Variant report

Variant	nsv576498
Chromosome Location	chr18:12650900-12658436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:470)
CpG islands
(count:551)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:470 , 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	chr18:12656801-12656872	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:12652724-12653356	K562	blood:	n/a	n/a
3	BACH1	chr18:12658233-12658814	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:12656956-12658031	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr18:12656832-12657146	K562	blood:	n/a	n/a
6	BHLHE40	chr18:12657711-12657720	HepG2	liver:	n/a	n/a
7	BHLHE40	chr18:12658112-12658339	GM12878	blood:	n/a	n/a
8	BHLHE40	chr18:12656971-12657245	K562	blood:	n/a	chr18:12657213-12657229
9	BHLHE40	chr18:12658019-12658356	HepG2	liver:	n/a	n/a
10	BHLHE40	chr18:12658128-12658361	K562	blood:	n/a	n/a
11	BRCA1	chr18:12656608-12656967	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr18:12657677-12657702	HepG2	liver:	n/a	n/a
13	CBX3	chr18:12656955-12657361	K562	blood:	n/a	n/a
14	CCNT2	chr18:12656952-12658330	K562	blood:	n/a	n/a
15	CEBPB	chr18:12658017-12658217	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr18:12652923-12653398	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr18:12653806-12653977	K562	blood:	n/a	n/a
18	CEBPB	chr18:12656689-12656975	IMR90	lung:	n/a	n/a
19	CEBPB	chr18:12656640-12656957	K562	blood:	n/a	n/a
20	CEBPB	chr18:12653806-12654027	IMR90	lung:	n/a	n/a
21	CEBPB	chr18:12656641-12657030	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr18:12652976-12653400	IMR90	lung:	n/a	n/a
23	CEBPB	chr18:12653142-12653309	HepG2	liver:	n/a	n/a
24	CHD1	chr18:12656380-12659102	IMR90	lung:	n/a	n/a
25	CHD2	chr18:12657035-12658381	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr18:12657439-12657480	HepG2	liver:	n/a	n/a
27	CREB1	chr18:12656957-12658467	HepG2	liver:	n/a	n/a
28	CREB1	chr18:12657351-12657811	K562	blood:	n/a	n/a
29	CREB1	chr18:12657763-12658498	A549	lung:	n/a	n/a
30	CREB1	chr18:12657013-12657382	A549	lung:	n/a	n/a
31	CREB1	chr18:12658035-12658519	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr18:12657860-12658806	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr18:12658212-12658419	GM12891	blood:	n/a	n/a
34	CTCF	chr18:12658120-12658270	GM12869	blood:	n/a	n/a
35	CTCF	chr18:12657236-12657305	MCF-7	breast:	n/a	n/a
36	CTCF	chr18:12658140-12658290	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr18:12658220-12658370	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr18:12658280-12658430	GM12871	blood:	n/a	n/a
39	CTCF	chr18:12658256-12658261	Fibrobl	skin:	n/a	n/a
40	CTCF	chr18:12658160-12658310	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr18:12658160-12658310	BJ	skin:	n/a	n/a
42	CTCF	chr18:12657828-12657947	MCF-7	breast:	n/a	n/a
43	CTCF	chr18:12657874-12657948	Fibrobl	skin:	n/a	n/a
44	CTCF	chr18:12657846-12657961	MCF-7	breast:	n/a	n/a
45	CTCF	chr18:12658148-12658420	GM19238	blood:	n/a	n/a
46	CTCF	chr18:12658220-12658370	GM06990	blood:	n/a	n/a
47	CTCF	chr18:12658280-12658430	GM12867	blood:	n/a	n/a
48	CTCF	chr18:12658205-12658444	GM19239	blood:	n/a	n/a
49	CTCF	chr18:12657160-12657310	SAEC	small airway:	n/a	n/a
50	CTCF	chr18:12658260-12658410	HMEC	breast:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12657909-12657959	HCF	heart:	n/a
2	chr18:12657692-12657742	GM12892	blood:	n/a
3	chr18:12657909-12657959	HCF	heart:	n/a
4	chr18:12657692-12657742	GM12892	blood:	n/a
5	chr18:12656910-12656960	AG09319	gingival:	n/a
6	chr18:12657749-12657799	MCF10A-Er-Src	breast:	n/a
7	chr18:12657749-12657799	HCPEpiC	choroid plexus:	n/a
8	chr18:12654742-12654792	HCF	heart:	n/a
9	chr18:12657166-12657216	PFSK-1	brain:	n/a
10	chr18:12654742-12654792	IMR90	lung:	fetal
11	chr18:12656910-12656960	CMK	blood:	n/a
12	chr18:12657056-12657106	SAEC	small airway:	n/a
13	chr18:12657056-12657106	HCT-116	colon:	n/a
14	chr18:12657056-12657106	GM12891	blood:	n/a
15	chr18:12657692-12657742	HRE	kidney:	n/a
16	chr18:12657749-12657799	PrEC	prostate:	n/a
