Variant report

Variant	nsv516237
Chromosome Location	chr14:24793762-24799358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:269)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr14:24797177-24797408	GM12878	blood:	n/a	n/a
2	BHLHE40	chr14:24799060-24799189	K562	blood:	n/a	n/a
3	CTCF	chr14:24797260-24797410	HEEpiC	esophagus:	n/a	n/a
4	CTCF	chr14:24797360-24797510	NHEK	skin:	n/a	n/a
5	CTCF	chr14:24797100-24797250	AG09309	skin:	n/a	n/a
6	CTCF	chr14:24797280-24797430	GM06990	blood:	n/a	n/a
7	CTCF	chr14:24797340-24797490	K562	blood:	n/a	n/a
8	CTCF	chr14:24797260-24797410	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr14:24797360-24797510	NHDF-neo	bronchial:	n/a	n/a
10	CTCF	chr14:24797185-24797423	Medullo	brain:	n/a	n/a
11	CTCF	chr14:24797194-24797425	K562	blood:	n/a	n/a
12	CTCF	chr14:24797300-24797450	AG09309	skin:	n/a	n/a
13	CTCF	chr14:24797260-24797410	SAEC	small airway:	n/a	n/a
14	CTCF	chr14:24796800-24796950	GM12872	blood:	n/a	n/a
15	CTCF	chr14:24797340-24797490	HRE	kidney:	n/a	n/a
16	CTCF	chr14:24797147-24797426	Lung_OC	lung:	n/a	n/a
17	CTCF	chr14:24797088-24797497	A549	lung:	n/a	n/a
18	CTCF	chr14:24797260-24797410	GM12875	blood:	n/a	n/a
19	CTCF	chr14:24796520-24796670	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr14:24797000-24797150	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr14:24797100-24797250	A549	lung:	n/a	n/a
22	CTCF	chr14:24797177-24797424	GM10248	blood:	n/a	n/a
23	CTCF	chr14:24797360-24797510	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr14:24796615-24796665	GM19239	blood:	n/a	n/a
25	CTCF	chr14:24797260-24797410	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr14:24797300-24797450	GM12867	blood:	n/a	n/a
27	CTCF	chr14:24797300-24797450	GM12871	blood:	n/a	n/a
28	CTCF	chr14:24797260-24797410	HepG2	liver:	n/a	n/a
29	CTCF	chr14:24796720-24796870	HMF	breast:	n/a	n/a
30	CTCF	chr14:24797340-24797490	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr14:24797000-24797150	NHEK	skin:	n/a	n/a
32	CTCF	chr14:24797221-24797401	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr14:24796900-24797150	GM12873	blood:	n/a	n/a
34	CTCF	chr14:24797340-24797490	GM06990	blood:	n/a	n/a
35	CTCF	chr14:24796920-24797070	GM12864	blood:	n/a	n/a
36	CTCF	chr14:24797167-24797426	GM13977	blood:	n/a	n/a
37	CTCF	chr14:24797100-24797250	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr14:24796921-24797031	GM19238	blood:	n/a	n/a
39	CTCF	chr14:24797240-24797390	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr14:24797340-24797490	NHLF	lung:	n/a	n/a
41	CTCF	chr14:24797185-24797406	A549	lung:	n/a	n/a
42	CTCF	chr14:24797230-24797414	Fibrobl	skin:	n/a	n/a
43	CTCF	chr14:24797260-24797410	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr14:24797213-24797393	GM20000	blood:	n/a	n/a
45	CTCF	chr14:24797320-24797470	GM12870	blood:	n/a	n/a
46	CTCF	chr14:24797167-24797436	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr14:24797223-24797419	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:24797320-24797470	HCM	heart:	n/a	n/a
49	CTCF	chr14:24797300-24797450	GM12869	blood:	n/a	n/a
50	CTCF	chr14:24797340-24797490	BE2_C	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24797871-24797921	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:24797871-24797921	BE2_C	brain:	n/a
3	chr14:24797871-24797921	Caco-2	colon:	n/a
4	chr14:24797871-24797921	SKMC	muscle:	n/a
5	chr14:24797871-24797921	T-47D	breast:	n/a
6	chr14:24797871-24797921	GM12892	blood:	n/a
7	chr14:24797871-24797921	ECC-1	luminal epithelium:	n/a
8	chr14:24797871-24797921	HAEpiC	amniotic membrane:	n/a
9	chr14:24797871-24797921	MCF10A-Er-Src	breast:	n/a
10	chr14:24797871-24797921	ovcar-3	ovarian:	n/a
11	chr14:24797871-24797921	HCT-116	colon:	n/a
12	chr14:24797871-24797921	GM12878	blood:	n/a
13	chr14:24797871-24797921	HUVEC	blood vessel:	n/a
14	chr14:24797871-24797921	LNCaP	prostate:	n/a
15	chr14:24797871-24797921	NB4	blood:	n/a
16	chr14:24797871-24797921	HNPCEpiC	eye:	n/a
17	chr14:24797871-24797921	BJ	skin:	n/a
18	chr14:24797871-24797921	ProgFib	skin:	n/a
19	chr14:24797871-24797921	HMEC	breast:	n/a
20	chr14:24797871-24797921	NH-A	brain:	n/a
21	chr14:24797871-24797921	PFSK-1	brain:	n/a
22	chr14:24797871-24797921	AG10803	skin:	n/a
23	chr14:24797871-24797921	HCM	heart:	n/a
24	chr14:24797871-24797921	CMK	blood:	n/a
25	chr14:24797871-24797921	U87	brain:	n/a
26	chr14:24797871-24797921	SAEC	small airway:	n/a
27	chr14:24797871-24797921	SK-N-SH	brain:	n/a
28	chr14:24797871-24797921	PANC-1	pancreas:	n/a
29	chr14:24797871-24797921	NHBE	bronchial:	n/a
30	chr14:24797871-24797921	RPTEC	kidney:	n/a
31	chr14:24797871-24797921	AoSMC	blood vessel:	n/a
32	chr14:24797871-24797921	A549	lung:	n/a
33	chr14:24797871-24797921	HIPEpiC	eye:	n/a
34	chr14:24797871-24797921	HepG2	liver:	n/a
35	chr14:24797871-24797921	IMR90	lung:	fetal
36	chr14:24797871-24797921	AG09319	gingival:	n/a
37	chr14:24797871-24797921	K562	blood:	n/a
38	chr14:24797871-24797921	SK-N-MC	brain:	n/a
39	chr14:24797871-24797921	HL-60	blood:	n/a
40	chr14:24797871-24797921	PrEC	prostate:	n/a
41	chr14:24797871-24797921	HRPEpiC	eye:	n/a
42	chr14:24797871-24797921	HRE	kidney:	n/a
43	chr14:24797871-24797921	HEEpiC	esophagus:	n/a
44	chr14:24797871-24797921	AG04449	skin:	fetal
45	chr14:24797871-24797921	HCF	heart:	n/a
46	chr14:24797871-24797921	HCPEpiC	choroid plexus:	n/a
47	chr14:24797871-24797921	MCF-7	breast:	n/a
48	chr14:24797871-24797921	Hepatocyte	liver:	n/a
49	chr14:24797871-24797921	GM06990	blood:	n/a
50	chr14:24797871-24797921	HEK293	kidney:	embryo

