Variant report

Variant	nsv1057105
Chromosome Location	chr18:143546-235928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1060)
CpG islands
(count:976)
Chromatin interactive
region (count:97)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:150435-150550	K562	blood:	n/a	n/a
2	ARID3A	chr18:199881-200096	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:158435-158687	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:189173-189528	HepG2	liver:	n/a	n/a
5	ATF1	chr18:158332-158983	K562	blood:	n/a	n/a
6	ATF3	chr18:158130-158721	HepG2	liver:	n/a	chr18:158290-158310
7	ATF3	chr18:158422-158737	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr18:158111-158789	GM12878	blood:	n/a	chr18:158290-158310
9	ATF3	chr18:158218-158388	GM12878	blood:	n/a	chr18:158290-158310
10	ATF3	chr18:158407-159043	K562	blood:	n/a	n/a
11	ATF3	chr18:158161-158396	K562	blood:	n/a	chr18:158290-158310
12	ATF3	chr18:158269-158734	HepG2	liver:	n/a	chr18:158290-158310
13	ATF3	chr18:158306-158739	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr18:158201-158395	H1-hESC	embryonic stem cell:	n/a	chr18:158290-158310
15	ATF3	chr18:158422-158663	GM12878	blood:	n/a	n/a
16	ATF3	chr18:158258-158725	K562	blood:	n/a	chr18:158290-158310
17	BACH1	chr18:158368-159507	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr18:158476-158601	K562	blood:	n/a	n/a
19	BACH1	chr18:158834-159144	K562	blood:	n/a	n/a
20	BCL11A	chr18:219072-219489	GM12878	blood:	n/a	n/a
21	BCL3	chr18:217619-218231	K562	blood:	n/a	n/a
22	BCLAF1	chr18:157980-158727	K562	blood:	n/a	n/a
23	BHLHE40	chr18:158221-158775	HepG2	liver:	n/a	n/a
24	BHLHE40	chr18:158165-158808	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:158201-159060	K562	blood:	n/a	n/a
26	BRCA1	chr18:158537-158560	HepG2	liver:	n/a	n/a
27	BRCA1	chr18:158364-158687	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr18:158389-158626	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr18:157970-158758	K562	blood:	n/a	n/a
30	CBX3	chr18:157987-158664	K562	blood:	n/a	n/a
31	CBX3	chr18:157972-158829	HCT-116	colon:	n/a	n/a
32	CCNT2	chr18:158176-159035	K562	blood:	n/a	n/a
33	CEBPB	chr18:155811-155939	HepG2	liver:	n/a	chr18:155888-155899
34	CEBPB	chr18:159455-159778	K562	blood:	n/a	n/a
35	CEBPB	chr18:212845-213060	K562	blood:	n/a	chr18:212950-212961
36	CEBPB	chr18:212854-213068	H1-hESC	embryonic stem cell:	n/a	chr18:212950-212961
37	CEBPB	chr18:212745-213108	MCF-7	breast:	n/a	chr18:212950-212961
38	CEBPB	chr18:227537-227565	HepG2	liver:	n/a	chr18:227540-227551 chr18:227540-227553
39	CEBPB	chr18:212939-213007	Hela-S3	cervix:	n/a	chr18:212950-212961
40	CEBPB	chr18:155773-156010	HepG2	liver:	n/a	chr18:155888-155899
41	CEBPB	chr18:212779-213059	MCF-7	breast:	n/a	chr18:212950-212961
42	CEBPB	chr18:155843-155953	H1-hESC	embryonic stem cell:	n/a	chr18:155888-155899
43	CEBPB	chr18:227512-227598	K562	blood:	n/a	chr18:227540-227551 chr18:227540-227553
44	CEBPB	chr18:155807-155958	K562	blood:	n/a	chr18:155888-155899
45	CEBPB	chr18:159554-159721	K562	blood:	n/a	n/a
46	CEBPB	chr18:159568-159751	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr18:212882-213012	A549	lung:	n/a	chr18:212950-212961
48	CEBPB	chr18:212894-213037	HepG2	liver:	n/a	chr18:212950-212961
49	CEBPD	chr18:158420-158717	HepG2	liver:	n/a	n/a
50	CEBPD	chr18:158337-158765	HepG2	liver:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:213653-213703	Hela-S3	cervix:	n/a
2	chr18:158011-158061	AG04449	skin:	fetal
3	chr18:165402-165452	AG04449	skin:	fetal
4	chr18:159793-159843	HL-60	blood:	n/a
5	chr18:159310-159360	NT2-D1	testis:	n/a
6	chr18:158567-158617	ECC-1	luminal epithelium:	n/a
7	chr18:213653-213703	HCT-116	colon:	n/a
8	chr18:158292-158342	PANC-1	pancreas:	n/a
9	chr18:158463-158513	A549	lung:	n/a
10	chr18:158011-158061	PFSK-1	brain:	n/a
11	chr18:158567-158617	HEEpiC	esophagus:	n/a
12	chr18:159310-159360	SK-N-MC	brain:	n/a
13	chr18:163067-163117	NHBE	bronchial:	n/a
14	chr18:159793-159843	HRPEpiC	eye:	n/a
15	chr18:155309-155359	Hela-S3	cervix:	n/a
16	chr18:158294-158344	U87	brain:	n/a
17	chr18:158229-158279	HCM	heart:	n/a
18	chr18:158294-158344	LNCaP	prostate:	n/a
19	chr18:158011-158061	GM06990	blood:	n/a
20	chr18:155309-155359	HL-60	blood:	n/a
