Variant report

Variant	nsv2201
Chromosome Location	chr18:9247631-9279825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:154)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:154 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr18:9273240-9273386	HepG2	liver:	n/a	chr18:9273296-9273307
2	CHD2	chr18:9258989-9259011	K562	blood:	n/a	n/a
3	CTCF	chr18:9275961-9276081	MCF-7	breast:	n/a	chr18:9276008-9276024
4	CTCF	chr18:9270900-9271050	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr18:9275940-9276090	MCF-7	breast:	n/a	chr18:9276008-9276024
6	CTCF	chr18:9275989-9276049	Pancreas_OC	pancreas:	n/a	chr18:9276008-9276024
7	CTCF	chr18:9261640-9261790	GM12873	blood:	n/a	n/a
8	CTCF	chr18:9275934-9276091	LNCaP	prostate:	n/a	chr18:9276008-9276024
9	CTCF	chr18:9252180-9252330	HRPEpiC	eye:	n/a	n/a
10	CTCF	chr18:9275892-9276154	GM12878	blood:	n/a	chr18:9276008-9276024
11	CTCF	chr18:9275951-9276070	LNCaP	prostate:	n/a	chr18:9276008-9276024
12	CTCF	chr18:9275060-9275210	GM12869	blood:	n/a	n/a
13	CTCF	chr18:9275994-9276046	MCF-7	breast:	n/a	chr18:9276008-9276024
14	CTCF	chr18:9275974-9276026	Hela-S3	cervix:	n/a	chr18:9276008-9276024
15	CTCF	chr18:9276006-9276047	K562	blood:	n/a	chr18:9276008-9276024
16	EBF1	chr18:9260552-9260802	GM12878	blood:	n/a	n/a
17	EGR1	chr18:9264896-9265110	K562	blood:	n/a	n/a
18	EP300	chr18:9259008-9259075	K562	blood:	n/a	n/a
19	GABPA	chr18:9267446-9267539	Hela-S3	cervix:	n/a	n/a
20	GATA3	chr18:9251195-9251353	SH-SY5Y	brain:	n/a	chr18:9251238-9251255
21	GATA3	chr18:9279748-9279850	SH-SY5Y	brain:	n/a	n/a
22	GTF2F1	chr18:9260878-9261090	H1-hESC	embryonic stem cell:	n/a	n/a
23	GTF2F1	chr18:9255933-9256118	H1-hESC	embryonic stem cell:	n/a	n/a
24	GTF2F1	chr18:9257853-9257885	H1-hESC	embryonic stem cell:	n/a	n/a
25	GTF2F1	chr18:9256965-9256985	H1-hESC	embryonic stem cell:	n/a	n/a
26	GTF2F1	chr18:9263543-9263554	K562	blood:	n/a	n/a
27	GTF2F1	chr18:9256928-9257047	K562	blood:	n/a	n/a
28	GTF2F1	chr18:9261736-9261748	H1-hESC	embryonic stem cell:	n/a	n/a
29	HDAC2	chr18:9260445-9260677	K562	blood:	n/a	n/a
30	KAP1	chr18:9256064-9256603	K562	blood:	n/a	n/a
31	KAP1	chr18:9258242-9258498	K562	blood:	n/a	n/a
32	KAP1	chr18:9255196-9255443	K562	blood:	n/a	n/a
33	MAFF	chr18:9275623-9275799	K562	blood:	n/a	n/a
34	MAFK	chr18:9275620-9275862	HepG2	liver:	n/a	n/a
35	MAFK	chr18:9275576-9275827	HepG2	liver:	n/a	n/a
36	MAFK	chr18:9255901-9255972	HepG2	liver:	n/a	n/a
37	MAX	chr18:9261027-9261180	H1-hESC	embryonic stem cell:	n/a	n/a
38	MYC	chr18:9261379-9261402	H1-hESC	embryonic stem cell:	n/a	n/a
39	NFYB	chr18:9249604-9249748	GM12878	blood:	n/a	n/a
40	NFYB	chr18:9279702-9279877	GM12878	blood:	n/a	n/a
41	POLR2A	chr18:9271901-9272068	GM12878	blood:	n/a	n/a
42	POLR2A	chr18:9276553-9276558	ProgFib	skin:	n/a	n/a
43	POLR2A	chr18:9248520-9248556	K562	blood:	n/a	n/a
44	POLR2A	chr18:9256948-9257340	GM12891	blood:	n/a	n/a
45	POLR2A	chr18:9276611-9276656	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr18:9275150-9275252	ProgFib	skin:	n/a	n/a
47	POLR2A	chr18:9258965-9258975	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr18:9258423-9258436	HepG2	liver:	n/a	n/a
49	POLR2A	chr18:9263086-9263997	GM12878	blood:	n/a	n/a
50	POLR2A	chr18:9260764-9261307	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:9261071-9261121	HRCEpiC	kidney:	n/a
2	chr18:9261071-9261121	GM12878	blood:	n/a
3	chr18:9261071-9261121	SKMC	muscle:	n/a
4	chr18:9261071-9261121	PANC-1	pancreas:	n/a
5	chr18:9261071-9261121	HRE	kidney:	n/a
6	chr18:9261071-9261121	PFSK-1	brain:	n/a
7	chr18:9261071-9261121	PrEC	prostate:	n/a
8	chr18:9261071-9261121	HEK293	kidney:	embryo
9	chr18:9261071-9261121	NT2-D1	testis:	n/a
10	chr18:9261071-9261121	NB4	blood:	n/a
11	chr18:9261071-9261121	HEEpiC	esophagus:	n/a
