Variant report

Variant	esv1828473
Chromosome Location	chr2:127653376-127717477
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:127699996-127700663	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:127700046-127700520	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:127699917-127700711	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr2:127700112-127700370	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr2:127693467-127693745	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:127662893-127663051	HepG2	liver:	n/a	n/a
7	BRCA1	chr2:127660620-127660631	HepG2	liver:	n/a	n/a
8	BRCA1	chr2:127704109-127704563	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr2:127701197-127701616	K562	blood:	n/a	n/a
10	CEBPB	chr2:127690181-127690364	A549	lung:	n/a	n/a
11	CEBPB	chr2:127690134-127690410	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:127715617-127715651	HepG2	liver:	n/a	chr2:127715635-127715646
13	CEBPB	chr2:127700142-127700504	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:127696904-127696939	GM10248	blood:	n/a	n/a
15	CTCF	chr2:127714633-127714752	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr2:127709920-127710070	Caco-2	colon:	n/a	n/a
17	CTCF	chr2:127703920-127704070	SK-N-SH_RA	brain:	n/a	chr2:127704018-127704039 chr2:127704023-127704041
18	CTCF	chr2:127700500-127700650	HEK293	kidney:	n/a	chr2:127700574-127700583
19	CTCF	chr2:127703920-127704070	RPTEC	kidney:	n/a	chr2:127704018-127704039 chr2:127704023-127704041
20	CTCF	chr2:127690900-127691050	WERI-Rb-1	eye:	n/a	chr2:127690914-127690927 chr2:127690912-127690930
21	CTCF	chr2:127683421-127683474	GM20000	blood:	n/a	n/a
22	CTCF	chr2:127691780-127691930	HEK293	kidney:	n/a	n/a
23	CTCF	chr2:127691740-127691890	HepG2	liver:	n/a	n/a
24	CTCF	chr2:127703980-127704130	WERI-Rb-1	eye:	n/a	chr2:127704018-127704039 chr2:127704023-127704041
25	CTCF	chr2:127704000-127704150	SK-N-SH_RA	brain:	n/a	chr2:127704018-127704039 chr2:127704023-127704041
26	CTCF	chr2:127690869-127690965	H1-hESC	embryonic stem cell:	n/a	chr2:127690914-127690927 chr2:127690912-127690930
27	CTCF	chr2:127679046-127679068	Lung_OC	lung:	n/a	n/a
28	CTCF	chr2:127700511-127700642	H1-hESC	embryonic stem cell:	n/a	chr2:127700574-127700583
29	E2F4	chr2:127678129-127678423	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr2:127655155-127655205	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F6	chr2:127699901-127700380	H1-hESC	embryonic stem cell:	n/a	n/a
32	E2F6	chr2:127699763-127700818	H1-hESC	embryonic stem cell:	n/a	n/a
33	ELK1	chr2:127668347-127668350	GM12878	blood:	n/a	n/a
34	EP300	chr2:127699968-127700408	H1-hESC	embryonic stem cell:	n/a	n/a
35	EP300	chr2:127703806-127704203	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr2:127693434-127693747	GM12878	blood:	n/a	chr2:127693715-127693729
37	EP300	chr2:127702716-127703002	SK-N-SH_RA	brain:	n/a	chr2:127702796-127702810
38	EP300	chr2:127703791-127704240	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr2:127665821-127667275	SK-N-SH	brain:	n/a	n/a
40	EP300	chr2:127702803-127703035	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr2:127702291-127704709	SK-N-SH	brain:	n/a	chr2:127702796-127702810
42	FAM48A	chr2:127699971-127700131	GM12878	blood:	n/a	n/a
43	FOS	chr2:127690106-127690387	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr2:127690114-127690388	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr2:127709928-127710005	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr2:127709799-127710121	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr2:127709909-127710107	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr2:127690109-127690387	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr2:127709839-127710059	MCF10A-Er-Src	breast:	n/a	n/a
50	FOXA1	chr2:127692255-127692642	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127699673-127699723	HEK293	kidney:	embryo
2	chr2:127713082-127713132	GM12891	blood:	n/a
3	chr2:127705908-127705958	NH-A	brain:	n/a
4	chr2:127705908-127705958	K562	blood:	n/a
5	chr2:127705908-127705958	HL-60	blood:	n/a
6	chr2:127705908-127705958	GM12878	blood:	n/a
7	chr2:127705908-127705958	SK-N-SH_RA	brain:	n/a
8	chr2:127713082-127713132	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:127713082-127713132	ECC-1	luminal epithelium:	n/a
10	chr2:127713082-127713132	HCPEpiC	choroid plexus:	n/a
11	chr2:127699673-127699723	HIPEpiC	eye:	n/a
12	chr2:127699673-127699723	PrEC	prostate:	n/a
13	chr2:127699673-127699723	SK-N-SH	brain:	n/a
14	chr2:127699673-127699723	SK-N-SH_RA	brain:	n/a
15	chr2:127705908-127705958	AG09309	skin:	n/a
16	chr2:127713082-127713132	NHBE	bronchial:	n/a
17	chr2:127699673-127699723	GM12892	blood:	n/a
18	chr2:127713082-127713132	SK-N-MC	brain:	n/a
19	chr2:127705908-127705958	SKMC	muscle:	n/a
20	chr2:127699673-127699723	HCF	heart:	n/a
21	chr2:127699673-127699723	BJ	skin:	n/a
22	chr2:127699673-127699723	GM12878	blood:	n/a
23	chr2:127699673-127699723	PANC-1	pancreas:	n/a
24	chr2:127699673-127699723	HCT-116	colon:	n/a
25	chr2:127705908-127705958	HCPEpiC	choroid plexus:	n/a
26	chr2:127699673-127699723	NT2-D1	testis:	n/a
