Variant report

Variant	nsv895046
Chromosome Location	chr10:42708898-42964207
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1752)
CpG islands
(count:1466)
Chromatin interactive
region (count:15)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:42799540-42800192	HepG2	liver:	n/a	n/a
2	ATF1	chr10:42815222-42815574	K562	blood:	n/a	n/a
3	ATF1	chr10:42817203-42817917	K562	blood:	n/a	n/a
4	ATF1	chr10:42801380-42801410	K562	blood:	n/a	n/a
5	ATF1	chr10:42799538-42800192	K562	blood:	n/a	n/a
6	ATF1	chr10:42797113-42797490	K562	blood:	n/a	n/a
7	BACH1	chr10:42813274-42813746	K562	blood:	n/a	n/a
8	BATF	chr10:42791080-42791784	GM12878	blood:	n/a	n/a
9	BATF	chr10:42843878-42844039	GM12878	blood:	n/a	chr10:42843938-42843949
10	BATF	chr10:42843892-42844051	GM12878	blood:	n/a	chr10:42843938-42843949
11	BATF	chr10:42734245-42734464	GM12878	blood:	n/a	n/a
12	BATF	chr10:42790414-42790906	GM12878	blood:	n/a	n/a
13	BATF	chr10:42796760-42798052	GM12878	blood:	n/a	n/a
14	BATF	chr10:42790411-42790908	GM12878	blood:	n/a	n/a
15	BATF	chr10:42794103-42794967	GM12878	blood:	n/a	n/a
16	BATF	chr10:42791867-42792344	GM12878	blood:	n/a	n/a
17	BATF	chr10:42815938-42818365	GM12878	blood:	n/a	n/a
18	BATF	chr10:42816795-42818369	GM12878	blood:	n/a	n/a
19	BATF	chr10:42775977-42776265	GM12878	blood:	n/a	n/a
20	BATF	chr10:42802384-42802603	GM12878	blood:	n/a	n/a
21	BATF	chr10:42799191-42800355	GM12878	blood:	n/a	n/a
22	BATF	chr10:42814968-42815467	GM12878	blood:	n/a	n/a
23	BATF	chr10:42791008-42791549	GM12878	blood:	n/a	n/a
24	BATF	chr10:42765314-42765560	GM12878	blood:	n/a	n/a
25	BATF	chr10:42792510-42793190	GM12878	blood:	n/a	n/a
26	BATF	chr10:42794125-42794872	GM12878	blood:	n/a	n/a
27	BATF	chr10:42801201-42801861	GM12878	blood:	n/a	n/a
28	BATF	chr10:42799184-42800297	GM12878	blood:	n/a	n/a
29	BATF	chr10:42810326-42810760	GM12878	blood:	n/a	n/a
30	BCL11A	chr10:42794300-42794905	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:42738846-42739017	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:42797687-42798021	GM12878	blood:	n/a	n/a
33	BCL11A	chr10:42734310-42734513	GM12878	blood:	n/a	n/a
34	BCL11A	chr10:42799172-42800370	GM12878	blood:	n/a	n/a
35	BCL11A	chr10:42816269-42818366	GM12878	blood:	n/a	n/a
36	BCL11A	chr10:42790997-42791796	GM12878	blood:	n/a	n/a
37	BCL11A	chr10:42790409-42790946	GM12878	blood:	n/a	n/a
38	BCL11A	chr10:42816771-42818395	GM12878	blood:	n/a	n/a
39	BCL3	chr10:42797112-42797375	K562	blood:	n/a	n/a
40	BHLHE40	chr10:42816960-42818341	HepG2	liver:	n/a	n/a
41	BHLHE40	chr10:42799294-42800192	HepG2	liver:	n/a	n/a
42	BHLHE40	chr10:42805345-42805717	K562	blood:	n/a	n/a
43	BHLHE40	chr10:42815145-42815520	HepG2	liver:	n/a	n/a
44	BHLHE40	chr10:42810371-42810796	HepG2	liver:	n/a	n/a
45	BRCA1	chr10:42813274-42813759	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr10:42809116-42809143	GM12878	blood:	n/a	n/a
47	BRCA1	chr10:42805344-42805718	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr10:42813274-42813756	GM12878	blood:	n/a	n/a
49	CBX3	chr10:42832408-42832737	K562	blood:	n/a	n/a
50	CBX3	chr10:42799259-42800350	K562	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42777375-42777425	PANC-1	pancreas:	n/a
2	chr10:42745966-42746016	SK-N-SH_RA	brain:	n/a
3	chr10:42777375-42777425	PANC-1	pancreas:	n/a
4	chr10:42745966-42746016	SK-N-SH_RA	brain:	n/a
5	chr10:42777375-42777425	IMR90	lung:	fetal
6	chr10:42739066-42739116	HRPEpiC	eye:	n/a
7	chr10:42737582-42737632	GM06990	blood:	n/a
8	chr10:42738815-42738865	T-47D	breast:	n/a
9	chr10:42777525-42777575	HAEpiC	amniotic membrane:	n/a
10	chr10:42863173-42863223	HMEC	breast:	n/a
11	chr10:42863068-42863118	HRCEpiC	kidney:	n/a
12	chr10:42777403-42777453	PANC-1	pancreas:	n/a
13	chr10:42859004-42859054	GM19239	blood:	n/a
14	chr10:42859004-42859054	Jurkat	blood:	n/a
15	chr10:42745966-42746016	MCF10A-Er-Src	breast:	n/a
16	chr10:42863068-42863118	HAEpiC	amniotic membrane:	n/a
17	chr10:42737139-42737189	PFSK-1	brain:	n/a
18	chr10:42737139-42737189	AG09309	skin:	n/a
19	chr10:42738815-42738865	SK-N-MC	brain:	n/a
20	chr10:42863550-42863600	PFSK-1	brain:	n/a
21	chr10:42863594-42863644	AG10803	skin:	n/a
22	chr10:42864633-42864683	HRCEpiC	kidney:	n/a
23	chr10:42864633-42864683	NT2-D1	testis:	n/a
24	chr10:42738538-42738588	SK-N-SH_RA	brain:	n/a
25	chr10:42739066-42739116	HRE	kidney:	n/a
26	chr10:42739066-42739116	Caco-2	colon:	n/a
27	chr10:42737322-42737372	BJ	skin:	n/a
28	chr10:42931123-42931173	HRCEpiC	kidney:	n/a
29	chr10:42737139-42737189	AG04450	lung:	fetal
30	chr10:42737139-42737189	SK-N-SH	brain:	n/a
31	chr10:42863539-42863589	HepG2	liver:	n/a
32	chr10:42745966-42746016	ProgFib	skin:	n/a
33	chr10:42864912-42864962	HCF	heart:	n/a
34	chr10:42777525-42777575	CMK	blood:	n/a
35	chr10:42737139-42737189	HCT-116	colon:	n/a
36	chr10:42864633-42864683	AG09319	gingival:	n/a
37	chr10:42863068-42863118	PrEC	prostate:	n/a
38	chr10:42739066-42739116	AoSMC	blood vessel:	n/a
39	chr10:42739066-42739116	HRCEpiC	kidney:	n/a
40	chr10:42738815-42738865	NT2-D1	testis:	n/a
41	chr10:42739066-42739116	A549	lung:	n/a
42	chr10:42737582-42737632	HRPEpiC	eye:	n/a
43	chr10:42777375-42777425	SK-N-SH	brain:	n/a
