Variant report

Variant	esv2757386
Chromosome Location	chr10:55357136-55531037
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	chr10:55379164-55379197	K562	blood:	n/a	n/a
2	ARID3A	chr10:55361088-55361391	HepG2	liver:	n/a	n/a
3	ATF2	chr10:55358549-55359145	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:55357496-55358125	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr10:55357030-55358165	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:55410674-55410823	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr10:55358747-55359028	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr10:55358639-55359002	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr10:55357742-55358035	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr10:55436651-55436653	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr10:55407553-55407753	K562	blood:	n/a	n/a
12	CEBPB	chr10:55407097-55407340	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:55411759-55412117	Hela-S3	cervix:	n/a	chr10:55411925-55411936
14	CEBPB	chr10:55482351-55482593	HepG2	liver:	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
15	CEBPB	chr10:55440189-55440480	HepG2	liver:	n/a	chr10:55440348-55440359
16	CEBPB	chr10:55495107-55495314	A549	lung:	n/a	n/a
17	CEBPB	chr10:55495099-55495137	K562	blood:	n/a	n/a
18	CEBPB	chr10:55440562-55440588	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr10:55494993-55495303	IMR90	lung:	n/a	n/a
20	CEBPB	chr10:55456808-55457116	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:55361129-55361360	A549	lung:	n/a	n/a
22	CEBPB	chr10:55411770-55412027	HepG2	liver:	n/a	chr10:55411925-55411936
23	CEBPB	chr10:55484473-55484797	IMR90	lung:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
24	CEBPB	chr10:55484474-55484818	HepG2	liver:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
25	CEBPB	chr10:55440217-55440437	IMR90	lung:	n/a	chr10:55440348-55440359
26	CEBPB	chr10:55484526-55484810	A549	lung:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
27	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
28	CEBPB	chr10:55440212-55440489	A549	lung:	n/a	chr10:55440348-55440359
29	CEBPB	chr10:55495022-55495339	HepG2	liver:	n/a	n/a
30	CHD1	chr10:55357813-55359280	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr10:55509966-55509970	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr10:55358578-55359145	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr10:55357387-55358301	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr10:55358584-55359169	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr10:55361140-55361290	HMEC	breast:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
36	CTCF	chr10:55361140-55361290	GM12875	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
37	CTCF	chr10:55361120-55361270	HCM	heart:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
38	CTCF	chr10:55361160-55361310	GM12874	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
39	CTCF	chr10:55361120-55361270	GM12868	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
40	CTCF	chr10:55361140-55361290	HMF	breast:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
41	CTCF	chr10:55361016-55361451	K562	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
42	CTCF	chr10:55361112-55361317	Kidney_OC	kidney:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
43	CTCF	chr10:55361100-55361250	GM12801	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
44	CTCF	chr10:55361120-55361270	HEK293	kidney:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
45	CTCF	chr10:55361100-55361250	WERI-Rb-1	eye:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
46	CTCF	chr10:55361160-55361310	HRPEpiC	eye:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
47	CTCF	chr10:55361093-55361356	GM13977	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
48	CTCF	chr10:55361120-55361270	NHLF	lung:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
49	CTCF	chr10:55361159-55361235	GM19240	blood:	n/a	chr10:55361217-55361233 chr10:55361216-55361234
50	CTCF	chr10:55361140-55361290	HRPEpiC	eye:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55419714-55419764	HepG2	liver:	n/a
2	chr10:55419714-55419764	MCF-7	breast:	n/a
3	chr10:55357618-55357668	AoSMC	blood vessel:	n/a
4	chr10:55357618-55357668	AG09319	gingival:	n/a
5	chr10:55419927-55419977	LNCaP	prostate:	n/a
6	chr10:55357618-55357668	GM12878	blood:	n/a
7	chr10:55393450-55393500	HMEC	breast:	n/a
8	chr10:55419714-55419764	HIPEpiC	eye:	n/a
9	chr10:55419714-55419764	HL-60	blood:	n/a
10	chr10:55393450-55393500	HPAEpiC	pulmonary alveolar:	n/a
11	chr10:55357618-55357668	MCF-7	breast:	n/a
12	chr10:55419714-55419764	T-47D	breast:	n/a
13	chr10:55357618-55357668	HepG2	liver:	n/a
14	chr10:55357618-55357668	HEEpiC	esophagus:	n/a
15	chr10:55357618-55357668	PANC-1	pancreas:	n/a
16	chr10:55393450-55393500	PrEC	prostate:	n/a
17	chr10:55419927-55419977	GM12892	blood:	n/a
18	chr10:55419927-55419977	NB4	blood:	n/a
19	chr10:55419714-55419764	ECC-1	luminal epithelium:	n/a
20	chr10:55419927-55419977	MCF10A-Er-Src	breast:	n/a
21	chr10:55419927-55419977	AoSMC	blood vessel:	n/a
22	chr10:55393450-55393500	ProgFib	skin:	n/a
23	chr10:55357618-55357668	AG04450	lung:	fetal
24	chr10:55393450-55393500	HL-60	blood:	n/a
25	chr10:55419714-55419764	CMK	blood:	n/a
26	chr10:55357618-55357668	NT2-D1	testis:	n/a
27	chr10:55419714-55419764	GM12892	blood:	n/a
28	chr10:55393450-55393500	IMR90	lung:	fetal
29	chr10:55419927-55419977	Caco-2	colon:	n/a
30	chr10:55393450-55393500	RPTEC	kidney:	n/a
31	chr10:55419714-55419764	HCM	heart:	n/a
32	chr10:55419714-55419764	SK-N-SH	brain:	n/a
33	chr10:55419927-55419977	PANC-1	pancreas:	n/a
34	chr10:55393450-55393500	AG10803	skin:	n/a
35	chr10:55419714-55419764	Caco-2	colon:	n/a
36	chr10:55419927-55419977	Jurkat	blood:	n/a
37	chr10:55357618-55357668	HMEC	breast:	n/a
38	chr10:55419714-55419764	SK-N-SH_RA	brain:	n/a
39	chr10:55357618-55357668	GM19239	blood:	n/a
40	chr10:55357618-55357668	IMR90	lung:	fetal
41	chr10:55419927-55419977	HRPEpiC	eye:	n/a
42	chr10:55393450-55393500	BE2_C	brain:	n/a
43	chr10:55419714-55419764	AG09309	skin:	n/a
44	chr10:55393450-55393500	CMK	blood:	n/a
45	chr10:55357618-55357668	Hela-S3	cervix:	n/a
46	chr10:55357618-55357668	HEK293	kidney:	embryo
47	chr10:55393450-55393500	HCT-116	colon:	n/a
48	chr10:55393450-55393500	PFSK-1	brain:	n/a
49	chr10:55357618-55357668	HCT-116	colon:	n/a
50	chr10:55357618-55357668	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:55481740..55482260-chr20:52673713..52674214,2	MCF-7	breast:
2	chr10:55360709..55361787-chr10:55606233..55607054,5	MCF-7	breast:
3	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
4	chr10:55360883..55361625-chr10:55568215..55569121,2	MCF-7	breast:
5	chr10:55405153..55407581-chr5:63345532..63348450,2	MCF-7	breast:
6	10:55527193-55535408..10:55949104-55956834	K562	blood:
7	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:

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

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

Extended variants
information (count: 3881 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3881 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1932011	chr10:55357136-55357137	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs199615361	chr10:55357233-55357234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570318661	chr10:55357236-55357237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559114523	chr10:55357250-55357251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11003695	chr10:55357257-55357258	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs189568927	chr10:55357278-55357279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555232218	chr10:55357318-55357319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34964627	chr10:55357379-55357380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374962539	chr10:55357382-55357383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112845891	chr10:55357385-55357386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560495968	chr10:55357408-55357409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74134707	chr10:55357465-55357466	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs538195772	chr10:55357503-55357504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10762996	chr10:55357560-55357561	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545470979	chr10:55357570-55357571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562277850	chr10:55357575-55357576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531394059	chr10:55357658-55357659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548132826	chr10:55357708-55357709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149357761	chr10:55357709-55357710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76416507	chr10:55357717-55357718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547688142	chr10:55357803-55357804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73232478	chr10:55357869-55357870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs72791377	chr10:55357903-55357904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs552686793	chr10:55357946-55357947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569413058	chr10:55357950-55357951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144676165	chr10:55357982-55357983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554816840	chr10:55357995-55357996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192401165	chr10:55358127-55358128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534191868	chr10:55358214-55358215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs117431357	chr10:55358238-55358239	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs576414833	chr10:55358257-55358258	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs545434251	chr10:55358360-55358361	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs373624397	chr10:55358401-55358402	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs184742015	chr10:55358529-55358530	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs200862693	chr10:55358585-55358586	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs561700844	chr10:55358621-55358622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527505467	chr10:55358622-55358623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs61859934	chr10:55358626-55358627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564405419	chr10:55358739-55358740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78023060	chr10:55358794-55358795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558832492	chr10:55358845-55358846	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs569276342	chr10:55358907-55358908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs531670092	chr10:55358960-55358961	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs376046162	chr10:55358974-55358975	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs188704896	chr10:55359032-55359033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369732617	chr10:55359036-55359037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181440774	chr10:55359071-55359072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532233066	chr10:55359077-55359078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570857668	chr10:55359156-55359157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186263686	chr10:55359236-55359237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55350400-55357400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr10:55353400-55357400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr10:55354000-55359400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:55354000-55359600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:55355400-55359600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr10:55355600-55357400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr10:55355600-55359400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr10:55355800-55359800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr10:55355800-55360000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr10:55356000-55358200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr10:55356200-55358400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:55356200-55359800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr10:55356400-55359200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:55356400-55359600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr10:55356600-55358800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr10:55356800-55357600	Enhancers	Placenta Amnion	Placenta Amnion
17	chr10:55357000-55357400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr10:55357000-55357600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr10:55357000-55359600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr10:55357400-55358400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr10:55357400-55358400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr10:55357400-55359200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr10:55357400-55359600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr10:55357600-55358000	Enhancers	HSMMtube	muscle
25	chr10:55357600-55359200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr10:55357600-55359600	Enhancers	HMEC	breast
27	chr10:55357600-55359800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:55357600-55361000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr10:55357800-55359600	Enhancers	NHEK	skin
30	chr10:55357800-55359800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr10:55358000-55359800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr10:55358200-55358600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr10:55358200-55359400	Enhancers	NH-A	brain
34	chr10:55358400-55359200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr10:55358400-55359200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:55358600-55359800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr10:55358800-55359000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr10:55359000-55359400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr10:55359000-55359800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr10:55359200-55359600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr10:55359200-55359800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr10:55359200-55361200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr10:55359400-55359600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr10:55359400-55359800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr10:55359600-55359800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr10:55359600-55359800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr10:55359600-55360800	Weak transcription	NHEK	skin
48	chr10:55359600-55362200	Weak transcription	HMEC	breast
49	chr10:55359600-55366800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr10:55359800-55360200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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