Variant report

Variant	nsv1019911
Chromosome Location	chr7:110505973-110570241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:245)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:110559170-110559447	GM12878	blood:	n/a	n/a
2	BACH1	chr7:110566972-110567002	K562	blood:	n/a	n/a
3	BATF	chr7:110559152-110559518	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
4	BATF	chr7:110559184-110559475	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
5	BATF	chr7:110554297-110554621	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:110559197-110559496	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:110559122-110559539	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:110559153-110559472	GM12878	blood:	n/a	n/a
9	CCNT2	chr7:110511063-110511211	K562	blood:	n/a	n/a
10	CEBPB	chr7:110506417-110506734	HepG2	liver:	n/a	chr7:110506562-110506573
11	CEBPB	chr7:110524419-110524763	HepG2	liver:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
12	CEBPB	chr7:110562920-110563368	A549	lung:	n/a	n/a
13	CEBPB	chr7:110524467-110524738	A549	lung:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
14	CEBPB	chr7:110561985-110562300	IMR90	lung:	n/a	chr7:110562028-110562041
15	CEBPB	chr7:110524427-110524734	K562	blood:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
16	CEBPB	chr7:110506562-110506564	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:110529398-110529581	K562	blood:	n/a	n/a
18	CEBPB	chr7:110524438-110524770	IMR90	lung:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
19	CEBPB	chr7:110506409-110506739	H1-hESC	embryonic stem cell:	n/a	chr7:110506562-110506573
20	CEBPB	chr7:110562932-110563401	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:110563061-110563322	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:110529337-110529519	A549	lung:	n/a	n/a
23	CEBPB	chr7:110562837-110563369	MCF-7	breast:	n/a	n/a
24	CHD2	chr7:110559239-110559431	GM12878	blood:	n/a	n/a
25	CTCF	chr7:110511100-110511250	BE2_C	brain:	n/a	n/a
26	CTCF	chr7:110529460-110529610	A549	lung:	n/a	n/a
27	CTCF	chr7:110511033-110511282	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:110511101-110511277	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:110567981-110567988	K562	blood:	n/a	n/a
30	CTCF	chr7:110529320-110529470	BE2_C	brain:	n/a	n/a
31	CTCF	chr7:110529387-110529474	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:110511120-110511270	BE2_C	brain:	n/a	n/a
33	CTCF	chr7:110511184-110511222	Medullo	brain:	n/a	n/a
34	CTCF	chr7:110511060-110511210	A549	lung:	n/a	n/a
35	CTCF	chr7:110529440-110529590	K562	blood:	n/a	n/a
36	CTCF	chr7:110506465-110506555	GM20000	blood:	n/a	n/a
37	CTCF	chr7:110511173-110511258	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr7:110567060-110567210	GM12872	blood:	n/a	n/a
39	CTCF	chr7:110529360-110529510	RPTEC	kidney:	n/a	n/a
40	CTCF	chr7:110529416-110529477	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:110511120-110511270	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:110511200-110511350	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:110529420-110529570	MCF-7	breast:	n/a	n/a
44	CUX1	chr7:110528611-110528634	K562	blood:	n/a	n/a
45	CUX1	chr7:110559414-110559446	GM12878	blood:	n/a	n/a
46	CUX1	chr7:110556118-110556195	K562	blood:	n/a	n/a
47	E2F4	chr7:110562988-110563388	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr7:110518639-110518839	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr7:110534332-110534518	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr7:110567941-110568080	MCF10A-Er-Src	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110511335-110511385	LNCaP	prostate:	n/a
2	chr7:110511335-110511385	LNCaP	prostate:	n/a
3	chr7:110547138-110547188	PrEC	prostate:	n/a
4	chr7:110511335-110511385	BJ	skin:	n/a
5	chr7:110562986-110563036	SK-N-SH	brain:	n/a
6	chr7:110511335-110511385	BE2_C	brain:	n/a
7	chr7:110506411-110506461	H1-hESC	embryonic stem cell:	embryo
8	chr7:110562986-110563036	GM12892	blood:	n/a
9	chr7:110511335-110511385	SAEC	small airway:	n/a
10	chr7:110511335-110511385	NB4	blood:	n/a
11	chr7:110506411-110506461	SKMC	muscle:	n/a
12	chr7:110511335-110511385	HNPCEpiC	eye:	n/a
13	chr7:110547138-110547188	LNCaP	prostate:	n/a
14	chr7:110506411-110506461	NHBE	bronchial:	n/a
15	chr7:110506411-110506461	A549	lung:	n/a
16	chr7:110506411-110506461	AG09309	skin:	n/a
17	chr7:110547138-110547188	SK-N-SH_RA	brain:	n/a
18	chr7:110511335-110511385	RPTEC	kidney:	n/a
19	chr7:110547138-110547188	AG09319	gingival:	n/a
20	chr7:110547138-110547188	Hepatocyte	liver:	n/a
21	chr7:110547138-110547188	H1-hESC	embryonic stem cell:	embryo
22	chr7:110511335-110511385	PFSK-1	brain:	n/a
23	chr7:110506411-110506461	GM12878	blood:	n/a
24	chr7:110547138-110547188	AG04450	lung:	fetal
25	chr7:110562986-110563036	GM19239	blood:	n/a
26	chr7:110562986-110563036	Jurkat	blood:	n/a
27	chr7:110562986-110563036	NHDF-neo	bronchial:	n/a
28	chr7:110547138-110547188	HUVEC	blood vessel:	n/a
29	chr7:110562986-110563036	H1-hESC	embryonic stem cell:	embryo
30	chr7:110547138-110547188	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:110547138-110547188	HRPEpiC	eye:	n/a
32	chr7:110506411-110506461	AG04449	skin:	fetal
33	chr7:110511335-110511385	Hela-S3	cervix:	n/a
34	chr7:110547138-110547188	NHDF-neo	bronchial:	n/a
35	chr7:110511335-110511385	SK-N-MC	brain:	n/a
36	chr7:110547138-110547188	PFSK-1	brain:	n/a
