Variant report

Variant	esv1808701
Chromosome Location	chr17:45610793-45675401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:268)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:268 , 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	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
2	CEBPB	chr17:45665577-45665788	HepG2	liver:	n/a	n/a
3	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
4	CEBPB	chr17:45632282-45632410	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
6	CEBPB	chr17:45616208-45616423	IMR90	lung:	n/a	chr17:45616275-45616286
7	CEBPB	chr17:45616172-45616360	K562	blood:	n/a	chr17:45616275-45616286
8	CEBPB	chr17:45644646-45644894	Hela-S3	cervix:	n/a	chr17:45644788-45644801
9	CEBPB	chr17:45665734-45665783	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr17:45665566-45665892	A549	lung:	n/a	n/a
11	CEBPB	chr17:45616218-45616423	HepG2	liver:	n/a	chr17:45616275-45616286
12	CEBPB	chr17:45616203-45616429	Hela-S3	cervix:	n/a	chr17:45616275-45616286
13	CEBPB	chr17:45665580-45665831	IMR90	lung:	n/a	n/a
14	CEBPB	chr17:45665734-45665763	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr17:45616205-45616431	K562	blood:	n/a	chr17:45616275-45616286
16	CEBPB	chr17:45665732-45665756	K562	blood:	n/a	n/a
17	CTCF	chr17:45639939-45639941	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr17:45655360-45655510	K562	blood:	n/a	n/a
19	CTCF	chr17:45639580-45639730	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr17:45639752-45639953	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr17:45669308-45669361	MCF-7	breast:	n/a	n/a
22	CTCF	chr17:45639760-45639940	K562	blood:	n/a	n/a
23	CTCF	chr17:45639620-45639770	HepG2	liver:	n/a	n/a
24	CTCF	chr17:45639620-45639770	HEK293	kidney:	n/a	n/a
25	CTCF	chr17:45639794-45639931	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr17:45633424-45633495	GM10248	blood:	n/a	n/a
27	CTCF	chr17:45639608-45639654	GM19240	blood:	n/a	n/a
28	CTCF	chr17:45639735-45639948	MCF-7	breast:	n/a	n/a
29	CTCF	chr17:45639786-45639888	HepG2	liver:	n/a	n/a
30	CTCF	chr17:45639787-45639938	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr17:45655314-45655358	ProgFib	skin:	n/a	n/a
32	CTCF	chr17:45639653-45639953	A549	lung:	n/a	n/a
33	CTCF	chr17:45639620-45639770	GM12869	blood:	n/a	n/a
34	CTCF	chr17:45639768-45639951	GM12878	blood:	n/a	n/a
35	CTCF	chr17:45639600-45639750	HAc	cerebellar:	n/a	n/a
36	CTCF	chr17:45639819-45639881	GM10248	blood:	n/a	n/a
37	CTCF	chr17:45639691-45639984	K562	blood:	n/a	n/a
38	CTCF	chr17:45639791-45639953	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr17:45639761-45639910	MCF-7	breast:	n/a	n/a
40	CTCF	chr17:45639761-45639816	ProgFib	skin:	n/a	n/a
41	CTCF	chr17:45639466-45640016	A549	lung:	n/a	n/a
42	CTCF	chr17:45639640-45639790	HFF	foreskin:	n/a	n/a
43	CTCF	chr17:45639821-45639905	GM13977	blood:	n/a	n/a
44	CTCF	chr17:45639800-45639917	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr17:45639756-45639890	Gliobla	brain:	n/a	n/a
46	CTCF	chr17:45639350-45639422	MCF-7	breast:	n/a	n/a
47	CTCF	chr17:45639841-45639902	LNCaP	prostate:	n/a	n/a
48	FOS	chr17:45644661-45644829	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr17:45644661-45644875	MCF10A-Er-Src	breast:	n/a	chr17:45644839-45644846
50	FOS	chr17:45644631-45644985	MCF10A-Er-Src	breast:	n/a	chr17:45644839-45644846

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45612338-45612388	SAEC	small airway:	n/a
2	chr17:45612338-45612388	MCF-7	breast:	n/a
3	chr17:45612338-45612388	HEEpiC	esophagus:	n/a
4	chr17:45612338-45612388	SK-N-SH_RA	brain:	n/a
5	chr17:45612338-45612388	H1-hESC	embryonic stem cell:	embryo
6	chr17:45612338-45612388	T-47D	breast:	n/a
7	chr17:45612338-45612388	NHBE	bronchial:	n/a
8	chr17:45612338-45612388	K562	blood:	n/a
9	chr17:45612338-45612388	NHDF-neo	bronchial:	n/a
10	chr17:45612338-45612388	BJ	skin:	n/a
11	chr17:45612338-45612388	BE2_C	brain:	n/a
12	chr17:45612338-45612388	HMEC	breast:	n/a
13	chr17:45612338-45612388	HepG2	liver:	n/a
14	chr17:45612338-45612388	ProgFib	skin:	n/a
15	chr17:45612338-45612388	A549	lung:	n/a
16	chr17:45612338-45612388	SKMC	muscle:	n/a
17	chr17:45612338-45612388	HRPEpiC	eye:	n/a
18	chr17:45612338-45612388	IMR90	lung:	fetal
19	chr17:45612338-45612388	HUVEC	blood vessel:	n/a
20	chr17:45612338-45612388	HL-60	blood:	n/a
21	chr17:45612338-45612388	GM12892	blood:	n/a
22	chr17:45612338-45612388	SK-N-MC	brain:	n/a
23	chr17:45612338-45612388	HCPEpiC	choroid plexus:	n/a
24	chr17:45612338-45612388	GM06990	blood:	n/a
25	chr17:45612338-45612388	AG10803	skin:	n/a
26	chr17:45612338-45612388	NH-A	brain:	n/a
27	chr17:45612338-45612388	HRCEpiC	kidney:	n/a
28	chr17:45612338-45612388	AG04449	skin:	fetal
