Variant report

Variant	nsv901852
Chromosome Location	chr14:46187306-46361344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:533)
CpG islands
(count:366)
Chromatin interactive
region (count:12)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:46336378-46337127	GM12878	blood:	n/a	n/a
2	ATF2	chr14:46337595-46337969	GM12878	blood:	n/a	n/a
3	ATF2	chr14:46337571-46338159	GM12878	blood:	n/a	n/a
4	BACH1	chr14:46351093-46351107	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr14:46337483-46338059	GM12878	blood:	n/a	chr14:46337729-46337740
6	BATF	chr14:46337483-46337971	GM12878	blood:	n/a	chr14:46337729-46337740
7	BATF	chr14:46336397-46337076	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:46337474-46337979	GM12878	blood:	n/a	n/a
9	BCL11A	chr14:46337580-46337867	GM12878	blood:	n/a	n/a
10	BCL11A	chr14:46338183-46338481	GM12878	blood:	n/a	n/a
11	BCL3	chr14:46337522-46337975	GM12878	blood:	n/a	n/a
12	BCL3	chr14:46337578-46337949	GM12878	blood:	n/a	n/a
13	BCL3	chr14:46336621-46336979	GM12878	blood:	n/a	n/a
14	BCLAF1	chr14:46337617-46337960	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:46337665-46337965	GM12878	blood:	n/a	n/a
16	CBX3	chr14:46256472-46256659	K562	blood:	n/a	n/a
17	CBX3	chr14:46213002-46213438	HCT-116	colon:	n/a	n/a
18	CEBPB	chr14:46242906-46243113	HepG2	liver:	n/a	chr14:46243004-46243015
19	CEBPB	chr14:46270324-46270772	HepG2	liver:	n/a	chr14:46270518-46270529
20	CEBPB	chr14:46248535-46248671	HepG2	liver:	n/a	chr14:46248607-46248618
21	CEBPB	chr14:46195157-46195161	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr14:46309387-46309957	HepG2	liver:	n/a	chr14:46309800-46309811
23	CEBPB	chr14:46270325-46270606	IMR90	lung:	n/a	chr14:46270518-46270529
24	CEBPB	chr14:46357543-46357739	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:46309406-46309962	A549	lung:	n/a	chr14:46309800-46309811
26	CEBPB	chr14:46321607-46321769	A549	lung:	n/a	n/a
27	CEBPB	chr14:46270317-46270820	A549	lung:	n/a	chr14:46270518-46270529
28	CEBPB	chr14:46242879-46243131	IMR90	lung:	n/a	chr14:46243004-46243015
29	CEBPB	chr14:46232907-46233168	HepG2	liver:	n/a	n/a
30	CHD2	chr14:46360235-46360350	HepG2	liver:	n/a	n/a
31	CREB1	chr14:46276327-46276806	GM12878	blood:	n/a	n/a
32	CREB1	chr14:46337522-46338032	GM12878	blood:	n/a	n/a
33	CTCF	chr14:46340320-46340470	BE2_C	brain:	n/a	n/a
34	CTCF	chr14:46279840-46279990	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr14:46187837-46188304	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:46307940-46308090	BJ	skin:	n/a	chr14:46307991-46308009 chr14:46307993-46308014
37	CTCF	chr14:46340360-46340510	GM12874	blood:	n/a	n/a
38	CTCF	chr14:46279440-46279590	NHEK	skin:	n/a	n/a
39	CTCF	chr14:46279760-46279910	GM12873	blood:	n/a	n/a
40	CTCF	chr14:46188020-46188170	HCT-116	colon:	n/a	n/a
41	CTCF	chr14:46326836-46326874	GM10266	blood:	n/a	n/a
42	CTCF	chr14:46340300-46340450	HEK293	kidney:	n/a	n/a
43	CTCF	chr14:46279820-46279970	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr14:46279840-46279990	BJ	skin:	n/a	n/a
45	CTCF	chr14:46279780-46279930	HRE	kidney:	n/a	n/a
46	CTCF	chr14:46340340-46340490	HCT-116	colon:	n/a	n/a
47	CTCF	chr14:46187944-46188147	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr14:46310934-46311190	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr14:46279858-46279970	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:46308009-46308027	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46241576-46241626	SAEC	small airway:	n/a
2	chr14:46241576-46241626	AG04449	skin:	fetal
3	chr14:46241576-46241626	HMEC	breast:	n/a
4	chr14:46358139-46358189	Hela-S3	cervix:	n/a
5	chr14:46300358-46300408	HAEpiC	amniotic membrane:	n/a
6	chr14:46241576-46241626	BJ	skin:	n/a
7	chr14:46300358-46300408	Hela-S3	cervix:	n/a
8	chr14:46283172-46283222	PrEC	prostate:	n/a
9	chr14:46300358-46300408	HUVEC	blood vessel:	n/a
10	chr14:46283117-46283167	HIPEpiC	eye:	n/a
11	chr14:46358279-46358329	HRCEpiC	kidney:	n/a
12	chr14:46300358-46300408	HRE	kidney:	n/a
13	chr14:46241576-46241626	BE2_C	brain:	n/a
14	chr14:46358139-46358189	HCPEpiC	choroid plexus:	n/a
15	chr14:46283172-46283222	HepG2	liver:	n/a
16	chr14:46241576-46241626	AG04450	lung:	fetal
17	chr14:46241576-46241626	HUVEC	blood vessel:	n/a
18	chr14:46241576-46241626	NT2-D1	testis:	n/a
19	chr14:46358279-46358329	SK-N-SH	brain:	n/a
20	chr14:46283172-46283222	RPTEC	kidney:	n/a
21	chr14:46241576-46241626	HEK293	kidney:	embryo
22	chr14:46283172-46283222	HRCEpiC	kidney:	n/a
23	chr14:46283172-46283222	AG04449	skin:	fetal
24	chr14:46358279-46358329	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:46283172-46283222	IMR90	lung:	fetal
26	chr14:46283172-46283222	AG09309	skin:	n/a
27	chr14:46241576-46241626	MCF-7	breast:	n/a
28	chr14:46358139-46358189	HRE	kidney:	n/a
29	chr14:46358279-46358329	HCT-116	colon:	n/a
30	chr14:46283117-46283167	AG09319	gingival:	n/a
31	chr14:46283172-46283222	HUVEC	blood vessel:	n/a
32	chr14:46358139-46358189	HCM	heart:	n/a
33	chr14:46300358-46300408	T-47D	breast:	n/a
34	chr14:46358139-46358189	HCT-116	colon:	n/a
35	chr14:46358279-46358329	SKMC	muscle:	n/a
36	chr14:46283172-46283222	HRE	kidney:	n/a
