Variant report

Variant	nsv895111
Chromosome Location	chr10:45989745-46071900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:440)
CpG islands
(count:550)
Chromatin interactive
region (count:40)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:45991298-45991617	K562	blood:	n/a	n/a
2	ARID3A	chr10:46010295-46010462	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:46053837-46054169	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:46023610-46023809	K562	blood:	n/a	n/a
5	ARID3A	chr10:45997886-45998301	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:46071413-46072318	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:46014629-46014791	K562	blood:	n/a	n/a
8	ARID3A	chr10:46053147-46053169	HepG2	liver:	n/a	n/a
9	ATF1	chr10:45991282-45991486	K562	blood:	n/a	n/a
10	ATF3	chr10:45991291-45991618	K562	blood:	n/a	n/a
11	BACH1	chr10:45991333-45991541	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:45991253-45991595	K562	blood:	n/a	n/a
13	BATF	chr10:45991303-45991500	GM12878	blood:	n/a	chr10:45991372-45991383
14	BATF	chr10:46048777-46048912	GM12878	blood:	n/a	n/a
15	BATF	chr10:46048680-46048912	GM12878	blood:	n/a	n/a
16	BATF	chr10:45991259-45991524	GM12878	blood:	n/a	chr10:45991372-45991383
17	BHLHE40	chr10:46049120-46049135	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:45991365-45991519	K562	blood:	n/a	n/a
19	BHLHE40	chr10:46071505-46071697	HepG2	liver:	n/a	n/a
20	CBX3	chr10:46052948-46053303	K562	blood:	n/a	n/a
21	CBX3	chr10:46052839-46053381	K562	blood:	n/a	n/a
22	CBX3	chr10:46070238-46070703	K562	blood:	n/a	n/a
23	CBX3	chr10:45991285-45991678	HCT-116	colon:	n/a	n/a
24	CBX3	chr10:45990866-45991680	K562	blood:	n/a	n/a
25	CBX3	chr10:45991212-45991639	K562	blood:	n/a	n/a
26	CEBPB	chr10:46040674-46040941	A549	lung:	n/a	chr10:46040811-46040822
27	CEBPB	chr10:46051286-46051631	Hela-S3	cervix:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
28	CEBPB	chr10:46040650-46040978	HepG2	liver:	n/a	chr10:46040811-46040822
29	CEBPB	chr10:46040656-46041003	K562	blood:	n/a	chr10:46040811-46040822
30	CEBPB	chr10:46051298-46051581	A549	lung:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
31	CEBPB	chr10:46051316-46051621	HepG2	liver:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
32	CEBPB	chr10:46051289-46051641	IMR90	lung:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
33	CEBPB	chr10:45993545-45993764	A549	lung:	n/a	chr10:45993685-45993696
34	CEBPB	chr10:45993570-45993775	HepG2	liver:	n/a	chr10:45993685-45993696
35	CEBPB	chr10:45993525-45993848	K562	blood:	n/a	chr10:45993685-45993696
36	CEBPB	chr10:46051317-46051601	K562	blood:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
37	CEBPB	chr10:45993517-45993811	IMR90	lung:	n/a	chr10:45993685-45993696
38	CEBPB	chr10:46064920-46065043	HepG2	liver:	n/a	chr10:46064929-46064940
39	CEBPB	chr10:45991322-45991595	K562	blood:	n/a	n/a
40	CHD2	chr10:46010281-46010481	HepG2	liver:	n/a	n/a
41	CTCF	chr10:46016100-46016250	HMEC	breast:	n/a	chr10:46016130-46016140
42	CTCF	chr10:46015940-46016090	GM12872	blood:	n/a	n/a
43	CTCF	chr10:46016040-46016190	HRPEpiC	eye:	n/a	chr10:46016130-46016140
44	CTCF	chr10:46016054-46016252	MCF-7	breast:	n/a	chr10:46016130-46016140
45	CTCF	chr10:46015960-46016110	HCM	heart:	n/a	n/a
46	CTCF	chr10:46016060-46016210	HMEC	breast:	n/a	chr10:46016130-46016140
47	CTCF	chr10:46016088-46016123	K562	blood:	n/a	n/a
48	CTCF	chr10:46053940-46054090	HepG2	liver:	n/a	n/a
49	CTCF	chr10:46015980-46016130	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:46009898-46009922	NHEK	skin:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:46010523-46010573	HMEC	breast:	n/a
2	chr10:46010523-46010573	HMEC	breast:	n/a
3	chr10:46065860-46065910	H1-hESC	embryonic stem cell:	embryo
4	chr10:46065860-46065910	SKMC	muscle:	n/a
5	chr10:46010523-46010573	T-47D	breast:	n/a
6	chr10:46032181-46032231	GM12891	blood:	n/a
7	chr10:46029359-46029409	SK-N-SH_RA	brain:	n/a
8	chr10:46032181-46032231	ovcar-3	ovarian:	n/a
9	chr10:46010523-46010573	ProgFib	skin:	n/a
10	chr10:46010025-46010075	PFSK-1	brain:	n/a
11	chr10:46010523-46010573	NH-A	brain:	n/a
12	chr10:46032181-46032231	NT2-D1	testis:	n/a
13	chr10:46032181-46032231	SKMC	muscle:	n/a
14	chr10:46010025-46010075	HIPEpiC	eye:	n/a
15	chr10:46010523-46010573	MCF-7	breast:	n/a
16	chr10:46065860-46065910	K562	blood:	n/a
