Variant report

Variant	nsv888968
Chromosome Location	chr7:110144415-110204292
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	ARID3A	chr7:110162717-110163545	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:110161251-110162197	HepG2	liver:	n/a	n/a
3	ATF3	chr7:110162799-110163299	A549	lung:	n/a	n/a
4	BACH1	chr7:110151378-110151411	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr7:110162678-110163384	A549	lung:	n/a	n/a
6	BCL3	chr7:110162740-110163442	A549	lung:	n/a	n/a
7	BHLHE40	chr7:110162911-110163273	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:110162913-110163306	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:110171283-110171565	IMR90	lung:	n/a	n/a
10	CEBPB	chr7:110184991-110185228	HepG2	liver:	n/a	chr7:110185096-110185107
11	CEBPB	chr7:110169270-110169612	IMR90	lung:	n/a	chr7:110169430-110169441
12	CEBPB	chr7:110169245-110169615	HepG2	liver:	n/a	chr7:110169430-110169441
13	CEBPB	chr7:110169268-110169575	A549	lung:	n/a	chr7:110169430-110169441
14	CEBPB	chr7:110162775-110163289	A549	lung:	n/a	n/a
15	CEBPB	chr7:110176259-110176422	HepG2	liver:	n/a	chr7:110176317-110176328 chr7:110176319-110176330 chr7:110176317-110176330 chr7:110176317-110176330
16	CEBPB	chr7:110182130-110182398	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:110169292-110169556	Hela-S3	cervix:	n/a	chr7:110169430-110169441
18	CEBPB	chr7:110168937-110169627	HepG2	liver:	n/a	chr7:110169430-110169441
19	CEBPB	chr7:110162874-110163235	A549	lung:	n/a	n/a
20	CEBPB	chr7:110182172-110182372	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:110184991-110185190	A549	lung:	n/a	chr7:110185096-110185107
22	CEBPB	chr7:110179284-110179632	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:110166663-110166922	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:110161316-110161827	HepG2	liver:	n/a	chr7:110161465-110161478
25	CEBPB	chr7:110169305-110169550	HepG2	liver:	n/a	chr7:110169430-110169441
26	CEBPD	chr7:110169295-110169515	HepG2	liver:	n/a	n/a
27	CEBPD	chr7:110162957-110163255	HepG2	liver:	n/a	n/a
28	CREB1	chr7:110162763-110163354	HepG2	liver:	n/a	n/a
29	CREB1	chr7:110162960-110163204	A549	lung:	n/a	n/a
30	CREB1	chr7:110162749-110163280	HepG2	liver:	n/a	n/a
31	CTCF	chr7:110155363-110155437	GM13976	blood:	n/a	n/a
32	CTCF	chr7:110174820-110174970	HEEpiC	esophagus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
33	CTCF	chr7:110174791-110174942	Hela-S3	cervix:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
34	CTCF	chr7:110174780-110174930	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
35	CTCF	chr7:110174722-110174989	A549	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
36	CTCF	chr7:110174752-110174933	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
37	CTCF	chr7:110174780-110174930	HCPEpiC	choroid plexus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
38	CTCF	chr7:110174767-110174933	LNCaP	prostate:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
39	CTCF	chr7:110174780-110174930	HEEpiC	esophagus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
40	CTCF	chr7:110174800-110174950	BE2_C	brain:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
41	CTCF	chr7:110174760-110174910	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
42	CTCF	chr7:110174780-110174930	SAEC	small airway:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
43	CTCF	chr7:110174780-110174930	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
44	CTCF	chr7:110184400-110184550	AG04449	skin:	n/a	n/a
45	CTCF	chr7:110174787-110174911	ProgFib	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
46	CTCF	chr7:110174757-110174955	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
47	CTCF	chr7:110174800-110174950	HMEC	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
48	CTCF	chr7:110174740-110174890	AG04450	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
49	CTCF	chr7:110184440-110184590	BJ	skin:	n/a	n/a
50	CTCF	chr7:110174720-110174870	HepG2	liver:	n/a	chr7:110174856-110174869 chr7:110174858-110174868

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110174780-110174830	SK-N-SH	brain:	n/a
2	chr7:110174780-110174830	A549	lung:	n/a
3	chr7:110174780-110174830	SK-N-MC	brain:	n/a
4	chr7:110174780-110174830	GM12878	blood:	n/a
5	chr7:110174780-110174830	ProgFib	skin:	n/a
6	chr7:110174780-110174830	BE2_C	brain:	n/a
7	chr7:110174780-110174830	SKMC	muscle:	n/a
8	chr7:110174780-110174830	HCF	heart:	n/a
9	chr7:110174780-110174830	SAEC	small airway:	n/a
10	chr7:110174780-110174830	HRPEpiC	eye:	n/a
11	chr7:110174780-110174830	NHDF-neo	bronchial:	n/a
12	chr7:110174780-110174830	HEEpiC	esophagus:	n/a
13	chr7:110174780-110174830	GM12891	blood:	n/a
14	chr7:110174780-110174830	ECC-1	luminal epithelium:	n/a
15	chr7:110174780-110174830	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:110174780-110174830	AG04449	skin:	fetal
17	chr7:110174780-110174830	NT2-D1	testis:	n/a
18	chr7:110174780-110174830	HCM	heart:	n/a
19	chr7:110174780-110174830	Jurkat	blood:	n/a
20	chr7:110174780-110174830	HUVEC	blood vessel:	n/a
21	chr7:110174780-110174830	GM12892	blood:	n/a
22	chr7:110174780-110174830	MCF-7	breast:	n/a
23	chr7:110174780-110174830	PFSK-1	brain:	n/a
24	chr7:110174780-110174830	CMK	blood:	n/a
25	chr7:110174780-110174830	K562	blood:	n/a
26	chr7:110174780-110174830	RPTEC	kidney:	n/a
27	chr7:110174780-110174830	Hela-S3	cervix:	n/a
