Variant report

Variant	esv1812440
Chromosome Location	chr17:44676478-44802774
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:406)
CpG islands
(count:428)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:406 , 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	ARID3A	chr17:44791224-44791474	K562	blood:	n/a	chr17:44791227-44791242
2	BATF	chr17:44680386-44680933	GM12878	blood:	n/a	chr17:44680402-44680411
3	BATF	chr17:44680387-44680931	GM12878	blood:	n/a	chr17:44680402-44680411
4	BATF	chr17:44729691-44729946	GM12878	blood:	n/a	n/a
5	BATF	chr17:44706376-44706744	GM12878	blood:	n/a	n/a
6	BCL11A	chr17:44706447-44706675	GM12878	blood:	n/a	n/a
7	BCL11A	chr17:44680508-44680869	GM12878	blood:	n/a	chr17:44680542-44680551
8	BCL11A	chr17:44729690-44730017	GM12878	blood:	n/a	n/a
9	BCL11A	chr17:44729666-44729907	GM12878	blood:	n/a	n/a
10	BCL11A	chr17:44706471-44706784	GM12878	blood:	n/a	n/a
11	BCL11A	chr17:44680433-44680905	GM12878	blood:	n/a	chr17:44680542-44680551 chr17:44680475-44680482
12	CEBPB	chr17:44712957-44713150	IMR90	lung:	n/a	n/a
13	CEBPB	chr17:44790985-44790993	IMR90	lung:	n/a	n/a
14	CEBPD	chr17:44737046-44737486	K562	blood:	n/a	n/a
15	CEBPZ	chr17:44797673-44797692	HepG2	liver:	n/a	n/a
16	CTCF	chr17:44724730-44724942	Hela-S3	cervix:	n/a	chr17:44724821-44724828
17	CTCF	chr17:44692984-44693063	GM12891	blood:	n/a	n/a
18	CTCF	chr17:44750230-44750403	K562	blood:	n/a	n/a
19	CTCF	chr17:44746761-44746803	Pancreas_OC	pancreas:	n/a	n/a
20	CTCF	chr17:44724724-44724924	GM12892	blood:	n/a	chr17:44724821-44724828
21	CTCF	chr17:44719733-44719989	A549	lung:	n/a	n/a
22	CTCF	chr17:44719346-44719506	GM13977	blood:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719435-44719448
23	CTCF	chr17:44704327-44704354	GM13976	blood:	n/a	n/a
24	CTCF	chr17:44719213-44719590	A549	lung:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719526-44719534 chr17:44719435-44719448
25	CTCF	chr17:44692985-44693051	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:44724731-44724928	A549	lung:	n/a	chr17:44724821-44724828
27	CTCF	chr17:44724730-44724926	HepG2	liver:	n/a	chr17:44724821-44724828
28	CTCF	chr17:44719771-44719939	GM10248	blood:	n/a	n/a
29	CTCF	chr17:44719764-44719872	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr17:44766054-44766080	GM10266	blood:	n/a	n/a
31	CTCF	chr17:44719620-44719770	RPTEC	kidney:	n/a	n/a
32	CTCF	chr17:44750217-44750414	ProgFib	skin:	n/a	n/a
33	CTCF	chr17:44719326-44719545	GM10248	blood:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719526-44719534 chr17:44719435-44719448
34	CTCF	chr17:44693014-44693025	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr17:44719700-44719850	HMEC	breast:	n/a	n/a
36	CTCF	chr17:44719802-44719875	GM12878	blood:	n/a	n/a
37	CTCF	chr17:44751551-44751632	GM13976	blood:	n/a	n/a
38	CTCF	chr17:44724754-44724897	HUVEC	blood vessel:	n/a	chr17:44724821-44724828
39	CTCF	chr17:44719272-44719573	K562	blood:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719526-44719534 chr17:44719435-44719448
40	CTCF	chr17:44769690-44769852	K562	blood:	n/a	n/a
41	CTCF	chr17:44719772-44719943	GM10266	blood:	n/a	n/a
42	CTCF	chr17:44719700-44719850	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr17:44719825-44719902	GM13976	blood:	n/a	n/a
44	CTCF	chr17:44766616-44766671	GM13976	blood:	n/a	n/a
45	CTCF	chr17:44719343-44719540	LNCaP	prostate:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719526-44719534 chr17:44719435-44719448
46	CTCF	chr17:44745430-44745433	GM13977	blood:	n/a	n/a
47	CTCF	chr17:44724747-44724897	H1-hESC	embryonic stem cell:	n/a	chr17:44724821-44724828
48	CTCF	chr17:44719697-44719959	Medullo	brain:	n/a	n/a
49	CTCF	chr17:44724713-44724929	GM12878	blood:	n/a	chr17:44724821-44724828
50	CTCF	chr17:44719304-44719524	GM12878	blood:	n/a	chr17:44719434-44719455 chr17:44719432-44719450 chr17:44719435-44719448

