Variant report

Variant	nsv817851
Chromosome Location	chr2:48941428-48973127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:305)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:48953356-48953556	K562	blood:	n/a	n/a
2	BHLHE40	chr2:48942448-48942774	K562	blood:	n/a	n/a
3	CEBPB	chr2:48950315-48950600	H1-hESC	embryonic stem cell:	n/a	chr2:48950437-48950450 chr2:48950379-48950391
4	CEBPB	chr2:48948433-48948535	A549	lung:	n/a	n/a
5	CEBPB	chr2:48945012-48945293	HepG2	liver:	n/a	chr2:48945177-48945188
6	CEBPB	chr2:48944996-48945351	IMR90	lung:	n/a	chr2:48945177-48945188
7	CEBPB	chr2:48945017-48945336	K562	blood:	n/a	chr2:48945177-48945188
8	CEBPB	chr2:48945080-48945346	ECC-1	luminal epithelium:	n/a	chr2:48945177-48945188
9	CEBPB	chr2:48962168-48962257	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:48942390-48942990	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:48948846-48948944	HepG2	liver:	n/a	chr2:48948890-48948901
12	CEBPB	chr2:48945061-48945333	H1-hESC	embryonic stem cell:	n/a	chr2:48945177-48945188
13	CEBPB	chr2:48950088-48950754	IMR90	lung:	n/a	chr2:48950437-48950450 chr2:48950379-48950391
14	CEBPB	chr2:48962045-48962384	IMR90	lung:	n/a	n/a
15	CHD1	chr2:48965950-48966331	IMR90	lung:	n/a	n/a
16	CTCF	chr2:48954795-48955017	LNCaP	prostate:	n/a	chr2:48954895-48954916
17	CTCF	chr2:48952977-48953097	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr2:48944879-48944905	GM10248	blood:	n/a	n/a
19	CTCF	chr2:48952972-48953074	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:48954721-48954986	H1-hESC	embryonic stem cell:	n/a	chr2:48954895-48954916
21	CTCF	chr2:48952920-48953070	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr2:48966000-48966150	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr2:48952971-48953166	GM12878	blood:	n/a	n/a
24	CTCF	chr2:48954840-48954990	HCM	heart:	n/a	chr2:48954895-48954916
25	CTCF	chr2:48954800-48954950	MCF-7	breast:	n/a	chr2:48954895-48954916
26	CTCF	chr2:48954580-48954730	HCM	heart:	n/a	n/a
27	CTCF	chr2:48954842-48954990	Hela-S3	cervix:	n/a	chr2:48954895-48954916
28	CTCF	chr2:48952949-48953130	HepG2	liver:	n/a	n/a
29	CTCF	chr2:48954880-48955030	HCM	heart:	n/a	chr2:48954895-48954916
30	CTCF	chr2:48954786-48955014	MCF-7	breast:	n/a	chr2:48954895-48954916
31	CTCF	chr2:48954798-48955011	Gliobla	brain:	n/a	chr2:48954895-48954916
32	CTCF	chr2:48952980-48953098	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:48954620-48954910	AG09309	skin:	n/a	n/a
34	CTCF	chr2:48955060-48955210	GM12870	blood:	n/a	n/a
35	CTCF	chr2:48954757-48955011	ECC-1	luminal epithelium:	n/a	chr2:48954895-48954916
36	CTCF	chr2:48954820-48954970	WERI-Rb-1	eye:	n/a	chr2:48954895-48954916
37	CTCF	chr2:48952900-48953050	A549	lung:	n/a	n/a
38	CTCF	chr2:48953040-48953190	HCM	heart:	n/a	n/a
39	CTCF	chr2:48954880-48955030	HVMF	connective:	n/a	chr2:48954895-48954916
40	CTCF	chr2:48964940-48965090	HMF	breast:	n/a	n/a
41	CTCF	chr2:48952986-48953075	GM12892	blood:	n/a	n/a
42	CTCF	chr2:48952920-48953084	T-47D	breast:	n/a	n/a
43	CTCF	chr2:48952977-48953060	GM12878	blood:	n/a	n/a
44	CTCF	chr2:48952900-48953133	HepG2	liver:	n/a	n/a
45	CTCF	chr2:48952920-48953070	HepG2	liver:	n/a	n/a
46	CTCF	chr2:48954800-48954950	GM12870	blood:	n/a	chr2:48954895-48954916
47	CTCF	chr2:48954815-48954997	GM12878	blood:	n/a	chr2:48954895-48954916
48	CTCF	chr2:48954816-48955009	SK-N-SH_RA	brain:	n/a	chr2:48954895-48954916
49	CTCF	chr2:48952865-48953141	K562	blood:	n/a	n/a
50	CTCF	chr2:48954820-48954970	GM12872	blood:	n/a	chr2:48954895-48954916

