Variant report

Variant	esv994931
Chromosome Location	chr14:21947144-21956367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:62)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:21954795-21955377	IMR90	lung:	n/a	chr14:21955213-21955224 chr14:21955212-21955223
2	CEBPB	chr14:21955145-21955321	HepG2	liver:	n/a	chr14:21955213-21955224 chr14:21955212-21955223
3	FAM48A	chr14:21950425-21950550	GM12878	blood:	n/a	n/a
4	FOXA1	chr14:21949512-21949988	HepG2	liver:	n/a	n/a
5	FOXA2	chr14:21949627-21949863	HepG2	liver:	n/a	n/a
6	MAFK	chr14:21951310-21951495	HepG2	liver:	n/a	n/a
7	MAFK	chr14:21951293-21951567	HepG2	liver:	n/a	n/a
8	MAZ	chr14:21954957-21954961	HepG2	liver:	n/a	n/a
9	POLR2A	chr14:21953086-21953226	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr14:21955649-21955697	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr14:21955853-21955874	MCF-7	breast:	n/a	n/a
12	POLR2A	chr14:21955756-21955837	MCF-7	breast:	n/a	n/a
13	POLR2A	chr14:21951940-21951956	MCF-7	breast:	n/a	n/a
14	POLR2A	chr14:21949428-21949537	HepG2	liver:	n/a	n/a
15	POLR2A	chr14:21955731-21955827	A549	lung:	n/a	n/a
16	POLR2A	chr14:21955752-21955859	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr14:21951917-21952193	HepG2	liver:	n/a	n/a
18	POLR2A	chr14:21955722-21955842	MCF-7	breast:	n/a	n/a
19	STAT3	chr14:21950523-21950620	MCF10A-Er-Src	breast:	n/a	n/a
20	STAT3	chr14:21955386-21955421	MCF10A-Er-Src	breast:	n/a	n/a
21	STAT3	chr14:21951773-21951804	MCF10A-Er-Src	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21949306-21949356	T-47D	breast:	n/a
2	chr14:21949306-21949356	T-47D	breast:	n/a
3	chr14:21949306-21949356	Caco-2	colon:	n/a
4	chr14:21949306-21949356	Hepatocyte	liver:	n/a
5	chr14:21949306-21949356	HCM	heart:	n/a
6	chr14:21949306-21949356	A549	lung:	n/a
7	chr14:21949306-21949356	HCF	heart:	n/a
8	chr14:21949306-21949356	HNPCEpiC	eye:	n/a
9	chr14:21949306-21949356	NHBE	bronchial:	n/a
10	chr14:21949306-21949356	ECC-1	luminal epithelium:	n/a
11	chr14:21949306-21949356	HUVEC	blood vessel:	n/a
12	chr14:21949306-21949356	SKMC	muscle:	n/a
13	chr14:21949306-21949356	HRPEpiC	eye:	n/a
14	chr14:21949306-21949356	RPTEC	kidney:	n/a
15	chr14:21949306-21949356	U87	brain:	n/a
16	chr14:21949306-21949356	NT2-D1	testis:	n/a
17	chr14:21949306-21949356	HL-60	blood:	n/a
18	chr14:21949306-21949356	AoSMC	blood vessel:	n/a
19	chr14:21949306-21949356	NHDF-neo	bronchial:	n/a
20	chr14:21949306-21949356	Jurkat	blood:	n/a
21	chr14:21949306-21949356	AG09309	skin:	n/a
22	chr14:21949306-21949356	H1-hESC	embryonic stem cell:	embryo
23	chr14:21949306-21949356	SK-N-SH	brain:	n/a
