Variant report

Variant	esv3379697
Chromosome Location	chr16:12011449-12049700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:123)
Chromatin interactive
region (count:22)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr16:12043478-12043482	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr16:12043444-12043912	GM12878	blood:	n/a	n/a
3	BHLHE40	chr16:12043531-12043826	K562	blood:	n/a	n/a
4	CEBPB	chr16:12014912-12015127	K562	blood:	n/a	chr16:12014987-12014998
5	CEBPB	chr16:12014976-12015000	IMR90	lung:	n/a	chr16:12014987-12014998
6	CEBPB	chr16:12014945-12015096	A549	lung:	n/a	chr16:12014987-12014998
7	CEBPB	chr16:12014960-12015012	HepG2	liver:	n/a	chr16:12014987-12014998
8	CEBPB	chr16:12040374-12040519	IMR90	lung:	n/a	n/a
9	CEBPB	chr16:12046996-12047188	HepG2	liver:	n/a	chr16:12047058-12047069
10	CEBPB	chr16:12049474-12050227	IMR90	lung:	n/a	chr16:12050003-12050011
11	CTCF	chr16:12043580-12043730	GM12865	blood:	n/a	n/a
12	CTCF	chr16:12043580-12043730	GM12866	blood:	n/a	n/a
13	CTCF	chr16:12043412-12043872	A549	lung:	n/a	n/a
14	CTCF	chr16:12043520-12043670	NHEK	skin:	n/a	n/a
15	CTCF	chr16:12043220-12043370	NHDF-neo	bronchial:	n/a	n/a
16	CTCF	chr16:12043580-12043730	HMF	breast:	n/a	n/a
17	CTCF	chr16:12043538-12043788	LNCaP	prostate:	n/a	n/a
18	CTCF	chr16:12043561-12043766	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr16:12043506-12043800	MCF-7	breast:	n/a	n/a
20	CTCF	chr16:12043580-12043730	GM12868	blood:	n/a	n/a
21	CTCF	chr16:12043600-12043750	GM12875	blood:	n/a	n/a
22	CTCF	chr16:12043527-12043792	Medullo	brain:	n/a	n/a
23	CTCF	chr16:12043540-12043690	MCF-7	breast:	n/a	n/a
24	CTCF	chr16:12043600-12043750	HMF	breast:	n/a	n/a
25	CTCF	chr16:12043536-12043759	MCF-7	breast:	n/a	n/a
26	CTCF	chr16:12043600-12043750	GM12873	blood:	n/a	n/a
27	CTCF	chr16:12043491-12043833	A549	lung:	n/a	n/a
28	CTCF	chr16:12043580-12043730	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr16:12043620-12043770	AG09309	skin:	n/a	n/a
30	CTCF	chr16:12043580-12043730	RPTEC	kidney:	n/a	n/a
31	CTCF	chr16:12043567-12043736	GM20000	blood:	n/a	n/a
32	CTCF	chr16:12043580-12043730	BE2_C	brain:	n/a	n/a
33	CTCF	chr16:12043391-12043891	GM12878	blood:	n/a	n/a
34	CTCF	chr16:12043580-12043730	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr16:12043544-12043856	T-47D	breast:	n/a	n/a
36	CTCF	chr16:12043620-12043770	HCM	heart:	n/a	n/a
37	CTCF	chr16:12043600-12043750	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr16:12043516-12043782	GM19240	blood:	n/a	n/a
39	CTCF	chr16:12043560-12043710	GM12867	blood:	n/a	n/a
40	CTCF	chr16:12043600-12043750	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr16:12043526-12043793	LNCaP	prostate:	n/a	n/a
42	CTCF	chr16:12043620-12043770	GM12878	blood:	n/a	n/a
43	CTCF	chr16:12043580-12043730	A549	lung:	n/a	n/a
44	CTCF	chr16:12043580-12043730	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr16:12043580-12043730	K562	blood:	n/a	n/a
46	CTCF	chr16:12043580-12043730	GM12871	blood:	n/a	n/a
47	CTCF	chr16:12043530-12043744	A549	lung:	n/a	n/a
48	CTCF	chr16:12043407-12043855	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr16:12043560-12043710	WI-38	lung:	n/a	n/a
50	CTCF	chr16:12043459-12043891	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12043656-12043706	BJ	skin:	n/a
2	chr16:12043656-12043706	BJ	skin:	n/a
3	chr16:12043656-12043706	HRCEpiC	kidney:	n/a
4	chr16:12043656-12043706	AG04449	skin:	fetal
5	chr16:12012117-12012167	MCF10A-Er-Src	breast:	n/a
6	chr16:12043656-12043706	NT2-D1	testis:	n/a
7	chr16:12043656-12043706	GM12878	blood:	n/a
8	chr16:12012117-12012167	NT2-D1	testis:	n/a
9	chr16:12012117-12012167	GM19239	blood:	n/a
10	chr16:12012117-12012167	SK-N-SH_RA	brain:	n/a
11	chr16:12043656-12043706	IMR90	lung:	fetal
12	chr16:12012117-12012167	NHDF-neo	bronchial:	n/a
13	chr16:12043656-12043706	HAEpiC	amniotic membrane:	n/a
14	chr16:12012117-12012167	ovcar-3	ovarian:	n/a
15	chr16:12012117-12012167	NHBE	bronchial:	n/a
16	chr16:12043656-12043706	K562	blood:	n/a
17	chr16:12012117-12012167	HCT-116	colon:	n/a