17	chr18:12657166-12657216	NB4	blood:	n/a
18	chr18:12657056-12657106	HPAEpiC	pulmonary alveolar:	n/a
19	chr18:12657056-12657106	IMR90	lung:	fetal
20	chr18:12657749-12657799	HRPEpiC	eye:	n/a
21	chr18:12657056-12657106	AG10803	skin:	n/a
22	chr18:12657909-12657959	HEEpiC	esophagus:	n/a
23	chr18:12657909-12657959	K562	blood:	n/a
24	chr18:12657692-12657742	Caco-2	colon:	n/a
25	chr18:12654742-12654792	HCM	heart:	n/a
26	chr18:12656824-12656874	AG04449	skin:	fetal
27	chr18:12657692-12657742	GM06990	blood:	n/a
28	chr18:12657056-12657106	CMK	blood:	n/a
29	chr18:12656824-12656874	HCPEpiC	choroid plexus:	n/a
30	chr18:12657056-12657106	HAEpiC	amniotic membrane:	n/a
31	chr18:12656824-12656874	ECC-1	luminal epithelium:	n/a
32	chr18:12658233-12658283	Hepatocyte	liver:	n/a
33	chr18:12657909-12657959	U87	brain:	n/a
34	chr18:12658233-12658283	HNPCEpiC	eye:	n/a
35	chr18:12657749-12657799	ovcar-3	ovarian:	n/a
36	chr18:12657056-12657106	HCPEpiC	choroid plexus:	n/a
37	chr18:12656824-12656874	ProgFib	skin:	n/a
38	chr18:12657692-12657742	HepG2	liver:	n/a
39	chr18:12657749-12657799	BJ	skin:	n/a
40	chr18:12657749-12657799	GM12892	blood:	n/a
41	chr18:12656910-12656960	T-47D	breast:	n/a
42	chr18:12657166-12657216	PANC-1	pancreas:	n/a
43	chr18:12654742-12654792	HIPEpiC	eye:	n/a
44	chr18:12657749-12657799	Jurkat	blood:	n/a
45	chr18:12657749-12657799	HEK293	kidney:	embryo
46	chr18:12657749-12657799	K562	blood:	n/a
47	chr18:12656910-12656960	Hela-S3	cervix:	n/a
48	chr18:12657692-12657742	AG04449	skin:	fetal
49	chr18:12658233-12658283	ProgFib	skin:	n/a
50	chr18:12654742-12654792	PANC-1	pancreas:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12654302..12656873-chr18:12657659..12659911,2	MCF-7	breast:
2	chr18:12651259..12653780-chr18:12656567..12658681,4	MCF-7	breast:
3	chr18:12651259..12653780-chr18:12656567..12658681,4	MCF-7	breast:
4	chr18:12657085..12659648-chr18:12882376..12884207,2	K562	blood:
5	chr18:12443233..12445110-chr18:12655911..12658418,2	MCF-7	breast:
6	chr18:12657668..12659639-chr18:12701302..12703566,3	MCF-7	breast:
7	chr18:12643422..12646156-chr18:12653146..12655533,3	MCF-7	breast:
8	chr18:12657540..12658417-chr22:46475896..46476854,2	Hela-S3	cervix:
9	chr18:12418998..12421842-chr18:12658407..12660489,3	MCF-7	breast:
10	chr18:12648702..12654959-chr18:12655130..12658770,8	K562	blood:
11	chr18:12375564..12378929-chr18:12655169..12659722,7	MCF-7	breast:
12	chr18:12374049..12378632-chr18:12655494..12660049,8	K562	blood:
13	chr18:12656018..12659900-chr18:12701056..12705601,5	K562	blood:
14	chr18:12654302..12656873-chr18:12657659..12659911,2	MCF-7	breast:
15	chr18:12649857..12654959-chr18:12655130..12658770,11	K562	blood:
16	chr18:12418519..12420831-chr18:12657213..12660140,3	MCF-7	breast:
17	chr18:12648702..12654959-chr18:12655130..12658770,8	K562	blood:
18	chr18:12372972..12377735-chr18:12656683..12660675,6	K562	blood:
19	chr18:12404079..12409500-chr18:12655702..12659746,9	K562	blood:
20	chr18:12307735..12310451-chr18:12655693..12658579,2	MCF-7	breast:
21	chr18:12406559..12410304-chr18:12656888..12659730,4	MCF-7	breast:
22	chr18:12649454..12651212-chr18:12654910..12658304,3	MCF-7	breast:
23	chr18:12543497..12545408-chr18:12653876..12656459,2	MCF-7	breast:
24	chr18:12646496..12648953-chr18:12649691..12651231,2	K562	blood:
25	chr18:12435991..12438957-chr18:12658317..12660163,2	MCF-7	breast:
26	chr18:12375685..12377446-chr18:12655932..12658656,3	MCF-7	breast:
27	chr18:12649857..12654959-chr18:12655130..12658770,11	K562	blood:

No data

Variant related genes	Relation type
PSMG2	TF binding region
SPIRE1	TF binding region
ENSG00000215527	TF binding region
PSMG2	CpG island
SPIRE1	CpG island
ENSG00000215527	CpG island
ENSG00000141385	chromatin interactions
ENSG00000141391	chromatin interactions
ENSG00000128789	chromatin interactions
ENSG00000215527	chromatin interactions
ENSG00000101624	chromatin interactions
ENSG00000134278	chromatin interactions
ENSG00000175354	chromatin interactions
ENSG00000197182	chromatin interactions
ENSG00000267199	chromatin interactions
