Variant report

Variant	esv1849526
Chromosome Location	chr17:45087601-45132750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:438)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr17:45127603-45127849	GM12878	blood:	n/a	n/a
2	BATF	chr17:45127560-45127755	GM12878	blood:	n/a	n/a
3	BCL11A	chr17:45127435-45128324	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:45125999-45126154	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:45127623-45127792	GM12878	blood:	n/a	n/a
6	BCL11A	chr17:45127023-45127200	GM12878	blood:	n/a	n/a
7	BCL11A	chr17:45096313-45096563	GM12878	blood:	n/a	n/a
8	BCL11A	chr17:45126159-45126397	GM12878	blood:	n/a	n/a
9	BHLHE40	chr17:45100421-45100689	HepG2	liver:	n/a	n/a
10	CTCF	chr17:45100084-45100112	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr17:45088195-45088264	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr17:45092932-45092976	LNCaP	prostate:	n/a	n/a
13	CTCF	chr17:45089076-45089086	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr17:45129800-45129950	SAEC	small airway:	n/a	n/a
15	CTCF	chr17:45088197-45088234	K562	blood:	n/a	n/a
16	EBF1	chr17:45128015-45128266	GM12878	blood:	n/a	n/a
17	EBF1	chr17:45096518-45096768	GM12878	blood:	n/a	n/a
18	EBF1	chr17:45126885-45127082	GM12878	blood:	n/a	chr17:45127021-45127034 chr17:45127023-45127033 chr17:45127023-45127032
19	EBF1	chr17:45118420-45118630	GM12878	blood:	n/a	n/a
20	EBF1	chr17:45127582-45127804	GM12878	blood:	n/a	n/a
21	EBF1	chr17:45127978-45128282	GM12878	blood:	n/a	n/a
22	EBF1	chr17:45098980-45099148	GM12878	blood:	n/a	n/a
23	EP300	chr17:45128985-45130054	GM12878	blood:	n/a	n/a
24	EP300	chr17:45129270-45129419	GM12878	blood:	n/a	n/a
25	EP300	chr17:45127569-45127779	GM12878	blood:	n/a	n/a
26	EP300	chr17:45119165-45119413	GM12878	blood:	n/a	n/a
27	EP300	chr17:45126452-45126851	GM12878	blood:	n/a	n/a
28	EP300	chr17:45125793-45126372	GM12878	blood:	n/a	n/a
29	EP300	chr17:45109845-45110076	GM12878	blood:	n/a	n/a
30	EP300	chr17:45127075-45128666	GM12878	blood:	n/a	n/a
31	FOSL2	chr17:45130113-45130336	HepG2	liver:	n/a	n/a
32	FOSL2	chr17:45127458-45128193	HepG2	liver:	n/a	n/a
33	FOSL2	chr17:45096161-45096723	HepG2	liver:	n/a	n/a
34	FOSL2	chr17:45095094-45095686	HepG2	liver:	n/a	chr17:45095495-45095504
35	FOSL2	chr17:45099565-45099866	HepG2	liver:	n/a	n/a
36	FOSL2	chr17:45096486-45096821	HepG2	liver:	n/a	n/a
37	FOSL2	chr17:45112276-45112555	HepG2	liver:	n/a	chr17:45112400-45112410 chr17:45112400-45112410 chr17:45112402-45112413 chr17:45112399-45112411 chr17:45112401-45112409
38	FOSL2	chr17:45107928-45108172	HepG2	liver:	n/a	n/a
39	FOSL2	chr17:45093746-45094001	HepG2	liver:	n/a	n/a
40	FOSL2	chr17:45107593-45107848	HepG2	liver:	n/a	chr17:45107828-45107837
41	FOSL2	chr17:45118319-45118621	HepG2	liver:	n/a	n/a
42	FOSL2	chr17:45128968-45130056	HepG2	liver:	n/a	n/a
43	FOSL2	chr17:45103477-45103723	HepG2	liver:	n/a	n/a
44	FOSL2	chr17:45109834-45110156	HepG2	liver:	n/a	n/a
45	FOSL2	chr17:45125983-45126818	HepG2	liver:	n/a	n/a
46	FOSL2	chr17:45124277-45124624	HepG2	liver:	n/a	n/a
47	FOSL2	chr17:45116644-45116986	HepG2	liver:	n/a	n/a
48	FOSL2	chr17:45094327-45094566	HepG2	liver:	n/a	n/a
49	FOSL2	chr17:45109738-45110081	HepG2	liver:	n/a	n/a
50	FOSL2	chr17:45129449-45129784	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45126661-45126711	ECC-1	luminal epithelium:	n/a
2	chr17:45094513-45094563	HL-60	blood:	n/a
3	chr17:45126661-45126711	ovcar-3	ovarian:	n/a
4	chr17:45126661-45126711	PANC-1	pancreas:	n/a
