Variant report

Variant	nsv1031497
Chromosome Location	chr7:150547113-150572570
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	BCL3	chr7:150548656-150548890	GM12878	blood:	n/a	n/a
2	BCL3	chr7:150571848-150572248	GM12878	blood:	n/a	n/a
3	BCL3	chr7:150571844-150572195	GM12878	blood:	n/a	n/a
4	CEBPB	chr7:150568768-150568949	IMR90	lung:	n/a	n/a
5	CEBPB	chr7:150563533-150563818	A549	lung:	n/a	chr7:150563663-150563674 chr7:150563633-150563644
6	CEBPB	chr7:150568779-150568972	K562	blood:	n/a	n/a
7	CEBPB	chr7:150563618-150563803	HepG2	liver:	n/a	chr7:150563663-150563674 chr7:150563633-150563644
8	CEBPB	chr7:150568807-150568991	A549	lung:	n/a	n/a
9	CTCF	chr7:150557876-150558053	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
10	CTCF	chr7:150557790-150558241	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
11	CTCF	chr7:150557860-150558010	HMF	breast:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
12	CTCF	chr7:150557924-150558056	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
13	CTCF	chr7:150555200-150555350	K562	blood:	n/a	n/a
14	CTCF	chr7:150557798-150558063	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
15	CTCF	chr7:150557860-150558010	WERI-Rb-1	eye:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
16	CTCF	chr7:150557900-150558050	Caco-2	colon:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
17	CTCF	chr7:150557948-150557984	K562	blood:	n/a	n/a
18	CTCF	chr7:150557880-150558030	Caco-2	colon:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
19	CTCF	chr7:150557941-150558069	H1-hESC	embryonic stem cell:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
20	CTCF	chr7:150557920-150558070	WERI-Rb-1	eye:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
21	CTCF	chr7:150557914-150558043	SK-N-SH_RA	brain:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
22	CTCF	chr7:150556024-150556177	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr7:150572024-150572106	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:150557938-150558041	Kidney_OC	kidney:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
25	CTCF	chr7:150557840-150557990	NHDF-neo	bronchial:	n/a	chr7:150557965-150557986
26	CTCF	chr7:150558120-150558270	K562	blood:	n/a	n/a
27	CTCF	chr7:150557980-150558034	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:150557900-150558050	RPTEC	kidney:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
29	CTCF	chr7:150557898-150558031	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
30	CTCF	chr7:150572049-150572100	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:150557920-150558070	HUVEC	blood vessel:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
32	CTCF	chr7:150557720-150557870	K562	blood:	n/a	n/a
33	CTCF	chr7:150557900-150558050	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
34	CTCF	chr7:150557945-150558092	Pancreas_OC	pancreas:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
35	CTCF	chr7:150557920-150558070	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
36	CTCF	chr7:150557844-150558071	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
37	CTCF	chr7:150557900-150558050	SK-N-SH_RA	brain:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
38	CTCF	chr7:150558460-150558541	GM19239	blood:	n/a	n/a
39	CTCF	chr7:150556066-150556144	GM19239	blood:	n/a	n/a
40	EGR1	chr7:150566544-150566897	MCF-7	breast:	n/a	chr7:150566749-150566759 chr7:150566743-150566765
41	EGR1	chr7:150566468-150566967	MCF-7	breast:	n/a	chr7:150566749-150566759 chr7:150566743-150566765
42	EP300	chr7:150564771-150564965	GM12878	blood:	n/a	n/a
43	FOS	chr7:150571586-150571671	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr7:150552576-150553386	MCF10A-Er-Src	breast:	n/a	chr7:150553229-150553238
45	FOS	chr7:150552597-150553327	MCF10A-Er-Src	breast:	n/a	chr7:150553229-150553238
46	FOS	chr7:150568745-150568999	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr7:150547424-150547624	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr7:150547524-150547684	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr7:150547482-150547667	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:150552617-150553359	MCF10A-Er-Src	breast:	n/a	chr7:150553229-150553238

