Variant report

Variant	nsv1024899
Chromosome Location	chr5:101475627-101522225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:101489024-101489385	HepG2	liver:	n/a	n/a
2	CCNT2	chr5:101518922-101519122	K562	blood:	n/a	n/a
3	CEBPB	chr5:101506875-101507212	HepG2	liver:	n/a	n/a
4	CEBPB	chr5:101492747-101492947	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:101506879-101507168	A549	lung:	n/a	n/a
6	CTCF	chr5:101489160-101489310	Caco-2	colon:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
7	CTCF	chr5:101489140-101489290	HEEpiC	esophagus:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
8	CTCF	chr5:101489080-101489355	HepG2	liver:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
9	CTCF	chr5:101489140-101489290	HMF	breast:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
10	CTCF	chr5:101489120-101489270	HVMF	connective:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
11	CTCF	chr5:101489120-101489270	BJ	skin:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
12	CTCF	chr5:101489460-101489610	GM12864	blood:	n/a	n/a
13	CTCF	chr5:101489053-101489368	HepG2	liver:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
14	CTCF	chr5:101489480-101489630	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr5:101489200-101489350	HA-sp	spinal cord:	n/a	chr5:101489200-101489218 chr5:101489201-101489217
16	CTCF	chr5:101489160-101489310	HepG2	liver:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
17	CTCF	chr5:101489100-101489250	GM12865	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
18	CTCF	chr5:101489160-101489310	HFF-Myc	foreskin:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
19	CTCF	chr5:101489080-101489230	HMF	breast:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
20	CTCF	chr5:101489160-101489310	GM12866	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
21	CTCF	chr5:101489160-101489310	SK-N-SH_RA	brain:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
22	CTCF	chr5:101489200-101489350	K562	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217
23	CTCF	chr5:101489112-101489348	A549	lung:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
24	CTCF	chr5:101488800-101488950	GM12873	blood:	n/a	n/a
25	CTCF	chr5:101489140-101489290	GM12870	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
26	CTCF	chr5:101488840-101488990	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr5:101489196-101489319	GM12891	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217
28	CTCF	chr5:101489140-101489290	AG04449	skin:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
29	CTCF	chr5:101489088-101489295	Spleen_OC	spleen:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
30	CTCF	chr5:101489160-101489310	HL-60	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
31	CTCF	chr5:101489125-101489290	K562	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
32	CTCF	chr5:101489100-101489250	GM06990	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
33	CTCF	chr5:101489160-101489310	NHEK	skin:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
34	CTCF	chr5:101489160-101489310	HA-sp	spinal cord:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
35	CTCF	chr5:101488996-101489613	GM12878	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
36	CTCF	chr5:101489077-101489337	Hela-S3	cervix:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
37	CTCF	chr5:101489100-101489250	HRE	kidney:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
38	CTCF	chr5:101488915-101489440	MCF-7	breast:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
39	CTCF	chr5:101489100-101489250	BE2_C	brain:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
40	CTCF	chr5:101489140-101489290	HMEC	breast:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
41	CTCF	chr5:101489121-101489308	LNCaP	prostate:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
42	CTCF	chr5:101488880-101489030	Caco-2	colon:	n/a	n/a
43	CTCF	chr5:101489150-101489309	GM13976	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
44	CTCF	chr5:101489160-101489310	GM12869	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
45	CTCF	chr5:101489180-101489330	NB4	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
46	CTCF	chr5:101489160-101489310	GM12874	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
47	CTCF	chr5:101482338-101482366	Lung_OC	lung:	n/a	n/a
48	CTCF	chr5:101489028-101489379	T-47D	breast:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
49	CTCF	chr5:101489120-101489270	GM06990	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216
50	CTCF	chr5:101489120-101489270	GM12865	blood:	n/a	chr5:101489200-101489218 chr5:101489201-101489217 chr5:101489195-101489216

No.	Distal block	Cell Line	Cell type
1	chr5:101476598..101478204-chr5:101481147..101483100,2	MCF-7	breast:
2	chr5:101476598..101478204-chr5:101481147..101483100,2	MCF-7	breast:
3	chr5:101475498..101477506-chr5:101479656..101481283,2	K562	blood:
4	chr5:101277790..101278635-chr5:101488732..101489585,4	MCF-7	breast:
5	chr5:101277636..101278379-chr5:101489093..101489664,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAM-5	chr5:101479781-101479847	XLOC_004491
2	lnc-PAM-5	chr5:101482019-101482276	XLOC_004491
3	lnc-PAM-5	chr5:101482018-101482276	NONHSAT103022
4	lnc-PAM-5	chr5:101479780-101479847	NONHSAT103022

Variant related genes	Relation type
ENSG00000248261	TF binding region
ENSG00000248261	chromatin interactions

