Variant report

Variant	esv1846002
Chromosome Location	chr17:44841209-44849188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:44848118..44848659-chr5:65439946..65440535,2	Hela-S3	cervix:
2	chr17:44840766..44847017-chr17:44847800..44851001,9	MCF-7	breast:
3	chr17:44846645..44849185-chr17:44896689..44899109,2	MCF-7	breast:
4	chr17:44848239..44850963-chr17:44871575..44873481,2	K562	blood:
5	chr17:44841770..44845110-chr17:44871532..44873744,3	K562	blood:
6	chr17:44834549..44837328-chr17:44842622..44845050,2	K562	blood:
7	chr17:44832715..44835385-chr17:44845501..44848268,3	K562	blood:
8	chr17:44054020..44055535-chr17:44843944..44845683,2	K562	blood:
9	chr17:44821369..44826185-chr17:44846753..44849990,6	K562	blood:
10	chr17:44801247..44804412-chr17:44846741..44850099,3	K562	blood:
11	chr17:44812780..44815644-chr17:44839923..44842823,2	K562	blood:
12	chr17:44267872..44270663-chr17:44839838..44842513,2	K562	blood:
13	chr17:44816270..44819088-chr17:44845691..44848257,2	MCF-7	breast:
14	chr17:44804689..44809871-chr17:44845472..44850072,6	K562	blood:
15	chr17:44848565..44850557-chr17:44896605..44898581,4	K562	blood:
16	chr17:44839344..44841120-chr17:44841937..44843876,2	K562	blood:
17	chr17:44819607..44821857-chr17:44848285..44851793,3	MCF-7	breast:
18	chr17:44848344..44850894-chr17:44852175..44854837,4	MCF-7	breast:
19	chr17:44840704..44842981-chr17:44847991..44849653,2	MCF-7	breast:
20	chr17:44820992..44822869-chr17:44847358..44849527,2	K562	blood:
21	chr17:44845310..44847853-chr17:44872083..44874051,2	K562	blood:
22	chr17:44847986..44850923-chr17:44874927..44876461,2	K562	blood:
23	chr17:44847668..44852830-chr17:44858394..44861796,5	MCF-7	breast:
24	chr17:44842407..44844540-chr17:44901586..44903730,2	K562	blood:
25	chr17:44846693..44849612-chr17:44868202..44870057,2	K562	blood:
26	chr17:44846353..44850075-chr17:44870910..44874671,5	K562	blood:
27	chr17:44830114..44832534-chr17:44845890..44849410,4	K562	blood:
28	chr17:44843310..44845974-chr17:44848991..44851957,3	MCF-7	breast:
29	chr17:44848371..44851556-chr17:44854343..44857073,3	MCF-7	breast:
30	chr17:44845867..44850393-chr17:44893846..44898781,9	K562	blood:
31	chr17:44843310..44845974-chr17:44848991..44851957,3	MCF-7	breast:
32	chr17:44848624..44851339-chr17:44893104..44896024,3	K562	blood:
33	chr17:44842963..44844961-chr17:44998826..45000868,2	K562	blood:
34	chr17:44848117..44849092-chr4:25235386..25236084,2	Hela-S3	cervix:
35	chr17:44848117..44849210-chr5:40835373..40836312,3	Hela-S3	cervix:
36	chr17:44840766..44847017-chr17:44847800..44851001,9	MCF-7	breast:
37	chr17:44847827..44849684-chr17:44903325..44905972,2	K562	blood:
38	chr17:44847670..44850061-chr17:44912249..44914668,3	K562	blood:
39	chr17:44848353..44849074-chr6:26158086..26158790,2	Hela-S3	cervix:
40	chr17:44841367..44842987-chr17:44894656..44897026,2	K562	blood:
41	chr17:44808673..44811660-chr17:44847775..44850081,2	K562	blood:
42	chr17:44837102..44839238-chr17:44845941..44848841,2	K562	blood:
43	chr17:44845867..44847496-chr17:44895029..44897224,2	K562	blood:
44	chr11:61559555..61560161-chr17:44848660..44849342,2	Hela-S3	cervix:
45	chr17:44846909..44848699-chr17:44886329..44888882,2	K562	blood:
46	chr17:44848363..44849947-chr17:45003750..45005877,2	K562	blood:
47	chr17:44840704..44842981-chr17:44847991..44849653,2	MCF-7	breast:
48	chr17:44836082..44838287-chr17:44847835..44850037,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000261886	chromatin interactions
ENSG00000262633	chromatin interactions
ENSG00000134825	chromatin interactions
ENSG00000153914	chromatin interactions
ENSG00000207601	chromatin interactions
ENSG00000168496	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000073969	chromatin interactions
ENSG00000120071	chromatin interactions
ENSG00000108433	chromatin interactions
ENSG00000108379	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000038210	chromatin interactions

