Variant report

Variant	nsv961678
Chromosome Location	chr2:127961305-127979990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:291)
CpG islands
(count:1220)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:127978469-127978928	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:127978610-127978921	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:127977021-127977221	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:127976536-127976757	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:127978408-127978681	A549	lung:	n/a	n/a
6	CEBPB	chr2:127978376-127978690	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:127974884-127975840	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr2:127964619-127964663	K562	blood:	n/a	n/a
9	CEBPB	chr2:127978350-127978767	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr2:127977925-127978781	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr2:127976706-127977050	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr2:127966057-127966280	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr2:127966010-127966272	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr2:127976626-127976629	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr2:127978295-127978965	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr2:127975550-127975833	Hela-S3	cervix:	n/a	n/a
17	CREB1	chr2:127975536-127975824	A549	lung:	n/a	n/a
18	CTBP2	chr2:127978461-127978935	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr2:127976359-127977309	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr2:127977380-127977530	AG04449	skin:	n/a	n/a
21	CTCF	chr2:127976456-127976468	A549	lung:	n/a	n/a
22	CTCF	chr2:127976409-127976539	NHEK	skin:	n/a	n/a
23	CTCF	chr2:127977840-127977990	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr2:127976500-127976650	AG04449	skin:	n/a	chr2:127976619-127976635 chr2:127976618-127976636
25	CTCF	chr2:127977220-127977370	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr2:127976580-127976730	HEEpiC	esophagus:	n/a	chr2:127976619-127976635 chr2:127976618-127976636
27	CTCF	chr2:127967258-127967361	LNCaP	prostate:	n/a	n/a
28	CTCF	chr2:127976420-127976570	A549	lung:	n/a	n/a
29	CTCF	chr2:127977080-127977230	HRE	kidney:	n/a	chr2:127977149-127977158
30	CTCF	chr2:127976560-127976710	HUVEC	blood vessel:	n/a	chr2:127976619-127976635 chr2:127976618-127976636
31	CTCF	chr2:127977320-127977470	HMEC	breast:	n/a	n/a
32	CTCF	chr2:127976500-127976650	BJ	skin:	n/a	chr2:127976619-127976635 chr2:127976618-127976636
33	CTCF	chr2:127968296-127968336	LNCaP	prostate:	n/a	n/a
34	CTCF	chr2:127965640-127965790	HMEC	breast:	n/a	n/a
35	CTCF	chr2:127976480-127976630	AG04449	skin:	n/a	n/a
36	CTCF	chr2:127965640-127965790	HRE	kidney:	n/a	n/a
37	CTCF	chr2:127976760-127976910	AG04449	skin:	n/a	chr2:127976889-127976898 chr2:127976889-127976902
38	CTCF	chr2:127977920-127978070	A549	lung:	n/a	n/a
39	CTCF	chr2:127976470-127976487	A549	lung:	n/a	n/a
40	CTCF	chr2:127975460-127975610	HMEC	breast:	n/a	chr2:127975534-127975552
41	CTCF	chr2:127963140-127963290	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr2:127965660-127965810	A549	lung:	n/a	n/a
43	CTCF	chr2:127976418-127976522	Fibrobl	skin:	n/a	n/a
44	CTCF	chr2:127963180-127963330	NHEK	skin:	n/a	n/a
45	CTCF	chr2:127976500-127976650	SK-N-SH_RA	brain:	n/a	chr2:127976619-127976635 chr2:127976618-127976636
46	CTCF	chr2:127976520-127976670	HMEC	breast:	n/a	chr2:127976618-127976636 chr2:127976619-127976635
47	CTCF	chr2:127968902-127969018	GM10248	blood:	n/a	n/a
48	CTCF	chr2:127965680-127965830	HEK293	kidney:	n/a	n/a
49	CTCF	chr2:127976480-127976630	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr2:127976580-127976730	HBMEC	blood vessel:	n/a	chr2:127976619-127976635 chr2:127976618-127976636

