Variant report

Variant	nsv882823
Chromosome Location	chr5:124569471-124639468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:183)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr5:124613108-124613668	A549	lung:	n/a	n/a
2	ATF3	chr5:124613278-124613732	HCT-116	colon:	n/a	n/a
3	BATF	chr5:124631188-124631480	GM12878	blood:	n/a	chr5:124631330-124631341 chr5:124631331-124631341 chr5:124631295-124631303
4	BATF	chr5:124631192-124631551	GM12878	blood:	n/a	chr5:124631493-124631503 chr5:124631330-124631341 chr5:124631331-124631341 chr5:124631295-124631303
5	CBX3	chr5:124613076-124613800	HCT-116	colon:	n/a	n/a
6	CBX3	chr5:124613114-124613658	HCT-116	colon:	n/a	n/a
7	CEBPB	chr5:124627111-124627481	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:124627171-124627389	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:124580124-124580430	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:124627181-124627437	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:124594418-124594662	HepG2	liver:	n/a	chr5:124594548-124594559
12	CEBPB	chr5:124619213-124619708	MCF-7	breast:	n/a	chr5:124619473-124619484
13	CEBPB	chr5:124627152-124627433	A549	lung:	n/a	n/a
14	CEBPB	chr5:124627221-124627436	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:124572005-124572184	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:124627105-124627535	A549	lung:	n/a	n/a
17	CEBPB	chr5:124613095-124613541	IMR90	lung:	n/a	n/a
18	CEBPB	chr5:124613148-124613813	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr5:124613223-124613558	Hela-S3	cervix:	n/a	n/a
20	CTBP2	chr5:124572729-124573167	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr5:124579095-124579157	GM20000	blood:	n/a	n/a
22	CTCF	chr5:124572260-124572410	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr5:124572360-124572510	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:124572320-124572470	AG09319	gingival:	n/a	n/a
25	CTCF	chr5:124634060-124634210	NHEK	skin:	n/a	n/a
26	CTCF	chr5:124634100-124634250	SAEC	small airway:	n/a	n/a
27	CTCF	chr5:124572560-124572710	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr5:124634080-124634230	HMEC	breast:	n/a	n/a
29	CTCF	chr5:124633980-124634130	HMEC	breast:	n/a	n/a
30	CTCF	chr5:124638379-124638430	GM13976	blood:	n/a	n/a
31	CTCF	chr5:124572340-124572490	AG09319	gingival:	n/a	n/a
32	CTCF	chr5:124615920-124616070	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr5:124613216-124613270	LNCaP	prostate:	n/a	n/a
34	CTCF	chr5:124634154-124634226	NHEK	skin:	n/a	n/a
35	E2F4	chr5:124634045-124634206	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr5:124619433-124619611	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr5:124613246-124613634	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr5:124580892-124581311	H1-hESC	embryonic stem cell:	n/a	n/a
39	E2F6	chr5:124580768-124581330	H1-hESC	embryonic stem cell:	n/a	n/a
40	EGR1	chr5:124613164-124613671	HCT-116	colon:	n/a	n/a
41	EP300	chr5:124631206-124631655	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr5:124611807-124612215	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr5:124612912-124613993	SK-N-SH	brain:	n/a	n/a
44	EP300	chr5:124610864-124611394	SK-N-SH_RA	brain:	n/a	chr5:124611376-124611390 chr5:124611377-124611391
45	EP300	chr5:124613046-124613812	SK-N-SH	brain:	n/a	n/a
