Variant report

Variant	nsv901851
Chromosome Location	chr14:46184595-46361884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:641)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr14:46336397-46337076	GM12878	blood:	n/a	n/a
7	BATF	chr14:46337483-46337971	GM12878	blood:	n/a	chr14:46337729-46337740
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	chr14:46336621-46336979	GM12878	blood:	n/a	n/a
12	BCL3	chr14:46337578-46337949	GM12878	blood:	n/a	n/a
13	BCL3	chr14:46337522-46337975	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	chr14:46195157-46195161	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:46270324-46270772	HepG2	liver:	n/a	chr14:46270518-46270529
20	CEBPB	chr14:46242879-46243131	IMR90	lung:	n/a	chr14:46243004-46243015
21	CEBPB	chr14:46309387-46309957	HepG2	liver:	n/a	chr14:46309800-46309811
22	CEBPB	chr14:46270325-46270606	IMR90	lung:	n/a	chr14:46270518-46270529
23	CEBPB	chr14:46321607-46321769	A549	lung:	n/a	n/a
24	CEBPB	chr14:46242906-46243113	HepG2	liver:	n/a	chr14:46243004-46243015
25	CEBPB	chr14:46248535-46248671	HepG2	liver:	n/a	chr14:46248607-46248618
26	CEBPB	chr14:46309406-46309962	A549	lung:	n/a	chr14:46309800-46309811
27	CEBPB	chr14:46270317-46270820	A549	lung:	n/a	chr14:46270518-46270529
28	CEBPB	chr14:46357543-46357739	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr14:46232907-46233168	HepG2	liver:	n/a	n/a
30	CHD2	chr14:46360235-46360350	HepG2	liver:	n/a	n/a
31	CREB1	chr14:46337522-46338032	GM12878	blood:	n/a	n/a
32	CREB1	chr14:46276327-46276806	GM12878	blood:	n/a	n/a
33	CTCF	chr14:46279760-46279910	NB4	blood:	n/a	n/a
34	CTCF	chr14:46185860-46186010	GM12864	blood:	n/a	chr14:46185903-46185921 chr14:46185906-46185915
35	CTCF	chr14:46292925-46292950	LNCaP	prostate:	n/a	n/a
36	CTCF	chr14:46340360-46340510	GM12874	blood:	n/a	n/a
37	CTCF	chr14:46187960-46188110	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:46349860-46350010	HEK293	kidney:	n/a	n/a
39	CTCF	chr14:46185836-46186061	MCF-7	breast:	n/a	chr14:46185903-46185921 chr14:46185906-46185915
40	CTCF	chr14:46185860-46186010	HEK293	kidney:	n/a	chr14:46185903-46185921 chr14:46185906-46185915
41	CTCF	chr14:46340340-46340490	GM12864	blood:	n/a	n/a
42	CTCF	chr14:46307914-46308084	HUVEC	blood vessel:	n/a	chr14:46307991-46308009 chr14:46307993-46308014
43	CTCF	chr14:46279820-46279970	HAc	cerebellar:	n/a	n/a
44	CTCF	chr14:46279840-46279990	BJ	skin:	n/a	n/a
45	CTCF	chr14:46279858-46279970	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:46185860-46186010	A549	lung:	n/a	chr14:46185903-46185921 chr14:46185906-46185915
47	CTCF	chr14:46279803-46280000	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:46310920-46311070	GM12871	blood:	n/a	n/a
49	CTCF	chr14:46340340-46340490	HCT-116	colon:	n/a	n/a
50	CTCF	chr14:46185860-46186010	BJ	skin:	n/a	chr14:46185903-46185921 chr14:46185906-46185915

