Variant report

Variant	esv3460557
Chromosome Location	chr2:112675200-112684076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112675986-112676431	K562	blood:	n/a	n/a
2	ARID3A	chr2:112677585-112678236	HepG2	liver:	n/a	n/a
3	BACH1	chr2:112680681-112680804	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:112675663-112676483	K562	blood:	n/a	n/a
5	BHLHE40	chr2:112676060-112676749	K562	blood:	n/a	n/a
6	BHLHE40	chr2:112677044-112677355	K562	blood:	n/a	n/a
7	BRCA1	chr2:112682375-112682657	HepG2	liver:	n/a	n/a
8	BRCA1	chr2:112677810-112678131	HepG2	liver:	n/a	n/a
9	CCNT2	chr2:112675983-112676723	K562	blood:	n/a	n/a
10	CEBPB	chr2:112677108-112677246	K562	blood:	n/a	n/a
11	CEBPB	chr2:112675902-112676388	MCF-7	breast:	n/a	chr2:112676014-112676031
12	CEBPB	chr2:112675897-112676565	K562	blood:	n/a	chr2:112676519-112676536 chr2:112676014-112676031
13	CEBPB	chr2:112675923-112676392	IMR90	lung:	n/a	chr2:112676014-112676031
14	CEBPB	chr2:112675941-112676456	K562	blood:	n/a	chr2:112676014-112676031
15	CEBPB	chr2:112684068-112684622	HepG2	liver:	n/a	chr2:112684254-112684265
16	CEBPB	chr2:112677815-112678162	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:112675965-112676279	HepG2	liver:	n/a	chr2:112676014-112676031
18	CEBPD	chr2:112676018-112676488	K562	blood:	n/a	n/a
19	CEBPD	chr2:112677717-112678106	HepG2	liver:	n/a	n/a
20	CHD2	chr2:112677738-112678105	HepG2	liver:	n/a	n/a
21	CHD2	chr2:112676680-112676728	K562	blood:	n/a	n/a
22	CTCF	chr2:112681500-112681564	K562	blood:	n/a	n/a
23	CTCF	chr2:112677060-112677210	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr2:112677110-112677165	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr2:112677053-112677221	HepG2	liver:	n/a	n/a
26	CTCF	chr2:112680960-112681110	AG09319	gingival:	n/a	n/a
27	CTCF	chr2:112677020-112677170	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr2:112677140-112677155	GM19239	blood:	n/a	n/a
29	CTCF	chr2:112677080-112677230	HAc	cerebellar:	n/a	n/a
30	CTCF	chr2:112677080-112677230	GM12864	blood:	n/a	n/a
31	CTCF	chr2:112680840-112680990	AG04450	lung:	n/a	n/a
32	CTCF	chr2:112677540-112677690	HPF	lung:	n/a	n/a
33	CTCF	chr2:112677100-112677250	GM12864	blood:	n/a	n/a
34	CTCF	chr2:112680880-112681030	HMF	breast:	n/a	n/a
35	CTCF	chr2:112677700-112677850	HPF	lung:	n/a	n/a
36	CTCF	chr2:112677040-112677190	GM12868	blood:	n/a	n/a
37	CTCF	chr2:112677119-112677181	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:112677100-112677250	GM12873	blood:	n/a	n/a
39	CTCF	chr2:112677040-112677190	HCM	heart:	n/a	n/a
40	CTCF	chr2:112677083-112677175	GM10266	blood:	n/a	n/a
41	CTCF	chr2:112677075-112677199	ProgFib	skin:	n/a	n/a
42	CTCF	chr2:112677120-112677270	Caco-2	colon:	n/a	n/a
43	CTCF	chr2:112680620-112680770	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr2:112676972-112677255	HepG2	liver:	n/a	n/a
45	CTCF	chr2:112676965-112677237	K562	blood:	n/a	n/a
46	CTCF	chr2:112677740-112677890	HepG2	liver:	n/a	n/a