46	EP300	chr5:124617299-124617751	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr5:124617308-124617755	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr5:124633967-124634287	SK-N-SH_RA	brain:	n/a	chr5:124634083-124634097 chr5:124633996-124634010
49	EP300	chr5:124613183-124613688	Hela-S3	cervix:	n/a	n/a
50	EP300	chr5:124631240-124631651	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:124606359-124606409	BJ	skin:	n/a
2	chr5:124636554-124636604	U87	brain:	n/a
3	chr5:124606359-124606409	HCM	heart:	n/a
4	chr5:124636554-124636604	AG04449	skin:	fetal
5	chr5:124636554-124636604	BJ	skin:	n/a
6	chr5:124606359-124606409	HRE	kidney:	n/a
7	chr5:124627753-124627803	PrEC	prostate:	n/a
8	chr5:124636554-124636604	AG04450	lung:	fetal
9	chr5:124606359-124606409	GM12878	blood:	n/a
10	chr5:124636554-124636604	HUVEC	blood vessel:	n/a
11	chr5:124627753-124627803	K562	blood:	n/a
12	chr5:124636554-124636604	AG09309	skin:	n/a
13	chr5:124636554-124636604	HCPEpiC	choroid plexus:	n/a
14	chr5:124606359-124606409	U87	brain:	n/a
15	chr5:124636554-124636604	ovcar-3	ovarian:	n/a
16	chr5:124627753-124627803	AG09319	gingival:	n/a
17	chr5:124606359-124606409	HL-60	blood:	n/a
18	chr5:124606359-124606409	CMK	blood:	n/a
19	chr5:124606359-124606409	NHBE	bronchial:	n/a
20	chr5:124606359-124606409	A549	lung:	n/a
21	chr5:124636554-124636604	NB4	blood:	n/a
22	chr5:124627753-124627803	HEEpiC	esophagus:	n/a
23	chr5:124627753-124627803	AG09309	skin:	n/a
24	chr5:124627753-124627803	NB4	blood:	n/a
25	chr5:124627753-124627803	HCM	heart:	n/a
26	chr5:124636554-124636604	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:124606359-124606409	IMR90	lung:	fetal
28	chr5:124606359-124606409	SK-N-SH	brain:	n/a
29	chr5:124627753-124627803	AoSMC	blood vessel:	n/a
30	chr5:124636554-124636604	SAEC	small airway:	n/a
31	chr5:124636554-124636604	HCM	heart:	n/a
32	chr5:124606359-124606409	MCF10A-Er-Src	breast:	n/a
33	chr5:124636554-124636604	HEK293	kidney:	embryo
34	chr5:124636554-124636604	AG09319	gingival:	n/a
35	chr5:124636554-124636604	RPTEC	kidney:	n/a
36	chr5:124627753-124627803	GM12891	blood:	n/a
37	chr5:124636554-124636604	AG10803	skin:	n/a
38	chr5:124636554-124636604	A549	lung:	n/a
39	chr5:124606359-124606409	GM06990	blood:	n/a
40	chr5:124636554-124636604	GM19239	blood:	n/a
41	chr5:124627753-124627803	CMK	blood:	n/a
42	chr5:124606359-124606409	MCF-7	breast:	n/a
43	chr5:124627753-124627803	HCT-116	colon:	n/a
44	chr5:124627753-124627803	HCF	heart:	n/a
45	chr5:124627753-124627803	Jurkat	blood:	n/a
46	chr5:124636554-124636604	NHDF-neo	bronchial:	n/a
47	chr5:124606359-124606409	SAEC	small airway:	n/a
48	chr5:124627753-124627803	HRPEpiC	eye:	n/a
49	chr5:124627753-124627803	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:124627753-124627803	HIPEpiC	eye:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:124584569..124586370-chr5:124590104..124592665,2	K562	blood:
2	chr5:124608857..124611312-chr5:124615964..124618402,2	MCF-7	breast:
3	chr5:124591558..124593226-chr5:124597239..124598785,2	K562	blood:
4	chr5:124591558..124593226-chr5:124597239..124598785,2	K562	blood:
5	chr5:124608857..124611312-chr5:124615964..124618402,2	MCF-7	breast:
6	chr5:123070152..123070765-chr5:124595660..124596171,2	K562	blood:
7	chr5:124584569..124586370-chr5:124590104..124592665,2	K562	blood:

No data

Variant related genes	Relation type
HMGB1P22	TF binding region
HMGB1P22	CpG island

Extended variants
information (count: 2830 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2830 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1439607	chr5:124569471-124569472	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560643477	chr5:124569493-124569494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572676839	chr5:124569504-124569505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115323232	chr5:124569510-124569511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11960748	chr5:124569563-124569564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185360556	chr5:124569572-124569573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188113021	chr5:124569582-124569583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561731765	chr5:124569644-124569645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528904725	chr5:124569676-124569677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534413156	chr5:124569686-124569687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542700984	chr5:124569690-124569691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150227973	chr5:124569709-124569710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555499855	chr5:124569717-124569718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181463404	chr5:124569747-124569748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575447520	chr5:124569860-124569861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13190088	chr5:124569876-124569877	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551211462	chr5:124569890-124569891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138700019	chr5:124569961-124569962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186504133	chr5:124569970-124569971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149362891	chr5:124569982-124569983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34398053	chr5:124569995-124569996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72778783	chr5:124570010-124570011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10463792	chr5:124570015-124570016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191729729	chr5:124570027-124570028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572689342	chr5:124570064-124570065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369778775	chr5:124570078-124570079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528334173	chr5:124570079-124570080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546515527	chr5:124570081-124570082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1272102	chr5:124570085-124570086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377033021	chr5:124570089-124570090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558452705	chr5:124570143-124570144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73311010	chr5:124570150-124570151	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs72778784	chr5:124570188-124570189	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs538705708	chr5:124570262-124570263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1439606	chr5:124570354-124570355	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs144596902	chr5:124570371-124570372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139364100	chr5:124570413-124570414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6867985	chr5:124570426-124570427	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185759250	chr5:124570490-124570491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550831148	chr5:124570533-124570534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570845844	chr5:124570590-124570591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551268896	chr5:124570651-124570652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374795422	chr5:124570677-124570678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530638184	chr5:124570708-124570709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111304685	chr5:124570729-124570730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561342097	chr5:124570731-124570732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190926465	chr5:124570752-124570753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535935494	chr5:124570822-124570823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538852962	chr5:124570844-124570845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375082085	chr5:124570857-124570858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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

Chromatin state (count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124546600-124585200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:124561400-124572600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:124567400-124569600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:124567800-124570000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:124568000-124569800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:124568000-124570000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr5:124568200-124569800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr5:124568200-124570200	Enhancers	Stomach Mucosa	stomach
9	chr5:124568600-124569600	Enhancers	Brain Substantia Nigra	brain
10	chr5:124568600-124573400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:124568800-124571000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:124568800-124571600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr5:124568800-124571600	Weak transcription	Brain Anterior Caudate	brain
14	chr5:124569200-124569800	Enhancers	Brain Angular Gyrus	brain
15	chr5:124569200-124570200	Enhancers	Fetal Heart	heart
16	chr5:124569400-124569600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:124569400-124569800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr5:124569400-124570000	Enhancers	Colon Smooth Muscle	Colon
19	chr5:124569400-124570000	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr5:124569600-124569800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:124569600-124569800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr5:124569600-124569800	Enhancers	Left Ventricle	heart
23	chr5:124569600-124570000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr5:124569600-124570000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:124569600-124570000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr5:124569600-124570200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr5:124569600-124570800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr5:124569600-124572400	Weak transcription	Brain Substantia Nigra	brain
29	chr5:124569800-124570000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:124569800-124571600	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr5:124569800-124571800	Weak transcription	Left Ventricle	heart
32	chr5:124569800-124572600	Weak transcription	Brain Angular Gyrus	brain
33	chr5:124570000-124570200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr5:124570000-124571200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr5:124570000-124571200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr5:124570000-124571200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr5:124570000-124571800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr5:124570000-124571800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:124570000-124572000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr5:124570000-124572400	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr5:124570200-124571200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr5:124570200-124571400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr5:124570200-124571400	Weak transcription	Fetal Heart	heart
44	chr5:124570200-124571600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr5:124570800-124571200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr5:124571000-124571400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:124571200-124571600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr5:124571200-124573200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr5:124571200-124573400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:124571200-124573600	Enhancers	HUES64 Cell Line	embryonic stem cell

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