Variant report

Variant	nsv543644
Chromosome Location	chr18:9576145-9612516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:0)
Chromatin interactive
region (count:62)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:9608225-9609199	K562	blood:	n/a	n/a
2	ARID3A	chr18:9605332-9605800	K562	blood:	n/a	n/a
3	ARID3A	chr18:9612249-9612537	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:9608351-9609353	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:9609469-9609484	K562	blood:	n/a	n/a
6	ARID3A	chr18:9606251-9606255	K562	blood:	n/a	n/a
7	ARID3A	chr18:9612362-9612525	K562	blood:	n/a	n/a
8	ARID3A	chr18:9599684-9599993	HepG2	liver:	n/a	n/a
9	ATF1	chr18:9608218-9608706	K562	blood:	n/a	n/a
10	ATF1	chr18:9609216-9609513	K562	blood:	n/a	n/a
11	ATF3	chr18:9608249-9608720	K562	blood:	n/a	chr18:9608534-9608549
12	BACH1	chr18:9608836-9608975	K562	blood:	n/a	n/a
13	BACH1	chr18:9609384-9609592	K562	blood:	n/a	n/a
14	BATF	chr18:9594757-9595023	GM12878	blood:	n/a	chr18:9594897-9594908
15	BATF	chr18:9594728-9595078	GM12878	blood:	n/a	chr18:9594897-9594908
16	BCLAF1	chr18:9612190-9612625	GM12878	blood:	n/a	n/a
17	BHLHE40	chr18:9608738-9609121	HepG2	liver:	n/a	n/a
18	BRCA1	chr18:9612216-9612548	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr18:9581637-9582041	K562	blood:	n/a	n/a
20	CBX3	chr18:9600201-9600529	K562	blood:	n/a	n/a
21	CBX3	chr18:9600131-9600847	K562	blood:	n/a	n/a
22	CCNT2	chr18:9609382-9609594	K562	blood:	n/a	n/a
23	CCNT2	chr18:9608340-9608608	K562	blood:	n/a	n/a
24	CCNT2	chr18:9608825-9609049	K562	blood:	n/a	n/a
25	CEBPB	chr18:9612221-9612609	MCF-7	breast:	n/a	n/a
26	CEBPB	chr18:9612277-9612522	HepG2	liver:	n/a	n/a
27	CEBPB	chr18:9612162-9612626	A549	lung:	n/a	n/a
28	CEBPB	chr18:9609337-9609426	K562	blood:	n/a	n/a
29	CEBPB	chr18:9612327-9612516	K562	blood:	n/a	n/a
30	CEBPB	chr18:9612232-9612639	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr18:9608320-9608682	K562	blood:	n/a	n/a
32	CEBPB	chr18:9612277-9612596	A549	lung:	n/a	n/a
33	CEBPB	chr18:9612273-9612616	A549	lung:	n/a	n/a
34	CEBPB	chr18:9608180-9608676	K562	blood:	n/a	n/a
35	CEBPD	chr18:9608150-9608725	K562	blood:	n/a	chr18:9608504-9608515
36	CEBPD	chr18:9608167-9608720	K562	blood:	n/a	chr18:9608504-9608515
37	CHD2	chr18:9612277-9612401	K562	blood:	n/a	n/a
38	CHD2	chr18:9594956-9594995	GM12878	blood:	n/a	n/a
39	CREB1	chr18:9608120-9608832	K562	blood:	n/a	chr18:9608535-9608548
40	CTCF	chr18:9612360-9612510	HA-sp	spinal cord:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
41	CTCF	chr18:9612340-9612490	HMF	breast:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
42	CTCF	chr18:9612320-9612470	AG10803	skin:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
43	CTCF	chr18:9612240-9612390	WI-38	lung:	n/a	n/a
44	CTCF	chr18:9612233-9612536	H1-hESC	embryonic stem cell:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
45	CTCF	chr18:9612284-9612510	LNCaP	prostate:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
46	CTCF	chr18:9612320-9612470	HRE	kidney:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
47	CTCF	chr18:9612340-9612490	RPTEC	kidney:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
48	CTCF	chr18:9612274-9612555	ProgFib	skin:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
49	CTCF	chr18:9612320-9612470	GM12867	blood:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412
50	CTCF	chr18:9612340-9612490	SK-N-SH_RA	brain:	n/a	chr18:9612399-9612417 chr18:9612400-9612416 chr18:9612401-9612422 chr18:9612404-9612412

