Variant report

Variant	esv3384774
Chromosome Location	chr14:24435212-24478110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:762)
CpG islands
(count:1344)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:24439122-24439137	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
7	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
9	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
10	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
12	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
13	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
14	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
15	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
16	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
17	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
18	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
19	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
20	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
21	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
22	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
24	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
25	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
26	CEBPD	chr14:24439025-24439361	HepG2	liver:	n/a	n/a
27	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
28	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
29	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
30	CHD2	chr14:24439126-24439200	GM12878	blood:	n/a	chr14:24439140-24439150
31	CTCF	chr14:24446380-24446530	A549	lung:	n/a	n/a
32	CTCF	chr14:24446380-24446530	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:24457589-24457742	MCF-7	breast:	n/a	chr14:24457659-24457668
34	CTCF	chr14:24446500-24446650	HepG2	liver:	n/a	n/a
35	CTCF	chr14:24446529-24446697	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr14:24457606-24457720	MCF-7	breast:	n/a	chr14:24457659-24457668
37	CTCF	chr14:24457961-24458093	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr14:24446520-24446681	A549	lung:	n/a	n/a
39	CTCF	chr14:24446600-24446750	NHLF	lung:	n/a	n/a
40	CTCF	chr14:24458043-24458099	GM19239	blood:	n/a	n/a
41	CTCF	chr14:24457480-24457630	GM12864	blood:	n/a	n/a
42	CTCF	chr14:24457673-24457713	GM13976	blood:	n/a	n/a
43	CTCF	chr14:24446580-24446730	GM12865	blood:	n/a	n/a
44	CTCF	chr14:24457980-24458130	GM12865	blood:	n/a	n/a
45	CTCF	chr14:24446380-24446530	HCT-116	colon:	n/a	n/a
46	CTCF	chr14:24446620-24446770	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr14:24468738-24468758	LNCaP	prostate:	n/a	n/a
48	CTCF	chr14:24458380-24458530	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr14:24446500-24446650	BJ	skin:	n/a	n/a
50	CTCF	chr14:24446485-24446736	Hela-S3	cervix:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24476559-24476609	CMK	blood:	n/a
2	chr14:24475906-24475956	SK-N-MC	brain:	n/a
3	chr14:24476559-24476609	CMK	blood:	n/a
4	chr14:24475906-24475956	SK-N-MC	brain:	n/a
5	chr14:24476478-24476528	Caco-2	colon:	n/a
6	chr14:24438909-24438959	HRE	kidney:	n/a
7	chr14:24439430-24439480	AG09319	gingival:	n/a
8	chr14:24458004-24458054	NH-A	brain:	n/a
9	chr14:24439430-24439480	MCF-7	breast:	n/a
10	chr14:24475906-24475956	MCF-7	breast:	n/a
11	chr14:24438909-24438959	H1-hESC	embryonic stem cell:	embryo
12	chr14:24438136-24438186	BJ	skin:	n/a
13	chr14:24458004-24458054	ProgFib	skin:	n/a
14	chr14:24458208-24458258	HRE	kidney:	n/a
15	chr14:24458000-24458050	AG10803	skin:	n/a
16	chr14:24438909-24438959	HCM	heart:	n/a
17	chr14:24458208-24458258	HCPEpiC	choroid plexus:	n/a
18	chr14:24476082-24476132	Jurkat	blood:	n/a
19	chr14:24458000-24458050	GM12892	blood:	n/a
20	chr14:24438909-24438959	MCF10A-Er-Src	breast:	n/a
21	chr14:24457509-24457559	AG09309	skin:	n/a
22	chr14:24476559-24476609	PrEC	prostate:	n/a
23	chr14:24458345-24458395	ProgFib	skin:	n/a
24	chr14:24454443-24454493	HCPEpiC	choroid plexus:	n/a
25	chr14:24438136-24438186	SK-N-SH_RA	brain:	n/a
26	chr14:24457993-24458043	HCT-116	colon:	n/a
27	chr14:24473832-24473882	HCM	heart:	n/a
28	chr14:24475906-24475956	HRCEpiC	kidney:	n/a
29	chr14:24438909-24438959	GM12891	blood:	n/a
30	chr14:24476478-24476528	Hepatocyte	liver:	n/a
31	chr14:24458299-24458349	SK-N-MC	brain:	n/a
32	chr14:24475906-24475956	MCF10A-Er-Src	breast:	n/a
33	chr14:24458299-24458349	SAEC	small airway:	n/a
34	chr14:24439430-24439480	HepG2	liver:	n/a
35	chr14:24439157-24439207	AG09319	gingival:	n/a
36	chr14:24457915-24457965	HIPEpiC	eye:	n/a
37	chr14:24457993-24458043	GM19239	blood:	n/a
38	chr14:24476478-24476528	HIPEpiC	eye:	n/a
39	chr14:24457509-24457559	GM06990	blood:	n/a
40	chr14:24458099-24458149	MCF-7	breast:	n/a
41	chr14:24458014-24458064	HIPEpiC	eye:	n/a
42	chr14:24476478-24476528	ECC-1	luminal epithelium:	n/a
43	chr14:24438909-24438959	HRCEpiC	kidney:	n/a
44	chr14:24458014-24458064	PFSK-1	brain:	n/a
45	chr14:24458208-24458258	HRCEpiC	kidney:	n/a
46	chr14:24475906-24475956	Hepatocyte	liver:	n/a
47	chr14:24454443-24454493	HRPEpiC	eye:	n/a
48	chr14:24454443-24454493	RPTEC	kidney:	n/a
49	chr14:24458004-24458054	BE2_C	brain:	n/a
50	chr14:24438909-24438959	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
2	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	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
ENSG00000100889	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000187630	chromatin interactions

Extended variants
information (count: 2133 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2133 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202069784	chr14:24435219-24435220	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs541545483	chr14:24435254-24435255	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs368160634	chr14:24435265-24435266	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs138982419	chr14:24435308-24435309	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs533583799	chr14:24435323-24435324	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs550469897	chr14:24435334-24435335	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs570368429	chr14:24435344-24435345	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs528855171	chr14:24435363-24435364	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs548692926	chr14:24435373-24435374	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs144699441	chr14:24435379-24435380	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs534398964	chr14:24435435-24435436	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs371622188	chr14:24435463-24435464	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs376187061	chr14:24435477-24435478	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs201751120	chr14:24435493-24435494	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs140619145	chr14:24435507-24435508	