27	chr2:127699673-127699723	LNCaP	prostate:	n/a
28	chr2:127705908-127705958	HEEpiC	esophagus:	n/a
29	chr2:127699673-127699723	SAEC	small airway:	n/a
30	chr2:127705908-127705958	HepG2	liver:	n/a
31	chr2:127699673-127699723	HRE	kidney:	n/a
32	chr2:127705908-127705958	HCT-116	colon:	n/a
33	chr2:127699673-127699723	HMEC	breast:	n/a
34	chr2:127699673-127699723	BE2_C	brain:	n/a
35	chr2:127705908-127705958	Hela-S3	cervix:	n/a
36	chr2:127713082-127713132	HUVEC	blood vessel:	n/a
37	chr2:127705908-127705958	MCF-7	breast:	n/a
38	chr2:127713082-127713132	GM12892	blood:	n/a
39	chr2:127699673-127699723	ovcar-3	ovarian:	n/a
40	chr2:127705908-127705958	AG04450	lung:	fetal
41	chr2:127713082-127713132	IMR90	lung:	fetal
42	chr2:127699673-127699723	HUVEC	blood vessel:	n/a
43	chr2:127699673-127699723	A549	lung:	n/a
44	chr2:127713082-127713132	HIPEpiC	eye:	n/a
45	chr2:127713082-127713132	BE2_C	brain:	n/a
46	chr2:127699673-127699723	SKMC	muscle:	n/a
47	chr2:127699673-127699723	Hepatocyte	liver:	n/a
48	chr2:127713082-127713132	AG10803	skin:	n/a
49	chr2:127699673-127699723	AG04449	skin:	fetal
50	chr2:127713082-127713132	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:127663020..127665879-chr2:127676391..127678881,2	MCF-7	breast:
2	chr2:127662850..127664564-chr2:127666506..127668375,2	K562	blood:
3	chr2:127662850..127664564-chr2:127666506..127668375,2	K562	blood:
4	chr2:127663020..127665879-chr2:127676391..127678881,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114783.1.1-1	chr2:127656510-127656693	ENSG00000237524
2	lnc-AC114783.1.1-1	chr2:127657412-127657429	ENSG00000237524
3	lnc-AC114783.1.1-1	chr2:127656793-127657003	ENSG00000237524
4	lnc-AC114783.1.1-1	chr2:127656795-127656867	ENSG00000237524
5	lnc-AC114783.1.1-1	chr2:127658786-127658854	ENSG00000237524
6	lnc-AC114783.1.1-1	chr2:127657099-127657188	ENSG00000237524
7	lnc-AC114783.1.1-1	chr2:127657098-127657188	ENSG00000237524
8	lnc-AC114783.1.1-1	chr2:127658786-127658858	ENSG00000237524
9	lnc-AC114783.1.1-1	chr2:127659445-127659673	ENSG00000237524
10	lnc-AC114783.1.1-1	chr2:127659445-127659673	ENSG00000237524

No data

Variant related genes	Relation type
ENSG00000237524	TF binding region
ENSG00000237524	CpG island

Extended variants
information (count: 1807 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1807 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12469732	chr2:127653376-127653377	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528419065	chr2:127653402-127653403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551529710	chr2:127653430-127653431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370242936	chr2:127653431-127653432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555823024	chr2:127653475-127653476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533431236	chr2:127653480-127653481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143982915	chr2:127653485-127653486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534387917	chr2:127653513-127653514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535842010	chr2:127653514-127653515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555846651	chr2:127653550-127653551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369979711	chr2:127653566-127653567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557412630	chr2:127653607-127653608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566340907	chr2:127653669-127653670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535042778	chr2:127653690-127653691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147334735	chr2:127653705-127653706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373610555	chr2:127653737-127653738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185685736	chr2:127653750-127653751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543068817	chr2:127653773-127653774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6721526	chr2:127653813-127653814	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs116861303	chr2:127653838-127653839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189623434	chr2:127653845-127653846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142476998	chr2:127653846-127653847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559111494	chr2:127653998-127653999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115436839	chr2:127654005-127654006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571049806	chr2:127654038-127654039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565062770	chr2:127654061-127654062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141425480	chr2:127654071-127654072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550257081	chr2:127654076-127654077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570161826	chr2:127654120-127654121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368147158	chr2:127654121-127654122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549383638	chr2:127654152-127654153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565956519	chr2:127654183-127654184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535301945	