Variant report

Variant	nsv1054951
Chromosome Location	chr10:54115222-54175982
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	chr10:54116813-54117088	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:54151854-54152011	HepG2	liver:	n/a	n/a
3	BHLHE40	chr10:54159642-54159726	GM12878	blood:	n/a	n/a
4	BHLHE40	chr10:54137814-54138087	HepG2	liver:	n/a	chr10:54137897-54137918 chr10:54137904-54137913
5	BRCA1	chr10:54159646-54159717	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr10:54138028-54138221	HepG2	liver:	n/a	chr10:54138127-54138138
7	CEBPB	chr10:54137993-54138284	H1-hESC	embryonic stem cell:	n/a	chr10:54138127-54138138
8	CEBPB	chr10:54137968-54138310	HepG2	liver:	n/a	chr10:54138127-54138138
9	CEBPB	chr10:54137942-54138319	HepG2	liver:	n/a	chr10:54138127-54138138
10	CEBPB	chr10:54137962-54138183	A549	lung:	n/a	chr10:54138127-54138138
11	CEBPB	chr10:54168907-54169458	MCF-7	breast:	n/a	n/a
12	CEBPB	chr10:54137925-54138270	HepG2	liver:	n/a	chr10:54138127-54138138
13	CEBPB	chr10:54168997-54169412	MCF-7	breast:	n/a	n/a
14	CEBPB	chr10:54142962-54143167	HepG2	liver:	n/a	chr10:54143027-54143038 chr10:54143028-54143039
15	CHD2	chr10:54150312-54150345	K562	blood:	n/a	n/a
16	CHD2	chr10:54125462-54125735	HepG2	liver:	n/a	n/a
17	CTCF	chr10:54128583-54128791	Gliobla	brain:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
18	CTCF	chr10:54128580-54128730	HVMF	connective:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
19	CTCF	chr10:54128640-54128739	Fibrobl	skin:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
20	CTCF	chr10:54128560-54128710	MCF-7	breast:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
21	CTCF	chr10:54137440-54137590	Caco-2	colon:	n/a	n/a
22	CTCF	chr10:54128541-54128850	GM12878	blood:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
23	CTCF	chr10:54128591-54128768	MCF-7	breast:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
24	CTCF	chr10:54128540-54128690	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr10:54128580-54128730	NHEK	skin:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
26	CTCF	chr10:54128620-54128770	RPTEC	kidney:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
27	CTCF	chr10:54128641-54128718	ProgFib	skin:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
28	CTCF	chr10:54128611-54128759	MCF-7	breast:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
29	CTCF	chr10:54128640-54128790	BE2_C	brain:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
30	CTCF	chr10:54128616-54128742	HepG2	liver:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
31	CTCF	chr10:54128640-54128790	Caco-2	colon:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
32	CTCF	chr10:54128540-54128690	GM12873	blood:	n/a	n/a
33	CTCF	chr10:54128660-54128714	A549	lung:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
34	CTCF	chr10:54128636-54128739	GM19239	blood:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
35	CTCF	chr10:54128560-54128710	HCPEpiC	choroid plexus:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
36	CTCF	chr10:54128560-54128710	GM06990	blood:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
37	CTCF	chr10:54128645-54128706	Spleen_OC	spleen:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
38	CTCF	chr10:54128520-54128670	BE2_C	brain:	n/a	n/a
39	CTCF	chr10:54128620-54128770	SK-N-SH_RA	brain:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
40	CTCF	chr10:54171750-54171842	GM10248	blood:	n/a	n/a
41	CTCF	chr10:54128560-54128710	HRE	kidney:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
42	CTCF	chr10:54128591-54128733	HepG2	liver:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
43	CTCF	chr10:54128646-54128749	GM19238	blood:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
44	CTCF	chr10:54128580-54128730	GM12869	blood:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
45	CTCF	chr10:54143755-54143841	GM20000	blood:	n/a	n/a
46	CTCF	chr10:54128616-54128760	HUVEC	blood vessel:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
47	CTCF	chr10:54128640-54128790	GM12864	blood:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
48	CTCF	chr10:54128580-54128730	HMEC	breast:	n/a	chr10:54128679-54128692 chr10:54128676-54128694 chr10:54128679-54128692
49	CTCF	chr10:54128540-54128690	HMF	breast:	n/a	n/a
50	CTCF	chr10:54128680-54128830	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:54170928-54170978	AoSMC	blood vessel:	n/a
2	chr10:54172718-54172768	HRE	kidney:	n/a
3	chr10:54172718-54172768	GM06990	blood:	n/a
4	chr10:54170977-54171027	SK-N-SH	brain:	n/a
5	chr10:54166783-54166833	HRPEpiC	eye:	n/a
6	chr10:54172718-54172768	PFSK-1	brain:	n/a
7	chr10:54170928-54170978	HRE	kidney:	n/a
8	chr10:54170977-54171027	PrEC	prostate:	n/a
9	chr10:54172718-54172768	HepG2	liver:	n/a
10	chr10:54172718-54172768	PANC-1	pancreas:	n/a
11	chr10:54170977-54171027	AG09319	gingival:	n/a
12	chr10:54170977-54171027	HRE	kidney:	n/a
13	chr10:54166783-54166833	ECC-1	luminal epithelium:	n/a
14	chr10:54170977-54171027	NHBE	bronchial:	n/a
15	chr10:54170928-54170978	GM12878	blood:	n/a
16	chr10:54172718-54172768	HUVEC	blood vessel:	n/a
17	chr10:54172718-54172768	Hela-S3	cervix:	n/a
18	chr10:54172718-54172768	HRCEpiC	kidney:	n/a
19	chr10:54170977-54171027	SK-N-MC	brain:	n/a
20	chr10:54172718-54172768	SAEC	small airway:	n/a
21	chr10:54170928-54170978	SK-N-MC	brain:	n/a
