Variant report

Variant	nsv1050323
Chromosome Location	chr10:55190079-55546575
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	chr10:55546113-55546324	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:55379164-55379197	K562	blood:	n/a	n/a
3	ARID3A	chr10:55361088-55361391	HepG2	liver:	n/a	n/a
4	ATF2	chr10:55357030-55358165	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr10:55357496-55358125	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr10:55238974-55239521	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr10:55236413-55237624	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr10:55358549-55359145	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:55410674-55410823	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:55217223-55217233	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr10:55239200-55239377	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
12	BCL11A	chr10:55358639-55359002	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr10:55357742-55358035	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr10:55239117-55239415	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
15	BCL11A	chr10:55358747-55359028	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr10:55190762-55191068	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:55191987-55192023	GM12878	blood:	n/a	n/a
18	BRCA1	chr10:55236620-55237424	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr10:55239096-55239406	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr10:55436651-55436653	Hela-S3	cervix:	n/a	n/a
21	CCNT2	chr10:55407553-55407753	K562	blood:	n/a	n/a
22	CEBPB	chr10:55539511-55539751	HepG2	liver:	n/a	n/a
23	CEBPB	chr10:55250360-55250591	A549	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
24	CEBPB	chr10:55312702-55312890	A549	lung:	n/a	chr10:55312751-55312762 chr10:55312749-55312766
25	CEBPB	chr10:55440212-55440489	A549	lung:	n/a	chr10:55440348-55440359
26	CEBPB	chr10:55250388-55250668	H1-hESC	embryonic stem cell:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
27	CEBPB	chr10:55411759-55412117	Hela-S3	cervix:	n/a	chr10:55411925-55411936
28	CEBPB	chr10:55531788-55532061	IMR90	lung:	n/a	chr10:55531918-55531929
29	CEBPB	chr10:55233744-55234036	HepG2	liver:	n/a	chr10:55233869-55233880
30	CEBPB	chr10:55495099-55495137	K562	blood:	n/a	n/a
31	CEBPB	chr10:55239054-55239539	H1-hESC	embryonic stem cell:	n/a	chr10:55239464-55239475 chr10:55239371-55239383
32	CEBPB	chr10:55440562-55440588	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr10:55407097-55407340	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr10:55312604-55312917	HepG2	liver:	n/a	chr10:55312751-55312762 chr10:55312749-55312766
35	CEBPB	chr10:55250389-55250679	Hela-S3	cervix:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
36	CEBPB	chr10:55440217-55440437	IMR90	lung:	n/a	chr10:55440348-55440359
37	CEBPB	chr10:55495022-55495339	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:55482323-55482573	IMR90	lung:	n/a	chr10:55482450-55482463 chr10:55482451-55482462 chr10:55482452-55482461 chr10:55482452-55482461 chr10:55482450-55482461 chr10:55482452-55482461 chr10:55482450-55482463 chr10:55482452-55482461 chr10:55482450-55482463
39	CEBPB	chr10:55494993-55495303	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:55495107-55495314	A549	lung:	n/a	n/a
41	CEBPB	chr10:55456808-55457116	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:55411770-55412027	HepG2	liver:	n/a	chr10:55411925-55411936
43	CEBPB	chr10:55316193-55316425	HepG2	liver:	n/a	chr10:55316279-55316290
44	CEBPB	chr10:55531808-55532061	HepG2	liver:	n/a	chr10:55531918-55531929
45	CEBPB	chr10:55312660-55312904	H1-hESC	embryonic stem cell:	n/a	chr10:55312751-55312762 chr10:55312749-55312766
46	CEBPB	chr10:55250346-55250673	IMR90	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
47	CEBPB	chr10:55311076-55311349	HepG2	liver:	n/a	chr10:55311194-55311205
48	CEBPB	chr10:55484473-55484797	IMR90	lung:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
49	CEBPB	chr10:55250334-55250666	K562	blood:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
50	CEBPB	chr10:55361129-55361360	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55419927-55419977	GM12891	blood:	n/a
2	chr10:55419714-55419764	ovcar-3	ovarian:	n/a
3	chr10:55419927-55419977	HIPEpiC	eye:	n/a
4	chr10:55357618-55357668	NT2-D1	testis:	n/a
5	chr10:55259527-55259577	GM06990	blood:	n/a
6	chr10:55259527-55259577	AoSMC	blood vessel:	n/a
7	chr10:55393450-55393500	NB4	blood:	n/a
8	chr10:55419714-55419764	GM12878	blood:	n/a
9	chr10:55357618-55357668	H1-hESC	embryonic stem cell:	embryo
10	chr10:55259527-55259577	SAEC	small airway:	n/a
11	chr10:55419927-55419977	HCPEpiC	choroid plexus:	n/a
12	chr10:55419927-55419977	RPTEC	kidney:	n/a
13	chr10:55259527-55259577	Jurkat	blood:	n/a
14	chr10:55259527-55259577	GM12892	blood:	n/a
15	chr10:55357618-55357668	SK-N-SH_RA	brain:	n/a
16	chr10:55259527-55259577	T-47D	breast:	n/a
17	chr10:55419927-55419977	MCF-7	breast:	n/a
18	chr10:55393450-55393500	HRCEpiC	kidney:	n/a
19	chr10:55259527-55259577	GM12891	blood:	n/a
20	chr10:55419714-55419764	Hela-S3	cervix:	n/a
21	chr10:55419927-55419977	NHBE	bronchial:	n/a
22	chr10:55357618-55357668	AG04449	skin:	fetal
23	chr10:55419927-55419977	ECC-1	luminal epithelium:	n/a
24	chr10:55419714-55419764	NHDF-neo	bronchial:	n/a
25	chr10:55357618-55357668	HRE	kidney:	n/a
