Variant report

Variant	nsv515878
Chromosome Location	chr18:13122618-13142415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:545)
CpG islands
(count:550)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:13138749-13139008	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:13137735-13138495	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:13139762-13140120	HepG2	liver:	n/a	n/a
4	BACH1	chr18:13133897-13133921	K562	blood:	n/a	n/a
5	BHLHE40	chr18:13137018-13137501	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:13136243-13136758	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:13137720-13138170	GM12878	blood:	n/a	n/a
8	BHLHE40	chr18:13137839-13139016	HepG2	liver:	n/a	n/a
9	BRCA1	chr18:13139965-13140122	HepG2	liver:	n/a	n/a
10	BRCA1	chr18:13138809-13138943	HepG2	liver:	n/a	n/a
11	BRCA1	chr18:13137837-13138037	HepG2	liver:	n/a	n/a
12	CEBPB	chr18:13135996-13136102	HepG2	liver:	n/a	n/a
13	CEBPB	chr18:13137929-13138378	HepG2	liver:	n/a	n/a
14	CEBPD	chr18:13137218-13137439	HepG2	liver:	n/a	n/a
15	CEBPD	chr18:13138098-13138607	HepG2	liver:	n/a	n/a
16	CHD1	chr18:13137440-13137888	GM12878	blood:	n/a	n/a
17	CHD2	chr18:13139926-13140338	HepG2	liver:	n/a	n/a
18	CHD2	chr18:13138379-13138979	HepG2	liver:	n/a	n/a
19	CHD2	chr18:13137600-13137605	HepG2	liver:	n/a	n/a
20	CHD2	chr18:13137248-13138387	GM12878	blood:	n/a	chr18:13137340-13137350
21	CTCF	chr18:13139754-13140118	K562	blood:	n/a	n/a
22	CTCF	chr18:13139762-13140084	K562	blood:	n/a	n/a
23	CTCF	chr18:13139926-13139982	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr18:13139889-13140019	GM10266	blood:	n/a	n/a
25	CTCF	chr18:13139820-13140082	MCF-7	breast:	n/a	n/a
26	CTCF	chr18:13139855-13140050	GM19239	blood:	n/a	n/a
27	CTCF	chr18:13136720-13136870	GM12864	blood:	n/a	n/a
28	CTCF	chr18:13139876-13140016	Gliobla	brain:	n/a	n/a
29	CTCF	chr18:13139860-13140010	Caco-2	colon:	n/a	n/a
30	CTCF	chr18:13137220-13137370	GM12871	blood:	n/a	n/a
31	CTCF	chr18:13139786-13140017	A549	lung:	n/a	n/a
32	CTCF	chr18:13139860-13140010	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr18:13139848-13140012	GM10248	blood:	n/a	n/a
34	CTCF	chr18:13136080-13136230	GM12878	blood:	n/a	chr18:13136215-13136224
35	CTCF	chr18:13139861-13139998	LNCaP	prostate:	n/a	n/a
36	CTCF	chr18:13139780-13140083	HepG2	liver:	n/a	n/a
37	CTCF	chr18:13139860-13140010	HEK293	kidney:	n/a	n/a
38	CTCF	chr18:13139800-13139950	GM12865	blood:	n/a	n/a
39	CTCF	chr18:13139800-13139950	GM12870	blood:	n/a	n/a
40	CTCF	chr18:13137140-13137290	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr18:13139880-13140030	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr18:13136140-13136290	GM12874	blood:	n/a	chr18:13136215-13136224
43	CTCF	chr18:13139920-13140070	GM12866	blood:	n/a	n/a
44	CTCF	chr18:13139860-13140010	GM12878	blood:	n/a	n/a
45	CTCF	chr18:13139829-13140027	A549	lung:	n/a	n/a
46	CTCF	chr18:13139867-13140047	GM12892	blood:	n/a	n/a
47	CTCF	chr18:13137220-13137370	HepG2	liver:	n/a	n/a
48	CTCF	chr18:13137160-13137310	NHEK	skin:	n/a	n/a
49	CTCF	chr18:13139880-13140030	HepG2	liver:	n/a	n/a
50	CTCF	chr18:13142240-13142390	GM06990	blood:	n/a	chr18:13142251-13142259