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:44799588-44799638	HPAEpiC	pulmonary alveolar:	n/a
2	chr17:44799588-44799638	HPAEpiC	pulmonary alveolar:	n/a
3	chr17:44799588-44799638	AG04450	lung:	fetal
4	chr17:44799588-44799638	SK-N-MC	brain:	n/a
5	chr17:44799470-44799520	Caco-2	colon:	n/a
6	chr17:44799518-44799568	Hepatocyte	liver:	n/a
7	chr17:44702619-44702669	ProgFib	skin:	n/a
8	chr17:44799588-44799638	ovcar-3	ovarian:	n/a
9	chr17:44802702-44802752	HIPEpiC	eye:	n/a
10	chr17:44799470-44799520	GM12891	blood:	n/a
11	chr17:44799470-44799520	MCF-7	breast:	n/a
12	chr17:44799470-44799520	HRPEpiC	eye:	n/a
13	chr17:44802702-44802752	SK-N-SH_RA	brain:	n/a
14	chr17:44802702-44802752	HMEC	breast:	n/a
15	chr17:44799470-44799520	HL-60	blood:	n/a
16	chr17:44799518-44799568	IMR90	lung:	fetal
17	chr17:44785029-44785079	SK-N-SH	brain:	n/a
18	chr17:44799470-44799520	BE2_C	brain:	n/a
19	chr17:44785029-44785079	HAEpiC	amniotic membrane:	n/a
20	chr17:44802702-44802752	HL-60	blood:	n/a
21	chr17:44802702-44802752	AG04450	lung:	fetal
22	chr17:44785029-44785079	GM12891	blood:	n/a
23	chr17:44702619-44702669	HUVEC	blood vessel:	n/a
24	chr17:44702619-44702669	Jurkat	blood:	n/a
25	chr17:44702619-44702669	AG04449	skin:	fetal
26	chr17:44799518-44799568	GM12891	blood:	n/a
27	chr17:44790735-44790785	HAEpiC	amniotic membrane:	n/a
28	chr17:44799518-44799568	ECC-1	luminal epithelium:	n/a
29	chr17:44799588-44799638	PANC-1	pancreas:	n/a
30	chr17:44785029-44785079	Hepatocyte	liver:	n/a
31	chr17:44799588-44799638	LNCaP	prostate:	n/a
32	chr17:44799518-44799568	NHBE	bronchial:	n/a
33	chr17:44790735-44790785	AG04449	skin:	fetal
34	chr17:44702619-44702669	HRE	kidney:	n/a
35	chr17:44802702-44802752	BE2_C	brain:	n/a
36	chr17:44702619-44702669	PFSK-1	brain:	n/a
37	chr17:44799470-44799520	GM19239	blood:	n/a
38	chr17:44799518-44799568	SAEC	small airway:	n/a
39	chr17:44799518-44799568	HCM	heart:	n/a
40	chr17:44702619-44702669	H1-hESC	embryonic stem cell:	embryo
41	chr17:44799470-44799520	SK-N-SH_RA	brain:	n/a
42	chr17:44702619-44702669	CMK	blood:	n/a
43	chr17:44799470-44799520	AG04449	skin:	fetal
44	chr17:44799518-44799568	K562	blood:	n/a
45	chr17:44799470-44799520	NHBE	bronchial:	n/a
46	chr17:44785029-44785079	HRCEpiC	kidney:	n/a
47	chr17:44802702-44802752	HCT-116	colon:	n/a
48	chr17:44785029-44785079	LNCaP	prostate:	n/a
49	chr17:44802702-44802752	MCF-7	breast:	n/a
50	chr17:44785029-44785079	IMR90	lung:	fetal

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:44801336..44803073-chr17:44904905..44907821,2	K562	blood:
2	chr17:44789439..44791140-chr17:44792595..44794517,2	MCF-7	breast:
3	chr17:44791299..44793121-chr17:44854894..44857732,2	MCF-7	breast:
4	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
5	chr17:44801354..44803469-chr17:44805636..44807734,2	K562	blood:
6	chr17:44793480..44795717-chr17:44798517..44800537,2	MCF-7	breast:
7	chr17:44797929..44800251-chr17:44801008..44803313,2	K562	blood:
8	chr17:44787498..44790449-chr17:44797075..44799216,2	MCF-7	breast:
9	chr17:44799962..44803131-chr17:44820339..44824064,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC37A2-1	chr17:44684607-44685035	ucscGeneNc_uc002iot_1
2	lnc-LRRC37A2-1	chr17:44685215-44685279	ucscGeneNc_uc002iot_1
3	lnc-LRRC37A2-1	chr17:44687052-44688810	ucscGeneNc_uc002iot_1
4	lnc-LRRC37A2-1	chr17:44680600-44680663	ucscGeneNc_uc002iot_1
5	lnc-WNT3-3	chr17:44793046-44793367	expReg_chr17_8945_-
6	lnc-WNT3-2	chr17:44793730-44793944	expReg_chr17_8951_-

