Variant report

Variant	nsv508585
Chromosome Location	chr10:54769376-54796804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:156)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:156 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:54782245-54782835	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr10:54782216-54782718	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr10:54782292-54782638	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr10:54773034-54773276	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:54782709-54782744	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:54789662-54789889	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:54772825-54773371	GM12878	blood:	n/a	n/a
8	CEBPB	chr10:54790215-54790565	IMR90	lung:	n/a	n/a
9	CHD2	chr10:54789549-54789899	GM12878	blood:	n/a	n/a
10	CTCF	chr10:54788566-54788619	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr10:54795020-54795170	GM12869	blood:	n/a	n/a
12	CTCF	chr10:54788534-54788565	GM19240	blood:	n/a	n/a
13	CTCF	chr10:54788501-54788615	GM19238	blood:	n/a	n/a
14	CTCF	chr10:54788534-54788584	HepG2	liver:	n/a	n/a
15	CTCF	chr10:54782440-54782590	Caco-2	colon:	n/a	n/a
16	CTCF	chr10:54788549-54788553	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr10:54782680-54782830	Caco-2	colon:	n/a	n/a
18	CTCF	chr10:54770400-54770550	AG10803	skin:	n/a	n/a
19	CUX1	chr10:54772800-54773567	GM12878	blood:	n/a	n/a
20	E2F4	chr10:54794671-54794808	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F6	chr10:54789184-54790029	H1-hESC	embryonic stem cell:	n/a	n/a
22	E2F6	chr10:54789198-54789460	H1-hESC	embryonic stem cell:	n/a	n/a
23	EBF1	chr10:54789785-54789872	GM12878	blood:	n/a	n/a
24	EBF1	chr10:54776657-54776891	GM12878	blood:	n/a	chr10:54776786-54776795 chr10:54776784-54776797 chr10:54776786-54776795 chr10:54776786-54776796
25	EBF1	chr10:54776847-54776886	GM12878	blood:	n/a	n/a
26	EBF1	chr10:54773077-54773453	GM12878	blood:	n/a	n/a
27	EBF1	chr10:54775757-54775897	GM12878	blood:	n/a	n/a
28	EP300	chr10:54770028-54770549	HepG2	liver:	n/a	chr10:54770219-54770233
29	EP300	chr10:54789684-54789996	GM12878	blood:	n/a	n/a
30	EP300	chr10:54789652-54789956	GM12878	blood:	n/a	n/a
31	EP300	chr10:54782240-54782939	ECC-1	luminal epithelium:	n/a	n/a
32	EP300	chr10:54785083-54785320	HepG2	liver:	n/a	n/a
33	EP300	chr10:54781911-54781975	K562	blood:	n/a	n/a
34	EP300	chr10:54782275-54782782	ECC-1	luminal epithelium:	n/a	n/a
35	EP300	chr10:54770014-54770522	HepG2	liver:	n/a	chr10:54770219-54770233
36	EP300	chr10:54785075-54785080	Hela-S3	cervix:	n/a	n/a
37	EP300	chr10:54785067-54785206	GM12878	blood:	n/a	n/a
38	EP300	chr10:54789557-54790279	ECC-1	luminal epithelium:	n/a	n/a
39	EP300	chr10:54782263-54782761	H1-hESC	embryonic stem cell:	n/a	n/a
40	EP300	chr10:54772964-54773391	GM12878	blood:	n/a	chr10:54773097-54773106 chr10:54773064-54773078
41	EP300	chr10:54772929-54773422	GM12878	blood:	n/a	chr10:54773097-54773106 chr10:54773064-54773078
42	FOS	chr10:54790238-54790506	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr10:54790145-54790652	HUVEC	blood vessel:	n/a	n/a
44	FOS	chr10:54772962-54773394	HUVEC	blood vessel:	n/a	chr10:54773095-54773106 chr10:54773095-54773107 chr10:54773097-54773106
45	FOS	chr10:54790236-54790505	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr10:54790236-54790507	MCF10A-Er-Src	breast:	n/a	n/a
47	FOSL2	chr10:54790315-54790639	SK-N-SH	brain:	n/a	n/a
48	FOXA1	chr10:54770107-54770411	HepG2	liver:	n/a	n/a
49	FOXA1	chr10:54789951-54790288	HepG2	liver:	n/a	n/a
50	FOXA1	chr10:54789948-54790202	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:54782631-54782681	HAEpiC	amniotic membrane:	n/a
2	chr10:54782631-54782681	MCF-7	breast:	n/a
3	chr10:54782631-54782681	MCF10A-Er-Src	breast:	n/a
4	chr10:54782631-54782681	NHBE	bronchial:	n/a
5	chr10:54782631-54782681	HEK293	kidney:	embryo
6	chr10:54782631-54782681	NHDF-neo	bronchial:	n/a
7	chr10:54782631-54782681	Caco-2	colon:	n/a
8	chr10:54782631-54782681	SAEC	small airway:	n/a
9	chr10:54782631-54782681	HEEpiC	esophagus:	n/a
10	chr10:54782631-54782681	HIPEpiC	eye:	n/a
11	chr10:54782631-54782681	HCM	heart:	n/a
12	chr10:54782631-54782681	NT2-D1	testis:	n/a
13	chr10:54782631-54782681	SKMC	muscle:	n/a
14	chr10:54782631-54782681	K562	blood:	n/a
15	chr10:54782631-54782681	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:54782631-54782681	LNCaP	prostate:	n/a
17	chr10:54782631-54782681	HNPCEpiC	eye:	n/a
18	chr10:54782631-54782681	ovcar-3	ovarian:	n/a
19	chr10:54782631-54782681	HL-60	blood:	n/a
20	chr10:54782631-54782681	AG09319	gingival:	n/a
21	chr10:54782631-54782681	GM19239	blood:	n/a
22	chr10:54782631-54782681	IMR90	lung:	fetal
23	chr10:54782631-54782681	NH-A	brain:	n/a
24	chr10:54782631-54782681	H1-hESC	embryonic stem cell:	embryo
25	chr10:54782631-54782681	GM12891	blood:	n/a
26	chr10:54782631-54782681	Hela-S3	cervix:	n/a
27	chr10:54782631-54782681	HCPEpiC	choroid plexus:	n/a
28	chr10:54782631-54782681	NB4	blood:	n/a
29	chr10:54782631-54782681	HepG2	liver:	n/a
30	chr10:54782631-54782681	BJ	skin:	n/a
31	chr10:54782631-54782681	Hepatocyte	liver:	n/a