Extended variants
information (count: 310 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:310 , 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	rs35359801	chr17:44841209-44841210	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs61006195	chr17:44841212-44841213	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs151339884	chr17:44841213-44841214	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369875455	chr17:44841216-44841217	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35839619	chr17:44841217-44841218	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs200786450	chr17:44841221-44841222	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574949900	chr17:44841241-44841242	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543763838	chr17:44841242-44841243	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532601642	chr17:44841292-44841293	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73987025	chr17:44841293-44841294	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs575994894	chr17:44841301-44841302	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544600499	chr17:44841320-44841321	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577549121	chr17:44841326-44841327	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538608202	chr17:44841337-44841338	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188748281	chr17:44841352-44841353	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs527367632	chr17:44841359-44841360	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547052640	chr17:44841445-44841446	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374576514	chr17:44841498-44841499	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143326731	chr17:44841499-44841500	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs146256056	chr17:44841556-44841557	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550758209	chr17:44841557-44841558	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs191542999	chr17:44841569-44841570	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148425936	chr17:44841601-44841602	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs552591996	chr17:44841607-44841608	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs566048226	chr17:44841725-44841726	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs147030694	chr17:44841767-44841768	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs9908452	chr17:44841786-44841787	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs555003133	chr17:44841799-44841800	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs1062339	chr17:44841818-44841819	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs568568645	chr17:44841872-44841873	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182563719	chr17:44841910-44841911	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs557413190	chr17:44841915-44841916	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577096848	chr17:44841916-44841917	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs544639075	chr17:44841934-44841935	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569194037	chr17:44841946-44841947	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114693722	chr17:44841967-44841968	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540729739	chr17:44841980-44841981	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561030760	chr17:44841984-44841985	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs529894831	chr17:44842164-44842165	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553905731	chr17:44842201-44842202	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150925039	chr17:44842219-44842220	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs140671995	chr17:44842258-44842259	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144213821	chr17:44842270-44842271	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552475548	chr17:44842310-44842311	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566085108	chr17:44842311-44842312	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs147733956	chr17:44842357-44842358	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs548433047	chr17:44842363-44842364	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs4968240	chr17:44842381-44842382	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs77790426	chr17:44842390-44842391	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs537273277	chr17:44842407-44842408	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	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
Breast cancer	21858162	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
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	19156837	CNVD
Williams-beuren syndrome	18553513	CNVD
Mental retardation	17847001	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
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44793600-44842200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr17:44798600-44841800	Weak transcription	Right Ventricle	heart
3	chr17:44818800-44842200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr17:44819200-44841400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr17:44820600-44844400	Weak transcription	Small Intestine	intestine
6	chr17:44820800-44841800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr17:44821200-44841800	Weak transcription	NHLF	lung
8	chr17:44826200-44841800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr17:44828400-44847800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr17:44829600-44844000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr17:44829800-44842000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr17:44829800-44848000	Weak transcription	Fetal Kidney	kidney
13	chr17:44830200-44841800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr17:44832400-44847800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr17:44833600-44841800	Weak transcription	Fetal Brain Male	brain
16	chr17:44833600-44842000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr17:44833600-44842400	Weak transcription	Brain Anterior Caudate	brain
18	chr17:44833800-44841400	Weak transcription	Brain Germinal Matrix	brain
19	chr17:44833800-44841800	Weak transcription	HMEC	breast
20	chr17:44834000-44842200	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr17:44834000-44846800	Weak transcription	Ovary	ovary
22	chr17:44834200-44841800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr17:44834400-44841400	Weak transcription	Colonic Mucosa	Colon
24	chr17:44834400-44841400	Weak transcription	Lung	lung
25	chr17:44834400-44841800	Weak transcription	Fetal Lung	lung
26	chr17:44834400-44842000	Weak transcription	Psoas Muscle	Psoas
27	chr17:44834400-44842200	Weak transcription	Brain Substantia Nigra	brain
28	chr17:44834400-44846400	Strong transcription	Fetal Intestine Small	intestine
29	chr17:44834600-44841800	Weak transcription	Osteobl	bone
30	chr17:44834600-44842000	Weak transcription	Brain Angular Gyrus	brain
31	chr17:44834600-44842000	Weak transcription	Colon Smooth Muscle	Colon
32	chr17:44834600-44842600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr17:44834600-44843800	Weak transcription	Stomach Smooth Muscle	stomach
34	chr17:44834600-44846400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr17:44834600-44847200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr17:44834600-44848000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr17:44834600-44848400	Weak transcription	Aorta	Aorta
38	chr17:44834800-44841800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr17:44834800-44842400	Weak transcription	HSMMtube	muscle
40	chr17:44834800-44847000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr17:44834800-44847800	Weak transcription	Dnd41	blood
42	chr17:44835000-44846800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr17:44835800-44841800	Weak transcription	Left Ventricle	heart
44	chr17:44836000-44841800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr17:44836000-44841800	Weak transcription	HSMM	muscle
46	chr17:44836200-44841800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr17:44836400-44842000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr17:44836400-44842600	Weak transcription	Placenta	Placenta
49	chr17:44836400-44846800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr17:44836800-44841800	Weak transcription	Pancreas	Pancrea

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