Variant report

Variant	esv1807564
Chromosome Location	chr17:44648058-44800046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:893)
CpG islands
(count:550)
Chromatin interactive
region (count:6)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:44791224-44791474	K562	blood:	n/a	chr17:44791227-44791242
2	BATF	chr17:44675761-44676320	GM12878	blood:	n/a	n/a
3	BATF	chr17:44654451-44654736	GM12878	blood:	n/a	n/a
4	BATF	chr17:44675819-44676288	GM12878	blood:	n/a	n/a
5	BATF	chr17:44680386-44680933	GM12878	blood:	n/a	chr17:44680402-44680411
6	BATF	chr17:44680387-44680931	GM12878	blood:	n/a	chr17:44680402-44680411
7	BATF	chr17:44706376-44706744	GM12878	blood:	n/a	n/a
8	BATF	chr17:44729691-44729946	GM12878	blood:	n/a	n/a
9	BCL11A	chr17:44729666-44729907	GM12878	blood:	n/a	n/a
10	BCL11A	chr17:44729690-44730017	GM12878	blood:	n/a	n/a
11	BCL11A	chr17:44706447-44706675	GM12878	blood:	n/a	n/a
12	BCL11A	chr17:44706471-44706784	GM12878	blood:	n/a	n/a
13	BCL11A	chr17:44675843-44676322	GM12878	blood:	n/a	n/a
14	BCL11A	chr17:44680508-44680869	GM12878	blood:	n/a	chr17:44680542-44680551
15	BCL11A	chr17:44680433-44680905	GM12878	blood:	n/a	chr17:44680542-44680551 chr17:44680475-44680482
16	BHLHE40	chr17:44658897-44659167	HepG2	liver:	n/a	n/a
17	CBX3	chr17:44656873-44657506	K562	blood:	n/a	n/a
18	CBX3	chr17:44656415-44656822	K562	blood:	n/a	n/a
19	CEBPB	chr17:44790985-44790993	IMR90	lung:	n/a	n/a
20	CEBPB	chr17:44712957-44713150	IMR90	lung:	n/a	n/a
21	CEBPB	chr17:44657149-44657159	HepG2	liver:	n/a	n/a
22	CEBPD	chr17:44737046-44737486	K562	blood:	n/a	n/a
23	CEBPZ	chr17:44797673-44797692	HepG2	liver:	n/a	n/a
24	CTCF	chr17:44706501-44706723	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr17:44750283-44750305	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:44719317-44719551	Pancreas_OC	pancreas:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719526-44719534 chr17:44719435-44719448
27	CTCF	chr17:44676190-44676274	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr17:44719679-44720008	A549	lung:	n/a	n/a
29	CTCF	chr17:44724756-44724908	GM12891	blood:	n/a	chr17:44724821-44724828
30	CTCF	chr17:44717129-44717161	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr17:44662366-44662441	LNCaP	prostate:	n/a	n/a
32	CTCF	chr17:44706623-44706659	GM12878	blood:	n/a	n/a
33	CTCF	chr17:44719668-44720001	K562	blood:	n/a	n/a
34	CTCF	chr17:44656468-44656639	GM12891	blood:	n/a	n/a
35	CTCF	chr17:44724743-44724891	GM13977	blood:	n/a	chr17:44724821-44724828
36	CTCF	chr17:44719624-44720004	A549	lung:	n/a	n/a
37	CTCF	chr17:44719354-44719499	GM13976	blood:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719435-44719448
38	CTCF	chr17:44656409-44656626	GM19240	blood:	n/a	n/a
39	CTCF	chr17:44671776-44671858	GM13976	blood:	n/a	n/a
40	CTCF	chr17:44719802-44719875	GM12878	blood:	n/a	n/a
41	CTCF	chr17:44706012-44706019	GM13977	blood:	n/a	n/a
42	CTCF	chr17:44719213-44719590	A549	lung:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719526-44719534 chr17:44719435-44719448
43	CTCF	chr17:44706027-44706088	GM13977	blood:	n/a	n/a
44	CTCF	chr17:44667875-44668040	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr17:44719346-44719506	GM13977	blood:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719435-44719448
46	CTCF	chr17:44719269-44719615	A549	lung:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719526-44719534 chr17:44719435-44719448
47	CTCF	chr17:44719700-44719850	AG09319	gingival:	n/a	n/a
48	CTCF	chr17:44769722-44769880	MCF-7	breast:	n/a	n/a