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:13136426-13136476	LNCaP	prostate:	n/a
2	chr18:13136426-13136476	LNCaP	prostate:	n/a
3	chr18:13136899-13136949	HNPCEpiC	eye:	n/a
4	chr18:13136340-13136390	HRCEpiC	kidney:	n/a
5	chr18:13137315-13137365	AG04450	lung:	fetal
6	chr18:13136597-13136647	SK-N-MC	brain:	n/a
7	chr18:13136899-13136949	LNCaP	prostate:	n/a
8	chr18:13138034-13138084	HUVEC	blood vessel:	n/a
9	chr18:13136340-13136390	Caco-2	colon:	n/a
10	chr18:13136899-13136949	NT2-D1	testis:	n/a
11	chr18:13136597-13136647	ProgFib	skin:	n/a
12	chr18:13136597-13136647	HCF	heart:	n/a
13	chr18:13136340-13136390	HUVEC	blood vessel:	n/a
14	chr18:13137315-13137365	GM12892	blood:	n/a
15	chr18:13137315-13137365	MCF-7	breast:	n/a
16	chr18:13137315-13137365	AG10803	skin:	n/a
17	chr18:13138034-13138084	GM19239	blood:	n/a
18	chr18:13133368-13133418	LNCaP	prostate:	n/a
19	chr18:13136426-13136476	RPTEC	kidney:	n/a
20	chr18:13139942-13139992	SK-N-MC	brain:	n/a
21	chr18:13138034-13138084	SK-N-SH	brain:	n/a
22	chr18:13137129-13137179	ovcar-3	ovarian:	n/a
23	chr18:13139942-13139992	HEK293	kidney:	embryo
24	chr18:13139942-13139992	SK-N-SH_RA	brain:	n/a
25	chr18:13133368-13133418	K562	blood:	n/a
26	chr18:13139942-13139992	Caco-2	colon:	n/a
27	chr18:13137129-13137179	Hela-S3	cervix:	n/a
28	chr18:13136426-13136476	HRCEpiC	kidney:	n/a
29	chr18:13137315-13137365	HCPEpiC	choroid plexus:	n/a
30	chr18:13138034-13138084	PrEC	prostate:	n/a
31	chr18:13138034-13138084	A549	lung:	n/a
32	chr18:13138034-13138084	T-47D	breast:	n/a
33	chr18:13137129-13137179	CMK	blood:	n/a
34	chr18:13137315-13137365	HUVEC	blood vessel:	n/a
35	chr18:13137129-13137179	NHDF-neo	bronchial:	n/a
36	chr18:13138034-13138084	HCF	heart:	n/a
37	chr18:13137129-13137179	K562	blood:	n/a
38	chr18:13136899-13136949	GM06990	blood:	n/a
39	chr18:13137129-13137179	RPTEC	kidney:	n/a
40	chr18:13139942-13139992	Hela-S3	cervix:	n/a
41	chr18:13133368-13133418	SK-N-SH_RA	brain:	n/a
42	chr18:13136340-13136390	T-47D	breast:	n/a
43	chr18:13133368-13133418	SKMC	muscle:	n/a
44	chr18:13133368-13133418	HCPEpiC	choroid plexus:	n/a
45	chr18:13133368-13133418	AG04449	skin:	fetal
46	chr18:13136426-13136476	U87	brain:	n/a
47	chr18:13139942-13139992	NH-A	brain:	n/a
48	chr18:13138034-13138084	AG09309	skin:	n/a
49	chr18:13136899-13136949	AG04449	skin:	fetal
50	chr18:13133368-13133418	AoSMC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:13128234..13129969-chr18:13130472..13133331,2	K562	blood:
2	chr18:13139722..13141913-chr18:13426612..13428353,2	MCF-7	breast:
3	chr18:13099273..13102130-chr18:13123064..13124628,2	MCF-7	breast:
4	chr18:13140854..13145257-chr18:13540228..13543130,4	MCF-7	breast:
5	chr18:13124233..13126010-chr18:13129729..13132355,2	K562	blood:
6	chr18:13124233..13126010-chr18:13129729..13132355,2	K562	blood:
7	chr18:13122649..13124818-chr18:13125733..13129086,3	K562	blood:
8	chr18:13130413..13132086-chr18:13135033..13137817,2	MCF-7	breast:
9	chr18:13130413..13132086-chr18:13135033..13137817,2	MCF-7	breast:
10	chr18:13139784..13142937-chr18:13215706..13218370,3	MCF-7	breast:
11	chr18:13129145..13130942-chr18:13543662..13545815,2	MCF-7	breast:
12	chr18:13128234..13129969-chr18:13130472..13133331,2	K562	blood:
13	chr18:13134910..13136836-chr18:13149613..13152006,2	K562	blood:
14	chr18:13122649..13124818-chr18:13125733..13129086,3	K562	blood:
15	chr18:13142218..13144930-chr18:13215209..13217622,2	MCF-7	breast:
16	chr18:13133544..13136413-chr18:13146335..13148164,2	K562	blood:
17	chr18:13138041..13140192-chr18:13216726..13219205,3	MCF-7	breast:
18	chr18:13141699..13142727-chr18:13159347..13160164,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP192-1	chr18:13140141-13140373	NONHSAT058414

No data

Variant related genes	Relation type
ENSG00000267656	TF binding region
ENSG00000267656	CpG island
ENSG00000267690	chromatin interactions
ENSG00000168675	chromatin interactions
ENSG00000267239	chromatin interactions