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46358279-46358329	SKMC	muscle:	n/a
2	chr14:46241576-46241626	SK-N-SH	brain:	n/a
3	chr14:46358139-46358189	AG04449	skin:	fetal
4	chr14:46358139-46358189	HCF	heart:	n/a
5	chr14:46300358-46300408	U87	brain:	n/a
6	chr14:46283117-46283167	HCPEpiC	choroid plexus:	n/a
7	chr14:46300358-46300408	PrEC	prostate:	n/a
8	chr14:46358279-46358329	HRPEpiC	eye:	n/a
9	chr14:46358279-46358329	HCPEpiC	choroid plexus:	n/a
10	chr14:46300358-46300408	GM12892	blood:	n/a
11	chr14:46241576-46241626	ProgFib	skin:	n/a
12	chr14:46300358-46300408	HEK293	kidney:	embryo
13	chr14:46283117-46283167	GM19239	blood:	n/a
14	chr14:46241576-46241626	MCF10A-Er-Src	breast:	n/a
15	chr14:46283172-46283222	HPAEpiC	pulmonary alveolar:	n/a
16	chr14:46241576-46241626	BE2_C	brain:	n/a
17	chr14:46300358-46300408	Hepatocyte	liver:	n/a
18	chr14:46300358-46300408	H1-hESC	embryonic stem cell:	embryo
19	chr14:46358139-46358189	HAEpiC	amniotic membrane:	n/a
20	chr14:46241576-46241626	AG04450	lung:	fetal
21	chr14:46283172-46283222	MCF10A-Er-Src	breast:	n/a
22	chr14:46241576-46241626	PrEC	prostate:	n/a
23	chr14:46241576-46241626	A549	lung:	n/a
24	chr14:46283172-46283222	Hepatocyte	liver:	n/a
25	chr14:46358139-46358189	SK-N-MC	brain:	n/a
26	chr14:46358279-46358329	HNPCEpiC	eye:	n/a
27	chr14:46358279-46358329	HAEpiC	amniotic membrane:	n/a
28	chr14:46283117-46283167	NB4	blood:	n/a
29	chr14:46358139-46358189	IMR90	lung:	fetal
30	chr14:46283172-46283222	SK-N-SH	brain:	n/a
31	chr14:46283117-46283167	NH-A	brain:	n/a
32	chr14:46358139-46358189	AoSMC	blood vessel:	n/a
33	chr14:46283117-46283167	MCF10A-Er-Src	breast:	n/a
34	chr14:46358279-46358329	K562	blood:	n/a
35	chr14:46358139-46358189	HRPEpiC	eye:	n/a
36	chr14:46241576-46241626	ovcar-3	ovarian:	n/a
37	chr14:46358139-46358189	HCPEpiC	choroid plexus:	n/a
38	chr14:46300358-46300408	NH-A	brain:	n/a
39	chr14:46283117-46283167	ProgFib	skin:	n/a
40	chr14:46300358-46300408	NB4	blood:	n/a
41	chr14:46241576-46241626	AG09319	gingival:	n/a
42	chr14:46283117-46283167	HEK293	kidney:	embryo
43	chr14:46283172-46283222	HCM	heart:	n/a
44	chr14:46283172-46283222	HIPEpiC	eye:	n/a
45	chr14:46300358-46300408	GM12891	blood:	n/a
46	chr14:46283117-46283167	GM12892	blood:	n/a
47	chr14:46241576-46241626	CMK	blood:	n/a
48	chr14:46358139-46358189	HIPEpiC	eye:	n/a
49	chr14:46283172-46283222	GM12892	blood:	n/a
50	chr14:46358139-46358189	HRE	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
2	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
3	chr14:46147376..46147982-chr14:46279500..46280082,2	MCF-7	breast:
4	chr14:46185365..46185918-chr14:46409681..46410218,2	MCF-7	breast:
5	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
6	chr14:46119850..46120526-chr14:46279646..46280307,2	MCF-7	breast:
7	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
8	chr10:29154738..29155346-chr14:46193775..46194564,2	MCF-7	breast:
9	chr14:46182590..46185086-chr14:46185381..46187428,2	MCF-7	breast:
10	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:
11	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
12	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
13	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
14	chr14:46079191..46080200-chr14:46279301..46280311,3	MCF-7	breast:
15	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-5	chr14:46217809-46217840	NONHSAT036670
2	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
3	lnc-FANCM-5	chr14:46241338-46241424	NONHSAT036671
4	lnc-FANCM-5	chr14:46213166-46213370	NONHSAT036671
5	lnc-FANCM-5	chr14:46241339-46241424	XLOC_010816
6	lnc-MIS18BP1-1	chr14:46184553-46185084	NONHSAT036669
7	lnc-FANCM-5	chr14:46241613-46241659	XLOC_010816
8	lnc-FANCM-5	chr14:46213325-46213370	XLOC_010816
9	lnc-FANCM-5	chr14:46241612-46241659	NONHSAT036671
10	lnc-FANCM-5	chr14:46217539-46217865	NONHSAT036671
11	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036670
12	lnc-FANCM-5	chr14:46217809-46217893	NONHSAT036668
13	lnc-FANCM-5	chr14:46217809-46217860	XLOC_010816
14	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036668
15	lnc-MIS18BP1-1	chr14:46184553-46185155	ENSG00000258616
16	lnc-MIS18BP1-1	chr14:46184553-46184894	ENSG00000258616
17	lnc-FANCM-5	chr14:46195358-46195474	NONHSAT036670
18	lnc-MIS18BP1-1	chr14:46184553-46185114	NONHSAT036666
19	lnc-MIS18BP1-1	chr14:46184553-46184690	ENSG00000258616

No data

Variant related genes	Relation type
ENSG00000258616	TF binding region
ENSG00000264420	TF binding region
ENSG00000258616	CpG island
ENSG00000264420	CpG island
ENSG00000258700	chromatin interactions
ENSG00000258616	chromatin interactions