32	chr10:54782631-54782681	SK-N-SH_RA	brain:	n/a
33	chr10:54782631-54782681	SK-N-MC	brain:	n/a
34	chr10:54782631-54782681	AoSMC	blood vessel:	n/a
35	chr10:54782631-54782681	AG09309	skin:	n/a
36	chr10:54782631-54782681	HRE	kidney:	n/a
37	chr10:54782631-54782681	PFSK-1	brain:	n/a
38	chr10:54782631-54782681	BE2_C	brain:	n/a
39	chr10:54782631-54782681	HRPEpiC	eye:	n/a
40	chr10:54782631-54782681	HCT-116	colon:	n/a
41	chr10:54782631-54782681	U87	brain:	n/a
42	chr10:54782631-54782681	SK-N-SH	brain:	n/a
43	chr10:54782631-54782681	HCF	heart:	n/a
44	chr10:54782631-54782681	GM12892	blood:	n/a
45	chr10:54782631-54782681	ECC-1	luminal epithelium:	n/a
46	chr10:54782631-54782681	HRCEpiC	kidney:	n/a
47	chr10:54782631-54782681	AG04449	skin:	fetal
48	chr10:54782631-54782681	PANC-1	pancreas:	n/a
49	chr10:54782631-54782681	T-47D	breast:	n/a
50	chr10:54782631-54782681	CMK	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:
2	chr10:54769210..54771714-chr10:54777628..54779140,2	K562	blood:
3	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:
4	chr10:54793499..54796412-chr10:54801093..54803641,2	MCF-7	breast:
5	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:
6	chr10:54764008..54766836-chr10:54772750..54774326,2	K562	blood:
7	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:
8	chr10:54769210..54771714-chr10:54777628..54779140,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBL2-2	chr10:54789671-54789810	NONHSAT013446
2	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
3	lnc-MBL2-2	chr10:54789652-54790030	XLOC_008826
4	lnc-MBL2-2	chr10:54782584-54782768	XLOC_008826
5	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
6	lnc-MBL2-2	chr10:54785024-54785887	XLOC_008826
7	lnc-MBL2-2	chr10:54789671-54789855	XLOC_008826
8	lnc-MBL2-2	chr10:54789671-54789884	XLOC_008826
9	lnc-MBL2-2	chr10:54782584-54782720	NONHSAT013446

No data

Variant related genes	Relation type
SNRPEP8	TF binding region
SNRPEP8	CpG island
MYB	miRNA target sites

Extended variants
information (count: 985 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:985 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544649857	chr10:54769394-54769395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576937562	chr10:54769411-54769412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148740781	chr10:54769450-54769451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185489677	chr10:54769451-54769452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531304060	chr10:54769463-54769464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547786521	chr10:54769466-54769467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371008352	chr10:54769473-54769474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375448991	chr10:54769475-54769476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564852766	chr10:54769479-54769480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190153374	chr10:54769521-54769522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182798981	chr10:54769645-54769646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548041380	chr10:54769652-54769653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571035611	chr10:54769655-54769656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185957452	chr10:54769674-54769675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11003329	chr10:54769687-54769688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191969404	chr10:54769754-54769755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570208986	chr10:54769773-54769774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144447402	chr10:54769780-54769781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs578258612	chr10:54769793-54769794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555805828	chr10:54769823-54769824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572368192	chr10:54769826-54769827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533863379	chr10:54769894-54769895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112178033	chr10:54769956-54769957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577055990	chr10:54770029-54770030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183650374	chr10:54770050-54770051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555895390	chr10:54770064-54770065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369697152	chr10:54770081-54770082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575743159	chr10:54770119-54770120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10508984	chr10:54770122-54770123	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs561553455	chr10:54770159-54770160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73353665	chr10:54770210-54770211	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540654660	chr10:54770222-54770223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs72800360	chr10:54770295-54770296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7074652	chr10:54770299-54770300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550399536	