24	chr14:21949306-21949356	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:21949306-21949356	HEEpiC	esophagus:	n/a
26	chr14:21949306-21949356	GM06990	blood:	n/a
27	chr14:21949306-21949356	ProgFib	skin:	n/a
28	chr14:21949306-21949356	AG04449	skin:	fetal
29	chr14:21949306-21949356	HAEpiC	amniotic membrane:	n/a
30	chr14:21949306-21949356	PANC-1	pancreas:	n/a
31	chr14:21949306-21949356	MCF10A-Er-Src	breast:	n/a
32	chr14:21949306-21949356	BJ	skin:	n/a
33	chr14:21949306-21949356	GM12891	blood:	n/a
34	chr14:21949306-21949356	SK-N-MC	brain:	n/a
35	chr14:21949306-21949356	Hela-S3	cervix:	n/a
36	chr14:21949306-21949356	HCT-116	colon:	n/a
37	chr14:21949306-21949356	AG10803	skin:	n/a
38	chr14:21949306-21949356	HepG2	liver:	n/a
39	chr14:21949306-21949356	HCPEpiC	choroid plexus:	n/a
40	chr14:21949306-21949356	PFSK-1	brain:	n/a
41	chr14:21949306-21949356	NH-A	brain:	n/a
42	chr14:21949306-21949356	SK-N-SH_RA	brain:	n/a
43	chr14:21949306-21949356	HRE	kidney:	n/a
44	chr14:21949306-21949356	AG09319	gingival:	n/a
45	chr14:21949306-21949356	HMEC	breast:	n/a
46	chr14:21949306-21949356	SAEC	small airway:	n/a
47	chr14:21949306-21949356	BE2_C	brain:	n/a
48	chr14:21949306-21949356	NB4	blood:	n/a
49	chr14:21949306-21949356	MCF-7	breast:	n/a
50	chr14:21949306-21949356	K562	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21949289..21951385-chr14:21959586..21961238,2	MCF-7	breast:
2	chr14:21923120..21925863-chr14:21948762..21952189,3	MCF-7	breast:
3	chr14:21922721..21925394-chr14:21943917..21947287,10	MCF-7	breast:
4	chr14:21945641..21947338-chr14:21977414..21979762,2	K562	blood:
5	chr14:21943174..21947446-chr14:21976603..21980796,8	K562	blood:
6	chr14:21941797..21947093-chr14:21954513..21961521,11	MCF-7	breast:
7	chr14:21953304..21957637-chr14:21977622..21980273,4	K562	blood:
8	chr14:21944239..21947571-chr14:21970430..21973821,4	MCF-7	breast:
9	chr14:21948837..21951421-chr14:21953212..21956640,4	MCF-7	breast:
10	chr14:21949379..21951265-chr14:21955547..21957612,2	K562	blood:
11	chr14:21954693..21956685-chr14:21971149..21973765,2	MCF-7	breast:
12	chr14:21942911..21947036-chr14:21948493..21952401,7	MCF-7	breast:
13	chr14:21923260..21925455-chr14:21943748..21947334,4	K562	blood:
14	chr14:21922608..21930261-chr14:21941288..21947915,21	MCF-7	breast:
15	chr14:21948837..21951421-chr14:21953212..21956640,4	MCF-7	breast:
16	chr14:21945001..21948392-chr14:21948946..21951939,4	K562	blood:
17	chr14:21944743..21947528-chr14:21994092..21996767,2	MCF-7	breast:
18	chr14:21950181..21952493-chr14:21954450..21957059,4	MCF-7	breast:

No data

Variant related genes	Relation type
TOX4	TF binding region
RAB2B	TF binding region
TOX4	CpG island
RAB2B	CpG island
ENSG00000129472	chromatin interactions
ENSG00000165821	chromatin interactions
ENSG00000092203	chromatin interactions
ENSG00000165819	chromatin interactions
ENSG00000100888	chromatin interactions

Extended variants
information (count: 340 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:340 , 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	rs139722495	chr14:21947184-21947185	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs10633914	chr14:21947185-21947186	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs34972892	chr14:21947186-21947187	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs537506543	chr14:21947201-21947202	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs188067681	chr14:21947217-21947218	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs574276622	chr14:21947244-21947245	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs543377604	chr14:21947249-21947250	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs553682923	chr14:21947290-21947291	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs150497169	chr14:21947292-21947293	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs573457183	chr14:21947295-21947296	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs376852106	chr14:21947298-21947299	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs540689341	chr14:21947317-21947318	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs139620920	chr14:21947321-21947322	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs35357403	chr14:21947324-21947325	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs564061034	chr14:21947356-21947357	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs531948107	chr14:21947390-21947391	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs370656218	chr14:21947429-21947430	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs148028678	chr14:21947469-21947470	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs7150948	chr14:21947531-21947532	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs568813157	chr14:21947538-21947539	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs529030818	chr14:21947564-21947565	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539342208	chr14:21947605-21947606	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181018938	chr14:21947617-21947618	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565653340	chr14:21947632-21947633	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs12889546	chr14:21947633-21947634	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs551488526	chr14:21947648-21947649	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs572934367	chr14:21947679-21947680	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571611945	chr14:21947721-21947722	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs7157961	chr14:21947761-21947762	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs187247294	chr14:21947762-21947763	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs28415160	chr14:21947778-21947779	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536861923	chr14:21947781-21947782	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190479389	chr14:21947814-21947815	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181619027	chr14:21947853-21947854	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10135215	chr14:21947857-21947858	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs557505297	chr14:21947897-21947898	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs76468881	chr14:21948013-21948014	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147342593	chr14:21948022-21948023	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368927078	chr14:21948073-21948074	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563065119	chr14:21948075-21948076	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528919834	chr14:21948076-21948077	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559451123	chr14:21948086-21948087	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528423082	chr14:21948114-21948115	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548060295	chr14:21948115-21948116	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536204131	chr14:21948123-21948124	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79408522	chr14:21948135-21948136	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565171029	chr14:21948162-21948163	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139475650	chr14:21948203-21948204	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550968158	chr14:21948222-21948223	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567778335	chr14:21948227-21948228	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	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
Developmental delay	21147756	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
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ewing''s sarcoma	18628472	CNVD
Rheumatoid arthritis	23223014	CNVD
Ependymoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21946000-21960600	Weak transcription	Small Intestine	intestine
2	chr14:21946200-21947400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr14:21946200-21947400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr14:21946200-21949200	Weak transcription	Esophagus	oesophagus
5	chr14:21946200-21949200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr14:21946200-21955600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:21946200-21955600	Weak transcription	Gastric	stomach
8	chr14:21946200-21955600	Weak transcription	Left Ventricle	heart
9	chr14:21946200-21955600	Weak transcription	Ovary	ovary
10	chr14:21946200-21955600	Weak transcription	Thymus	Thymus
11	chr14:21946200-21977600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr14:21946400-21947200	Enhancers	Primary T cells fromperipheralblood	blood
13	chr14:21946400-21947200	Enhancers	Liver	Liver
14	chr14:21946400-21947400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr14:21946400-21947400	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr14:21946400-21948200	Weak transcription	HSMM	muscle
17	chr14:21946400-21948800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr14:21946400-21952000	Weak transcription	Lung	lung
19	chr14:21946400-21952600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:21946400-21952800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr14:21946400-21955400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:21946400-21955600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr14:21946400-21958000	Weak transcription	Pancreas	Pancrea
24	chr14:21946400-21958800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr14:21946400-21960800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr14:21946400-21971400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:21946600-21947200	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr14:21946600-21947200	Weak transcription	Fetal Intestine Small	intestine
29	chr14:21946600-21947400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:21946600-21947600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr14:21946600-21947600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr14:21946600-21947600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr14:21946600-21947800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr14:21946600-21947800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr14:21946600-21947800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr14:21946600-21948000	Weak transcription	Placenta	Placenta
37	chr14:21946600-21949200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr14:21946600-21949200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr14:21946600-21949400	Weak transcription	Brain Anterior Caudate	brain
40	chr14:21946600-21949400	Weak transcription	Fetal Kidney	kidney
41	chr14:21946600-21949600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:21946600-21950400	Weak transcription	Primary B cells from cord blood	blood
43	chr14:21946600-21954600	Weak transcription	HSMMtube	muscle
44	chr14:21946600-21954800	Weak transcription	Rectal Smooth Muscle	rectum
45	chr14:21946600-21954800	Weak transcription	K562	blood
46	chr14:21946600-21955000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr14:21946600-21955000	Weak transcription	Fetal Thymus	thymus
48	chr14:21946600-21955400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr14:21946600-21955400	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr14:21946600-21955600	Weak transcription	Brain Germinal Matrix	brain

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