49	CTCF	chr17:44751551-44751632	GM13976	blood:	n/a	n/a
50	CTCF	chr17:44789140-44789290	BE2_C	brain:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:44657154-44657204	CMK	blood:	n/a
2	chr17:44657154-44657204	CMK	blood:	n/a
3	chr17:44799470-44799520	SK-N-SH	brain:	n/a
4	chr17:44785029-44785079	HCM	heart:	n/a
5	chr17:44648385-44648435	SK-N-MC	brain:	n/a
6	chr17:44799588-44799638	AG10803	skin:	n/a
7	chr17:44799518-44799568	ECC-1	luminal epithelium:	n/a
8	chr17:44657394-44657444	A549	lung:	n/a
9	chr17:44702619-44702669	RPTEC	kidney:	n/a
10	chr17:44657154-44657204	PANC-1	pancreas:	n/a
11	chr17:44702619-44702669	ECC-1	luminal epithelium:	n/a
12	chr17:44648385-44648435	HNPCEpiC	eye:	n/a
13	chr17:44799518-44799568	ovcar-3	ovarian:	n/a
14	chr17:44657394-44657444	HL-60	blood:	n/a
15	chr17:44790735-44790785	SKMC	muscle:	n/a
16	chr17:44790735-44790785	BJ	skin:	n/a
17	chr17:44799588-44799638	PFSK-1	brain:	n/a
18	chr17:44790735-44790785	NB4	blood:	n/a
19	chr17:44790735-44790785	A549	lung:	n/a
20	chr17:44785029-44785079	SK-N-SH	brain:	n/a
21	chr17:44648385-44648435	BJ	skin:	n/a
22	chr17:44799518-44799568	GM19239	blood:	n/a
23	chr17:44657154-44657204	MCF-7	breast:	n/a
24	chr17:44799588-44799638	AG04449	skin:	fetal
25	chr17:44648385-44648435	IMR90	lung:	fetal
26	chr17:44702619-44702669	HCF	heart:	n/a
27	chr17:44785029-44785079	HRCEpiC	kidney:	n/a
28	chr17:44799588-44799638	LNCaP	prostate:	n/a
29	chr17:44648385-44648435	ovcar-3	ovarian:	n/a
30	chr17:44657154-44657204	RPTEC	kidney:	n/a
31	chr17:44799518-44799568	HepG2	liver:	n/a
32	chr17:44799588-44799638	CMK	blood:	n/a
33	chr17:44657154-44657204	HCPEpiC	choroid plexus:	n/a
34	chr17:44648385-44648435	GM12892	blood:	n/a
35	chr17:44657154-44657204	NB4	blood:	n/a
36	chr17:44799518-44799568	HRE	kidney:	n/a
37	chr17:44790735-44790785	SK-N-SH_RA	brain:	n/a
38	chr17:44790735-44790785	HCF	heart:	n/a
39	chr17:44799470-44799520	GM12892	blood:	n/a
40	chr17:44648385-44648435	HRE	kidney:	n/a
41	chr17:44657394-44657444	SAEC	small airway:	n/a
42	chr17:44799518-44799568	T-47D	breast:	n/a
43	chr17:44799518-44799568	HCT-116	colon:	n/a
44	chr17:44648385-44648435	U87	brain:	n/a
45	chr17:44657154-44657204	Caco-2	colon:	n/a
46	chr17:44657154-44657204	SAEC	small airway:	n/a
47	chr17:44799470-44799520	IMR90	lung:	fetal
48	chr17:44799470-44799520	Jurkat	blood:	n/a
49	chr17:44799470-44799520	NT2-D1	testis:	n/a
50	chr17:44657394-44657444	HPAEpiC	pulmonary alveolar:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:44793480..44795717-chr17:44798517..44800537,2	MCF-7	breast:
2	chr17:44791299..44793121-chr17:44854894..44857732,2	MCF-7	breast:
3	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
4	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
5	chr17:44789439..44791140-chr17:44792595..44794517,2	MCF-7	breast:
6	chr17:44799962..44803131-chr17:44820339..44824064,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WNT3-3	chr17:44793046-44793367	expReg_chr17_8945_-
2	lnc-LRRC37A2-1	chr17:44685215-44685279	ucscGeneNc_uc002iot_1
3	lnc-NSF-1	chr17:44668501-44668700	l_1459_chr17:44663232-44671620_testes
4	lnc-WNT3-2	chr17:44793730-44793944	expReg_chr17_8951_-
5	lnc-NSF-1	chr17:44663233-44663284	l_1459_chr17:44663232-44671620_testes
6	lnc-LRRC37A2-1	chr17:44687052-44688810	ucscGeneNc_uc002iot_1
7	lnc-NSF-1	chr17:44671411-44671620	l_1459_chr17:44663232-44671620_testes
8	lnc-NSF-1	chr17:44670559-44670675	l_1459_chr17:44663232-44671620_testes
9	lnc-LRRC37A2-1	chr17:44680600-44680663	ucscGeneNc_uc002iot_1
10	lnc-LRRC37A2-1	chr17:44684607-44685035	ucscGeneNc_uc002iot_1

