Variant report

Variant	nsv1013338
Chromosome Location	chr2:144806920-144969818
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1374)
CpG islands
(count:489)
Chromatin interactive
region (count:89)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1374 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:144908751-144909800	K562	blood:	n/a	chr2:144909235-144909251 chr2:144909236-144909252
2	ARID3A	chr2:144891393-144891682	K562	blood:	n/a	n/a
3	ARID3A	chr2:144921102-144921451	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:144910290-144910897	K562	blood:	n/a	n/a
5	ARID3A	chr2:144907854-144908054	K562	blood:	n/a	n/a
6	ARID3A	chr2:144895357-144895907	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:144955704-144956090	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:144895265-144895277	K562	blood:	n/a	n/a
9	ATF1	chr2:144910447-144910802	K562	blood:	n/a	n/a
10	ATF1	chr2:144891442-144891664	K562	blood:	n/a	n/a
11	ATF1	chr2:144908994-144909342	K562	blood:	n/a	n/a
12	ATF1	chr2:144955717-144956108	K562	blood:	n/a	n/a
13	ATF2	chr2:144941155-144941769	GM12878	blood:	n/a	n/a
14	ATF3	chr2:144955664-144956103	K562	blood:	n/a	n/a
15	ATF3	chr2:144908943-144909278	K562	blood:	n/a	n/a
16	BACH1	chr2:144920265-144920548	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr2:144941255-144941630	GM12878	blood:	n/a	n/a
18	BATF	chr2:144941269-144941565	GM12878	blood:	n/a	n/a
19	BCL11A	chr2:144941399-144941632	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:144960613-144960792	K562	blood:	n/a	n/a
21	BHLHE40	chr2:144941310-144941789	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:144910435-144910665	K562	blood:	n/a	n/a
23	BHLHE40	chr2:144920331-144920509	K562	blood:	n/a	n/a
24	BHLHE40	chr2:144895720-144895875	HepG2	liver:	n/a	n/a
25	CBX3	chr2:144908911-144909379	K562	blood:	n/a	n/a
26	CBX3	chr2:144861840-144862174	K562	blood:	n/a	n/a
27	CBX3	chr2:144910307-144910775	K562	blood:	n/a	n/a
28	CCNT2	chr2:144910447-144910874	K562	blood:	n/a	n/a
29	CCNT2	chr2:144908971-144909788	K562	blood:	n/a	n/a
30	CEBPB	chr2:144901126-144901406	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:144955722-144956078	HepG2	liver:	n/a	chr2:144955892-144955903
32	CEBPB	chr2:144955733-144956062	K562	blood:	n/a	chr2:144955892-144955903
33	CEBPB	chr2:144940529-144940617	HepG2	liver:	n/a	chr2:144940547-144940560 chr2:144940548-144940559
34	CEBPB	chr2:144946973-144947123	A549	lung:	n/a	n/a
35	CEBPB	chr2:144823838-144823865	HepG2	liver:	n/a	chr2:144823849-144823862 chr2:144823849-144823860 chr2:144823849-144823862 chr2:144823851-144823862
36	CEBPB	chr2:144948782-144949095	HepG2	liver:	n/a	chr2:144948954-144948967 chr2:144948955-144948966 chr2:144948954-144948965 chr2:144948956-144948965 chr2:144948954-144948967
37	CEBPB	chr2:144922008-144922260	Hela-S3	cervix:	n/a	chr2:144922025-144922038 chr2:144922173-144922186
38	CEBPB	chr2:144948861-144949088	A549	lung:	n/a	chr2:144948954-144948967 chr2:144948955-144948966 chr2:144948954-144948965 chr2:144948956-144948965 chr2:144948954-144948967
39	CEBPB	chr2:144909021-144909492	K562	blood:	n/a	n/a
40	CEBPB	chr2:144928018-144928120	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:144904937-144905263	A549	lung:	n/a	chr2:144905114-144905123 chr2:144905112-144905125 chr2:144905112-144905125 chr2:144905112-144905123 chr2:144905114-144905123 chr2:144905114-144905123
42	CEBPB	chr2:144920244-144920546	MCF-7	breast:	n/a	n/a
43	CEBPB	chr2:144832006-144832266	A549	lung:	n/a	chr2:144832110-144832123
44	CEBPB	chr2:144832050-144832234	H1-hESC	embryonic stem cell:	n/a	chr2:144832110-144832123
45	CEBPB	chr2:144911847-144912162	HepG2	liver:	n/a	chr2:144912080-144912091 chr2:144912016-144912027
46	CEBPB	chr2:144904931-144905312	HepG2	liver:	n/a	chr2:144905114-144905123 chr2:144905112-144905125 chr2:144905112-144905125 chr2:144905112-144905123 chr2:144905114-144905123 chr2:144905114-144905123
