Variant report

Variant	esv2752377
Chromosome Location	chr3:139163302-139188302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:211 , 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	CEBPB	chr3:139177200-139177563	HepG2	liver:	n/a	n/a
2	CEBPB	chr3:139177198-139177560	K562	blood:	n/a	n/a
3	CEBPB	chr3:139177205-139177555	IMR90	lung:	n/a	n/a
4	CEBPB	chr3:139177237-139177559	A549	lung:	n/a	n/a
5	CEBPB	chr3:139177153-139177627	A549	lung:	n/a	n/a
6	CEBPB	chr3:139177245-139177545	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr3:139174780-139174930	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr3:139174660-139174810	GM12871	blood:	n/a	chr3:139174695-139174703
9	CTCF	chr3:139174700-139174850	K562	blood:	n/a	n/a
10	CTCF	chr3:139174760-139174910	GM12873	blood:	n/a	n/a
11	CTCF	chr3:139174830-139174916	GM19238	blood:	n/a	n/a
12	CTCF	chr3:139174780-139174930	GM06990	blood:	n/a	n/a
13	CTCF	chr3:139174740-139174890	HFF	foreskin:	n/a	n/a
14	CTCF	chr3:139174820-139174970	GM12872	blood:	n/a	n/a
15	CTCF	chr3:139174720-139174870	GM12865	blood:	n/a	n/a
16	CTCF	chr3:139174820-139174970	GM12878	blood:	n/a	n/a
17	CTCF	chr3:139174824-139175016	GM12878	blood:	n/a	n/a
18	CTCF	chr3:139174809-139174900	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr3:139174824-139174948	LNCaP	prostate:	n/a	n/a
20	CTCF	chr3:139174766-139174934	GM12878	blood:	n/a	n/a
21	CTCF	chr3:139174822-139174920	MCF-7	breast:	n/a	n/a
22	CTCF	chr3:139174800-139174950	GM12875	blood:	n/a	n/a
23	CTCF	chr3:139174800-139174950	GM12864	blood:	n/a	n/a
24	CTCF	chr3:139174880-139175030	GM12870	blood:	n/a	n/a
25	CTCF	chr3:139174720-139174870	AG04450	lung:	n/a	n/a
26	CTCF	chr3:139174700-139174850	A549	lung:	n/a	n/a
27	CTCF	chr3:139174620-139174770	GM12870	blood:	n/a	chr3:139174695-139174703
28	CTCF	chr3:139174700-139174850	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr3:139174760-139174910	GM12872	blood:	n/a	n/a
30	CTCF	chr3:139174799-139174924	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:139185340-139185490	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr3:139180597-139180659	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:139174800-139174950	BE2_C	brain:	n/a	n/a
34	CTCF	chr3:139174820-139174970	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr3:139174740-139175010	HVMF	connective:	n/a	n/a
36	CTCF	chr3:139174700-139174850	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr3:139174760-139174910	AG04449	skin:	n/a	n/a
38	CTCF	chr3:139174820-139174970	BJ	skin:	n/a	n/a
39	CTCF	chr3:139174719-139174942	HepG2	liver:	n/a	n/a
40	CTCF	chr3:139174780-139174930	GM12873	blood:	n/a	n/a
41	CTCF	chr3:139174740-139174890	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr3:139174780-139174930	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr3:139174740-139174890	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr3:139174760-139174910	RPTEC	kidney:	n/a	n/a
45	CTCF	chr3:139174813-139174952	NHEK	skin:	n/a	n/a
46	CTCF	chr3:139174660-139174810	HCM	heart:	n/a	chr3:139174695-139174703
47	CTCF	chr3:139174800-139174950	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr3:139174740-139174890	HRE	kidney:	n/a	n/a
49	CTCF	chr3:139174740-139174890	HepG2	liver:	n/a	n/a
50	CTCF	chr3:139174811-139174899	GM13977	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:139173779-139173829	ProgFib	skin:	n/a
2	chr3:139173779-139173829	BE2_C	brain:	n/a
3	chr3:139173779-139173829	GM12891	blood:	n/a
4	chr3:139173779-139173829	AG09309	skin:	n/a
5	chr3:139173779-139173829	SK-N-MC	brain:	n/a
6	chr3:139173779-139173829	HAEpiC	amniotic membrane:	n/a
7	chr3:139173779-139173829	HNPCEpiC	eye:	n/a
8	chr3:139173779-139173829	PANC-1	pancreas:	n/a
9	chr3:139173779-139173829	Jurkat	blood:	n/a
10	chr3:139173779-139173829	ovcar-3	ovarian:	n/a
11	chr3:139173779-139173829	LNCaP	prostate:	n/a
12	chr3:139173779-139173829	NHDF-neo	bronchial:	n/a
13	chr3:139173779-139173829	HL-60	blood:	n/a
14	chr3:139173779-139173829	NB4	blood:	n/a
15	chr3:139173779-139173829	K562	blood:	n/a
16	chr3:139173779-139173829	GM19239	blood:	n/a
17	chr3:139173779-139173829	AG09319	gingival:	n/a
18	chr3:139173779-139173829	AG10803	skin:	n/a
19	chr3:139173779-139173829	SAEC	small airway:	n/a
20	chr3:139173779-139173829	U87	brain:	n/a
21	chr3:139173779-139173829	IMR90	lung:	fetal
22	chr3:139173779-139173829	HIPEpiC	eye:	n/a
23	chr3:139173779-139173829	CMK	blood:	n/a
24	chr3:139173779-139173829	HRPEpiC	eye:	n/a
25	chr3:139173779-139173829	HEEpiC	esophagus:	n/a
26	chr3:139173779-139173829	GM12878	blood:	n/a
27	chr3:139173779-139173829	MCF10A-Er-Src	breast:	n/a
28	chr3:139173779-139173829	NH-A	brain:	n/a
29	chr3:139173779-139173829	HUVEC	blood vessel:	n/a
30	chr3:139173779-139173829	Hela-S3	cervix:	n/a
31	chr3:139173779-139173829	A549	lung:	n/a
32	chr3:139173779-139173829	ECC-1	luminal epithelium:	n/a
33	chr3:139173779-139173829	SK-N-SH_RA	brain:	n/a
34	chr3:139173779-139173829	HRCEpiC	kidney:	n/a
35	chr3:139173779-139173829	HCF	heart:	n/a
36	chr3:139173779-139173829	AG04449	skin:	fetal
37	chr3:139173779-139173829	GM12892	blood:	n/a
38	chr3:139173779-139173829	HCM	heart:	n/a
