Variant report

Variant	nsv888967
Chromosome Location	chr7:110133558-110183622
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	chr7:110161251-110162197	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:110162717-110163545	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	chr7:110162740-110163442	A549	lung:	n/a	n/a
6	BCL3	chr7:110162678-110163384	A549	lung:	n/a	n/a
7	BHLHE40	chr7:110162911-110163273	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:110162874-110163235	A549	lung:	n/a	n/a
9	CEBPB	chr7:110171283-110171565	IMR90	lung:	n/a	n/a
10	CEBPB	chr7:110182130-110182398	IMR90	lung:	n/a	n/a
11	CEBPB	chr7:110176259-110176422	HepG2	liver:	n/a	chr7:110176317-110176328 chr7:110176319-110176330 chr7:110176317-110176330 chr7:110176317-110176330
12	CEBPB	chr7:110169245-110169615	HepG2	liver:	n/a	chr7:110169430-110169441
13	CEBPB	chr7:110169292-110169556	Hela-S3	cervix:	n/a	chr7:110169430-110169441
14	CEBPB	chr7:110168937-110169627	HepG2	liver:	n/a	chr7:110169430-110169441
15	CEBPB	chr7:110179284-110179632	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:110162913-110163306	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:110169268-110169575	A549	lung:	n/a	chr7:110169430-110169441
18	CEBPB	chr7:110166663-110166922	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:110162775-110163289	A549	lung:	n/a	n/a
20	CEBPB	chr7:110169270-110169612	IMR90	lung:	n/a	chr7:110169430-110169441
21	CEBPB	chr7:110169305-110169550	HepG2	liver:	n/a	chr7:110169430-110169441
22	CEBPB	chr7:110161316-110161827	HepG2	liver:	n/a	chr7:110161465-110161478
23	CEBPB	chr7:110182172-110182372	Hela-S3	cervix:	n/a	n/a
24	CEBPD	chr7:110169295-110169515	HepG2	liver:	n/a	n/a
25	CEBPD	chr7:110162957-110163255	HepG2	liver:	n/a	n/a
26	CREB1	chr7:110162960-110163204	A549	lung:	n/a	n/a
27	CREB1	chr7:110162763-110163354	HepG2	liver:	n/a	n/a
28	CREB1	chr7:110162749-110163280	HepG2	liver:	n/a	n/a
29	CTCF	chr7:110174760-110174910	HCPEpiC	choroid plexus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
30	CTCF	chr7:110174760-110174910	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
31	CTCF	chr7:110159697-110159754	Fibrobl	skin:	n/a	n/a
32	CTCF	chr7:110174760-110174910	HMF	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
33	CTCF	chr7:110174760-110174910	AG04450	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
34	CTCF	chr7:110174787-110174911	ProgFib	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
35	CTCF	chr7:110174777-110174948	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
36	CTCF	chr7:110174653-110175102	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
37	CTCF	chr7:110174800-110174950	HMEC	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
38	CTCF	chr7:110174820-110174970	AG10803	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
39	CTCF	chr7:110158870-110158908	GM20000	blood:	n/a	n/a
40	CTCF	chr7:110174762-110174953	LNCaP	prostate:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
41	CTCF	chr7:110174720-110174870	HepG2	liver:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
42	CTCF	chr7:110174757-110174955	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
43	CTCF	chr7:110174780-110174930	BE2_C	brain:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
44	CTCF	chr7:110174780-110174930	HCPEpiC	choroid plexus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
45	CTCF	chr7:110174780-110174930	AG09319	gingival:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
46	CTCF	chr7:110174780-110174930	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
47	CTCF	chr7:110174780-110174930	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
48	CTCF	chr7:110174717-110175031	IMR90	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
49	CTCF	chr7:110155363-110155437	GM13976	blood:	n/a	n/a
50	CTCF	chr7:110174780-110174930	SAEC	small airway:	n/a	chr7:110174856-110174869 chr7:110174858-110174868

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110174780-110174830	NHBE	bronchial:	n/a
2	chr7:110174780-110174830	AG04449	skin:	fetal
3	chr7:110174780-110174830	GM12891	blood:	n/a
4	chr7:110174780-110174830	GM06990	blood:	n/a
5	chr7:110174780-110174830	HAEpiC	amniotic membrane:	n/a
6	chr7:110174780-110174830	BJ	skin:	n/a
7	chr7:110174780-110174830	HRCEpiC	kidney:	n/a
8	chr7:110174780-110174830	MCF10A-Er-Src	breast:	n/a
9	chr7:110174780-110174830	H1-hESC	embryonic stem cell:	embryo
10	chr7:110174780-110174830	ECC-1	luminal epithelium:	n/a
11	chr7:110174780-110174830	HCT-116	colon:	n/a
12	chr7:110174780-110174830	HRPEpiC	eye:	n/a
13	chr7:110174780-110174830	NHDF-neo	bronchial:	n/a
14	chr7:110174780-110174830	SK-N-SH_RA	brain:	n/a
15	chr7:110174780-110174830	Jurkat	blood:	n/a
16	chr7:110174780-110174830	IMR90	lung:	fetal
17	chr7:110174780-110174830	AG04450	lung:	fetal
18	chr7:110174780-110174830	SK-N-SH	brain:	n/a
19	chr7:110174780-110174830	NH-A	brain:	n/a
20	chr7:110174780-110174830	HL-60	blood:	n/a
21	chr7:110174780-110174830	SAEC	small airway:	n/a
22	chr7:110174780-110174830	NT2-D1	testis:	n/a
23	chr7:110174780-110174830	HIPEpiC	eye:	n/a
24	chr7:110174780-110174830	PFSK-1	brain:	n/a