17	chr10:46032264-46032314	NB4	blood:	n/a
18	chr10:46032264-46032314	GM06990	blood:	n/a
19	chr10:46032264-46032314	HNPCEpiC	eye:	n/a
20	chr10:46032264-46032314	K562	blood:	n/a
21	chr10:46010025-46010075	CMK	blood:	n/a
22	chr10:46010523-46010573	HL-60	blood:	n/a
23	chr10:46032181-46032231	PFSK-1	brain:	n/a
24	chr10:46010523-46010573	HCT-116	colon:	n/a
25	chr10:46010025-46010075	HRPEpiC	eye:	n/a
26	chr10:46029359-46029409	GM06990	blood:	n/a
27	chr10:46029359-46029409	HPAEpiC	pulmonary alveolar:	n/a
28	chr10:46029359-46029409	HRPEpiC	eye:	n/a
29	chr10:46065860-46065910	ovcar-3	ovarian:	n/a
30	chr10:46010025-46010075	PrEC	prostate:	n/a
31	chr10:46010523-46010573	HCPEpiC	choroid plexus:	n/a
32	chr10:46032264-46032314	H1-hESC	embryonic stem cell:	embryo
33	chr10:46029359-46029409	GM12878	blood:	n/a
34	chr10:46010523-46010573	BE2_C	brain:	n/a
35	chr10:46030793-46030843	LNCaP	prostate:	n/a
36	chr10:46030793-46030843	HRPEpiC	eye:	n/a
37	chr10:46032264-46032314	SAEC	small airway:	n/a
38	chr10:46053734-46053784	ProgFib	skin:	n/a
39	chr10:46010523-46010573	HCM	heart:	n/a
40	chr10:46032181-46032231	HIPEpiC	eye:	n/a
41	chr10:46053734-46053784	HRCEpiC	kidney:	n/a
42	chr10:46032202-46032252	ovcar-3	ovarian:	n/a
43	chr10:46030793-46030843	AG10803	skin:	n/a
44	chr10:46032202-46032252	Jurkat	blood:	n/a
45	chr10:46032181-46032231	HEEpiC	esophagus:	n/a
46	chr10:46029359-46029409	AG04449	skin:	fetal
47	chr10:46065860-46065910	HCF	heart:	n/a
48	chr10:46030793-46030843	HCM	heart:	n/a
49	chr10:46065860-46065910	HL-60	blood:	n/a
50	chr10:46032264-46032314	HCF	heart:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:46010308..46013233-chr10:46016249..46018005,2	MCF-7	breast:
2	chr10:46017813..46021385-chr10:46021525..46026200,4	K562	blood:
3	chr10:46045209..46047210-chr10:46049150..46053014,3	K562	blood:
4	chr10:45983824..45985525-chr10:45988162..45991006,2	K562	blood:
5	chr10:46045209..46047210-chr10:46049150..46053014,3	K562	blood:
6	chr10:46043857..46045748-chr10:46047438..46049398,2	K562	blood:
7	chr10:46009283..46011028-chr10:46011723..46015001,3	K562	blood:
8	chr10:45990901..45993266-chr10:45994025..45996239,2	K562	blood:
9	chr10:46010308..46013233-chr10:46016249..46018005,2	MCF-7	breast:
10	chr10:46013794..46015809-chr10:46017694..46020673,2	K562	blood:
11	chr10:45964249..45966447-chr10:46001375..46005597,3	K562	blood:
12	chr10:46013794..46016102-chr10:46018304..46020673,2	K562	blood:
13	chr10:46015623..46016577-chr10:46167502..46168534,4	MCF-7	breast:
14	chr10:46049227..46053354-chr10:46053983..46058180,6	K562	blood:
15	chr10:46070111..46072532-chr10:46080912..46083330,2	K562	blood:
16	chr10:46042311..46044795-chr10:46052336..46053839,2	K562	blood:
17	chr10:46009283..46011028-chr10:46011723..46015001,3	K562	blood:
18	chr10:45983415..45984921-chr10:45987489..45990303,2	K562	blood:
19	chr10:46047681..46050727-chr10:46051442..46055483,4	K562	blood:
20	chr10:45990901..45993266-chr10:45994025..45997013,3	K562	blood:
21	chr10:46009283..46010923-chr10:46013025..46015001,2	K562	blood:
22	chr10:46054558..46056066-chr10:46056809..46059379,2	K562	blood:
23	chr10:45990901..45993266-chr10:45994025..45997013,3	K562	blood:
24	chr10:46016593..46020414-chr10:46030454..46032226,3	K562	blood:
25	chr10:46018607..46021116-chr10:46021525..46024218,2	K562	blood:
26	chr10:46009283..46010923-chr10:46013025..46015001,2	K562	blood:
27	chr10:46047681..46050727-chr10:46051442..46055483,4	K562	blood:
28	chr10:45990901..45993266-chr10:45994025..45996239,2	K562	blood:
29	chr10:46042311..46044795-chr10:46052336..46053839,2	K562	blood:
30	chr10:46017813..46021385-chr10:46021525..46026200,4	K562	blood:
31	chr10:46015710..46016361-chr10:46167710..46168363,2	MCF-7	breast:
32	chr10:46038014..46040186-chr10:46047906..46049912,2	K562	blood:
33	chr10:46013794..46015809-chr10:46017694..46020673,2	K562	blood:
34	chr10:46043857..46045748-chr10:46047438..46049398,2	K562	blood:
35	chr10:46049227..46053354-chr10:46053983..46058180,6	K562	blood:
36	chr10:46018607..46021116-chr10:46021525..46024218,2	K562	blood:
37	chr10:46014012..46015571-chr10:46081118..46083546,2	K562	blood:
38	chr10:46013794..46016102-chr10:46018304..46020673,2	K562	blood:
39	chr10:46054558..46056066-chr10:46056809..46059379,2	K562	blood:
40	chr10:46038014..46040186-chr10:46047906..46049912,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALOX5-1	chr10:46056139-46056282	NONHSAT013106
