Variant report

Variant	nsv961869
Chromosome Location	chr2:112645626-112660962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:974)
CpG islands
(count:854)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112658309-112658903	K562	blood:	n/a	n/a
2	ARID3A	chr2:112658342-112659025	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:112645334-112645686	K562	blood:	n/a	n/a
4	ARID3A	chr2:112645308-112645752	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:112654996-112655925	HepG2	liver:	n/a	n/a
6	ATF1	chr2:112645254-112645673	K562	blood:	n/a	n/a
7	BACH1	chr2:112655304-112655930	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:112656498-112657001	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:112652132-112652417	K562	blood:	n/a	n/a
10	BHLHE40	chr2:112645324-112645694	HepG2	liver:	n/a	n/a
11	BHLHE40	chr2:112645369-112645646	K562	blood:	n/a	n/a
12	BHLHE40	chr2:112655170-112656761	HepG2	liver:	n/a	chr2:112655836-112655852
13	BHLHE40	chr2:112656584-112656777	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:112652322-112652327	K562	blood:	n/a	n/a
15	BHLHE40	chr2:112655488-112655881	GM12878	blood:	n/a	chr2:112655836-112655852
16	BHLHE40	chr2:112656228-112656290	K562	blood:	n/a	n/a
17	BHLHE40	chr2:112655271-112655681	K562	blood:	n/a	n/a
18	BRCA1	chr2:112657912-112657943	GM12878	blood:	n/a	n/a
19	BRCA1	chr2:112655360-112655921	HepG2	liver:	n/a	n/a
20	CCNT2	chr2:112655405-112656949	K562	blood:	n/a	chr2:112655529-112655538 chr2:112656403-112656412
21	CEBPB	chr2:112653197-112653545	HepG2	liver:	n/a	chr2:112653372-112653381 chr2:112653394-112653405 chr2:112653370-112653381
22	CEBPB	chr2:112658570-112658934	K562	blood:	n/a	n/a
23	CEBPB	chr2:112658595-112658892	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:112653264-112654209	K562	blood:	n/a	chr2:112653372-112653381 chr2:112653394-112653405 chr2:112653370-112653381
25	CEBPB	chr2:112656787-112656987	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:112658585-112658910	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:112653311-112653449	Hela-S3	cervix:	n/a	chr2:112653372-112653381 chr2:112653394-112653405 chr2:112653370-112653381
28	CEBPB	chr2:112653277-112653551	A549	lung:	n/a	chr2:112653372-112653381 chr2:112653394-112653405 chr2:112653370-112653381
29	CEBPB	chr2:112658590-112658924	MCF-7	breast:	n/a	n/a
30	CEBPD	chr2:112655541-112656317	HepG2	liver:	n/a	n/a
31	CEBPD	chr2:112655408-112656644	HepG2	liver:	n/a	n/a
32	CEBPZ	chr2:112648193-112648203	HepG2	liver:	n/a	n/a
33	CHD1	chr2:112655489-112655910	H1-hESC	embryonic stem cell:	n/a	chr2:112655551-112655561
34	CHD1	chr2:112655689-112655764	GM12878	blood:	n/a	n/a
35	CHD1	chr2:112656207-112656862	H1-hESC	embryonic stem cell:	n/a	chr2:112656828-112656838
36	CHD1	chr2:112656196-112656396	GM12878	blood:	n/a	n/a
37	CHD2	chr2:112656125-112657001	GM12878	blood:	n/a	chr2:112656828-112656838
38	CHD2	chr2:112655303-112655914	GM12878	blood:	n/a	chr2:112655551-112655561
39	CHD2	chr2:112656521-112656532	K562	blood:	n/a	n/a
40	CHD2	chr2:112654841-112655933	HepG2	liver:	n/a	chr2:112655551-112655561
41	CHD2	chr2:112660156-112660270	HepG2	liver:	n/a	n/a
42	CHD2	chr2:112653618-112653866	K562	blood:	n/a	n/a
43	CHD2	chr2:112656180-112656907	HepG2	liver:	n/a	chr2:112656828-112656838
44	CHD2	chr2:112655461-112655709	K562	blood:	n/a	chr2:112655551-112655561
45	CHD2	chr2:112658560-112658827	HepG2	liver:	n/a	n/a
46	CREB1	chr2:112654908-112656986	HepG2	liver:	n/a	n/a
47	CREB1	chr2:112655380-112655854	A549	lung:	n/a	n/a
48	CTBP2	chr2:112655267-112656984	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr2:112655500-112655650	HL-60	blood:	n/a	n/a
50	CTCF	chr2:112658660-112658810	HMEC	breast:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112654017-112654067	MCF-7	breast:	n/a
2	chr2:112655112-112655162	NHBE	bronchial:	n/a
3	chr2:112659978-112660028	ECC-1	luminal epithelium:	n/a
4	chr2:112656262-112656312	MCF10A-Er-Src	breast:	n/a
5	chr2:112655153-112655203	AG04450	lung:	fetal
6	chr2:112655713-112655763	HIPEpiC	eye:	n/a
7	chr2:112656629-112656679	HRPEpiC	eye:	n/a
8	chr2:112658759-112658809	HL-60	blood:	n/a
9	chr2:112658759-112658809	Caco-2	colon:	n/a
10	chr2:112658759-112658809	HMEC	breast:	n/a
11	chr2:112654017-112654067	PANC-1	pancreas:	n/a