12	chr18:9261071-9261121	HIPEpiC	eye:	n/a
13	chr18:9261071-9261121	HNPCEpiC	eye:	n/a
14	chr18:9261071-9261121	A549	lung:	n/a
15	chr18:9261071-9261121	BJ	skin:	n/a
16	chr18:9261071-9261121	Caco-2	colon:	n/a
17	chr18:9261071-9261121	BE2_C	brain:	n/a
18	chr18:9261071-9261121	ECC-1	luminal epithelium:	n/a
19	chr18:9261071-9261121	HCT-116	colon:	n/a
20	chr18:9261071-9261121	AG04450	lung:	fetal
21	chr18:9261071-9261121	H1-hESC	embryonic stem cell:	embryo
22	chr18:9261071-9261121	U87	brain:	n/a
23	chr18:9261071-9261121	NHDF-neo	bronchial:	n/a
24	chr18:9261071-9261121	LNCaP	prostate:	n/a
25	chr18:9261071-9261121	HPAEpiC	pulmonary alveolar:	n/a
26	chr18:9261071-9261121	NHBE	bronchial:	n/a
27	chr18:9261071-9261121	ovcar-3	ovarian:	n/a
28	chr18:9261071-9261121	HepG2	liver:	n/a
29	chr18:9261071-9261121	HRPEpiC	eye:	n/a
30	chr18:9261071-9261121	RPTEC	kidney:	n/a
31	chr18:9261071-9261121	HMEC	breast:	n/a
32	chr18:9261071-9261121	Jurkat	blood:	n/a
33	chr18:9261071-9261121	T-47D	breast:	n/a
34	chr18:9261071-9261121	HL-60	blood:	n/a
35	chr18:9261071-9261121	GM06990	blood:	n/a
36	chr18:9261071-9261121	MCF-7	breast:	n/a
37	chr18:9261071-9261121	HCM	heart:	n/a
38	chr18:9261071-9261121	HUVEC	blood vessel:	n/a
39	chr18:9261071-9261121	AoSMC	blood vessel:	n/a
40	chr18:9261071-9261121	SK-N-SH_RA	brain:	n/a
41	chr18:9261071-9261121	HCF	heart:	n/a
42	chr18:9261071-9261121	AG04449	skin:	fetal
43	chr18:9261071-9261121	SAEC	small airway:	n/a
44	chr18:9261071-9261121	IMR90	lung:	fetal
45	chr18:9261071-9261121	K562	blood:	n/a
46	chr18:9261071-9261121	HAEpiC	amniotic membrane:	n/a
47	chr18:9261071-9261121	GM12892	blood:	n/a
48	chr18:9261071-9261121	GM12891	blood:	n/a
49	chr18:9261071-9261121	AG09319	gingival:	n/a
50	chr18:9261071-9261121	SK-N-MC	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:9250388..9251906-chr18:9254855..9256434,2	K562	blood:
2	chr18:9258105..9261280-chr18:9261761..9265772,3	K562	blood:
3	chr18:9252289..9254016-chr18:9256022..9258799,2	MCF-7	breast:
4	chr18:9250388..9251906-chr18:9254855..9256434,2	K562	blood:
5	chr18:9257452..9259305-chr18:9285325..9287150,2	K562	blood:
6	chr18:9275475..9277686-chr18:9279833..9282533,2	K562	blood:
7	chr18:9262107..9264956-chr18:9417331..9418844,2	K562	blood:
8	chr18:9272647..9274830-chr18:9278892..9281463,2	MCF-7	breast:
9	chr18:9272647..9274830-chr18:9278892..9281463,2	MCF-7	breast:
10	chr18:9252289..9254016-chr18:9256022..9258799,2	MCF-7	breast:
11	chr18:9240868..9242942-chr18:9247072..9249031,2	K562	blood:
12	chr18:9249091..9251466-chr18:9256573..9259954,3	K562	blood:
13	chr18:9252879..9257377-chr18:9257965..9263892,6	K562	blood:
14	chr18:9249091..9251466-chr18:9256573..9259954,3	K562	blood:
15	chr18:9246217..9247723-chr18:9249489..9251834,2	K562	blood:
16	chr18:9258135..9261280-chr18:9262408..9265307,3	K562	blood:
17	chr18:9240868..9244297-chr18:9247072..9249031,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TWSG1-2	chr18:9259386-9260388	ENSG00000273284.1

No data

Variant related genes	Relation type
ENSG00000273284	TF binding region
ENSG00000239087	TF binding region
ENSG00000200883	TF binding region
ENSG00000207092	TF binding region
ENSG00000273284	CpG island
ENSG00000239087	CpG island
ENSG00000200883	CpG island
ENSG00000207092	CpG island
ENSG00000273284	chromatin interactions
ENSG00000207092	chromatin interactions
ENSG00000200883	chromatin interactions

Extended variants