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127963590-127963640	HIPEpiC	eye:	n/a
2	chr2:127976400-127976450	AG10803	skin:	n/a
3	chr2:127977385-127977435	AG10803	skin:	n/a
4	chr2:127963653-127963703	BJ	skin:	n/a
5	chr2:127975738-127975788	HEK293	kidney:	embryo
6	chr2:127976928-127976978	AG10803	skin:	n/a
7	chr2:127976400-127976450	AG09319	gingival:	n/a
8	chr2:127976351-127976401	NHBE	bronchial:	n/a
9	chr2:127963590-127963640	U87	brain:	n/a
10	chr2:127963330-127963380	HNPCEpiC	eye:	n/a
11	chr2:127977559-127977609	LNCaP	prostate:	n/a
12	chr2:127964374-127964424	HCM	heart:	n/a
13	chr2:127963653-127963703	SAEC	small airway:	n/a
14	chr2:127976928-127976978	SAEC	small airway:	n/a
15	chr2:127977385-127977435	HCPEpiC	choroid plexus:	n/a
16	chr2:127978579-127978629	AG09319	gingival:	n/a
17	chr2:127976351-127976401	HNPCEpiC	eye:	n/a
18	chr2:127977385-127977435	IMR90	lung:	fetal
19	chr2:127963330-127963380	HRPEpiC	eye:	n/a
20	chr2:127963503-127963553	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:127978579-127978629	Hepatocyte	liver:	n/a
22	chr2:127976351-127976401	MCF10A-Er-Src	breast:	n/a
23	chr2:127976928-127976978	GM12892	blood:	n/a
24	chr2:127978579-127978629	HepG2	liver:	n/a
25	chr2:127976738-127976788	RPTEC	kidney:	n/a
26	chr2:127963489-127963539	HepG2	liver:	n/a
27	chr2:127976613-127976663	GM12891	blood:	n/a
28	chr2:127963653-127963703	LNCaP	prostate:	n/a
29	chr2:127977385-127977435	H1-hESC	embryonic stem cell:	embryo
30	chr2:127977849-127977899	Jurkat	blood:	n/a
31	chr2:127976613-127976663	AG04449	skin:	fetal
32	chr2:127976400-127976450	Hela-S3	cervix:	n/a
33	chr2:127963503-127963553	GM12878	blood:	n/a
34	chr2:127973314-127973364	BJ	skin:	n/a
35	chr2:127978490-127978540	GM12878	blood:	n/a
36	chr2:127975738-127975788	HUVEC	blood vessel:	n/a
37	chr2:127963330-127963380	BJ	skin:	n/a
38	chr2:127978579-127978629	HCPEpiC	choroid plexus:	n/a
39	chr2:127978490-127978540	NB4	blood:	n/a
40	chr2:127963489-127963539	AoSMC	blood vessel:	n/a
41	chr2:127976351-127976401	A549	lung:	n/a
42	chr2:127963512-127963562	RPTEC	kidney:	n/a
43	chr2:127975738-127975788	NT2-D1	testis:	n/a
44	chr2:127963590-127963640	BJ	skin:	n/a
45	chr2:127963489-127963539	HCT-116	colon:	n/a
46	chr2:127977849-127977899	SK-N-SH_RA	brain:	n/a
47	chr2:127977559-127977609	NHDF-neo	bronchial:	n/a
48	chr2:127976613-127976663	AG10803	skin:	n/a
49	chr2:127976351-127976401	HCF	heart:	n/a
50	chr2:127963067-127963117	HUVEC	blood vessel:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:127965809..127968370-chr2:127982231..127984174,2	K562	blood:
2	chr2:127978350..127980779-chr2:127984214..127985920,2	MCF-7	breast:
3	chr2:127972542..127975941-chr2:127982453..127985678,4	MCF-7	breast:
4	chr2:127973375..127977110-chr2:128049967..128052200,3	MCF-7	breast:
5	chr2:127961531..127964078-chr2:127974115..127976124,2	MCF-7	breast:
6	chr2:127975205..127977314-chr2:127992465..127995136,2	K562	blood:
7	chr2:127974300..127976848-chr2:127983797..127985574,2	MCF-7	breast:
8	chr2:127957550..127959520-chr2:127975505..127977152,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERCC3-1	chr2:127975143-127976209	ucscGeneNc_uc002too_1

No data

Variant related genes	Relation type
CYP27C1	TF binding region
CYP27C1	CpG island
ENSG00000186684	chromatin interactions
ENSG00000163161	chromatin interactions