5	chr17:45094513-45094563	NB4	blood:	n/a
6	chr17:45126661-45126711	RPTEC	kidney:	n/a
7	chr17:45126661-45126711	HCT-116	colon:	n/a
8	chr17:45094513-45094563	HRPEpiC	eye:	n/a
9	chr17:45094513-45094563	Caco-2	colon:	n/a
10	chr17:45094513-45094563	GM12892	blood:	n/a
11	chr17:45126661-45126711	U87	brain:	n/a
12	chr17:45126661-45126711	Hela-S3	cervix:	n/a
13	chr17:45126661-45126711	GM12892	blood:	n/a
14	chr17:45094513-45094563	MCF10A-Er-Src	breast:	n/a
15	chr17:45094513-45094563	K562	blood:	n/a
16	chr17:45094513-45094563	HAEpiC	amniotic membrane:	n/a
17	chr17:45126661-45126711	H1-hESC	embryonic stem cell:	embryo
18	chr17:45094513-45094563	LNCaP	prostate:	n/a
19	chr17:45094513-45094563	HCT-116	colon:	n/a
20	chr17:45126661-45126711	NT2-D1	testis:	n/a
21	chr17:45126661-45126711	A549	lung:	n/a
22	chr17:45094513-45094563	PrEC	prostate:	n/a
23	chr17:45126661-45126711	HepG2	liver:	n/a
24	chr17:45126661-45126711	HEK293	kidney:	embryo
25	chr17:45126661-45126711	NHDF-neo	bronchial:	n/a
26	chr17:45126661-45126711	T-47D	breast:	n/a
27	chr17:45094513-45094563	H1-hESC	embryonic stem cell:	embryo
28	chr17:45126661-45126711	AG10803	skin:	n/a
29	chr17:45094513-45094563	AG04450	lung:	fetal
30	chr17:45126661-45126711	SAEC	small airway:	n/a
31	chr17:45094513-45094563	SAEC	small airway:	n/a
32	chr17:45094513-45094563	HCF	heart:	n/a
33	chr17:45126661-45126711	HEEpiC	esophagus:	n/a
34	chr17:45094513-45094563	SK-N-SH	brain:	n/a
35	chr17:45126661-45126711	HCF	heart:	n/a
36	chr17:45126661-45126711	NB4	blood:	n/a
37	chr17:45126661-45126711	SK-N-SH_RA	brain:	n/a
38	chr17:45094513-45094563	CMK	blood:	n/a
39	chr17:45094513-45094563	HIPEpiC	eye:	n/a
40	chr17:45094513-45094563	GM12878	blood:	n/a
41	chr17:45126661-45126711	HMEC	breast:	n/a
42	chr17:45094513-45094563	HNPCEpiC	eye:	n/a
43	chr17:45094513-45094563	Hela-S3	cervix:	n/a
44	chr17:45126661-45126711	MCF-7	breast:	n/a
45	chr17:45094513-45094563	HCPEpiC	choroid plexus:	n/a
46	chr17:45094513-45094563	U87	brain:	n/a
47	chr17:45094513-45094563	HepG2	liver:	n/a
48	chr17:45094513-45094563	AG10803	skin:	n/a
49	chr17:45094513-45094563	HRCEpiC	kidney:	n/a
50	chr17:45126661-45126711	GM19239	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45035542..45037686-chr17:45103345..45105555,2	K562	blood:
2	chr17:45085709..45088129-chr17:45091783..45094489,2	K562	blood:
3	chr17:45085709..45088129-chr17:45091783..45094489,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPRML-3	chr17:45098948-45098989	ENSG00000262879.1
2	lnc-GOSR2-2	chr17:45099216-45099287	NONHSAT054231
3	lnc-GOSR2-2	chr17:45131638-45133274	NONHSAT054261
4	lnc-GOSR2-2	chr17:45126422-45126511	NONHSAT054231
5	lnc-CDC27-2	chr17:45128639-45128968	ENSG00000250104
6	lnc-GOSR2-2	chr17:45124512-45124630	NONHSAT054231
7	lnc-GOSR2-2	chr17:45131884-45134124	NONHSAT054246
8	lnc-RPRML-3	chr17:45128652-45128968	NONHSAT054254
9	lnc-RPRML-3	chr17:45129892-45131988	NONHSAT054259
10	lnc-GOSR2-2	chr17:45131093-45131559	NONHSAT054261
11	lnc-CDC27-1	chr17:45099553-45100857	ENSG00000249029
12	lnc-CDC27-2	chr17:45129070-45129168	ENSG00000250104
13	lnc-RPRML-3	chr17:45126241-45127901	NONHSAT054248
14	lnc-RPRML-3	chr17:45129070-45129168	NONHSAT054254
15	lnc-RPRML-3	chr17:45098948-45099032	ENSG00000262879.1
16	lnc-RPRML-3	chr17:45087830-45088102	ENSG00000262879.1
17	lnc-GOSR2-2	chr17:45124167-45124630	NONHSAT054246
18	lnc-GOSR2-2	chr17:45126422-45131777	NONHSAT054246
19	lnc-GOSR2-1	chr17:45119191-45119483	NONHSAT054245