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:48960164-48960214	HEK293	kidney:	embryo
2	chr2:48956876-48956926	ovcar-3	ovarian:	n/a
3	chr2:48946375-48946425	AG10803	skin:	n/a
4	chr2:48956876-48956926	SAEC	small airway:	n/a
5	chr2:48960164-48960214	MCF10A-Er-Src	breast:	n/a
6	chr2:48956876-48956926	NH-A	brain:	n/a
7	chr2:48956876-48956926	MCF10A-Er-Src	breast:	n/a
8	chr2:48956876-48956926	AG04450	lung:	fetal
9	chr2:48956876-48956926	HUVEC	blood vessel:	n/a
10	chr2:48950153-48950203	HCPEpiC	choroid plexus:	n/a
11	chr2:48960164-48960214	A549	lung:	n/a
12	chr2:48946375-48946425	SK-N-MC	brain:	n/a
13	chr2:48946375-48946425	HAEpiC	amniotic membrane:	n/a
14	chr2:48962273-48962323	SAEC	small airway:	n/a
15	chr2:48956876-48956926	H1-hESC	embryonic stem cell:	embryo
16	chr2:48962273-48962323	AG09319	gingival:	n/a
17	chr2:48960164-48960214	ovcar-3	ovarian:	n/a
18	chr2:48956876-48956926	NT2-D1	testis:	n/a
19	chr2:48946375-48946425	HUVEC	blood vessel:	n/a
20	chr2:48946375-48946425	Hela-S3	cervix:	n/a
21	chr2:48956876-48956926	AG10803	skin:	n/a
22	chr2:48956876-48956926	BJ	skin:	n/a
23	chr2:48946375-48946425	HRPEpiC	eye:	n/a
24	chr2:48950153-48950203	CMK	blood:	n/a
25	chr2:48946375-48946425	HL-60	blood:	n/a
26	chr2:48956876-48956926	HCPEpiC	choroid plexus:	n/a
27	chr2:48960164-48960214	AG04449	skin:	fetal
28	chr2:48962273-48962323	HAEpiC	amniotic membrane:	n/a
29	chr2:48950153-48950203	SK-N-MC	brain:	n/a
30	chr2:48946375-48946425	U87	brain:	n/a
31	chr2:48960164-48960214	HepG2	liver:	n/a
32	chr2:48956876-48956926	Hepatocyte	liver:	n/a
33	chr2:48946375-48946425	ovcar-3	ovarian:	n/a
34	chr2:48946375-48946425	Hepatocyte	liver:	n/a
35	chr2:48956876-48956926	ProgFib	skin:	n/a
36	chr2:48962273-48962323	NB4	blood:	n/a
37	chr2:48950153-48950203	SK-N-SH	brain:	n/a
38	chr2:48946375-48946425	H1-hESC	embryonic stem cell:	embryo
39	chr2:48956876-48956926	GM19239	blood:	n/a
40	chr2:48960164-48960214	IMR90	lung:	fetal
41	chr2:48962273-48962323	ovcar-3	ovarian:	n/a
42	chr2:48956876-48956926	HRE	kidney:	n/a
43	chr2:48956876-48956926	PrEC	prostate:	n/a
44	chr2:48962273-48962323	SKMC	muscle:	n/a
45	chr2:48956876-48956926	HCF	heart:	n/a
46	chr2:48946375-48946425	BJ	skin:	n/a
47	chr2:48956876-48956926	GM12891	blood:	n/a
48	chr2:48946375-48946425	ProgFib	skin:	n/a
49	chr2:48950153-48950203	HMEC	breast:	n/a
50	chr2:48962273-48962323	HCM	heart:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:48947110..48949799-chr2:48950949..48954085,3	K562	blood:
2	chr2:48947110..48949799-chr2:48950949..48954085,3	K562	blood:
3	chr2:48955353..48957599-chr2:48959365..48961603,2	MCF-7	breast:
4	chr2:48899103..48900749-chr2:48945263..48947505,2	MCF-7	breast:
5	chr2:48938808..48941243-chr2:48942125..48945142,3	K562	blood:
6	chr2:48955353..48957599-chr2:48959365..48961603,2	MCF-7	breast:
7	chr2:48959559..48961435-chr2:48964209..48965937,2	K562	blood:
8	chr2:48947110..48950890-chr2:48950949..48954085,5	K562	blood:
9	chr2:48959559..48961435-chr2:48964209..48965937,2	K562	blood:

No data

Variant related genes	Relation type
LHCGR	TF binding region
LHCGR	CpG island
ENSG00000138039	chromatin interactions