37	chr14:46283117-46283167	T-47D	breast:	n/a
38	chr14:46283117-46283167	AG04450	lung:	fetal
39	chr14:46358139-46358189	SK-N-SH_RA	brain:	n/a
40	chr14:46358279-46358329	AG09309	skin:	n/a
41	chr14:46358139-46358189	BE2_C	brain:	n/a
42	chr14:46358139-46358189	PFSK-1	brain:	n/a
43	chr14:46283172-46283222	HEK293	kidney:	embryo
44	chr14:46283172-46283222	PFSK-1	brain:	n/a
45	chr14:46358279-46358329	GM12878	blood:	n/a
46	chr14:46283117-46283167	HEK293	kidney:	embryo
47	chr14:46283172-46283222	A549	lung:	n/a
48	chr14:46358139-46358189	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:46300358-46300408	MCF-7	breast:	n/a
50	chr14:46300358-46300408	GM12892	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
2	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
3	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:
4	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
5	chr10:29154738..29155346-chr14:46193775..46194564,2	MCF-7	breast:
6	chr14:46119850..46120526-chr14:46279646..46280307,2	MCF-7	breast:
7	chr14:46147376..46147982-chr14:46279500..46280082,2	MCF-7	breast:
8	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
9	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
10	chr14:46079191..46080200-chr14:46279301..46280311,3	MCF-7	breast:
11	chr14:46182590..46185086-chr14:46185381..46187428,2	MCF-7	breast:
12	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036668
2	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
3	lnc-FANCM-5	chr14:46213166-46213370	NONHSAT036671
4	lnc-FANCM-5	chr14:46241339-46241424	XLOC_010816
5	lnc-FANCM-5	chr14:46217809-46217860	XLOC_010816
6	lnc-FANCM-5	chr14:46213325-46213370	XLOC_010816
7	lnc-FANCM-5	chr14:46241338-46241424	NONHSAT036671
8	lnc-FANCM-5	chr14:46241613-46241659	XLOC_010816
9	lnc-FANCM-5	chr14:46241612-46241659	NONHSAT036671
10	lnc-FANCM-5	chr14:46195358-46195474	NONHSAT036670
11	lnc-FANCM-5	chr14:46217809-46217840	NONHSAT036670
12	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036670
13	lnc-FANCM-5	chr14:46217809-46217893	NONHSAT036668
14	lnc-FANCM-5	chr14:46217539-46217865	NONHSAT036671

No data

Variant related genes	Relation type
ENSG00000258616	TF binding region
ENSG00000264420	TF binding region
ENSG00000258616	CpG island
ENSG00000264420	CpG island
ENSG00000258616	chromatin interactions

Extended variants
information (count: 2655 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2655 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1266261	chr14:46187306-46187307	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1266260	chr14:46187363-46187364	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs564452930	chr14:46187389-46187390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531774562	chr14:46187430-46187431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190905753	chr14:46187454-46187455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562016077	chr14:46187468-46187469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529394774	chr14:46187495-46187496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149626758	chr14:46187504-46187505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565912035	chr14:46187526-46187527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534555944	chr14:46187583-46187584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551295121	chr14:46187704-46187705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144342733	chr14:46187707-46187708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140633300	chr14:46187727-46187728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182754866	chr14:46187733-46187734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185213628	chr14:46187738-46187739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201687125	chr14:46187743-46187744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554122302	chr14:46187777-46187778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534754034	chr14:46187779-46187780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554071001	chr14:46187796-46187797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567857069	chr14:46187828-46187829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536807182	chr14:46187853-46187854	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs35080792	chr14:46187862-46187863	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs546505096	chr14:46187876-46187877	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs575439616	chr14:46187893-46187894	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374167639	chr14:46187934-46187935	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558455964	chr14:46187985-46187986	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs191102490	chr14:46188021-46188022	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs139105875	chr14:46188025-46188026	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs143132766	chr14:46188044-46188045	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs549919514	chr14:46188096-46188097	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs541541239	chr14:46188137-46188138	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs559264986	