28	chr7:110174780-110174830	AG10803	skin:	n/a
29	chr7:110174780-110174830	GM19239	blood:	n/a
30	chr7:110174780-110174830	ovcar-3	ovarian:	n/a
31	chr7:110174780-110174830	GM06990	blood:	n/a
32	chr7:110174780-110174830	HRCEpiC	kidney:	n/a
33	chr7:110174780-110174830	H1-hESC	embryonic stem cell:	embryo
34	chr7:110174780-110174830	HCPEpiC	choroid plexus:	n/a
35	chr7:110174780-110174830	AG09309	skin:	n/a
36	chr7:110174780-110174830	HCT-116	colon:	n/a
37	chr7:110174780-110174830	PrEC	prostate:	n/a
38	chr7:110174780-110174830	U87	brain:	n/a
39	chr7:110174780-110174830	LNCaP	prostate:	n/a
40	chr7:110174780-110174830	BJ	skin:	n/a
41	chr7:110174780-110174830	AG04450	lung:	fetal
42	chr7:110174780-110174830	HL-60	blood:	n/a
43	chr7:110174780-110174830	T-47D	breast:	n/a
44	chr7:110174780-110174830	SK-N-SH_RA	brain:	n/a
45	chr7:110174780-110174830	HRE	kidney:	n/a
46	chr7:110174780-110174830	HepG2	liver:	n/a
47	chr7:110174780-110174830	AG09319	gingival:	n/a
48	chr7:110174780-110174830	NH-A	brain:	n/a
49	chr7:110174780-110174830	HMEC	breast:	n/a
50	chr7:110174780-110174830	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:110148252..110150649-chr7:110845950..110847481,2	K562	blood:
2	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
3	chr7:110204286..110206261-chr7:110213162..110216015,2	MCF-7	breast:
4	chr7:110175478..110177187-chr7:110400882..110403616,2	MCF-7	breast:
5	chr7:86847727..86850173-chr7:110164264..110166076,2	K562	blood:
6	chr4:4482219..4482825-chr7:110184645..110185165,2	MCF-7	breast:
7	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
8	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
9	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:
10	chr7:110202555..110205359-chr7:110210937..110215614,4	K562	blood:
11	chr7:109858826..109860608-chr7:110161184..110163464,2	MCF-7	breast:
12	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
13	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
14	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
15	chr17:57931575..57933892-chr7:110150089..110152912,2	MCF-7	breast:
16	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:
17	chr7:110203860..110205462-chr7:110210314..110213055,2	K562	blood:
18	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
19	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMMP2L-1	chr7:110151117-110151171	XLOC_006561
2	lnc-IMMP2L-1	chr7:110165513-110165618	XLOC_006561
3	lnc-IMMP2L-1	chr7:110151117-110151171	XLOC_006561
4	lnc-IMMP2L-1	chr7:110174646-110174811	XLOC_006561
5	lnc-IMMP2L-1	chr7:110165513-110165618	XLOC_006561

Variant related genes	Relation type
ENSG00000226965	TF binding region
ENSG00000226965	CpG island
ENSG00000135185	chromatin interactions
ENSG00000200397	chromatin interactions
XIRP2	miRNA target sites
GULP1	miRNA target sites
LCA5	miRNA target sites

Extended variants
information (count: 2230 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2230 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7811230	chr7:110144415-110144416	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377204122	chr7:110144425-110144426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370582118	chr7:110144507-110144508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191864964	chr7:110144544-110144545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10235251	chr7:110144623-110144624	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6961576	chr7:110144651-110144652	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs112685015	chr7:110144653-110144654	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs534621709	chr7:110144674-110144675	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs367814310	chr7:110144710-110144711	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs568279922	chr7:110144719-110144720	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs184483272	chr7:110144770-110144771	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs557071292	chr7:110144771-110144772	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs576912338	chr7:110144809-110144810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539410137	chr7:110144837-110144838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552704737	chr7:110144842-110144843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572650277	chr7:110144895-110144896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541346454	chr7:110144913-110144914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1948990	chr7:110144930-110144931	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148677908	chr7:110144934-110144935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563797985	chr7:110144943-110144944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532536547	chr7:110144978-110144979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112200553	chr7:110144986-110144987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11307411	chr7:110144987-110144988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200793669	chr7:110145000-110145001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369445393	chr7:110145066-110145067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546136751	chr7:110145079-110145080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559511330	chr7:110145126-110145127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73205251	