Variant report

Variant	nsv962334
Chromosome Location	chr17:45600707-45632564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
2	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
3	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
4	BHLHE40	chr17:45605793-45605974	HepG2	liver:	n/a	n/a
5	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
6	CCNT2	chr17:45608329-45608370	K562	blood:	n/a	n/a
7	CEBPB	chr17:45616205-45616431	K562	blood:	n/a	chr17:45616275-45616286
8	CEBPB	chr17:45632282-45632410	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr17:45616208-45616423	IMR90	lung:	n/a	chr17:45616275-45616286
10	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
11	CEBPB	chr17:45616172-45616360	K562	blood:	n/a	chr17:45616275-45616286
12	CEBPB	chr17:45616218-45616423	HepG2	liver:	n/a	chr17:45616275-45616286
13	CEBPB	chr17:45609557-45609591	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
15	CEBPB	chr17:45616203-45616429	Hela-S3	cervix:	n/a	chr17:45616275-45616286
16	CEBPD	chr17:45608348-45608658	HepG2	liver:	n/a	n/a
17	CHD2	chr17:45608212-45608501	HepG2	liver:	n/a	n/a
18	CHD2	chr17:45608171-45608525	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr17:45608212-45608653	A549	lung:	n/a	n/a
20	CTCF	chr17:45608674-45608723	MCF-7	breast:	n/a	n/a
21	CTCF	chr17:45608677-45608717	Fibrobl	skin:	n/a	n/a
22	CTCF	chr17:45609146-45609247	GM19240	blood:	n/a	n/a
23	CTCF	chr17:45608622-45608710	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr17:45609163-45609272	GM10248	blood:	n/a	n/a
25	CTCF	chr17:45608670-45608672	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:45608264-45608280	GM13977	blood:	n/a	n/a
27	E2F4	chr17:45608301-45608415	MCF10A-Er-Src	breast:	n/a	chr17:45608389-45608398
28	E2F4	chr17:45609441-45609604	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F6	chr17:45608192-45608625	K562	blood:	n/a	chr17:45608459-45608469 chr17:45608389-45608398 chr17:45608610-45608619 chr17:45608607-45608619
30	E2F6	chr17:45608254-45608467	K562	blood:	n/a	chr17:45608389-45608398
31	EBF1	chr17:45608125-45608837	GM12878	blood:	n/a	n/a
32	EBF1	chr17:45609270-45609512	GM12878	blood:	n/a	n/a
33	EGR1	chr17:45608263-45608647	K562	blood:	n/a	chr17:45608609-45608619 chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608279-45608292 chr17:45608605-45608618 chr17:45608521-45608535
34	EGR1	chr17:45608386-45608617	GM12878	blood:	n/a	chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608503-45608517 chr17:45608521-45608535
35	EGR1	chr17:45608321-45608635	K562	blood:	n/a	chr17:45608609-45608619 chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608605-45608618 chr17:45608521-45608535
36	EGR1	chr17:45609243-45609701	K562	blood:	n/a	chr17:45609549-45609562 chr17:45609550-45609560 chr17:45609549-45609562 chr17:45609388-45609403 chr17:45609548-45609563
37	EGR1	chr17:45608435-45608626	GM12878	blood:	n/a	chr17:45608609-45608619 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608605-45608618 chr17:45608521-45608535
38	EGR1	chr17:45608104-45608955	GM12878	blood:	n/a	chr17:45608609-45608619 chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608203-45608227 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608279-45608292 chr17:45608605-45608618 chr17:45608521-45608535
39	ELF1	chr17:45608201-45608669	GM12878	blood:	n/a	chr17:45608392-45608404
40	ELF1	chr17:45608235-45608651	K562	blood:	n/a	chr17:45608392-45608404
41	ELF1	chr17:45608330-45608613	K562	blood:	n/a	chr17:45608392-45608404
42	EP300	chr17:45609481-45609594	GM12878	blood:	n/a	n/a
43	EP300	chr17:45609301-45609491	GM12878	blood:	n/a	chr17:45609343-45609357
44	FOS	chr17:45603588-45603851	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr17:45609954-45610163	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr17:45603587-45603787	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr17:45603587-45603859	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr17:45609954-45610153	MCF10A-Er-Src	breast:	n/a	n/a
49	FOSL2	chr17:45603580-45603872	HepG2	liver:	n/a	n/a
50	FOSL2	chr17:45607924-45608918	HepG2	liver:	n/a	chr17:45608611-45608620 chr17:45608547-45608556

