Variant report

Variant	nsv888009
Chromosome Location	chr7:48750857-48936143
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	chr7:48821475-48821666	GM12878	blood:	n/a	n/a
2	BRCA1	chr7:48829561-48829585	GM12878	blood:	n/a	n/a
3	BRCA1	chr7:48919396-48919460	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr7:48900095-48900399	K562	blood:	n/a	n/a
5	CBX3	chr7:48900123-48900352	K562	blood:	n/a	n/a
6	CEBPB	chr7:48758403-48758619	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:48918492-48918690	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr7:48758482-48758670	A549	lung:	n/a	n/a
9	CEBPB	chr7:48759675-48759935	HepG2	liver:	n/a	chr7:48759775-48759786
10	CEBPB	chr7:48753679-48753939	IMR90	lung:	n/a	chr7:48753822-48753833
11	CEBPB	chr7:48849803-48849906	HepG2	liver:	n/a	chr7:48849846-48849857
12	CEBPB	chr7:48896152-48896236	HepG2	liver:	n/a	chr7:48896174-48896183 chr7:48896174-48896183 chr7:48896172-48896185 chr7:48896174-48896183
13	CEBPB	chr7:48872368-48872474	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:48795633-48795833	HepG2	liver:	n/a	chr7:48795707-48795720 chr7:48795708-48795719
15	CEBPB	chr7:48753680-48754000	HepG2	liver:	n/a	chr7:48753822-48753833
16	CEBPB	chr7:48759753-48759860	H1-hESC	embryonic stem cell:	n/a	chr7:48759775-48759786
17	CEBPB	chr7:48896162-48896194	IMR90	lung:	n/a	chr7:48896174-48896183 chr7:48896174-48896183 chr7:48896172-48896185 chr7:48896174-48896183
18	CEBPB	chr7:48753715-48753954	A549	lung:	n/a	chr7:48753822-48753833
19	CEBPB	chr7:48756456-48756730	A549	lung:	n/a	chr7:48756597-48756608
20	CEBPB	chr7:48758377-48758670	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:48851684-48851844	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:48758402-48758657	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:48806460-48806573	A549	lung:	n/a	chr7:48806526-48806537
24	CEBPB	chr7:48878800-48879033	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:48753765-48753962	K562	blood:	n/a	chr7:48753822-48753833
26	CEBPB	chr7:48806398-48806609	HepG2	liver:	n/a	chr7:48806526-48806537
27	CEBPB	chr7:48756455-48756759	HepG2	liver:	n/a	chr7:48756723-48756734 chr7:48756597-48756608
28	CEBPB	chr7:48847193-48847277	A549	lung:	n/a	chr7:48847205-48847218
29	CREB1	chr7:48914922-48915311	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:48914996-48915205	SK-N-SH_RA	brain:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
31	CTCF	chr7:48934315-48934779	GM12878	blood:	n/a	n/a
32	CTCF	chr7:48915060-48915210	HEEpiC	esophagus:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
33	CTCF	chr7:48914900-48915050	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr7:48934300-48934450	AG09319	gingival:	n/a	n/a
35	CTCF	chr7:48915040-48915190	HCPEpiC	choroid plexus:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
36	CTCF	chr7:48934360-48934389	K562	blood:	n/a	n/a
37	CTCF	chr7:48915820-48915970	GM12872	blood:	n/a	chr7:48915883-48915892
38	CTCF	chr7:48934240-48934390	HepG2	liver:	n/a	n/a
39	CTCF	chr7:48915080-48915230	AoAF	blood vessel:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
40	CTCF	chr7:48915065-48915146	HUVEC	blood vessel:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
41	CTCF	chr7:48915060-48915210	GM12865	blood:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
42	CTCF	chr7:48915020-48915170	HEEpiC	esophagus:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
43	CTCF	chr7:48915060-48915210	HL-60	blood:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
44	CTCF	chr7:48915020-48915170	Hela-S3	cervix:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
45	CTCF	chr7:48915000-48915150	GM12873	blood:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
46	CTCF	chr7:48915800-48915950	GM12875	blood:	n/a	chr7:48915883-48915892
47	CTCF	chr7:48915780-48915930	MCF-7	breast:	n/a	chr7:48915883-48915892
48	CTCF	chr7:48915100-48915250	GM12875	blood:	n/a	chr7:48915107-48915125
49	CTCF	chr7:48915806-48915953	Gliobla	brain:	n/a	chr7:48915883-48915892
50	CTCF	chr7:48931010-48931096	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48887640-48887690	HIPEpiC	eye:	n/a
2	chr7:48915086-48915136	SK-N-SH	brain:	n/a
3	chr7:48887640-48887690	HIPEpiC	eye:	n/a
4	chr7:48915086-48915136	SK-N-SH	brain:	n/a
5	chr7:48884523-48884573	SKMC	muscle:	n/a
6	chr7:48887585-48887635	PFSK-1	brain:	n/a
7	chr7:48915086-48915136	SKMC	muscle:	n/a
8	chr7:48887640-48887690	AoSMC	blood vessel:	n/a
9	chr7:48889641-48889691	NB4	blood:	n/a
10	chr7:48915086-48915136	HCT-116	colon:	n/a
11	chr7:48887640-48887690	HRE	kidney:	n/a
12	chr7:48887585-48887635	SK-N-SH_RA	brain:	n/a
13	chr7:48884523-48884573	ProgFib	skin:	n/a
14	chr7:48889641-48889691	MCF-7	breast:	n/a
15	chr7:48887585-48887635	AG04449	skin:	fetal
16	chr7:48889641-48889691	H1-hESC	embryonic stem cell:	embryo
17	chr7:48884523-48884573	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:48887421-48887471	PANC-1	pancreas:	n/a
19	chr7:48887640-48887690	H1-hESC	embryonic stem cell:	embryo
20	chr7:48889641-48889691	T-47D	breast:	n/a
21	chr7:48887640-48887690	HL-60	blood:	n/a
22	chr7:48915086-48915136	HNPCEpiC	eye:	n/a
23	chr7:48915086-48915136	GM12878	blood:	n/a
