prostate:	n/a
22	chr13:80233183-80233233	U87	brain:	n/a
23	chr13:80233183-80233233	HRPEpiC	eye:	n/a
24	chr13:80233183-80233233	HepG2	liver:	n/a
25	chr13:80173719-80173769	BJ	skin:	n/a
26	chr13:80173719-80173769	HRPEpiC	eye:	n/a
27	chr13:80173719-80173769	HNPCEpiC	eye:	n/a
28	chr13:80233183-80233233	ECC-1	luminal epithelium:	n/a
29	chr13:80233183-80233233	NT2-D1	testis:	n/a
30	chr13:80173719-80173769	HEEpiC	esophagus:	n/a
31	chr13:80233183-80233233	HUVEC	blood vessel:	n/a
32	chr13:80174349-80174399	AG09319	gingival:	n/a
33	chr13:80173719-80173769	AG04449	skin:	fetal
34	chr13:80233183-80233233	HNPCEpiC	eye:	n/a
35	chr13:80174349-80174399	Jurkat	blood:	n/a
36	chr13:80233183-80233233	NHBE	bronchial:	n/a
37	chr13:80174349-80174399	HEK293	kidney:	embryo
38	chr13:80174349-80174399	PANC-1	pancreas:	n/a
39	chr13:80174349-80174399	AoSMC	blood vessel:	n/a
40	chr13:80174349-80174399	RPTEC	kidney:	n/a
41	chr13:80173719-80173769	GM06990	blood:	n/a
42	chr13:80174349-80174399	SK-N-MC	brain:	n/a
43	chr13:80173719-80173769	HRCEpiC	kidney:	n/a
44	chr13:80174349-80174399	HMEC	breast:	n/a
45	chr13:80173719-80173769	MCF10A-Er-Src	breast:	n/a
46	chr13:80173719-80173769	U87	brain:	n/a
47	chr13:80174349-80174399	GM12892	blood:	n/a
48	chr13:80233183-80233233	GM12878	blood:	n/a
49	chr13:80233183-80233233	SK-N-MC	brain:	n/a
50	chr13:80174349-80174399	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:80141740..80145180-chr13:80145215..80148510,3	K562	blood:
2	chr13:80141740..80145180-chr13:80145215..80148510,3	K562	blood:
3	chr13:80120811..80122493-chr13:80123557..80126338,2	K562	blood:
4	chr13:80123748..80125276-chr13:80125653..80128359,2	K562	blood:
5	chr13:80123748..80125276-chr13:80125653..80128359,2	K562	blood:
6	chr13:79978813..79981256-chr13:80124756..80127721,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDFIP2-1	chr13:80144923-80146077	NONHSAT034493
2	lnc-NDFIP2-3	chr13:80211603-80211770	XLOC_010447
3	lnc-NDFIP2-1	chr13:80145215-80145923	XLOC_010446
4	lnc-RBM26-3	chr13:80144698-80144983	XLOC_010668
5	lnc-NDFIP2-1	chr13:80144698-80144983	ENSG00000227676.2
6	lnc-NDFIP2-1	chr13:80140837-80140942	XLOC_010446
7	lnc-RBM26-3	chr13:80140881-80140942	XLOC_010668
8	lnc-NDFIP2-1	chr13:80145215-80145335	NONHSAT034489
9	lnc-NDFIP2-1	chr13:80132494-80132526	NONHSAT034489
10	lnc-NDFIP2-1	chr13:80144698-80144885	NONHSAT034489
11	lnc-NDFIP2-3	chr13:80240740-80240876	XLOC_010447
12	lnc-NDFIP2-1	chr13:80144698-80144885	XLOC_010446
13	lnc-NDFIP2-1	chr13:80140881-80140942	ENSG00000227676.2
14	lnc-NDFIP2-1	chr13:80144654-80144915	NONHSAT034493

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NDFIP2	hsa-miR-7-5p	chr13:80125592-80125599
2	NDFIP2	hsa-miR-7-5p	chr13:80126970-80126992
3	NDFIP2	hsa-miR-378a-3p	chr13:80126910-80126931

Variant related genes	Relation type
LINC01068	TF binding region
LINC01068	CpG island
ENSG00000139746	chromatin interactions
ENSG00000227354	chromatin interactions