Extended variants
information (count: 999 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7227681	chr18:13122618-13122619	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142676570	chr18:13122710-13122711	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540057264	chr18:13122738-13122739	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114255009	chr18:13122759-13122760	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs369690646	chr18:13122832-13122833	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs398032028	chr18:13122852-13122853	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76882544	chr18:13122854-13122855	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573599358	chr18:13122877-13122878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183825870	chr18:13122904-13122905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561945459	chr18:13122949-13122950	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188417907	chr18:13123040-13123041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114588801	chr18:13123073-13123074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547534357	chr18:13123129-13123130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544655981	chr18:13123169-13123170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541910840	chr18:13123177-13123178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560226820	chr18:13123245-13123246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559986682	chr18:13123251-13123252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73419545	chr18:13123318-13123319	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs193209386	chr18:13123322-13123323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568630013	chr18:13123357-13123358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529499746	chr18:13123363-13123364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373412112	chr18:13123387-13123388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185005215	chr18:13123411-13123412	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188162021	chr18:13123457-13123458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539853473	chr18:13123488-13123489	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557829971	chr18:13123494-13123495	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575750919	chr18:13123526-13123527	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144853102	chr18:13123530-13123531	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542853387	chr18:13123555-13123556	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111952497	chr18:13123574-13123575	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573543096	chr18:13123577-13123578	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138671524	chr18:13123631-13123632	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547084	chr18:13123645-13123646	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs564065584	chr18:13123667-13123668	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373004077	chr18:13123732-13123733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545004191	chr18:13123777-13123778	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116548648	chr18:13123875-13123876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529620	chr18:13123876-13123877	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs542784066	chr18:13123887-13123888	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375713747	chr18:13123940-13123941	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369488215	chr18:13123970-13123971	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373501244	chr18:13123972-13123973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560960897	chr18:13123987-13123988	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550131941	chr18:13124010-13124011	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529537555	chr18:13124022-13124023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191572095	chr18:13124032-13124033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550877313	chr18:13124042-13124043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141699500	chr18:13124071-13124072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540615089	chr18:13124073-13124074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377666306	chr18:13124079-13124080	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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	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
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:13086400-13128000	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr18:13099200-13124800	Strong transcription	Fetal Thymus	thymus
3	chr18:13099200-13127800	Strong transcription	Dnd41	blood
4	chr18:13099200-13128200	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr18:13099400-13129400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr18:13106200-13130000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr18:13106800-13135400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr18:13107000-13130400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr18:13109600-13126600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr18:13112000-13122800	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr18:13112200-13125600	Weak transcription	Fetal Brain Female	brain
12	chr18:13115600-13125400	Weak transcription	Colon Smooth Muscle	Colon
13	chr18:13116200-13126200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr18:13116200-13126800	Weak transcription	Esophagus	oesophagus
15	chr18:13116200-13128800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr18:13116200-13130000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr18:13118000-13126400	Weak transcription	Pancreas	Pancrea
18	chr18:13118000-13126400	Weak transcription	Right Ventricle	heart
19	chr18:13118000-13126800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr18:13118000-13126800	Weak transcription	Aorta	Aorta
21	chr18:13118000-13130000	Weak transcription	Small Intestine	intestine
22	chr18:13118200-13126800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr18:13118200-13132600	Weak transcription	HepG2	liver
24	chr18:13118400-13124400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr18:13118400-13135600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr18:13118400-13136200	Weak transcription	Psoas Muscle	Psoas
27	chr18:13118800-13126400	Weak transcription	Lung	lung
28	chr18:13118800-13130600	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr18:13118800-13136800	Weak transcription	HSMMtube	muscle
30	chr18:13119000-13126400	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr18:13119000-13127200	Weak transcription	Colonic Mucosa	Colon
32	chr18:13119000-13130800	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr18:13119000-13133400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr18:13119000-13134200	Weak transcription	Fetal Lung	lung
35	chr18:13119000-13136400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr18:13119200-13123400	Weak transcription	Left Ventricle	heart
37	chr18:13119200-13123400	Weak transcription	HSMM	muscle
38	chr18:13119200-13124600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr18:13119200-13124800	Weak transcription	Fetal Heart	heart
40	chr18:13119200-13126400	Weak transcription	Spleen	Spleen
41	chr18:13119200-13126800	Weak transcription	Fetal Muscle Leg	muscle
42	chr18:13119200-13135800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr18:13119200-13136400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr18:13119400-13123400	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr18:13119400-13124000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr18:13119400-13124200	Weak transcription	Liver	Liver
47	chr18:13119400-13124400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr18:13119400-13126400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr18:13119400-13126600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr18:13119400-13127000	Weak transcription	NHLF	lung

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