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150554420-150554470	HRE	kidney:	n/a
2	chr7:150554628-150554678	U87	brain:	n/a
3	chr7:150554420-150554470	HRE	kidney:	n/a
4	chr7:150554628-150554678	U87	brain:	n/a
5	chr7:150549175-150549225	HNPCEpiC	eye:	n/a
6	chr7:150554628-150554678	NH-A	brain:	n/a
7	chr7:150554113-150554163	HRPEpiC	eye:	n/a
8	chr7:150548765-150548815	HAEpiC	amniotic membrane:	n/a
9	chr7:150555302-150555352	Hela-S3	cervix:	n/a
10	chr7:150554628-150554678	NT2-D1	testis:	n/a
11	chr7:150554915-150554965	RPTEC	kidney:	n/a
12	chr7:150549175-150549225	A549	lung:	n/a
13	chr7:150548934-150548984	K562	blood:	n/a
14	chr7:150549472-150549522	NT2-D1	testis:	n/a
15	chr7:150549560-150549610	HCPEpiC	choroid plexus:	n/a
16	chr7:150554628-150554678	SKMC	muscle:	n/a
17	chr7:150554113-150554163	SK-N-MC	brain:	n/a
18	chr7:150549175-150549225	AG04450	lung:	fetal
19	chr7:150551373-150551423	HepG2	liver:	n/a
20	chr7:150554420-150554470	NB4	blood:	n/a
21	chr7:150554420-150554470	PANC-1	pancreas:	n/a
22	chr7:150554113-150554163	HRCEpiC	kidney:	n/a
23	chr7:150549406-150549456	HCT-116	colon:	n/a
24	chr7:150554915-150554965	NB4	blood:	n/a
25	chr7:150554420-150554470	SK-N-SH	brain:	n/a
26	chr7:150549472-150549522	BJ	skin:	n/a
27	chr7:150548765-150548815	SK-N-MC	brain:	n/a
28	chr7:150554915-150554965	MCF-7	breast:	n/a
29	chr7:150548765-150548815	A549	lung:	n/a
30	chr7:150549370-150549420	HRE	kidney:	n/a
31	chr7:150554113-150554163	HEK293	kidney:	embryo
32	chr7:150549406-150549456	MCF-7	breast:	n/a
33	chr7:150554420-150554470	GM12891	blood:	n/a
34	chr7:150554113-150554163	BJ	skin:	n/a
35	chr7:150555302-150555352	H1-hESC	embryonic stem cell:	embryo
36	chr7:150549560-150549610	MCF10A-Er-Src	breast:	n/a
37	chr7:150554628-150554678	HCPEpiC	choroid plexus:	n/a
38	chr7:150549472-150549522	HRPEpiC	eye:	n/a
39	chr7:150549406-150549456	GM06990	blood:	n/a
40	chr7:150549370-150549420	SK-N-SH	brain:	n/a
41	chr7:150558377-150558427	HIPEpiC	eye:	n/a
42	chr7:150549560-150549610	SK-N-SH_RA	brain:	n/a
43	chr7:150548765-150548815	BJ	skin:	n/a
44	chr7:150549370-150549420	Hepatocyte	liver:	n/a
45	chr7:150549175-150549225	LNCaP	prostate:	n/a
46	chr7:150549175-150549225	BE2_C	brain:	n/a
47	chr7:150548934-150548984	ECC-1	luminal epithelium:	n/a
48	chr7:150551373-150551423	GM12892	blood:	n/a
49	chr7:150549472-150549522	NH-A	brain:	n/a
50	chr7:150548765-150548815	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150542584..150544794-chr7:150560485..150563293,2	MCF-7	breast:
2	chr7:150562856..150565769-chr7:150566346..150570295,3	K562	blood:
3	chr7:150568033..150570583-chr7:150684396..150686354,2	MCF-7	breast:
4	chr7:150570270..150572638-chr7:150573385..150575681,2	K562	blood:
5	chr7:150567773..150569879-chr7:150653213..150655593,2	K562	blood:
6	chr7:150521643..150523890-chr7:150556049..150558134,2	K562	blood:
7	chr7:150541762..150544255-chr7:150551164..150553467,2	K562	blood:
8	chr7:150546933..150549270-chr7:150550109..150551654,2	K562	blood:
9	chr7:150556165..150558158-chr7:150561303..150563873,2	K562	blood:
10	chr7:150539254..150541517-chr7:150546331..150548334,2	K562	blood:
11	chr7:150564458..150567179-chr7:150567861..150571641,4	K562	blood:
12	chr7:150572299..150575283-chr7:150617480..150621735,3	K562	blood:
13	chr7:150556165..150558158-chr7:150561303..150563873,2	K562	blood:
14	chr7:150547227..150549974-chr7:150551519..150553271,2	K562	blood:
15	chr7:150550808..150555015-chr7:150558384..150561943,5	K562	blood:
16	chr7:150562856..150565769-chr7:150566346..150570295,3	K562	blood:
17	chr7:150540017..150541716-chr7:150546331..150547904,2	K562	blood:
18	chr7:150550808..150553153-chr7:150558456..150560989,3	K562	blood:
19	chr7:150570280..150573172-chr7:150702825..150704695,2	K562	blood:
20	chr7:150550808..150553153-chr7:150558456..150560989,3	K562	blood:
21	chr7:150546391..150548614-chr7:150875114..150878211,3	K562	blood:
22	chr7:150564868..150567649-chr7:150590717..150593691,2	K562	blood:
23	chr12:58153738..58156431-chr7:150562978..150565095,2	MCF-7	breast:
24	chr7:150550808..150555015-chr7:150558384..150561943,5	K562	blood:
25	chr7:150564458..150567179-chr7:150567861..150571641,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABP1-1	chr7:150568035-150568307	expRegAs_chr7_12357_+
2	lnc-ABP1-2	chr7:150568389-150569059	predAs_engstrom06_BM715580_1

Variant related genes	Relation type
AOC1	TF binding region
AOC1	CpG island
ENSG00000002726	chromatin interactions