chr7:110145171-110145172	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs142064456	chr7:110145178-110145179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376126134	chr7:110145182-110145183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116891148	chr7:110145226-110145227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192517406	chr7:110145241-110145242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73429249	chr7:110145335-110145336	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185388738	chr7:110145338-110145339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545363366	chr7:110145445-110145446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531976168	chr7:110145499-110145500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190674724	chr7:110145565-110145566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368284542	chr7:110145586-110145587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552904026	chr7:110145592-110145593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566360002	chr7:110145616-110145617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139232868	chr7:110145636-110145637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554819942	chr7:110145645-110145646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574837689	chr7:110145670-110145671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543597776	chr7:110145697-110145698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372489512	chr7:110145729-110145730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557280097	chr7:110145739-110145740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577218980	chr7:110145756-110145757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570344185	chr7:110145759-110145760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545998726	chr7:110145794-110145795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559832311	chr7:110145809-110145810	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Acute myeloid leukemia	16864856	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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110142200-110144600	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr7:110143800-110144600	Enhancers	Dnd41	blood
3	chr7:110144600-110144800	Flanking Active TSS	Dnd41	blood
4	chr7:110144800-110146200	Enhancers	Dnd41	blood
5	chr7:110146200-110147000	Genic enhancers	Dnd41	blood
6	chr7:110147000-110149800	Enhancers	Dnd41	blood
7	chr7:110148000-110148400	Enhancers	Liver	Liver
8	chr7:110149800-110150200	Weak transcription	Dnd41	blood
9	chr7:110150200-110150400	Enhancers	Dnd41	blood
10	chr7:110150400-110151200	Weak transcription	Dnd41	blood
11	chr7:110151200-110152600	Genic enhancers	Dnd41	blood
12	chr7:110152200-110152400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:110152600-110154600	Weak transcription	Dnd41	blood
14	chr7:110154600-110155400	Enhancers	Dnd41	blood
15	chr7:110155000-110155400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:110155200-110155400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:110155400-110156000	Enhancers	Right Atrium	heart
18	chr7:110155400-110156000	Genic enhancers	Dnd41	blood
19	chr7:110155400-110162600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:110155600-110155800	Enhancers	Pancreas	Pancrea
21	chr7:110155800-110158800	Weak transcription	Pancreas	Pancrea
22	chr7:110156000-110157600	Enhancers	Dnd41	blood
23	chr7:110157000-110158800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:110157200-110158600	Enhancers	Liver	Liver
25	chr7:110157400-110157600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:110157600-110158400	Weak transcription	Dnd41	blood
27	chr7:110158400-110161600	ZNF genes & repeats	Dnd41	blood
28	chr7:110158600-110161000	Weak transcription	Liver	Liver
29	chr7:110158800-110159400	ZNF genes & repeats	Pancreas	Pancrea
30	chr7:110158800-110159800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:110158800-110160200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:110159400-110161600	Weak transcription	Pancreas	Pancrea
33	chr7:110159800-110170400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:110160000-110160200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
35	chr7:110160200-110163000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr7:110160800-110163600	Enhancers	HepG2	liver
37	chr7:110160800-110163800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:110161000-110161600	Enhancers	Liver	Liver
39	chr7:110161200-110162600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:110161200-110163200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr7:110161400-110163400	Enhancers	Fetal Intestine Large	intestine
42	chr7:110161600-110162000	Enhancers	Psoas Muscle	Psoas
43	chr7:110161600-110162000	Transcr. at gene 5' and 3'	Dnd41	blood
44	chr7:110161600-110162200	Flanking Active TSS	Liver	Liver
45	chr7:110161600-110162200	Enhancers	Duodenum Mucosa	Duodenum
46	chr7:110161600-110162800	Enhancers	Brain Hippocampus Middle	brain
47	chr7:110161600-110163200	Enhancers	Pancreas	Pancrea
48	chr7:110161600-110163400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr7:110161600-110163600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:110161600-110163800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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