26	chr10:55393450-55393500	AG04450	lung:	fetal
27	chr10:55419927-55419977	HEEpiC	esophagus:	n/a
28	chr10:55419714-55419764	H1-hESC	embryonic stem cell:	embryo
29	chr10:55259527-55259577	CMK	blood:	n/a
30	chr10:55357618-55357668	PANC-1	pancreas:	n/a
31	chr10:55393450-55393500	LNCaP	prostate:	n/a
32	chr10:55259527-55259577	MCF-7	breast:	n/a
33	chr10:55393450-55393500	AG04449	skin:	fetal
34	chr10:55259527-55259577	Caco-2	colon:	n/a
35	chr10:55357618-55357668	NHDF-neo	bronchial:	n/a
36	chr10:55419714-55419764	SK-N-MC	brain:	n/a
37	chr10:55259527-55259577	SKMC	muscle:	n/a
38	chr10:55259527-55259577	RPTEC	kidney:	n/a
39	chr10:55357618-55357668	PFSK-1	brain:	n/a
40	chr10:55419927-55419977	AG09309	skin:	n/a
41	chr10:55419927-55419977	HCM	heart:	n/a
42	chr10:55259527-55259577	ProgFib	skin:	n/a
43	chr10:55393450-55393500	PANC-1	pancreas:	n/a
44	chr10:55419714-55419764	Hepatocyte	liver:	n/a
45	chr10:55259527-55259577	GM12878	blood:	n/a
46	chr10:55393450-55393500	K562	blood:	n/a
47	chr10:55419927-55419977	GM12892	blood:	n/a
48	chr10:55357618-55357668	LNCaP	prostate:	n/a
49	chr10:55259527-55259577	ovcar-3	ovarian:	n/a
50	chr10:55259527-55259577	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
2	chr10:55481740..55482260-chr20:52673713..52674214,2	MCF-7	breast:
3	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:
4	chr10:55303514..55305516-chr10:55305569..55307810,2	K562	blood:
5	chr10:55278002..55279503-chr7:30548599..30550148,2	MCF-7	breast:
6	chr10:55303514..55305516-chr10:55305569..55307810,2	K562	blood:
7	chr10:55360883..55361625-chr10:55568215..55569121,2	MCF-7	breast:
8	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:
9	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
10	chr10:55313361..55315052-chr10:55318156..55320737,2	K562	blood:
11	10:55527193-55535408..10:55949104-55956834	K562	blood:
12	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
13	chr10:55405153..55407581-chr5:63345532..63348450,2	MCF-7	breast:
14	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
15	chr10:55298474..55301304-chr10:55304357..55306392,2	MCF-7	breast:
16	chr10:55360709..55361787-chr10:55606233..55607054,5	MCF-7	breast:
17	chr10:55298474..55301304-chr10:55304357..55306392,2	MCF-7	breast:
18	chr10:55313361..55315052-chr10:55318156..55320737,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DKK1-4	chr10:55526160-55526374	NONHSAT013453

Variant related genes	Relation type
RNA5SP318	TF binding region
ENSG00000233805	TF binding region
RNA5SP318	CpG island
ENSG00000233805	CpG island

Extended variants
information (count: 10607 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:10607 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149166549	chr10:55190102-55190103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs17620117	chr10:55190182-55190183	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs553959561	chr10:55190224-55190225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375164196	chr10:55190228-55190229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372346598	chr10:55190248-55190249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551237992	chr10:55190285-55190286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374065934	chr10:55190286-55190287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1198120	chr10:55190288-55190289	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs117539585	chr10:55190309-55190310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1198119	chr10:55190325-55190326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
11	rs34392536	chr10:55190350-55190351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541892828	chr10:55190357-55190358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375131826	chr10:55190396-55190397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561719275	chr10:55190405-55190406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577560793	chr10:55190425-55190426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527390923	chr10:55190434-55190435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547581304	chr10:55190460-55190461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141693439	chr10:55190469-55190470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188640635	chr10:55190535-55190536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77803576	chr10:55190589-55190590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186782337	chr10:55190599-55190600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549792922	chr10:55190627-55190628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191623578	chr10:55190640-55190641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533824707	chr10:55190663-55190664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537848227	chr10:55190670-55190671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532687953	chr10:55190789-55190790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1211298	chr10:55190839-55190840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs116651904	chr10:55190894-55190895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565234357	chr10:55190915-55190916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183925796	chr10:55190950-55190951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554266333	chr10:55191025-55191026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187309488	