chr14:46188181-46188182	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs114294267	chr14:46188189-46188190	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551180924	chr14:46188202-46188203	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs569567706	chr14:46188223-46188224	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs530723405	chr14:46188235-46188236	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563764411	chr14:46188258-46188259	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs544310842	chr14:46188278-46188279	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs183254392	chr14:46188331-46188332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187527185	chr14:46188357-46188358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557776300	chr14:46188364-46188365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577564555	chr14:46188373-46188374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534399273	chr14:46188393-46188394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571270026	chr14:46188454-46188455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs530579101	chr14:46188485-46188486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs376638436	chr14:46188489-46188490	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs540013910	chr14:46188493-46188494	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201804788	chr14:46188494-46188495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs147451184	chr14:46188500-46188501	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs1266259	chr14:46188553-46188554	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Glioblastoma multiforme	21390271	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46185400-46187600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr14:46187600-46188400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr14:46203400-46204400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:46212000-46212200	Enhancers	Esophagus	oesophagus
5	chr14:46212200-46213000	Weak transcription	Esophagus	oesophagus
6	chr14:46213000-46213400	Enhancers	Esophagus	oesophagus
7	chr14:46213200-46213400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:46225000-46225400	Enhancers	Esophagus	oesophagus
9	chr14:46231800-46232800	Enhancers	Colon Smooth Muscle	Colon
10	chr14:46232800-46241200	Weak transcription	Colon Smooth Muscle	Colon
11	chr14:46237600-46238000	Enhancers	Rectal Smooth Muscle	rectum
12	chr14:46241200-46242000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr14:46241200-46242200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr14:46241200-46242200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr14:46241200-46242200	Enhancers	Colon Smooth Muscle	Colon
16	chr14:46241200-46242400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr14:46241200-46242400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr14:46241200-46242400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr14:46252200-46252600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:46252600-46252800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr14:46252800-46253600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr14:46253200-46256800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:46253400-46253800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr14:46253400-46254000	ZNF genes & repeats	NHEK	skin
25	chr14:46253400-46254200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:46253600-46253800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr14:46253600-46254000	Enhancers	Stomach Mucosa	stomach
28	chr14:46253600-46255600	Enhancers	HMEC	breast
29	chr14:46253800-46254000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr14:46253800-46254200	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr14:46253800-46255400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr14:46254000-46254200	Enhancers	NHEK	skin
33	chr14:46254000-46254800	Weak transcription	Stomach Mucosa	stomach
34	chr14:46254000-46255400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr14:46254200-46254400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr14:46254200-46254600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:46254200-46254600	Flanking Active TSS	NHEK	skin
38	chr14:46254400-46254600	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr14:46254600-46255000	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr14:46254600-46255000	Enhancers	NHEK	skin
41	chr14:46254600-46255600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr14:46254800-46255600	Enhancers	Stomach Mucosa	stomach
43	chr14:46254800-46256400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:46255000-46255600	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr14:46255000-46256000	ZNF genes & repeats	NHEK	skin
46	chr14:46255200-46255800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr14:46255400-46255600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr14:46255400-46256400	ZNF genes & repeats	Liver	Liver
49	chr14:46255600-46255800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:46255800-46256200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links