24	chr7:48884523-48884573	RPTEC	kidney:	n/a
25	chr7:48889641-48889691	AG10803	skin:	n/a
26	chr7:48915086-48915136	AG04450	lung:	fetal
27	chr7:48887640-48887690	A549	lung:	n/a
28	chr7:48889641-48889691	AG04450	lung:	fetal
29	chr7:48887421-48887471	BJ	skin:	n/a
30	chr7:48884523-48884573	HL-60	blood:	n/a
31	chr7:48915086-48915136	GM12892	blood:	n/a
32	chr7:48887421-48887471	AG09319	gingival:	n/a
33	chr7:48915086-48915136	NHBE	bronchial:	n/a
34	chr7:48889641-48889691	BE2_C	brain:	n/a
35	chr7:48887640-48887690	NH-A	brain:	n/a
36	chr7:48884523-48884573	HIPEpiC	eye:	n/a
37	chr7:48889641-48889691	HCT-116	colon:	n/a
38	chr7:48915086-48915136	HEK293	kidney:	embryo
39	chr7:48889641-48889691	SK-N-MC	brain:	n/a
40	chr7:48884523-48884573	BE2_C	brain:	n/a
41	chr7:48889641-48889691	LNCaP	prostate:	n/a
42	chr7:48915086-48915136	Caco-2	colon:	n/a
43	chr7:48887585-48887635	PrEC	prostate:	n/a
44	chr7:48915086-48915136	H1-hESC	embryonic stem cell:	embryo
45	chr7:48915086-48915136	ProgFib	skin:	n/a
46	chr7:48887585-48887635	H1-hESC	embryonic stem cell:	embryo
47	chr7:48887585-48887635	GM06990	blood:	n/a
48	chr7:48884523-48884573	ovcar-3	ovarian:	n/a
49	chr7:48889641-48889691	NH-A	brain:	n/a
50	chr7:48884523-48884573	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:48375884..48377251-chr7:48914594..48915844,5	MCF-7	breast:
2	chr7:48882427..48884923-chr7:49456665..49458198,2	MCF-7	breast:
3	chr7:48464066..48464994-chr7:48914675..48915561,3	MCF-7	breast:
4	chr7:48863351..48865401-chr7:48869144..48870913,2	K562	blood:
5	chr7:48350873..48351428-chr7:48826215..48827185,2	MCF-7	breast:
6	chr7:48338977..48339698-chr7:48914621..48915709,3	MCF-7	breast:
7	chr7:48464147..48465026-chr7:48914660..48915807,4	MCF-7	breast:
8	chr7:48863351..48865401-chr7:48869144..48870913,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCA13-1	chr7:48750753-48751116	NONHSAT120531
2	lnc-ABCA13-3	chr7:48855232-48855837	l_3412_chr7:48854077-48855837_testes
3	lnc-ABCA13-2	chr7:48883532-48883578	XLOC_006092
4	lnc-ABCA13-2	chr7:48884686-48885282	XLOC_006092
5	lnc-ABCA13-3	chr7:48854078-48854124	l_3412_chr7:48854077-48855837_testes

Variant related genes	Relation type
ENSG00000225705	TF binding region
ENSG00000267970	TF binding region
ENSG00000225705	CpG island
ENSG00000267970	CpG island

Extended variants
information (count: 1452 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:1452 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4504584	chr7:48750857-48750858	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537840162	chr7:48750862-48750863	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs1136636	chr7:48750984-48750985	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560537545	chr7:48751000-48751001	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs557690181	chr7:48751019-48751020	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs185911051	chr7:48751030-48751031	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs139857116	chr7:48751037-48751038	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs554085641	chr7:48751040-48751041	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs373133491	chr7:48751087-48751088	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs189928248	chr7:48751098-48751099	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs531445327	chr7:48751105-48751106	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs562590978	chr7:48758625-48758626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192615352	chr7:48758631-48758632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148962234	chr7:48758634-48758635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551319917	chr7:48758669-48758670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372940052	chr7:48758670-48758671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571911081	chr7:48758672-48758673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374472189	chr7:48758691-48758692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143647108	chr7:48758692-48758693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182587376	chr7:48758703-48758704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138256925	chr7:48758741-48758742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187148305	chr7:48758742-48758743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191195525	chr7:48758762-48758763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111540662	chr7:48758870-48758871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367705578	chr7:48758887-48758888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73098461	chr7:48758909-48758910	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs142659437	chr7:48758941-48758942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200845546	chr7:48758970-48758971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs57336355	chr7:48758998-48758999	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs540143424	chr7:48759013-48759014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553961273	chr7:48759056-48759057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573498360	