Variant report

Variant	nsv1029101
Chromosome Location	chr7:137952620-138005671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:137963629-137963637	K562	blood:	n/a	n/a
2	ARID3A	chr7:137998866-137999439	K562	blood:	n/a	n/a
3	ARID3A	chr7:138000832-138002097	HepG2	liver:	n/a	chr7:138001986-138002002
4	ARID3A	chr7:137982261-137982550	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:137979278-137979630	HepG2	liver:	n/a	n/a
6	ATF1	chr7:137970315-137970429	K562	blood:	n/a	n/a
7	ATF1	chr7:137998883-137999397	K562	blood:	n/a	n/a
8	BACH1	chr7:137998973-137999022	K562	blood:	n/a	n/a
9	BHLHE40	chr7:137979859-137979883	K562	blood:	n/a	n/a
10	BHLHE40	chr7:138001263-138001418	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:137998872-137999388	K562	blood:	n/a	n/a
12	CBX3	chr7:137974456-137974990	K562	blood:	n/a	n/a
13	CBX3	chr7:137998634-137999978	K562	blood:	n/a	n/a
14	CBX3	chr7:138005588-138006011	K562	blood:	n/a	n/a
15	CBX3	chr7:137974549-137975036	K562	blood:	n/a	n/a
16	CBX3	chr7:137998847-137999452	K562	blood:	n/a	n/a
17	CCNT2	chr7:137999128-137999386	K562	blood:	n/a	n/a
18	CEBPB	chr7:137952706-137952980	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:137971625-137971846	K562	blood:	n/a	chr7:137971799-137971812 chr7:137971798-137971815
20	CEBPB	chr7:137971691-137971834	IMR90	lung:	n/a	chr7:137971799-137971812 chr7:137971798-137971815
21	CEBPB	chr7:138001292-138001669	A549	lung:	n/a	n/a
22	CEBPB	chr7:137991204-137991426	K562	blood:	n/a	chr7:137991287-137991298
23	CEBPB	chr7:138001024-138001735	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:138001155-138001560	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:137991142-137991389	A549	lung:	n/a	chr7:137991287-137991298
26	CEBPB	chr7:138001253-138001807	A549	lung:	n/a	n/a
27	CEBPB	chr7:137976030-137976153	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:137971630-137971914	Hela-S3	cervix:	n/a	chr7:137971799-137971812 chr7:137971798-137971815
29	CEBPB	chr7:137988577-137989198	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:137963902-137963929	K562	blood:	n/a	n/a
31	CEBPB	chr7:137998956-137999220	K562	blood:	n/a	n/a
32	CEBPB	chr7:137971615-137971849	A549	lung:	n/a	chr7:137971799-137971812 chr7:137971798-137971815
33	CEBPB	chr7:138000920-138002142	HepG2	liver:	n/a	chr7:138002034-138002045
34	CEBPB	chr7:138001299-138001710	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:137971629-137971889	HepG2	liver:	n/a	chr7:137971799-137971812 chr7:137971798-137971815
36	CEBPB	chr7:137991179-137991427	HepG2	liver:	n/a	chr7:137991287-137991298
37	CEBPB	chr7:137979404-137979576	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:137998843-137999463	K562	blood:	n/a	n/a
39	CEBPD	chr7:137998824-137999481	K562	blood:	n/a	n/a
40	CEBPD	chr7:137998856-137999504	K562	blood:	n/a	n/a
41	CTCF	chr7:137952815-137952911	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:137968301-137968343	GM10248	blood:	n/a	n/a
43	CTCF	chr7:137967516-137967575	GM20000	blood:	n/a	n/a
44	CTCF	chr7:137969108-137969186	GM20000	blood:	n/a	n/a
45	CTCF	chr7:137983103-137983113	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:137952809-137952949	H1-hESC	embryonic stem cell:	n/a	chr7:137952913-137952926
47	CTCF	chr7:137999960-138000110	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:137961820-137961970	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:138000040-138000190	GM12872	blood:	n/a	n/a
50	CTCF	chr7:138000060-138000210	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137983235-137983285	HNPCEpiC	eye:	n/a
2	chr7:137983235-137983285	AG04450	lung:	fetal
3	chr7:137984018-137984068	CMK	blood:	n/a
4	chr7:137983235-137983285	CMK	blood:	n/a
5	chr7:137984018-137984068	NHBE	bronchial:	n/a
6	chr7:137984018-137984068	SK-N-SH_RA	brain:	n/a
7	chr7:137983235-137983285	AG09309	skin:	n/a
8	chr7:137984018-137984068	RPTEC	kidney:	n/a
9	chr7:137984018-137984068	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:137983235-137983285	GM19239	blood:	n/a
11	chr7:137984018-137984068	BE2_C	brain:	n/a
12	chr7:137984018-137984068	AG09309	skin:	n/a
13	chr7:137983235-137983285	HCPEpiC	choroid plexus:	n/a
14	chr7:137984018-137984068	H1-hESC	embryonic stem cell:	embryo
15	chr7:137983235-137983285	Hela-S3	cervix:	n/a
16	chr7:137984018-137984068	HL-60	blood:	n/a
17	chr7:137984018-137984068	A549	lung:	n/a
18	chr7:137984018-137984068	GM12892	blood:	n/a
19	chr7:137983235-137983285	NHBE	bronchial:	n/a
20	chr7:137983235-137983285	Caco-2	colon:	n/a
21	chr7:137984018-137984068	HRPEpiC	eye:	n/a
22	chr7:137983235-137983285	GM12878	blood:	n/a
23	chr7:137984018-137984068	NHDF-neo	bronchial:	n/a
24	chr7:137983235-137983285	AG09319	gingival:	n/a
25	chr7:137983235-137983285	NHDF-neo	bronchial:	n/a
26	chr7:137984018-137984068	NH-A	brain:	n/a
27	chr7:137984018-137984068	NT2-D1	testis:	n/a
28	chr7:137984018-137984068	PANC-1	pancreas:	n/a
29	chr7:137983235-137983285	PFSK-1	brain:	n/a
30	chr7:137983235-137983285	HEEpiC	esophagus:	n/a
31	chr7:137983235-137983285	MCF10A-Er-Src	breast:	n/a
32	chr7:137984018-137984068	GM12891	blood:	n/a