No data

Variant related genes	Relation type
NSF	TF binding region
ARL17A	TF binding region
RPS7P11	TF binding region
NSF	CpG island
ARL17A	CpG island
RPS7P11	CpG island
ENSG00000073969	chromatin interactions
ENSG00000213326	chromatin interactions

Extended variants
information (count: 804 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139705193	chr17:44648193-44648194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376377247	chr17:44648366-44648367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149763288	chr17:44648997-44648998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145780376	chr17:44649083-44649084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377246705	chr17:44649552-44649553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139496288	chr17:44649557-44649558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148949611	chr17:44649652-44649653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370937840	chr17:44649975-44649976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373763808	chr17:44650138-44650139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367554357	chr17:44650381-44650382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370389793	chr17:44650385-44650386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375675405	chr17:44650814-44650815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113858404	chr17:44650958-44650959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564383380	chr17:44651239-44651240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533050474	chr17:44651355-44651356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558710130	chr17:44652348-44652349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566828438	chr17:44652411-44652412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529407758	chr17:44652419-44652420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544495128	chr17:44652462-44652463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549492819	chr17:44652472-44652473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372645904	chr17:44652561-44652562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367960686	chr17:44652645-44652646	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538414914	chr17:44652651-44652652	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576827993	chr17:44652673-44652674	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140199629	chr17:44652701-44652702	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145269005	chr17:44652731-44652732	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534187352	chr17:44652735-44652736	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149724338	chr17:44652756-44652757	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190080210	chr17:44652784-44652785	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552552506	chr17:44653036-44653037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572503045	chr17:44653094-44653095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144562016	chr17:44653340-44653341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372807415	chr17:44653351-44653352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147612473	chr17:44653929-44653930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369231328	chr17:44654366-44654367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567113551	chr17:44655822-44655823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142128947	chr17:44656701-44656702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146163868	chr17:44656828-44656829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74465702	chr17:44656973-44656974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148265451	chr17:44657024-44657025	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs374830138	chr17:44657065-44657066	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs140107079	chr17:44657154-44657155	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs541566426	chr17:44657191-44657192	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs555027818	chr17:44657277-44657278	Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs575374900	chr17:44657387-44657388	Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs544417730	chr17:44657415-44657416	Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs564091758	chr17:44657451-44657452	Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs533263407	chr17:44657567-44657568	Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs540482744	chr17:44657653-44657654	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs150292772	chr17:44657706-44657707	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	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
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22817714	CNVD
Non-syndromic sensorineural hearing loss	21084979	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	16397240	CNVD
Prostate cancer	17217626	CNVD
Autism	22817714	CNVD

Chromatin state (count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44621200-44657400	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr17:44647600-44652400	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr17:44649600-44657200	Weak transcription	Fetal Stomach	stomach
4	chr17:44649600-44657400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr17:44650600-44652400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr17:44650600-44657400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr17:44650600-44657600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr17:44651000-44657400	Weak transcription	Fetal Muscle Leg	muscle
9	chr17:44651000-44657600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr17:44651000-44657600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr17:44651200-44657000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr17:44651200-44657400	Weak transcription	Liver	Liver
13	chr17:44651200-44657400	Weak transcription	Spleen	Spleen
14	chr17:44651400-44652800	Weak transcription	Gastric	stomach
15	chr17:44651400-44657400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr17:44651400-44657400	Weak transcription	Ovary	ovary
17	chr17:44651600-44652600	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr17:44651600-44654000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr17:44652400-44653000	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr17:44652400-44653000	Strong transcription	Primary B cells from peripheral blood	blood
21	chr17:44652600-44652800	Enhancers	Left Ventricle	heart
22	chr17:44652600-44653000	Genic enhancers	Primary T cells fromperipheralblood	blood
23	chr17:44652800-44653000	Genic enhancers	Gastric	stomach
24	chr17:44652800-44657400	Weak transcription	Left Ventricle	heart
25	chr17:44653000-44657400	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr17:44653000-44657400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr17:44653000-44657400	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr17:44653000-44657600	Weak transcription	Gastric	stomach
29	chr17:44657000-44657400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr17:44657000-44657800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
31	chr17:44657000-44657800	Active TSS	Fetal Brain Female	brain
32	chr17:44657000-44657800	Active TSS	Fetal Intestine Large	intestine
33	chr17:44657000-44657800	Active TSS	Fetal Intestine Small	intestine
34	chr17:44657000-44657800	Active TSS	Thymus	Thymus
35	chr17:44657200-44657600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr17:44657200-44657600	Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr17:44657200-44657800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr17:44657200-44657800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr17:44657200-44657800	Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr17:44657200-44657800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr17:44657200-44657800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr17:44657200-44657800	Active TSS	Brain Anterior Caudate	brain
43	chr17:44657200-44657800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr17:44657200-44657800	Active TSS	Fetal Stomach	stomach
45	chr17:44657400-44657600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr17:44657400-44657600	Active TSS	Primary monocytes fromperipheralblood	blood
47	chr17:44657400-44657600	Active TSS	Primary B cells from peripheral blood	blood
48	chr17:44657400-44657600	Active TSS	Primary T cells fromperipheralblood	blood
49	chr17:44657400-44657600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr17:44657400-44657600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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