37	chr7:110511335-110511385	U87	brain:	n/a
38	chr7:110547138-110547188	NH-A	brain:	n/a
39	chr7:110506411-110506461	AG10803	skin:	n/a
40	chr7:110511335-110511385	ECC-1	luminal epithelium:	n/a
41	chr7:110547138-110547188	SK-N-SH	brain:	n/a
42	chr7:110506411-110506461	NH-A	brain:	n/a
43	chr7:110506411-110506461	GM19239	blood:	n/a
44	chr7:110506411-110506461	Caco-2	colon:	n/a
45	chr7:110506411-110506461	SK-N-MC	brain:	n/a
46	chr7:110506411-110506461	HRPEpiC	eye:	n/a
47	chr7:110562986-110563036	HCPEpiC	choroid plexus:	n/a
48	chr7:110562986-110563036	HUVEC	blood vessel:	n/a
49	chr7:110562986-110563036	AoSMC	blood vessel:	n/a
50	chr7:110547138-110547188	HCM	heart:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:110505153..110508497-chr7:110509523..110512758,4	K562	blood:
2	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
3	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
4	chr7:110506997..110509461-chr7:110511258..110513064,2	K562	blood:
5	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
6	chr7:110506997..110509461-chr7:110511258..110513064,2	K562	blood:
7	chr7:110514426..110517089-chr7:110544753..110547740,2	K562	blood:
8	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
9	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
10	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
11	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
12	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
13	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:
14	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
15	chr7:110505153..110508497-chr7:110509523..110512758,4	K562	blood:
16	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
17	chr1:244816363..244816913-chr7:110550021..110550823,2	MCF-7	breast:
18	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
19	chr7:110497630..110499420-chr7:110504943..110507709,2	K562	blood:
20	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
21	chr6:22768459..22769224-chr7:110535482..110536237,2	MCF-7	breast:
22	chr7:110514426..110517089-chr7:110544753..110547740,2	K562	blood:
23	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
24	chr7:110562762..110564605-chr7:110608157..110609660,2	K562	blood:
25	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
26	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
27	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000221279	TF binding region
ENSG00000221279	CpG island
ENSG00000121644	chromatin interactions

Extended variants
information (count: 1655 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1655 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17158058	chr7:110505973-110505974	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142760410	chr7:110506011-110506012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555932939	chr7:110506028-110506029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10235732	chr7:110506045-110506046	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs112689503	chr7:110506094-110506095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10235831	chr7:110506097-110506098	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182984678	chr7:110506152-110506153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563662332	chr7:110506162-110506163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532494745	chr7:110506244-110506245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552165013	chr7:110506256-110506257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186703411	chr7:110506352-110506353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567730274	chr7:110506353-110506354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535039993	chr7:110506366-110506367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147341611	chr7:110506369-110506370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548271240	chr7:110506394-110506395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567776484	chr7:110506411-110506412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536742722	chr7:110506412-110506413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550210964	chr7:110506419-110506420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191848549	chr7:110506451-110506452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539355259	chr7:110506492-110506493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184026967	chr7:110506578-110506579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544041548	chr7:110506585-110506586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572620791	chr7:110506697-110506698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139458060	chr7:110506698-110506699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555107734	chr7:110506710-110506711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7780566	chr7:110506712-110506713	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs78008024	chr7:110506809-110506810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189114405	chr7:110506914-110506915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577151891	chr7:110506915-110506916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546102031	chr7:110506943-110506944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193020332	chr7:110506986-110506987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551667189	