33	chr7:137984018-137984068	SAEC	small airway:	n/a
34	chr7:137983235-137983285	HRCEpiC	kidney:	n/a
35	chr7:137983235-137983285	BJ	skin:	n/a
36	chr7:137983235-137983285	RPTEC	kidney:	n/a
37	chr7:137983235-137983285	HEK293	kidney:	embryo
38	chr7:137984018-137984068	SK-N-MC	brain:	n/a
39	chr7:137984018-137984068	HIPEpiC	eye:	n/a
40	chr7:137983235-137983285	U87	brain:	n/a
41	chr7:137984018-137984068	LNCaP	prostate:	n/a
42	chr7:137983235-137983285	NT2-D1	testis:	n/a
43	chr7:137984018-137984068	PrEC	prostate:	n/a
44	chr7:137984018-137984068	Hela-S3	cervix:	n/a
45	chr7:137983235-137983285	T-47D	breast:	n/a
46	chr7:137983235-137983285	HIPEpiC	eye:	n/a
47	chr7:137984018-137984068	HCT-116	colon:	n/a
48	chr7:137984018-137984068	Caco-2	colon:	n/a
49	chr7:137984018-137984068	HCF	heart:	n/a
50	chr7:137984018-137984068	SKMC	muscle:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:137969521..137971635-chr7:138143799..138146467,2	K562	blood:
2	chr7:137988083..137990941-chr7:138145037..138146557,2	MCF-7	breast:
3	chr7:137978354..137980372-chr7:137985691..137988661,2	K562	blood:
4	chr7:137947555..137949067-chr7:137952751..137956382,3	K562	blood:
5	chr7:137956498..137958305-chr7:137960190..137962007,2	K562	blood:
6	chr7:137995053..137999099-chr7:138144129..138146392,3	K562	blood:
7	chr7:137978354..137980372-chr7:137985691..137988661,2	K562	blood:
8	chr7:137978354..137980840-chr7:137985937..137988661,2	K562	blood:
9	chr7:137965863..137967594-chr7:137968478..137970711,2	MCF-7	breast:
10	chr7:137956498..137958305-chr7:137960190..137962007,2	K562	blood:
11	chr7:137978354..137980840-chr7:137985937..137988661,2	K562	blood:
12	chr7:137920098..137922481-chr7:137970184..137972526,2	MCF-7	breast:
13	chr7:137970347..137972756-chr7:137980665..137982972,2	K562	blood:
14	chr7:137965863..137967594-chr7:137968478..137970711,2	MCF-7	breast:
15	chr7:137970347..137972756-chr7:137980665..137982972,2	K562	blood:
16	chr7:137974611..137977011-chr7:138155722..138157358,2	K562	blood:
17	chr7:137926916..137928434-chr7:137998152..138000341,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000213238	TF binding region
ENSG00000213238	CpG island
ENSG00000122779	chromatin interactions

Extended variants
information (count: 2333 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2333 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111925696	chr7:137952663-137952664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183710290	chr7:137952733-137952734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559115807	chr7:137952755-137952756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77284101	chr7:137952816-137952817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541813343	chr7:137952852-137952853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561776421	chr7:137952854-137952855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs55956373	chr7:137952855-137952856	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs550153492	chr7:137952857-137952858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563897988	chr7:137952874-137952875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535370997	chr7:137952902-137952903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7803399	chr7:137952906-137952907	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs13438299	chr7:137952927-137952928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534711305	chr7:137952928-137952929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548134484	chr7:137952946-137952947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560015499	chr7:137952947-137952948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568215260	chr7:137952971-137952972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537141246	chr7:137952980-137952981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550433976	chr7:137953019-137953020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568829404	chr7:137953056-137953057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376568025	chr7:137953083-137953084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187334178	chr7:137953096-137953097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138682801	chr7:137953125-137953126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553249274	chr7:137953181-137953182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190287801	chr7:137953225-137953226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35068265	chr7:137953355-137953356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141148655	chr7:137953370-137953371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539210008	chr7:137953372-137953373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182478611	chr7:137953406-137953407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114112943	chr7:137953457-137953458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544279749	chr7:137953492-137953493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563757419	chr7:137953551-137953552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186886970	