Variant report

Variant	nsv5654
Chromosome Location	chr10:5868365-5930634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1417)
CpG islands
(count:918)
Chromatin interactive
region (count:114)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5930437-5930734	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5882378-5882749	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5887078-5887316	K562	blood:	n/a	n/a
4	ARID3A	chr10:5915469-5915783	K562	blood:	n/a	n/a
5	ARID3A	chr10:5895391-5895857	K562	blood:	n/a	n/a
6	ARID3A	chr10:5888296-5888348	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:5903253-5903873	HepG2	liver:	n/a	chr10:5903606-5903622
8	ARID3A	chr10:5915453-5915764	HepG2	liver:	n/a	n/a
9	ATF2	chr10:5882088-5883394	GM12878	blood:	n/a	n/a
10	ATF2	chr10:5904071-5905027	GM12878	blood:	n/a	n/a
11	ATF2	chr10:5894153-5894810	GM12878	blood:	n/a	n/a
12	ATF2	chr10:5904094-5905203	GM12878	blood:	n/a	n/a
13	ATF2	chr10:5895386-5895843	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr10:5887991-5888533	GM12878	blood:	n/a	n/a
15	ATF2	chr10:5885759-5886344	GM12878	blood:	n/a	n/a
16	ATF2	chr10:5882822-5883381	GM12878	blood:	n/a	n/a
17	ATF2	chr10:5882081-5882634	GM12878	blood:	n/a	n/a
18	ATF2	chr10:5888079-5888517	GM12878	blood:	n/a	n/a
19	ATF2	chr10:5894122-5894884	GM12878	blood:	n/a	n/a
20	ATF2	chr10:5872492-5872930	GM12878	blood:	n/a	n/a
21	ATF2	chr10:5885726-5886294	GM12878	blood:	n/a	n/a
22	ATF3	chr10:5895143-5896014	A549	lung:	n/a	n/a
23	ATF3	chr10:5887049-5887248	K562	blood:	n/a	chr10:5887191-5887200 chr10:5887191-5887211
24	ATF3	chr10:5895150-5896042	A549	lung:	n/a	n/a
25	ATF3	chr10:5895226-5895940	K562	blood:	n/a	n/a
26	ATF3	chr10:5895229-5895945	HCT-116	colon:	n/a	n/a
27	ATF3	chr10:5895238-5896003	HCT-116	colon:	n/a	n/a
28	BACH1	chr10:5883022-5883034	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr10:5904143-5905100	GM12878	blood:	n/a	n/a
30	BATF	chr10:5872567-5872931	GM12878	blood:	n/a	n/a
31	BATF	chr10:5888064-5888456	GM12878	blood:	n/a	n/a
32	BATF	chr10:5882191-5882590	GM12878	blood:	n/a	chr10:5882324-5882334
33	BATF	chr10:5904206-5904991	GM12878	blood:	n/a	n/a
34	BATF	chr10:5895558-5895813	GM12878	blood:	n/a	n/a
35	BATF	chr10:5872639-5872854	GM12878	blood:	n/a	n/a
36	BATF	chr10:5894178-5894732	GM12878	blood:	n/a	n/a
37	BATF	chr10:5888145-5888416	GM12878	blood:	n/a	n/a
38	BCL11A	chr10:5904278-5904614	GM12878	blood:	n/a	n/a
39	BCL11A	chr10:5885938-5886268	GM12878	blood:	n/a	n/a
40	BCL11A	chr10:5882223-5882654	GM12878	blood:	n/a	n/a
41	BCL11A	chr10:5894373-5894676	GM12878	blood:	n/a	n/a
42	BCL11A	chr10:5894328-5894755	GM12878	blood:	n/a	n/a
43	BCL11A	chr10:5888140-5888401	GM12878	blood:	n/a	n/a
44	BCL11A	chr10:5882236-5882572	GM12878	blood:	n/a	n/a
45	BCL11A	chr10:5904162-5905104	GM12878	blood:	n/a	n/a
46	BCL11A	chr10:5888070-5888508	GM12878	blood:	n/a	n/a
47	BCL11A	chr10:5882963-5883335	GM12878	blood:	n/a	n/a
48	BCL3	chr10:5897974-5898199	GM12878	blood:	n/a	n/a
49	BCL3	chr10:5904200-5904748	GM12878	blood:	n/a	n/a
50	BCL3	chr10:5882190-5882621	GM12878	blood:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5870888-5870938	HCT-116	colon:	n/a
2	chr10:5882466-5882516	K562	blood:	n/a
3	chr10:5920104-5920154	BJ	skin:	n/a
4	chr10:5870888-5870938	HCT-116	colon:	n/a
5	chr10:5882466-5882516	K562	blood:	n/a
6	chr10:5920104-5920154	BJ	skin:	n/a
7	chr10:5882304-5882354	HNPCEpiC	eye:	n/a
8	chr10:5882466-5882516	HRPEpiC	eye:	n/a
9	chr10:5870938-5870988	SK-N-MC	brain:	n/a
10	chr10:5884153-5884203	SK-N-SH	brain:	n/a
11	chr10:5870956-5871006	HCF	heart:	n/a
12	chr10:5870888-5870938	RPTEC	kidney:	n/a
13	chr10:5882304-5882354	Jurkat	blood:	n/a
14	chr10:5870888-5870938	HEK293	kidney:	embryo
15	chr10:5884153-5884203	PrEC	prostate:	n/a
16	chr10:5884105-5884155	A549	lung:	n/a
17	chr10:5884153-5884203	BE2_C	brain:	n/a
18	chr10:5882466-5882516	AoSMC	blood vessel:	n/a
19	chr10:5930543-5930593	AG09309	skin:	n/a
20	chr10:5884061-5884111	HCF	heart:	n/a
21	chr10:5904561-5904611	NB4	blood:	n/a
22	chr10:5884105-5884155	U87	brain:	n/a
23	chr10:5884061-5884111	HPAEpiC	pulmonary alveolar:	n/a
24	chr10:5882466-5882516	AG04450	lung:	fetal
25	chr10:5884153-5884203	NH-A	brain:	n/a
26	chr10:5882466-5882516	HMEC	breast:	n/a