21	chr18:159310-159360	GM12892	blood:	n/a
22	chr18:158551-158601	HCF	heart:	n/a
23	chr18:159265-159315	GM12891	blood:	n/a
24	chr18:165402-165452	Hepatocyte	liver:	n/a
25	chr18:158292-158342	AG09309	skin:	n/a
26	chr18:158551-158601	K562	blood:	n/a
27	chr18:159265-159315	HepG2	liver:	n/a
28	chr18:213653-213703	HMEC	breast:	n/a
29	chr18:158838-158888	AG09319	gingival:	n/a
30	chr18:158567-158617	PANC-1	pancreas:	n/a
31	chr18:159310-159360	NH-A	brain:	n/a
32	chr18:158294-158344	PFSK-1	brain:	n/a
33	chr18:158838-158888	HNPCEpiC	eye:	n/a
34	chr18:159310-159360	PrEC	prostate:	n/a
35	chr18:158292-158342	AoSMC	blood vessel:	n/a
36	chr18:158294-158344	HAEpiC	amniotic membrane:	n/a
37	chr18:155309-155359	ovcar-3	ovarian:	n/a
38	chr18:155309-155359	PFSK-1	brain:	n/a
39	chr18:158463-158513	HRE	kidney:	n/a
40	chr18:213653-213703	CMK	blood:	n/a
41	chr18:158294-158344	HCM	heart:	n/a
42	chr18:155309-155359	SK-N-SH	brain:	n/a
43	chr18:158551-158601	BJ	skin:	n/a
44	chr18:158551-158601	HPAEpiC	pulmonary alveolar:	n/a
45	chr18:158348-158398	HEK293	kidney:	embryo
46	chr18:158229-158279	Hela-S3	cervix:	n/a
47	chr18:159310-159360	NHBE	bronchial:	n/a
48	chr18:159310-159360	HUVEC	blood vessel:	n/a
49	chr18:159793-159843	ECC-1	luminal epithelium:	n/a
50	chr18:159793-159843	PANC-1	pancreas:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:145450..147918-chr18:815829..817789,2	K562	blood:
2	chr18:181732..184561-chr18:191775..193318,2	K562	blood:
3	chr18:191278..194179-chr18:207630..209643,2	K562	blood:
4	chr18:228215..230385-chr18:232509..234575,2	K562	blood:
5	chr18:199995..202051-chr18:204177..206910,3	MCF-7	breast:
6	chr18:219579..224693-chr18:231367..234811,5	K562	blood:
7	chr18:158132..161790-chr18:177799..183224,6	K562	blood:
8	chr18:185477..188373-chr18:192212..194752,2	K562	blood:
9	chr18:196681..199674-chr18:200190..202098,2	K562	blood:
10	chr18:181732..184561-chr18:191775..193318,2	K562	blood:
11	chr18:175173..178003-chr18:178964..182067,3	K562	blood:
12	chr18:208647..210877-chr18:212851..214807,2	MCF-7	breast:
13	chr18:225339..228063-chr18:231717..233482,2	K562	blood:
14	chr18:196681..199674-chr18:200190..202098,2	K562	blood:
15	chr18:139586..141641-chr18:148416..149949,2	K562	blood:
16	chr18:185477..188373-chr18:192212..194752,2	K562	blood:
17	chr18:175956..178936-chr18:178964..180560,2	K562	blood:
18	chr18:164137..168777-chr18:169771..171938,5	K562	blood:
19	chr18:141525..143923-chr18:160153..163099,2	K562	blood:
20	chr14:70233601..70234234-chr18:157797..158549,2	Hela-S3	cervix:
21	chr18:225092..228063-chr18:231717..233531,3	K562	blood:
22	chr18:218670..220555-chr18:223382..226341,3	K562	blood:
23	chr18:204844..208399-chr18:208509..211522,4	K562	blood:
24	chr18:226011..228697-chr18:258254..260700,2	K562	blood:
25	chr18:233093..235805-chr18:238186..240596,2	MCF-7	breast:
26	chr18:181284..183295-chr18:192261..194255,2	K562	blood:
27	chr18:226421..229879-chr18:235133..238634,3	K562	blood:
28	chr18:226421..229879-chr18:235133..238634,3	K562	blood:
29	chr18:233992..236480-chr18:246342..248551,2	K562	blood:
30	chr18:159584..161282-chr18:196677..199436,2	K562	blood:
31	chr18:169841..172227-chr18:180107..182467,2	K562	blood:
32	chr18:175956..178936-chr18:178964..180560,2	K562	blood:
33	chr18:172540..174181-chr18:176241..178456,2	K562	blood:
34	chr18:158417..159997-chr18:214475..216956,2	K562	blood:
35	chr18:172540..174181-chr18:176241..178456,2	K562	blood:
36	chr18:158226..159980-chr18:161322..163085,2	MCF-7	breast:
37	chr18:234980..237687-chr18:246158..248551,2	K562	blood:
38	chr18:181273..184246-chr18:226060..228939,2	K562	blood:
39	chr18:148615..151946-chr18:155352..158851,3	K562	blood:
40	chr18:141525..143923-chr18:160153..163099,2	K562	blood:
41	chr18:199995..202051-chr18:204177..206910,3	MCF-7	breast:
42	chr18:227929..230720-chr18:265725..267925,3	K562	blood:
43	chr18:204844..208179-chr18:208509..211348,3	K562	blood:
44	chr18:187241..189505-chr18:246011..247661,2	K562	blood:
45	chr18:197810..202080-chr18:202633..206358,5	K562	blood:
46	chr18:155065..156905-chr18:157468..160011,3	K562	blood:
47	chr18:227929..232043-chr18:265870..268355,3	K562	blood:
48	chr18:197810..202080-chr18:202633..206358,5	K562	blood:
49	chr18:173629..175507-chr18:185992..188221,2	MCF-7	breast:
50	chr18:160787..162407-chr18:176462..179044,2	K562	blood:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP14	hsa-miR-204-5p	chr18:213710-213731
2	THOC1	hsa-miR-186-5p	chr18:225149-225174
3	USP14	hsa-miR-204-5p	chr18:212024-212043
4	THOC1	hsa-miR-186-5p	chr18:214607-214625

Variant related genes	Relation type
THOC1	TF binding region
USP14	TF binding region
THOC1	CpG island
USP14	CpG island
ENSG00000100650	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000223635	chromatin interactions
ENSG00000069248	chromatin interactions
ENSG00000101557	chromatin interactions
ENSG00000263884	chromatin interactions

Extended variants
information (count: 3490 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3490 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76209227	chr18:143559-143560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574387560	chr18:143578-143579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11876622	chr18:143591-143592	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559898786	chr18:143635-143636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190711433	chr18:143639-143640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116788100	chr18:143658-143659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149019516	chr18:143673-143674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565184598	chr18:143701-143702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548654868	chr18:143737-143738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143820720	chr18:143798-143799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376035825	chr18:143918-143919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7232480	chr18:143973-143974	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs112638692	chr18:143987-143988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537203364	chr18:146652-146653	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs556704046	chr18:146676-146677	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs150945490	chr18:146783-146784	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs535899122	chr18:146792-146793	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs112648682	chr18:146823-146824	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs373959710	chr18:146824-146825	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs374764207	chr18:146834-146835	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs199840096	chr18:146835-146836	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs377182693	chr18:146839-146840	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs370425972	chr18:146843-146844	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs572370130	chr18:146850-146851	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs200125303	chr18:146855-146856	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs543010777	chr18:146861-146862	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs201238233	chr18:146865-146866	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369050007	chr18:146867-146868	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs372723610	chr18:146868-146869	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs546201531	chr18:146895-146896	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs573280508	chr18:146897-146898	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs372082012	chr18:146915-146916	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs562594427	chr18:146918-146919	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs150026918	chr18:146926-146927	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs57083463	chr18:146927-146928	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564953842	chr18:146944-146945	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs190961684	chr18:146949-146950	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs59741346	chr18:146953-146954	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs547025525	chr18:146965-146966	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs9965503	chr18:146966-146967	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs139023470	chr18:146978-146979	