22	chr10:54170928-54170978	IMR90	lung:	fetal
23	chr10:54172718-54172768	BE2_C	brain:	n/a
24	chr10:54170977-54171027	HEK293	kidney:	embryo
25	chr10:54166783-54166833	HEK293	kidney:	embryo
26	chr10:54166783-54166833	ovcar-3	ovarian:	n/a
27	chr10:54170977-54171027	Caco-2	colon:	n/a
28	chr10:54172718-54172768	HRPEpiC	eye:	n/a
29	chr10:54170977-54171027	A549	lung:	n/a
30	chr10:54170977-54171027	HRCEpiC	kidney:	n/a
31	chr10:54170928-54170978	NB4	blood:	n/a
32	chr10:54170928-54170978	HNPCEpiC	eye:	n/a
33	chr10:54170928-54170978	HCM	heart:	n/a
34	chr10:54172718-54172768	Caco-2	colon:	n/a
35	chr10:54170977-54171027	ECC-1	luminal epithelium:	n/a
36	chr10:54170928-54170978	HL-60	blood:	n/a
37	chr10:54172718-54172768	GM12892	blood:	n/a
38	chr10:54170928-54170978	PrEC	prostate:	n/a
39	chr10:54170928-54170978	NHDF-neo	bronchial:	n/a
40	chr10:54166783-54166833	T-47D	breast:	n/a
41	chr10:54166783-54166833	HNPCEpiC	eye:	n/a
42	chr10:54166783-54166833	PANC-1	pancreas:	n/a
43	chr10:54172718-54172768	U87	brain:	n/a
44	chr10:54170928-54170978	HIPEpiC	eye:	n/a
45	chr10:54170977-54171027	HCT-116	colon:	n/a
46	chr10:54166783-54166833	GM12878	blood:	n/a
47	chr10:54170928-54170978	H1-hESC	embryonic stem cell:	embryo
48	chr10:54170977-54171027	NB4	blood:	n/a
49	chr10:54172718-54172768	ECC-1	luminal epithelium:	n/a
50	chr10:54172718-54172768	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:54075730..54077425-chr10:54167077..54169136,2	MCF-7	breast:
2	chr10:54136741..54139715-chr10:54150116..54153046,2	MCF-7	breast:
3	chr10:54129947..54132591-chr10:54167991..54170801,2	MCF-7	breast:
4	chr10:54136741..54139715-chr10:54150116..54153046,2	MCF-7	breast:
5	chr10:54072676..54075890-chr10:54175491..54177804,3	MCF-7	breast:
6	chr10:54128254..54128951-chr10:54248414..54249406,2	MCF-7	breast:
7	chr10:54073525..54075924-chr10:54146848..54149629,2	MCF-7	breast:
8	chr10:54149526..54151091-chr10:54155620..54157632,2	K562	blood:
9	chr10:54116820..54117320-chr12:52463690..52464439,2	MCF-7	breast:
10	chr10:54170977..54173585-chr10:54198985..54203167,3	MCF-7	breast:
11	chr10:54149526..54151091-chr10:54155620..54157632,2	K562	blood:
12	chr10:54168310..54170304-chr10:54200960..54203183,2	MCF-7	breast:
13	chr10:54129947..54132591-chr10:54167991..54170801,2	MCF-7	breast:
14	chr10:54071543..54073516-chr10:54113139..54115614,2	MCF-7	breast:
15	chr10:54145859..54147775-chr10:54203869..54205399,2	MCF-7	breast:
16	chr10:54092984..54095026-chr10:54166953..54169179,2	MCF-7	breast:
17	chr10:54097318..54099271-chr10:54118313..54119934,2	MCF-7	breast:
18	chr10:54071490..54075450-chr10:54149766..54152641,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBL2-9	chr10:54148872-54149248	NONHSAT013425

Variant related genes	Relation type
ENSG00000213657	TF binding region
PRKRIRP3	TF binding region
ENSG00000213657	CpG island
PRKRIRP3	CpG island
ENSG00000123395	chromatin interactions
ENSG00000236671	chromatin interactions
ENSG00000107984	chromatin interactions

Extended variants
information (count: 2204 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2204 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191013528	chr10:54115241-54115242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550011706	chr10:54115243-54115244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567855789	chr10:54115275-54115276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144057603	chr10:54115373-54115374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554638393	chr10:54115399-54115400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182907786	chr10:54115422-54115423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573542390	chr10:54115467-54115468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147334895	chr10:54115468-54115469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558861866	chr10:54115532-54115533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575657651	chr10:54115534-54115535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116561538	chr10:54115535-54115536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139012725	chr10:54115554-54115555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149362250	chr10:54115595-54115596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542550970	chr10:54115603-54115604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559240853	chr10:54115685-54115686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542987106	chr10:54115686-54115687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528342658	chr10:54115712-54115713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551093893	chr10:54115754-54115755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571183613	chr10:54115778-54115779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554135748	chr10:54115797-54115798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530561650	chr10:54115821-54115822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76018872	chr10:54115855-54115856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186676703	chr10:54115944-54115945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377267586	chr10:54115948-54115949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556456395	chr10:54115976-54115977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145232869	chr10:54115978-54115979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200511566	