Variant report

Variant	nsv962331
Chromosome Location	chr17:45088443-45141744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45140347-45140388	K562	blood:	n/a	n/a
2	BATF	chr17:45127560-45127755	GM12878	blood:	n/a	n/a
3	BATF	chr17:45127603-45127849	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:45126159-45126397	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:45125999-45126154	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	chr17:45127623-45127792	GM12878	blood:	n/a	n/a
9	BCL11A	chr17:45127435-45128324	GM12878	blood:	n/a	n/a
10	BHLHE40	chr17:45100421-45100689	HepG2	liver:	n/a	n/a
11	CEBPB	chr17:45136819-45136906	HepG2	liver:	n/a	chr17:45136845-45136856
12	CTCF	chr17:45138000-45138104	GM20000	blood:	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	chr17:45100084-45100112	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr17:45092932-45092976	LNCaP	prostate:	n/a	n/a
17	EBF1	chr17:45128015-45128266	GM12878	blood:	n/a	n/a
18	EBF1	chr17:45098980-45099148	GM12878	blood:	n/a	n/a
19	EBF1	chr17:45127582-45127804	GM12878	blood:	n/a	n/a
20	EBF1	chr17:45118420-45118630	GM12878	blood:	n/a	n/a
21	EBF1	chr17:45096518-45096768	GM12878	blood:	n/a	n/a
22	EBF1	chr17:45127978-45128282	GM12878	blood:	n/a	n/a
23	EBF1	chr17:45126885-45127082	GM12878	blood:	n/a	chr17:45127021-45127034 chr17:45127023-45127033 chr17:45127023-45127032
24	EP300	chr17:45126452-45126851	GM12878	blood:	n/a	n/a
25	EP300	chr17:45119165-45119413	GM12878	blood:	n/a	n/a
26	EP300	chr17:45128985-45130054	GM12878	blood:	n/a	n/a
27	EP300	chr17:45109845-45110076	GM12878	blood:	n/a	n/a
28	EP300	chr17:45127075-45128666	GM12878	blood:	n/a	n/a
29	EP300	chr17:45127569-45127779	GM12878	blood:	n/a	n/a
30	EP300	chr17:45125793-45126372	GM12878	blood:	n/a	n/a
31	EP300	chr17:45129270-45129419	GM12878	blood:	n/a	n/a
32	EP300	chr17:45140359-45140391	K562	blood:	n/a	n/a
33	FOSL2	chr17:45135559-45136764	HepG2	liver:	n/a	n/a
34	FOSL2	chr17:45130113-45130336	HepG2	liver:	n/a	n/a
35	FOSL2	chr17:45127458-45128193	HepG2	liver:	n/a	n/a
36	FOSL2	chr17:45096161-45096723	HepG2	liver:	n/a	n/a
37	FOSL2	chr17:45118319-45118621	HepG2	liver:	n/a	n/a
38	FOSL2	chr17:45124277-45124624	HepG2	liver:	n/a	n/a
39	FOSL2	chr17:45129449-45129784	HepG2	liver:	n/a	n/a
40	FOSL2	chr17:45140814-45141139	HepG2	liver:	n/a	n/a
41	FOSL2	chr17:45109738-45110081	HepG2	liver:	n/a	n/a
42	FOSL2	chr17:45107593-45107848	HepG2	liver:	n/a	chr17:45107828-45107837
43	FOSL2	chr17:45094607-45094897	HepG2	liver:	n/a	n/a
44	FOSL2	chr17:45125846-45128653	HepG2	liver:	n/a	n/a
45	FOSL2	chr17:45103477-45103723	HepG2	liver:	n/a	n/a
46	FOSL2	chr17:45094327-45094566	HepG2	liver:	n/a	n/a
47	FOSL2	chr17:45125983-45126818	HepG2	liver:	n/a	n/a
48	FOSL2	chr17:45098901-45099149	HepG2	liver:	n/a	chr17:45099050-45099062
49	FOSL2	chr17:45116644-45116986	HepG2	liver:	n/a	n/a
50	FOSL2	chr17:45095094-45095686	HepG2	liver:	n/a	chr17:45095495-45095504

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45134721-45134771	HUVEC	blood vessel:	n/a
2	chr17:45134721-45134771	HUVEC	blood vessel:	n/a
3	chr17:45094513-45094563	SK-N-SH	brain:	n/a
4	chr17:45094513-45094563	AG04449	skin:	fetal
5	chr17:45126661-45126711	HCF	heart:	n/a
6	chr17:45094513-45094563	SK-N-SH_RA	brain:	n/a
7	chr17:45126661-45126711	Hepatocyte	liver:	n/a
8	chr17:45134721-45134771	HepG2	liver:	n/a
9	chr17:45094513-45094563	HCF	heart:	n/a
10	chr17:45126661-45126711	MCF-7	breast:	n/a
11	chr17:45134721-45134771	T-47D	breast:	n/a
12	chr17:45094513-45094563	CMK	blood:	n/a
13	chr17:45094513-45094563	PFSK-1	brain:	n/a
14	chr17:45094513-45094563	HEEpiC	esophagus:	n/a
15	chr17:45094513-45094563	HIPEpiC	eye:	n/a
16	chr17:45094513-45094563	BJ	skin:	n/a
17	chr17:45126661-45126711	T-47D	breast:	n/a
18	chr17:45126661-45126711	HMEC	breast:	n/a
19	chr17:45134721-45134771	IMR90	lung:	fetal
20	chr17:45094513-45094563	AG09309	skin:	n/a
21	chr17:45094513-45094563	T-47D	breast:	n/a
22	chr17:45126661-45126711	ProgFib	skin:	n/a
23	chr17:45094513-45094563	HRE	kidney:	n/a
24	chr17:45094513-45094563	AG09319	gingival:	n/a
25	chr17:45134721-45134771	HCF	heart:	n/a
26	chr17:45094513-45094563	GM12892	blood:	n/a
27	chr17:45126661-45126711	BE2_C	brain:	n/a
28	chr17:45134721-45134771	GM19239	blood:	n/a
29	chr17:45134721-45134771	HEEpiC	esophagus:	n/a
30	chr17:45126661-45126711	HCPEpiC	choroid plexus:	n/a
31	chr17:45126661-45126711	HEEpiC	esophagus:	n/a
32	chr17:45126661-45126711	SKMC	muscle:	n/a
33	chr17:45134721-45134771	NH-A	brain:	n/a
34	chr17:45094513-45094563	HEK293	kidney:	embryo
35	chr17:45094513-45094563	ovcar-3	ovarian:	n/a
36	chr17:45126661-45126711	SK-N-SH_RA	brain:	n/a
37	chr17:45126661-45126711	NH-A	brain:	n/a
38	chr17:45094513-45094563	MCF10A-Er-Src	breast:	n/a
