Variant report

Variant	nsv522126
Chromosome Location	chr17:66538239-66548457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr17:66540840-66540990	HepG2	liver:	n/a	n/a
2	ESR1	chr17:66546027-66546336	T-47D	breast:	n/a	n/a
3	FOS	chr17:66539134-66539490	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr17:66539170-66539443	MCF10A-Er-Src	breast:	n/a	n/a
5	FOS	chr17:66539177-66539431	MCF10A-Er-Src	breast:	n/a	n/a
6	FOSL2	chr17:66535224-66539318	HepG2	liver:	n/a	chr17:66536355-66536369 chr17:66537173-66537182
7	FOSL2	chr17:66540127-66540597	HepG2	liver:	n/a	n/a
8	FOSL2	chr17:66539523-66540107	HepG2	liver:	n/a	n/a
9	FOXA1	chr17:66546011-66546294	T-47D	breast:	n/a	n/a
10	FOXA2	chr17:66539120-66539563	A549	lung:	n/a	n/a
11	FOXA2	chr17:66539132-66539695	A549	lung:	n/a	n/a
12	MAX	chr17:66545930-66545982	NB4	blood:	n/a	chr17:66545930-66545940 chr17:66545965-66545975
13	NFYB	chr17:66543342-66543347	GM12878	blood:	n/a	n/a
14	PAX5	chr17:66538890-66539153	GM12878	blood:	n/a	chr17:66539069-66539078 chr17:66539062-66539079 chr17:66539060-66539078
15	PAX5	chr17:66538823-66539213	GM12878	blood:	n/a	chr17:66539069-66539078 chr17:66539062-66539079 chr17:66539060-66539078
16	PAX5	chr17:66538941-66539141	GM12891	blood:	n/a	chr17:66539069-66539078 chr17:66539062-66539079 chr17:66539060-66539078
17	POLR2A	chr17:66538577-66539138	HCT-116	colon:	n/a	n/a
18	POLR2A	chr17:66547301-66547732	HepG2	liver:	n/a	n/a
19	POLR2A	chr17:66546646-66546860	HepG2	liver:	n/a	n/a
20	POLR2A	chr17:66535303-66540040	HepG2	liver:	n/a	n/a
21	POLR2A	chr17:66528378-66541028	HepG2	liver:	n/a	n/a
22	POLR2A	chr17:66541489-66541738	HepG2	liver:	n/a	n/a
23	POLR2A	chr17:66539118-66539517	HepG2	liver:	n/a	n/a
24	POLR2A	chr17:66540097-66540351	HepG2	liver:	n/a	n/a
25	POLR2A	chr17:66538011-66538326	HepG2	liver:	n/a	n/a
26	POLR2A	chr17:66538040-66538351	A549	lung:	n/a	n/a
27	POLR2A	chr17:66543085-66543342	HepG2	liver:	n/a	n/a
28	POLR2A	chr17:66534939-66538247	PFSK-1	brain:	n/a	n/a
29	POLR2A	chr17:66538080-66538338	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr17:66537270-66538700	A549	lung:	n/a	n/a
31	POLR2A	chr17:66537905-66538416	HCT-116	colon:	n/a	n/a
32	POLR2A	chr17:66535238-66538921	HepG2	liver:	n/a	n/a
33	POLR2A	chr17:66540624-66540671	HepG2	liver:	n/a	n/a
34	POLR2A	chr17:66538040-66538322	MCF-7	breast:	n/a	n/a
35	POLR2A	chr17:66538069-66538794	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr17:66537945-66538465	H1-neurons	neurons:	n/a	n/a
37	POLR2A	chr17:66537282-66538908	HepG2	liver:	n/a	n/a
38	POLR2A	chr17:66544166-66544485	HepG2	liver:	n/a	n/a
39	POLR2A	chr17:66538112-66538283	A549	lung:	n/a	n/a
40	POLR2A	chr17:66538446-66539370	PFSK-1	brain:	n/a	n/a
41	POLR2A	chr17:66539132-66539162	HepG2	liver:	n/a	n/a
42	POLR2A	chr17:66533313-66538368	K562	blood:	n/a	n/a
43	POLR2A	chr17:66540679-66540758	HepG2	liver:	n/a	n/a
44	POLR2A	chr17:66538615-66538784	MCF-7	breast:	n/a	n/a
45	POLR2A	chr17:66538056-66538261	HCT-116	colon:	n/a	n/a
46	POLR2A	chr17:66539462-66539848	HepG2	liver:	n/a	n/a
47	POLR2A	chr17:66537968-66539466	HepG2	liver:	n/a	n/a
48	POLR2A	chr17:66546152-66546253	HepG2	liver:	n/a	n/a
49	POLR2A	chr17:66538587-66538885	HepG2	liver:	n/a	n/a
50	POLR2A	chr17:66539185-66539341	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:66545890..66547411-chr17:66550502..66553080,2	MCF-7	breast:
2	chr17:66509250..66511874-chr17:66538190..66540879,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269657	TF binding region
FAM20A	TF binding region
ENSG00000108946	chromatin interactions

