Variant report

Variant	esv2759554
Chromosome Location	chr7:110523298-110787849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2038)
CpG islands
(count:856)
Chromatin interactive
region (count:91)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2038 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110767136-110767361	K562	blood:	n/a	n/a
2	ARID3A	chr7:110665042-110665376	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:110714027-110714511	K562	blood:	n/a	n/a
4	ARID3A	chr7:110634723-110635192	K562	blood:	n/a	n/a
5	ARID3A	chr7:110666350-110666597	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:110707368-110708116	K562	blood:	n/a	n/a
7	ARID3A	chr7:110738705-110739063	K562	blood:	n/a	n/a
8	ARID3A	chr7:110714785-110715097	K562	blood:	n/a	n/a
9	ARID3A	chr7:110668832-110669461	HepG2	liver:	n/a	chr7:110669031-110669047
10	ARID3A	chr7:110748723-110748958	HepG2	liver:	n/a	chr7:110748905-110748921
11	ARID3A	chr7:110729855-110730276	K562	blood:	n/a	n/a
12	ATF1	chr7:110634674-110635014	K562	blood:	n/a	n/a
13	ATF1	chr7:110707277-110707577	K562	blood:	n/a	n/a
14	ATF1	chr7:110767089-110767407	K562	blood:	n/a	n/a
15	ATF1	chr7:110594853-110594948	K562	blood:	n/a	n/a
16	ATF1	chr7:110725357-110725359	K562	blood:	n/a	n/a
17	ATF2	chr7:110723284-110723973	GM12878	blood:	n/a	n/a
18	ATF2	chr7:110777861-110778654	GM12878	blood:	n/a	n/a
19	ATF2	chr7:110778132-110778718	GM12878	blood:	n/a	n/a
20	ATF2	chr7:110753630-110754135	GM12878	blood:	n/a	n/a
21	ATF2	chr7:110559170-110559447	GM12878	blood:	n/a	n/a
22	ATF2	chr7:110669473-110669931	GM12878	blood:	n/a	n/a
23	ATF2	chr7:110669475-110670098	GM12878	blood:	n/a	n/a
24	ATF2	chr7:110753575-110754112	GM12878	blood:	n/a	n/a
25	ATF2	chr7:110737027-110737471	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr7:110723314-110723993	GM12878	blood:	n/a	n/a
27	ATF3	chr7:110634636-110635037	K562	blood:	n/a	n/a
28	ATF3	chr7:110714103-110714516	K562	blood:	n/a	n/a
29	ATF3	chr7:110753707-110753971	K562	blood:	n/a	n/a
30	ATF3	chr7:110629178-110629445	K562	blood:	n/a	n/a
31	BACH1	chr7:110566972-110567002	K562	blood:	n/a	n/a
32	BACH1	chr7:110730041-110730145	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr7:110707871-110708042	K562	blood:	n/a	n/a
34	BACH1	chr7:110584962-110585666	H1-hESC	embryonic stem cell:	n/a	chr7:110585569-110585583
35	BATF	chr7:110559152-110559518	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
36	BATF	chr7:110777879-110778565	GM12878	blood:	n/a	n/a
37	BATF	chr7:110665136-110665403	GM12878	blood:	n/a	n/a
38	BATF	chr7:110753698-110753996	GM12878	blood:	n/a	chr7:110753878-110753891
39	BATF	chr7:110748731-110748903	GM12878	blood:	n/a	chr7:110748817-110748828
40	BATF	chr7:110653358-110653749	GM12878	blood:	n/a	n/a
41	BATF	chr7:110723453-110723935	GM12878	blood:	n/a	n/a
42	BATF	chr7:110723453-110723867	GM12878	blood:	n/a	n/a
43	BATF	chr7:110554297-110554621	GM12878	blood:	n/a	n/a
44	BATF	chr7:110559184-110559475	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
45	BATF	chr7:110669545-110669924	GM12878	blood:	n/a	chr7:110669743-110669752
46	BATF	chr7:110778240-110778523	GM12878	blood:	n/a	n/a
47	BATF	chr7:110653407-110653722	GM12878	blood:	n/a	n/a
48	BATF	chr7:110743737-110744141	GM12878	blood:	n/a	n/a
49	BATF	chr7:110725456-110725718	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:110559197-110559496	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110731201-110731251	LNCaP	prostate:	n/a
2	chr7:110658544-110658594	Hepatocyte	liver:	n/a
3	chr7:110731201-110731251	LNCaP	prostate:	n/a
4	chr7:110658544-110658594	Hepatocyte	liver:	n/a
5	chr7:110731527-110731577	Caco-2	colon:	n/a
6	chr7:110730805-110730855	HEEpiC	esophagus:	n/a
7	chr7:110722380-110722430	Jurkat	blood:	n/a
8	chr7:110658544-110658594	ovcar-3	ovarian:	n/a
9	chr7:110693055-110693105	HCPEpiC	choroid plexus:	n/a
10	chr7:110658544-110658594	HIPEpiC	eye:	n/a
11	chr7:110693055-110693105	ECC-1	luminal epithelium:	n/a
12	chr7:110738315-110738365	U87	brain:	n/a
13	chr7:110730805-110730855	HMEC	breast:	n/a
14	chr7:110585140-110585190	HCM	heart:	n/a
15	chr7:110753971-110754021	Hela-S3	cervix:	n/a
16	chr7:110562986-110563036	HEK293	kidney:	embryo
17	chr7:110730805-110730855	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:110658544-110658594	NH-A	brain:	n/a
19	chr7:110731201-110731251	HIPEpiC	eye:	n/a
20	chr7:110562986-110563036	AoSMC	blood vessel:	n/a
21	chr7:110722380-110722430	NHDF-neo	bronchial:	n/a
22	chr7:110730805-110730855	BJ	skin:	n/a
