Variant report

Variant	nsv1056191
Chromosome Location	chr17:45442007-45519072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:366)
Chromatin interactive
region (count:23)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45505316-45506040	HepG2	liver:	n/a	n/a
2	BCL11A	chr17:45504891-45505246	GM12878	blood:	n/a	n/a
3	CBX3	chr17:45450369-45450751	K562	blood:	n/a	n/a
4	CBX3	chr17:45450397-45450796	HCT-116	colon:	n/a	n/a
5	CBX3	chr17:45450400-45450697	K562	blood:	n/a	n/a
6	CEBPB	chr17:45482269-45482596	HepG2	liver:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
7	CEBPB	chr17:45491776-45491931	K562	blood:	n/a	n/a
8	CEBPB	chr17:45482271-45482609	K562	blood:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
9	CEBPB	chr17:45453922-45454159	HepG2	liver:	n/a	chr17:45454038-45454049
10	CEBPB	chr17:45505310-45505563	HepG2	liver:	n/a	n/a
11	CEBPB	chr17:45482316-45482557	A549	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
12	CEBPB	chr17:45493468-45493688	K562	blood:	n/a	chr17:45493564-45493575
13	CEBPB	chr17:45453915-45454146	K562	blood:	n/a	chr17:45454038-45454049
14	CEBPB	chr17:45482340-45482579	IMR90	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
15	CEBPB	chr17:45493445-45493683	A549	lung:	n/a	chr17:45493564-45493575
16	CEBPB	chr17:45493466-45493668	HepG2	liver:	n/a	chr17:45493564-45493575
17	CTCF	chr17:45454572-45454639	MCF-7	breast:	n/a	n/a
18	CTCF	chr17:45501075-45501150	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr17:45501124-45501145	GM12891	blood:	n/a	n/a
20	CTCF	chr17:45491577-45491639	Fibrobl	skin:	n/a	n/a
21	CTCF	chr17:45482723-45482749	GM10248	blood:	n/a	n/a
22	CTCF	chr17:45501099-45501153	A549	lung:	n/a	n/a
23	CTCF	chr17:45480700-45480850	HCT-116	colon:	n/a	n/a
24	CTCF	chr17:45480700-45480850	AG09309	skin:	n/a	n/a
25	CTCF	chr17:45500854-45500948	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:45500980-45501130	GM12865	blood:	n/a	n/a
27	CTCF	chr17:45501628-45501635	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr17:45454666-45454686	GM10248	blood:	n/a	n/a
29	CTCF	chr17:45480760-45480910	HCT-116	colon:	n/a	n/a
30	CTCF	chr17:45503813-45503939	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr17:45501060-45501210	GM12872	blood:	n/a	n/a
32	CTCF	chr17:45480800-45480950	AG09319	gingival:	n/a	n/a
33	CTCF	chr17:45480800-45480950	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr17:45480760-45480910	A549	lung:	n/a	n/a
35	CTCF	chr17:45501140-45501290	HEK293	kidney:	n/a	n/a
36	CTCF	chr17:45480680-45480830	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr17:45501040-45501190	GM12874	blood:	n/a	n/a
38	CTCF	chr17:45501240-45501390	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr17:45501180-45501330	SAEC	small airway:	n/a	n/a
40	CTCF	chr17:45495359-45495387	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr17:45480860-45481010	HCT-116	colon:	n/a	n/a
42	CTCF	chr17:45501040-45501190	GM12868	blood:	n/a	n/a
43	CTCF	chr17:45501637-45501674	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr17:45507446-45507452	A549	lung:	n/a	n/a
45	CTCF	chr17:45500839-45500928	MCF-7	breast:	n/a	n/a
46	CTCF	chr17:45501084-45501184	MCF-7	breast:	n/a	n/a
47	CTCF	chr17:45513628-45513693	Lung_OC	lung:	n/a	n/a
48	CTCF	chr17:45501146-45501167	GM12891	blood:	n/a	n/a
49	CTCF	chr17:45501060-45501210	GM12871	blood:	n/a	n/a
50	CTCF	chr17:45501099-45501101	GM12891	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45501697-45501747	RPTEC	kidney:	n/a
2	chr17:45501628-45501678	NH-A	brain:	n/a
3	chr17:45501030-45501080	NHBE	bronchial:	n/a
4	chr17:45502151-45502201	ovcar-3	ovarian:	n/a
5	chr17:45502151-45502201	PrEC	prostate:	n/a
6	chr17:45505249-45505299	SKMC	muscle:	n/a
7	chr17:45501242-45501292	GM12892	blood:	n/a
8	chr17:45505249-45505299	GM06990	blood:	n/a
9	chr17:45501697-45501747	NB4	blood:	n/a
10	chr17:45501030-45501080	HUVEC	blood vessel:	n/a
11	chr17:45501628-45501678	SK-N-SH	brain:	n/a
12	chr17:45501697-45501747	IMR90	lung:	fetal
13	chr17:45501628-45501678	HCPEpiC	choroid plexus:	n/a
14	chr17:45501697-45501747	AG09319	gingival:	n/a
15	chr17:45501628-45501678	AG04449	skin:	fetal
16	chr17:45501242-45501292	HL-60	blood:	n/a
17	chr17:45501697-45501747	MCF-7	breast:	n/a
18	chr17:45501697-45501747	SKMC	muscle:	n/a
19	chr17:45505249-45505299	MCF-7	breast:	n/a
20	chr17:45505249-45505299	AG04450	lung:	fetal
21	chr17:45502151-45502201	RPTEC	kidney:	n/a
22	chr17:45505249-45505299	HEEpiC	esophagus:	n/a
23	chr17:45501697-45501747	HEK293	kidney:	embryo
24	chr17:45501030-45501080	AoSMC	blood vessel:	n/a
25	chr17:45501697-45501747	Hepatocyte	liver:	n/a
26	chr17:45502151-45502201	CMK	blood:	n/a
27	chr17:45501242-45501292	GM06990	blood:	n/a
28	chr17:45501030-45501080	Caco-2	colon:	n/a
29	chr17:45505249-45505299	HepG2	liver:	n/a
30	chr17:45502151-45502201	GM12891	blood:	n/a
31	chr17:45501242-45501292	AG04450	lung:	fetal
32	chr17:45501030-45501080	HCF	heart:	n/a
33	chr17:45501030-45501080	MCF-7	breast:	n/a
34	chr17:45501242-45501292	GM19239	blood:	n/a
35	chr17:45501697-45501747	Hela-S3	cervix:	n/a
36	chr17:45505249-45505299	RPTEC	kidney:	n/a
37	chr17:45501030-45501080	HCM	heart:	n/a
38	chr17:45505249-45505299	SK-N-MC	brain:	n/a
39	chr17:45505249-45505299	HUVEC	blood vessel:	n/a
40	chr17:45501697-45501747	HIPEpiC	eye:	n/a
41	chr17:45501628-45501678	NHDF-neo	bronchial:	n/a
42	chr17:45505249-45505299	BJ	skin:	n/a