information (count: 1466 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1466 , 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	rs533356389	chr18:9247651-9247652	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs560494337	chr18:9247676-9247677	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557301281	chr18:9247710-9247711	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs565748778	chr18:9247751-9247752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186558697	chr18:9247765-9247766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540090578	chr18:9247766-9247767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201710394	chr18:9247781-9247782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558073267	chr18:9247809-9247810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72939224	chr18:9247849-9247850	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs368568183	chr18:9247850-9247851	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370994839	chr18:9247857-9247858	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs147829812	chr18:9247942-9247943	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552685639	chr18:9247952-9247953	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs72939226	chr18:9247996-9247997	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs568022561	chr18:9248035-9248036	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs190878266	chr18:9248043-9248044	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563263349	chr18:9248047-9248048	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs575456607	chr18:9248075-9248076	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs1893198	chr18:9248150-9248151	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs141297702	chr18:9248222-9248223	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528333447	chr18:9248244-9248245	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370726655	chr18:9248270-9248271	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34495373	chr18:9248279-9248280	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183700109	chr18:9248280-9248281	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531398707	chr18:9248287-9248288	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529358836	chr18:9248295-9248296	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142726362	chr18:9248310-9248311	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570746804	chr18:9248338-9248339	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79158655	chr18:9248357-9248358	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539447967	chr18:9248367-9248368	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552092534	chr18:9248459-9248460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188274123	chr18:9248464-9248465	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534155162	chr18:9248491-9248492	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555516068	chr18:9248493-9248494	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574210737	chr18:9248520-9248521	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs75643928	chr18:9248582-9248583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572555139	chr18:9248590-9248591	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs151004003	chr18:9248614-9248615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192949772	chr18:9248646-9248647	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140285700	chr18:9248725-9248726	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368129962	chr18:9248726-9248727	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199788114	chr18:9248731-9248732	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140961017	chr18:9248743-9248744	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564405356	chr18:9248760-9248761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574470392	chr18:9248777-9248778	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183140489	chr18:9248804-9248805	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs540454165	chr18:9248819-9248820	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs371315925	chr18:9248833-9248834	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs529377470	chr18:9248876-9248877	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs551101775	chr18:9248924-9248925	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:834 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9192200-9284000	Weak transcription	NHEK	skin