chr7:48759062-48759063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144884857	chr7:48759103-48759104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368177986	chr7:48759154-48759155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114497521	chr7:48759162-48759163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548937607	chr7:48759163-48759164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545406875	chr7:48759167-48759168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368019742	chr7:48762149-48762150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543093152	chr7:48762168-48762169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368477935	chr7:48762172-48762173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534812953	chr7:48762174-48762175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs193043845	chr7:48762179-48762180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185741894	chr7:48762181-48762182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545443567	chr7:48762182-48762183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559605107	chr7:48762191-48762192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528368484	chr7:48762205-48762206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10250303	chr7:48762240-48762241	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs534425273	chr7:48762269-48762270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553956002	chr7:48762281-48762282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531052795	chr7:48762332-48762333	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Abnormal phenotypes	18644119	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48750600-48751000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr7:48758600-48759000	Enhancers	HMEC	breast
3	chr7:48758600-48759200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:48762000-48762800	Enhancers	Thymus	Thymus
5	chr7:48762600-48762800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:48762800-48763200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:48773200-48773600	Enhancers	Fetal Heart	heart
8	chr7:48774600-48775600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:48781000-48781600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr7:48781200-48782000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:48781200-48782200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr7:48787600-48788000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:48787800-48788200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:48787800-48788200	ZNF genes & repeats	Pancreas	Pancrea
15	chr7:48788000-48788200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:48788000-48788400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:48788200-48788400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:48788200-48788400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:48788400-48788800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:48793400-48794400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:48793400-48794400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:48793600-48794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:48794000-48794200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr7:48794200-48795400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr7:48794400-48795200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:48794400-48795200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr7:48794800-48795200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:48795200-48795400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:48795400-48796400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr7:48798200-48799000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr7:48798800-48799200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr7:48800400-48801000	Enhancers	HSMMtube	muscle
33	chr7:48821400-48821600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:48821600-48822400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:48821800-48822200	Enhancers	NH-A	brain
36	chr7:48822000-48822200	Enhancers	Adipose Nuclei	Adipose
37	chr7:48822400-48822600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:48826600-48827000	Enhancers	Esophagus	oesophagus
39	chr7:48826800-48827200	Enhancers	Brain Germinal Matrix	brain
40	chr7:48826800-48827400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr7:48833000-48833200	Weak transcription	Pancreas	Pancrea
42	chr7:48833200-48833400	ZNF genes & repeats	Pancreas	Pancrea
43	chr7:48833400-48836400	Weak transcription	Pancreas	Pancrea
44	chr7:48850400-48850800	Enhancers	Primary T cells from cord blood	blood
45	chr7:48850400-48851400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:48850400-48851400	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr7:48850800-48851200	Weak transcription	Primary T cells from cord blood	blood
48	chr7:48851200-48851400	Enhancers	Primary T cells from cord blood	blood
49	chr7:48851400-48852400	Weak transcription	Primary T cells from cord blood	blood
50	chr7:48852400-48853400	Enhancers	Primary T cells from cord blood	blood

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