Variant report

Variant	esv1846948
Chromosome Location	chr18:7562317-7568860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:917)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
2	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
3	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
4	BACH1	chr18:7566548-7566660	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:7568581-7568843	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr18:7566784-7567400	HepG2	liver:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
8	BHLHE40	chr18:7567045-7567395	GM12878	blood:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
9	BHLHE40	chr18:7566522-7567366	K562	blood:	n/a	chr18:7567340-7567356 chr18:7566691-7566707 chr18:7567117-7567133
10	BRCA1	chr18:7566113-7566632	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr18:7566537-7567551	K562	blood:	n/a	n/a
12	CHD1	chr18:7568086-7568380	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr18:7567168-7567252	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr18:7566627-7566933	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr18:7565958-7569508	IMR90	lung:	n/a	chr18:7567084-7567094
16	CHD2	chr18:7566988-7567580	Hela-S3	cervix:	n/a	chr18:7567084-7567094
17	CHD2	chr18:7566856-7567052	HepG2	liver:	n/a	n/a
18	CHD2	chr18:7567294-7567335	HepG2	liver:	n/a	n/a
19	CHD2	chr18:7566721-7566935	K562	blood:	n/a	n/a
20	CHD2	chr18:7568188-7568727	Hela-S3	cervix:	n/a	n/a
21	CREB1	chr18:7566544-7566952	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr18:7566858-7567601	HepG2	liver:	n/a	n/a
23	CREB1	chr18:7566645-7567541	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr18:7567001-7567445	K562	blood:	n/a	n/a
25	CREB1	chr18:7568530-7568853	A549	lung:	n/a	n/a
26	CREB1	chr18:7567887-7568154	A549	lung:	n/a	n/a
27	CREB1	chr18:7567063-7567481	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr18:7567120-7567445	A549	lung:	n/a	n/a
29	CREB1	chr18:7566663-7567589	A549	lung:	n/a	n/a
30	CTBP2	chr18:7568128-7568834	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr18:7566540-7567821	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr18:7567200-7567350	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr18:7566700-7566850	HAc	cerebellar:	n/a	chr18:7566742-7566758
34	CTCF	chr18:7566736-7566973	Fibrobl	skin:	n/a	chr18:7566742-7566758
35	CTCF	chr18:7567160-7567310	GM12867	blood:	n/a	n/a
36	CTCF	chr18:7568240-7568390	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr18:7567160-7567310	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr18:7568120-7568270	BJ	skin:	n/a	n/a
39	CTCF	chr18:7567104-7567319	A549	lung:	n/a	n/a
40	CTCF	chr18:7568580-7568730	SAEC	small airway:	n/a	n/a
41	CTCF	chr18:7568520-7568670	SAEC	small airway:	n/a	n/a
42	CTCF	chr18:7567200-7567350	GM12872	blood:	n/a	n/a
43	CTCF	chr18:7568580-7568730	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr18:7567220-7567370	GM12872	blood:	n/a	n/a
