Variant report

Variant	nsv895406
Chromosome Location	chr10:54780677-54830687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:189)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:189 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:54812645-54812845	HepG2	liver:	n/a	n/a
2	ATF2	chr10:54782216-54782718	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr10:54782245-54782835	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr10:54828775-54829045	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:54782292-54782638	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr10:54828892-54829105	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:54782709-54782744	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:54789662-54789889	GM12878	blood:	n/a	n/a
9	CEBPB	chr10:54798974-54799011	IMR90	lung:	n/a	chr10:54798994-54799005 chr10:54798993-54799006 chr10:54798978-54798989
10	CEBPB	chr10:54806095-54806330	HepG2	liver:	n/a	chr10:54806203-54806216 chr10:54806204-54806215 chr10:54806203-54806214 chr10:54806203-54806216
11	CEBPB	chr10:54790215-54790565	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:54802424-54802606	IMR90	lung:	n/a	n/a
13	CEBPB	chr10:54812569-54812835	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:54802374-54802596	HepG2	liver:	n/a	chr10:54802395-54802407
15	CEBPB	chr10:54798877-54799130	HepG2	liver:	n/a	chr10:54798994-54799005 chr10:54798993-54799006 chr10:54798978-54798989
16	CHD1	chr10:54828900-54828903	GM12878	blood:	n/a	n/a
17	CHD2	chr10:54812157-54812247	HepG2	liver:	n/a	n/a
18	CHD2	chr10:54789549-54789899	GM12878	blood:	n/a	n/a
19	CHD2	chr10:54828795-54829022	GM12878	blood:	n/a	n/a
20	CTCF	chr10:54788549-54788553	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr10:54820034-54820118	GM20000	blood:	n/a	n/a
22	CTCF	chr10:54799346-54799409	GM10248	blood:	n/a	n/a
23	CTCF	chr10:54782680-54782830	Caco-2	colon:	n/a	n/a
24	CTCF	chr10:54788566-54788619	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr10:54782440-54782590	Caco-2	colon:	n/a	n/a
26	CTCF	chr10:54788534-54788565	GM19240	blood:	n/a	n/a
27	CTCF	chr10:54788534-54788584	HepG2	liver:	n/a	n/a
28	CTCF	chr10:54788501-54788615	GM19238	blood:	n/a	n/a
29	CTCF	chr10:54795020-54795170	GM12869	blood:	n/a	n/a
30	CUX1	chr10:54818130-54818131	GM12878	blood:	n/a	n/a
31	CUX1	chr10:54828642-54828821	GM12878	blood:	n/a	n/a
32	E2F4	chr10:54802182-54802408	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr10:54794671-54794808	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F6	chr10:54789184-54790029	H1-hESC	embryonic stem cell:	n/a	n/a
35	E2F6	chr10:54789198-54789460	H1-hESC	embryonic stem cell:	n/a	n/a
36	EBF1	chr10:54789785-54789872	GM12878	blood:	n/a	n/a
37	EBF1	chr10:54828906-54828946	GM12878	blood:	n/a	n/a
38	ELK1	chr10:54828915-54828926	GM12878	blood:	n/a	n/a
39	EP300	chr10:54789684-54789996	GM12878	blood:	n/a	n/a
40	EP300	chr10:54828759-54829122	GM12878	blood:	n/a	n/a
41	EP300	chr10:54828786-54829200	GM12878	blood:	n/a	n/a
42	EP300	chr10:54828849-54829030	GM12878	blood:	n/a	n/a
43	EP300	chr10:54824397-54824722	GM12878	blood:	n/a	n/a
44	EP300	chr10:54782263-54782761	H1-hESC	embryonic stem cell:	n/a	n/a
45	EP300	chr10:54781911-54781975	K562	blood:	n/a	n/a
46	EP300	chr10:54785075-54785080	Hela-S3	cervix:	n/a	n/a
47	EP300	chr10:54789652-54789956	GM12878	blood:	n/a	n/a
48	EP300	chr10:54785067-54785206	GM12878	blood:	n/a	n/a
49	EP300	chr10:54789557-54790279	ECC-1	luminal epithelium:	n/a	n/a
50	EP300	chr10:54782275-54782782	ECC-1	luminal epithelium:	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	SK-N-SH	brain:	n/a
2	chr10:54782631-54782681	BJ	skin:	n/a
3	chr10:54782631-54782681	RPTEC	kidney:	n/a
4	chr10:54782631-54782681	HEEpiC	esophagus:	n/a
5	chr10:54782631-54782681	LNCaP	prostate:	n/a
6	chr10:54782631-54782681	AG10803	skin:	n/a
7	chr10:54782631-54782681	HCPEpiC	choroid plexus:	n/a
8	chr10:54782631-54782681	BE2_C	brain:	n/a
9	chr10:54782631-54782681	HRCEpiC	kidney:	n/a
10	chr10:54782631-54782681	GM06990	blood:	n/a
11	chr10:54782631-54782681	HPAEpiC	pulmonary alveolar:	n/a
12	chr10:54782631-54782681	NB4	blood:	n/a
13	chr10:54782631-54782681	SK-N-SH_RA	brain:	n/a
14	chr10:54782631-54782681	U87	brain:	n/a
15	chr10:54782631-54782681	HepG2	liver:	n/a
16	chr10:54782631-54782681	PANC-1	pancreas:	n/a
17	chr10:54782631-54782681	ovcar-3	ovarian:	n/a
18	chr10:54782631-54782681	SAEC	small airway:	n/a
19	chr10:54782631-54782681	MCF10A-Er-Src	breast:	n/a
20	chr10:54782631-54782681	HL-60	blood:	n/a
21	chr10:54782631-54782681	CMK	blood:	n/a
22	chr10:54782631-54782681	AG04449	skin:	fetal
23	chr10:54782631-54782681	IMR90	lung:	fetal
24	chr10:54782631-54782681	NH-A	brain:	n/a
25	chr10:54782631-54782681	AG09319	gingival:	n/a
26	chr10:54782631-54782681	HEK293	kidney:	embryo
27	chr10:54782631-54782681	AoSMC	blood vessel:	n/a
28	chr10:54782631-54782681	H1-hESC	embryonic stem cell:	embryo
29	chr10:54782631-54782681	A549	lung:	n/a