12	chr2:112655713-112655763	HAEpiC	amniotic membrane:	n/a
13	chr2:112655072-112655122	T-47D	breast:	n/a
14	chr2:112659978-112660028	AG04450	lung:	fetal
15	chr2:112659978-112660028	IMR90	lung:	fetal
16	chr2:112655829-112655879	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:112656917-112656967	HCF	heart:	n/a
18	chr2:112655112-112655162	AG04450	lung:	fetal
19	chr2:112656262-112656312	HAEpiC	amniotic membrane:	n/a
20	chr2:112659978-112660028	AG10803	skin:	n/a
21	chr2:112655112-112655162	AG04449	skin:	fetal
22	chr2:112659978-112660028	GM12878	blood:	n/a
23	chr2:112656153-112656203	BJ	skin:	n/a
24	chr2:112655153-112655203	GM12891	blood:	n/a
25	chr2:112654017-112654067	AoSMC	blood vessel:	n/a
26	chr2:112655713-112655763	ProgFib	skin:	n/a
27	chr2:112659978-112660028	GM06990	blood:	n/a
28	chr2:112655072-112655122	HNPCEpiC	eye:	n/a
29	chr2:112655072-112655122	HL-60	blood:	n/a
30	chr2:112656629-112656679	NB4	blood:	n/a
31	chr2:112655492-112655542	SK-N-SH	brain:	n/a
32	chr2:112656917-112656967	Hela-S3	cervix:	n/a
33	chr2:112656949-112656999	HEEpiC	esophagus:	n/a
34	chr2:112655153-112655203	GM12878	blood:	n/a
35	chr2:112655153-112655203	HEEpiC	esophagus:	n/a
36	chr2:112659978-112660028	BJ	skin:	n/a
37	chr2:112655153-112655203	PANC-1	pancreas:	n/a
38	chr2:112655072-112655122	RPTEC	kidney:	n/a
39	chr2:112656262-112656312	HRE	kidney:	n/a
40	chr2:112656917-112656967	Caco-2	colon:	n/a
41	chr2:112656262-112656312	HepG2	liver:	n/a
42	chr2:112655713-112655763	GM12892	blood:	n/a
43	chr2:112655492-112655542	HepG2	liver:	n/a
44	chr2:112659978-112660028	MCF10A-Er-Src	breast:	n/a
45	chr2:112655829-112655879	AG04449	skin:	fetal
46	chr2:112656949-112656999	ProgFib	skin:	n/a
47	chr2:112658759-112658809	HIPEpiC	eye:	n/a
48	chr2:112655153-112655203	Jurkat	blood:	n/a
49	chr2:112656262-112656312	HUVEC	blood vessel:	n/a
50	chr2:112658759-112658809	Hela-S3	cervix:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:112648375..112650802-chr2:112777900..112780548,2	K562	blood:
2	chr2:112658215..112658830-chr2:112806155..112807049,3	K562	blood:
3	chr2:112657825..112659209-chr2:112806011..112807065,8	MCF-7	breast:
4	chr2:112640168..112643307-chr2:112651695..112653616,3	K562	blood:
5	chr2:112651539..112654934-chr2:112657187..112660968,3	K562	blood:
6	chr14:58893841..58894558-chr2:112655563..112656149,2	HCT-116	colon:
7	chr2:112659159..112661147-chr2:112720717..112723278,2	K562	blood:
8	chr2:112656058..112657680-chr2:112660254..112662224,2	K562	blood:
9	chr2:112639319..112643119-chr2:112654632..112657707,5	K562	blood:
10	chr2:112653818..112657765-chr2:112811676..112815783,10	MCF-7	breast:
11	chr2:112652127..112657107-chr2:112810449..112814378,4	K562	blood:
12	chr2:112640266..112649080-chr2:112649576..112660203,14	MCF-7	breast:
13	chr2:112655191..112655972-chr2:113339541..113340327,2	K562	blood:
14	chr2:112655301..112655903-chr2:112806007..112806643,3	MCF-7	breast:
15	chr2:112644062..112645639-chr2:112651109..112653676,3	K562	blood:
16	chr2:112659908..112662713-chr2:112675959..112678023,2	MCF-7	breast:
17	chr14:20937129..20937919-chr2:112655605..112656367,2	NB4	blood:
18	chr2:112660151..112661755-chr2:112668828..112671671,2	MCF-7	breast:
19	chr2:112650423..112652429-chr2:112810965..112814807,3	K562	blood:
20	chr2:112646919..112648669-chr2:112812919..112814641,2	MCF-7	breast:
21	chr1:144533868..144534647-chr2:112655787..112656607,2	HCT-116	colon:
22	chr2:112656058..112658724-chr2:112660197..112662923,3	K562	blood:
23	chr2:112645445..112647552-chr2:112653399..112655152,2	K562	blood:
24	chr2:112639278..112642827-chr2:112654632..112657057,4	K562	blood:
25	chr2:112655233..112656048-chr2:112716163..112716720,2	MCF-7	breast:
26	chr2:112646865..112650044-chr2:112654690..112657019,3	K562	blood:
27	chr2:112640266..112649080-chr2:112649576..112660203,14	MCF-7	breast:
28	chr2:112642663..112645475-chr2:112649811..112652343,2	MCF-7	breast:
29	chr2:112641916..112643475-chr2:112652986..112654770,2	MCF-7	breast:
30	chr2:112658476..112659217-chr2:112777886..112778574,2	MCF-7	breast:
31	chr2:112651539..112654934-chr2:112657187..112660968,3	K562	blood:
32	chr2:112641269..112644137-chr2:112654774..112658202,3	MCF-7	breast:
33	chr2:112654702..112658000-chr2:112810291..112813027,3	K562	blood:
34	chr2:112654612..112656528-chr2:112812544..112814421,2	MCF-7	breast:
35	chr2:112640261..112643657-chr2:112643710..112649158,9	MCF-7	breast:

No data

Variant related genes	Relation type
MERTK	TF binding region
ANAPC1	TF binding region
MERTK	CpG island
ANAPC1	CpG island
ENSG00000153208	chromatin interactions
ENSG00000153107	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000100575	chromatin interactions
ENSG00000153214	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000236307	chromatin interactions
ENSG00000100578	chromatin interactions

Extended variants
information (count: 594 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185268732	chr2:112645689-112645690	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs141505461	chr2:112645707-112645708	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs538713362	chr2:112645713-112645714	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs552927433	chr2:112645736-112645737	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs190129420	chr2:112645755-112645756	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535388470	chr2:112645776-112645777	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs79550551	chr2:112645787-112645788	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs77161370	chr2:112645788-112645789	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs13019359	chr2:112645792-112645793	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs575600033	chr2:112645793-112645794	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs111899451	chr2:112645801-112645802	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs182257653	chr2:112645872-112645873	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs577697538	chr2:112645895-112645896	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs549716414	chr2:112645901-112645902	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs184778696	chr2:112645915-112645916	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs529445072	chr2:112645918-112645919	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs142687036	chr2:112645947-112645948	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs529415341	chr2:112645990-112645991	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs4848835	chr2:112646016-112646017	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs531882329	chr2:112646026-112646027	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs551391392	chr2:112646035-112646036	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs571601493	chr2:112646045-112646046	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532526947	chr2:112646046-112646047	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375788555	chr2:112646054-112646055	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs528736299	chr2:112646057-112646058	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187967877	chr2:112646078-112646079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547823427	chr2:112646100-112646101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566557724	chr2:112646116-112646117	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138536319	chr2:112646129-112646130	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs111234046	chr2:112646163-112646164	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs569200869	chr2:112646174-112646175	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs539989105	chr2:112646175-112646176	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs538120775	chr2:112646186-112646187	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs557480767	chr2:112646196-112646197	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs113682031	chr2:112646224-112646225	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577535325	chr2:112646228-112646229	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs533657005	chr2:112646250-112646251	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs112435928	chr2:112646305-112646306	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs573646637	chr2:112646332-112646333	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs77656951	chr2:112646333-112646334	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs113983765	