Extended variants
information (count: 4363 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:4363 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555351793	chr13:80123610-80123611	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575442776	chr13:80123615-80123616	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182531955	chr13:80123641-80123642	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7998370	chr13:80123663-80123664	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569071599	chr13:80123766-80123767	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578157986	chr13:80123787-80123788	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559971307	chr13:80123791-80123792	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190530202	chr13:80123802-80123803	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536454269	chr13:80123811-80123812	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554172078	chr13:80123865-80123866	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573929919	chr13:80123870-80123871	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543348960	chr13:80123946-80123947	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35353924	chr13:80123949-80123950	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563028447	chr13:80123963-80123964	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs987284	chr13:80123984-80123985	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs572621772	chr13:80124015-80124016	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533677470	chr13:80124038-80124039	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57032852	chr13:80124096-80124097	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs532881510	chr13:80124099-80124100	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114881954	chr13:80124106-80124107	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566493652	chr13:80124215-80124216	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543836691	chr13:80124231-80124232	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73234700	chr13:80124241-80124242	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576802756	chr13:80124248-80124249	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549300788	chr13:80124255-80124256	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569067133	chr13:80124318-80124319	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538092285	chr13:80124340-80124341	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181740791	chr13:80124376-80124377	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571451138	chr13:80124493-80124494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11348493	chr13:80124559-80124560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533781119	chr13:80124676-80124677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546003114	chr13:80124677-80124678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1414156	chr13:80124707-80124708	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs1414155	chr13:80124717-80124718	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs574017319	chr13:80124720-80124721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370922077	chr13:80124791-80124792	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528736814	chr13:80124842-80124843	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs113412021	chr13:80124926-80124927	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574656741	chr13:80124975-80124976	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35584801	chr13:80124978-80124979	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542664915	chr13:80125002-80125003	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs373307406	chr13:80125041-80125042	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576349455	chr13:80125074-80125075	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs185945818	chr13:80125080-80125081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs545263129	chr13:80125223-80125224	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs565171814	chr13:80125275-80125276	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376204236	chr13:80125288-80125289	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs527857920	chr13:80125342-80125343	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540373255	chr13:80125352-80125353	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542060636	chr13:80125382-80125383	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	19490664	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Breast cancer	21364760	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Schizophrenia	19197363	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:778 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:80087400-80134000	Weak transcription	Aorta	Aorta
2	chr13:80087400-80134600	Weak transcription	Pancreas	Pancrea
3	chr13:80098600-80135000	Weak transcription	Placenta	Placenta
4	chr13:80099400-80133200	Weak transcription	Psoas Muscle	Psoas
5	chr13:80100600-80136400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr13:80100800-80133200	Weak transcription	Hela-S3	cervix
7	chr13:80101800-80133200	Weak transcription	Primary T cells from cord blood	blood
8	chr13:80102200-80133600	Weak transcription	Gastric	stomach
9	chr13:80104800-80133600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:80108400-80132200	Weak transcription	A549	lung
11	chr13:80109000-80129400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr13:80109000-80133200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr13:80109000-80133200	Weak transcription	HSMM	muscle
14	chr13:80109200-80133200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr13:80109600-80133200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr13:80109800-80128000	Weak transcription	NHDF-Ad	bronchial
17	chr13:80109800-80131600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr13:80110600-80133200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr13:80112600-80131800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr13:80112600-80133200	Weak transcription	Osteobl	bone
21	chr13:80113200-80123600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr13:80113200-80123600	Weak transcription	Fetal Intestine Small	intestine
23	chr13:80113200-80131600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr13:80113200-80133800	Weak transcription	Left Ventricle	heart
25	chr13:80114400-80130600	Weak transcription	NHEK	skin
26	chr13:80114400-80131600	Weak transcription	Duodenum Mucosa	Duodenum
27	chr13:80114600-80131800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr13:80115000-80133800	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr13:80115200-80127800	Strong transcription	Dnd41	blood
30	chr13:80117800-80123600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr13:80117800-80123600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr13:80120200-80132000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr13:80120200-80134200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr13:80121800-80123800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr13:80121800-80124200	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr13:80122000-80123600	Weak transcription	HSMMtube	muscle
37	chr13:80122000-80133200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr13:80122200-80123800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:80122200-80133000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr13:80122800-80124000	Enhancers	Fetal Lung	lung
41	chr13:80122800-80124200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr13:80122800-80124400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr13:80123000-80124200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr13:80123000-80124200	Enhancers	Fetal Heart	heart
45	chr13:80123000-80131600	Weak transcription	Liver	Liver
46	chr13:80123000-80135000	Weak transcription	Stomach Mucosa	stomach
47	chr13:80123200-80123600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr13:80123200-80124200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr13:80123200-80124200	Enhancers	Fetal Intestine Large	intestine
50	chr13:80123200-80124200	Enhancers	Fetal Kidney	kidney

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