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRC37A2	hsa-miR-92a-3p	chr17:45102113-45102117
2	LRRC37A2	hsa-miR-92a-3p	chr17:45104923-45104939

Variant related genes	Relation type
RN7SL270P	TF binding region
ENSG00000262879	TF binding region
LRRC37A17P	TF binding region
RN7SL270P	CpG island
ENSG00000262879	CpG island
LRRC37A17P	CpG island
UTP15	miRNA target sites
STARD7	miRNA target sites
AGMAT	miRNA target sites

Extended variants
information (count: 1354 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555511362	chr17:45087632-45087633	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575859678	chr17:45087633-45087634	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544600876	chr17:45087660-45087661	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182393589	chr17:45087678-45087679	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542188300	chr17:45087689-45087690	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2271790	chr17:45087706-45087707	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs578117667	chr17:45087731-45087732	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540871294	chr17:45087761-45087762	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140819092	chr17:45087858-45087859	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs118104219	chr17:45087882-45087883	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs149726164	chr17:45087898-45087899	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs11654119	chr17:45087902-45087903	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs561547742	chr17:45087934-45087935	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs530783469	chr17:45087974-45087975	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs147829351	chr17:45087983-45087984	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs188030021	chr17:45087994-45087995	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs539243113	chr17:45088034-45088035	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs11657803	chr17:45088042-45088043	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs141193803	chr17:45088055-45088056	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs11657519	chr17:45088064-45088065	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs376902872	chr17:45088112-45088113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555704298	chr17:45088140-45088141	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575553513	chr17:45088156-45088157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538490431	chr17:45088188-45088189	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549326348	chr17:45088192-45088193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558159240	chr17:45088209-45088210	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192484487	chr17:45088210-45088211	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570478258	chr17:45088241-45088242	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540810131	chr17:45088281-45088282	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560703088	chr17:45088302-45088303	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35384746	chr17:45088361-45088362	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370063272	chr17:45088417-45088418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572943858	chr17:45088453-45088454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7216950	chr17:45088455-45088456	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs547452663	chr17:45088467-45088468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368741407	chr17:45088489-45088490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530412846	chr17:45088542-45088543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146959404	chr17:45088547-45088548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565763454	chr17:45088597-45088598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533089631	chr17:45088621-45088622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183402522	chr17:45088629-45088630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs151101917	chr17:45088655-45088656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566351326	chr17:45088732-45088733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535510518	chr17:45088774-45088775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370201642	chr17:45088899-45088900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200995540	chr17:45088936-45088937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549218733	chr17:45088937-45088938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569923260	chr17:45088940-45088941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113675605	chr17:45088951-45088952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569375574	chr17:45088972-45088973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
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
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
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45057200-45100000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr17:45062200-45113200	Weak transcription	Ovary	ovary
3	chr17:45075200-45130200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr17:45079200-45098200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr17:45079400-45095800	Weak transcription	Fetal Intestine Small	intestine
6	chr17:45083000-45095600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr17:45083200-45092000	Weak transcription	Brain Substantia Nigra	brain
8	chr17:45083200-45095600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr17:45083400-45107000	Weak transcription	Lung	lung
10	chr17:45085200-45089800	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr17:45085200-45095600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr17:45085600-45088800	Weak transcription	Aorta	Aorta
13	chr17:45086000-45129600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr17:45086000-45129600	Weak transcription	Fetal Muscle Leg	muscle
15	chr17:45086600-45088600	Strong transcription	Fetal Stomach	stomach
16	chr17:45086800-45095800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr17:45086800-45129600	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr17:45087000-45088000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr17:45087000-45088200	Enhancers	Left Ventricle	heart
20	chr17:45087200-45111400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr17:45087200-45126600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr17:45087400-45097200	Weak transcription	Brain Hippocampus Middle	brain
23	chr17:45087400-45098200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr17:45087600-45087800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr17:45087600-45087800	Enhancers	HSMMtube	muscle
26	chr17:45087600-45088600	Strong transcription	Spleen	Spleen
27	chr17:45087600-45129600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr17:45087800-45088400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr17:45087800-45097200	Weak transcription	HSMMtube	muscle
30	chr17:45088000-45088200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr17:45088200-45088400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr17:45088400-45095600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr17:45088400-45097400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr17:45088600-45090200	Weak transcription	Spleen	Spleen
35	chr17:45088600-45095800	Weak transcription	Fetal Stomach	stomach
36	chr17:45088600-45128600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr17:45089800-45090000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr17:45089800-45090600	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr17:45090000-45090200	Enhancers	Dnd41	blood
40	chr17:45090000-45090400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr17:45090000-45090400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr17:45090000-45090600	Enhancers	Primary B cells from peripheral blood	blood
43	chr17:45090000-45090600	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr17:45090000-45091400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr17:45090000-45131600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr17:45090200-45090600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr17:45090200-45090600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr17:45090200-45131000	Weak transcription	Dnd41	blood
49	chr17:45090600-45100200	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr17:45090600-45103600	Weak transcription	Primary B cells from peripheral blood	blood

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