Variant report

Variant	esv3380733
Chromosome Location	chr18:12436852-12441150
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr18:12439194-12439448	GM12878	blood:	n/a	n/a
2	BCL3	chr18:12436768-12436982	GM12878	blood:	n/a	n/a
3	CCNT2	chr18:12439371-12439408	K562	blood:	n/a	n/a
4	CEBPB	chr18:12438821-12438972	K562	blood:	n/a	n/a
5	CTCF	chr18:12437940-12438090	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr18:12440080-12440230	HBMEC	blood vessel:	n/a	chr18:12440218-12440227
7	CTCF	chr18:12440100-12440250	HUVEC	blood vessel:	n/a	chr18:12440218-12440227
8	CTCF	chr18:12440100-12440250	HEK293	kidney:	n/a	chr18:12440218-12440227
9	CTCF	chr18:12440200-12440350	HBMEC	blood vessel:	n/a	chr18:12440218-12440227
10	MXI1	chr18:12441058-12442604	SK-N-SH	brain:	n/a	n/a
11	MXI1	chr18:12439142-12439148	GM12878	blood:	n/a	n/a
12	POLR2A	chr18:12439603-12439906	HepG2	liver:	n/a	n/a
13	POLR2A	chr18:12437028-12437042	ProgFib	skin:	n/a	n/a
14	POLR2A	chr18:12437833-12437963	HepG2	liver:	n/a	n/a
15	POLR2A	chr18:12437794-12438531	HepG2	liver:	n/a	n/a
16	POLR2A	chr18:12437350-12437525	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr18:12438375-12438431	GM12878	blood:	n/a	n/a
18	POLR2A	chr18:12440209-12440245	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr18:12438387-12438394	MCF-7	breast:	n/a	n/a
20	POLR2A	chr18:12438735-12439023	HUVEC	blood vessel:	n/a	n/a
21	POLR2A	chr18:12437446-12437606	HepG2	liver:	n/a	n/a
22	POLR2A	chr18:12440622-12440672	HepG2	liver:	n/a	n/a
23	POLR2A	chr18:12439956-12440144	HepG2	liver:	n/a	n/a
24	POLR2A	chr18:12440533-12440534	HepG2	liver:	n/a	n/a
25	POLR2A	chr18:12440702-12440923	HepG2	liver:	n/a	n/a
26	POLR2A	chr18:12440543-12440577	HepG2	liver:	n/a	n/a
27	POLR2A	chr18:12438069-12438136	MCF-7	breast:	n/a	n/a
28	POLR2A	chr18:12438861-12438978	HepG2	liver:	n/a	n/a
29	POLR2A	chr18:12440491-12440503	HepG2	liver:	n/a	n/a
30	POLR2A	chr18:12440153-12440205	HepG2	liver:	n/a	n/a
31	POLR2A	chr18:12437796-12438083	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr18:12440212-12440489	HepG2	liver:	n/a	n/a
33	POLR2A	chr18:12437001-12437042	MCF-7	breast:	n/a	n/a
34	POLR2A	chr18:12438599-12438815	HepG2	liver:	n/a	n/a
35	POLR2A	chr18:12436463-12437200	HepG2	liver:	n/a	n/a
36	RAD21	chr18:12440069-12440316	H1-hESC	embryonic stem cell:	n/a	n/a
37	RCOR1	chr18:12439049-12439095	K562	blood:	n/a	n/a
38	STAT5A	chr18:12439233-12439467	GM12878	blood:	n/a	n/a
39	TAL1	chr18:12438927-12439148	K562	blood:	n/a	chr18:12439029-12439047

