Variant report

Variant	nsv888966
Chromosome Location	chr7:110127814-110183622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 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	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	chr7:110162678-110163384	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	chr7:110169268-110169575	A549	lung:	n/a	chr7:110169430-110169441
9	CEBPB	chr7:110128091-110128277	K562	blood:	n/a	chr7:110128163-110128174
10	CEBPB	chr7:110128264-110128268	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr7:110169270-110169612	IMR90	lung:	n/a	chr7:110169430-110169441
12	CEBPB	chr7:110128025-110128284	IMR90	lung:	n/a	chr7:110128163-110128174
13	CEBPB	chr7:110171283-110171565	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:110128025-110128320	A549	lung:	n/a	chr7:110128163-110128174
15	CEBPB	chr7:110169245-110169615	HepG2	liver:	n/a	chr7:110169430-110169441
16	CEBPB	chr7:110127997-110128340	HepG2	liver:	n/a	chr7:110128163-110128174
17	CEBPB	chr7:110182130-110182398	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:110161316-110161827	HepG2	liver:	n/a	chr7:110161465-110161478
19	CEBPB	chr7:110169292-110169556	Hela-S3	cervix:	n/a	chr7:110169430-110169441
20	CEBPB	chr7:110179284-110179632	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:110182172-110182372	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:110176259-110176422	HepG2	liver:	n/a	chr7:110176317-110176328 chr7:110176319-110176330 chr7:110176317-110176330 chr7:110176317-110176330
23	CEBPB	chr7:110169305-110169550	HepG2	liver:	n/a	chr7:110169430-110169441
24	CEBPB	chr7:110132132-110132277	IMR90	lung:	n/a	chr7:110132184-110132195
25	CEBPB	chr7:110162913-110163306	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:110162874-110163235	A549	lung:	n/a	n/a
27	CEBPB	chr7:110132045-110132280	HepG2	liver:	n/a	chr7:110132184-110132195
28	CEBPB	chr7:110168937-110169627	HepG2	liver:	n/a	chr7:110169430-110169441
29	CEBPB	chr7:110162775-110163289	A549	lung:	n/a	n/a
30	CEBPB	chr7:110166663-110166922	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPD	chr7:110169295-110169515	HepG2	liver:	n/a	n/a
32	CEBPD	chr7:110162957-110163255	HepG2	liver:	n/a	n/a
33	CREB1	chr7:110162749-110163280	HepG2	liver:	n/a	n/a
34	CREB1	chr7:110162960-110163204	A549	lung:	n/a	n/a
35	CREB1	chr7:110162763-110163354	HepG2	liver:	n/a	n/a
36	CTCF	chr7:110174820-110174970	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
37	CTCF	chr7:110174820-110174970	HEEpiC	esophagus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
38	CTCF	chr7:110174760-110174910	AG04450	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
39	CTCF	chr7:110174752-110174933	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
40	CTCF	chr7:110158870-110158908	GM20000	blood:	n/a	n/a
41	CTCF	chr7:110174722-110174989	A549	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
42	CTCF	chr7:110174660-110174950	NHEK	skin:	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	chr7:110174777-110174948	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
