Variant report

Variant	nsv550812
Chromosome Location	chr10:49484698-49524715
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1458)
CpG islands
(count:488)
Chromatin interactive
region (count:59)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:49514699-49514899	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:49517762-49518319	K562	blood:	n/a	n/a
3	ARID3A	chr10:49514425-49514517	K562	blood:	n/a	n/a
4	ARID3A	chr10:49517881-49518317	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:49499283-49499420	HepG2	liver:	n/a	n/a
6	ATF1	chr10:49497714-49498043	K562	blood:	n/a	n/a
7	ATF1	chr10:49499290-49499629	K562	blood:	n/a	n/a
8	ATF2	chr10:49497607-49498044	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr10:49497434-49498032	GM12878	blood:	n/a	n/a
10	ATF2	chr10:49490829-49491340	GM12878	blood:	n/a	n/a
11	ATF2	chr10:49486941-49487901	GM12878	blood:	n/a	n/a
12	ATF2	chr10:49490835-49491395	GM12878	blood:	n/a	n/a
13	ATF2	chr10:49493627-49494187	GM12878	blood:	n/a	n/a
14	ATF2	chr10:49493624-49494189	GM12878	blood:	n/a	n/a
15	ATF2	chr10:49495897-49496410	GM12878	blood:	n/a	n/a
16	ATF2	chr10:49486865-49488015	GM12878	blood:	n/a	n/a
17	ATF3	chr10:49514255-49514895	K562	blood:	n/a	n/a
18	BACH1	chr10:49515040-49515249	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr10:49517737-49518300	GM12878	blood:	n/a	n/a
20	BATF	chr10:49490920-49491270	GM12878	blood:	n/a	n/a
21	BATF	chr10:49487504-49487868	GM12878	blood:	n/a	n/a
22	BATF	chr10:49493773-49494002	GM12878	blood:	n/a	n/a
23	BATF	chr10:49490859-49491377	GM12878	blood:	n/a	n/a
24	BATF	chr10:49486980-49487476	GM12878	blood:	n/a	n/a
25	BATF	chr10:49495983-49496331	GM12878	blood:	n/a	n/a
26	BATF	chr10:49493745-49494164	GM12878	blood:	n/a	n/a
27	BATF	chr10:49517766-49518251	GM12878	blood:	n/a	n/a
28	BATF	chr10:49486983-49487492	GM12878	blood:	n/a	n/a
29	BATF	chr10:49495976-49496300	GM12878	blood:	n/a	n/a
30	BCL11A	chr10:49487004-49487709	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:49493739-49494122	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:49490880-49491363	GM12878	blood:	n/a	n/a
33	BCL11A	chr10:49491010-49491334	GM12878	blood:	n/a	n/a
34	BCL11A	chr10:49487048-49487421	GM12878	blood:	n/a	n/a
35	BCL11A	chr10:49493743-49494064	GM12878	blood:	n/a	n/a
36	BCL3	chr10:49486950-49487924	GM12878	blood:	n/a	n/a
37	BCL3	chr10:49487002-49487402	GM12878	blood:	n/a	n/a
38	BCL3	chr10:49493625-49494224	GM12878	blood:	n/a	n/a
39	BCLAF1	chr10:49486925-49487605	GM12878	blood:	n/a	n/a
40	BCLAF1	chr10:49514444-49515017	GM12878	blood:	n/a	chr10:49514930-49514943 chr10:49514935-49514948 chr10:49514818-49514831 chr10:49514852-49514865 chr10:49514822-49514835 chr10:49514932-49514945 chr10:49514935-49514944 chr10:49514938-49514947 chr10:49514929-49514942
41	BCLAF1	chr10:49487006-49487512	GM12878	blood:	n/a	n/a
42	BCLAF1	chr10:49490826-49491321	GM12878	blood:	n/a	n/a
43	BCLAF1	chr10:49493768-49494172	GM12878	blood:	n/a	n/a
44	BHLHE40	chr10:49495972-49496403	GM12878	blood:	n/a	n/a
45	BHLHE40	chr10:49497707-49498099	K562	blood:	n/a	n/a
46	BHLHE40	chr10:49514067-49514896	K562	blood:	n/a	chr10:49514447-49514463
47	BHLHE40	chr10:49486921-49487764	GM12878	blood:	n/a	n/a
48	BHLHE40	chr10:49490913-49491483	GM12878	blood:	n/a	n/a
49	BHLHE40	chr10:49499333-49499616	K562	blood:	n/a	n/a
50	BHLHE40	chr10:49514087-49514854	HepG2	liver:	n/a	chr10:49514447-49514463

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49514337-49514387	GM19239	blood:	n/a
2	chr10:49516634-49516684	HCT-116	colon:	n/a
3	chr10:49514530-49514580	PrEC	prostate:	n/a
4	chr10:49514530-49514580	HCM	heart:	n/a
5	chr10:49515028-49515078	HRE	kidney:	n/a
6	chr10:49515374-49515424	HRCEpiC	kidney:	n/a
7	chr10:49515374-49515424	HEEpiC	esophagus:	n/a
8	chr10:49515028-49515078	AG09319	gingival:	n/a
9	chr10:49515374-49515424	BJ	skin:	n/a
10	chr10:49514546-49514596	AG04450	lung:	fetal
11	chr10:49514530-49514580	HRCEpiC	kidney:	n/a
12	chr10:49514273-49514323	HepG2	liver:	n/a
13	chr10:49515374-49515424	ProgFib	skin:	n/a
14	chr10:49517767-49517817	HNPCEpiC	eye:	n/a
15	chr10:49515374-49515424	HAEpiC	amniotic membrane:	n/a
16	chr10:49515374-49515424	AG09319	gingival:	n/a
17	chr10:49514337-49514387	MCF-7	breast:	n/a
18	chr10:49514546-49514596	PrEC	prostate:	n/a
19	chr10:49516634-49516684	U87	brain:	n/a
20	chr10:49514530-49514580	Hela-S3	cervix:	n/a
21	chr10:49514273-49514323	MCF-7	breast:	n/a
22	chr10:49514337-49514387	U87	brain:	n/a