27	chr10:5882739-5882789	ProgFib	skin:	n/a
28	chr10:5886111-5886161	Hepatocyte	liver:	n/a
29	chr10:5920104-5920154	SK-N-SH	brain:	n/a
30	chr10:5884153-5884203	HMEC	breast:	n/a
31	chr10:5884105-5884155	HEK293	kidney:	embryo
32	chr10:5884061-5884111	T-47D	breast:	n/a
33	chr10:5884153-5884203	HCT-116	colon:	n/a
34	chr10:5884105-5884155	AG04450	lung:	fetal
35	chr10:5879090-5879140	ProgFib	skin:	n/a
36	chr10:5882576-5882626	MCF-7	breast:	n/a
37	chr10:5884061-5884111	NH-A	brain:	n/a
38	chr10:5870956-5871006	LNCaP	prostate:	n/a
39	chr10:5870938-5870988	HNPCEpiC	eye:	n/a
40	chr10:5882466-5882516	ovcar-3	ovarian:	n/a
41	chr10:5882739-5882789	T-47D	breast:	n/a
42	chr10:5870888-5870938	ProgFib	skin:	n/a
43	chr10:5884061-5884111	PANC-1	pancreas:	n/a
44	chr10:5870938-5870988	CMK	blood:	n/a
45	chr10:5882304-5882354	HCT-116	colon:	n/a
46	chr10:5920104-5920154	HRE	kidney:	n/a
47	chr10:5886111-5886161	SKMC	muscle:	n/a
48	chr10:5884105-5884155	AG09309	skin:	n/a
49	chr10:5884105-5884155	NT2-D1	testis:	n/a
50	chr10:5884153-5884203	HEK293	kidney:	embryo

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:5854450..5857183-chr10:5867124..5872976,6	MCF-7	breast:
2	chr10:5852752..5856561-chr10:5907945..5911516,4	MCF-7	breast:
3	chr10:5910241..5913072-chr10:5913979..5917301,3	MCF-7	breast:
4	chr10:5902878..5905797-chr10:5909283..5911826,2	MCF-7	breast:
5	chr10:5854510..5857923-chr10:5911220..5914905,6	MCF-7	breast:
6	chr10:5919010..5920872-chr10:5921692..5924189,2	K562	blood:
7	chr10:5875866..5877647-chr10:5881023..5883616,2	K562	blood:
8	chr10:5870260..5872899-chr10:5873504..5877637,4	K562	blood:
9	chr10:5874179..5876350-chr10:5894206..5896113,2	K562	blood:
10	chr10:5853771..5858349-chr10:5915568..5920799,8	MCF-7	breast:
11	chr10:5925580..5929335-chr10:5933926..5939138,5	K562	blood:
12	chr10:5855088..5855608-chr10:5874999..5875621,2	MCF-7	breast:
13	chr10:5853822..5855522-chr10:5894959..5897047,2	MCF-7	breast:
14	chr10:5915609..5918597-chr10:5924591..5926431,2	K562	blood:
15	chr10:5854377..5856986-chr10:5893024..5895477,2	MCF-7	breast:
16	chr10:5853739..5856663-chr10:5888964..5891448,2	MCF-7	breast:
17	chr10:5918577..5924576-chr10:5927726..5932597,9	MCF-7	breast:
18	chr10:5853575..5857221-chr10:5900529..5905112,5	MCF-7	breast:
19	chr10:5853712..5856413-chr10:5877125..5879138,3	MCF-7	breast:
20	chr10:5854140..5855797-chr10:5921600..5924146,3	MCF-7	breast:
21	chr10:5725838..5728251-chr10:5915424..5916991,2	MCF-7	breast:
22	chr10:5916960..5919162-chr10:5939258..5940829,2	K562	blood:
23	chr10:5872995..5874657-chr10:5893099..5894735,2	K562	blood:
24	chr10:5867636..5869273-chr10:5869585..5872452,2	K562	blood:
25	chr10:5853075..5856620-chr10:5914833..5920117,6	K562	blood:
26	chr10:5850869..5856128-chr10:5879241..5885807,8	K562	blood:
27	chr10:5887749..5890618-chr10:5895657..5897180,2	K562	blood:
28	chr10:5910337..5913057-chr10:5913896..5915551,2	K562	blood:
29	chr10:5870260..5872899-chr10:5873504..5877637,4	K562	blood:
30	chr10:5852473..5857853-chr10:5880942..5888645,8	MCF-7	breast:
31	chr10:5867636..5869273-chr10:5869585..5872452,2	K562	blood:
32	chr10:5910241..5913072-chr10:5913979..5917301,3	MCF-7	breast:
33	chr10:5853267..5855548-chr10:5881785..5884894,3	MCF-7	breast:
34	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:
35	chr10:5857495..5859789-chr10:5881654..5883847,2	K562	blood:
36	chr10:5854140..5856929-chr10:5898558..5900231,2	MCF-7	breast:
37	chr10:5854620..5857118-chr10:5886149..5888419,4	K562	blood:
38	chr10:5912116..5915465-chr10:5917203..5919997,3	K562	blood:
39	chr10:5876253..5877969-chr10:5881683..5883648,2	K562	blood:
40	chr10:5912116..5915465-chr10:5917203..5919997,3	K562	blood:
41	chr10:5912116..5916503-chr10:5917203..5921455,4	K562	blood:
42	chr10:5917302..5921893-chr10:5926757..5932751,9	MCF-7	breast:
43	chr10:5869850..5872422-chr10:5929194..5931187,2	MCF-7	breast:
44	chr10:5853453..5857248-chr10:5914833..5919853,7	K562	blood:
45	chr10:5874179..5876350-chr10:5894206..5896113,2	K562	blood:
46	chr10:5867768..5870710-chr10:5870936..5873255,3	MCF-7	breast:
47	chr10:5889255..5891417-chr10:5903224..5906135,2	MCF-7	breast:
48	chr10:5929157..5931311-chr10:6018059..6019673,2	MCF-7	breast:
49	chr10:5851570..5858995-chr10:5881654..5887342,9	K562	blood:
50	chr10:5835385..5837024-chr10:5893151..5895747,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO18-1	chr10:5916643-5917392	NONHSAT011189
2	lnc-GDI2-2	chr10:5903768-5903859	NONHSAT011187
3	lnc-GDI2-3	chr10:5911773-5912346	NONHSAT011188
4	lnc-GDI2-2	chr10:5904161-5904557	NONHSAT011187

No data

Variant related genes	Relation type
ENSG00000240180	TF binding region
FBXO18	TF binding region
GDI2	TF binding region
ANKRD16	TF binding region
ENSG00000240180	CpG island
FBXO18	CpG island
GDI2	CpG island
ANKRD16	CpG island
ENSG00000134461	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000270427	chromatin interactions
ENSG00000170525	chromatin interactions
ENSG00000134470	chromatin interactions
ENSG00000240180	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000134452	chromatin interactions

Extended variants
information (count: 2846 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2846 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551320872	chr10:5868366-5868367	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs71499644	chr10:5868446-5868447	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs11592964	chr10:5868472-5868473	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs72774103	chr10:5868476-5868477	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs548953808	chr10:5868485-5868486	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs371216696	chr10:5868521-5868522	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs185478841	chr10:5868524-5868525	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs537882279	chr10:5868556-5868557	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs111620325	chr10:5868557-5868558	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs191020712	chr10:5868569-5868570	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557726044	chr10:5868583-5868584	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374016099	chr10:5868621-5868622	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs554089731	chr10:5868663-5868664	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572453352	chr10:5868702-5868703	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs566774161	chr10:5868721-5868722	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs542719281	chr10:5868753-5868754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554680972	chr10:5868765-5868766	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576022343	chr10:5868812-5868813	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142472347	chr10:5868837-5868838	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs562425533	chr10:5868910-5868911	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371365994	chr10:5868912-5868913	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs547033241	chr10:5868931-5868932	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545160237	chr10:5868938-5868939	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs7082223	chr10:5868968-5868969	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs200781177	chr10:5868978-5868979	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562597675	chr10:5868982-5868983	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200156264	chr10:5868985-5868986	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144924358	chr10:5868986-5868987	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549091037	chr10:5868990-5868991	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs182363092	chr10:5869024-5869025	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs150187243	chr10:5869054-5869055	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549839056	chr10:5869078-5869079	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533720852	chr10:5869146-5869147	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73614613	chr10:5869161-5869162	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538988061	chr10:5869205-5869206	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554298960	chr10:5869265-5869266	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs71479741	chr10:5869268-5869269	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566130989	chr10:5869303-5869304	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs553475639	