47	CEBPB	chr2:144831975-144832295	IMR90	lung:	n/a	chr2:144832110-144832123
48	CEBPB	chr2:144921939-144922334	IMR90	lung:	n/a	chr2:144922025-144922038 chr2:144922173-144922186
49	CEBPB	chr2:144955732-144956077	IMR90	lung:	n/a	chr2:144955892-144955903
50	CEBPB	chr2:144921912-144922367	HepG2	liver:	n/a	chr2:144922025-144922038 chr2:144922173-144922186

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:144827306-144827356	MCF10A-Er-Src	breast:	n/a
2	chr2:144827306-144827356	MCF10A-Er-Src	breast:	n/a
3	chr2:144895454-144895504	HIPEpiC	eye:	n/a
4	chr2:144841354-144841404	ovcar-3	ovarian:	n/a
5	chr2:144888877-144888927	HNPCEpiC	eye:	n/a
6	chr2:144827306-144827356	SK-N-SH	brain:	n/a
7	chr2:144855085-144855135	ProgFib	skin:	n/a
8	chr2:144895454-144895504	GM12891	blood:	n/a
9	chr2:144911452-144911502	H1-hESC	embryonic stem cell:	embryo
10	chr2:144827306-144827356	GM19239	blood:	n/a
11	chr2:144869361-144869411	HCF	heart:	n/a
12	chr2:144869361-144869411	AoSMC	blood vessel:	n/a
13	chr2:144869361-144869411	NHBE	bronchial:	n/a
14	chr2:144895454-144895504	HEK293	kidney:	embryo
15	chr2:144895454-144895504	HNPCEpiC	eye:	n/a
16	chr2:144888877-144888927	AG04449	skin:	fetal
17	chr2:144869361-144869411	MCF-7	breast:	n/a
18	chr2:144869361-144869411	GM19239	blood:	n/a
19	chr2:144841354-144841404	HAEpiC	amniotic membrane:	n/a
20	chr2:144869361-144869411	HMEC	breast:	n/a
21	chr2:144869361-144869411	HepG2	liver:	n/a
22	chr2:144888877-144888927	MCF-7	breast:	n/a
23	chr2:144869361-144869411	ovcar-3	ovarian:	n/a
24	chr2:144911452-144911502	ovcar-3	ovarian:	n/a
25	chr2:144869361-144869411	GM12878	blood:	n/a
26	chr2:144827306-144827356	HEEpiC	esophagus:	n/a
27	chr2:144911452-144911502	HCM	heart:	n/a
28	chr2:144841354-144841404	PFSK-1	brain:	n/a
29	chr2:144888877-144888927	NH-A	brain:	n/a
30	chr2:144869361-144869411	LNCaP	prostate:	n/a
31	chr2:144895454-144895504	HepG2	liver:	n/a
32	chr2:144827306-144827356	GM12892	blood:	n/a
33	chr2:144855085-144855135	Hela-S3	cervix:	n/a
34	chr2:144855085-144855135	PANC-1	pancreas:	n/a
35	chr2:144827306-144827356	AG10803	skin:	n/a
36	chr2:144915087-144915137	AG09309	skin:	n/a
37	chr2:144869361-144869411	H1-hESC	embryonic stem cell:	embryo
38	chr2:144911452-144911502	BJ	skin:	n/a
39	chr2:144855085-144855135	IMR90	lung:	fetal
40	chr2:144888877-144888927	HepG2	liver:	n/a
41	chr2:144841354-144841404	U87	brain:	n/a
42	chr2:144915087-144915137	RPTEC	kidney:	n/a
43	chr2:144888877-144888927	HRE	kidney:	n/a
44	chr2:144841354-144841404	GM12878	blood:	n/a
45	chr2:144888877-144888927	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:144855085-144855135	Jurkat	blood:	n/a
47	chr2:144888877-144888927	AoSMC	blood vessel:	n/a
48	chr2:144895454-144895504	BJ	skin:	n/a
49	chr2:144869361-144869411	ECC-1	luminal epithelium:	n/a
50	chr2:144888877-144888927	SK-N-SH	brain:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:144909064..144910928-chr2:144912495..144915157,2	K562	blood:
2	chr2:144333030..144333684-chr2:144828727..144829250,2	MCF-7	breast:
3	chr2:144907547..144909813-chr2:145165279..145167381,2	K562	blood:
4	chr2:144831724..144834117-chr2:144836393..144838658,2	K562	blood:
5	chr2:144909064..144910928-chr2:144912495..144915157,2	K562	blood:
6	chr2:144964243..144966732-chr2:144985702..144988124,2	K562	blood:
7	chr2:144892432..144894234-chr2:144907279..144909796,2	K562	blood:
8	chr2:144910287..144911946-chr2:144917070..144919325,2	K562	blood:
9	chr2:144839334..144841490-chr2:144858861..144860690,2	K562	blood:
10	chr2:144952090..144954781-chr2:145087114..145090082,2	K562	blood:
11	chr2:144892432..144894234-chr2:144907279..144909796,2	K562	blood:
12	chr2:144887546..144889474-chr2:144891117..144893763,2	K562	blood:
13	chr2:144915994..144918653-chr2:144928305..144930697,2	K562	blood:
14	chr2:144895471..144897745-chr2:144898659..144900274,2	K562	blood:
15	chr2:144871415..144873570-chr2:144877450..144879140,2	K562	blood:
16	chr2:144915994..144918653-chr2:144928305..144930697,2	K562	blood:
17	chr2:144825930..144827931-chr2:144829738..144833404,3	K562	blood:
18	chr2:144927685..144929852-chr2:145051639..145053932,2	K562	blood:
19	chr2:144839342..144841610-chr2:144842729..144844354,2	K562	blood:
20	chr2:144959046..144961054-chr2:144965383..144967301,2	K562	blood:
21	chr2:144809098..144811827-chr2:144812391..144814303,2	K562	blood:
22	chr2:144930645..144932924-chr2:144935124..144938054,2	K562	blood:
23	chr2:144331645..144332292-chr2:144828903..144829703,2	MCF-7	breast:
24	chr2:144904358..144906463-chr2:144910174..144912005,2	K562	blood:
25	chr2:144841519..144844337-chr2:144854788..144856843,2	K562	blood:
26	chr2:144958460..144960546-chr2:144965383..144967191,2	K562	blood:
27	chr2:144958460..144960546-chr2:144965383..144967191,2	K562	blood:
28	chr2:144879880..144882574-chr2:144884778..144888739,3	K562	blood:
29	chr2:144878632..144882574-chr2:144884432..144888739,5	K562	blood:
30	chr2:144925535..144928425-chr2:144928955..144931463,2	K562	blood:
31	chr2:144906956..144909639-chr2:145115493..145118052,3	K562	blood:
32	chr2:144909008..144910995-chr2:144934770..144936322,2	K562	blood:
33	chr2:144898663..144900343-chr2:146340645..146343317,2	MCF-7	breast:
34	chr2:144443861..144445344-chr2:144828239..144829556,5	MCF-7	breast:
35	chr2:144871415..144873570-chr2:144877450..144879140,2	K562	blood:
36	chr2:144887546..144889474-chr2:144891117..144893763,2	K562	blood:
37	chr2:144835744..144838498-chr2:144855384..144857120,2	K562	blood:
38	chr2:144961397..144965444-chr2:144966089..144968979,3	K562	blood:
39	chr2:144809098..144811827-chr2:144812391..144814303,2	K562	blood:
40	chr2:144909008..144910601-chr2:144933945..144936322,2	K562	blood:
41	chr2:144904358..144906463-chr2:144910174..144912005,2	K562	blood:
42	chr2:144909008..144910995-chr2:144934770..144936322,2	K562	blood:
43	chr2:144599305..144600135-chr2:144828924..144829696,2	MCF-7	breast:
44	chr2:144839342..144841610-chr2:144842729..144844354,2	K562	blood:
45	chr2:144848969..144851398-chr2:144852531..144855002,2	K562	blood:
46	chr2:144946214..144949112-chr2:144950562..144952419,2	MCF-7	breast:
47	chr2:144895471..144897745-chr2:144898659..144900274,2	K562	blood:
48	chr2:144961397..144965444-chr2:144966089..144968979,3	K562	blood:
49	chr2:144841519..144844337-chr2:144854788..144856843,2	K562	blood:
50	chr2:144758525..144761304-chr2:144910263..144913200,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP15-13	chr2:144917322-144917615	uc_80_+
2	lnc-ZEB2-8	chr2:144968402-144968804	NONHSAT074756
3	lnc-ARHGAP15-10	chr2:144877603-144877937	uc_76_+
4	lnc-ZEB2-8	chr2:144969082-144969146	NONHSAT074756
5	lnc-ARHGAP15-11	chr2:144904824-144905071	uc_78_+
6	lnc-ZEB2-15	chr2:144877603-144877937	uc_76_-
7	lnc-ZEB2-14	chr2:144883649-144885151	NONHSAT074755
8	lnc-ZEB2-11	chr2:144913647-144913941	uc_79_-
9	lnc-ZEB2-10	chr2:144917322-144917615	uc_80_-
10	lnc-ARHGAP15-12	chr2:144913647-144913941	uc_79_+
11	lnc-ZEB2-12	chr2:144904824-144905071	uc_78_-
12	lnc-ZEB2-9	chr2:144965559-144965921	expReg_chr2_10439_-

No data

Variant related genes	Relation type
GTDC1	TF binding region
GTDC1	CpG island
ENSG00000121964	chromatin interactions
ENSG00000238057	chromatin interactions
ENSG00000169554	chromatin interactions
G3BP2	miRNA target sites

Extended variants