43	chr17:45501697-45501747	HAEpiC	amniotic membrane:	n/a
44	chr17:45505249-45505299	PrEC	prostate:	n/a
45	chr17:45501697-45501747	SK-N-SH	brain:	n/a
46	chr17:45501030-45501080	PFSK-1	brain:	n/a
47	chr17:45501030-45501080	U87	brain:	n/a
48	chr17:45501242-45501292	HMEC	breast:	n/a
49	chr17:45501628-45501678	CMK	blood:	n/a
50	chr17:45505249-45505299	SK-N-SH	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45443966..45446911-chr17:45490507..45492639,3	K562	blood:
2	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
3	chr17:45422002..45424871-chr17:45443232..45445313,2	MCF-7	breast:
4	chr17:45443966..45446911-chr17:45490626..45492639,2	K562	blood:
5	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:
6	chr17:45433817..45436270-chr17:45439623..45442042,2	K562	blood:
7	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
8	chr17:45443966..45446911-chr17:45490626..45492639,2	K562	blood:
9	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
10	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
11	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
12	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:
13	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:
14	chr17:45499733..45501782-chr17:45502052..45504438,2	K562	blood:
15	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
16	chr17:45445857..45448249-chr17:45449955..45451934,2	MCF-7	breast:
17	chr17:45450399..45452853-chr17:45453985..45455878,3	K562	blood:
18	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
19	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:
20	chr17:45443966..45446911-chr17:45490507..45492639,3	K562	blood:
21	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
22	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:
23	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC040934.1-1	chr17:45500728-45500892	ENSG00000253347.1
2	lnc-ITGB3-1	chr17:45447803-45447874	NONHSAT054302
3	lnc-ITGB3-1	chr17:45451838-45452004	NONHSAT054302
4	lnc-AC040934.1-1	chr17:45486688-45487035	ENSG00000253347.1
5	lnc-ITGB3-1	chr17:45446982-45447290	NONHSAT054302

No data

Variant related genes	Relation type
EFCAB13	TF binding region
ENSG00000253347	TF binding region
EFCAB13	CpG island
ENSG00000253347	CpG island
ENSG00000253347	chromatin interactions
ENSG00000178852	chromatin interactions

Extended variants
information (count: 2583 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:2583 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541843862	chr17:45442018-45442019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs8079142	chr17:45442049-45442050	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs183480264	chr17:45442101-45442102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529608928	chr17:45442105-45442106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564277350	chr17:45442113-45442114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34562475	chr17:45442149-45442150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533264372	chr17:45442169-45442170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546645917	chr17:45442256-45442257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566527402	chr17:45442257-45442258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547889724	chr17:45442276-45442277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8075843	chr17:45442363-45442364	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs138640300	chr17:45442453-45442454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530663005	chr17:45442463-45442464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544862955	chr17:45442464-45442465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186657749	chr17:45442523-45442524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558085554	chr17:45442590-45442591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573910221	chr17:45442598-45442599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192371953	chr17:45442603-45442604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113245622	chr17:45442604-45442605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553150857	chr17:45442630-45442631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35767539	chr17:45442653-45442654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562611128	chr17:45442717-45442718	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs55879010	chr17:45442722-45442723	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185760021	chr17:45442803-45442804	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189934748	chr17:45442807-45442808	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575470604	chr17:45442808-45442809	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs182099505	chr17:45442824-45442825	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs76909769	chr17:45442840-45442841	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs532912994	chr17:45442882-45442883	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs546384062	chr17:45442890-45442891	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs144614507	chr17:45442906-45442907	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs184754497	chr17:45442949-45442950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549132823	chr17:45442965-45442966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148448334	