Variant report

Variant	nsv909596
Chromosome Location	chr18:44291419-44330604
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:212)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:212 , 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	ARID3A	chr18:44291594-44291809	K562	blood:	n/a	n/a
2	ATF1	chr18:44291355-44291752	K562	blood:	n/a	n/a
3	ATF2	chr18:44291349-44291738	GM12878	blood:	n/a	n/a
4	ATF2	chr18:44291343-44291737	GM12878	blood:	n/a	n/a
5	ATF3	chr18:44291373-44291757	K562	blood:	n/a	n/a
6	BACH1	chr18:44291404-44291604	K562	blood:	n/a	n/a
7	BHLHE40	chr18:44299297-44299305	K562	blood:	n/a	n/a
8	BHLHE40	chr18:44291404-44291771	K562	blood:	n/a	n/a
9	BHLHE40	chr18:44294139-44294257	HepG2	liver:	n/a	n/a
10	BRCA1	chr18:44318689-44318719	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr18:44291375-44291672	K562	blood:	n/a	n/a
12	CCNT2	chr18:44291435-44291748	K562	blood:	n/a	n/a
13	CEBPB	chr18:44298198-44298374	K562	blood:	n/a	n/a
14	CEBPB	chr18:44307201-44307385	HepG2	liver:	n/a	n/a
15	CEBPB	chr18:44291467-44291759	K562	blood:	n/a	n/a
16	CEBPB	chr18:44291358-44291613	K562	blood:	n/a	n/a
17	CEBPB	chr18:44299061-44299279	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr18:44298913-44299496	HCT-116	colon:	n/a	n/a
19	CEBPB	chr18:44298091-44298404	IMR90	lung:	n/a	n/a
20	CEBPD	chr18:44291359-44291881	K562	blood:	n/a	n/a
21	CEBPD	chr18:44291321-44291792	K562	blood:	n/a	n/a
22	CHD2	chr18:44291348-44291684	K562	blood:	n/a	n/a
23	CHD2	chr18:44291380-44291723	GM12878	blood:	n/a	n/a
24	CTCF	chr18:44291525-44291719	K562	blood:	n/a	n/a
25	CTCF	chr18:44302588-44302717	GM12878	blood:	n/a	n/a
26	CTCF	chr18:44295069-44295451	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr18:44319649-44319791	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr18:44324641-44324687	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr18:44295231-44295323	K562	blood:	n/a	n/a
30	CTCF	chr18:44295196-44295309	GM12892	blood:	n/a	n/a
31	CTCF	chr18:44302520-44302670	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr18:44295125-44295325	GM12878	blood:	n/a	n/a
33	CTCF	chr18:44294960-44295110	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr18:44295201-44295314	HepG2	liver:	n/a	n/a
35	CTCF	chr18:44298480-44298630	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr18:44310460-44310564	Lung_OC	lung:	n/a	n/a
37	CTCF	chr18:44325696-44325713	GM20000	blood:	n/a	n/a
38	CTCF	chr18:44295256-44295321	Medullo	brain:	n/a	n/a
39	CTCF	chr18:44295200-44295350	GM12866	blood:	n/a	n/a
40	CTCF	chr18:44295237-44295278	GM19238	blood:	n/a	n/a
41	CTCF	chr18:44298560-44298710	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr18:44295062-44295357	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr18:44319692-44319734	GM12891	blood:	n/a	n/a
44	CTCF	chr18:44295180-44295330	GM12875	blood:	n/a	n/a
45	CTCF	chr18:44302580-44302730	GM12871	blood:	n/a	n/a
46	CTCF	chr18:44295200-44295350	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr18:44295180-44295330	GM12872	blood:	n/a	n/a
48	CTCF	chr18:44295160-44295310	HepG2	liver:	n/a	n/a
49	CTCF	chr18:44298320-44298470	HAc	cerebellar:	n/a	n/a
50	CTCF	chr18:44295159-44295354	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr18:44290160..44292978-chr18:44295020..44296704,2	K562	blood:
2	chr18:44295920..44298422-chr18:44298971..44300843,2	K562	blood:
3	chr18:44290160..44292978-chr18:44295020..44296704,2	K562	blood:
4	chr18:44295920..44298422-chr18:44298971..44300843,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-10	chr18:44302938-44303186	NONHSAT059136

No data

Variant related genes	Relation type
ST8SIA5	TF binding region
ENSG00000240983	TF binding region