chr2:127654196-127654197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150814827	chr2:127654207-127654208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139310066	chr2:127654225-127654226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371698015	chr2:127654253-127654254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573807708	chr2:127654259-127654260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542918158	chr2:127654262-127654263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557177065	chr2:127654284-127654285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573378267	chr2:127654322-127654323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558097022	chr2:127654387-127654388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542344927	chr2:127654432-127654433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552898025	chr2:127654440-127654441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569267529	chr2:127654441-127654442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551935787	chr2:127654448-127654449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375185224	chr2:127654470-127654471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528029835	chr2:127654506-127654507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144347578	chr2:127654575-127654576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375746541	chr2:127654594-127654595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146089646	chr2:127654628-127654629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127653000-127653800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:127653200-127657400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:127653800-127654400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:127657400-127657800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:127657800-127658200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:127658800-127659000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:127659200-127660400	Enhancers	Fetal Muscle Trunk	muscle
8	chr2:127659600-127660400	Enhancers	Fetal Stomach	stomach
9	chr2:127659800-127660200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
10	chr2:127659800-127660400	Enhancers	Colon Smooth Muscle	Colon
11	chr2:127660000-127660400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:127660000-127660400	Enhancers	Fetal Muscle Leg	muscle
13	chr2:127660200-127661800	Enhancers	HepG2	liver
14	chr2:127662400-127663800	Enhancers	Primary B cells from peripheral blood	blood
15	chr2:127662800-127664000	Enhancers	Primary B cells from cord blood	blood
16	chr2:127663000-127663400	Enhancers	Fetal Brain Male	brain
17	chr2:127663000-127663800	Enhancers	Brain Germinal Matrix	brain
18	chr2:127663400-127663800	Weak transcription	Fetal Brain Male	brain
19	chr2:127663400-127664400	Enhancers	Fetal Stomach	stomach
20	chr2:127663800-127664000	Enhancers	Fetal Brain Male	brain
21	chr2:127663800-127665800	Enhancers	Stomach Smooth Muscle	stomach
22	chr2:127664000-127666000	Weak transcription	Fetal Brain Male	brain
23	chr2:127664400-127664600	Enhancers	Fetal Brain Female	brain
24	chr2:127664400-127665600	Bivalent Enhancer	Fetal Stomach	stomach
25	chr2:127664600-127666200	Weak transcription	Fetal Brain Female	brain
26	chr2:127664800-127665000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:127665000-127669600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr2:127665400-127667600	Enhancers	Rectal Smooth Muscle	rectum
29	chr2:127665600-127665800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr2:127665600-127665800	Enhancers	Colon Smooth Muscle	Colon
31	chr2:127665600-127669800	Enhancers	Fetal Stomach	stomach
32	chr2:127665800-127666200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
33	chr2:127665800-127666600	Enhancers	Brain Germinal Matrix	brain
34	chr2:127665800-127666800	Weak transcription	Colon Smooth Muscle	Colon
35	chr2:127666000-127667000	Enhancers	Fetal Brain Male	brain
36	chr2:127666200-127666600	Enhancers	Ovary	ovary
37	chr2:127666200-127666600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
38	chr2:127666200-127667000	Enhancers	Fetal Lung	lung
39	chr2:127666200-127667200	Enhancers	Fetal Brain Female	brain
40	chr2:127666400-127666600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:127666400-127667600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:127666600-127666800	Active TSS	Stomach Smooth Muscle	stomach
43	chr2:127666800-127667000	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr2:127666800-127667600	Enhancers	Colon Smooth Muscle	Colon
45	chr2:127667000-127667600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
46	chr2:127667000-127671600	Weak transcription	Fetal Brain Male	brain
47	chr2:127667200-127672600	Weak transcription	Fetal Brain Female	brain
48	chr2:127668200-127668800	Enhancers	Primary hematopoietic stem cells	blood
49	chr2:127668200-127668800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr2:127669600-127669800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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