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24791657..24793644-chr14:24793834..24797111,3	MCF-7	breast:
2	chr14:24796890..24797637-chr14:24900960..24901588,2	MCF-7	breast:
3	chr14:24796718..24800207-chr14:24803965..24807105,3	MCF-7	breast:
4	chr14:24794139..24796164-chr14:24797754..24799865,2	K562	blood:
5	chr14:24796459..24799989-chr14:24897944..24901736,5	K562	blood:
6	chr14:24629199..24631872-chr14:24798413..24800219,2	MCF-7	breast:
7	chr14:24683967..24686751-chr14:24798225..24800322,2	MCF-7	breast:
8	chr14:24789439..24822082-chr14:24898039..24913135,99	MCF-7	breast:
9	chr14:24794139..24796164-chr14:24797754..24799865,2	K562	blood:
10	chr14:24781460..24810019-chr14:24892340..24914262,110	MCF-7	breast:
11	chr14:24796552..24799266-chr14:24908909..24911628,3	K562	blood:
12	chr14:24768871..24772362-chr14:24798723..24803416,4	MCF-7	breast:
13	chr14:24798684..24800642-chr14:24867625..24869190,2	K562	blood:
14	chr14:24791358..24808812-chr14:24895309..24913599,55	K562	blood:
15	chr14:24796879..24804920-chr14:24831628..24840088,12	MCF-7	breast:
16	chr14:24767930..24771021-chr14:24792565..24795803,5	MCF-7	breast:

No data

Variant related genes	Relation type
ADCY4	TF binding region
ADCY4	CpG island
ENSG00000260669	chromatin interactions
ENSG00000129467	chromatin interactions
ENSG00000100445	chromatin interactions
ENSG00000258973	chromatin interactions
ENSG00000196943	chromatin interactions
ENSG00000213920	chromatin interactions
ENSG00000100441	chromatin interactions
ENSG00000213928	chromatin interactions
ENSG00000092098	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000100968	chromatin interactions
ENSG00000129465	chromatin interactions
ENSG00000139899	chromatin interactions
ENSG00000205978	chromatin interactions