2	lnc-ALOX5-1	chr10:46045257-46045361	NONHSAT013106
3	lnc-ALOX5-1	chr10:46043743-46043887	NONHSAT013106
4	lnc-ZFAND4-1	chr10:46048560-46048652	NONHSAT013107

No data

Variant related genes	Relation type
MARCH8	TF binding region
MARCH8	CpG island
ENSG00000165406	chromatin interactions
ENSG00000172671	chromatin interactions

Extended variants
information (count: 2981 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2981 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12774690	chr10:45989745-45989746	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532805931	chr10:45989764-45989765	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs189047115	chr10:45989868-45989869	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs200199490	chr10:45989883-45989884	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs35560623	chr10:45989884-45989885	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs563670566	chr10:45989893-45989894	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs531096623	chr10:45989914-45989915	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs550556672	chr10:45989956-45989957	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs568478792	chr10:45990021-45990022	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs549207999	chr10:45990083-45990084	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs564432120	chr10:45990107-45990108	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs567757276	chr10:45990108-45990109	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs535177961	chr10:45990126-45990127	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs546792076	chr10:45990172-45990173	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs571683444	chr10:45990186-45990187	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs539060098	chr10:45990247-45990248	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs371400163	chr10:45990248-45990249	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs150544355	chr10:45990294-45990295	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs4949004	chr10:45990295-45990296	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs192002496	chr10:45990373-45990374	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs555589058	chr10:45990377-45990378	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs184917120	chr10:45990394-45990395	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs541186811	chr10:45990428-45990429	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs35488254	chr10:45990437-45990438	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs371852105	chr10:45990444-45990445	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs577645553	chr10:45990509-45990510	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs544641292	chr10:45990523-45990524	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs144170192	chr10:45990524-45990525	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs113432182	chr10:45990622-45990623	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs531158319	chr10:45990624-45990625	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs570805449	chr10:45990625-45990626	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs549271146	chr10:45990656-45990657	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs561591002	chr10:45990673-45990674	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs529004708	chr10:45990674-45990675	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs60572230	chr10:45990686-45990687	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs578036170	chr10:45990761-45990762	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs547146303	chr10:45990774-45990775	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs571684578	chr10:45990826-45990827	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs111585183	chr10:45990831-45990832	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs551040079	chr10:45990857-45990858	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs569276383	chr10:45990859-45990860	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs536609886	chr10:45990899-45990900	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs116929075	chr10:45990917-45990918	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs17157861	chr10:45990925-45990926	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs534543929	chr10:45991047-45991048	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs553120521	chr10:45991097-45991098	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs577361758	chr10:45991125-45991126	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs71494796	chr10:45991221-45991222	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	mRNA abundance