Extended variants
information (count: 1499 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1499 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11082551	chr18:44291419-44291420	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs41471844	chr18:44291440-44291441	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs114889591	chr18:44291477-44291478	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs386802907	chr18:44291478-44291479	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs12605659	chr18:44291479-44291480	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs571627293	chr18:44291481-44291482	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs138732058	chr18:44291490-44291491	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs547858221	chr18:44291548-44291549	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs185169851	chr18:44291549-44291550	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs531864543	chr18:44291575-44291576	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs149297751	chr18:44291576-44291577	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs144572059	chr18:44291683-44291684	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs113122101	chr18:44291714-44291715	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs572454597	chr18:44291715-44291716	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs539823264	chr18:44291746-44291747	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs372836691	chr18:44291747-44291748	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs553523024	chr18:44291767-44291768	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs573645294	chr18:44291818-44291819	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs542378170	chr18:44291819-44291820	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs562653506	chr18:44291831-44291832	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs78863685	chr18:44291834-44291835	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs545263626	chr18:44291844-44291845	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs17778939	chr18:44291905-44291906	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs148452839	chr18:44291930-44291931	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs372829844	chr18:44291977-44291978	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs527934787	chr18:44291986-44291987	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs8099322	chr18:44292026-44292027	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs567574418	chr18:44292068-44292069	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs530162896	chr18:44292216-44292217	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs550016070	chr18:44292220-44292221	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs570172806	chr18:44292355-44292356	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs187994213	chr18:44292362-44292363	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs552384306	chr18:44292366-44292367	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs142581567	chr18:44292384-44292385	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs535000469	chr18:44292397-44292398	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs553698582	chr18:44292440-44292441	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs573557911	chr18:44292476-44292477	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs536302018	chr18:44292493-44292494	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs56190504	chr18:44292509-44292510	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs576251451	chr18:44292580-44292581	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs191519339	chr18:44292594-44292595	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs948570	chr18:44292598-44292599	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs183767336	chr18:44292609-44292610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs540972472	chr18:44292647-44292648	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs756032	chr18:44292667-44292668	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530033476	chr18:44292684-44292685	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs550199167	chr18:44292686-44292687	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs563422086	chr18:44292695-44292696	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs532505930	chr18:44292742-44292743	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs552320807	chr18:44292743-44292744	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Prostate cancer	22341455	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44285200-44291600	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr18:44286800-44291600	Weak transcription	Brain Hippocampus Middle	brain
3	chr18:44286800-44291600	Weak transcription	Brain Substantia Nigra	brain
4	chr18:44286800-44298800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr18:44287400-44291600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr18:44287400-44291800	Weak transcription	NHLF	lung
7	chr18:44287800-44298800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr18:44288400-44292000	Weak transcription	Brain Germinal Matrix	brain
9	chr18:44290000-44293600	Enhancers	Psoas Muscle	Psoas
10	chr18:44290000-44295400	Enhancers	Fetal Muscle Leg	muscle
11	chr18:44290600-44293200	Enhancers	Right Atrium	heart
12	chr18:44290600-44293600	Enhancers	Fetal Muscle Trunk	muscle
13	chr18:44290600-44293600	Enhancers	Left Ventricle	heart
14	chr18:44290600-44294600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr18:44290800-44292600	Enhancers	K562	blood
16	chr18:44290800-44292800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr18:44290800-44293800	Enhancers	HSMMtube	muscle
18	chr18:44291000-44292000	Flanking Active TSS	Fetal Heart	heart
19	chr18:44291000-44293000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr18:44291000-44293400	Enhancers	NHDF-Ad	bronchial
21	chr18:44291000-44293600	Enhancers	Brain Angular Gyrus	brain
22	chr18:44291200-44291800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr18:44291200-44291800	Bivalent Enhancer	GM12878-XiMat	blood
24	chr18:44291200-44292600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr18:44291200-44293000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr18:44291200-44293000	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr18:44291200-44293400	Enhancers	HSMM	muscle
28	chr18:44291400-44291800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr18:44291400-44291800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr18:44291400-44292000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr18:44291400-44292400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr18:44291400-44292600	Enhancers	Fetal Brain Male	brain
33	chr18:44291400-44292800	Bivalent Enhancer	Fetal Stomach	stomach
34	chr18:44291400-44293000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr18:44291400-44293000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr18:44291400-44293200	Enhancers	Brain Cingulate Gyrus	brain
37	chr18:44291600-44292000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr18:44291600-44292200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr18:44291600-44292200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
40	chr18:44291600-44293000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr18:44291600-44293000	Enhancers	Brain Hippocampus Middle	brain
42	chr18:44291600-44293000	Enhancers	Ovary	ovary
43	chr18:44291600-44293200	Enhancers	Brain Substantia Nigra	brain
44	chr18:44291600-44293400	Enhancers	NH-A	brain
45	chr18:44291600-44293600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr18:44291800-44292400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr18:44291800-44292400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr18:44291800-44293000	Enhancers	Right Ventricle	heart
49	chr18:44291800-44293200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr18:44291800-44293200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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