chr17:45443040-45443041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146456327	chr17:45443198-45443199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199885786	chr17:45443199-45443200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538166655	chr17:45443230-45443231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78099539	chr17:45443344-45443345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552006010	chr17:45443398-45443399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1912483	chr17:45443494-45443495	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs144106050	chr17:45443503-45443504	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs371663725	chr17:45443561-45443562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1912484	chr17:45443664-45443665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs546704982	chr17:45443681-45443682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369323932	chr17:45443684-45443685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200810377	chr17:45443694-45443695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373613414	chr17:45443738-45443739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535804911	chr17:45443797-45443798	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs73324432	chr17:45443828-45443829	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs555082553	chr17:45443841-45443842	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Urothelial carcinoma	21177765	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
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45402000-45442600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr17:45402200-45446400	Weak transcription	Colon Smooth Muscle	Colon
3	chr17:45402200-45500800	Weak transcription	Aorta	Aorta
4	chr17:45411600-45468200	Weak transcription	Left Ventricle	heart
5	chr17:45412400-45463400	Weak transcription	Gastric	stomach
6	chr17:45413400-45463800	Weak transcription	Ovary	ovary
7	chr17:45421800-45449800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr17:45423000-45450000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr17:45423000-45465400	Weak transcription	Adipose Nuclei	Adipose
10	chr17:45423200-45450000	Weak transcription	Primary B cells from cord blood	blood
11	chr17:45435000-45463200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr17:45435200-45447600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr17:45435400-45449600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr17:45440200-45442600	Strong transcription	Primary B cells from peripheral blood	blood
15	chr17:45440600-45457200	Weak transcription	Fetal Intestine Small	intestine
16	chr17:45440800-45449400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr17:45440800-45449800	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr17:45442600-45449400	Weak transcription	Primary B cells from peripheral blood	blood
19	chr17:45442800-45449800	Weak transcription	Primary hematopoietic stem cells	blood
20	chr17:45444600-45445400	Enhancers	Esophagus	oesophagus
21	chr17:45445600-45446000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr17:45445600-45447800	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr17:45449400-45451000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
24	chr17:45449400-45451600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr17:45449600-45451000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr17:45449800-45450800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
27	chr17:45449800-45451000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
28	chr17:45450000-45450400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
29	chr17:45450000-45451000	ZNF genes & repeats	Primary B cells from cord blood	blood
30	chr17:45450400-45461000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr17:45450800-45470400	Weak transcription	Liver	Liver
32	chr17:45451000-45455400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr17:45451000-45460000	Weak transcription	Primary hematopoietic stem cells	blood
34	chr17:45451000-45463000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr17:45451000-45463400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr17:45451000-45464600	Weak transcription	Primary B cells from cord blood	blood
37	chr17:45451600-45453200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr17:45453200-45454000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr17:45454000-45454400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr17:45454400-45458800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr17:45455400-45456200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr17:45456200-45459200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr17:45458800-45459200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr17:45459200-45460200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr17:45460000-45460400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
46	chr17:45460200-45460400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr17:45460400-45462800	Weak transcription	Primary hematopoietic stem cells	blood
48	chr17:45460600-45467400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr17:45460800-45463200	Weak transcription	Lung	lung
50	chr17:45460800-45466600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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