Extended variants
information (count: 819 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12659729	chr5:101475627-101475628	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575437456	chr5:101475642-101475643	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12659731	chr5:101475656-101475657	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs141428303	chr5:101475679-101475680	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs190402796	chr5:101475732-101475733	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs541732975	chr5:101475834-101475835	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs146942522	chr5:101475847-101475848	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553089314	chr5:101475850-101475851	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557512024	chr5:101475859-101475860	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545303013	chr5:101475862-101475863	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563440862	chr5:101475878-101475879	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs202193906	chr5:101475990-101475991	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11740476	chr5:101476014-101476015	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs548923792	chr5:101476027-101476028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs560947759	chr5:101476031-101476032	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114785993	chr5:101476065-101476066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs75149300	chr5:101476067-101476068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571485020	chr5:101476088-101476089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538804509	chr5:101476089-101476090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550839747	chr5:101476092-101476093	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200781232	chr5:101476107-101476108	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568963090	chr5:101476117-101476118	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573441631	chr5:101476151-101476152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs112812798	chr5:101476283-101476284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs554577678	chr5:101476292-101476293	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572812528	chr5:101476320-101476321	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533587122	chr5:101476321-101476322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553611286	chr5:101476424-101476425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs371674391	chr5:101476429-101476430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149067897	chr5:101476449-101476450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545577064	chr5:101476458-101476459	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs563550410	chr5:101476464-101476465	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143060480	chr5:101476479-101476480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542733314	chr5:101476586-101476587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569730156	chr5:101476602-101476603	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572941890	chr5:101476617-101476618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs56283402	chr5:101476620-101476621	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs546705974	chr5:101476631-101476632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148357012	chr5:101476658-101476659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs142097573	chr5:101476699-101476700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145901951	chr5:101476700-101476701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369428326	chr5:101476732-101476733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs535263155	chr5:101476755-101476756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569096343	chr5:101476757-101476758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553289304	chr5:101476788-101476789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs536319467	chr5:101476790-101476791	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs79685738	chr5:101476862-101476863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181401137	chr5:101476876-101476877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576202296	chr5:101476880-101476881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79969100	chr5:101476884-101476885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101474600-101476000	Enhancers	HepG2	liver
2	chr5:101475400-101475800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr5:101476000-101480800	Weak transcription	HepG2	liver
4	chr5:101477600-101477800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr5:101478000-101480000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:101480000-101481200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:101480600-101481000	Enhancers	Hela-S3	cervix
8	chr5:101480800-101481800	Enhancers	HepG2	liver
9	chr5:101481200-101488800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:101481800-101487600	Weak transcription	HepG2	liver
11	chr5:101487600-101489600	Enhancers	HepG2	liver
12	chr5:101488400-101488800	Enhancers	Fetal Intestine Large	intestine
13	chr5:101488800-101489000	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr5:101488800-101489000	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr5:101488800-101489200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:101488800-101489200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:101488800-101489200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:101488800-101489200	Flanking Active TSS	Fetal Intestine Large	intestine
19	chr5:101488800-101489200	Enhancers	Fetal Kidney	kidney
20	chr5:101488800-101489400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr5:101488800-101489800	Enhancers	Fetal Intestine Small	intestine
22	chr5:101488800-101491200	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr5:101489000-101490400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr5:101489200-101489600	Enhancers	Fetal Intestine Large	intestine
25	chr5:101489200-101490400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:101489200-101490400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr5:101489400-101490400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr5:101489600-101490000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:101489600-101490200	Weak transcription	Fetal Intestine Large	intestine
30	chr5:101489800-101490200	Weak transcription	Fetal Intestine Small	intestine
31	chr5:101490000-101490400	Active TSS	Primary T cells from cord blood	blood
32	chr5:101490000-101491200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:101490200-101491200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr5:101490200-101491200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr5:101490200-101491200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
36	chr5:101490200-101491200	Active TSS	Fetal Intestine Large	intestine
37	chr5:101490200-101491200	Active TSS	Fetal Intestine Small	intestine
38	chr5:101490200-101491200	Active TSS	Stomach Smooth Muscle	stomach
39	chr5:101490400-101491000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr5:101490400-101491000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr5:101490400-101491000	Active TSS	Esophagus	oesophagus
42	chr5:101490400-101491000	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr5:101490400-101491200	Active TSS	H1 Cell Line	embryonic stem cell
44	chr5:101490400-101491200	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr5:101490400-101491200	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr5:101490400-101491200	Active TSS	Pancreas	Pancrea
47	chr5:101490400-101491200	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr5:101490400-101491200	Active TSS	Osteobl	bone
49	chr5:101490600-101491000	Active TSS	Right Ventricle	heart
50	chr5:101491000-101493600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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