chr2:112646337-112646338	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs576364078	chr2:112646360-112646361	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs554859039	chr2:112646451-112646452	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200068135	chr2:112646493-112646494	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs545262904	chr2:112646495-112646496	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200906429	chr2:112646507-112646508	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560325163	chr2:112646508-112646509	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs185244091	chr2:112646511-112646512	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs12711665	chr2:112646524-112646525	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs191416931	chr2:112646533-112646534	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112642600-112646200	Weak transcription	Fetal Intestine Large	intestine
2	chr2:112642600-112654400	Weak transcription	Fetal Intestine Small	intestine
3	chr2:112642600-112655000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:112642600-112655000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:112642600-112655000	Weak transcription	Right Atrium	heart
6	chr2:112642800-112655000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:112643000-112653600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:112645200-112645800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:112645200-112645800	Enhancers	Liver	Liver
10	chr2:112645200-112645800	Enhancers	Brain Substantia Nigra	brain
11	chr2:112645200-112645800	Enhancers	HepG2	liver
12	chr2:112645200-112645800	Enhancers	HSMMtube	muscle
13	chr2:112645400-112653200	Weak transcription	K562	blood
14	chr2:112645600-112646200	Enhancers	Duodenum Mucosa	Duodenum
15	chr2:112645600-112646200	Enhancers	Stomach Mucosa	stomach
16	chr2:112645800-112650800	Weak transcription	Liver	Liver
17	chr2:112645800-112653600	Weak transcription	HepG2	liver
18	chr2:112646200-112646400	Enhancers	Fetal Intestine Large	intestine
19	chr2:112646200-112655000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr2:112650800-112651600	Enhancers	Liver	Liver
21	chr2:112651000-112651400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr2:112651400-112653200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr2:112651600-112655000	Weak transcription	Liver	Liver
24	chr2:112653200-112654000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr2:112653200-112655000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr2:112653200-112655000	Enhancers	K562	blood
27	chr2:112653400-112653600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:112653400-112655000	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr2:112653600-112653800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:112653600-112653800	Enhancers	Colonic Mucosa	Colon
31	chr2:112653600-112653800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr2:112653600-112654000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:112653600-112654000	Enhancers	Stomach Mucosa	stomach
34	chr2:112653600-112654800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:112653600-112654800	Enhancers	HepG2	liver
36	chr2:112653600-112655000	Enhancers	Fetal Heart	heart
37	chr2:112653600-112655200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:112653600-112655400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:112653600-112655400	Enhancers	Esophagus	oesophagus
40	chr2:112653600-112655400	Enhancers	Spleen	Spleen
41	chr2:112653800-112654000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:112653800-112654000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr2:112653800-112654000	Enhancers	Lung	lung
44	chr2:112653800-112654200	Enhancers	Fetal Thymus	thymus
45	chr2:112653800-112654600	Enhancers	HMEC	breast
46	chr2:112653800-112654600	Enhancers	NHEK	skin
47	chr2:112653800-112654800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:112653800-112655000	Weak transcription	Colonic Mucosa	Colon
49	chr2:112653800-112655200	Enhancers	Placenta	Placenta
50	chr2:112654000-112654600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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