23	chr7:110731201-110731251	ovcar-3	ovarian:	n/a
24	chr7:110738315-110738365	AG04449	skin:	fetal
25	chr7:110731527-110731577	RPTEC	kidney:	n/a
26	chr7:110731201-110731251	GM12878	blood:	n/a
27	chr7:110693055-110693105	HIPEpiC	eye:	n/a
28	chr7:110658544-110658594	HCPEpiC	choroid plexus:	n/a
29	chr7:110731527-110731577	T-47D	breast:	n/a
30	chr7:110585140-110585190	BJ	skin:	n/a
31	chr7:110753971-110754021	SAEC	small airway:	n/a
32	chr7:110731201-110731251	HCM	heart:	n/a
33	chr7:110738836-110738886	Caco-2	colon:	n/a
34	chr7:110722380-110722430	RPTEC	kidney:	n/a
35	chr7:110547138-110547188	Caco-2	colon:	n/a
36	chr7:110764536-110764586	NHDF-neo	bronchial:	n/a
37	chr7:110731527-110731577	PrEC	prostate:	n/a
38	chr7:110730805-110730855	HepG2	liver:	n/a
39	chr7:110730805-110730855	GM12891	blood:	n/a
40	chr7:110658544-110658594	AoSMC	blood vessel:	n/a
41	chr7:110658544-110658594	GM12892	blood:	n/a
42	chr7:110562986-110563036	U87	brain:	n/a
43	chr7:110547138-110547188	SK-N-MC	brain:	n/a
44	chr7:110693055-110693105	ovcar-3	ovarian:	n/a
45	chr7:110738836-110738886	HEK293	kidney:	embryo
46	chr7:110730805-110730855	NHDF-neo	bronchial:	n/a
47	chr7:110585140-110585190	AG09319	gingival:	n/a
48	chr7:110738836-110738886	HCT-116	colon:	n/a
49	chr7:110547138-110547188	MCF10A-Er-Src	breast:	n/a
50	chr7:110693055-110693105	ProgFib	skin:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:110699046..110701763-chr7:110705311..110708989,4	K562	blood:
2	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
3	chr7:110729473..110730895-chr7:111126285..111127252,5	MCF-7	breast:
4	chr7:110679780..110681548-chr7:110685158..110686912,2	K562	blood:
5	chr7:110644466..110647207-chr7:110661227..110663752,2	MCF-7	breast:
6	chr7:110738735..110741219-chr7:110742996..110745706,3	K562	blood:
7	chr7:110780555..110783082-chr7:110783527..110786521,2	K562	blood:
8	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
9	chr7:110685337..110687591-chr7:111322599..111325063,2	K562	blood:
10	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:
11	chr7:110749058..110751591-chr7:110755370..110758452,3	K562	blood:
12	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
13	chr7:110650313..110653197-chr7:110655896..110658694,2	K562	blood:
14	chr7:110684762..110686902-chr7:110689607..110691796,2	K562	blood:
15	chr7:110699046..110700709-chr7:110705786..110708655,2	K562	blood:
16	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
17	chr7:110630007..110632205-chr7:110633801..110636131,2	K562	blood:
18	chr7:110645729..110647636-chr7:110649973..110652991,3	K562	blood:
19	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
20	chr7:110707719..110710533-chr7:110715072..110716624,2	K562	blood:
21	chr7:110766284..110768061-chr7:110775175..110776979,2	K562	blood:
22	chr7:110780555..110783082-chr7:110783527..110786521,2	K562	blood:
23	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
24	chr7:110641915..110646048-chr7:110658516..110661977,3	K562	blood:
25	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
26	chr7:110562762..110564605-chr7:110608157..110609660,2	K562	blood:
27	chr7:110734986..110737421-chr7:110741175..110743179,2	K562	blood:
28	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
29	chr7:110726126..110728780-chr7:110733291..110735049,2	K562	blood:
30	chr7:110654683..110656937-chr7:110658000..110660146,2	K562	blood:
31	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:
32	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:
33	chr7:110784339..110787250-chr7:110788420..110790472,2	K562	blood:
34	chr7:110645729..110647636-chr7:110649973..110652991,3	K562	blood:
35	chr7:110667611..110669471-chr7:110672812..110675111,2	K562	blood:
36	chr7:110707719..110710533-chr7:110715072..110716624,2	K562	blood:
37	chr7:110755598..110757748-chr7:110758221..110760832,2	K562	blood:
38	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
39	chr7:110730162..110730849-chr7:111126372..111127229,2	MCF-7	breast:
40	chr7:110642788..110644757-chr7:111200772..111203526,2	K562	blood:
41	chr7:110730146..110732609-chr7:110768211..110770026,2	K562	blood:
42	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
43	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
44	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
45	chr7:110634034..110636972-chr7:110638479..110640199,3	K562	blood:
46	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
47	chr7:110667611..110669471-chr7:110672812..110675111,2	K562	blood:
48	chr7:110654683..110656937-chr7:110658000..110660146,2	K562	blood:
49	chr7:110684762..110686902-chr7:110689607..110691796,2	K562	blood:
50	chr7:110634034..110636972-chr7:110638479..110640199,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF277-4	chr7:110731150-110731560	NONHSAT122768
2	lnc-ZNF277-4	chr7:110737226-110737372	NONHSAT122768

No data

Variant related genes	Relation type
ENSG00000238922	TF binding region
IMMP2L	TF binding region
ENSG00000221279	TF binding region
LRRN3	TF binding region
ENSG00000238922	CpG island
IMMP2L	CpG island
ENSG00000221279	CpG island
LRRN3	CpG island
ENSG00000121644	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000238922	chromatin interactions

Extended variants
information (count: 8997 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:8997 , 50 per page) page: 1 2 3 4 5 6 7 ... 180

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556436183	chr7:110528014-110528015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115881298	chr7:110528015-110528016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139648337	chr7:110528033-110528034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559918657	chr7:110528045-110528046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573310834	chr7:110528084-110528085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116295081	chr7:110528112-110528113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192056156	chr7:110528163-110528164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143671762	chr7:110528164-110528165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183942439	chr7:110528165-110528166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75162436	chr7:110528166-110528167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17158114	chr7:110528168-110528169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149712443	chr7:110528178-110528179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533275603	chr7:110528232-110528233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549625161	chr7:110528257-110528258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189692553	chr7:110528270-110528271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372826976	chr7:110528277-110528278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182698102	chr7:110528286-110528287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566666322	chr7:110528293-110528294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529115063	chr7:110528294-110528295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79177219	chr7:110528308-110528309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145573421	chr7:110528322-110528323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569004030	chr7:110528329-110528330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537927108	chr7:110528407-110528408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557803737	chr7:110528462-110528463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571235591	chr7:110528469-110528470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540130430	chr7:110528478-110528479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536032055	chr7:110528520-110528521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573477506	chr7:110528521-110528522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542085455	chr7:110528557-110528558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs258977	chr7:110528567-110528568	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372675952	chr7:110528584-110528585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575350027	chr7:110528587-110528588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544268704	chr7:110528592-110528593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115824166	chr7:110528599-110528600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187344970	chr7:110528648-110528649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540611232	chr7:110528655-110528656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572455357	chr7:110528721-110528722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560235480	chr7:110528739-110528740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192877095	chr7:110528743-110528744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549236009	chr7:110528764-110528765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185274751	chr7:110528768-110528769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139155340	