Variant report

Variant	esv3444902
Chromosome Location	chr7:48778643-49027602
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	BACH1	chr7:48944648-48944936	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr7:48821475-48821666	GM12878	blood:	n/a	n/a
3	BRCA1	chr7:48919396-48919460	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr7:48829561-48829585	GM12878	blood:	n/a	n/a
5	CBX3	chr7:48900095-48900399	K562	blood:	n/a	n/a
6	CBX3	chr7:48900123-48900352	K562	blood:	n/a	n/a
7	CBX3	chr7:48951078-48951343	K562	blood:	n/a	n/a
8	CEBPB	chr7:48806398-48806609	HepG2	liver:	n/a	chr7:48806526-48806537
9	CEBPB	chr7:48984359-48984602	MCF-7	breast:	n/a	chr7:48984516-48984525 chr7:48984514-48984525 chr7:48984514-48984527 chr7:48984515-48984526
10	CEBPB	chr7:48918492-48918690	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:48878800-48879033	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:48851684-48851844	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:48984347-48984682	IMR90	lung:	n/a	chr7:48984516-48984525 chr7:48984514-48984525 chr7:48984514-48984527 chr7:48984515-48984526
14	CEBPB	chr7:48984331-48984693	HepG2	liver:	n/a	chr7:48984516-48984525 chr7:48984514-48984525 chr7:48984514-48984527 chr7:48984515-48984526
15	CEBPB	chr7:48849803-48849906	HepG2	liver:	n/a	chr7:48849846-48849857
16	CEBPB	chr7:48795633-48795833	HepG2	liver:	n/a	chr7:48795707-48795720 chr7:48795708-48795719
17	CEBPB	chr7:48896162-48896194	IMR90	lung:	n/a	chr7:48896174-48896183 chr7:48896174-48896183 chr7:48896172-48896185 chr7:48896174-48896183
18	CEBPB	chr7:48872368-48872474	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:48896152-48896236	HepG2	liver:	n/a	chr7:48896174-48896183 chr7:48896174-48896183 chr7:48896172-48896185 chr7:48896174-48896183
20	CEBPB	chr7:48847193-48847277	A549	lung:	n/a	chr7:48847205-48847218
21	CEBPB	chr7:48806460-48806573	A549	lung:	n/a	chr7:48806526-48806537
22	CEBPB	chr7:48984346-48984669	A549	lung:	n/a	chr7:48984516-48984525 chr7:48984514-48984525 chr7:48984514-48984527 chr7:48984515-48984526
23	CEBPB	chr7:48984349-48984676	H1-hESC	embryonic stem cell:	n/a	chr7:48984516-48984525 chr7:48984514-48984525 chr7:48984514-48984527 chr7:48984515-48984526
24	CREB1	chr7:48914922-48915311	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:48915760-48916050	NHEK	skin:	n/a	chr7:48915883-48915892
26	CTCF	chr7:48915060-48915210	NB4	blood:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
27	CTCF	chr7:48934292-48934461	GM12878	blood:	n/a	n/a
28	CTCF	chr7:48915020-48915170	HMF	breast:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
29	CTCF	chr7:48915080-48915230	AoAF	blood vessel:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
30	CTCF	chr7:48915060-48915210	GM06990	blood:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
31	CTCF	chr7:48934160-48934310	GM12874	blood:	n/a	n/a
32	CTCF	chr7:48934260-48934410	GM12874	blood:	n/a	n/a
33	CTCF	chr7:48934300-48934450	GM12873	blood:	n/a	n/a
34	CTCF	chr7:48912180-48912330	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:48915806-48915953	Gliobla	brain:	n/a	chr7:48915883-48915892
36	CTCF	chr7:48914982-48915233	LNCaP	prostate:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
37	CTCF	chr7:48915021-48915206	Medullo	brain:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
38	CTCF	chr7:48915880-48916030	HMF	breast:	n/a	chr7:48915883-48915892
39	CTCF	chr7:48915065-48915146	HUVEC	blood vessel:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
40	CTCF	chr7:48915020-48915170	HBMEC	blood vessel:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
41	CTCF	chr7:48884571-48884667	Lung_OC	lung:	n/a	n/a
42	CTCF	chr7:48934240-48934390	GM12864	blood:	n/a	n/a
43	CTCF	chr7:48934240-48934390	NB4	blood:	n/a	n/a
44	CTCF	chr7:48914971-48915236	MCF-7	breast:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
45	CTCF	chr7:48915000-48915150	HepG2	liver:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
46	CTCF	chr7:48954323-48954366	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr7:48915760-48915910	GM12873	blood:	n/a	chr7:48915883-48915892
48	CTCF	chr7:48914680-48916238	SK-N-SH	brain:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915883-48915892 chr7:48915089-48915110
49	CTCF	chr7:48914884-48915260	MCF-7	breast:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110
50	CTCF	chr7:48915040-48915190	GM12865	blood:	n/a	chr7:48915107-48915125 chr7:48915094-48915112 chr7:48915089-48915110

