Variant report

Variant	nsv1033349
Chromosome Location	chr7:126010250-126168918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:126019383-126019479	K562	blood:	n/a	n/a
2	ATF1	chr7:126148916-126149043	K562	blood:	n/a	n/a
3	BACH1	chr7:126120721-126120800	K562	blood:	n/a	n/a
4	BATF	chr7:126141768-126142023	GM12878	blood:	n/a	n/a
5	BATF	chr7:126084070-126084326	GM12878	blood:	n/a	chr7:126084174-126084185
6	BCLAF1	chr7:126090272-126090898	GM12878	blood:	n/a	n/a
7	BCLAF1	chr7:126090235-126090798	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:126018785-126018989	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:126051887-126051999	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:126089835-126090907	GM12878	blood:	n/a	n/a
11	BRCA1	chr7:126090538-126090546	GM12878	blood:	n/a	n/a
12	BRCA1	chr7:126090013-126090032	GM12878	blood:	n/a	n/a
13	CCNT2	chr7:126134074-126134168	K562	blood:	n/a	n/a
14	CCNT2	chr7:126151253-126151311	K562	blood:	n/a	n/a
15	CCNT2	chr7:126099340-126099539	K562	blood:	n/a	n/a
16	CEBPB	chr7:126024589-126024864	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:126024630-126024852	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:126034447-126034803	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:126159752-126159820	K562	blood:	n/a	chr7:126159770-126159781 chr7:126159769-126159782
20	CEBPB	chr7:126159605-126159898	A549	lung:	n/a	chr7:126159770-126159781 chr7:126159769-126159782
21	CEBPB	chr7:126042017-126042357	IMR90	lung:	n/a	chr7:126042182-126042193
22	CEBPB	chr7:126068403-126068603	Hela-S3	cervix:	n/a	chr7:126068481-126068492
23	CEBPB	chr7:126122653-126122853	H1-hESC	embryonic stem cell:	n/a	chr7:126122780-126122791
24	CEBPB	chr7:126042119-126042350	H1-hESC	embryonic stem cell:	n/a	chr7:126042182-126042193
25	CEBPB	chr7:126122626-126122947	HepG2	liver:	n/a	chr7:126122780-126122791
26	CEBPB	chr7:126042010-126042361	HepG2	liver:	n/a	chr7:126042182-126042193
27	CEBPB	chr7:126084073-126084284	Hela-S3	cervix:	n/a	chr7:126084085-126084096
28	CEBPB	chr7:126042044-126042349	Hela-S3	cervix:	n/a	chr7:126042182-126042193
29	CEBPB	chr7:126068332-126068651	IMR90	lung:	n/a	chr7:126068481-126068492
30	CEBPB	chr7:126134219-126134277	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:126042031-126042354	K562	blood:	n/a	chr7:126042182-126042193
32	CEBPB	chr7:126042012-126042340	A549	lung:	n/a	chr7:126042182-126042193
33	CEBPB	chr7:126023220-126023260	A549	lung:	n/a	n/a
34	CEBPB	chr7:126122640-126122937	K562	blood:	n/a	chr7:126122780-126122791
35	CEBPB	chr7:126100510-126100809	K562	blood:	n/a	chr7:126100653-126100666 chr7:126100655-126100664 chr7:126100653-126100664 chr7:126100655-126100666
36	CEBPB	chr7:126159627-126159904	HepG2	liver:	n/a	chr7:126159770-126159781 chr7:126159769-126159782
37	CEBPB	chr7:126100511-126100809	IMR90	lung:	n/a	chr7:126100653-126100666 chr7:126100655-126100664 chr7:126100653-126100664 chr7:126100655-126100666
38	CEBPB	chr7:126068356-126068599	HepG2	liver:	n/a	chr7:126068481-126068492
39	CEBPB	chr7:126100471-126100834	HepG2	liver:	n/a	chr7:126100653-126100666 chr7:126100655-126100664 chr7:126100653-126100664 chr7:126100655-126100666
40	CEBPB	chr7:126122658-126122913	A549	lung:	n/a	chr7:126122780-126122791
41	CEBPB	chr7:126077316-126077456	HepG2	liver:	n/a	chr7:126077404-126077415
42	CEBPB	chr7:126122603-126122918	IMR90	lung:	n/a	chr7:126122780-126122791
43	CEBPB	chr7:126039435-126039635	A549	lung:	n/a	n/a
44	CEBPB	chr7:126035277-126035444	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:126100594-126100794	H1-hESC	embryonic stem cell:	n/a	chr7:126100653-126100666 chr7:126100655-126100664 chr7:126100653-126100664 chr7:126100655-126100666
46	CHD1	chr7:126089898-126091153	GM12878	blood:	n/a	n/a
47	CHD2	chr7:126089964-126090744	GM12878	blood:	n/a	n/a
48	CTCF	chr7:126064614-126064730	LNCaP	prostate:	n/a	n/a
49	CTCF	chr7:126066960-126067110	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:126013060-126013210	HBMEC	blood vessel:	n/a	chr7:126013174-126013192