39	chr3:139173779-139173829	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:139173779-139173829	HMEC	breast:	n/a
41	chr3:139173779-139173829	Hepatocyte	liver:	n/a
42	chr3:139173779-139173829	AG04450	lung:	fetal
43	chr3:139173779-139173829	RPTEC	kidney:	n/a
44	chr3:139173779-139173829	HCT-116	colon:	n/a
45	chr3:139173779-139173829	NT2-D1	testis:	n/a
46	chr3:139173779-139173829	NHBE	bronchial:	n/a
47	chr3:139173779-139173829	Caco-2	colon:	n/a
48	chr3:139173779-139173829	HEK293	kidney:	embryo
49	chr3:139173779-139173829	SKMC	muscle:	n/a
50	chr3:139173779-139173829	HepG2	liver:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46926680..46927202-chr3:139164975..139165475,2	HCT-116	colon:
2	chr3:139168645..139171256-chr3:139173067..139176313,3	K562	blood:
3	chr3:139164444..139166894-chr3:139178847..139180451,2	K562	blood:
4	chr3:139174418..139175114-chr3:139280608..139281156,2	MCF-7	breast:
5	chr3:139186237..139189203-chr3:139191374..139194272,2	K562	blood:
6	chr3:139165019..139166769-chr3:139169234..139171368,2	MCF-7	breast:
7	chr3:139187703..139190427-chr3:139192772..139195214,2	K562	blood:
8	chr3:139178292..139180286-chr3:139183692..139185516,2	K562	blood:
9	chr3:139164444..139166894-chr3:139178847..139180451,2	K562	blood:
10	chr3:139156554..139158574-chr3:139162722..139165410,2	MCF-7	breast:
11	chr3:139168645..139171256-chr3:139173067..139176313,3	K562	blood:
12	chr3:139165019..139166769-chr3:139169234..139171368,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS22-1	chr3:139163021-139165157	NONHSAT092369
2	lnc-MRPS22-1	chr3:139169474-139169503	NONHSAT092358
3	lnc-MRPS22-1	chr3:139170843-139171082	ENSG00000248932.1
4	lnc-MRPS22-2	chr3:139185415-139185637	ENSG00000248790.1
5	lnc-MRPS22-2	chr3:139185272-139185321	ENSG00000248790.1
6	lnc-MRPS22-1	chr3:139163136-139163452	NONHSAT092368
7	lnc-MRPS22-1	chr3:139163136-139163352	NONHSAT092358
8	lnc-MRPS22-1	chr3:139163136-139163429	NONHSAT092359
9	lnc-MRPS22-1	chr3:139169122-139169255	ENSG00000248932.1

No data

Variant related genes	Relation type
ENSG00000248790	TF binding region
ENSG00000248790	CpG island
ENSG00000248790	chromatin interactions

Extended variants
information (count: 869 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146037462	chr3:139163313-139163314	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs184641950	chr3:139163486-139163487	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs576588413	chr3:139163501-139163502	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs13325144	chr3:139163540-139163541	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs189912265	chr3:139163602-139163603	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs527807099	chr3:139163659-139163660	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs541387801	chr3:139163683-139163684	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs7635513	chr3:139163707-139163708	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs35168405	chr3:139163708-139163709	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs181472488	chr3:139163845-139163846	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs549856622	chr3:139163859-139163860	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs34701386	chr3:139163873-139163874	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs138777618	chr3:139163940-139163941	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs142763072	chr3:139163947-139163948	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs2289349	chr3:139163993-139163994	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs565409921	chr3:139164057-139164058	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs534420541	chr3:139164108-139164109	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs144477361	chr3:139164168-139164169	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs568495151	chr3:139164234-139164235	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs536929598	chr3:139164240-139164241	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs369405283	chr3:139164243-139164244	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs148003274	chr3:139164256-139164257	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs576686990	chr3:139164259-139164260	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs2289348	chr3:139164266-139164267	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559196557	chr3:139164284-139164285	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs572533213	chr3:139164375-139164376	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs2289347	chr3:139164391-139164392	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs561334837	chr3:139164426-139164427	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs531072338	chr3:139164448-139164449	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs574771239	chr3:139164450-139164451	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs141642959	chr3:139164451-139164452	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs116307387	chr3:139164458-139164459	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs529619653	chr3:139164559-139164560	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs532295933	