44	chr10:42931123-42931173	AG04449	skin:	fetal
45	chr10:42863594-42863644	HIPEpiC	eye:	n/a
46	chr10:42738538-42738588	SAEC	small airway:	n/a
47	chr10:42745966-42746016	PANC-1	pancreas:	n/a
48	chr10:42863068-42863118	HRE	kidney:	n/a
49	chr10:42863550-42863600	LNCaP	prostate:	n/a
50	chr10:42737139-42737189	BE2_C	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
2	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:
3	chr10:42861377..42864864-chr10:42876467..42879026,3	K562	blood:
4	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
5	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
6	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:
7	chr10:42822722..42825307-chr10:42828970..42830910,2	K562	blood:
8	chr10:42860335..42863039-chr10:43132551..43135299,2	K562	blood:
9	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
10	chr10:42846704..42848638-chr10:42856458..42859194,2	K562	blood:
11	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:
12	chr10:42822722..42825307-chr10:42828970..42830910,2	K562	blood:
13	chr10:42739123..42739644-chr10:101379768..101380454,2	HCT-116	colon:
14	chr10:42673795..42674377-chr10:42765091..42765784,2	MCF-7	breast:
15	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNYL2-6	chr10:42775182-42777267	NONHSAT012861
2	lnc-BMS1-7	chr10:42746444-42746645	NONHSAT012859
3	lnc-CCNYL2-5	chr10:42796822-42796961	NONHSAT012863
4	lnc-CCNYL2-5	chr10:42795737-42796013	NONHSAT012863
5	lnc-CCNYL2-5	chr10:42794471-42794553	NONHSAT012863
6	lnc-BMS1-7	chr10:42737930-42738014	NONHSAT012859
7	lnc-BMS1-6	chr10:42791078-42791322	NONHSAT012862

No data

Variant related genes	Relation type
ENSG00000264398	TF binding region
CCNYL2	TF binding region
PABPC1P8	TF binding region
ENSG00000215146	TF binding region
ENSG00000264398	CpG island
CCNYL2	CpG island
PABPC1P8	CpG island
ENSG00000215146	CpG island
ENSG00000272373	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000215146	chromatin interactions
ENSG00000155287	chromatin interactions

Extended variants
information (count: 6636 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6636 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77350837	chr10:42712202-42712203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535027272	chr10:42712210-42712211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140620949	chr10:42712216-42712217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79932502	chr10:42712241-42712242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370870019	chr10:42712246-42712247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548557089	chr10:42712258-42712259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568386833	chr10:42712261-42712262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537307503	chr10:42712271-42712272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77999482	chr10:42712289-42712290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370153058	chr10:42712314-42712315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76671591	chr10:42712317-42712318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs61853452	chr10:42712327-42712328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368269668	chr10:42712331-42712332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs61853453	chr10:42712334-42712335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs61854377	chr10:42712338-42712339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111552761	chr10:42712353-42712354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs61854378	chr10:42712362-42712363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536456413	chr10:42712375-42712376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190768507	chr10:42712395-42712396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79724646	chr10:42712427-42712428	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78432869	chr10:42712470-42712471	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12247604	chr10:42712487-42712488	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539255736	chr10:42712488-42712489	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs61854379	chr10:42712513-42712514	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61854380	chr10:42712540-42712541	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545107912	chr10:42712542-42712543	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77891254	chr10:42712552-42712553	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369456366	chr10:42712565-42712566	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553073855	chr10:42712572-42712573	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369410612	chr10:42712576-42712577	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74597368	chr10:42712592-42712593	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79514001	chr10:42712614-42712615	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs61854381	chr10:42712617-42712618	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12250563	chr10:42712621-42712622	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541425139	chr10:42712622-42712623	