Variant report

Variant	nsv1040467
Chromosome Location	chr14:24424032-24458931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:607)
CpG islands
(count:1222)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:607 , 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	ARID3A	chr14:24443416-24443612	HepG2	liver:	n/a	n/a
2	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
3	BACH1	chr14:24439122-24439137	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr14:24423720-24424085	GM12878	blood:	n/a	n/a
6	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
7	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:24423865-24424037	GM12878	blood:	n/a	n/a
9	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
10	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
13	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
14	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
15	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
17	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
19	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
20	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
21	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
22	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
23	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
24	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
25	CEBPD	chr14:24439025-24439361	HepG2	liver:	n/a	n/a
26	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
27	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
28	CHD2	chr14:24439126-24439200	GM12878	blood:	n/a	chr14:24439140-24439150
29	CTCF	chr14:24446600-24446750	GM12867	blood:	n/a	n/a
30	CTCF	chr14:24454220-24454370	NHEK	skin:	n/a	n/a
31	CTCF	chr14:24458043-24458099	GM19239	blood:	n/a	n/a
32	CTCF	chr14:24424310-24424354	LNCaP	prostate:	n/a	n/a
33	CTCF	chr14:24446480-24446630	AG09309	skin:	n/a	n/a
34	CTCF	chr14:24446380-24446530	GM12866	blood:	n/a	n/a
35	CTCF	chr14:24447767-24447837	Fibrobl	skin:	n/a	n/a
36	CTCF	chr14:24457937-24458015	Lung_OC	lung:	n/a	n/a
37	CTCF	chr14:24446380-24446530	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr14:24454180-24454330	NHEK	skin:	n/a	n/a
39	CTCF	chr14:24446492-24446709	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr14:24457655-24457707	GM10248	blood:	n/a	chr14:24457659-24457668
41	CTCF	chr14:24446520-24446693	Lung_OC	lung:	n/a	n/a
42	CTCF	chr14:24446500-24446650	BJ	skin:	n/a	n/a
43	CTCF	chr14:24446380-24446530	HMEC	breast:	n/a	n/a
44	CTCF	chr14:24446580-24446730	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr14:24457480-24457630	GM12873	blood:	n/a	n/a
46	CTCF	chr14:24454280-24454430	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr14:24436009-24436038	GM13976	blood:	n/a	n/a
48	CTCF	chr14:24446480-24446630	SAEC	small airway:	n/a	n/a
49	CTCF	chr14:24446380-24446530	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr14:24446480-24446630	HEEpiC	esophagus:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24457893-24457943	ECC-1	luminal epithelium:	n/a