39	chr17:45094513-45094563	HRPEpiC	eye:	n/a
40	chr17:45134721-45134771	A549	lung:	n/a
41	chr17:45134721-45134771	HRPEpiC	eye:	n/a
42	chr17:45134721-45134771	NHDF-neo	bronchial:	n/a
43	chr17:45094513-45094563	H1-hESC	embryonic stem cell:	embryo
44	chr17:45134721-45134771	HMEC	breast:	n/a
45	chr17:45134721-45134771	AG09309	skin:	n/a
46	chr17:45094513-45094563	NT2-D1	testis:	n/a
47	chr17:45134721-45134771	ECC-1	luminal epithelium:	n/a
48	chr17:45134721-45134771	CMK	blood:	n/a
49	chr17:45134721-45134771	HAEpiC	amniotic membrane:	n/a
50	chr17:45134721-45134771	SAEC	small airway:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45136707..45138287-chr17:45138390..45140418,2	K562	blood:
2	chr17:45137333..45141674-chr17:45143017..45146181,5	MCF-7	breast:
3	chr17:45035542..45037686-chr17:45103345..45105555,2	K562	blood:
4	chr17:45085709..45088129-chr17:45091783..45094489,2	K562	blood:
5	chr17:45138815..45142587-chr17:45143506..45146312,3	K562	blood:
6	chr17:45141024..45142587-chr17:45143013..45146312,3	K562	blood:
7	chr17:45136707..45138287-chr17:45138390..45140418,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOSR2-2	chr17:45124167-45124630	NONHSAT054246
2	lnc-GOSR2-1	chr17:45119191-45119483	NONHSAT054245
3	lnc-CDC27-1	chr17:45099553-45100857	ENSG00000249029
4	lnc-GOSR2-2	chr17:45124512-45124630	NONHSAT054231
5	lnc-CDC27-3	chr17:45135517-45136457	NONHSAT054275
6	lnc-RPRML-3	chr17:45126241-45127901	NONHSAT054248
7	lnc-RPRML-3	chr17:45133975-45134119	ENSG00000262879.1
8	lnc-GOSR2-2	chr17:45131638-45133274	NONHSAT054261
9	lnc-CDC27-2	chr17:45129070-45129168	ENSG00000250104
10	lnc-CDC27-2	chr17:45128639-45128968	ENSG00000250104
11	lnc-RPRML-3	chr17:45128652-45128968	NONHSAT054254
12	lnc-RPRML-3	chr17:45098948-45098989	ENSG00000262879.1
13	lnc-GOSR2-2	chr17:45131884-45134124	NONHSAT054246
14	lnc-GOSR2-2	chr17:45131093-45131559	NONHSAT054261
15	lnc-RPRML-3	chr17:45129892-45131988	NONHSAT054259
16	lnc-RPRML-3	chr17:45129070-45129168	NONHSAT054254
17	lnc-GOSR2-2	chr17:45126422-45131777	NONHSAT054246
18	lnc-GOSR2-2	chr17:45099216-45099287	NONHSAT054231
19	lnc-RPRML-3	chr17:45098948-45099032	ENSG00000262879.1
20	lnc-GOSR2-2	chr17:45126422-45126511	NONHSAT054231

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
ENSG00000262879	chromatin interactions
AGMAT	miRNA target sites
UTP15	miRNA target sites
STARD7	miRNA target sites

Extended variants
information (count: 1745 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1745 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572943858	chr17:45088453-45088454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7216950	chr17:45088455-45088456	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs547452663	chr17:45088467-45088468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368741407	chr17:45088489-45088490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530412846	chr17:45088542-45088543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146959404	chr17:45088547-45088548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565763454	chr17:45088597-45088598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533089631	chr17:45088621-45088622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183402522	chr17:45088629-45088630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151101917	chr17:45088655-45088656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566351326	chr17:45088732-45088733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535510518	chr17:45088774-45088775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370201642	chr17:45088899-45088900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200995540	chr17:45088936-45088937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549218733	chr17:45088937-45088938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569923260	chr17:45088940-45088941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113675605	chr17:45088951-45088952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569375574	chr17:45088972-45088973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537849022	chr17:45088973-45088974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558161910	chr17:45088993-45088994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571956958	chr17:45089000-45089001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374774051	chr17:45089021-45089022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534516077	chr17:45089047-45089048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554381341	chr17:45089050-45089051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574291025	chr17:45089052-45089053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs137857173	