Variant report

Variant	nsv830475
Chromosome Location	chr5:124387292-124550256
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	chr5:124450555-124451075	HepG2	liver:	n/a	n/a
2	ATF1	chr5:124396286-124396445	K562	blood:	n/a	n/a
3	BACH1	chr5:124526465-124526602	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:124470369-124470393	K562	blood:	n/a	n/a
5	BATF	chr5:124449049-124449341	GM12878	blood:	n/a	chr5:124449221-124449232
6	BATF	chr5:124549755-124550033	GM12878	blood:	n/a	n/a
7	BATF	chr5:124478189-124478438	GM12878	blood:	n/a	chr5:124478315-124478326
8	BATF	chr5:124549750-124550026	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:124449065-124449369	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:124450400-124450947	HepG2	liver:	n/a	n/a
11	BRCA1	chr5:124458433-124458470	GM12878	blood:	n/a	n/a
12	BRCA1	chr5:124482601-124482622	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:124401025-124401111	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr5:124408689-124409149	HCT-116	colon:	n/a	n/a
15	CEBPB	chr5:124511607-124512204	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:124511788-124512350	MCF-7	breast:	n/a	n/a
17	CEBPB	chr5:124513046-124513405	IMR90	lung:	n/a	chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513223-124513234 chr5:124513223-124513236
18	CEBPB	chr5:124452717-124452797	HepG2	liver:	n/a	chr5:124452756-124452769 chr5:124452756-124452767 chr5:124452757-124452768
19	CEBPB	chr5:124522211-124522499	A549	lung:	n/a	chr5:124522320-124522333
20	CEBPB	chr5:124511582-124512340	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr5:124511658-124512408	MCF-7	breast:	n/a	n/a
22	CEBPB	chr5:124394340-124394552	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:124522278-124522353	IMR90	lung:	n/a	chr5:124522320-124522333
24	CEBPB	chr5:124536368-124536643	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:124512007-124512287	A549	lung:	n/a	n/a
26	CEBPB	chr5:124513052-124513405	HepG2	liver:	n/a	chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513223-124513234 chr5:124513223-124513236
27	CEBPB	chr5:124537119-124537311	H1-hESC	embryonic stem cell:	n/a	chr5:124537287-124537298
28	CEBPB	chr5:124470105-124470757	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:124525107-124525428	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:124537218-124537512	IMR90	lung:	n/a	chr5:124537287-124537298
31	CEBPB	chr5:124475916-124476308	IMR90	lung:	n/a	chr5:124476044-124476057
32	CEBPB	chr5:124513058-124513394	H1-hESC	embryonic stem cell:	n/a	chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513223-124513234 chr5:124513223-124513236
33	CEBPB	chr5:124488783-124488794	IMR90	lung:	n/a	n/a
34	CEBPB	chr5:124513121-124513515	A549	lung:	n/a	chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513223-124513234 chr5:124513223-124513236
35	CEBPB	chr5:124469182-124469364	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr5:124511833-124512279	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr5:124392281-124392448	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr5:124450513-124450886	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:124391951-124392489	A549	lung:	n/a	chr5:124391979-124391992 chr5:124392030-124392043
40	CEBPB	chr5:124513090-124513405	K562	blood:	n/a	chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513223-124513234 chr5:124513223-124513236
41	CEBPB	chr5:124513018-124513411	MCF-7	breast:	n/a	chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513223-124513234 chr5:124513223-124513236
42	CEBPB	chr5:124529359-124529574	IMR90	lung:	n/a	chr5:124529449-124529460 chr5:124529450-124529459
43	CEBPB	chr5:124470273-124470761	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr5:124512012-124512345	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:124513046-124513414	A549	lung:	n/a	chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513225-124513234 chr5:124513223-124513234 chr5:124513223-124513236
46	CEBPB	chr5:124537263-124537468	HepG2	liver:	n/a	chr5:124537287-124537298
47	CEBPB	chr5:124529331-124529634	HepG2	liver:	n/a	chr5:124529449-124529460 chr5:124529450-124529459
48	CEBPB	chr5:124470111-124470667	IMR90	lung:	n/a	n/a
49	CHD2	chr5:124450778-124450973	HepG2	liver:	n/a	n/a
50	CHD2	chr5:124525630-124525701	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:124532763-124532813	GM12891	blood:	n/a
2	chr5:124487035-124487085	PANC-1	pancreas:	n/a
3	chr5:124461245-124461295	BE2_C	brain:	n/a
4	chr5:124532763-124532813	GM12891	blood:	n/a
5	chr5:124487035-124487085	PANC-1	pancreas:	n/a
6	chr5:124461245-124461295	BE2_C	brain:	n/a
7	chr5:124537511-124537561	BE2_C	brain:	n/a
8	chr5:124401393-124401443	HRCEpiC	kidney:	n/a
9	chr5:124401393-124401443	NHDF-neo	bronchial:	n/a
10	chr5:124401393-124401443	ProgFib	skin:	n/a
11	chr5:124537511-124537561	A549	lung:	n/a
12	chr5:124536183-124536233	SK-N-MC	brain:	n/a
13	chr5:124388456-124388506	AG04450	lung:	fetal
14	chr5:124487035-124487085	T-47D	breast:	n/a
15	chr5:124401393-124401443	GM12878	blood:	n/a
16	chr5:124537511-124537561	AoSMC	blood vessel:	n/a
17	chr5:124487035-124487085	ProgFib	skin:	n/a
18	chr5:124388456-124388506	HepG2	liver:	n/a
19	chr5:124526339-124526389	SK-N-SH_RA	brain:	n/a
20	chr5:124517583-124517633	K562	blood:	n/a
21	chr5:124388456-124388506	GM12891	blood:	n/a
22	chr5:124517583-124517633	HEEpiC	esophagus:	n/a
23	chr5:124394386-124394436	ovcar-3	ovarian:	n/a
24	chr5:124526339-124526389	HCM	heart:	n/a
25	chr5:124532763-124532813	HepG2	liver:	n/a
26	chr5:124517583-124517633	BJ	skin:	n/a
27	chr5:124487035-124487085	PrEC	prostate:	n/a