47	CTCF	chr2:112677003-112677435	A549	lung:	n/a	n/a
48	CTCF	chr2:112677080-112677230	GM12872	blood:	n/a	n/a
49	CTCF	chr2:112677100-112677250	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr2:112677111-112677202	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112676834-112676884	SK-N-MC	brain:	n/a
2	chr2:112676834-112676884	HCT-116	colon:	n/a
3	chr2:112676834-112676884	HMEC	breast:	n/a
4	chr2:112676834-112676884	BJ	skin:	n/a
5	chr2:112676834-112676884	K562	blood:	n/a
6	chr2:112676834-112676884	HIPEpiC	eye:	n/a
7	chr2:112676834-112676884	HEEpiC	esophagus:	n/a
8	chr2:112676834-112676884	HL-60	blood:	n/a
9	chr2:112676834-112676884	Jurkat	blood:	n/a
10	chr2:112676834-112676884	HRPEpiC	eye:	n/a
11	chr2:112676834-112676884	A549	lung:	n/a
12	chr2:112676834-112676884	LNCaP	prostate:	n/a
13	chr2:112676834-112676884	BE2_C	brain:	n/a
14	chr2:112676834-112676884	CMK	blood:	n/a
15	chr2:112676834-112676884	SK-N-SH_RA	brain:	n/a
16	chr2:112676834-112676884	ProgFib	skin:	n/a
17	chr2:112676834-112676884	HCM	heart:	n/a
18	chr2:112676834-112676884	HUVEC	blood vessel:	n/a
19	chr2:112676834-112676884	HNPCEpiC	eye:	n/a
20	chr2:112676834-112676884	AG09319	gingival:	n/a
21	chr2:112676834-112676884	AG09309	skin:	n/a
22	chr2:112676834-112676884	Caco-2	colon:	n/a
23	chr2:112676834-112676884	PrEC	prostate:	n/a
24	chr2:112676834-112676884	AoSMC	blood vessel:	n/a
25	chr2:112676834-112676884	MCF10A-Er-Src	breast:	n/a
26	chr2:112676834-112676884	Hela-S3	cervix:	n/a
27	chr2:112676834-112676884	NHDF-neo	bronchial:	n/a
28	chr2:112676834-112676884	NB4	blood:	n/a
29	chr2:112676834-112676884	PFSK-1	brain:	n/a
30	chr2:112676834-112676884	RPTEC	kidney:	n/a
31	chr2:112676834-112676884	ECC-1	luminal epithelium:	n/a
32	chr2:112676834-112676884	HAEpiC	amniotic membrane:	n/a
33	chr2:112676834-112676884	SK-N-SH	brain:	n/a
34	chr2:112676834-112676884	HCF	heart:	n/a
35	chr2:112676834-112676884	H1-hESC	embryonic stem cell:	embryo
36	chr2:112676834-112676884	GM12892	blood:	n/a
37	chr2:112676834-112676884	HCPEpiC	choroid plexus:	n/a
38	chr2:112676834-112676884	HRE	kidney:	n/a
39	chr2:112676834-112676884	HRCEpiC	kidney:	n/a
40	chr2:112676834-112676884	NT2-D1	testis:	n/a
41	chr2:112676834-112676884	T-47D	breast:	n/a
42	chr2:112676834-112676884	Hepatocyte	liver:	n/a
43	chr2:112676834-112676884	HepG2	liver:	n/a
44	chr2:112676834-112676884	MCF-7	breast:	n/a
45	chr2:112676834-112676884	SKMC	muscle:	n/a
46	chr2:112676834-112676884	GM12878	blood:	n/a
47	chr2:112676834-112676884	HPAEpiC	pulmonary alveolar:	n/a
48	chr2:112676834-112676884	ovcar-3	ovarian:	n/a
49	chr2:112676834-112676884	GM19239	blood:	n/a
50	chr2:112676834-112676884	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr2:112655330..112658154-chr2:112679462..112681101,2	K562	blood:
2	chr2:112680614..112683730-chr2:112685370..112687144,3	K562	blood:
3	chr2:112659908..112662713-chr2:112675959..112678023,2	MCF-7	breast:
4	chr2:112640047..112642030-chr2:112676094..112677687,2	K562	blood:

No data

Variant related genes	Relation type
RN7SL297P	TF binding region
RN7SL297P	CpG island
ENSG00000153107	chromatin interactions
ENSG00000153208	chromatin interactions

Extended variants
information (count: 318 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148925013	chr2:112675229-112675230	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531581854	chr2:112675230-112675231	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372602890	chr2:112675239-112675240	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532735472	chr2:112675291-112675292	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575135605	chr2:112675299-112675300	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184263136	chr2:112675306-112675307	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564020280	chr2:112675330-112675331	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188897487	chr2:112675334-112675335	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540617864	chr2:112675335-112675336	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143209968	chr2:112675376-112675377	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4290663	chr2:112675392-112675393	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs548305413	chr2:112675417-112675418	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181636073	chr2:112675432-112675433	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549682707	chr2:112675460-112675461	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11443176	chr2:112675461-112675462	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6541951	chr2:112675519-112675520	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs533235554	chr2:112675565-112675566	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549524225	chr2:112675606-112675607	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185320071	chr2:112675629-112675630	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190612568	chr2:112675697-112675698	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558536927	chr2:112675752-112675753	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140305297	chr2:112675755-112675756	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145401174	chr2:112675882-112675883	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554747642	chr2:112675916-112675917	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182222178	chr2:112675923-112675924	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543288392	chr2:112675940-112675941	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544036122	chr2:112675947-112675948	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557245520	chr2:112675991-112675992	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577482463	chr2:112675993-112675994	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546215382	chr2:112676021-112676022	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559975714	chr2:112676042-112676043	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528512346	chr2:112676059-112676060	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs137946694	chr2:112676071-112676072	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142419324	chr2:112676096-112676097	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7571447	chr2:112676128-112676129	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs549967333	chr2:112676182-112676183	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186018249	chr2:112676209-112676210	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145963844	chr2:112676260-112676261	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs552214136	chr2:112676271-112676272	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs189767881	chr2:112676292-112676293	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs534612794	chr2:112676300-112676301	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs548164883	chr2:112676306-112676307	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568186322	chr2:112676429-112676430	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569686808	chr2:112676476-112676477	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs138396824	chr2:112676486-112676487	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557002471	chr2:112676524-112676525	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577395711	chr2:112676529-112676530	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149244860	chr2:112676634-112676635	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181093739	chr2:112676641-112676642	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185481165	chr2:112676661-112676662	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112662800-112675800	Weak transcription	Fetal Muscle Leg	muscle
2	chr2:112662800-112677000	Weak transcription	Spleen	Spleen
3	chr2:112663000-112677800	Weak transcription	Right Ventricle	heart
4	chr2:112664600-112675800	Weak transcription	HUVEC	blood vessel
5	chr2:112664600-112676000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr2:112664600-112676600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr2:112664600-112687600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr2:112664600-112702200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr2:112664800-112675600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr2:112664800-112676200	Weak transcription	Thymus	Thymus
11	chr2:112664800-112676600	Weak transcription	Pancreas	Pancrea
12	chr2:112666400-112680200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr2:112666400-112681800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr2:112666400-112692800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:112666600-112680800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr2:112666800-112675600	Weak transcription	K562	blood
17	chr2:112666800-112677400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr2:112667000-112682000	Weak transcription	Aorta	Aorta
19	chr2:112667000-112684400	Weak transcription	Brain Angular Gyrus	brain
20	chr2:112667200-112675800	Weak transcription	Fetal Intestine Large	intestine
21	chr2:112667400-112676000	Weak transcription	Colon Smooth Muscle	Colon
22	chr2:112667800-112682000	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr2:112668800-112676000	Weak transcription	Adipose Nuclei	Adipose
24	chr2:112668800-112676400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr2:112668800-112676600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:112668800-112677200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr2:112668800-112680600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:112669000-112676000	Weak transcription	Brain Hippocampus Middle	brain
29	chr2:112669000-112677000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr2:112669000-112677400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:112670400-112675800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr2:112670400-112677000	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr2:112670600-112676000	Weak transcription	Small Intestine	intestine
34	chr2:112670600-112677200	Weak transcription	Left Ventricle	heart
35	chr2:112670600-112677400	Weak transcription	Ovary	ovary
36	chr2:112670600-112677800	Weak transcription	Right Atrium	heart
37	chr2:112670800-112684600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:112674400-112676800	Genic enhancers	HepG2	liver
39	chr2:112674600-112675200	Enhancers	Brain Substantia Nigra	brain
40	chr2:112674600-112675200	Strong transcription	Fetal Intestine Small	intestine
41	chr2:112674600-112675200	Enhancers	Gastric	stomach
42	chr2:112674600-112687400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:112674800-112675400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:112674800-112676000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr2:112674800-112687600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr2:112675000-112676000	Weak transcription	Brain Anterior Caudate	brain
47	chr2:112675000-112676000	Weak transcription	Placenta	Placenta
48	chr2:112675000-112676000	Weak transcription	Fetal Stomach	stomach
49	chr2:112675000-112676600	Weak transcription	Lung	lung
50	chr2:112675000-112679400	Enhancers	Liver	Liver

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