45	CTCF	chr7:110174780-110174930	SAEC	small airway:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
46	CTCF	chr7:110159697-110159754	Fibrobl	skin:	n/a	n/a
47	CTCF	chr7:110163060-110163210	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:110174780-110174930	BE2_C	brain:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
49	CTCF	chr7:110155363-110155437	GM13976	blood:	n/a	n/a
50	CTCF	chr7:110174760-110174910	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110174780-110174830	NHDF-neo	bronchial:	n/a
2	chr7:110174780-110174830	HCM	heart:	n/a
3	chr7:110174780-110174830	AG09309	skin:	n/a
4	chr7:110174780-110174830	H1-hESC	embryonic stem cell:	embryo
5	chr7:110174780-110174830	HEK293	kidney:	embryo
6	chr7:110174780-110174830	ECC-1	luminal epithelium:	n/a
7	chr7:110174780-110174830	HUVEC	blood vessel:	n/a
8	chr7:110174780-110174830	ProgFib	skin:	n/a
9	chr7:110174780-110174830	SK-N-SH_RA	brain:	n/a
10	chr7:110174780-110174830	GM12891	blood:	n/a
11	chr7:110174780-110174830	IMR90	lung:	fetal
12	chr7:110174780-110174830	MCF-7	breast:	n/a
13	chr7:110174780-110174830	HL-60	blood:	n/a
14	chr7:110174780-110174830	HNPCEpiC	eye:	n/a
15	chr7:110174780-110174830	PrEC	prostate:	n/a
16	chr7:110174780-110174830	U87	brain:	n/a
17	chr7:110174780-110174830	SK-N-MC	brain:	n/a
18	chr7:110174780-110174830	BJ	skin:	n/a
19	chr7:110174780-110174830	GM12892	blood:	n/a
20	chr7:110174780-110174830	HCT-116	colon:	n/a
21	chr7:110174780-110174830	AG04450	lung:	fetal
22	chr7:110174780-110174830	NH-A	brain:	n/a
23	chr7:110174780-110174830	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:110174780-110174830	PANC-1	pancreas:	n/a
25	chr7:110174780-110174830	HMEC	breast:	n/a
26	chr7:110174780-110174830	SAEC	small airway:	n/a
27	chr7:110174780-110174830	Jurkat	blood:	n/a
28	chr7:110174780-110174830	RPTEC	kidney:	n/a
29	chr7:110174780-110174830	HCPEpiC	choroid plexus:	n/a
30	chr7:110174780-110174830	LNCaP	prostate:	n/a
31	chr7:110174780-110174830	CMK	blood:	n/a
32	chr7:110174780-110174830	HRPEpiC	eye:	n/a
33	chr7:110174780-110174830	AG04449	skin:	fetal
34	chr7:110174780-110174830	AG10803	skin:	n/a
35	chr7:110174780-110174830	HRCEpiC	kidney:	n/a
36	chr7:110174780-110174830	AG09319	gingival:	n/a
37	chr7:110174780-110174830	NHBE	bronchial:	n/a
38	chr7:110174780-110174830	Hepatocyte	liver:	n/a
39	chr7:110174780-110174830	Hela-S3	cervix:	n/a
40	chr7:110174780-110174830	GM06990	blood:	n/a
41	chr7:110174780-110174830	GM12878	blood:	n/a
42	chr7:110174780-110174830	PFSK-1	brain:	n/a
43	chr7:110174780-110174830	HEEpiC	esophagus:	n/a
44	chr7:110174780-110174830	HAEpiC	amniotic membrane:	n/a
45	chr7:110174780-110174830	HRE	kidney:	n/a
46	chr7:110174780-110174830	SK-N-SH	brain:	n/a
47	chr7:110174780-110174830	K562	blood:	n/a
48	chr7:110174780-110174830	GM19239	blood:	n/a
49	chr7:110174780-110174830	A549	lung:	n/a
50	chr7:110174780-110174830	ovcar-3	ovarian:	n/a