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126165242-126165292	GM12891	blood:	n/a
2	chr7:126165242-126165292	MCF10A-Er-Src	breast:	n/a
3	chr7:126165242-126165292	NT2-D1	testis:	n/a
4	chr7:126165242-126165292	LNCaP	prostate:	n/a
5	chr7:126165242-126165292	GM06990	blood:	n/a
6	chr7:126079083-126079133	NHDF-neo	bronchial:	n/a
7	chr7:126079083-126079133	GM12878	blood:	n/a
8	chr7:126079083-126079133	NHBE	bronchial:	n/a
9	chr7:126079083-126079133	BE2_C	brain:	n/a
10	chr7:126079083-126079133	SK-N-SH	brain:	n/a
11	chr7:126165242-126165292	SAEC	small airway:	n/a
12	chr7:126165242-126165292	HEEpiC	esophagus:	n/a
13	chr7:126165242-126165292	T-47D	breast:	n/a
14	chr7:126079083-126079133	K562	blood:	n/a
15	chr7:126165242-126165292	HRPEpiC	eye:	n/a
16	chr7:126165242-126165292	HRCEpiC	kidney:	n/a
17	chr7:126165242-126165292	SK-N-MC	brain:	n/a
18	chr7:126165242-126165292	HNPCEpiC	eye:	n/a
19	chr7:126079083-126079133	HEEpiC	esophagus:	n/a
20	chr7:126165242-126165292	AG10803	skin:	n/a
21	chr7:126079083-126079133	SK-N-MC	brain:	n/a
22	chr7:126165242-126165292	SK-N-SH	brain:	n/a
23	chr7:126079083-126079133	HCM	heart:	n/a
24	chr7:126165242-126165292	AG09319	gingival:	n/a
25	chr7:126079083-126079133	HUVEC	blood vessel:	n/a
26	chr7:126079083-126079133	AG04450	lung:	fetal
27	chr7:126165242-126165292	U87	brain:	n/a
28	chr7:126079083-126079133	NH-A	brain:	n/a
29	chr7:126165242-126165292	SKMC	muscle:	n/a
30	chr7:126079083-126079133	PrEC	prostate:	n/a
31	chr7:126079083-126079133	GM06990	blood:	n/a
32	chr7:126165242-126165292	HCM	heart:	n/a
33	chr7:126165242-126165292	PrEC	prostate:	n/a
34	chr7:126079083-126079133	HepG2	liver:	n/a
35	chr7:126079083-126079133	AG09309	skin:	n/a
36	chr7:126165242-126165292	Caco-2	colon:	n/a
37	chr7:126079083-126079133	T-47D	breast:	n/a
38	chr7:126079083-126079133	HRPEpiC	eye:	n/a
39	chr7:126165242-126165292	BE2_C	brain:	n/a
40	chr7:126165242-126165292	HIPEpiC	eye:	n/a
41	chr7:126165242-126165292	SK-N-SH_RA	brain:	n/a
42	chr7:126079083-126079133	SAEC	small airway:	n/a
43	chr7:126165242-126165292	HCF	heart:	n/a
44	chr7:126079083-126079133	HNPCEpiC	eye:	n/a
45	chr7:126079083-126079133	Jurkat	blood:	n/a
46	chr7:126079083-126079133	HRCEpiC	kidney:	n/a
47	chr7:126079083-126079133	A549	lung:	n/a
48	chr7:126165242-126165292	Hepatocyte	liver:	n/a
49	chr7:126165242-126165292	RPTEC	kidney:	n/a
50	chr7:126165242-126165292	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:126136384..126139302-chr7:126250186..126252685,2	K562	blood:
2	chr7:126104127..126105778-chr7:126106556..126109113,2	K562	blood:
3	7:126130122-126133705..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
4	chr7:126127310..126130214-chr7:126150191..126152367,2	K562	blood:
5	chr7:126121758..126123459-chr7:126162475..126164735,2	K562	blood:
6	chr7:126028745..126031381-chr7:126035464..126038065,3	K562	blood:
7	chr7:126121758..126123459-chr7:126162475..126164735,2	K562	blood:
8	7:126133705-126138790..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
9	chr7:126082404..126082904-chr9:129703018..129703561,2	MCF-7	breast:
10	7:126148685-126150023..7:126733290-126737485	GM12878	blood:
11	chr7:126028745..126031381-chr7:126035464..126037060,2	K562	blood:
12	chr7:126147698..126150261-chr7:126203102..126205183,2	K562	blood:
13	chr7:126028745..126031381-chr7:126035464..126038065,3	K562	blood:
14	7:126154600-126176992..7:126756671-126761022	H1-hESC	embryonic stem cell:	embryo
15	7:126154600-126176992..7:127221502-127225864	Hela-S3	cervix:
16	chr7:126028745..126031381-chr7:126035464..126037060,2	K562	blood:
17	7:126154600-126176992..7:127009457-127018926	H1-hESC	embryonic stem cell:	embryo