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs75479712	chr14:24435536-24435537	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs11556285	chr14:24435542-24435543	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs1043650	chr14:24435564-24435565	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs138417192	chr14:24435565-24435566	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs141593871	chr14:24435577-24435578	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs201142570	chr14:24435579-24435580	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs573605554	chr14:24435582-24435583	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs536586387	chr14:24435597-24435598	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs372755007	chr14:24435598-24435599	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs377726588	chr14:24435605-24435606	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs370120638	chr14:24435611-24435612	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200665946	chr14:24435666-24435667	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200547090	chr14:24435672-24435673	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572441325	chr14:24435825-24435826	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs541134174	chr14:24435871-24435872	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs61999772	chr14:24435882-24435883	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs564594734	chr14:24435960-24435961	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs578183879	chr14:24435964-24435965	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs544040373	chr14:24435969-24435970	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs59242048	chr14:24435996-24435997	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141694248	chr14:24436047-24436048	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs61312537	chr14:24436048-24436049	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs146694003	chr14:24436074-24436075	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs571209669	chr14:24436092-24436093	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs563913189	chr14:24436094-24436095	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs566216565	chr14:24436112-24436113	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs71405820	chr14:24436130-24436131	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs549679038	chr14:24436135-24436136	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs559070578	chr14:24436221-24436222	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528104457	chr14:24436224-24436225	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs113819651	chr14:24436227-24436228	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs551161279	chr14:24436232-24436233	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs28620370	chr14:24436234-24436235	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs111644370	chr14:24436256-24436257	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs375984037	chr14:24436270-24436271	Weak transcription Enhancers Active TSS	TF binding region	1 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:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24423600-24438800	Weak transcription	Lung	lung
2	chr14:24423600-24438800	Weak transcription	Ovary	ovary
3	chr14:24423800-24435600	Weak transcription	Primary B cells from cord blood	blood
4	chr14:24423800-24438200	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr14:24423800-24438600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr14:24423800-24438600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr14:24423800-24438800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr14:24423800-24438800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr14:24423800-24438800	Weak transcription	Left Ventricle	heart
10	chr14:24423800-24438800	Weak transcription	Right Ventricle	heart
11	chr14:24423800-24438800	Weak transcription	Osteobl	bone
12	chr14:24424000-24435400	Weak transcription	Primary B cells from peripheral blood	blood
13	chr14:24424000-24437400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr14:24424000-24438200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr14:24424000-24438200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr14:24424000-24438800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr14:24424000-24438800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr14:24424000-24438800	Weak transcription	HSMM	muscle
19	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
20	chr14:24424200-24435400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr14:24424200-24438200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr14:24424200-24438800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr14:24424200-24438800	Weak transcription	NHEK	skin
24	chr14:24424400-24436600	Weak transcription	Gastric	stomach
25	chr14:24424400-24438000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr14:24424400-24438600	Weak transcription	Brain Hippocampus Middle	brain
27	chr14:24424400-24438800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:24424400-24438800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr14:24424400-24438800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr14:24424400-24438800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr14:24424400-24438800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr14:24424400-24438800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr14:24424400-24438800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr14:24424400-24438800	Weak transcription	Colonic Mucosa	Colon
35	chr14:24424400-24438800	Weak transcription	Fetal Muscle Leg	muscle
36	chr14:24424400-24438800	Weak transcription	Pancreas	Pancrea
37	chr14:24424400-24438800	Weak transcription	Spleen	Spleen
38	chr14:24424400-24438800	Weak transcription	HMEC	breast
39	chr14:24424800-24437600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:24424800-24439000	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr14:24425600-24438800	Weak transcription	Fetal Muscle Trunk	muscle
42	chr14:24425800-24438000	Weak transcription	HepG2	liver
43	chr14:24425800-24438800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr14:24426000-24438800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:24426800-24438600	Weak transcription	Adipose Nuclei	Adipose
46	chr14:24427800-24438800	Weak transcription	Fetal Intestine Large	intestine
47	chr14:24428000-24439200	Weak transcription	Liver	Liver
48	chr14:24428200-24438200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:24428600-24438000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr14:24429400-24439000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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