Variant report

Variant	esv1816307
Chromosome Location	chr5:59992305-60012235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:805)
CpG islands
(count:980)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59995305-59996360	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:59999797-60000151	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:59996034-59996038	K562	blood:	n/a	n/a
4	ATF1	chr5:59995447-59996702	K562	blood:	n/a	n/a
5	ATF2	chr5:59995349-59996155	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:59995701-59996325	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:59995674-59996236	GM12878	blood:	n/a	n/a
8	ATF3	chr5:59995819-59996207	K562	blood:	n/a	chr5:59996023-59996043 chr5:59996035-59996046
9	BACH1	chr5:59995416-59996305	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr5:59995402-59996329	A549	lung:	n/a	chr5:59995938-59995951 chr5:59995934-59995947 chr5:59996005-59996018 chr5:59995768-59995781 chr5:59995966-59995979
11	BCLAF1	chr5:59995423-59996324	GM12878	blood:	n/a	chr5:59995938-59995951 chr5:59995934-59995947 chr5:59996005-59996018 chr5:59995768-59995781 chr5:59995966-59995979
12	BCLAF1	chr5:59995291-59996358	GM12878	blood:	n/a	chr5:59995938-59995951 chr5:59995934-59995947 chr5:59996005-59996018 chr5:59995768-59995781 chr5:59995966-59995979
13	BHLHE40	chr5:59995469-59997496	K562	blood:	n/a	chr5:59995940-59995956 chr5:59995931-59995947
14	BHLHE40	chr5:59995711-59996635	GM12878	blood:	n/a	chr5:59995940-59995956 chr5:59995931-59995947
15	BRCA1	chr5:59995376-59996098	HepG2	liver:	n/a	n/a
16	BRCA1	chr5:59995808-59996235	GM12878	blood:	n/a	n/a
17	BRCA1	chr5:59995307-59996461	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr5:59995381-59996849	K562	blood:	n/a	n/a
19	CBX3	chr5:59995862-59996182	K562	blood:	n/a	n/a
20	CCNT2	chr5:59997685-59997818	K562	blood:	n/a	n/a
21	CCNT2	chr5:59995634-59996720	K562	blood:	n/a	chr5:59996179-59996188
22	CEBPB	chr5:59999872-60000091	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:59999783-60000117	MCF-7	breast:	n/a	n/a
24	CEBPB	chr5:60004676-60004744	HepG2	liver:	n/a	chr5:60004699-60004710
25	CEBPB	chr5:59995859-59996093	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:59997356-59997558	K562	blood:	n/a	n/a
27	CEBPB	chr5:59997360-59997660	K562	blood:	n/a	n/a
28	CEBPB	chr5:59999774-60000259	A549	lung:	n/a	n/a
29	CEBPB	chr5:59996231-59997044	K562	blood:	n/a	n/a
30	CEBPB	chr5:59995520-59996098	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:59999856-60000111	A549	lung:	n/a	n/a
32	CEBPD	chr5:59995781-59996215	HepG2	liver:	n/a	n/a
33	CHD1	chr5:59995176-59996387	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr5:59995518-59996260	GM12878	blood:	n/a	n/a
35	CHD2	chr5:59995422-59996575	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr5:59997166-59997206	K562	blood:	n/a	n/a
37	CHD2	chr5:59995240-59996437	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr5:59995370-59996235	K562	blood:	n/a	n/a
39	CHD2	chr5:59995380-59996189	HepG2	liver:	n/a	n/a
40	CHD2	chr5:59995439-59996328	GM12878	blood:	n/a	n/a
41	CREB1	chr5:59995293-59996595	HepG2	liver:	n/a	n/a
42	CREB1	chr5:59995801-59996300	ECC-1	luminal epithelium:	n/a	n/a
43	CREB1	chr5:59995198-59996501	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr5:59995652-59996713	K562	blood:	n/a	n/a
45	CREB1	chr5:59995525-59996327	A549	lung:	n/a	n/a
46	CREB1	chr5:59995228-59996421	GM12878	blood:	n/a	n/a
47	CREB1	chr5:59995736-59996401	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr5:59995569-59996463	K562	blood:	n/a	n/a
49	CREB1	chr5:59995331-59996379	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr5:59995384-59996553	HepG2	liver:	n/a	n/a