chr10:5869328-5869329	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs188301242	chr10:5869331-5869332	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536492438	chr10:5869333-5869334	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs554619604	chr10:5869335-5869336	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs371913501	chr10:5869353-5869354	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs555171620	chr10:5869373-5869374	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs573549070	chr10:5869394-5869395	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543376905	chr10:5869397-5869398	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373715706	chr10:5869426-5869427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs577822297	chr10:5869451-5869452	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs375770423	chr10:5869458-5869459	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs56102348	chr10:5869508-5869509	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5857400-5871400	Weak transcription	Pancreas	Pancrea
2	chr10:5869800-5871000	Enhancers	K562	blood
3	chr10:5870000-5870200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:5870200-5875000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:5870600-5871200	Flanking Bivalent TSS/Enh	HepG2	liver
6	chr10:5871000-5871400	Flanking Active TSS	K562	blood
7	chr10:5871200-5872800	Enhancers	HepG2	liver
8	chr10:5871400-5871800	Enhancers	Pancreas	Pancrea
9	chr10:5871400-5872400	Enhancers	K562	blood
10	chr10:5872200-5873600	Enhancers	Primary B cells from peripheral blood	blood
11	chr10:5872400-5873400	Enhancers	Primary B cells from cord blood	blood
12	chr10:5872400-5873400	Enhancers	Fetal Thymus	thymus
13	chr10:5872400-5875600	Weak transcription	K562	blood
14	chr10:5872600-5873400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr10:5872600-5873400	Enhancers	GM12878-XiMat	blood
16	chr10:5872800-5873200	Active TSS	Spleen	Spleen
17	chr10:5872800-5873600	Flanking Active TSS	HepG2	liver
18	chr10:5873000-5873200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr10:5873000-5873400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr10:5873200-5873400	Enhancers	Esophagus	oesophagus
21	chr10:5873200-5882400	Weak transcription	Spleen	Spleen
22	chr10:5873400-5873600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr10:5873400-5874400	Weak transcription	Esophagus	oesophagus
24	chr10:5873400-5875000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr10:5873400-5875600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr10:5873600-5875600	Enhancers	HepG2	liver
27	chr10:5874400-5875000	Weak transcription	Right Atrium	heart
28	chr10:5874400-5875200	Enhancers	Esophagus	oesophagus
29	chr10:5874600-5875000	Enhancers	Duodenum Mucosa	Duodenum
30	chr10:5874600-5875000	Enhancers	Placenta Amnion	Placenta Amnion
31	chr10:5874600-5875000	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr10:5874600-5875200	Enhancers	Stomach Mucosa	stomach
33	chr10:5874600-5876400	Enhancers	Placenta	Placenta
34	chr10:5874800-5875400	Enhancers	Colonic Mucosa	Colon
35	chr10:5874800-5875400	Enhancers	Gastric	stomach
36	chr10:5874800-5876000	Enhancers	Fetal Heart	heart
37	chr10:5875000-5875200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr10:5875000-5875200	Genic enhancers	Right Atrium	heart
39	chr10:5875000-5875400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr10:5875000-5875400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:5875000-5875400	Active TSS	Duodenum Mucosa	Duodenum
42	chr10:5875000-5875400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr10:5875000-5876000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr10:5875000-5886600	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr10:5875200-5875400	Enhancers	Left Ventricle	heart
46	chr10:5875200-5875800	Weak transcription	Stomach Mucosa	stomach
47	chr10:5875200-5877600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr10:5875200-5882200	Weak transcription	Right Atrium	heart
49	chr10:5875400-5876000	Weak transcription	Left Ventricle	heart
50	chr10:5875400-5876200	Weak transcription	Gastric	stomach

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