28	chr5:124487035-124487085	GM12891	blood:	n/a
29	chr5:124487035-124487085	SAEC	small airway:	n/a
30	chr5:124476664-124476714	K562	blood:	n/a
31	chr5:124517583-124517633	MCF10A-Er-Src	breast:	n/a
32	chr5:124461245-124461295	Hela-S3	cervix:	n/a
33	chr5:124388456-124388506	U87	brain:	n/a
34	chr5:124537511-124537561	HepG2	liver:	n/a
35	chr5:124537511-124537561	RPTEC	kidney:	n/a
36	chr5:124526339-124526389	SKMC	muscle:	n/a
37	chr5:124476664-124476714	HCPEpiC	choroid plexus:	n/a
38	chr5:124487035-124487085	RPTEC	kidney:	n/a
39	chr5:124388456-124388506	HEK293	kidney:	embryo
40	chr5:124517583-124517633	GM19239	blood:	n/a
41	chr5:124532763-124532813	SK-N-SH	brain:	n/a
42	chr5:124476664-124476714	HCT-116	colon:	n/a
43	chr5:124401393-124401443	ovcar-3	ovarian:	n/a
44	chr5:124461245-124461295	CMK	blood:	n/a
45	chr5:124532763-124532813	HCF	heart:	n/a
46	chr5:124526339-124526389	HMEC	breast:	n/a
47	chr5:124476664-124476714	HepG2	liver:	n/a
48	chr5:124536183-124536233	HepG2	liver:	n/a
49	chr5:124526339-124526389	GM19239	blood:	n/a
50	chr5:124401393-124401443	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:124515635..124517727-chr5:124517780..124520916,3	K562	blood:
2	chr5:124510130..124512819-chr5:124513957..124516828,2	MCF-7	breast:
3	chr5:124521759..124522261-chr5:124745524..124746309,2	MCF-7	breast:
4	chr5:124478793..124481294-chr5:124482364..124483984,2	K562	blood:
5	chr5:124385684..124387313-chr5:124391971..124393955,2	MCF-7	breast:
6	chr2:78716026..78716644-chr5:124520515..124521066,2	MCF-7	breast:
7	chr5:124441238..124443626-chr5:124448312..124451103,2	MCF-7	breast:
8	chr5:124478793..124481294-chr5:124482364..124483984,2	K562	blood:
9	chr5:124515635..124517727-chr5:124517780..124520916,3	K562	blood:
10	chr5:124510130..124512819-chr5:124513957..124516828,2	MCF-7	breast:
11	chr5:124441238..124443626-chr5:124448312..124451103,2	MCF-7	breast:
12	chr5:124517096..124519190-chr5:124529404..124532074,2	K562	blood:
13	chr5:124385684..124387313-chr5:124391971..124393955,2	MCF-7	breast:
14	chr3:64006147..64007783-chr5:124428420..124431254,2	MCF-7	breast:
15	chr5:124517096..124519190-chr5:124529404..124532074,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-43D2.2.1-13	chr5:124485221-124485622	ENSG00000249365
2	lnc-RP11-43D2.2.1-13	chr5:124443897-124443945	ENSG00000249365
3	lnc-RP11-43D2.2.1-12	chr5:124494346-124494515	NR_109882
4	lnc-RP11-43D2.2.1-12	chr5:124505231-124505319	NR_109882
5	lnc-RP11-43D2.2.1-14	chr5:124537581-124538223	ENSG00000248631
6	lnc-RP11-43D2.2.1-19	chr5:124410358-124410673	NONHSAT103549

Variant related genes	Relation type
ENSG00000250194	TF binding region
ENSG00000249365	TF binding region
ENSG00000248631	TF binding region
ENSG00000250194	CpG island
ENSG00000249365	CpG island
ENSG00000248631	CpG island

Extended variants
information (count: 6760 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6760 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114428039	chr5:124387293-124387294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183509649	chr5:124387302-124387303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532276361	chr5:124387320-124387321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550402348	chr5:124387337-124387338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563754818	chr5:124387405-124387406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568836331	chr5:124387417-124387418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114243571	chr5:124387418-124387419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561941084	chr5:124387448-124387449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187848349	chr5:124387473-124387474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566744453	chr5:124387477-124387478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77624833	chr5:124387478-124387479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190023046	chr5:124387516-124387517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145085738	chr5:124387583-124387584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71594396	chr5:124387604-124387605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs182098395	chr5:124387631-124387632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549169901	chr5:124387664-124387665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188292897	chr5:124387675-124387676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569208347	chr5:124387689-124387690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542628387	chr5:124387699-124387700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560927370	chr5:124387718-124387719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528796973	chr5:124387728-124387729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10071600	chr5:124387763-124387764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565187014	chr5:124387767-124387768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532548299	chr5:124387771-124387772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113134606	chr5:124387772-124387773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551763418	chr5:124387785-124387786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559623727	chr5:124387793-124387794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571649678	chr5:124387812-124387813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147650820	chr5:124387826-124387827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568822606	chr5:124387859-124387860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534211508	