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs551390235	chr18:146988-146989	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs369993503	chr18:147002-147003	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs183185723	chr18:147011-147012	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs537284607	chr18:147019-147020	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs549197235	chr18:147051-147052	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs568602188	chr18:147068-147069	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs535968299	chr18:147074-147075	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs111313872	chr18:147114-147115	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs56005815	chr18:147138-147139	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:70)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	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
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:143000-144000	Enhancers	K562	blood
2	chr18:146600-147800	Active TSS	Placenta	Placenta
3	chr18:155400-155600	Enhancers	HepG2	liver
4	chr18:155600-156000	Flanking Active TSS	HepG2	liver
5	chr18:156000-156200	Enhancers	K562	blood
6	chr18:156000-156400	Enhancers	HepG2	liver
7	chr18:156200-156800	Weak transcription	K562	blood
8	chr18:156400-156800	Weak transcription	HepG2	liver
9	chr18:156800-157200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr18:156800-158000	Enhancers	HepG2	liver
11	chr18:156800-158000	Enhancers	K562	blood
12	chr18:157200-158000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr18:157400-157800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr18:157400-157800	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr18:157400-157800	Enhancers	Brain Substantia Nigra	brain
16	chr18:157400-158000	Enhancers	Primary B cells from peripheral blood	blood
17	chr18:157400-158000	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr18:157400-158000	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr18:157600-158000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr18:157600-158000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr18:157600-158000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr18:157600-158000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr18:157600-158000	Enhancers	Brain Cingulate Gyrus	brain
24	chr18:157600-158000	Enhancers	Brain Hippocampus Middle	brain
25	chr18:157600-158000	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr18:157600-158000	Enhancers	Fetal Kidney	kidney
27	chr18:157600-158000	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr18:157600-158000	Enhancers	Dnd41	blood
29	chr18:157600-158200	Enhancers	Primary B cells from cord blood	blood
30	chr18:157800-158000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr18:157800-158600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr18:158000-158200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
33	chr18:158000-158200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr18:158000-158200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr18:158000-158200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr18:158000-158200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr18:158000-158200	Flanking Active TSS	Primary B cells from peripheral blood	blood
38	chr18:158000-158200	Enhancers	Primary hematopoietic stem cells	blood
39	chr18:158000-158200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr18:158000-158200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr18:158000-158200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr18:158000-158200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr18:158000-158200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr18:158000-158200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr18:158000-158200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr18:158000-158200	Flanking Active TSS	Fetal Thymus	thymus
47	chr18:158000-158200	Active TSS	Right Atrium	heart
48	chr18:158000-158200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr18:158000-158200	Flanking Active TSS	A549	lung
50	chr18:158000-158200	Flanking Active TSS	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links