chr3:139164616-139164617	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs551908336	chr3:139164636-139164637	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs113458468	chr3:139164696-139164697	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs559160911	chr3:139164716-139164717	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs113578097	chr3:139164734-139164735	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs528169436	chr3:139164790-139164791	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs13085888	chr3:139164874-139164875	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs116180452	chr3:139164893-139164894	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs536605365	chr3:139164919-139164920	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs550570564	chr3:139164981-139164982	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs570314640	chr3:139164993-139164994	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs539348594	chr3:139165011-139165012	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs150507936	chr3:139165031-139165032	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs139780110	chr3:139165057-139165058	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs535103639	chr3:139165089-139165090	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs12495890	chr3:139165108-139165109	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs574893170	chr3:139165246-139165247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139136400-139166200	Weak transcription	Fetal Brain Female	brain
2	chr3:139138600-139166200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:139138600-139170400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr3:139141400-139167000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr3:139142200-139172200	Weak transcription	Fetal Heart	heart
6	chr3:139142800-139169000	Weak transcription	Aorta	Aorta
7	chr3:139142800-139176800	Weak transcription	Fetal Stomach	stomach
8	chr3:139144800-139173200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr3:139145200-139164400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:139145200-139170400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr3:139149800-139170600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr3:139154000-139167000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr3:139154200-139165600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr3:139154200-139168200	Weak transcription	Fetal Intestine Small	intestine
15	chr3:139154200-139171200	Weak transcription	Right Atrium	heart
16	chr3:139154200-139173600	Weak transcription	Ovary	ovary
17	chr3:139154200-139178600	Weak transcription	Left Ventricle	heart
18	chr3:139154400-139166200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr3:139154400-139167000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr3:139154800-139165200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:139158600-139166200	Weak transcription	Fetal Muscle Leg	muscle
22	chr3:139158600-139172600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr3:139158600-139174800	Weak transcription	Adipose Nuclei	Adipose
24	chr3:139158800-139166000	Weak transcription	HSMMtube	muscle
25	chr3:139160200-139174800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:139160400-139163400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:139160600-139170200	Weak transcription	Lung	lung
28	chr3:139160600-139174800	Weak transcription	Fetal Brain Male	brain
29	chr3:139161000-139164800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr3:139161400-139166200	Weak transcription	Brain Germinal Matrix	brain
31	chr3:139161400-139168800	Weak transcription	Fetal Intestine Large	intestine
32	chr3:139162800-139163800	Enhancers	Brain Anterior Caudate	brain
33	chr3:139162800-139164200	Enhancers	Brain Substantia Nigra	brain
34	chr3:139162800-139164400	Enhancers	Brain Angular Gyrus	brain
35	chr3:139162800-139166600	Enhancers	Brain Hippocampus Middle	brain
36	chr3:139162800-139167600	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr3:139163000-139163400	Enhancers	Small Intestine	intestine
38	chr3:139163000-139170000	Weak transcription	Duodenum Mucosa	Duodenum
39	chr3:139163400-139163800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:139163400-139189000	Weak transcription	Small Intestine	intestine
41	chr3:139163800-139165400	Weak transcription	Brain Anterior Caudate	brain
42	chr3:139163800-139180200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:139164200-139165000	Weak transcription	Brain Substantia Nigra	brain
44	chr3:139164400-139166200	Weak transcription	Brain Angular Gyrus	brain
45	chr3:139164800-139165000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr3:139164800-139168200	Enhancers	Brain Cingulate Gyrus	brain
47	chr3:139165000-139168400	Enhancers	Brain Substantia Nigra	brain
48	chr3:139165400-139167400	Enhancers	Brain Anterior Caudate	brain
49	chr3:139165600-139165800	Enhancers	Right Ventricle	heart
50	chr3:139165600-139166000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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