(count:16 , 50 per page) page: 1

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

(count:5 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2094 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2094 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2966404	chr7:110127814-110127815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571917441	chr7:110127899-110127900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564595424	chr7:110127925-110127926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77046576	chr7:110128015-110128016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546996011	chr7:110128076-110128077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10275471	chr7:110128091-110128092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs10275476	chr7:110128094-110128095	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549260147	chr7:110128113-110128114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138638285	chr7:110128168-110128169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190413972	chr7:110128204-110128205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72203279	chr7:110128300-110128301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546947254	chr7:110128310-110128311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78905066	chr7:110128313-110128314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74917474	chr7:110128314-110128315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112800024	chr7:110128324-110128325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551331227	chr7:110128338-110128339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571297059	chr7:110128343-110128344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533674687	chr7:110128352-110128353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553317323	chr7:110128378-110128379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573323760	chr7:110128382-110128383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs386716811	chr7:110128405-110128406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112735061	chr7:110128406-110128407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7792588	chr7:110128407-110128408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77554946	chr7:110128426-110128427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544789570	chr7:110128469-110128470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7792740	chr7:110128474-110128475	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs112474133	chr7:110128516-110128517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540748786	chr7:110128528-110128529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560478095	chr7:110128573-110128574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529310851	chr7:110128591-110128592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180750872	chr7:110128604-110128605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531534663	chr7:110128624-110128625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530462284	chr7:110128659-110128660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571125129	chr7:110128700-110128701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536379392	chr7:110128718-110128719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144317094	chr7:110128723-110128724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148380742	chr7:110128724-110128725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142217180	chr7:110128744-110128745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554535639	chr7:110128785-110128786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536236722	chr7:110128830-110128831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555933381	chr7:110128883-110128884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186054063	chr7:110128907-110128908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377269464	chr7:110128915-110128916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146310645	chr7:110128925-110128926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558300443	chr7:110128959-110128960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578230968	chr7:110129086-110129087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540688055	chr7:110129093-110129094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554295530	chr7:110129109-110129110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534204828	chr7:110129119-110129120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12705695	chr7:110129145-110129146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110126400-110133400	Weak transcription	Dnd41	blood
2	chr7:110133400-110133600	ZNF genes & repeats	Dnd41	blood
3	chr7:110133600-110137200	Weak transcription	Dnd41	blood
4	chr7:110137200-110138800	Strong transcription	Dnd41	blood
5	chr7:110138800-110141200	Weak transcription	Dnd41	blood
6	chr7:110141200-110142200	Genic enhancers	Dnd41	blood
7	chr7:110142200-110142400	Enhancers	Dnd41	blood
8	chr7:110142200-110144600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr7:110142400-110143800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:110142400-110143800	Flanking Active TSS	Dnd41	blood
11	chr7:110142800-110143000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:110143000-110143600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:110143000-110143600	Enhancers	HMEC	breast
14	chr7:110143200-110143600	Enhancers	Primary hematopoietic stem cells	blood
15	chr7:110143200-110143600	Enhancers	NHEK	skin
16	chr7:110143800-110144600	Enhancers	Dnd41	blood
17	chr7:110144600-110144800	Flanking Active TSS	Dnd41	blood
18	chr7:110144800-110146200	Enhancers	Dnd41	blood
19	chr7:110146200-110147000	Genic enhancers	Dnd41	blood
20	chr7:110147000-110149800	Enhancers	Dnd41	blood
21	chr7:110148000-110148400	Enhancers	Liver	Liver
22	chr7:110149800-110150200	Weak transcription	Dnd41	blood
23	chr7:110150200-110150400	Enhancers	Dnd41	blood
24	chr7:110150400-110151200	Weak transcription	Dnd41	blood
25	chr7:110151200-110152600	Genic enhancers	Dnd41	blood
26	chr7:110152200-110152400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:110152600-110154600	Weak transcription	Dnd41	blood
28	chr7:110154600-110155400	Enhancers	Dnd41	blood
29	chr7:110155000-110155400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:110155200-110155400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:110155400-110156000	Enhancers	Right Atrium	heart
32	chr7:110155400-110156000	Genic enhancers	Dnd41	blood
33	chr7:110155400-110162600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:110155600-110155800	Enhancers	Pancreas	Pancrea
35	chr7:110155800-110158800	Weak transcription	Pancreas	Pancrea
36	chr7:110156000-110157600	Enhancers	Dnd41	blood
37	chr7:110157000-110158800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:110157200-110158600	Enhancers	Liver	Liver
39	chr7:110157400-110157600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:110157600-110158400	Weak transcription	Dnd41	blood
41	chr7:110158400-110161600	ZNF genes & repeats	Dnd41	blood
42	chr7:110158600-110161000	Weak transcription	Liver	Liver
43	chr7:110158800-110159400	ZNF genes & repeats	Pancreas	Pancrea
44	chr7:110158800-110159800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:110158800-110160200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:110159400-110161600	Weak transcription	Pancreas	Pancrea
47	chr7:110159800-110170400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:110160000-110160200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
49	chr7:110160200-110163000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr7:110160800-110163600	Enhancers	HepG2	liver

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