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-4	chr7:126058290-126058349	XLOC_006236
2	lnc-ARF5-4	chr7:126019024-126019055	XLOC_006236
3	lnc-ARF5-4	chr7:126061118-126061230	XLOC_006236
4	lnc-ARF5-4	chr7:126059887-126059999	XLOC_006236
5	lnc-ARF5-4	chr7:126061482-126061634	XLOC_006236
6	lnc-ARF5-4	chr7:126064175-126064239	XLOC_006236
7	lnc-ARF5-4	chr7:126055283-126055392	XLOC_006236
8	lnc-ARF5-17	chr7:126151189-126152933	NONHSAT123118

No data

Variant related genes	Relation type
ENSG00000241921	TF binding region
ENSG00000227249	TF binding region
GRM8	TF binding region
ENSG00000241921	CpG island
ENSG00000227249	CpG island
GRM8	CpG island
ENSG00000227249	chromatin interactions
ENSG00000179562	chromatin interactions
ENSG00000179603	chromatin interactions
ENSG00000048405	chromatin interactions

Extended variants
information (count: 2654 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2654 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536160292	chr7:126010258-126010259	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs115207838	chr7:126010259-126010260	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs569462128	chr7:126010261-126010262	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs150685190	chr7:126010309-126010310	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs201749472	chr7:126010311-126010312	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs114229441	chr7:126010324-126010325	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs139897907	chr7:126010364-126010365	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs576892462	chr7:126010376-126010377	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs534288603	chr7:126010450-126010451	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs561916303	chr7:126010454-126010455	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs1582280	chr7:126010502-126010503	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs143247288	chr7:126010515-126010516	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs541712322	chr7:126010525-126010526	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs1582281	chr7:126010529-126010530	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs560270879	chr7:126010587-126010588	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs575324082	chr7:126010600-126010601	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs371249504	chr7:126010622-126010623	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs74870191	chr7:126010632-126010633	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs147504486	chr7:126010664-126010665	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs75848172	chr7:126010715-126010716	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs7810406	chr7:126010781-126010782	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs529344411	chr7:126010789-126010790	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs547359997	chr7:126016602-126016603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540810663	chr7:126016649-126016650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568656602	chr7:126016650-126016651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536086448	chr7:126016665-126016666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554342991	chr7:126016676-126016677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6964312	chr7:126016773-126016774	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs184578552	chr7:126016792-126016793	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs536599171	chr7:126016796-126016797	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs189027699	chr7:126016810-126016811	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs181482545	chr7:126016831-126016832	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs541260806	chr7:126016838-126016839	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs557727835	chr7:126016880-126016881	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186591541	chr7:126016892-126016893	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs577519446	chr7:126016902-126016903	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs540915974	chr7:126016937-126016938	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs577318143	chr7:126016939-126016940	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs574269647	chr7:126016947-126016948	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs542029346	chr7:126016948-126016949	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs563596831	chr7:126016949-126016950	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs531037815	