Extended variants
information (count: 317 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17184682	chr14:24793762-24793763	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574680289	chr14:24793765-24793766	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs540209664	chr14:24793780-24793781	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs74038605	chr14:24793819-24793820	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs371091180	chr14:24793830-24793831	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs544979848	chr14:24793832-24793833	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs552793130	chr14:24793851-24793852	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs530872248	chr14:24793856-24793857	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs12435732	chr14:24793897-24793898	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs112561625	chr14:24793905-24793906	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs561275828	chr14:24793906-24793907	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs371100303	chr14:24793918-24793919	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs368514562	chr14:24793933-24793934	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs530311084	chr14:24793940-24793941	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs138002186	chr14:24793941-24793942	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs111944731	chr14:24793952-24793953	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs538663298	chr14:24793963-24793964	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs552170888	chr14:24793992-24793993	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs568983607	chr14:24794003-24794004	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs12431793	chr14:24794055-24794056	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs554646688	chr14:24794063-24794064	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs568204067	chr14:24794065-24794066	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs533972086	chr14:24794085-24794086	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs553677658	chr14:24794099-24794100	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs576697815	chr14:24794112-24794113	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs113441724	chr14:24794131-24794132	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs558480827	chr14:24794153-24794154	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs575694866	chr14:24794190-24794191	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs544424920	chr14:24794198-24794199	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs561420231	chr14:24794263-24794264	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs527684370	chr14:24794271-24794272	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs540804042	chr14:24794285-24794286	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs141979650	chr14:24794295-24794296	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs532814841	chr14:24794296-24794297	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs78269053	chr14:24794314-24794315	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	mRNA abundance
36	rs146160386	chr14:24794333-24794334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs183878497	chr14:24794335-24794336	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs188484235	chr14:24794386-24794387	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs568123285	chr14:24794395-24794396	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs386775681	chr14:24794412-24794413	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs57938687	chr14:24794427-24794428	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs8006514	chr14:24794428-24794429	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs17184689	chr14:24794440-24794441	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs375266449	chr14:24794444-24794445	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs557511420	chr14:24794453-24794454	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs566451139	chr14:24794470-24794471	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs533683881	chr14:24794512-24794513	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs180946987	chr14:24794528-24794529	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs373477958	chr14:24794540-24794541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs55928265	chr14:24794541-24794542	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24784600-24796400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr14:24784800-24796600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr14:24786200-24801600	Weak transcription	Left Ventricle	heart
4	chr14:24787000-24801200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr14:24787200-24796400	Weak transcription	Osteobl	bone
6	chr14:24788400-24801000	Weak transcription	Gastric	stomach
7	chr14:24790400-24796400	Weak transcription	Colonic Mucosa	Colon
8	chr14:24790600-24794400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr14:24790800-24795200	Strong transcription	Adipose Nuclei	Adipose
10	chr14:24791400-24794200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr14:24791600-24796600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:24792000-24793800	Strong transcription	Right Ventricle	heart
13	chr14:24792200-24798200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr14:24792600-24794400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr14:24792600-24794600	Weak transcription	Placenta	Placenta
16	chr14:24792600-24794800	Enhancers	K562	blood
17	chr14:24793200-24793800	Genic enhancers	Spleen	Spleen
18	chr14:24793400-24796400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr14:24793400-24796600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr14:24793400-24797400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr14:24793600-24793800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:24793600-24794000	Flanking Bivalent TSS/Enh	HepG2	liver
23	chr14:24793600-24794200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr14:24793600-24794800	Enhancers	Primary hematopoietic stem cells	blood
25	chr14:24793600-24796600	Weak transcription	Lung	lung
26	chr14:24793800-24796400	Weak transcription	Spleen	Spleen
27	chr14:24793800-24797200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr14:24793800-24801000	Weak transcription	Right Ventricle	heart
29	chr14:24794200-24795600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr14:24794200-24796400	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr14:24794200-24797200	Weak transcription	Fetal Stomach	stomach
32	chr14:24794400-24794800	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr14:24794400-24795400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr14:24794400-24796400	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr14:24794600-24794800	Enhancers	Placenta	Placenta
36	chr14:24794800-24795000	Enhancers	Fetal Thymus	thymus
37	chr14:24794800-24796400	Weak transcription	Primary hematopoietic stem cells	blood
38	chr14:24794800-24796400	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr14:24794800-24801200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr14:24794800-24801200	Weak transcription	K562	blood
41	chr14:24795000-24796400	Weak transcription	Fetal Thymus	thymus
42	chr14:24795000-24796400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr14:24795000-24801200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr14:24795200-24796400	Weak transcription	Adipose Nuclei	Adipose
45	chr14:24795400-24795600	Bivalent Enhancer	Brain Germinal Matrix	brain
46	chr14:24795400-24795800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr14:24795400-24796600	Weak transcription	Pancreas	Pancrea
48	chr14:24795600-24801600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr14:24795800-24797000	Enhancers	Primary B cells from cord blood	blood
50	chr14:24795800-24797000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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