ENSG00000176014	chromatin interactions

Extended variants
information (count: 265 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4796966	chr18:12650900-12650901	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112286784	chr18:12650938-12650939	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs184638793	chr18:12650939-12650940	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs554050158	chr18:12650958-12650959	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs113206760	chr18:12650966-12650967	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs115838413	chr18:12651044-12651045	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs71353220	chr18:12651053-12651054	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs149770727	chr18:12651073-12651074	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs569496015	chr18:12651080-12651081	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs565664583	chr18:12651094-12651095	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs79889188	chr18:12651106-12651107	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs189185318	chr18:12651112-12651113	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs149918545	chr18:12651122-12651123	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs369722089	chr18:12651168-12651169	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs529680728	chr18:12651181-12651182	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs556810147	chr18:12651256-12651257	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs578238418	chr18:12651270-12651271	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs545713839	chr18:12651320-12651321	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs182461130	chr18:12651333-12651334	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs146580077	chr18:12651351-12651352	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs146886877	chr18:12651367-12651368	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs546140593	chr18:12651378-12651379	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs9957278	chr18:12651404-12651405	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs561408169	chr18:12651413-12651414	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs375939661	chr18:12651423-12651424	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs531708883	chr18:12651426-12651427	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs576880996	chr18:12651448-12651449	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs373551188	chr18:12651491-12651492	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs549522283	chr18:12651501-12651502	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs141283203	chr18:12651530-12651531	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs143672873	chr18:12651574-12651575	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs547658158	chr18:12651604-12651605	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs565868314	chr18:12651650-12651651	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs548229664	chr18:12651659-12651660	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs113403601	chr18:12651685-12651686	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs544339780	chr18:12651691-12651692	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs185755966	chr18:12651693-12651694	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs115499485	chr18:12651715-12651716	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs562609986	chr18:12651768-12651769	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs189503647	chr18:12651789-12651790	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs34963673	chr18:12651821-12651822	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs537147046	chr18:12651866-12651867	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs76195993	chr18:12651887-12651888	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs542056168	chr18:12651899-12651900	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs370132584	chr18:12651901-12651902	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs146797794	chr18:12651942-12651943	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs115863039	chr18:12651987-12651988	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs148926885	chr18:12651992-12651993	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs114501593	chr18:12651999-12652000	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs74732619	chr18:12652016-12652017	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12607800-12651800	Weak transcription	Brain Germinal Matrix	brain