chr17:45089151-45089152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555164388	chr17:45089172-45089173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537443511	chr17:45089229-45089230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575323264	chr17:45089274-45089275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543846971	chr17:45089292-45089293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72823405	chr17:45089302-45089303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs533028894	chr17:45089329-45089330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540139608	chr17:45089330-45089331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149045038	chr17:45089373-45089374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529044573	chr17:45089380-45089381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577433139	chr17:45089493-45089494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs60813462	chr17:45089557-45089558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567960125	chr17:45089570-45089571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187818478	chr17:45089579-45089580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143813683	chr17:45089613-45089614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117783419	chr17:45089680-45089681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117343447	chr17:45089708-45089709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571692590	chr17:45089716-45089717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191964981	chr17:45089785-45089786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185293868	chr17:45089794-45089795	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs554493603	chr17:45089847-45089848	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs148176180	chr17:45089862-45089863	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs536421964	chr17:45089869-45089870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs189401550	chr17:45089876-45089877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs57446924	chr17:45089892-45089893	Weak transcription Enhancers	TF binding region	1 gene(s)	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:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr17:45087200-45111400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr17:45087200-45126600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr17:45087400-45097200	Weak transcription	Brain Hippocampus Middle	brain
21	chr17:45087400-45098200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr17:45087600-45088600	Strong transcription	Spleen	Spleen
23	chr17:45087600-45129600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr17:45087800-45097200	Weak transcription	HSMMtube	muscle
25	chr17:45088400-45095600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr17:45088400-45097400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr17:45088600-45090200	Weak transcription	Spleen	Spleen
28	chr17:45088600-45095800	Weak transcription	Fetal Stomach	stomach
29	chr17:45088600-45128600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr17:45089800-45090000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr17:45089800-45090600	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr17:45090000-45090200	Enhancers	Dnd41	blood
33	chr17:45090000-45090400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr17:45090000-45090400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr17:45090000-45090600	Enhancers	Primary B cells from peripheral blood	blood
36	chr17:45090000-45090600	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr17:45090000-45091400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr17:45090000-45131600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr17:45090200-45090600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr17:45090200-45090600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr17:45090200-45131000	Weak transcription	Dnd41	blood
42	chr17:45090600-45100200	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr17:45090600-45103600	Weak transcription	Primary B cells from peripheral blood	blood
44	chr17:45090600-45129600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr17:45091200-45129600	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr17:45093400-45095800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr17:45093400-45111200	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr17:45093800-45095800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr17:45094000-45098400	Weak transcription	HepG2	liver
50	chr17:45094200-45129600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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