No data

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:9610312..9611854-chr18:9611926..9614343,2	MCF-7	breast:
2	chr18:9579114..9582159-chr18:9598940..9602426,3	K562	blood:
3	chr18:9575576..9576151-chr18:9661257..9662212,2	MCF-7	breast:
4	chr18:9561840..9564033-chr18:9575235..9576918,2	K562	blood:
5	chr18:9582156..9584516-chr18:9588377..9590362,3	K562	blood:
6	chr18:9574087..9576896-chr18:9600490..9602058,2	K562	blood:
7	chr18:9573898..9575587-chr18:9599993..9601990,2	K562	blood:
8	chr18:9595087..9597869-chr18:9607007..9610720,3	MCF-7	breast:
9	chr18:9584648..9586476-chr18:9589220..9590730,2	K562	blood:
10	chr18:9612231..9612794-chr18:9683319..9684221,2	MCF-7	breast:
11	chr18:9612064..9613483-chr18:9661140..9662203,5	MCF-7	breast:
12	chr18:9581775..9584005-chr18:9596096..9598190,2	K562	blood:
13	chr18:9566461..9572065-chr18:9572620..9578759,7	K562	blood:
14	chr18:9583998..9586737-chr18:9586977..9590180,4	MCF-7	breast:
15	chr18:9585681..9587283-chr18:9614464..9616135,2	MCF-7	breast:
16	chr18:9603204..9605560-chr18:9708114..9710476,2	K562	blood:
17	chr18:9604425..9606972-chr18:9949570..9951578,2	K562	blood:
18	chr18:9580164..9581759-chr18:9584185..9586548,2	K562	blood:
19	chr18:9582156..9584516-chr18:9588377..9590362,3	K562	blood:
20	chr18:9580227..9582159-chr18:9599784..9602426,2	K562	blood:
21	chr18:9610247..9612763-chr18:9683592..9685519,2	K562	blood:
22	chr18:9608061..9610764-chr18:9617117..9619483,2	MCF-7	breast:
23	chr18:9594858..9597558-chr18:9614248..9616397,2	MCF-7	breast:
24	chr18:9596087..9600746-chr18:9613522..9617540,6	MCF-7	breast:
25	chr18:9581775..9584005-chr18:9596096..9598190,2	K562	blood:
26	chr18:9608014..9609757-chr18:9710686..9713009,2	K562	blood:
27	chr18:9578277..9581617-chr18:9743011..9745983,3	K562	blood:
28	chr18:9584648..9586476-chr18:9589220..9590730,2	K562	blood:
29	chr18:9593285..9595195-chr18:9598496..9600998,2	K562	blood:
30	chr18:9593285..9595195-chr18:9598496..9600998,2	K562	blood:
31	chr18:9602295..9606145-chr18:9613242..9615540,3	MCF-7	breast:
32	chr18:9575405..9579354-chr18:9587737..9592465,5	K562	blood:
33	chr18:9566461..9572540-chr18:9573224..9580743,8	K562	blood:
34	chr18:9552433..9554256-chr18:9573786..9576485,2	K562	blood:
35	chr18:9474317..9476491-chr18:9607261..9609060,2	K562	blood:
36	chr18:9612320..9612866-chr18:9673221..9674104,3	MCF-7	breast:
37	chr18:9586574..9588610-chr18:9591063..9593804,2	K562	blood:
38	chr18:9580164..9581759-chr18:9584185..9586548,2	K562	blood:
39	chr18:9611182..9615699-chr18:9705314..9711194,13	MCF-7	breast:
40	chr18:9595087..9597869-chr18:9607007..9610720,3	MCF-7	breast:
41	chr18:9612136..9615353-chr18:9912435..9915971,5	MCF-7	breast:
42	chr18:9569658..9574401-chr18:9612462..9616455,5	K562	blood:
43	chr18:9577278..9579746-chr18:9582108..9585693,4	K562	blood:
44	chr18:9577244..9580030-chr18:9613761..9615940,2	K562	blood:
45	chr18:9582694..9585330-chr18:9707569..9709416,2	K562	blood:
46	chr18:9606592..9610420-chr18:9613242..9616597,5	MCF-7	breast:
47	chr18:9580227..9582159-chr18:9599784..9602426,2	K562	blood:
48	chr18:9584735..9586577-chr18:9599877..9602634,2	K562	blood:
49	chr18:9574087..9576896-chr18:9600490..9602058,2	K562	blood:
50	chr18:9604914..9606998-chr18:9897522..9900316,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RALBP1-1	chr18:9589794-9590180	ENSG00000266541.1
2	lnc-RALBP1-4	chr18:9607146-9607283	l_1522_chr18:9604874-9609362_testes
3	lnc-RALBP1-4	chr18:9609193-9609362	l_1522_chr18:9604874-9609362_testes
4	lnc-RALBP1-1	chr18:9587384-9587530	ENSG00000266541.1
5	lnc-RALBP1-4	chr18:9604875-9605333	l_1522_chr18:9604874-9609362_testes
6	lnc-PIEZO2-14	chr18:9594823-9595151	NONHSAT057228