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12437948-12437998	NB4	blood:	n/a
2	chr18:12437948-12437998	HIPEpiC	eye:	n/a
3	chr18:12437948-12437998	PANC-1	pancreas:	n/a
4	chr18:12437948-12437998	PrEC	prostate:	n/a
5	chr18:12437948-12437998	ECC-1	luminal epithelium:	n/a
6	chr18:12437948-12437998	BE2_C	brain:	n/a
7	chr18:12437948-12437998	MCF-7	breast:	n/a
8	chr18:12437948-12437998	HRE	kidney:	n/a
9	chr18:12437948-12437998	AG09319	gingival:	n/a
10	chr18:12437948-12437998	HCF	heart:	n/a
11	chr18:12437948-12437998	NHBE	bronchial:	n/a
12	chr18:12437948-12437998	HCPEpiC	choroid plexus:	n/a
13	chr18:12437948-12437998	HL-60	blood:	n/a
14	chr18:12437948-12437998	Caco-2	colon:	n/a
15	chr18:12437948-12437998	SK-N-MC	brain:	n/a
16	chr18:12437948-12437998	ProgFib	skin:	n/a
17	chr18:12437948-12437998	PFSK-1	brain:	n/a
18	chr18:12437948-12437998	HepG2	liver:	n/a
19	chr18:12437948-12437998	AoSMC	blood vessel:	n/a
20	chr18:12437948-12437998	GM12891	blood:	n/a
21	chr18:12437948-12437998	MCF10A-Er-Src	breast:	n/a
22	chr18:12437948-12437998	HMEC	breast:	n/a
23	chr18:12437948-12437998	BJ	skin:	n/a
24	chr18:12437948-12437998	RPTEC	kidney:	n/a
25	chr18:12437948-12437998	HNPCEpiC	eye:	n/a
26	chr18:12437948-12437998	ovcar-3	ovarian:	n/a
27	chr18:12437948-12437998	U87	brain:	n/a
28	chr18:12437948-12437998	AG09309	skin:	n/a
29	chr18:12437948-12437998	AG04450	lung:	fetal
30	chr18:12437948-12437998	A549	lung:	n/a
31	chr18:12437948-12437998	GM12878	blood:	n/a
32	chr18:12437948-12437998	HCM	heart:	n/a
33	chr18:12437948-12437998	HAEpiC	amniotic membrane:	n/a
34	chr18:12437948-12437998	SAEC	small airway:	n/a
35	chr18:12437948-12437998	AG10803	skin:	n/a
36	chr18:12437948-12437998	Hela-S3	cervix:	n/a
37	chr18:12437948-12437998	HEEpiC	esophagus:	n/a
38	chr18:12437948-12437998	NH-A	brain:	n/a
39	chr18:12437948-12437998	LNCaP	prostate:	n/a
40	chr18:12437948-12437998	HRPEpiC	eye:	n/a
41	chr18:12437948-12437998	GM12892	blood:	n/a
42	chr18:12437948-12437998	Jurkat	blood:	n/a
43	chr18:12437948-12437998	HRCEpiC	kidney:	n/a
44	chr18:12437948-12437998	H1-hESC	embryonic stem cell:	embryo
45	chr18:12437948-12437998	GM19239	blood:	n/a
46	chr18:12437948-12437998	HCT-116	colon:	n/a
47	chr18:12437948-12437998	IMR90	lung:	fetal
48	chr18:12437948-12437998	SK-N-SH_RA	brain:	n/a
49	chr18:12437948-12437998	CMK	blood:	n/a
50	chr18:12437948-12437998	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:12436425..12438277-chr18:12439040..12441425,2	MCF-7	breast:
2	chr18:12421209..12423248-chr18:12437108..12438890,2	MCF-7	breast:
3	chr18:12436425..12438277-chr18:12439040..12441425,2	MCF-7	breast:
4	chr18:12436823..12439176-chr18:12440236..12443079,2	K562	blood:
5	chr18:12436823..12439176-chr18:12440236..12443079,2	K562	blood:
6	chr18:12435991..12438957-chr18:12658317..12660163,2	MCF-7	breast:
7	chr18:12427958..12434396-chr18:12436312..12440619,6	K562	blood:
8	chr18:12411709..12414167-chr18:12440258..12442480,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLMO1-1	chr18:12438889-12439122	NONHSAT058371
2	lnc-SLMO1-1	chr18:12438889-12439075	XLOC_012632
3	lnc-SLMO1-1	chr18:12438971-12439105	NONHSAT058374
4	lnc-SLMO1-1	chr18:12438889-12439105	ENSG00000267199.1
5	lnc-SLMO1-1	chr18:12437680-12437727	NONHSAT058371
6	lnc-SLMO1-1	chr18:12438422-12438623	XLOC_012632

No data

Variant related genes	Relation type
ENSG00000267199	TF binding region
ENSG00000267199	CpG island
ENSG00000256786	chromatin interactions
ENSG00000267108	chromatin interactions
ENSG00000141391	chromatin interactions
ENSG00000267199	chromatin interactions
ENSG00000128789	chromatin interactions
TWSG1	miRNA target sites
RNPEPL1	miRNA target sites