chr7:137953565-137953566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557674248	chr7:137953698-137953699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552458071	chr7:137953779-137953780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114751977	chr7:137953784-137953785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528711043	chr7:137953811-137953812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527611887	chr7:137953835-137953836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548221411	chr7:137953845-137953846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147226157	chr7:137953884-137953885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192759340	chr7:137953963-137953964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566706988	chr7:137953967-137953968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552035764	chr7:137953983-137953984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150703132	chr7:137953995-137953996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139995556	chr7:137954013-137954014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565453764	chr7:137954032-137954033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570823379	chr7:137954037-137954038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531070881	chr7:137954043-137954044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553389772	chr7:137954063-137954064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539630785	chr7:137954112-137954113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184124026	chr7:137954117-137954118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137942400-137953200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:137947600-137961600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:137952600-137952800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:137952600-137953000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:137953000-137974000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:137961800-137962000	Enhancers	NH-A	brain
7	chr7:137962200-137963400	Weak transcription	NH-A	brain
8	chr7:137963400-137963800	Enhancers	NH-A	brain
9	chr7:137963600-137963800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:137963800-137973600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:137967800-137968000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr7:137967800-137968200	Enhancers	Ovary	ovary
13	chr7:137968000-137968600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr7:137968200-137969400	Weak transcription	Ovary	ovary
15	chr7:137968600-137969200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:137968600-137971200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr7:137969200-137969800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:137969200-137971400	Enhancers	HepG2	liver
19	chr7:137969400-137970200	Enhancers	Ovary	ovary
20	chr7:137969800-137970000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:137970000-137971800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:137970200-137970600	Weak transcription	Ovary	ovary
23	chr7:137970600-137970800	Enhancers	Ovary	ovary
24	chr7:137970800-137979200	Weak transcription	Ovary	ovary
25	chr7:137971400-137979200	Weak transcription	HepG2	liver
26	chr7:137971800-137972000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:137973200-137976200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr7:137973600-137974800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:137973600-137975000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:137974000-137974200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr7:137977600-137978000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr7:137977800-137978000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:137978000-137978400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr7:137978000-137980400	Enhancers	Liver	Liver
35	chr7:137978000-137981000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:137978400-137979400	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr7:137978800-137979800	Enhancers	Colonic Mucosa	Colon
38	chr7:137978800-137979800	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr7:137978800-137980000	Enhancers	Adipose Nuclei	Adipose
40	chr7:137978800-137980000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr7:137978800-137980000	Enhancers	Placenta	Placenta
42	chr7:137978800-137980200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:137978800-137980400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr7:137979000-137979600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:137979000-137979800	Enhancers	Left Ventricle	heart
46	chr7:137979000-137979800	Enhancers	Lung	lung
47	chr7:137979000-137980200	Enhancers	Primary hematopoietic stem cells	blood
48	chr7:137979000-137980200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr7:137979200-137979400	Enhancers	GM12878-XiMat	blood
50	chr7:137979200-137979400	Enhancers	Monocytes-CD14+_RO01746	blood

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