18	chr16:12043656-12043706	HRE	kidney:	n/a
19	chr16:12043656-12043706	Hela-S3	cervix:	n/a
20	chr16:12043656-12043706	NHDF-neo	bronchial:	n/a
21	chr16:12012117-12012167	HCF	heart:	n/a
22	chr16:12043656-12043706	HCPEpiC	choroid plexus:	n/a
23	chr16:12043656-12043706	SAEC	small airway:	n/a
24	chr16:12012117-12012167	K562	blood:	n/a
25	chr16:12043656-12043706	GM12891	blood:	n/a
26	chr16:12043656-12043706	PANC-1	pancreas:	n/a
27	chr16:12043656-12043706	BE2_C	brain:	n/a
28	chr16:12012117-12012167	LNCaP	prostate:	n/a
29	chr16:12012117-12012167	T-47D	breast:	n/a
30	chr16:12043656-12043706	HL-60	blood:	n/a
31	chr16:12012117-12012167	AG04450	lung:	fetal
32	chr16:12012117-12012167	Caco-2	colon:	n/a
33	chr16:12012117-12012167	IMR90	lung:	fetal
34	chr16:12012117-12012167	HL-60	blood:	n/a
35	chr16:12012117-12012167	PANC-1	pancreas:	n/a
36	chr16:12043656-12043706	SK-N-MC	brain:	n/a
37	chr16:12043656-12043706	ProgFib	skin:	n/a
38	chr16:12012117-12012167	HNPCEpiC	eye:	n/a
39	chr16:12012117-12012167	HRCEpiC	kidney:	n/a
40	chr16:12043656-12043706	AG09309	skin:	n/a
41	chr16:12012117-12012167	AG09319	gingival:	n/a
42	chr16:12043656-12043706	HEEpiC	esophagus:	n/a
43	chr16:12043656-12043706	MCF-7	breast:	n/a
44	chr16:12012117-12012167	Hela-S3	cervix:	n/a
45	chr16:12043656-12043706	SKMC	muscle:	n/a
46	chr16:12012117-12012167	HMEC	breast:	n/a
47	chr16:12043656-12043706	Jurkat	blood:	n/a
48	chr16:12012117-12012167	ECC-1	luminal epithelium:	n/a
49	chr16:12043656-12043706	GM19239	blood:	n/a
50	chr16:12043656-12043706	NB4	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:11988100..11996073-chr16:12007143..12011577,10	MCF-7	breast:
2	chr16:12040634..12043579-chr16:12069006..12072022,3	K562	blood:
3	chr16:12044743..12047515-chr16:12054722..12057306,2	K562	blood:
4	chr16:12042157..12044609-chr16:12069694..12072152,2	MCF-7	breast:
5	chr16:12010494..12013016-chr16:12016316..12019639,3	MCF-7	breast:
6	chr16:10710065..10712953-chr16:12010240..12012086,2	MCF-7	breast:
7	chr16:12043121..12044152-chr16:12161482..12162455,10	MCF-7	breast:
8	chr16:12010691..12013114-chr16:12155698..12158691,2	MCF-7	breast:
9	chr16:12040634..12043075-chr16:12070522..12072619,2	K562	blood:
10	chr16:11831944..11836692-chr16:12007199..12011492,4	K562	blood:
11	chr16:12012124..12014555-chr16:12045355..12047902,2	K562	blood:
12	chr16:12012124..12014555-chr16:12045355..12047902,2	K562	blood:
13	chr16:12010494..12013016-chr16:12016316..12019639,3	MCF-7	breast:
14	chr16:11889469..11891900-chr16:12008639..12011975,4	MCF-7	breast:
15	chr16:11988764..11995180-chr16:12006980..12012068,9	MCF-7	breast:
16	chr16:11943912..11945965-chr16:12008319..12011491,4	MCF-7	breast:
17	chr16:12010326..12012796-chr16:12069017..12071833,3	MCF-7	breast:
18	chr16:12008911..12011067-chr16:12016765..12018435,3	MCF-7	breast:
19	chr16:11835219..11836957-chr16:12010044..12011553,2	MCF-7	breast:
20	chr16:12008780..12010777-chr16:12013125..12015097,2	MCF-7	breast:
21	chr16:12043208..12044500-chr16:12161423..12162347,8	K562	blood:
22	chr16:12006809..12011472-chr16:12069677..12072698,7	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSPT1-1	chr16:12021452-12021736	NONHSAT140608
2	lnc-GSPT1-1	chr16:12022838-12023132	NONHSAT140609
3	lnc-GSPT1-1	chr16:12023242-12023494	NONHSAT140609
4	lnc-GSPT1-1	chr16:12023097-12023200	NONHSAT140608
5	lnc-RP11-166B2.1.1-2	chr16:12027480-12027518	NONHSAT140610
6	lnc-RP11-166B2.1.1-2	chr16:12027682-12027781	NONHSAT140610
7	lnc-RP11-166B2.1.1-2	chr16:12031397-12031525	NONHSAT140610

No data

Variant related genes	Relation type
GSPT1	TF binding region
ENSG00000266163	TF binding region
ENSG00000234719	TF binding region
GSPT1	CpG island
ENSG00000266163	CpG island
ENSG00000234719	CpG island
ENSG00000153066	chromatin interactions
ENSG00000103342	chromatin interactions
ENSG00000262420	chromatin interactions
ENSG00000171490	chromatin interactions
ENSG00000263307	chromatin interactions
ENSG00000048471	chromatin interactions
ENSG00000234719	chromatin interactions
ENSG00000260488	chromatin interactions