45	CTCF	chr18:7568140-7568290	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr18:7568542-7568861	Gliobla	brain:	n/a	n/a
47	CTCF	chr18:7567200-7567350	GM12869	blood:	n/a	n/a
48	CTCF	chr18:7568204-7568285	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr18:7568580-7568730	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr18:7567160-7567310	AG09319	gingival:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7567799-7567849	HepG2	liver:	n/a
2	chr18:7567638-7567688	BJ	skin:	n/a
3	chr18:7567799-7567849	HepG2	liver:	n/a
4	chr18:7567638-7567688	BJ	skin:	n/a
5	chr18:7566656-7566706	MCF-7	breast:	n/a
6	chr18:7566781-7566831	HCPEpiC	choroid plexus:	n/a
7	chr18:7566258-7566308	MCF10A-Er-Src	breast:	n/a
8	chr18:7568265-7568315	HIPEpiC	eye:	n/a
9	chr18:7568829-7568879	BE2_C	brain:	n/a
10	chr18:7567799-7567849	ovcar-3	ovarian:	n/a
11	chr18:7568539-7568589	PANC-1	pancreas:	n/a
12	chr18:7568539-7568589	BJ	skin:	n/a
13	chr18:7568829-7568879	Jurkat	blood:	n/a
14	chr18:7566781-7566831	MCF10A-Er-Src	breast:	n/a
15	chr18:7566258-7566308	IMR90	lung:	fetal
16	chr18:7568829-7568879	ProgFib	skin:	n/a
17	chr18:7567426-7567476	NHBE	bronchial:	n/a
18	chr18:7567426-7567476	PFSK-1	brain:	n/a
19	chr18:7567799-7567849	PANC-1	pancreas:	n/a
20	chr18:7566558-7566608	MCF-7	breast:	n/a
21	chr18:7567548-7567598	HCM	heart:	n/a
22	chr18:7567799-7567849	BJ	skin:	n/a
23	chr18:7566558-7566608	ovcar-3	ovarian:	n/a
24	chr18:7563847-7563897	AG04450	lung:	fetal
25	chr18:7567638-7567688	HUVEC	blood vessel:	n/a
26	chr18:7566781-7566831	SKMC	muscle:	n/a
27	chr18:7568265-7568315	SK-N-MC	brain:	n/a
28	chr18:7568829-7568879	HRE	kidney:	n/a
29	chr18:7566558-7566608	HIPEpiC	eye:	n/a
30	chr18:7567426-7567476	IMR90	lung:	fetal
31	chr18:7568186-7568236	PFSK-1	brain:	n/a
32	chr18:7568159-7568209	SK-N-SH_RA	brain:	n/a
33	chr18:7563847-7563897	HRPEpiC	eye:	n/a
34	chr18:7568159-7568209	SAEC	small airway:	n/a
35	chr18:7563847-7563897	CMK	blood:	n/a
36	chr18:7566258-7566308	GM19239	blood:	n/a
37	chr18:7567799-7567849	HEK293	kidney:	embryo
38	chr18:7568265-7568315	AG09309	skin:	n/a
39	chr18:7566258-7566308	HCM	heart:	n/a
40	chr18:7567717-7567767	BE2_C	brain:	n/a
41	chr18:7567638-7567688	GM06990	blood:	n/a
42	chr18:7566558-7566608	HUVEC	blood vessel:	n/a
43	chr18:7563847-7563897	GM06990	blood:	n/a
44	chr18:7567799-7567849	U87	brain:	n/a
45	chr18:7568829-7568879	T-47D	breast:	n/a
46	chr18:7568265-7568315	MCF10A-Er-Src	breast:	n/a
47	chr18:7568186-7568236	GM12891	blood:	n/a
48	chr18:7567548-7567598	AG09309	skin:	n/a
49	chr18:7567548-7567598	HCT-116	colon:	n/a
50	chr18:7566558-7566608	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:7561940..7563899-chr18:7566456..7568145,3	K562	blood:
2	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
3	chr18:7560178..7562976-chr18:7564673..7567118,2	MCF-7	breast:
4	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:
5	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
6	chr18:7560671..7563899-chr18:7566458..7568145,4	K562	blood:

No data

Variant related genes	Relation type
PTPRM	TF binding region
PTPRM	CpG island
ENSG00000173482	chromatin interactions
ENSG00000149658	chromatin interactions

Extended variants
information (count: 205 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:205 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58953090	chr18:7562317-7562318	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs116893516	chr18:7562330-7562331	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567259649	chr18:7562340-7562341	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs535914040	chr18:7562375-7562376	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs73385357	chr18:7562397-7562398	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189337005	chr18:7562401-7562402	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113651368	chr18:7562466-7562467	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78852401	chr18:7562526-7562527	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557739279	chr18:7562582-7562583	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs556677379	chr18:7562598-7562599	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs561711395	chr18:7562709-7562710	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs577821816	chr18:7562713-7562714	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375743713	chr18:7562741-7562742	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs577728980	chr18:7562783-7562784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182387328	chr18:7562875-7562876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557074818	chr18:7562890-7562891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573696009	chr18:7562915-7562916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542685328	chr18:7562927-7562928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371622419	chr18:7562934-7562935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559582838	chr18:7562937-7562938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs528346521	chr18:7562985-7562986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545291084	chr18:7562994-7562995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571261180	chr18:7563059-7563060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534074725	chr18:7563101-7563102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565031155	chr18:7563130-7563131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530765389	chr18:7563131-7563132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373755908	chr18:7563173-7563174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140236926	chr18:7563174-7563175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567395820	chr18:7563198-7563199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs529674055	chr18:7563207-7563208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186539601	chr18:7563350-7563351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191092364	chr18:7563382-7563383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566487588	chr18:7563396-7563397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534963130	chr18:7563427-7563428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369174589	chr18:7563436-7563437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs367561504	chr18:7563495-7563496	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146953196	chr18:7563743-7563744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571500347	chr18:7563756-7563757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116381988	chr18:7563761-7563762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs138133710	chr18:7563762-7563763	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553832800	chr18:7563769-7563770	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs77894090	chr18:7563784-7563785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573806929	chr18:7563789-7563790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575267549	chr18:7563809-7563810	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375508871	chr18:7563842-7563843	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143592191	chr18:7563853-7563854	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368373992	chr18:7563873-7563874	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544964572	chr18:7563901-7563902	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200782705	chr18:7563945-7563946	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs146179190	chr18:7563948-7563949	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
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
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
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Breast cancer	17133270	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7558200-7566000	Weak transcription	Right Atrium	heart
2	chr18:7560200-7564600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr18:7560200-7565200	Weak transcription	Psoas Muscle	Psoas
4	chr18:7560200-7566200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr18:7560400-7565200	Weak transcription	Left Ventricle	heart
6	chr18:7560400-7566000	Weak transcription	Lung	lung
7	chr18:7560400-7566000	Weak transcription	Pancreas	Pancrea
8	chr18:7561400-7562400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr18:7561600-7562600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr18:7561600-7562600	Enhancers	HepG2	liver
11	chr18:7561600-7562800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr18:7561600-7562800	Enhancers	HUVEC	blood vessel
13	chr18:7561600-7565600	Enhancers	Colon Smooth Muscle	Colon
14	chr18:7561800-7562400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr18:7561800-7562400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr18:7561800-7562400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr18:7561800-7562600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr18:7561800-7562600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr18:7561800-7562800	Enhancers	Adipose Nuclei	Adipose
20	chr18:7561800-7562800	Enhancers	Brain Anterior Caudate	brain
21	chr18:7561800-7563200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr18:7561800-7563200	Enhancers	Rectal Smooth Muscle	rectum
23	chr18:7562000-7562400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr18:7562000-7562400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr18:7562000-7562400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr18:7562000-7562400	Enhancers	Brain Hippocampus Middle	brain
27	chr18:7562000-7562400	Enhancers	Brain Substantia Nigra	brain
28	chr18:7562000-7562400	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr18:7562000-7562600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr18:7562000-7562600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr18:7562000-7562600	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr18:7562000-7562800	Enhancers	Fetal Heart	heart
33	chr18:7562000-7563200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr18:7562000-7564400	Weak transcription	Thymus	Thymus
35	chr18:7562200-7562600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr18:7562200-7564800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr18:7562200-7564800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr18:7562200-7564800	Weak transcription	Spleen	Spleen
39	chr18:7562200-7565000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr18:7562200-7565600	Weak transcription	Brain Angular Gyrus	brain
41	chr18:7562200-7565800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr18:7562200-7566000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr18:7562400-7564600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr18:7562400-7564800	Weak transcription	Brain Hippocampus Middle	brain
45	chr18:7562400-7565200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr18:7562400-7565600	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr18:7562400-7565800	Weak transcription	Brain Substantia Nigra	brain
48	chr18:7562400-7566000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr18:7562600-7565600	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr18:7562800-7564600	Weak transcription	Adipose Nuclei	Adipose

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