30	chr10:54782631-54782681	HUVEC	blood vessel:	n/a
31	chr10:54782631-54782681	GM19239	blood:	n/a
32	chr10:54782631-54782681	ECC-1	luminal epithelium:	n/a
33	chr10:54782631-54782681	SKMC	muscle:	n/a
34	chr10:54782631-54782681	GM12891	blood:	n/a
35	chr10:54782631-54782681	K562	blood:	n/a
36	chr10:54782631-54782681	SK-N-MC	brain:	n/a
37	chr10:54782631-54782681	HRE	kidney:	n/a
38	chr10:54782631-54782681	HNPCEpiC	eye:	n/a
39	chr10:54782631-54782681	Hela-S3	cervix:	n/a
40	chr10:54782631-54782681	Hepatocyte	liver:	n/a
41	chr10:54782631-54782681	GM12878	blood:	n/a
42	chr10:54782631-54782681	HIPEpiC	eye:	n/a
43	chr10:54782631-54782681	AG04450	lung:	fetal
44	chr10:54782631-54782681	HAEpiC	amniotic membrane:	n/a
45	chr10:54782631-54782681	HRPEpiC	eye:	n/a
46	chr10:54782631-54782681	HCF	heart:	n/a
47	chr10:54782631-54782681	PFSK-1	brain:	n/a
48	chr10:54782631-54782681	MCF-7	breast:	n/a
49	chr10:54782631-54782681	HCM	heart:	n/a
50	chr10:54782631-54782681	NHBE	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:
2	chr10:54793499..54796412-chr10:54801093..54803641,2	MCF-7	breast:
3	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:
4	chr10:54793499..54796412-chr10:54801093..54803641,2	MCF-7	breast:
5	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBL2-2	chr10:54782584-54782720	NONHSAT013446
2	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
3	lnc-MBL2-2	chr10:54789671-54789855	XLOC_008826
4	lnc-MBL2-2	chr10:54789671-54789810	NONHSAT013446
5	lnc-MBL2-2	chr10:54789671-54789884	XLOC_008826
6	lnc-MBL2-2	chr10:54789652-54790030	XLOC_008826
7	lnc-MBL2-2	chr10:54785024-54785887	XLOC_008826
8	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
9	lnc-DKK1-3	chr10:54798045-54798304	NONHSAT013449
10	lnc-MBL2-2	chr10:54782584-54782768	XLOC_008826

No data

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

Extended variants
information (count: 915 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2249349	chr10:54780677-54780678	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544584681	chr10:54780699-54780700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542230077	chr10:54780704-54780705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148290669	chr10:54780740-54780741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61669173	chr10:54780742-54780743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548912438	chr10:54780750-54780751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76078532	chr10:54780807-54780808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1917195	chr10:54780827-54780828	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs543362201	chr10:54780830-54780831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2249356	chr10:54780836-54780837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs1917194	chr10:54780847-54780848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs571358536	chr10:54780861-54780862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536697014	chr10:54780879-54780880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556871114	chr10:54780935-54780936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567876816	chr10:54781008-54781009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78328097	chr10:54781019-54781020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12263217	chr10:54781020-54781021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs538833964	chr10:54781048-54781049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552432447	chr10:54781125-54781126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371081041	chr10:54781129-54781130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73334922	chr10:54781142-54781143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1344275	chr10:54781196-54781197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186038537	chr10:54781197-54781198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113541349	chr10:54781206-54781207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189230843	chr10:54781240-54781241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561292542	chr10:54781257-54781258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374378239	chr10:54781335-54781336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs80217585	chr10:54781356-54781357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114372413	chr10:54781357-54781358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182247555	chr10:54781363-54781364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185942171	chr10:54781386-54781387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190862668	chr10:54781391-54781392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183074143	chr10:54781402-54781403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185739621	chr10:54781423-54781424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374237080	