No data

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

Extended variants
information (count: 794 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150240286	chr17:44678188-44678189	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs371045439	chr17:44679423-44679424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs147276352	chr17:44685009-44685010	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs62074063	chr17:44685241-44685242	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs541165288	chr17:44687059-44687060	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs554625542	chr17:44687136-44687137	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs574717748	chr17:44687145-44687146	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs543671882	chr17:44687176-44687177	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs563867471	chr17:44687177-44687178	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs149189608	chr17:44687193-44687194	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs532699777	chr17:44687253-44687254	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs546475746	chr17:44687263-44687264	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs564913762	chr17:44687284-44687285	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs112854183	chr17:44687304-44687305	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs527262267	chr17:44687319-44687320	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs375865743	chr17:44687373-44687374	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs146917667	chr17:44687381-44687382	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs371481638	chr17:44687392-44687393	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs150047702	chr17:44687393-44687394	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs528412035	chr17:44687395-44687396	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs200774023	chr17:44687396-44687397	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs200975719	chr17:44687397-44687398	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs545055767	chr17:44687407-44687408	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs367984138	chr17:44687408-44687409	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs7209664	chr17:44687411-44687412	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs200172346	chr17:44687415-44687416	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs370864982	chr17:44687434-44687435	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs373494174	chr17:44687437-44687438	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs549718729	chr17:44687447-44687448	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs192847700	chr17:44687454-44687455	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs62074064	chr17:44687461-44687462	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs369452486	chr17:44687465-44687466	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs372221529	chr17:44687466-44687467	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs62074066	chr17:44687477-44687478	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs9889297	chr17:44687696-44687697	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs538603006	chr17:44687766-44687767	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs552041296	chr17:44688256-44688257	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs145040742	chr17:44688285-44688286	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs565768410	chr17:44688322-44688323	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs139302329	chr17:44688687-44688688	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs140818683	chr17:44688707-44688708	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs202052261	chr17:44702987-44702988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573585370	chr17:44703042-44703043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542493483	chr17:44703047-44703048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558548035	chr17:44703382-44703383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184810529	chr17:44703411-44703412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139961331	chr17:44703461-44703462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563373970	chr17:44703530-44703531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200750878	chr17:44703794-44703795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545484531	chr17:44704233-44704234	Weak transcription	n/a	n/a	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
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	16397240	CNVD
Prostate cancer	17217626	CNVD
Autism	22817714	CNVD

Chromatin state (count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44702800-44704600	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr17:44704200-44707200	Weak transcription	Dnd41	blood
3	chr17:44704600-44705200	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr17:44705200-44712600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr17:44707200-44707600	Enhancers	Primary T cells fromperipheralblood	blood
6	chr17:44707200-44707600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:44707200-44707600	Enhancers	Dnd41	blood
8	chr17:44712600-44713400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr17:44743200-44743600	Enhancers	Pancreas	Pancrea
10	chr17:44768800-44784600	Weak transcription	Fetal Stomach	stomach
11	chr17:44769200-44787200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr17:44770000-44785000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr17:44770200-44782000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr17:44770200-44784400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr17:44770200-44787800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr17:44770400-44784400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr17:44770400-44784600	Weak transcription	Primary B cells from peripheral blood	blood
18	chr17:44770400-44785000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr17:44770600-44782000	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr17:44771600-44784600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr17:44771600-44784800	Weak transcription	Primary T cells from cord blood	blood
22	chr17:44771600-44785000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr17:44773600-44784400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr17:44777800-44784800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr17:44779200-44794400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr17:44780400-44782000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr17:44780400-44784400	Weak transcription	Osteobl	bone
28	chr17:44780400-44789000	Weak transcription	Fetal Muscle Leg	muscle
29	chr17:44780600-44784400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr17:44780600-44784400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr17:44780600-44784400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr17:44780600-44803600	Weak transcription	K562	blood
33	chr17:44780600-44809800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr17:44780800-44784400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr17:44780800-44784400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr17:44780800-44784600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr17:44780800-44787200	Weak transcription	Primary hematopoietic stem cells	blood
38	chr17:44780800-44787200	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr17:44780800-44787600	Weak transcription	Primary B cells from cord blood	blood
40	chr17:44780800-44790200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr17:44780800-44790800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr17:44780800-44794400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr17:44780800-44794600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr17:44780800-44797400	Weak transcription	NH-A	brain
45	chr17:44780800-44798000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr17:44780800-44835200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr17:44781000-44797400	Weak transcription	NHEK	skin
48	chr17:44781400-44784400	Weak transcription	Fetal Thymus	thymus
49	chr17:44781600-44787800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr17:44781800-44784600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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