29	chr17:45612338-45612388	U87	brain:	n/a
30	chr17:45612338-45612388	RPTEC	kidney:	n/a
31	chr17:45612338-45612388	AG04450	lung:	fetal
32	chr17:45612338-45612388	Jurkat	blood:	n/a
33	chr17:45612338-45612388	Hepatocyte	liver:	n/a
34	chr17:45612338-45612388	MCF10A-Er-Src	breast:	n/a
35	chr17:45612338-45612388	HCM	heart:	n/a
36	chr17:45612338-45612388	HCT-116	colon:	n/a
37	chr17:45612338-45612388	ECC-1	luminal epithelium:	n/a
38	chr17:45612338-45612388	AG09319	gingival:	n/a
39	chr17:45612338-45612388	CMK	blood:	n/a
40	chr17:45612338-45612388	PANC-1	pancreas:	n/a
41	chr17:45612338-45612388	PrEC	prostate:	n/a
42	chr17:45612338-45612388	HNPCEpiC	eye:	n/a
43	chr17:45612338-45612388	HCF	heart:	n/a
44	chr17:45612338-45612388	LNCaP	prostate:	n/a
45	chr17:45612338-45612388	HIPEpiC	eye:	n/a
46	chr17:45612338-45612388	HEK293	kidney:	embryo
47	chr17:45612338-45612388	Hela-S3	cervix:	n/a
48	chr17:45612338-45612388	NT2-D1	testis:	n/a
49	chr17:45612338-45612388	Caco-2	colon:	n/a
50	chr17:45612338-45612388	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
2	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000206734	TF binding region
NPEPPS	CpG island
ENSG00000206734	CpG island
ENSG00000141279	chromatin interactions

Extended variants
information (count: 2383 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:2383 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549998893	chr17:45610847-45610848	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569895608	chr17:45610882-45610883	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531354615	chr17:45610886-45610887	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185071953	chr17:45611016-45611017	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs571232004	chr17:45611018-45611019	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs367573708	chr17:45611037-45611038	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs533509268	chr17:45611065-45611066	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs539103430	chr17:45611071-45611072	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189135182	chr17:45611074-45611075	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567415302	chr17:45611106-45611107	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs180704494	chr17:45611173-45611174	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs2611975	chr17:45611178-45611179	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs189361759	chr17:45611257-45611258	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs181975258	chr17:45611359-45611360	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs186695531	chr17:45611405-45611406	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192005174	chr17:45611418-45611419	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572424310	chr17:45611485-45611486	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371757670	chr17:45611496-45611497	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541030003	chr17:45611516-45611517	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561322485	chr17:45611518-45611519	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574823341	chr17:45611520-45611521	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543706482	chr17:45611559-45611560	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181277554	chr17:45611580-45611581	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551460205	chr17:45611606-45611607	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564801328	chr17:45611642-45611643	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527298135	chr17:45611667-45611668	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566232522	chr17:45611679-45611680	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547104634	chr17:45611695-45611696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs8079821	chr17:45611704-45611705	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs145796837	chr17:45611708-45611709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555226031	chr17:45611718-45611719	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569866632	chr17:45611786-45611787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538423950	chr17:45611809-45611810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559024585	chr17:45611815-45611816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142859928	chr17:45611820-45611821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535098109	chr17:45611847-45611848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573582059	chr17:45611857-45611858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554714587	