Extended variants
information (count: 486 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2302234	chr17:66538239-66538240	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374633547	chr17:66538251-66538252	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs372486448	chr17:66538259-66538260	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs150508189	chr17:66538260-66538261	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs368814272	chr17:66538271-66538272	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs139437162	chr17:66538286-66538287	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs149246756	chr17:66538289-66538290	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs367996001	chr17:66538299-66538300	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs141405038	chr17:66538318-66538319	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78681907	chr17:66538359-66538360	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs76499529	chr17:66538384-66538385	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs568633790	chr17:66538416-66538417	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs182324207	chr17:66538417-66538418	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs2302235	chr17:66538418-66538419	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs554192643	chr17:66538427-66538428	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576243251	chr17:66538436-66538437	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs543538141	chr17:66538450-66538451	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs558294201	chr17:66538466-66538467	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576754585	chr17:66538478-66538479	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs540634415	chr17:66538494-66538495	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs139956199	chr17:66538495-66538496	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs529891184	chr17:66538514-66538515	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs541631796	chr17:66538547-66538548	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs186053004	chr17:66538571-66538572	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs530939835	chr17:66538585-66538586	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs530280321	chr17:66538597-66538598	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs143391371	chr17:66538610-66538611	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs374654023	chr17:66538673-66538674	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs78241877	chr17:66538714-66538715	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs72845862	chr17:66538790-66538791	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs146230912	chr17:66538792-66538793	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs75550131	chr17:66538793-66538794	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs372299359	chr17:66538808-66538809	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs16973042	chr17:66538819-66538820	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs369571869	chr17:66538820-66538821	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs372280569	chr17:66538864-66538865	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs373618718	chr17:66538882-66538883	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs372691559	chr17:66538919-66538920	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs199630924	chr17:66538933-66538934	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs570338353	chr17:66538934-66538935	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs147371993	chr17:66538936-66538937	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs387907215	chr17:66538937-66538938	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs201900897	chr17:66538970-66538971	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs537459979	chr17:66538997-66538998	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs9910528	chr17:66539012-66539013	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576833825	chr17:66539017-66539018	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs149917082	chr17:66539026-66539027	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs552653545	chr17:66539031-66539032	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs574432789	chr17:66539057-66539058	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs144942126	chr17:66539066-66539067	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
Chordoma	18071362	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21858162	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Cancer	21129771	CNVD
Congenital generalized hypertrichosis terminalis	19463983	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
XY gonadal dysgenesis	20685758	CNVD
Gingival hyperplasia	19463983	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neuroblastoma	20406844	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Breast cancer	21045282	CNVD
Epilepsy	22083797	CNVD
Sezary syndrome	18413736	CNVD
Honadal dysgenesis	21408189	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66520400-66539800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr17:66523200-66542200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr17:66523600-66538800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
4	chr17:66525400-66538600	Strong transcription	HUES64 Cell Line	embryonic stem cell
5	chr17:66526000-66539400	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr17:66526600-66539800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr17:66526800-66540600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr17:66527600-66554200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr17:66527800-66538400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr17:66530800-66539200	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr17:66531200-66552400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr17:66531400-66538800	Strong transcription	Fetal Stomach	stomach
13	chr17:66531400-66539200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
14	chr17:66531400-66540000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr17:66531600-66538400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr17:66531800-66540000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr17:66532400-66538400	Weak transcription	HUVEC	blood vessel
18	chr17:66532400-66540200	Strong transcription	Osteobl	bone
19	chr17:66532800-66538400	Weak transcription	Brain Angular Gyrus	brain
20	chr17:66532800-66539600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr17:66533000-66555200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr17:66533200-66539200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
23	chr17:66533400-66538400	Strong transcription	Adipose Nuclei	Adipose
24	chr17:66533600-66539000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr17:66533800-66545400	Weak transcription	Psoas Muscle	Psoas
26	chr17:66533800-66549800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr17:66534000-66541400	Weak transcription	Colon Smooth Muscle	Colon
28	chr17:66534000-66541800	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr17:66534000-66552800	Weak transcription	Fetal Kidney	kidney
30	chr17:66534200-66563200	Weak transcription	Ovary	ovary
31	chr17:66534600-66538800	Weak transcription	GM12878-XiMat	blood
32	chr17:66534600-66539800	Weak transcription	Primary B cells from cord blood	blood
33	chr17:66534800-66554200	Weak transcription	NHDF-Ad	bronchial
34	chr17:66535000-66540000	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr17:66535200-66542800	Weak transcription	Fetal Brain Female	brain
36	chr17:66535400-66538400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr17:66535400-66540200	Genic enhancers	Liver	Liver
38	chr17:66536200-66538800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr17:66536200-66539200	Weak transcription	Brain Substantia Nigra	brain
40	chr17:66536200-66540200	Weak transcription	Right Atrium	heart
41	chr17:66536400-66540000	Strong transcription	Fetal Muscle Leg	muscle
42	chr17:66536400-66541400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr17:66536600-66538800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr17:66536600-66539800	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr17:66536600-66542600	Weak transcription	Pancreas	Pancrea
46	chr17:66536800-66538400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr17:66536800-66538400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr17:66536800-66538400	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr17:66536800-66538400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr17:66536800-66538400	Weak transcription	HMEC	breast

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