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45612338-45612388	PrEC	prostate:	n/a
2	chr17:45608114-45608164	SK-N-MC	brain:	n/a
3	chr17:45612338-45612388	PrEC	prostate:	n/a
4	chr17:45608114-45608164	SK-N-MC	brain:	n/a
5	chr17:45609121-45609171	CMK	blood:	n/a
6	chr17:45609121-45609171	AG04450	lung:	fetal
7	chr17:45608114-45608164	SK-N-SH	brain:	n/a
8	chr17:45608114-45608164	GM12878	blood:	n/a
9	chr17:45612338-45612388	HCPEpiC	choroid plexus:	n/a
10	chr17:45612338-45612388	RPTEC	kidney:	n/a
11	chr17:45608315-45608365	GM19239	blood:	n/a
12	chr17:45612338-45612388	MCF-7	breast:	n/a
13	chr17:45608823-45608873	AG04449	skin:	fetal
14	chr17:45604514-45604564	AoSMC	blood vessel:	n/a
15	chr17:45608315-45608365	AG04450	lung:	fetal
16	chr17:45608114-45608164	AG04450	lung:	fetal
17	chr17:45604514-45604564	Caco-2	colon:	n/a
18	chr17:45612338-45612388	ProgFib	skin:	n/a
19	chr17:45609121-45609171	HEEpiC	esophagus:	n/a
20	chr17:45608315-45608365	AG09309	skin:	n/a
21	chr17:45608114-45608164	HUVEC	blood vessel:	n/a
22	chr17:45608823-45608873	K562	blood:	n/a
23	chr17:45609121-45609171	AG04449	skin:	fetal
24	chr17:45608315-45608365	ProgFib	skin:	n/a
25	chr17:45608114-45608164	CMK	blood:	n/a
26	chr17:45608315-45608365	PrEC	prostate:	n/a
27	chr17:45608823-45608873	NH-A	brain:	n/a
28	chr17:45608315-45608365	NHDF-neo	bronchial:	n/a
29	chr17:45604514-45604564	ovcar-3	ovarian:	n/a
30	chr17:45608823-45608873	SK-N-MC	brain:	n/a
31	chr17:45604514-45604564	HPAEpiC	pulmonary alveolar:	n/a
32	chr17:45604514-45604564	GM12891	blood:	n/a
33	chr17:45608114-45608164	NB4	blood:	n/a
34	chr17:45608114-45608164	AoSMC	blood vessel:	n/a
35	chr17:45604514-45604564	ProgFib	skin:	n/a
36	chr17:45608114-45608164	HRE	kidney:	n/a
37	chr17:45608315-45608365	HAEpiC	amniotic membrane:	n/a
38	chr17:45608114-45608164	Hela-S3	cervix:	n/a
39	chr17:45604514-45604564	HNPCEpiC	eye:	n/a
40	chr17:45604514-45604564	GM12878	blood:	n/a
41	chr17:45608114-45608164	Caco-2	colon:	n/a
42	chr17:45608315-45608365	GM12892	blood:	n/a
43	chr17:45608315-45608365	HEK293	kidney:	embryo
44	chr17:45609121-45609171	ovcar-3	ovarian:	n/a
45	chr17:45609121-45609171	HRCEpiC	kidney:	n/a
46	chr17:45608823-45608873	GM06990	blood:	n/a
47	chr17:45608823-45608873	HUVEC	blood vessel:	n/a
48	chr17:45608114-45608164	HCT-116	colon:	n/a
49	chr17:45608114-45608164	HNPCEpiC	eye:	n/a
50	chr17:45609121-45609171	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
2	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
3	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
4	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000206734	TF binding region
NPEPPS	CpG island
ENSG00000206734	CpG island
ENSG00000141279	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000228782	chromatin interactions