25	chr7:110174780-110174830	NB4	blood:	n/a
26	chr7:110174780-110174830	AoSMC	blood vessel:	n/a
27	chr7:110174780-110174830	SKMC	muscle:	n/a
28	chr7:110174780-110174830	HEEpiC	esophagus:	n/a
29	chr7:110174780-110174830	BE2_C	brain:	n/a
30	chr7:110174780-110174830	PrEC	prostate:	n/a
31	chr7:110174780-110174830	HMEC	breast:	n/a
32	chr7:110174780-110174830	CMK	blood:	n/a
33	chr7:110174780-110174830	RPTEC	kidney:	n/a
34	chr7:110174780-110174830	AG10803	skin:	n/a
35	chr7:110174780-110174830	HCF	heart:	n/a
36	chr7:110174780-110174830	Hepatocyte	liver:	n/a
37	chr7:110174780-110174830	A549	lung:	n/a
38	chr7:110174780-110174830	ovcar-3	ovarian:	n/a
39	chr7:110174780-110174830	AG09319	gingival:	n/a
40	chr7:110174780-110174830	HRE	kidney:	n/a
41	chr7:110174780-110174830	HCPEpiC	choroid plexus:	n/a
42	chr7:110174780-110174830	HNPCEpiC	eye:	n/a
43	chr7:110174780-110174830	T-47D	breast:	n/a
44	chr7:110174780-110174830	GM12892	blood:	n/a
45	chr7:110174780-110174830	AG09309	skin:	n/a
46	chr7:110174780-110174830	Hela-S3	cervix:	n/a
47	chr7:110174780-110174830	Caco-2	colon:	n/a
48	chr7:110174780-110174830	HUVEC	blood vessel:	n/a
49	chr7:110174780-110174830	ProgFib	skin:	n/a
50	chr7:110174780-110174830	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:
2	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
3	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
4	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
5	chr7:86847727..86850173-chr7:110164264..110166076,2	K562	blood:
6	chr7:110148252..110150649-chr7:110845950..110847481,2	K562	blood:
7	chr7:110130797..110132612-chr7:110136260..110138401,2	K562	blood:
8	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:
9	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
10	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
11	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
12	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
13	chr17:57931575..57933892-chr7:110150089..110152912,2	MCF-7	breast:
14	chr7:109858826..109860608-chr7:110161184..110163464,2	MCF-7	breast:
15	chr7:110175478..110177187-chr7:110400882..110403616,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMMP2L-1	chr7:110151117-110151171	XLOC_006561
2	lnc-IMMP2L-1	chr7:110151117-110151171	XLOC_006561
3	lnc-IMMP2L-1	chr7:110165513-110165618	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
ENSG00000200397	chromatin interactions
ENSG00000135185	chromatin interactions
XIRP2	miRNA target sites
GULP1	miRNA target sites
LCA5	miRNA target sites

Extended variants
information (count: 1877 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1877 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10270301	chr7:110133558-110133559	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530954967	chr7:110133590-110133591	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs117278020	chr7:110133592-110133593	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs564480692	chr7:110133597-110133598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs138262864	chr7:110133609-110133610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73714187	chr7:110133640-110133641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566511930	chr7:110133649-110133650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188321996	chr7:110133764-110133765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144203677	chr7:110133785-110133786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148750384	chr7:110133793-110133794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546437470	chr7:110133818-110133819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557287196	chr7:110133848-110133849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577242071	chr7:110133865-110133866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181192712	chr7:110133913-110133914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368602842	chr7:110133937-110133938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113419235	chr7:110133984-110133985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573487468	chr7:110134016-110134017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73429218	chr7:110134052-110134053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370476941	chr7:110134153-110134154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562185598	chr7:110134156-110134157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2966406	chr7:110134191-110134192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs188583661	chr7:110134197-110134198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73717104	chr7:110134204-110134205	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs533379056	chr7:110134224-110134225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142324465	chr7:110134263-110134264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560371157	chr7:110134339-110134340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368657971	chr7:110134347-110134348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567992716	chr7:110134350-110134351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150572203	