chr10:54115979-54115980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201599790	chr10:54115981-54115982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200063117	chr10:54115983-54115984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11001749	chr10:54115985-54115986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553575484	chr10:54116032-54116033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114225721	chr10:54116102-54116103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs16929708	chr10:54116123-54116124	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs545587460	chr10:54116142-54116143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558721059	chr10:54116159-54116160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs66594753	chr10:54116233-54116234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575589430	chr10:54116262-54116263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192604700	chr10:54116297-54116298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554629688	chr10:54116309-54116310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574560413	chr10:54116317-54116318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562484014	chr10:54116366-54116367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144726279	chr10:54116373-54116374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148522902	chr10:54116397-54116398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10762715	chr10:54116418-54116419	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs545279068	chr10:54116452-54116453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564754318	chr10:54116470-54116471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10762716	chr10:54116478-54116479	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs142871962	chr10:54116484-54116485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74133318	chr10:54116519-54116520	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs529766198	chr10:54116520-54116521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54112400-54115600	Weak transcription	HUVEC	blood vessel
2	chr10:54113400-54117200	Enhancers	HepG2	liver
3	chr10:54113800-54116000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:54114000-54116200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:54114000-54116400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:54114000-54118600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:54114200-54115600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:54114200-54117400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:54114400-54115400	Weak transcription	NHDF-Ad	bronchial
10	chr10:54114400-54115400	Weak transcription	Osteobl	bone
11	chr10:54114400-54115600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:54114400-54115600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr10:54114400-54115600	Weak transcription	HSMM	muscle
14	chr10:54114400-54118800	Weak transcription	HMEC	breast
15	chr10:54114400-54119200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr10:54114600-54115400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:54114600-54115800	Enhancers	NHEK	skin
18	chr10:54115000-54116400	Enhancers	Fetal Intestine Small	intestine
19	chr10:54115400-54116200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr10:54115400-54116400	Enhancers	Osteobl	bone
21	chr10:54115600-54115800	Enhancers	A549	lung
22	chr10:54115600-54115800	Enhancers	NHDF-Ad	bronchial
23	chr10:54115600-54116000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:54115600-54116200	Enhancers	HUVEC	blood vessel
25	chr10:54115600-54116400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr10:54115600-54117000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr10:54115800-54119600	Weak transcription	NHEK	skin
28	chr10:54116000-54116200	Enhancers	HSMM	muscle
29	chr10:54116000-54119400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr10:54116200-54120000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:54116400-54118000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr10:54117200-54117600	Weak transcription	HepG2	liver
33	chr10:54117400-54120000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr10:54117600-54118200	Enhancers	HepG2	liver
35	chr10:54117800-54118000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr10:54117800-54118200	Enhancers	Fetal Heart	heart
37	chr10:54118000-54118800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr10:54118400-54119800	Enhancers	Primary hematopoietic stem cells	blood
39	chr10:54118600-54119000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:54118600-54119600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr10:54118800-54120000	Enhancers	HMEC	breast
42	chr10:54119200-54119600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr10:54119200-54119800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr10:54119200-54119800	Enhancers	NH-A	brain
45	chr10:54119400-54119800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:54119600-54119800	Enhancers	NHEK	skin
47	chr10:54125200-54125400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr10:54125200-54125800	Enhancers	HepG2	liver
49	chr10:54125200-54127400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:54125400-54126000	Active TSS	HUES6 Cell Line	embryonic stem cell

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