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48887640-48887690	BJ	skin:	n/a
2	chr7:48887640-48887690	BJ	skin:	n/a
3	chr7:48887421-48887471	NH-A	brain:	n/a
4	chr7:48965301-48965351	BE2_C	brain:	n/a
5	chr7:48963443-48963493	AG09309	skin:	n/a
6	chr7:48967106-48967156	HIPEpiC	eye:	n/a
7	chr7:48884523-48884573	AG09319	gingival:	n/a
8	chr7:48887421-48887471	HMEC	breast:	n/a
9	chr7:48887421-48887471	BE2_C	brain:	n/a
10	chr7:48884523-48884573	SK-N-SH	brain:	n/a
11	chr7:48884523-48884573	K562	blood:	n/a
12	chr7:48887640-48887690	AoSMC	blood vessel:	n/a
13	chr7:48962376-48962426	HCPEpiC	choroid plexus:	n/a
14	chr7:48915086-48915136	GM12891	blood:	n/a
15	chr7:48887421-48887471	HIPEpiC	eye:	n/a
16	chr7:48962376-48962426	HCM	heart:	n/a
17	chr7:48887421-48887471	HRCEpiC	kidney:	n/a
18	chr7:48962376-48962426	NT2-D1	testis:	n/a
19	chr7:48967106-48967156	NB4	blood:	n/a
20	chr7:48962376-48962426	ProgFib	skin:	n/a
21	chr7:48887640-48887690	HCF	heart:	n/a
22	chr7:48887585-48887635	GM12878	blood:	n/a
23	chr7:48887421-48887471	RPTEC	kidney:	n/a
24	chr7:48887585-48887635	GM12892	blood:	n/a
25	chr7:48889641-48889691	HEEpiC	esophagus:	n/a
26	chr7:48887640-48887690	H1-hESC	embryonic stem cell:	embryo
27	chr7:48963408-48963458	AG04449	skin:	fetal
28	chr7:48964325-48964375	SKMC	muscle:	n/a
29	chr7:48963408-48963458	H1-hESC	embryonic stem cell:	embryo
30	chr7:48963443-48963493	Jurkat	blood:	n/a
31	chr7:48967106-48967156	HCPEpiC	choroid plexus:	n/a
32	chr7:48889641-48889691	U87	brain:	n/a
33	chr7:48887585-48887635	K562	blood:	n/a
34	chr7:48967106-48967156	SK-N-SH_RA	brain:	n/a
35	chr7:48964325-48964375	HMEC	breast:	n/a
36	chr7:48967106-48967156	HCF	heart:	n/a
37	chr7:48889641-48889691	HUVEC	blood vessel:	n/a
38	chr7:48964051-48964101	A549	lung:	n/a
39	chr7:48887585-48887635	HCPEpiC	choroid plexus:	n/a
40	chr7:48963443-48963493	SKMC	muscle:	n/a
41	chr7:48964051-48964101	SKMC	muscle:	n/a
42	chr7:48967106-48967156	NHBE	bronchial:	n/a
43	chr7:48884523-48884573	SK-N-SH_RA	brain:	n/a
44	chr7:48964325-48964375	PrEC	prostate:	n/a
45	chr7:48963443-48963493	HCM	heart:	n/a
46	chr7:48967106-48967156	HCM	heart:	n/a
47	chr7:48887640-48887690	HRCEpiC	kidney:	n/a
48	chr7:48963408-48963458	HRPEpiC	eye:	n/a
49	chr7:48959999-48960049	NT2-D1	testis:	n/a
50	chr7:48887640-48887690	ProgFib	skin:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCA13-3	chr7:48854078-48854124	l_3412_chr7:48854077-48855837_testes
2	lnc-ABCA13-2	chr7:48884686-48885282	XLOC_006092
3	lnc-ABCA13-4	chr7:48964157-48967049	NR_003595
4	lnc-ABCA13-3	chr7:48855232-48855837	l_3412_chr7:48854077-48855837_testes
5	lnc-ABCA13-2	chr7:48883532-48883578	XLOC_006092

Variant related genes	Relation type
GDI2P1	TF binding region
ENSG00000218305	TF binding region
ENSG00000267970	TF binding region
ENSG00000225705	TF binding region
GDI2P1	CpG island
ENSG00000218305	CpG island
ENSG00000267970	CpG island
ENSG00000225705	CpG island