chr7:110134367-110134368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560660594	chr7:110134406-110134407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568962792	chr7:110134437-110134438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531280535	chr7:110134455-110134456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140497799	chr7:110134495-110134496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571045901	chr7:110134516-110134517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535395011	chr7:110134517-110134518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533524671	chr7:110134538-110134539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553399120	chr7:110134587-110134588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4455768	chr7:110134590-110134591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs181664047	chr7:110134603-110134604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555882434	chr7:110134631-110134632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575770106	chr7:110134648-110134649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28516641	chr7:110134654-110134655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544681509	chr7:110134665-110134666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558266255	chr7:110134767-110134768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1508180	chr7:110134807-110134808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs144566790	chr7:110134819-110134820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80048517	chr7:110134826-110134827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147851427	chr7:110134853-110134854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371591250	chr7:110134893-110134894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201735335	chr7:110134905-110134906	Weak transcription	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:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110133400-110133600	ZNF genes & repeats	Dnd41	blood
2	chr7:110133600-110137200	Weak transcription	Dnd41	blood
3	chr7:110137200-110138800	Strong transcription	Dnd41	blood
4	chr7:110138800-110141200	Weak transcription	Dnd41	blood
5	chr7:110141200-110142200	Genic enhancers	Dnd41	blood
6	chr7:110142200-110142400	Enhancers	Dnd41	blood
7	chr7:110142200-110144600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr7:110142400-110143800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:110142400-110143800	Flanking Active TSS	Dnd41	blood
10	chr7:110142800-110143000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:110143000-110143600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:110143000-110143600	Enhancers	HMEC	breast
13	chr7:110143200-110143600	Enhancers	Primary hematopoietic stem cells	blood
14	chr7:110143200-110143600	Enhancers	NHEK	skin
15	chr7:110143800-110144600	Enhancers	Dnd41	blood
16	chr7:110144600-110144800	Flanking Active TSS	Dnd41	blood
17	chr7:110144800-110146200	Enhancers	Dnd41	blood
18	chr7:110146200-110147000	Genic enhancers	Dnd41	blood
19	chr7:110147000-110149800	Enhancers	Dnd41	blood
20	chr7:110148000-110148400	Enhancers	Liver	Liver
21	chr7:110149800-110150200	Weak transcription	Dnd41	blood
22	chr7:110150200-110150400	Enhancers	Dnd41	blood
23	chr7:110150400-110151200	Weak transcription	Dnd41	blood
24	chr7:110151200-110152600	Genic enhancers	Dnd41	blood
25	chr7:110152200-110152400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:110152600-110154600	Weak transcription	Dnd41	blood
27	chr7:110154600-110155400	Enhancers	Dnd41	blood
28	chr7:110155000-110155400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:110155200-110155400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:110155400-110156000	Enhancers	Right Atrium	heart
31	chr7:110155400-110156000	Genic enhancers	Dnd41	blood
32	chr7:110155400-110162600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:110155600-110155800	Enhancers	Pancreas	Pancrea
34	chr7:110155800-110158800	Weak transcription	Pancreas	Pancrea
35	chr7:110156000-110157600	Enhancers	Dnd41	blood
36	chr7:110157000-110158800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:110157200-110158600	Enhancers	Liver	Liver
38	chr7:110157400-110157600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:110157600-110158400	Weak transcription	Dnd41	blood
40	chr7:110158400-110161600	ZNF genes & repeats	Dnd41	blood
41	chr7:110158600-110161000	Weak transcription	Liver	Liver
42	chr7:110158800-110159400	ZNF genes & repeats	Pancreas	Pancrea
43	chr7:110158800-110159800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:110158800-110160200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:110159400-110161600	Weak transcription	Pancreas	Pancrea
46	chr7:110159800-110170400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:110160000-110160200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
48	chr7:110160200-110163000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr7:110160800-110163600	Enhancers	HepG2	liver
50	chr7:110160800-110163800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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