2	chr18:12633600-12655800	Weak transcription	Fetal Stomach	stomach
3	chr18:12637800-12652000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr18:12640400-12652000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr18:12643600-12651800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr18:12643800-12653000	Weak transcription	A549	lung
7	chr18:12644400-12651800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr18:12646000-12652200	Weak transcription	NH-A	brain
9	chr18:12646000-12653000	Weak transcription	Thymus	Thymus
10	chr18:12646000-12654000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr18:12646200-12651000	Weak transcription	Brain Substantia Nigra	brain
12	chr18:12646200-12651600	Weak transcription	HSMM	muscle
13	chr18:12646200-12651600	Weak transcription	HSMMtube	muscle
14	chr18:12646200-12651800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr18:12646200-12651800	Weak transcription	Fetal Kidney	kidney
16	chr18:12646200-12652600	Weak transcription	HMEC	breast
17	chr18:12646200-12652800	Weak transcription	Brain Anterior Caudate	brain
18	chr18:12646200-12652800	Weak transcription	K562	blood
19	chr18:12646200-12653000	Weak transcription	Right Atrium	heart
20	chr18:12646200-12653000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr18:12646200-12653000	Weak transcription	NHLF	lung
22	chr18:12646200-12657000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr18:12646200-12657000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr18:12646400-12651000	Weak transcription	NHDF-Ad	bronchial
25	chr18:12646400-12651800	Weak transcription	Brain Hippocampus Middle	brain
26	chr18:12646400-12652000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr18:12646400-12652000	Weak transcription	Fetal Intestine Small	intestine
28	chr18:12646400-12652200	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr18:12646400-12652400	Weak transcription	Brain Angular Gyrus	brain
30	chr18:12646400-12652800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr18:12646400-12652800	Weak transcription	Ovary	ovary
32	chr18:12646400-12653000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr18:12646400-12653000	Weak transcription	Fetal Thymus	thymus
34	chr18:12646400-12653000	Weak transcription	Psoas Muscle	Psoas
35	chr18:12646400-12656600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr18:12646400-12656600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr18:12646400-12657000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr18:12646600-12651400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr18:12646600-12651800	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr18:12646600-12652200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr18:12646600-12653000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr18:12646800-12652200	Weak transcription	Fetal Brain Male	brain
43	chr18:12647000-12651200	Weak transcription	Fetal Heart	heart
44	chr18:12647000-12653000	Weak transcription	Lung	lung
45	chr18:12648000-12651000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr18:12648000-12656800	Weak transcription	Left Ventricle	heart
47	chr18:12648400-12651800	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr18:12648400-12652600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr18:12648400-12656600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr18:12648600-12651000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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