Extended variants
information (count: 3331 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:3331 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367951526	chr7:48781061-48781062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551269645	chr7:48781063-48781064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376324213	chr7:48781089-48781090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554076831	chr7:48781122-48781123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35807069	chr7:48781123-48781124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574850451	chr7:48781133-48781134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs118059227	chr7:48781204-48781205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547852131	chr7:48781239-48781240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567672002	chr7:48781257-48781258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373474777	chr7:48781304-48781305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372566141	chr7:48781332-48781333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375598182	chr7:48781335-48781336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536601529	chr7:48781367-48781368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556920236	chr7:48781372-48781373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576776496	chr7:48781437-48781438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368276604	chr7:48781475-48781476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542798640	chr7:48781552-48781553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539256590	chr7:48781557-48781558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189162257	chr7:48781562-48781563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181878481	chr7:48781597-48781598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17388204	chr7:48781605-48781606	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs185738562	chr7:48781643-48781644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544377919	chr7:48781674-48781675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573307106	chr7:48781680-48781681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542179780	chr7:48781692-48781693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188885078	chr7:48781705-48781706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531482677	chr7:48781714-48781715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373892815	chr7:48781729-48781730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371503790	chr7:48781730-48781731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545235813	chr7:48781736-48781737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564922556	chr7:48781746-48781747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527439428	chr7:48781756-48781757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547913548	chr7:48781771-48781772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567736254	chr7:48781791-48781792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554278551	chr7:48781825-48781826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562928365	chr7:48781866-48781867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530134638	chr7:48781876-48781877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140244448	chr7:48781877-48781878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs17388239	chr7:48781878-48781879	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs538963501	chr7:48781936-48781937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145147720	chr7:48781937-48781938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114667444	chr7:48782006-48782007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535175803	chr7:48782014-48782015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139004344	chr7:48782030-48782031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573384338	chr7:48782034-48782035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542240652	chr7:48782057-48782058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141595161	chr7:48782062-48782063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564829780	chr7:48782064-48782065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367578214	chr7:48782123-48782124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113189810	chr7:48782124-48782125	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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
Acute lymphoblastic leukemia	18768390	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48781000-48781600	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr7:48781200-48782000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr7:48781200-48782200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:48787600-48788000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:48787800-48788200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:48787800-48788200	ZNF genes & repeats	Pancreas	Pancrea
7	chr7:48788000-48788200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:48788000-48788400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:48788200-48788400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:48788200-48788400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:48788400-48788800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:48793400-48794400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:48793400-48794400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:48793600-48794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:48794000-48794200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr7:48794200-48795400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr7:48794400-48795200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr7:48794400-48795200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:48794800-48795200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr7:48795200-48795400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:48795400-48796400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr7:48798200-48799000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:48798800-48799200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:48800400-48801000	Enhancers	HSMMtube	muscle
25	chr7:48821400-48821600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:48821600-48822400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:48821800-48822200	Enhancers	NH-A	brain
28	chr7:48822000-48822200	Enhancers	Adipose Nuclei	Adipose
29	chr7:48822400-48822600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:48826600-48827000	Enhancers	Esophagus	oesophagus
31	chr7:48826800-48827200	Enhancers	Brain Germinal Matrix	brain
32	chr7:48826800-48827400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr7:48833000-48833200	Weak transcription	Pancreas	Pancrea
34	chr7:48833200-48833400	ZNF genes & repeats	Pancreas	Pancrea
35	chr7:48833400-48836400	Weak transcription	Pancreas	Pancrea
36	chr7:48850400-48850800	Enhancers	Primary T cells from cord blood	blood
37	chr7:48850400-48851400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:48850400-48851400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr7:48850800-48851200	Weak transcription	Primary T cells from cord blood	blood
40	chr7:48851200-48851400	Enhancers	Primary T cells from cord blood	blood
41	chr7:48851400-48852400	Weak transcription	Primary T cells from cord blood	blood
42	chr7:48852400-48853400	Enhancers	Primary T cells from cord blood	blood
43	chr7:48852600-48853400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:48857200-48858000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr7:48871200-48872800	Enhancers	Brain Angular Gyrus	brain
46	chr7:48871600-48872000	Enhancers	Brain Hippocampus Middle	brain
47	chr7:48871600-48872800	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr7:48871800-48872800	Enhancers	Brain Substantia Nigra	brain
49	chr7:48872000-48872400	Flanking Active TSS	Brain Cingulate Gyrus	brain
50	chr7:48872000-48872400	Flanking Active TSS	Brain Hippocampus Middle	brain

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