23	chr10:49514337-49514387	GM12891	blood:	n/a
24	chr10:49514530-49514580	HCT-116	colon:	n/a
25	chr10:49514273-49514323	IMR90	lung:	fetal
26	chr10:49514337-49514387	ProgFib	skin:	n/a
27	chr10:49514273-49514323	AG04450	lung:	fetal
28	chr10:49515028-49515078	SKMC	muscle:	n/a
29	chr10:49516634-49516684	HCM	heart:	n/a
30	chr10:49514530-49514580	NT2-D1	testis:	n/a
31	chr10:49514546-49514596	BE2_C	brain:	n/a
32	chr10:49515028-49515078	Hepatocyte	liver:	n/a
33	chr10:49517767-49517817	SK-N-SH_RA	brain:	n/a
34	chr10:49514546-49514596	NB4	blood:	n/a
35	chr10:49515028-49515078	U87	brain:	n/a
36	chr10:49515374-49515424	T-47D	breast:	n/a
37	chr10:49514546-49514596	NHBE	bronchial:	n/a
38	chr10:49514530-49514580	HEK293	kidney:	embryo
39	chr10:49515028-49515078	NHBE	bronchial:	n/a
40	chr10:49514530-49514580	T-47D	breast:	n/a
41	chr10:49514273-49514323	H1-hESC	embryonic stem cell:	embryo
42	chr10:49516634-49516684	HIPEpiC	eye:	n/a
43	chr10:49514530-49514580	HepG2	liver:	n/a
44	chr10:49515374-49515424	HNPCEpiC	eye:	n/a
45	chr10:49514546-49514596	HAEpiC	amniotic membrane:	n/a
46	chr10:49514530-49514580	NHBE	bronchial:	n/a
47	chr10:49514273-49514323	HL-60	blood:	n/a
48	chr10:49514530-49514580	GM19239	blood:	n/a
49	chr10:49516634-49516684	SK-N-SH_RA	brain:	n/a
50	chr10:49514530-49514580	AG10803	skin:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:49502225..49505206-chr10:49511176..49513041,2	MCF-7	breast:
2	chr10:49422440..49425186-chr10:49494550..49500073,5	MCF-7	breast:
3	chr10:49423481..49424232-chr10:49497847..49498349,2	K562	blood:
4	chr10:49523430..49525253-chr10:49550597..49552808,2	K562	blood:
5	chr10:49505338..49509227-chr10:49512971..49515977,6	K562	blood:
6	chr10:49489462..49491590-chr10:49496144..49498930,2	MCF-7	breast:
7	chr10:49442419..49445275-chr10:49506224..49508061,2	K562	blood:
8	chr10:49498367..49502317-chr10:49513526..49516072,3	MCF-7	breast:
9	chr10:49423127..49424126-chr10:49497102..49498218,5	MCF-7	breast:
10	chr10:49494826..49497610-chr10:49513560..49515926,2	MCF-7	breast:
11	chr10:49515905..49518176-chr10:49521604..49523677,2	MCF-7	breast:
12	chr10:49496582..49501262-chr10:49513244..49517429,4	K562	blood:
13	chr10:49514688..49515207-chr5:33441143..33441743,2	Hela-S3	cervix:
14	chr10:49522636..49524628-chr10:49534736..49536666,2	K562	blood:
15	chr10:49496582..49501262-chr10:49513244..49517429,4	K562	blood:
16	chr10:49518153..49519864-chr10:49521781..49524737,2	MCF-7	breast:
17	chr10:49489462..49491590-chr10:49496144..49498930,2	MCF-7	breast:
18	chr10:49517657..49518610-chr10:49713350..49714126,2	MCF-7	breast:
19	chr10:49497874..49500351-chr10:49502359..49504964,2	MCF-7	breast:
20	chr10:49513387..49516033-chr10:49518059..49520914,3	MCF-7	breast:
21	chr10:49516260..49519086-chr10:49729762..49732585,2	K562	blood:
22	chr10:49459652..49462139-chr10:49513267..49515617,2	K562	blood:
23	chr10:49495690..49496196-chr10:51547486..51547990,2	MCF-7	breast:
24	chr10:49506365..49508904-chr10:49509611..49511777,2	K562	blood:
25	chr10:49423144..49424160-chr10:49497116..49498379,10	MCF-7	breast:
26	chr10:49518153..49519864-chr10:49521781..49524737,2	MCF-7	breast:
27	chr10:49498367..49502317-chr10:49513526..49516072,3	MCF-7	breast:
28	chr10:49495793..49496380-chr10:49514095..49514687,2	MCF-7	breast:
29	chr10:49509543..49512452-chr10:49513184..49514985,2	K562	blood:
30	chr10:49495793..49496380-chr10:49514095..49514687,2	MCF-7	breast:
31	chr10:49462023..49464427-chr10:49493283..49495844,2	MCF-7	breast:
32	chr10:49514655..49517342-chr10:49637868..49640207,2	K562	blood:
33	chr10:49508706..49510479-chr10:49512304..49514227,2	MCF-7	breast:
34	chr10:49504955..49507590-chr10:49509692..49512990,3	MCF-7	breast:
35	chr10:49514463..49514994-chr17:62501665..62502574,2	HCT-116	colon:
36	chr10:49505437..49509227-chr10:49512303..49516954,6	K562	blood:
37	chr10:49520506..49525716-chr10:49528736..49531606,6	K562	blood:
38	chr10:49514520..49515023-chr9:91933231..91933828,2	Hela-S3	cervix:
39	chr10:49506365..49508904-chr10:49509611..49511777,2	K562	blood:
40	chr10:49517027..49519236-chr10:49642083..49643882,2	K562	blood:
41	chr10:49488285..49491107-chr10:49498371..49500631,2	MCF-7	breast:
42	chr10:49508706..49510479-chr10:49512304..49514227,2	MCF-7	breast:
43	chr10:49517751..49518571-chr10:49540674..49541220,2	MCF-7	breast:
44	chr10:49518947..49521091-chr10:49533089..49535117,2	K562	blood:
45	chr10:49488285..49491107-chr10:49498371..49500631,2	MCF-7	breast:
46	chr10:49497874..49500351-chr10:49502359..49504964,2	MCF-7	breast:
47	chr10:49517538..49519332-chr10:49540338..49542175,2	MCF-7	breast:
48	chr10:49507404..49509732-chr10:49510277..49512510,2	K562	blood:
49	chr10:49502225..49505206-chr10:49511176..49513041,2	MCF-7	breast:
50	chr10:49504955..49507590-chr10:49509692..49512990,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAPK8-3	chr10:49500742-49501460	NONHSAT013264

No data

Variant related genes	Relation type
MAPK8	TF binding region
FRMPD2	TF binding region
ENSG00000225482	TF binding region
MAPK8	CpG island
FRMPD2	CpG island
ENSG00000225482	CpG island
ENSG00000187742	chromatin interactions
ENSG00000113407	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000128805	chromatin interactions
ENSG00000170324	chromatin interactions
ENSG00000111371	chromatin interactions
ENSG00000107643	chromatin interactions
ENSG00000225482	chromatin interactions

Extended variants
information (count: 1471 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1471 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7071413	chr10:49484698-49484699	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs180782335	chr10:49484724-49484725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183958747	chr10:49484769-49484770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148537216	chr10:49484821-49484822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564887110	chr10:49484896-49484897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113184657	chr10:49484941-49484942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189423077	chr10:49484955-49484956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182421863	chr10:49485010-49485011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79952797	chr10:49485150-49485151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186537819	chr10:49485154-49485155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374503810	chr10:49485163-49485164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557658207	chr10:49485169-49485170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577363963	chr10:49485172-49485173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569417322	chr10:49485177-49485178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368775561	chr10:49485198-49485199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112560315	chr10:49485249-49485250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369805098	chr10:49485252-49485253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117352829	chr10:49485284-49485285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572650769	chr10:49485370-49485371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7096711	chr10:49485421-49485422	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs117011462	chr10:49485454-49485455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191954648	chr10:49485531-49485532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543825574	chr10:49485538-49485539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562809517	chr10:49485556-49485557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574596213	chr10:49485612-49485613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200459265	chr10:49485673-49485674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542089328	chr10:49485679-49485680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115860342	chr10:49485692-49485693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528631810	chr10:49485732-49485733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547093177	chr10:49485796-49485797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141306240	chr10:49485806-49485807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565204937	chr10:49485810-49485811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373382755	chr10:49485811-49485812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113604704	chr10:49485812-49485813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144245927	chr10:49485868-49485869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550661710	chr10:49485870-49485871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569537478	chr10:49485880-49485881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376321952	chr10:49485938-49485939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536545811	chr10:49485945-49485946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549189460	