chr7:126016971-126016972	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs552438793	chr7:126016988-126016989	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs564465336	chr7:126017012-126017013	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191340026	chr7:126017020-126017021	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs77005232	chr7:126017045-126017046	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs547293918	chr7:126017048-126017049	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs372479848	chr7:126017054-126017055	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs544847333	chr7:126017056-126017057	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs143034618	chr7:126017088-126017089	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Autism	22495311	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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	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
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Autism	19246517	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126009800-126010800	ZNF genes & repeats	GM12878-XiMat	blood
2	chr7:126016600-126017200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:126017000-126017400	Enhancers	Adipose Nuclei	Adipose
4	chr7:126017600-126018000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:126018400-126020000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr7:126018600-126019000	Flanking Active TSS	GM12878-XiMat	blood
7	chr7:126038400-126039400	Enhancers	HSMMtube	muscle
8	chr7:126038800-126039600	Enhancers	Fetal Heart	heart
9	chr7:126039000-126039800	Enhancers	GM12878-XiMat	blood
10	chr7:126040800-126041600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:126041600-126042800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:126042800-126043600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:126050200-126050400	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:126051000-126051600	Active TSS	A549	lung
15	chr7:126051200-126051600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:126051200-126051600	Active TSS	Duodenum Mucosa	Duodenum
17	chr7:126051200-126051800	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr7:126051400-126051600	Active TSS	GM12878-XiMat	blood
19	chr7:126051400-126051600	Enhancers	Hela-S3	cervix
20	chr7:126051400-126052000	Active TSS	Brain Angular Gyrus	brain
21	chr7:126051600-126052000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr7:126051600-126052200	Flanking Active TSS	GM12878-XiMat	blood
23	chr7:126052200-126052400	Enhancers	GM12878-XiMat	blood
24	chr7:126055600-126056000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:126070800-126071200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:126070800-126071400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:126070800-126071600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:126071400-126076200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:126076200-126076400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:126076200-126076400	Enhancers	Fetal Heart	heart
31	chr7:126076400-126076600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:126076400-126076800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr7:126076400-126076800	Flanking Active TSS	Fetal Heart	heart
34	chr7:126076400-126077200	Enhancers	Fetal Intestine Large	intestine
35	chr7:126076600-126076800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:126076600-126077200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr7:126076800-126077000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:126076800-126077400	Enhancers	Fetal Heart	heart
39	chr7:126076800-126081800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr7:126077000-126082000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:126077200-126080200	Weak transcription	Fetal Intestine Large	intestine
42	chr7:126077400-126077800	Weak transcription	Fetal Heart	heart
43	chr7:126077400-126078200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr7:126077800-126078000	Enhancers	Fetal Heart	heart
45	chr7:126078000-126081800	Weak transcription	Fetal Heart	heart
46	chr7:126080200-126081000	Enhancers	Fetal Intestine Large	intestine
47	chr7:126081000-126082000	Weak transcription	Fetal Intestine Large	intestine
48	chr7:126081400-126082400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr7:126081800-126082200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:126081800-126082200	Enhancers	Fetal Heart	heart

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