chr5:124387861-124387862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573055720	chr5:124387868-124387869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7700716	chr5:124387905-124387906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs138645598	chr5:124387906-124387907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192579684	chr5:124387915-124387916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35678138	chr5:124387946-124387947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs558887663	chr5:124387948-124387949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs70991657	chr5:124387976-124387977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111945089	chr5:124387977-124387978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6595572	chr5:124388012-124388013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556741993	chr5:124388084-124388085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557450405	chr5:124388096-124388097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185367714	chr5:124388115-124388116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368587910	chr5:124388173-124388174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574962668	chr5:124388202-124388203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372621203	chr5:124388217-124388218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137941533	chr5:124388232-124388233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572900077	chr5:124388233-124388234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561950483	chr5:124388234-124388235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540530157	chr5:124388274-124388275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	16397240	CNVD
Parathyroid adenoma	22454399	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1482 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124379000-124388200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr5:124380600-124388400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:124381800-124388600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr5:124382800-124388400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:124382800-124394200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:124382800-124394200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr5:124383000-124389400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:124387000-124389800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:124387200-124392200	Weak transcription	Brain Anterior Caudate	brain
10	chr5:124387200-124392400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr5:124387200-124392400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr5:124387200-124392400	Weak transcription	Brain Substantia Nigra	brain
13	chr5:124387400-124392400	Weak transcription	Aorta	Aorta
14	chr5:124388200-124390600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr5:124388400-124388600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr5:124388400-124389000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr5:124388400-124389200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr5:124388400-124390000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:124388400-124390200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr5:124388400-124396400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr5:124388400-124396400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:124388600-124390000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:124388600-124392400	Weak transcription	Left Ventricle	heart
24	chr5:124388600-124395000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr5:124388800-124390400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:124389000-124389400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr5:124389200-124389600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr5:124389400-124390200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr5:124389400-124390200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:124389600-124389800	Enhancers	HMEC	breast
31	chr5:124389600-124390000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:124389600-124390200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:124389600-124390400	Enhancers	NHEK	skin
34	chr5:124389600-124396200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:124389800-124390600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:124390000-124390200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:124390000-124390200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:124390000-124390200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr5:124390000-124390800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr5:124390000-124391200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr5:124390000-124391200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr5:124390000-124392200	Weak transcription	HMEC	breast
43	chr5:124390200-124390600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr5:124390200-124391400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr5:124390200-124392400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:124390200-124392400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:124390200-124392400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr5:124390400-124392200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr5:124390400-124392200	Weak transcription	NHEK	skin
50	chr5:124390400-124392600	Weak transcription	Right Atrium	heart

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