chr10:54781425-54781426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190408606	chr10:54781515-54781516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530589761	chr10:54781538-54781539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550320625	chr10:54781554-54781555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567227087	chr10:54781561-54781562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2249478	chr10:54781562-54781563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs546925225	chr10:54781646-54781647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546349611	chr10:54781655-54781656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143123393	chr10:54781683-54781684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377015471	chr10:54781766-54781767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10824857	chr10:54781771-54781772	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs558677537	chr10:54781894-54781895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57494549	chr10:54781930-54781931	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs538303104	chr10:54781952-54781953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376949978	chr10:54781998-54781999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183033022	chr10:54782047-54782048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54765200-54782600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:54767600-54782200	Weak transcription	Fetal Kidney	kidney
3	chr10:54773400-54781200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr10:54773600-54782200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr10:54781200-54782200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr10:54781800-54782200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr10:54781800-54782200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr10:54782000-54782200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr10:54782000-54782200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr10:54782000-54783400	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr10:54782000-54783600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr10:54782000-54783800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr10:54782200-54782400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr10:54782200-54782400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr10:54782200-54782600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr10:54782200-54783000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr10:54782200-54783000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr10:54782200-54783200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr10:54782200-54783400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr10:54782200-54783600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr10:54782200-54784400	Enhancers	Fetal Kidney	kidney
22	chr10:54782400-54782600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr10:54782400-54782600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr10:54782400-54782800	Weak transcription	Lung	lung
25	chr10:54782400-54783000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr10:54782400-54783400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr10:54782400-54783600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr10:54782400-54784000	Enhancers	Placenta	Placenta
29	chr10:54782400-54786000	Enhancers	Fetal Stomach	stomach
30	chr10:54782600-54782800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr10:54782600-54783000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:54782600-54783000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:54782600-54783000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr10:54782600-54783000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr10:54782600-54783200	Enhancers	Stomach Mucosa	stomach
36	chr10:54782600-54783400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr10:54782600-54783400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr10:54782600-54783600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr10:54782600-54783600	Enhancers	H9 Cell Line	embryonic stem cell
40	chr10:54782600-54783600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr10:54782600-54783600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr10:54782600-54783600	Enhancers	NHEK	skin
43	chr10:54782800-54783600	Enhancers	Fetal Intestine Small	intestine
44	chr10:54782800-54783600	Enhancers	Fetal Lung	lung
45	chr10:54782800-54783800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr10:54783000-54783200	Enhancers	Ovary	ovary
47	chr10:54783000-54783400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr10:54783000-54783600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr10:54783000-54783600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr10:54783200-54783400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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