chr10:55191037-55191038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191009695	chr10:55191044-55191045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77064357	chr10:55191116-55191117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs398096958	chr10:55191121-55191122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144616805	chr10:55191154-55191155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148070914	chr10:55191155-55191156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541805205	chr10:55191237-55191238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141785051	chr10:55191241-55191242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542429532	chr10:55191264-55191265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200249544	chr10:55191268-55191269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572143271	chr10:55191317-55191318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541106711	chr10:55191367-55191368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79442971	chr10:55191368-55191369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532975113	chr10:55191436-55191437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576040822	chr10:55191437-55191438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543650757	chr10:55191459-55191460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563393119	chr10:55191511-55191512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529163745	chr10:55191520-55191521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182158217	chr10:55191588-55191589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55182400-55200400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:55184600-55200600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:55186000-55206600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr10:55189200-55190200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr10:55190000-55190400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr10:55190000-55190800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr10:55190000-55190800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr10:55190200-55190600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr10:55190400-55190600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr10:55190400-55194000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr10:55190600-55198600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr10:55190600-55199200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr10:55191200-55191400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr10:55191400-55192000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr10:55192000-55192200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr10:55192200-55194600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr10:55194000-55194200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr10:55194200-55194800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr10:55194600-55195200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr10:55194800-55195000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr10:55194800-55195000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr10:55195200-55198800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr10:55198600-55199400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr10:55198600-55199400	Enhancers	Fetal Kidney	kidney
25	chr10:55198800-55199200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr10:55198800-55199200	Enhancers	Placenta	Placenta
27	chr10:55198800-55199200	Active TSS	Fetal Stomach	stomach
28	chr10:55198800-55199400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr10:55198800-55199400	Enhancers	Fetal Heart	heart
30	chr10:55199200-55199400	Enhancers	H9 Cell Line	embryonic stem cell
31	chr10:55199200-55199600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr10:55199400-55200600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr10:55199400-55206800	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr10:55200400-55200800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr10:55200600-55200800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr10:55200600-55200800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr10:55200800-55201200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr10:55200800-55206200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr10:55201200-55201400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr10:55201400-55206600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr10:55205400-55205800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr10:55205800-55208000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr10:55205800-55208200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr10:55206000-55206600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr10:55206200-55208000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr10:55206600-55207800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
47	chr10:55206600-55207800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr10:55206600-55207800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
49	chr10:55206600-55208000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
50	chr10:55206600-55208400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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