No data

Variant related genes	Relation type
ENSG00000263627	TF binding region
ENSG00000266541	TF binding region
PPP4R1	TF binding region
ENSG00000212572	chromatin interactions
ENSG00000168461	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000263627	chromatin interactions
ENSG00000266541	chromatin interactions
ENSG00000154845	chromatin interactions
ENSG00000272799	chromatin interactions
ENSG00000101558	chromatin interactions

Extended variants
information (count: 1336 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1336 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370793331	chr18:9576150-9576151	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs528959306	chr18:9576220-9576221	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550640389	chr18:9576277-9576278	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143788438	chr18:9576334-9576335	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs7240277	chr18:9576350-9576351	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551707055	chr18:9576364-9576365	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183348024	chr18:9576420-9576421	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs143952698	chr18:9576472-9576473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533766935	chr18:9576473-9576474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549147830	chr18:9576475-9576476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567683187	chr18:9576493-9576494	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533320733	chr18:9576587-9576588	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538333997	chr18:9576643-9576644	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556180986	chr18:9576677-9576678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188081887	chr18:9576697-9576698	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538619830	chr18:9576703-9576704	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs554057558	chr18:9576706-9576707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191348955	chr18:9576720-9576721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374475786	chr18:9576731-9576732	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546701210	chr18:9576748-9576749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143048580	chr18:9576751-9576752	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs35776972	chr18:9576752-9576753	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs72091988	chr18:9576753-9576754	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs57129395	chr18:9576754-9576755	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs62087459	chr18:9576755-9576756	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200878338	chr18:9576789-9576790	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs147330884	chr18:9576804-9576805	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532980805	chr18:9576817-9576818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs551363310	chr18:9576818-9576819	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560225513	chr18:9576841-9576842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527563927	chr18:9576898-9576899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10616192	chr18:9576901-9576902	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs398059039	chr18:9576906-9576907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548953547	chr18:9576951-9576952	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567446309	chr18:9576953-9576954	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182451469	chr18:9576968-9576969	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370217850	chr18:9577019-9577020	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373639726	chr18:9577058-9577059	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201899657	chr18:9577145-9577146	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs571372092	chr18:9577187-9577188	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs371794287	chr18:9577219-9577220	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538680224	chr18:9577223-9577224	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs374695098	chr18:9577227-9577228	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs329000	chr18:9577352-9577353	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs551489599	chr18:9577384-9577385	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139322621	chr18:9577389-9577390	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372333489	chr18:9577414-9577415	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs569144453	chr18:9577420-9577421	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538172463	chr18:9577442-9577443	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576581051	chr18:9577443-9577444	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
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
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1694 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9545800-9583600	Strong transcription	Primary T cells fromperipheralblood	blood
2	chr18:9545800-9595200	Strong transcription	Dnd41	blood
3	chr18:9549600-9581800	Weak transcription	Psoas Muscle	Psoas
4	chr18:9551000-9612200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr18:9553800-9582000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr18:9553800-9613600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr18:9554400-9578400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr18:9555400-9580600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr18:9558000-9580600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr18:9559000-9586800	Weak transcription	Small Intestine	intestine
11	chr18:9559600-9580600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr18:9559600-9587000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr18:9560200-9577600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr18:9560400-9577600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr18:9563000-9581600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr18:9563200-9580600	Weak transcription	Aorta	Aorta
17	chr18:9563600-9577400	Weak transcription	Spleen	Spleen
18	chr18:9563600-9580600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr18:9563600-9591600	Weak transcription	Colonic Mucosa	Colon
20	chr18:9563600-9594800	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr18:9564200-9579600	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr18:9565000-9579400	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr18:9565200-9594200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr18:9565600-9578000	Strong transcription	Placenta	Placenta
25	chr18:9566400-9577600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr18:9566600-9577000	Strong transcription	HMEC	breast
27	chr18:9566800-9592600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr18:9566800-9594600	Strong transcription	HSMM	muscle
29	chr18:9567000-9576400	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr18:9567200-9577800	Strong transcription	NHEK	skin
31	chr18:9568600-9587600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr18:9569200-9578200	Weak transcription	Gastric	stomach
33	chr18:9569800-9576200	Strong transcription	Fetal Thymus	thymus
34	chr18:9569800-9582400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr18:9570400-9594400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr18:9570600-9577400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr18:9570600-9577400	Weak transcription	Lung	lung
38	chr18:9570600-9577400	Weak transcription	Pancreas	Pancrea
39	chr18:9570600-9580600	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr18:9570600-9580600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr18:9570600-9580800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr18:9570600-9580800	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr18:9570600-9580800	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr18:9570800-9577400	Weak transcription	Fetal Brain Female	brain
45	chr18:9570800-9579400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr18:9571000-9577200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr18:9571800-9579400	Weak transcription	Right Ventricle	heart
48	chr18:9572000-9577200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr18:9572000-9580800	Weak transcription	GM12878-XiMat	blood
50	chr18:9572200-9577400	Weak transcription	Left Ventricle	heart

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