information (count: 5319 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:5319 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190468293	chr2:144806931-144806932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs151243143	chr2:144806966-144806967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539847372	chr2:144806967-144806968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557848567	chr2:144806971-144806972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576711372	chr2:144806975-144806976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543759450	chr2:144807059-144807060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77027536	chr2:144807103-144807104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183276061	chr2:144807107-144807108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574295172	chr2:144807122-144807123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35222605	chr2:144807123-144807124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs58057530	chr2:144807152-144807153	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs560312782	chr2:144807212-144807213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187550399	chr2:144807299-144807300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192403070	chr2:144807331-144807332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184307518	chr2:144807414-144807415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531288932	chr2:144807461-144807462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549673419	chr2:144807471-144807472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567978487	chr2:144807517-144807518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187544776	chr2:144807521-144807522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192967017	chr2:144807522-144807523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13008005	chr2:144807555-144807556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75183674	chr2:144807659-144807660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547256139	chr2:144807691-144807692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539538968	chr2:144807713-144807714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372671669	chr2:144807714-144807715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376935643	chr2:144807770-144807771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558182041	chr2:144807772-144807773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576364743	chr2:144807773-144807774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537413650	chr2:144807782-144807783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556114373	chr2:144807880-144807881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562010402	chr2:144807923-144807924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553243593	chr2:144807943-144807944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574360563	chr2:144807987-144807988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541674453	chr2:144808035-144808036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140651189	chr2:144808056-144808057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528193256	chr2:144808092-144808093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184152046	chr2:144808167-144808168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77238217	chr2:144808168-144808169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145891483	chr2:144808205-144808206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531222248	chr2:144808249-144808250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542985103	chr2:144808257-144808258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561673750	chr2:144808319-144808320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143689340	chr2:144808348-144808349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144067407	chr2:144808349-144808350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529133895	chr2:144808392-144808393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370597051	chr2:144808439-144808440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547226858	chr2:144808453-144808454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565730704	chr2:144808454-144808455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189224053	chr2:144808489-144808490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548040768	chr2:144808533-144808534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Non-syndromic sensorineural hearing loss	20456320	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1207 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:144783600-144817000	Weak transcription	Aorta	Aorta