Extended variants
information (count: 1038 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556964448	chr17:45603451-45603452	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs147805380	chr17:45603455-45603456	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs546098247	chr17:45603470-45603471	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs187938276	chr17:45603541-45603542	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs573405676	chr17:45603550-45603551	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs113457742	chr17:45603620-45603621	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs562290942	chr17:45603760-45603761	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs529777306	chr17:45603784-45603785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs549896234	chr17:45603878-45603879	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201513188	chr17:45604028-45604029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532106541	chr17:45604096-45604097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552506297	chr17:45604192-45604193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532943320	chr17:45604217-45604218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565810274	chr17:45604219-45604220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2611998	chr17:45604290-45604291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs560037965	chr17:45604348-45604349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527547247	chr17:45604358-45604359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548120413	chr17:45604379-45604380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568225734	chr17:45604380-45604381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549116681	chr17:45604392-45604393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145051507	chr17:45604398-45604399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557025937	chr17:45604445-45604446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373225839	chr17:45604552-45604553	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs113773265	chr17:45604652-45604653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576829157	chr17:45604707-45604708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539419488	chr17:45604773-45604774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553643511	chr17:45604787-45604788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573489865	chr17:45604907-45604908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542486132	chr17:45604987-45604988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560919746	chr17:45605101-45605102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28678440	chr17:45605108-45605109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28444320	chr17:45605109-45605110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531559217	chr17:45605110-45605111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562188009	chr17:45605118-45605119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575781653	chr17:45605126-45605127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561757539	chr17:45605131-45605132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543554315	chr17:45605175-45605176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563329351	chr17:45605202-45605203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532167855	chr17:45605243-45605244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143632811	chr17:45605247-45605248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559286751	chr17:45605302-45605303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188523111	chr17:45605397-45605398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567603260	chr17:45605402-45605403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375579696	chr17:45605434-45605435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528404633	chr17:45605482-45605483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548461486	chr17:45605504-45605505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193076003	chr17:45605534-45605535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538003571	chr17:45605536-45605537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530572104	chr17:45605578-45605579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369672479	chr17:45605591-45605592	Weak 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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Epithelial cancer	20478067	CNVD

Chromatin state (count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45603800-45604200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr17:45604200-45608000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr17:45607600-45607800	Enhancers	Placenta	Placenta
4	chr17:45607600-45607800	Enhancers	Dnd41	blood
5	chr17:45607600-45607800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr17:45607600-45608000	Enhancers	Primary T cells fromperipheralblood	blood
7	chr17:45607600-45609400	Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr17:45607600-45610800	Active TSS	A549	lung
9	chr17:45607800-45608000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr17:45607800-45608000	Enhancers	Primary B cells from peripheral blood	blood
11	chr17:45607800-45608000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:45607800-45608000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr17:45607800-45608000	Enhancers	Fetal Muscle Leg	muscle
14	chr17:45607800-45608200	Enhancers	Primary B cells from cord blood	blood
15	chr17:45607800-45608200	Flanking Active TSS	Placenta	Placenta
16	chr17:45607800-45608200	Flanking Active TSS	Dnd41	blood
17	chr17:45607800-45609400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr17:45607800-45609800	Active TSS	Monocytes-CD14+_RO01746	blood
19	chr17:45607800-45610000	Active TSS	Colonic Mucosa	Colon
20	chr17:45607800-45610200	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr17:45607800-45610400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr17:45608000-45608200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr17:45608000-45608200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
24	chr17:45608000-45608200	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr17:45608000-45608200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
26	chr17:45608000-45608200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr17:45608000-45608200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
28	chr17:45608000-45608200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr17:45608000-45608200	Flanking Active TSS	Fetal Muscle Leg	muscle
30	chr17:45608000-45608200	Enhancers	K562	blood
31	chr17:45608000-45608400	Active TSS	Brain Angular Gyrus	brain
32	chr17:45608000-45609200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr17:45608000-45609200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells	blood
35	chr17:45608000-45609400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
36	chr17:45608000-45609400	Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr17:45608000-45609400	Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr17:45608000-45609400	Active TSS	Liver	Liver
41	chr17:45608000-45609600	Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr17:45608000-45609600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr17:45608000-45609600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr17:45608000-45609600	Active TSS	Fetal Muscle Trunk	muscle
45	chr17:45608000-45609600	Active TSS	Fetal Thymus	thymus
46	chr17:45608000-45609800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr17:45608000-45609800	Active TSS	Primary T cells from cord blood	blood
48	chr17:45608000-45609800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr17:45608000-45609800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr17:45608000-45609800	Active TSS	Colon Smooth Muscle	Colon

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