chr7:110506995-110506996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556953650	chr7:110507005-110507006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528298542	chr7:110507006-110507007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77011358	chr7:110507010-110507011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10240065	chr7:110507051-110507052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs17158071	chr7:110507124-110507125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs78524388	chr7:110507166-110507167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550247790	chr7:110507193-110507194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528496547	chr7:110507195-110507196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34664563	chr7:110507247-110507248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114745694	chr7:110507310-110507311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532761400	chr7:110507397-110507398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149469709	chr7:110507401-110507402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566198719	chr7:110507410-110507411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575130878	chr7:110507484-110507485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185158231	chr7:110507518-110507519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555248805	chr7:110507564-110507565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144384623	chr7:110507625-110507626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190798524	chr7:110507653-110507654	Weak transcription 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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110503600-110508400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:110505400-110506600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr7:110505400-110506600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:110505600-110506000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:110505600-110506000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:110505600-110506200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:110506000-110506400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:110506000-110511000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr7:110506200-110506800	Enhancers	Dnd41	blood
10	chr7:110506200-110507600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:110506400-110506600	Enhancers	H9 Cell Line	embryonic stem cell
12	chr7:110506400-110506600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:110506400-110506600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:110506600-110507800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:110506600-110507800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr7:110506600-110511000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:110506600-110511200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:110506600-110512200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr7:110507400-110508200	Weak transcription	Primary T cells from cord blood	blood
20	chr7:110507600-110508600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:110507800-110508000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:110507800-110508000	Enhancers	Fetal Thymus	thymus
23	chr7:110507800-110508200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:110507800-110508200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:110507800-110508400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr7:110508000-110508800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr7:110508000-110511200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr7:110508200-110508400	Enhancers	Primary T cells from cord blood	blood
29	chr7:110508200-110511000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr7:110508400-110508800	Enhancers	Colon Smooth Muscle	Colon
31	chr7:110508400-110508800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr7:110508400-110509000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:110508400-110509000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr7:110508400-110509400	Weak transcription	Primary T cells from cord blood	blood
35	chr7:110508400-110510800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr7:110508800-110512800	Weak transcription	Psoas Muscle	Psoas
37	chr7:110509400-110510200	Enhancers	Primary T cells from cord blood	blood
38	chr7:110510000-110513000	Enhancers	Fetal Thymus	thymus
39	chr7:110510200-110510600	Weak transcription	Primary T cells from cord blood	blood
40	chr7:110510200-110511600	Enhancers	Aorta	Aorta
41	chr7:110510600-110511200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:110510600-110511600	Enhancers	Dnd41	blood
43	chr7:110510600-110511800	Enhancers	Primary T cells from cord blood	blood
44	chr7:110510800-110511800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:110510800-110512600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr7:110510800-110512600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:110511000-110511800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:110511000-110512800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr7:110511000-110512800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr7:110511200-110511600	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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