chr17:45611867-45611868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151075713	chr17:45611897-45611898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369234168	chr17:45611947-45611948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537866416	chr17:45612009-45612010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200465069	chr17:45612018-45612019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186328049	chr17:45612026-45612027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577046041	chr17:45612027-45612028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190107702	chr17:45612062-45612063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559883615	chr17:45612083-45612084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527440780	chr17:45612198-45612199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547458803	chr17:45612225-45612226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560875316	chr17:45612293-45612294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536093120	chr17:45612311-45612312	Weak transcription Strong transcription	n/a	n/a	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	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Epithelial cancer	20478067	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45607600-45610800	Active TSS	A549	lung
2	chr17:45608000-45610800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr17:45608000-45610800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr17:45608000-45610800	Active TSS	Fetal Brain Female	brain
5	chr17:45608000-45610800	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr17:45608000-45610800	Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr17:45608000-45610800	Active TSS	NH-A	brain
8	chr17:45608000-45610800	Active TSS	NHEK	skin
9	chr17:45608000-45611000	Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr17:45608000-45611000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr17:45608000-45611000	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr17:45608000-45611000	Active TSS	HUVEC	blood vessel
13	chr17:45608000-45611000	Active TSS	NHLF	lung
14	chr17:45608000-45611200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr17:45608000-45611200	Active TSS	Muscle Satellite Cultured Cells	--
16	chr17:45608000-45611200	Active TSS	HMEC	breast
17	chr17:45608000-45611200	Active TSS	HSMMtube	muscle
18	chr17:45608000-45611400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr17:45609200-45611000	Active TSS	Brain Angular Gyrus	brain
20	chr17:45609200-45611400	Active TSS	GM12878-XiMat	blood
21	chr17:45609600-45613400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr17:45609800-45611000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr17:45609800-45611200	Enhancers	Primary B cells from cord blood	blood
24	chr17:45609800-45611400	Enhancers	Liver	Liver
25	chr17:45609800-45624800	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr17:45610000-45610800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr17:45610000-45611000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr17:45610000-45611000	Enhancers	Fetal Lung	lung
29	chr17:45610000-45617400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr17:45610000-45623400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr17:45610000-45624000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr17:45610000-45624400	Weak transcription	Placenta	Placenta
33	chr17:45610000-45624800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr17:45610000-45630000	Weak transcription	Gastric	stomach
35	chr17:45610000-45638600	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr17:45610000-45639000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr17:45610000-45670600	Weak transcription	Lung	lung
38	chr17:45610000-45670600	Weak transcription	Pancreas	Pancrea
39	chr17:45610000-45676800	Weak transcription	Ovary	ovary
40	chr17:45610200-45611000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr17:45610200-45611000	Enhancers	Fetal Heart	heart
42	chr17:45610200-45674200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr17:45610400-45611000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr17:45610400-45611000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr17:45610400-45611000	Enhancers	Rectal Smooth Muscle	rectum
46	chr17:45610400-45611000	Enhancers	Hela-S3	cervix
47	chr17:45610400-45611400	Weak transcription	Fetal Intestine Small	intestine
48	chr17:45610400-45611400	Weak transcription	Fetal Muscle Leg	muscle
49	chr17:45610400-45611600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr17:45610400-45617800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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