2	chr2:144798000-144808000	Weak transcription	Primary B cells from cord blood	blood
3	chr2:144805200-144807000	Enhancers	K562	blood
4	chr2:144805600-144807400	Enhancers	Fetal Heart	heart
5	chr2:144806200-144807000	Enhancers	Fetal Lung	lung
6	chr2:144806600-144813000	Weak transcription	Left Ventricle	heart
7	chr2:144806800-144807200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:144807000-144812000	Weak transcription	Fetal Lung	lung
9	chr2:144809600-144810200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:144809800-144810200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr2:144809800-144810200	Enhancers	Adipose Nuclei	Adipose
12	chr2:144810200-144812200	Weak transcription	Adipose Nuclei	Adipose
13	chr2:144812000-144813200	Enhancers	Fetal Lung	lung
14	chr2:144812200-144812600	Enhancers	Adipose Nuclei	Adipose
15	chr2:144813000-144813200	Enhancers	Left Ventricle	heart
16	chr2:144813200-144814200	Weak transcription	Left Ventricle	heart
17	chr2:144816800-144817200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr2:144821800-144822200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:144822200-144826200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:144823400-144824200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr2:144824200-144825400	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr2:144825000-144825600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:144825200-144826800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:144825400-144825800	Enhancers	Fetal Brain Male	brain
25	chr2:144825400-144827600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr2:144825600-144826400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr2:144825600-144826600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:144825600-144826600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:144825600-144828800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:144825600-144839600	Enhancers	Fetal Lung	lung
31	chr2:144825800-144826600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:144826000-144826600	Enhancers	Fetal Heart	heart
33	chr2:144826200-144826800	Enhancers	Brain Germinal Matrix	brain
34	chr2:144826200-144827200	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr2:144826200-144827200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:144826400-144827200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr2:144826600-144827200	Enhancers	Primary hematopoietic stem cells	blood
38	chr2:144826600-144830200	Weak transcription	Fetal Heart	heart
39	chr2:144826800-144839000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr2:144828000-144828600	Enhancers	Fetal Kidney	kidney
41	chr2:144828000-144829800	Enhancers	NHLF	lung
42	chr2:144828400-144828600	Enhancers	Brain Angular Gyrus	brain
43	chr2:144828600-144834800	Weak transcription	Fetal Kidney	kidney
44	chr2:144828800-144829200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:144828800-144829400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:144829000-144829200	Enhancers	Osteobl	bone
47	chr2:144829000-144830200	Enhancers	Fetal Stomach	stomach
48	chr2:144829000-144830200	Enhancers	Ovary	ovary
49	chr2:144829000-144830400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr2:144829200-144829400	Enhancers	Brain Angular Gyrus	brain

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