(count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59995715-59995765	NHBE	bronchial:	n/a
2	chr5:59996455-59996505	GM19239	blood:	n/a
3	chr5:59996421-59996471	IMR90	lung:	fetal
4	chr5:59996028-59996078	HRPEpiC	eye:	n/a
5	chr5:59995715-59995765	NHBE	bronchial:	n/a
6	chr5:59996455-59996505	GM19239	blood:	n/a
7	chr5:59996421-59996471	IMR90	lung:	fetal
8	chr5:59996028-59996078	HRPEpiC	eye:	n/a
9	chr5:59995433-59995483	GM12892	blood:	n/a
10	chr5:59992788-59992838	SKMC	muscle:	n/a
11	chr5:59996120-59996170	GM12892	blood:	n/a
12	chr5:59996240-59996290	MCF-7	breast:	n/a
13	chr5:59996455-59996505	Caco-2	colon:	n/a
14	chr5:59996025-59996075	AG09319	gingival:	n/a
15	chr5:59992788-59992838	NT2-D1	testis:	n/a
16	chr5:59996115-59996165	CMK	blood:	n/a
17	chr5:59996328-59996378	HMEC	breast:	n/a
18	chr5:59996328-59996378	HRE	kidney:	n/a
19	chr5:59996328-59996378	IMR90	lung:	fetal
20	chr5:59996105-59996155	SK-N-SH	brain:	n/a
21	chr5:59995715-59995765	HCM	heart:	n/a
22	chr5:59996328-59996378	GM06990	blood:	n/a
23	chr5:59996120-59996170	CMK	blood:	n/a
24	chr5:59995837-59995887	U87	brain:	n/a
25	chr5:59996025-59996075	RPTEC	kidney:	n/a
26	chr5:59996066-59996116	HCF	heart:	n/a
27	chr5:59995433-59995483	SKMC	muscle:	n/a
28	chr5:59996328-59996378	LNCaP	prostate:	n/a
29	chr5:59996455-59996505	HL-60	blood:	n/a
30	chr5:59996328-59996378	HepG2	liver:	n/a
31	chr5:59996455-59996505	SKMC	muscle:	n/a
32	chr5:59996028-59996078	NB4	blood:	n/a
33	chr5:59995433-59995483	GM12891	blood:	n/a
34	chr5:59995354-59995404	HCM	heart:	n/a
35	chr5:59999842-59999892	AG09319	gingival:	n/a
36	chr5:59996105-59996155	IMR90	lung:	fetal
37	chr5:59996105-59996155	HCF	heart:	n/a
38	chr5:59996328-59996378	BE2_C	brain:	n/a
39	chr5:59996105-59996155	HNPCEpiC	eye:	n/a
40	chr5:59996066-59996116	HRE	kidney:	n/a
41	chr5:59995715-59995765	GM12892	blood:	n/a
42	chr5:59996025-59996075	SK-N-MC	brain:	n/a
43	chr5:59995354-59995404	K562	blood:	n/a
44	chr5:59995354-59995404	HCPEpiC	choroid plexus:	n/a
45	chr5:59995837-59995887	IMR90	lung:	fetal
46	chr5:59995354-59995404	T-47D	breast:	n/a
47	chr5:59996028-59996078	AG09319	gingival:	n/a
48	chr5:59996328-59996378	HRCEpiC	kidney:	n/a
49	chr5:59995715-59995765	HMEC	breast:	n/a
50	chr5:59996421-59996471	SK-N-SH	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:59994459..59997012-chr5:59999943..60002207,3	K562	blood:
2	chr5:59994474..59997876-chr5:60455928..60460228,5	K562	blood:
3	chr5:59994210..59996553-chr5:60627404..60629725,2	MCF-7	breast:
4	chr5:59998583..60001649-chr5:60008376..60010857,3	K562	blood:
5	chr5:59984165..59985932-chr5:59998391..60001093,2	K562	blood:
6	chr5:59998796..60001597-chr5:60005006..60007976,2	MCF-7	breast:
7	chr5:59978724..59981449-chr5:59990551..59993454,2	K562	blood:
8	chr5:59996423..59998684-chr5:60001090..60003995,3	MCF-7	breast:
9	chr5:59998796..60001597-chr5:60005006..60007976,2	MCF-7	breast:
10	chr5:59994766..59997434-chr5:59998869..60000673,3	MCF-7	breast:
11	chr5:59990643..59992382-chr5:60006988..60008746,2	K562	blood:
12	chr5:59997848..60001535-chr5:60002216..60006200,5	K562	blood:
13	chr5:59998145..60001535-chr5:60003151..60006329,3	K562	blood:
14	chr5:59968561..59971245-chr5:59997935..60000093,2	MCF-7	breast:
15	chr5:59994096..59995835-chr5:60107793..60109955,2	MCF-7	breast:
16	chr5:60006154..60007664-chr5:60138828..60140875,2	MCF-7	breast:
17	chr5:59994018..59997409-chr5:59998010..60001591,3	MCF-7	breast:
18	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
19	chr5:59997848..60001535-chr5:60002216..60006200,5	K562	blood:
20	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
21	chr5:59994459..59997087-chr5:60000577..60002875,2	K562	blood:
22	chr5:59933171..59934818-chr5:59991480..59994360,2	K562	blood:
23	chr10:75385509..75386409-chr5:59996058..59996562,2	HCT-116	colon:
24	chr5:59998583..60001649-chr5:60008376..60010857,3	K562	blood:
25	chr5:59994332..59996148-chr5:60627447..60629730,3	K562	blood:
26	chr5:59986799..59989085-chr5:59989251..59992450,3	MCF-7	breast:
27	chr5:59993591..59996148-chr5:60625919..60628980,4	K562	blood:
28	chr5:59990643..59992382-chr5:60006988..60008746,2	K562	blood:
29	chr5:59996423..59998684-chr5:60001090..60003995,3	MCF-7	breast:
30	chr5:59998145..60001535-chr5:60003151..60006329,3	K562	blood:

No data

Variant related genes	Relation type
DEPDC1B	TF binding region
DEPDC1B	CpG island
ENSG00000164182	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000130449	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000268584	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000166348	chromatin interactions
ENSG00000035499	chromatin interactions

Extended variants
information (count: 464 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10471483	chr5:59992305-59992306	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541117722	chr5:59992306-59992307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182811445	chr5:59992443-59992444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566275468	chr5:59992453-59992454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534876694	chr5:59992501-59992502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542384858	chr5:59992530-59992531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113099682	chr5:59992570-59992571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555121660	chr5:59992627-59992628	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs187135362	chr5:59992628-59992629	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs190879212	chr5:59992630-59992631	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs573691347	chr5:59992651-59992652	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs563870248	chr5:59992665-59992666	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs375358271	chr5:59992699-59992700	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs118078371	chr5:59992728-59992729	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs555789256	chr5:59992732-59992733	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs559793147	chr5:59992785-59992786	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs575588813	chr5:59992789-59992790	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs79736154	chr5:59992874-59992875	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs544912419	chr5:59992887-59992888	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs79814060	chr5:59992901-59992902	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182687313	chr5:59992921-59992922	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs188872799	chr5:59992983-59992984	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs561125594	chr5:59993031-59993032	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs530180418	chr5:59993075-59993076	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs59337855	chr5:59993111-59993112	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs142003600	chr5:59993130-59993131	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570074254	chr5:59993131-59993132	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs370077050	chr5:59993136-59993137	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs377168927	chr5:59993184-59993185	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs552891183	chr5:59993207-59993208	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs532511681	chr5:59993227-59993228	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs552923878	chr5:59993253-59993254	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs12517207	chr5:59993268-59993269	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs2124751	chr5:59993291-59993292	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531201732	chr5:59993296-59993297	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs568637412	chr5:59993320-59993321	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs549713333	chr5:59993438-59993439	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs535948846	chr5:59993444-59993445	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs554997685	chr5:59993476-59993477	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs555803178	chr5:59993488-59993489	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs561421452	chr5:59993529-59993530	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs193209266	chr5:59993561-59993562	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs145767656	chr5:59993592-59993593	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs544577639	chr5:59993629-59993630	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558504993	chr5:59993651-59993652	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528683226	chr5:59993757-59993758	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546918764	chr5:59993791-59993792	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs726268	chr5:59993850-59993851	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs572289320	chr5:59993853-59993854	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs200688717	chr5:59993856-59993857	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59969600-59994800	Weak transcription	Fetal Lung	lung
2	chr5:59971000-59993800	Weak transcription	NHLF	lung
3	chr5:59971000-59994000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr5:59971000-59994200	Weak transcription	NH-A	brain
5	chr5:59974200-59994200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr5:59974400-59993600	Weak transcription	Hela-S3	cervix
7	chr5:59977200-59994800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:59980200-59995200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr5:59981800-59994200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr5:59982400-59993600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr5:59982600-59994800	Weak transcription	Fetal Muscle Leg	muscle
12	chr5:59982800-59992400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:59982800-59993800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:59982800-59994800	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr5:59982800-59994800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr5:59983000-59992800	Weak transcription	NHEK	skin
17	chr5:59983000-59994000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr5:59983000-59994000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr5:59983000-59994000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr5:59983000-59994200	Weak transcription	Thymus	Thymus
21	chr5:59983000-59994600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr5:59983000-59994800	Weak transcription	Fetal Thymus	thymus
23	chr5:59983000-59994800	Weak transcription	HSMM	muscle
24	chr5:59983200-59993800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr5:59983200-59993800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr5:59984200-59993000	Weak transcription	NHDF-Ad	bronchial
27	chr5:59984600-59993000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr5:59984600-59994000	Weak transcription	Fetal Heart	heart
29	chr5:59984600-59994800	Weak transcription	Fetal Intestine Small	intestine
30	chr5:59986800-59992400	Weak transcription	HepG2	liver
31	chr5:59986800-59994000	Weak transcription	Osteobl	bone
32	chr5:59991400-59992600	Weak transcription	GM12878-XiMat	blood
33	chr5:59991400-59993000	Weak transcription	Placenta	Placenta
34	chr5:59991400-59993200	Weak transcription	Dnd41	blood
35	chr5:59991400-59993200	Weak transcription	K562	blood
36	chr5:59991400-59993400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:59991400-59993400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:59991400-59993400	Weak transcription	A549	lung
39	chr5:59991400-59994000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr5:59991400-59994000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:59991400-59994200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr5:59991400-59994200	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr5:59991400-59994800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:59991400-59994800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:59991400-59995000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:59991400-59995000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:59991400-59995200	Weak transcription	Pancreas	Pancrea
48	chr5:59991600-59993000	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr5:59991600-59994000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:59991600-59994200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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