chr7:110528823-110528824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188542625	chr7:110528842-110528843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144044724	chr7:110528848-110528849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193113700	chr7:110528859-110528860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533594607	chr7:110528914-110528915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78708598	chr7:110528991-110528992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567085599	chr7:110528993-110528994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536111478	chr7:110528995-110528996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140790205	chr7:110528998-110528999	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Attention deficit hyperactivity disorder	19546859	CNVD

Chromatin state (count:2291 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110528000-110529000	Enhancers	Fetal Lung	lung
2	chr7:110528200-110528600	Enhancers	Brain Germinal Matrix	brain
3	chr7:110529600-110529800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr7:110529800-110530400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:110530200-110530800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:110530200-110531000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:110530400-110530800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:110530400-110531000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:110531000-110531600	Enhancers	Dnd41	blood
10	chr7:110540400-110540800	Enhancers	HSMMtube	muscle
11	chr7:110541000-110541400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:110542800-110545600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr7:110544800-110546000	Enhancers	Primary T cells from cord blood	blood
14	chr7:110545400-110546400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr7:110545600-110546000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr7:110545600-110546600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr7:110545800-110546600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr7:110546000-110546400	Flanking Active TSS	Primary T cells from cord blood	blood
19	chr7:110546000-110546600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr7:110546000-110546600	Active TSS	Primary T killer memory cells from peripheral blood	blood
21	chr7:110546400-110546600	Enhancers	Primary T cells from cord blood	blood
22	chr7:110549000-110549200	Enhancers	A549	lung
23	chr7:110549000-110549400	Enhancers	Liver	Liver
24	chr7:110549000-110549400	Enhancers	HepG2	liver
25	chr7:110549000-110550200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr7:110549800-110550200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:110550000-110550200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
28	chr7:110550200-110562000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:110552800-110553000	Enhancers	Esophagus	oesophagus
30	chr7:110556000-110561200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr7:110556600-110557000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:110557000-110557400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:110557000-110557600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:110557000-110557800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:110557200-110557400	Enhancers	Esophagus	oesophagus
36	chr7:110557400-110558400	Enhancers	Adipose Nuclei	Adipose
37	chr7:110557400-110559800	Weak transcription	Esophagus	oesophagus
38	chr7:110557400-110561200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:110557600-110561200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:110557800-110558400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:110558400-110560400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:110558400-110561400	Weak transcription	Adipose Nuclei	Adipose
43	chr7:110559400-110559600	Enhancers	GM12878-XiMat	blood
44	chr7:110559400-110560000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr7:110559800-110560200	Enhancers	Esophagus	oesophagus
46	chr7:110560400-110561600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:110561200-110561400	Enhancers	Aorta	Aorta
48	chr7:110561200-110561800	Enhancers	Fetal Lung	lung
49	chr7:110561200-110562000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:110561200-110563800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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