2	chr14:24435159-24435209	K562	blood:	n/a
3	chr14:24457893-24457943	ECC-1	luminal epithelium:	n/a
4	chr14:24435159-24435209	K562	blood:	n/a
5	chr14:24458099-24458149	GM19239	blood:	n/a
6	chr14:24458000-24458050	HCPEpiC	choroid plexus:	n/a
7	chr14:24439157-24439207	AoSMC	blood vessel:	n/a
8	chr14:24458208-24458258	NHDF-neo	bronchial:	n/a
9	chr14:24435159-24435209	GM12878	blood:	n/a
10	chr14:24457915-24457965	HPAEpiC	pulmonary alveolar:	n/a
11	chr14:24454443-24454493	HCF	heart:	n/a
12	chr14:24439430-24439480	HNPCEpiC	eye:	n/a
13	chr14:24425012-24425062	SK-N-SH	brain:	n/a
14	chr14:24457915-24457965	IMR90	lung:	fetal
15	chr14:24435159-24435209	BE2_C	brain:	n/a
16	chr14:24458000-24458050	CMK	blood:	n/a
17	chr14:24458099-24458149	GM12892	blood:	n/a
18	chr14:24425012-24425062	GM12878	blood:	n/a
19	chr14:24438136-24438186	ProgFib	skin:	n/a
20	chr14:24425012-24425062	MCF-7	breast:	n/a
21	chr14:24438909-24438959	HEEpiC	esophagus:	n/a
22	chr14:24439430-24439480	GM06990	blood:	n/a
23	chr14:24425012-24425062	NB4	blood:	n/a
24	chr14:24458345-24458395	GM19239	blood:	n/a
25	chr14:24457509-24457559	IMR90	lung:	fetal
26	chr14:24438136-24438186	NH-A	brain:	n/a
27	chr14:24439157-24439207	Jurkat	blood:	n/a
28	chr14:24425012-24425062	HPAEpiC	pulmonary alveolar:	n/a
29	chr14:24424191-24424241	ProgFib	skin:	n/a
30	chr14:24424191-24424241	HAEpiC	amniotic membrane:	n/a
31	chr14:24458208-24458258	HL-60	blood:	n/a
32	chr14:24458345-24458395	HepG2	liver:	n/a
33	chr14:24439157-24439207	GM12891	blood:	n/a
34	chr14:24438909-24438959	BJ	skin:	n/a
35	chr14:24439430-24439480	AoSMC	blood vessel:	n/a
36	chr14:24438136-24438186	PFSK-1	brain:	n/a
37	chr14:24438136-24438186	SK-N-SH_RA	brain:	n/a
38	chr14:24458299-24458349	BJ	skin:	n/a
39	chr14:24457915-24457965	AG09309	skin:	n/a
40	chr14:24439430-24439480	HRCEpiC	kidney:	n/a
41	chr14:24424191-24424241	SKMC	muscle:	n/a
42	chr14:24458208-24458258	AG10803	skin:	n/a
43	chr14:24454443-24454493	A549	lung:	n/a
44	chr14:24425142-24425192	H1-hESC	embryonic stem cell:	embryo
45	chr14:24435159-24435209	U87	brain:	n/a
46	chr14:24425012-24425062	HAEpiC	amniotic membrane:	n/a
47	chr14:24458099-24458149	ECC-1	luminal epithelium:	n/a
48	chr14:24458299-24458349	IMR90	lung:	fetal
49	chr14:24457893-24457943	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:24438909-24438959	Caco-2	colon:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24197895..24200996-chr14:24421897..24424681,3	MCF-7	breast:
2	chr14:24422915..24424427-chr14:24563237..24565374,2	MCF-7	breast:
3	chr14:24421589..24424746-chr14:24425153..24428957,4	MCF-7	breast:
4	chr14:24036767..24038500-chr14:24420729..24424068,4	MCF-7	breast:
5	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:
6	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24423957-24424298	NONHSAT035953
2	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3