chr10:49485969-49485970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548417372	chr10:49486032-49486033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146066914	chr10:49486033-49486034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375804903	chr10:49486034-49486035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549762688	chr10:49486035-49486036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7098618	chr10:49486037-49486038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538517010	chr10:49486053-49486054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576821413	chr10:49486090-49486091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537849837	chr10:49486098-49486099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555880147	chr10:49486104-49486105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111949913	chr10:49486168-49486169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Cancer	21183584	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
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1003 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49466800-49492400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:49480600-49484800	Enhancers	GM12878-XiMat	blood
3	chr10:49482600-49484800	Enhancers	Dnd41	blood
4	chr10:49486200-49486800	Enhancers	GM12878-XiMat	blood
5	chr10:49486800-49487200	Flanking Active TSS	GM12878-XiMat	blood
6	chr10:49487200-49487400	Enhancers	GM12878-XiMat	blood
7	chr10:49487400-49487600	Flanking Active TSS	GM12878-XiMat	blood
8	chr10:49487600-49488800	Enhancers	GM12878-XiMat	blood
9	chr10:49488800-49489200	Weak transcription	GM12878-XiMat	blood
10	chr10:49489200-49493200	ZNF genes & repeats	GM12878-XiMat	blood
11	chr10:49491200-49492400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:49492000-49492400	ZNF genes & repeats	Dnd41	blood
13	chr10:49492400-49493600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:49492400-49494000	Enhancers	Dnd41	blood
15	chr10:49492400-49495400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:49492400-49498200	Enhancers	Fetal Thymus	thymus
17	chr10:49493200-49493800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr10:49493200-49499800	Enhancers	GM12878-XiMat	blood
19	chr10:49493400-49494200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr10:49493600-49504200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr10:49493800-49494000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr10:49493800-49494000	Enhancers	Fetal Muscle Leg	muscle
23	chr10:49493800-49494000	Enhancers	Right Atrium	heart
24	chr10:49493800-49494200	Enhancers	Ovary	ovary
25	chr10:49493800-49494200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
26	chr10:49493800-49494400	Enhancers	Adipose Nuclei	Adipose
27	chr10:49494000-49494200	Bivalent Enhancer	Fetal Muscle Leg	muscle
28	chr10:49494000-49494200	Flanking Active TSS	Dnd41	blood
29	chr10:49494000-49495600	Weak transcription	Fetal Heart	heart
30	chr10:49494000-49495600	Weak transcription	Right Atrium	heart
31	chr10:49494000-49497600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr10:49494200-49494600	Enhancers	Dnd41	blood
33	chr10:49494200-49495600	Weak transcription	Fetal Muscle Leg	muscle
34	chr10:49494400-49498000	Weak transcription	Adipose Nuclei	Adipose
35	chr10:49494600-49496800	Flanking Active TSS	Dnd41	blood
36	chr10:49495000-49496400	Enhancers	Brain Germinal Matrix	brain
37	chr10:49495000-49498000	Enhancers	Brain Hippocampus Middle	brain
38	chr10:49495200-49496800	Enhancers	Brain Angular Gyrus	brain
39	chr10:49495200-49497800	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr10:49495200-49498200	Enhancers	Brain Substantia Nigra	brain
41	chr10:49495400-49495600	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr10:49495400-49495600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr10:49495400-49496400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:49495400-49496600	Enhancers	Colon Smooth Muscle	Colon
45	chr10:49495400-49496600	Enhancers	Lung	lung
46	chr10:49495400-49496600	Enhancers	Right Ventricle	heart
47	chr10:49495400-49497000	Enhancers	Fetal Stomach	stomach
48	chr10:49495400-49497200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr10:49495400-49497200	Enhancers	Pancreas	Pancrea
50	chr10:49495400-49497400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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