Extended variants
information (count: 1327 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1327 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4953616	chr2:48941428-48941429	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371442320	chr2:48941431-48941432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189575021	chr2:48941473-48941474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180802531	chr2:48941477-48941478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553496147	chr2:48941507-48941508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183931454	chr2:48941536-48941537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546783378	chr2:48941549-48941550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189546550	chr2:48941555-48941556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181374493	chr2:48941561-48941562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17326446	chr2:48941564-48941565	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs186586474	chr2:48941600-48941601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544060685	chr2:48941605-48941606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565350860	chr2:48941608-48941609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375335258	chr2:48941623-48941624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532514599	chr2:48941629-48941630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61510695	chr2:48941636-48941637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200567974	chr2:48941639-48941640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541376423	chr2:48941664-48941665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10445930	chr2:48941670-48941671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559492765	chr2:48941677-48941678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530148416	chr2:48941698-48941699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548849617	chr2:48941719-48941720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567250816	chr2:48941742-48941743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531375352	chr2:48941744-48941745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139106663	chr2:48941781-48941782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545313673	chr2:48941800-48941801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116329600	chr2:48941814-48941815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538355991	chr2:48941824-48941825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370192934	chr2:48941849-48941850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547514181	chr2:48941866-48941867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140441677	chr2:48941879-48941880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367600055	chr2:48941880-48941881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62135393	chr2:48941881-48941882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113272578	chr2:48941891-48941892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200627856	chr2:48941893-48941894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368299031	chr2:48941895-48941896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565532349	chr2:48941899-48941900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536281651	chr2:48941903-48941904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372057357	chr2:48941905-48941906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4337523	chr2:48941910-48941911	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576834399	chr2:48941934-48941935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191947558	chr2:48942036-48942037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181801068	chr2:48942047-48942048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568908074	chr2:48942069-48942070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149929451	chr2:48942074-48942075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557755063	chr2:48942088-48942089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571125507	chr2:48942097-48942098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374888937	chr2:48942127-48942128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112042300	chr2:48942156-48942157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574719941	chr2:48942157-48942158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48921600-48949600	Weak transcription	Ovary	ovary
2	chr2:48938000-48944400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:48940400-48942800	Enhancers	Rectal Smooth Muscle	rectum
4	chr2:48940400-48943400	Enhancers	Colon Smooth Muscle	Colon
5	chr2:48940400-48943400	Enhancers	Fetal Stomach	stomach
6	chr2:48940600-48941600	Enhancers	Left Ventricle	heart
7	chr2:48940600-48943400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:48940600-48943400	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr2:48940600-48943400	Enhancers	Fetal Muscle Leg	muscle
10	chr2:48940600-48945600	Enhancers	Fetal Lung	lung
11	chr2:48940800-48942000	Weak transcription	Right Ventricle	heart
12	chr2:48940800-48943400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:48941000-48942000	Weak transcription	Fetal Thymus	thymus
14	chr2:48941000-48942000	Weak transcription	Right Atrium	heart
15	chr2:48941000-48942800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:48941000-48942800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:48941000-48943400	Enhancers	NHLF	lung
18	chr2:48941000-48943600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:48941000-48944800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:48941000-48945000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:48941000-48946400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr2:48941200-48941600	Weak transcription	K562	blood
23	chr2:48941200-48943400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr2:48941200-48944400	Enhancers	Stomach Smooth Muscle	stomach
25	chr2:48941200-48944800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:48941400-48941600	Enhancers	Lung	lung
27	chr2:48941400-48941600	Enhancers	NH-A	brain
28	chr2:48941400-48942000	Weak transcription	Adipose Nuclei	Adipose
29	chr2:48941400-48942600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr2:48941400-48942600	Weak transcription	Fetal Heart	heart
31	chr2:48941400-48943200	Enhancers	Osteobl	bone
32	chr2:48941600-48942200	Weak transcription	NH-A	brain
33	chr2:48941600-48942600	Weak transcription	Left Ventricle	heart
34	chr2:48941600-48943200	Enhancers	K562	blood
35	chr2:48941600-48945600	Weak transcription	Lung	lung
36	chr2:48942000-48942800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:48942000-48942800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr2:48942000-48942800	Enhancers	Right Atrium	heart
39	chr2:48942000-48943200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr2:48942000-48943200	Enhancers	Adipose Nuclei	Adipose
41	chr2:48942000-48943200	Enhancers	Fetal Thymus	thymus
42	chr2:48942000-48943200	Enhancers	Right Ventricle	heart
43	chr2:48942000-48943400	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr2:48942000-48943400	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr2:48942200-48943200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr2:48942200-48943200	Enhancers	Fetal Kidney	kidney
47	chr2:48942200-48943400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr2:48942200-48943600	Enhancers	NH-A	brain
49	chr2:48942600-48943000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr2:48942600-48943000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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