Extended variants
information (count: 1124 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139685486	chr7:150547119-150547120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11766970	chr7:150547144-150547145	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs537049427	chr7:150547176-150547177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189618642	chr7:150547182-150547183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144237812	chr7:150547188-150547189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542545775	chr7:150547290-150547291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372411026	chr7:150547294-150547295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563933427	chr7:150547318-150547319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191411316	chr7:150547330-150547331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111621723	chr7:150547339-150547340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552923667	chr7:150547348-150547349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573007653	chr7:150547365-150547366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531172320	chr7:150547402-150547403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573018140	chr7:150547404-150547405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115399828	chr7:150547459-150547460	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs575796815	chr7:150547472-150547473	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs578003787	chr7:150547543-150547544	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs543452350	chr7:150547591-150547592	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs183890174	chr7:150547592-150547593	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs529571311	chr7:150547653-150547654	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs188351878	chr7:150547663-150547664	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs149385351	chr7:150547722-150547723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs45490299	chr7:150547723-150547724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551637791	chr7:150547729-150547730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546081002	chr7:150547731-150547732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs45597433	chr7:150547747-150547748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35411492	chr7:150547769-150547770	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs567253211	chr7:150547809-150547810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536217974	chr7:150547812-150547813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553251645	chr7:150547965-150547966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2373876	chr7:150547968-150547969	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs376993142	chr7:150548021-150548022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564340874	chr7:150548032-150548033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181181211	chr7:150548034-150548035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376376179	chr7:150548040-150548041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558463143	chr7:150548059-150548060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577763899	chr7:150548111-150548112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543489369	chr7:150548112-150548113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563377639	chr7:150548123-150548124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573714347	chr7:150548146-150548147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551220648	chr7:150548156-150548157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148668548	chr7:150548157-150548158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs45563633	chr7:150548195-150548196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373904169	chr7:150548248-150548249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143333328	chr7:150548259-150548260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10273148	chr7:150548272-150548273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551993941	chr7:150548323-150548324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186362849	chr7:150548329-150548330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs45600938	chr7:150548335-150548336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190081694	chr7:150548384-150548385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150539600-150553800	Weak transcription	Liver	Liver
2	chr7:150543200-150548600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:150543200-150551200	Weak transcription	Fetal Lung	lung
4	chr7:150543200-150557600	Weak transcription	Right Atrium	heart
5	chr7:150543800-150549200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:150544400-150549200	Weak transcription	Adipose Nuclei	Adipose
7	chr7:150544800-150549000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr7:150545000-150548800	Weak transcription	Fetal Intestine Small	intestine
9	chr7:150546200-150548400	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr7:150548200-150549000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:150548400-150549400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr7:150548400-150549400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:150548400-150549400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr7:150548400-150550000	Enhancers	Primary hematopoietic stem cells	blood
15	chr7:150548600-150549200	Enhancers	Stomach Mucosa	stomach
16	chr7:150548600-150550000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr7:150548600-150550400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:150548800-150549400	Enhancers	Fetal Intestine Small	intestine
19	chr7:150549000-150549200	Enhancers	Colonic Mucosa	Colon
20	chr7:150549000-150549200	Enhancers	Duodenum Mucosa	Duodenum
21	chr7:150549000-150549200	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
22	chr7:150549000-150549200	Enhancers	Fetal Intestine Large	intestine
23	chr7:150549000-150549200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr7:150549000-150549200	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr7:150549000-150550000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr7:150549200-150549400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:150549200-150549400	Enhancers	Adipose Nuclei	Adipose
28	chr7:150549200-150549400	Flanking Active TSS	Colonic Mucosa	Colon
29	chr7:150549200-150549400	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr7:150549200-150549400	Flanking Active TSS	Fetal Intestine Large	intestine
31	chr7:150549200-150549400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
32	chr7:150549200-150549400	Flanking Active TSS	Stomach Mucosa	stomach
33	chr7:150549200-150549600	Bivalent Enhancer	Placenta	Placenta
34	chr7:150549200-150549600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr7:150549200-150549800	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr7:150549400-150549600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:150549400-150549600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr7:150549400-150549600	Enhancers	Colonic Mucosa	Colon
39	chr7:150549400-150549600	Flanking Active TSS	Fetal Intestine Small	intestine
40	chr7:150549400-150549600	Enhancers	Spleen	Spleen
41	chr7:150549400-150549800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr7:150549400-150549800	Bivalent Enhancer	Adipose Nuclei	Adipose
43	chr7:150549400-150549800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr7:150549400-150550000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:150549400-150550000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr7:150549400-150550000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:150549400-150550000	Enhancers	Fetal Muscle Leg	muscle
48	chr7:150549400-150550000	Active TSS	Stomach Mucosa	stomach
49	chr7:150549400-150550600	Active TSS	Fetal Intestine Large	intestine
50	chr7:150549400-150550600	Active TSS	Rectal Mucosa Donor 29	rectum

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