ENSG00000122299	chromatin interactions
ENSG00000266163	chromatin interactions

Extended variants
information (count: 989 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:989 , 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	rs57871000	chr16:12011516-12011517	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185496594	chr16:12011551-12011552	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs144277789	chr16:12011553-12011554	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs531855216	chr16:12011667-12011668	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs548848691	chr16:12011719-12011720	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs568688817	chr16:12011734-12011735	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs113361660	chr16:12011751-12011752	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs386384256	chr16:12011752-12011753	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs35154046	chr16:12011753-12011754	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs374250129	chr16:12011769-12011770	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs374269990	chr16:12011775-12011776	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs559710023	chr16:12011825-12011826	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs564619634	chr16:12011832-12011833	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs367988970	chr16:12011834-12011835	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs561580662	chr16:12011883-12011884	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs369712112	chr16:12011889-12011890	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs527267019	chr16:12011890-12011891	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs547006855	chr16:12011898-12011899	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs111405423	chr16:12011900-12011901	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs538999211	chr16:12011920-12011921	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs555748415	chr16:12011922-12011923	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs377270260	chr16:12011925-12011926	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs575672597	chr16:12011928-12011929	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs535365394	chr16:12011964-12011965	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs535315778	chr16:12011994-12011995	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs148724077	chr16:12011995-12011996	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs379936	chr16:12012013-12012014	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs534140243	chr16:12012060-12012061	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs554213587	chr16:12012148-12012149	Enhancers Weak transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs189204796	chr16:12012190-12012191	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs181959446	chr16:12012228-12012229	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs185690528	chr16:12012259-12012260	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs188982756	chr16:12012382-12012383	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs542079679	chr16:12012384-12012385	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs201475180	chr16:12012397-12012398	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs569755498	chr16:12012451-12012452	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs59306656	chr16:12012452-12012453	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs113901233	chr16:12012457-12012458	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs186741759	chr16:12012464-12012465	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs367724994	chr16:12012474-12012475	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs190683643	chr16:12012478-12012479	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs140198038	chr16:12012493-12012494	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs182986982	chr16:12012501-12012502	