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs61854382	chr10:42712625-42712626	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74669438	chr10:42712626-42712627	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561317209	chr10:42712628-42712629	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574806850	chr10:42712640-42712641	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543741152	chr10:42712648-42712649	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs61854383	chr10:42712649-42712650	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563806204	chr10:42712657-42712658	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532786902	chr10:42712659-42712660	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76921872	chr10:42712660-42712661	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559801179	chr10:42712661-42712662	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75317540	chr10:42712678-42712679	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528569662	chr10:42712679-42712680	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs61854384	chr10:42712685-42712686	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79814739	chr10:42712688-42712689	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78981242	chr10:42712695-42712696	Flanking Active TSS Enhancers	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
Lung cancer	18438408	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
Breast cancer	21509527	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	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
Obesity	20622171	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD
Melanoma	20877625	CNVD
Hirschsprung''s Disease	19925665	CNVD
Hirschsprung''s Disease	20456320	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42712200-42712400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:42712200-42712800	Enhancers	HepG2	liver
3	chr10:42712400-42712800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:42712400-42712800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:42712400-42712800	Enhancers	Adipose Nuclei	Adipose
6	chr10:42712400-42712800	Enhancers	Aorta	Aorta
7	chr10:42712400-42712800	Enhancers	Hela-S3	cervix
8	chr10:42725600-42726200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:42725600-42726200	Enhancers	Pancreas	Pancrea
10	chr10:42725600-42726800	ZNF genes & repeats	Esophagus	oesophagus
11	chr10:42726200-42726800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:42726800-42728200	Weak transcription	Esophagus	oesophagus
13	chr10:42728200-42730600	Enhancers	Esophagus	oesophagus
14	chr10:42728800-42729400	ZNF genes & repeats	Spleen	Spleen
15	chr10:42728800-42730400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:42729000-42729400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr10:42729400-42732200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:42732200-42732400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr10:42732200-42732400	Enhancers	Gastric	stomach
20	chr10:42732400-42742600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr10:42736600-42737000	Weak transcription	HSMMtube	muscle
22	chr10:42737000-42737200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
23	chr10:42737000-42737200	Active TSS	HSMM	muscle
24	chr10:42737000-42737400	Enhancers	Primary hematopoietic stem cells	blood
25	chr10:42737000-42737400	Active TSS	HMEC	breast
26	chr10:42737000-42737400	ZNF genes & repeats	HSMMtube	muscle
27	chr10:42737000-42737400	Bivalent Enhancer	NHEK	skin
28	chr10:42737000-42737600	Enhancers	Osteobl	bone
29	chr10:42737000-42738400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:42737000-42738400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr10:42737200-42737400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr10:42737200-42737400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
33	chr10:42737200-42737400	Enhancers	Brain Substantia Nigra	brain
34	chr10:42737200-42737400	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr10:42737200-42737400	Flanking Active TSS	HSMM	muscle
36	chr10:42737200-42737400	ZNF genes & repeats	NH-A	brain
37	chr10:42737200-42737600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
38	chr10:42737200-42738200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
39	chr10:42737400-42738000	Weak transcription	HSMM	muscle
40	chr10:42737400-42739000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr10:42737600-42737800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr10:42737600-42737800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr10:42737600-42738000	Active TSS	Esophagus	oesophagus
44	chr10:42737600-42738000	Active TSS	Pancreas	Pancrea
45	chr10:42737600-42738000	Bivalent/Poised TSS	Right Ventricle	heart
46	chr10:42737600-42738000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
47	chr10:42737600-42738400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr10:42737600-42738400	Active TSS	Colon Smooth Muscle	Colon
49	chr10:42737600-42738800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr10:42737600-42739200	Active TSS	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links