No data

Variant related genes	Relation type
DHRS4-AS1	TF binding region
DHRS4	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	CpG island
DHRS4	CpG island
DHRS4L2	CpG island
ENSG00000215256	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000258464	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000187630	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000213983	chromatin interactions

Extended variants
information (count: 1783 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1783 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527714467	chr14:24424033-24424034	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
2	rs547466225	chr14:24424035-24424036	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
3	rs149860092	chr14:24424062-24424063	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
4	rs539603870	chr14:24424080-24424081	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
5	rs556719649	chr14:24424098-24424099	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs561117787	chr14:24424111-24424112	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs570201640	chr14:24424128-24424129	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs536134518	chr14:24424147-24424148	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs180985433	chr14:24424155-24424156	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs572047087	chr14:24424161-24424162	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs146356650	chr14:24424181-24424182	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs61999765	chr14:24424182-24424183	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs61999766	chr14:24424186-24424187	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs557854878	chr14:24424209-24424210	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
15	rs139708761	chr14:24424224-24424225	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
16	rs373010678	chr14:24424225-24424226	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
17	rs146373042	chr14:24424247-24424248	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs543208779	chr14:24424248-24424249	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs563498507	chr14:24424252-24424253	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs138564114	chr14:24424253-24424254	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs374151392	chr14:24424260-24424261	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs377038259	chr14:24424264-24424265	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs199663128	chr14:24424266-24424267	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs559251300	chr14:24424267-24424268	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs527652442	chr14:24424280-24424281	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs1127278	chr14:24424281-24424282	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs1127279	chr14:24424289-24424290	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs533460137	chr14:24424292-24424293	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs550046703	chr14:24424305-24424306	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs79086208	chr14:24424306-24424307	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs148405684	chr14:24424326-24424327	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs142533242	chr14:24424331-24424332	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs150588702	chr14:24424333-24424334	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs139648244	chr14:24424339-24424340	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs549668516	chr14:24424340-24424341	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs4981491	chr14:24424346-24424347	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs566393352	chr14:24424362-24424363	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs12147221	chr14:24424367-24424368	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs375092227	chr14:24424374-24424375	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs370061276	chr14:24424379-24424380	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs557791502	chr14:24424391-24424392	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs577612599	chr14:24424394-24424395	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs373307909	chr14:24424407-24424408	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs537144117	chr14:24424420-24424421	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs139945419	chr14:24424421-24424422	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs376438168	chr14:24424441-24424442	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs542436847	chr14:24424458-24424459	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs559179305	chr14:24424464-24424465	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs572801973	chr14:24424519-24424520	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544946991	chr14:24424527-24424528	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24421600-24424200	Active TSS	Duodenum Mucosa	Duodenum
2	chr14:24421800-24424200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr14:24422200-24424200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:24422600-24424200	Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr14:24423000-24424400	Active TSS	Fetal Brain Female	brain
6	chr14:24423200-24424200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
7	chr14:24423400-24424200	Flanking Active TSS	Liver	Liver
8	chr14:24423400-24424200	Weak transcription	Gastric	stomach
9	chr14:24423400-24424200	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr14:24423400-24424400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr14:24423400-24424400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
12	chr14:24423400-24424400	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr14:24423400-24429000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr14:24423400-24431000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:24423600-24424200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr14:24423600-24424200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr14:24423600-24424200	Weak transcription	Pancreas	Pancrea
18	chr14:24423600-24424400	Flanking Active TSS	Brain Hippocampus Middle	brain
19	chr14:24423600-24424400	Enhancers	Fetal Muscle Leg	muscle
20	chr14:24423600-24424400	Enhancers	Placenta	Placenta
21	chr14:24423600-24425200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:24423600-24426600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr14:24423600-24430800	Weak transcription	Psoas Muscle	Psoas
24	chr14:24423600-24438800	Weak transcription	Lung	lung
25	chr14:24423600-24438800	Weak transcription	Ovary	ovary
26	chr14:24423800-24424200	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr14:24423800-24424200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr14:24423800-24424200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr14:24423800-24424200	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr14:24423800-24424400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:24423800-24424400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr14:24423800-24424400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr14:24423800-24424400	Enhancers	Adipose Nuclei	Adipose
34	chr14:24423800-24424400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr14:24423800-24424400	Enhancers	Esophagus	oesophagus
36	chr14:24423800-24424400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr14:24423800-24424400	Enhancers	Fetal Intestine Large	intestine
38	chr14:24423800-24424400	Enhancers	Fetal Muscle Trunk	muscle
39	chr14:24423800-24424400	Enhancers	GM12878-XiMat	blood
40	chr14:24423800-24424400	Flanking Active TSS	HMEC	breast
41	chr14:24423800-24425000	Weak transcription	Fetal Kidney	kidney
42	chr14:24423800-24425600	Weak transcription	HUVEC	blood vessel
43	chr14:24423800-24426400	Weak transcription	Fetal Lung	lung
44	chr14:24423800-24427400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:24423800-24427400	Weak transcription	HSMMtube	muscle
46	chr14:24423800-24429200	Weak transcription	Fetal Intestine Small	intestine
47	chr14:24423800-24430800	Weak transcription	Fetal Thymus	thymus
48	chr14:24423800-24432400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:24423800-24435600	Weak transcription	Primary B cells from cord blood	blood
50	chr14:24423800-24438200	Weak transcription	Primary T helper cells PMA-I stimulated	--

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