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs560526513	chr16:12012535-12012536	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs532798283	chr16:12012540-12012541	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs456325	chr16:12012562-12012563	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs186017372	chr16:12012574-12012575	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs535601019	chr16:12012623-12012624	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs546362343	chr16:12012706-12012707	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs145614769	chr16:12012751-12012752	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12010800-12011600	Enhancers	Fetal Intestine Large	intestine
2	chr16:12010800-12011800	Weak transcription	Placenta	Placenta
3	chr16:12011200-12011600	Enhancers	HepG2	liver
4	chr16:12011200-12012400	Weak transcription	A549	lung
5	chr16:12011200-12012400	Weak transcription	Hela-S3	cervix
6	chr16:12011600-12014600	Weak transcription	HepG2	liver
7	chr16:12012000-12012200	Enhancers	Placenta	Placenta
8	chr16:12012600-12012800	Enhancers	A549	lung
9	chr16:12012600-12012800	Enhancers	Hela-S3	cervix
10	chr16:12014600-12014800	Enhancers	Right Ventricle	heart
11	chr16:12014600-12015000	Enhancers	HepG2	liver
12	chr16:12015000-12016000	Weak transcription	HepG2	liver
13	chr16:12016000-12016200	Enhancers	HepG2	liver
14	chr16:12021200-12021400	Enhancers	K562	blood
15	chr16:12030000-12030200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr16:12030800-12031000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr16:12030800-12031600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr16:12035400-12035800	Enhancers	H1 Cell Line	embryonic stem cell
19	chr16:12038600-12038800	Enhancers	HepG2	liver
20	chr16:12039400-12039800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr16:12039600-12040000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr16:12039600-12040400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr16:12040000-12040200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr16:12040000-12040400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr16:12040200-12040600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr16:12040400-12040600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr16:12040400-12040600	Enhancers	K562	blood
28	chr16:12040400-12041600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr16:12040400-12065400	Weak transcription	Fetal Intestine Small	intestine
30	chr16:12040600-12041600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr16:12040600-12042800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr16:12041600-12041800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr16:12041600-12042000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr16:12041600-12042000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr16:12041600-12042200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr16:12041600-12042200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr16:12041600-12042600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr16:12041800-12042000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr16:12041800-12042000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:12041800-12042000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr16:12041800-12042000	Enhancers	A549	lung
42	chr16:12041800-12042000	Bivalent Enhancer	K562	blood
43	chr16:12041800-12042200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr16:12041800-12042200	Strong transcription	Fetal Stomach	stomach
45	chr16:12042000-12042200	Bivalent Enhancer	HepG2	liver
46	chr16:12042000-12043200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr16:12042000-12049200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:12042000-12049600	Weak transcription	A549	lung
49	chr16:12042200-12043200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr16:12042200-12043400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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