Extended variants
information (count: 2783 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2783 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1266264	chr14:46184595-46184596	ZNF genes & repeats Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74575824	chr14:46184613-46184614	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs1061124	chr14:46184620-46184621	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs371187980	chr14:46184629-46184630	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs540375242	chr14:46184639-46184640	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs187405547	chr14:46184649-46184650	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs574241193	chr14:46184651-46184652	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs1001234	chr14:46184681-46184682	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs562443261	chr14:46184683-46184684	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs529747299	chr14:46184746-46184747	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs1001233	chr14:46184750-46184751	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs1266263	chr14:46184791-46184792	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs148888218	chr14:46184815-46184816	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs547133575	chr14:46184829-46184830	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs571791448	chr14:46184849-46184850	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs532666512	chr14:46184850-46184851	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs578215297	chr14:46184851-46184852	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs568123141	chr14:46184860-46184861	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs191819422	chr14:46184868-46184869	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs80058800	chr14:46184906-46184907	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs143497832	chr14:46184916-46184917	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs566914771	chr14:46184942-46184943	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs112201347	chr14:46185074-46185075	ZNF genes & repeats Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs558712785	chr14:46185075-46185076	ZNF genes & repeats Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs577136464	chr14:46185095-46185096	ZNF genes & repeats Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs544499694	chr14:46185128-46185129	ZNF genes & repeats Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs556460986	chr14:46185148-46185149	ZNF genes & repeats Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs574804898	chr14:46185179-46185180	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs184698925	chr14:46185183-46185184	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs559905042	chr14:46185239-46185240	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs527373077	chr14:46185240-46185241	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs545629079	chr14:46185243-46185244	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs565454329	chr14:46185287-46185288	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs532602162	chr14:46185342-46185343	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs374679835	chr14:46185359-46185360	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550777957	chr14:46185360-46185361	ZNF genes & repeats Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs368140664	chr14:46185409-46185410	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs530335181	chr14:46185411-46185412	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548553216	chr14:46185418-46185419	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs566798646	chr14:46185441-46185442	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554382951	chr14:46185444-46185445	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs534278852	chr14:46185477-46185478	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113996205	chr14:46185530-46185531	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570971314	chr14:46185585-46185586	ZNF genes & repeats Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs574148656	chr14:46185794-46185795	ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs538008458	chr14:46185815-46185816	ZNF genes & repeats Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556395482	chr14:46185827-46185828	ZNF genes & repeats Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs189362615	chr14:46185870-46185871	ZNF genes & repeats Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs541948051	chr14:46185929-46185930	ZNF genes & repeats Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192690492	chr14:46185934-46185935	ZNF genes & repeats Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	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:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46180000-46185000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:46183000-46185800	Weak transcription	Fetal Kidney	kidney
3	chr14:46183600-46184600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:46183600-46186200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:46184600-46185400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr14:46185000-46185600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:46185400-46185600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr14:46185400-46187600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr14:46185600-46186200	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr14:46185800-46186200	Enhancers	Adipose Nuclei	Adipose
11	chr14:46185800-46186400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:46185800-46186400	Enhancers	Fetal Kidney	kidney
13	chr14:46187600-46188400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr14:46203400-46204400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr14:46212000-46212200	Enhancers	Esophagus	oesophagus
16	chr14:46212200-46213000	Weak transcription	Esophagus	oesophagus
17	chr14:46213000-46213400	Enhancers	Esophagus	oesophagus
18	chr14:46213200-46213400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr14:46225000-46225400	Enhancers	Esophagus	oesophagus
20	chr14:46231800-46232800	Enhancers	Colon Smooth Muscle	Colon
21	chr14:46232800-46241200	Weak transcription	Colon Smooth Muscle	Colon
22	chr14:46237600-46238000	Enhancers	Rectal Smooth Muscle	rectum
23	chr14:46241200-46242000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr14:46241200-46242200	Enhancers	H1 Cell Line	embryonic stem cell
25	chr14:46241200-46242200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr14:46241200-46242200	Enhancers	Colon Smooth Muscle	Colon
27	chr14:46241200-46242400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr14:46241200-46242400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr14:46241200-46242400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr14:46252200-46252600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr14:46252600-46252800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:46252800-46253600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr14:46253200-46256800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:46253400-46253800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr14:46253400-46254000	ZNF genes & repeats	NHEK	skin
36	chr14:46253400-46254200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:46253600-46253800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr14:46253600-46254000	Enhancers	Stomach Mucosa	stomach
39	chr14:46253600-46255600	Enhancers	HMEC	breast
40	chr14:46253800-46254000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr14:46253800-46254200	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr14:46253800-46255400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr14:46254000-46254200	Enhancers	NHEK	skin
44	chr14:46254000-46254800	Weak transcription	Stomach Mucosa	stomach
45	chr14:46254000-46255400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr14:46254200-46254400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
47	chr14:46254200-46254600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:46254200-46254600	Flanking Active TSS	NHEK	skin
49	chr14:46254400-46254600	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr14:46254600-46255000	Weak transcription	Rectal Mucosa Donor 31	rectum

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