49	rs139722001	chr10:45991229-45991230	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs574907283	chr10:45991230-45991231	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
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
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21138945	CNVD
Autism	19287141	CNVD
Intellectual disability	21948486	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45974800-45990600	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr10:45978600-46000800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:45984000-45989800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr10:45984000-45991400	Weak transcription	Fetal Lung	lung
5	chr10:45984200-45990400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr10:45984200-45991400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr10:45984200-46011000	Weak transcription	Left Ventricle	heart
8	chr10:45984600-45989800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr10:45984600-45990800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr10:45984800-45990600	Weak transcription	Primary T cells from cord blood	blood
11	chr10:45984800-45991600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr10:45984800-45993400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr10:45988400-45996000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:45989200-45991000	Weak transcription	Primary hematopoietic stem cells	blood
15	chr10:45989200-46015200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr10:45989400-45990000	ZNF genes & repeats	K562	blood
17	chr10:45990600-45991200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
18	chr10:45990800-45991000	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
19	chr10:45991000-45995600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr10:45991400-45991600	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr10:45993200-45994400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr10:45993600-45994000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr10:45995800-45998600	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr10:45997200-45998800	Enhancers	HepG2	liver
25	chr10:45997800-45998200	Enhancers	A549	lung
26	chr10:45997800-45998800	Enhancers	Liver	Liver
27	chr10:45998200-45998600	Enhancers	HUVEC	blood vessel
28	chr10:45998600-45998800	Enhancers	Pancreas	Pancrea
29	chr10:45998600-46000000	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr10:45998800-46000800	Weak transcription	Liver	Liver
31	chr10:45998800-46009600	Weak transcription	Pancreas	Pancrea
32	chr10:45999000-46025600	Weak transcription	Primary hematopoietic stem cells	blood
33	chr10:46000000-46000600	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr10:46000600-46001400	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr10:46000600-46001400	Enhancers	NHDF-Ad	bronchial
36	chr10:46000800-46001200	Enhancers	Liver	Liver
37	chr10:46000800-46001200	Enhancers	Brain Cingulate Gyrus	brain
38	chr10:46000800-46001200	Enhancers	Brain Hippocampus Middle	brain
39	chr10:46000800-46019800	Weak transcription	Primary B cells from cord blood	blood
40	chr10:46001000-46001400	Enhancers	Brain Substantia Nigra	brain
41	chr10:46001200-46001400	Enhancers	Brain Angular Gyrus	brain
42	chr10:46001200-46004600	Weak transcription	Brain Hippocampus Middle	brain
43	chr10:46001200-46009000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr10:46001200-46009800	Weak transcription	Liver	Liver
45	chr10:46001400-46003800	Weak transcription	Brain Substantia Nigra	brain
46	chr10:46001400-46005600	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr10:46001400-46008800	Weak transcription	Brain Angular Gyrus	brain
48	chr10:46003800-46004800	Enhancers	Brain Substantia Nigra	brain
49	chr10:46004400-46005800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr10:46004400-46005800	Enhancers	HMEC	breast

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