chr10:54770353-54770354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570221221	chr10:54770372-54770373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147818894	chr10:54770381-54770382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531756690	chr10:54770384-54770385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549425743	chr10:54770385-54770386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566015767	chr10:54770400-54770401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535060488	chr10:54770411-54770412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557866851	chr10:54770421-54770422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141464305	chr10:54770477-54770478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7086840	chr10:54770513-54770514	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs189098128	chr10:54770524-54770525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575804964	chr10:54770617-54770618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs193142788	chr10:54770620-54770621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555472838	chr10:54770658-54770659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145279869	chr10:54770690-54770691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541066366	chr10:54770801-54770802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Chronic lymphocytic leukemia	21546498	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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54764400-54771200	Enhancers	HepG2	liver
2	chr10:54765200-54782600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:54766800-54770000	Weak transcription	Stomach Mucosa	stomach
4	chr10:54767400-54769600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr10:54767600-54770000	Weak transcription	Fetal Lung	lung
6	chr10:54767600-54770200	Weak transcription	Liver	Liver
7	chr10:54767600-54782200	Weak transcription	Fetal Kidney	kidney
8	chr10:54769200-54772600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr10:54769800-54770800	Enhancers	Fetal Brain Female	brain
10	chr10:54770000-54770600	Enhancers	Stomach Mucosa	stomach
11	chr10:54770000-54770800	Enhancers	Fetal Lung	lung
12	chr10:54771400-54772800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr10:54771600-54774800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr10:54771800-54772200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr10:54772200-54773000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr10:54772400-54773800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr10:54772600-54772800	Enhancers	GM12878-XiMat	blood
18	chr10:54772600-54773600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr10:54772600-54774000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr10:54772800-54773400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr10:54772800-54773600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr10:54772800-54774000	Flanking Active TSS	GM12878-XiMat	blood
23	chr10:54772800-54774200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr10:54773000-54773400	Active TSS	Monocytes-CD14+_RO01746	blood
25	chr10:54773400-54773800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr10:54773400-54781200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr10:54773600-54782200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr10:54773800-54774400	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr10:54774000-54774400	Enhancers	GM12878-XiMat	blood
30	chr10:54781200-54782200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr10:54781800-54782200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr10:54781800-54782200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr10:54782000-54782200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr10:54782000-54782200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr10:54782000-54783400	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr10:54782000-54783600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr10:54782000-54783800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr10:54782200-54782400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr10:54782200-54782400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr10:54782200-54782600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr10:54782200-54783000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr10:54782200-54783000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr10:54782200-54783200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr10:54782200-54783400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr10:54782200-54783600	Enhancers	Placenta Amnion	Placenta Amnion
46	chr10:54782200-54784400	Enhancers	Fetal Kidney	kidney
47	chr10:54782400-54782600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr10:54782400-54782600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr10:54782400-54782800	Weak transcription	Lung	lung
50	chr10:54782400-54783000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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