Extended variants
information (count: 660 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560399750	chr2:127961305-127961306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532168294	chr2:127961309-127961310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184250857	chr2:127961331-127961332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188312598	chr2:127961404-127961405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531064272	chr2:127961420-127961421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550548745	chr2:127961424-127961425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116450162	chr2:127961440-127961441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113815201	chr2:127961479-127961480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201850556	chr2:127961491-127961492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553207143	chr2:127961590-127961591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144047746	chr2:127961591-127961592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538826167	chr2:127961607-127961608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559133165	chr2:127961647-127961648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181809501	chr2:127961698-127961699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377003183	chr2:127961709-127961710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544363143	chr2:127961758-127961759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111403484	chr2:127961821-127961822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150945515	chr2:127961829-127961830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371053819	chr2:127961852-127961853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373742078	chr2:127961857-127961858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557108069	chr2:127961900-127961901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28457590	chr2:127961967-127961968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373446642	chr2:127961970-127961971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199875635	chr2:127961971-127961972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189574827	chr2:127961978-127961979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs59482629	chr2:127962017-127962018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs70985437	chr2:127962029-127962030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373380422	chr2:127962047-127962048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377389810	chr2:127962055-127962056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369842924	chr2:127962062-127962063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13007073	chr2:127962065-127962066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200541036	chr2:127962069-127962070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370776278	chr2:127962072-127962073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375073806	chr2:127962076-127962077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367996775	chr2:127962080-127962081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112411551	chr2:127962084-127962085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71343621	chr2:127962088-127962089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371754035	chr2:127962089-127962090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186935649	chr2:127962092-127962093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191415124	chr2:127962096-127962097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373646876	chr2:127962106-127962107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199976034	chr2:127962111-127962112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372686054	chr2:127962112-127962113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183018394	chr2:127962119-127962120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12692062	chr2:127962131-127962132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377497623	chr2:127962134-127962135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189775700	chr2:127962166-127962167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150046806	chr2:127962178-127962179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560155113	chr2:127962180-127962181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145335260	chr2:127962182-127962183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Breast cancer	22522925	CNVD

Chromatin state (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127934600-127965600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:127941000-127963000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:127948800-127973400	Weak transcription	HMEC	breast
4	chr2:127951200-127965800	Weak transcription	Esophagus	oesophagus
5	chr2:127951400-127962200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:127952000-127963000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr2:127952200-127964400	Weak transcription	Right Atrium	heart
8	chr2:127952200-127975200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:127954200-127964000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr2:127954600-127962800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr2:127954800-127965600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:127955000-127965600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr2:127955600-127962800	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:127955800-127963000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr2:127956000-127961400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:127956400-127975800	Weak transcription	Fetal Kidney	kidney
17	chr2:127957200-127962600	Weak transcription	Fetal Brain Female	brain
18	chr2:127957400-127962200	Weak transcription	Fetal Lung	lung
19	chr2:127957400-127965800	Weak transcription	NHEK	skin
20	chr2:127957800-127963200	Weak transcription	Fetal Intestine Small	intestine
21	chr2:127959200-127963000	Weak transcription	Fetal Muscle Leg	muscle
22	chr2:127959400-127962200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr2:127959400-127962400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:127959400-127962600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:127959400-127963000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:127959400-127965800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr2:127959600-127962400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:127959600-127963000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr2:127960800-127961400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:127960800-127961600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:127961000-127962400	Weak transcription	Fetal Stomach	stomach
32	chr2:127961000-127963200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:127961200-127965800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:127961400-127961800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:127961400-127961800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:127961400-127965800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:127961600-127962400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:127961800-127963000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:127962200-127962600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr2:127962200-127962800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:127962200-127963000	Enhancers	Fetal Lung	lung
42	chr2:127962400-127962800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr2:127962400-127963200	Enhancers	Fetal Brain Male	brain
44	chr2:127962400-127963400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:127962400-127963400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr2:127962400-127963600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:127962400-127963600	Enhancers	Placenta	Placenta
48	chr2:127962400-127963600	Genic enhancers	Fetal Stomach	stomach
49	chr2:127962600-127963000	Enhancers	Fetal Brain Female	brain
50	chr2:127962600-127963600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links