2	chr18:9211800-9254800	Weak transcription	NH-A	brain
3	chr18:9212200-9254200	Weak transcription	Hela-S3	cervix
4	chr18:9216000-9250000	Weak transcription	Small Intestine	intestine
5	chr18:9216000-9289600	Weak transcription	HMEC	breast
6	chr18:9228200-9258000	Weak transcription	Fetal Heart	heart
7	chr18:9232600-9254200	Weak transcription	HUVEC	blood vessel
8	chr18:9232600-9261400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr18:9232800-9248000	Weak transcription	Fetal Brain Male	brain
10	chr18:9232800-9273000	Weak transcription	Fetal Kidney	kidney
11	chr18:9233200-9249600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr18:9233200-9264200	Weak transcription	Brain Anterior Caudate	brain
13	chr18:9233400-9256400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr18:9233400-9265800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr18:9234200-9253600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:9234200-9264200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr18:9234400-9254200	Weak transcription	Fetal Thymus	thymus
18	chr18:9234400-9280400	Weak transcription	Psoas Muscle	Psoas
19	chr18:9234600-9256400	Weak transcription	Brain Germinal Matrix	brain
20	chr18:9234600-9264800	Weak transcription	Colonic Mucosa	Colon
21	chr18:9234600-9278000	Weak transcription	Brain Angular Gyrus	brain
22	chr18:9234800-9252200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr18:9234800-9252200	Weak transcription	Ovary	ovary
24	chr18:9234800-9254200	Weak transcription	A549	lung
25	chr18:9234800-9256800	Weak transcription	Fetal Brain Female	brain
26	chr18:9234800-9264200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr18:9234800-9264800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr18:9234800-9264800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr18:9234800-9264800	Weak transcription	Lung	lung
30	chr18:9234800-9264800	Weak transcription	Pancreas	Pancrea
31	chr18:9234800-9290000	Weak transcription	NHLF	lung
32	chr18:9235000-9251400	Weak transcription	Fetal Intestine Small	intestine
33	chr18:9235000-9257000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr18:9235000-9264600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr18:9235000-9264800	Weak transcription	Gastric	stomach
36	chr18:9235000-9264800	Weak transcription	Right Ventricle	heart
37	chr18:9235000-9285400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr18:9235200-9260800	Weak transcription	Esophagus	oesophagus
39	chr18:9235200-9264200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr18:9235200-9264600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr18:9235400-9264800	Weak transcription	Fetal Stomach	stomach
42	chr18:9235400-9270800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr18:9235600-9258200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr18:9235600-9264600	Weak transcription	Stomach Smooth Muscle	stomach
45	chr18:9235800-9260800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr18:9235800-9264800	Weak transcription	Thymus	Thymus
47	chr18:9236200-9253400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr18:9236600-9264200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr18:9237000-9264200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr18:9239600-9264600	Weak transcription	HepG2	liver

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