Extended variants
information (count: 200 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:200 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12954436	chr18:12436863-12436864	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566446987	chr18:12436876-12436877	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs192420122	chr18:12436887-12436888	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs542778348	chr18:12436898-12436899	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs372302294	chr18:12436904-12436905	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs375397852	chr18:12436911-12436912	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs564023729	chr18:12436946-12436947	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs367769342	chr18:12436979-12436980	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs531257338	chr18:12436990-12436991	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs549409983	chr18:12436993-12436994	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs535119810	chr18:12437006-12437007	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs549696218	chr18:12437015-12437016	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs141167808	chr18:12437030-12437031	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs184755139	chr18:12437081-12437082	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs536462291	chr18:12437108-12437109	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs548358490	chr18:12437133-12437134	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs117251324	chr18:12437227-12437228	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs187980885	chr18:12437229-12437230	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs371231781	chr18:12437241-12437242	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs375498197	chr18:12437272-12437273	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs547815817	chr18:12437300-12437301	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs560241888	chr18:12437303-12437304	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs577946576	chr18:12437368-12437369	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs555038086	chr18:12437419-12437420	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs1977937	chr18:12437424-12437425	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs138243792	chr18:12437427-12437428	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs542813307	chr18:12437445-12437446	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs143724051	chr18:12437460-12437461	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs574944521	chr18:12437469-12437470	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs60709238	chr18:12437470-12437471	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs147195753	chr18:12437543-12437544	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs542140371	chr18:12437550-12437551	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs3056883	chr18:12437567-12437568	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs71985943	chr18:12437568-12437569	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs576435590	chr18:12437594-12437595	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs564803004	chr18:12437623-12437624	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs113655721	chr18:12437629-12437630	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs36066588	chr18:12437630-12437631	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs375737235	chr18:12437639-12437640	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs532150948	chr18:12437653-12437654	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs184684303	chr18:12437657-12437658	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs559605085	chr18:12437670-12437671	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs530012929	chr18:12437681-12437682	Weak transcription Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs548446477	chr18:12437814-12437815	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs569850511	chr18:12437832-12437833	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs372333141	chr18:12437860-12437861	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs189396664	chr18:12437868-12437869	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs138561436	chr18:12437878-12437879	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs77329691	chr18:12437887-12437888	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs182003195	chr18:12437909-12437910	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12420600-12443600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr18:12420600-12477600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr18:12421200-12443400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr18:12421200-12447600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr18:12421200-12452800	Weak transcription	Colonic Mucosa	Colon
6	chr18:12421400-12444200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr18:12421800-12442400	Weak transcription	GM12878-XiMat	blood
8	chr18:12426600-12438600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr18:12428200-12440200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr18:12428200-12440600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr18:12428400-12437400	Strong transcription	Fetal Intestine Small	intestine
12	chr18:12428400-12439600	Weak transcription	Primary B cells from cord blood	blood
13	chr18:12428400-12443400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr18:12428600-12443800	Weak transcription	HSMMtube	muscle
15	chr18:12430800-12443400	Weak transcription	A549	lung
16	chr18:12431000-12438000	Weak transcription	HSMM	muscle
17	chr18:12431000-12443400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr18:12431000-12443600	Weak transcription	Fetal Heart	heart
19	chr18:12431000-12447600	Weak transcription	NH-A	brain
20	chr18:12431000-12449200	Weak transcription	Pancreas	Pancrea
21	chr18:12431200-12438800	Weak transcription	K562	blood
22	chr18:12431200-12443400	Weak transcription	Fetal Kidney	kidney
23	chr18:12431200-12447800	Weak transcription	NHEK	skin
24	chr18:12431400-12443400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr18:12432000-12443800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr18:12432600-12439000	Strong transcription	Fetal Stomach	stomach
27	chr18:12432600-12447000	Weak transcription	HMEC	breast
28	chr18:12433000-12438000	Weak transcription	Osteobl	bone
29	chr18:12433000-12441400	Weak transcription	Brain Substantia Nigra	brain
30	chr18:12433000-12441600	Weak transcription	NHDF-Ad	bronchial
31	chr18:12433000-12442800	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr18:12433000-12443200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr18:12433000-12443600	Weak transcription	Fetal Brain Male	brain
34	chr18:12433000-12448800	Weak transcription	HUVEC	blood vessel
35	chr18:12433200-12441400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr18:12433200-12443400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr18:12433200-12443400	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr18:12433200-12443600	Weak transcription	Brain Angular Gyrus	brain
39	chr18:12433200-12444000	Weak transcription	Left Ventricle	heart
40	chr18:12433200-12444000	Weak transcription	Right Ventricle	heart
41	chr18:12433200-12449200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr18:12433200-12449200	Weak transcription	Gastric	stomach
43	chr18:12433200-12449200	Weak transcription	Spleen	Spleen
44	chr18:12433200-12450200	Weak transcription	Thymus	Thymus
45	chr18:12433200-12464600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr18:12433400-12443600	Weak transcription	Brain Cingulate Gyrus	brain
47	chr18:12433400-12458600	Weak transcription	HepG2	liver
48	chr18:12434000-12437800	Weak transcription	Stomach Smooth Muscle	stomach
49	chr18:12434200-12443600	Weak transcription	Fetal Intestine Large	intestine
50	chr18:12434200-12477000	Weak transcription	Esophagus	oesophagus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links