Variant report

Variant	nsv608109
Chromosome Location	chr7:109542198-109642442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:217)
CpG islands
(count:488)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:217 , 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	BACH1	chr7:109590985-109591005	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:109574018-109574056	K562	blood:	n/a	n/a
3	CEBPB	chr7:109600727-109601032	IMR90	lung:	n/a	chr7:109600899-109600910
4	CEBPB	chr7:109600756-109601006	HepG2	liver:	n/a	chr7:109600899-109600910
5	CEBPB	chr7:109600731-109601037	K562	blood:	n/a	chr7:109600899-109600910
6	CEBPB	chr7:109569232-109569428	A549	lung:	n/a	chr7:109569324-109569333 chr7:109569324-109569333 chr7:109569324-109569333
7	CEBPB	chr7:109624910-109625197	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr7:109596973-109597531	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr7:109541285-109542360	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:109569274-109569479	HepG2	liver:	n/a	chr7:109569324-109569333 chr7:109569324-109569333 chr7:109569324-109569333
11	CEBPB	chr7:109595794-109595902	A549	lung:	n/a	n/a
12	CEBPB	chr7:109611851-109612073	A549	lung:	n/a	n/a
13	CEBPB	chr7:109611839-109612086	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:109611846-109612084	IMR90	lung:	n/a	n/a
15	CTCF	chr7:109604771-109604794	ProgFib	skin:	n/a	n/a
16	CTCF	chr7:109606520-109606670	NB4	blood:	n/a	n/a
17	CTCF	chr7:109641840-109641990	BE2_C	brain:	n/a	n/a
18	CTCF	chr7:109543154-109543200	GM13977	blood:	n/a	n/a
19	CTCF	chr7:109579179-109579265	Lung_OC	lung:	n/a	n/a
20	CTCF	chr7:109551945-109552024	LNCaP	prostate:	n/a	n/a
21	CTCF	chr7:109580110-109580146	GM20000	blood:	n/a	n/a
22	E2F4	chr7:109624340-109625130	MCF10A-Er-Src	breast:	n/a	chr7:109624611-109624622
23	E2F4	chr7:109629552-109629572	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr7:109544531-109544548	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr7:109574070-109574232	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr7:109571634-109571811	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr7:109594913-109595113	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F6	chr7:109579331-109579976	H1-hESC	embryonic stem cell:	n/a	n/a
29	E2F6	chr7:109579418-109579812	H1-hESC	embryonic stem cell:	n/a	n/a
30	EP300	chr7:109641487-109642042	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr7:109623766-109624012	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr7:109641633-109642023	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr7:109596585-109597705	ECC-1	luminal epithelium:	n/a	n/a
34	EP300	chr7:109640925-109642949	SK-N-SH	brain:	n/a	chr7:109642399-109642406
35	EP300	chr7:109566449-109567447	SK-N-SH	brain:	n/a	n/a
36	EP300	chr7:109596718-109597626	ECC-1	luminal epithelium:	n/a	n/a
37	EP300	chr7:109623049-109624314	SK-N-SH	brain:	n/a	chr7:109623206-109623216 chr7:109624024-109624038 chr7:109624014-109624028 chr7:109624018-109624032
38	EP300	chr7:109541993-109542339	Hela-S3	cervix:	n/a	n/a
39	EP300	chr7:109566805-109567109	SK-N-SH_RA	brain:	n/a	n/a
40	ESR1	chr7:109596870-109597384	ECC-1	luminal epithelium:	n/a	n/a
41	ESR1	chr7:109596865-109597376	ECC-1	luminal epithelium:	n/a	n/a
42	ESR1	chr7:109596977-109597340	ECC-1	luminal epithelium:	n/a	n/a
43	ESR1	chr7:109591458-109591714	T-47D	breast:	n/a	n/a
44	FOS	chr7:109604909-109605056	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr7:109624673-109625108	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr7:109624737-109625044	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr7:109541944-109542248	MCF10A-Er-Src	breast:	n/a	chr7:109541946-109541958 chr7:109542078-109542087 chr7:109542076-109542088 chr7:109542135-109542144 chr7:109542079-109542086
48	FOS	chr7:109607520-109607818	MCF10A-Er-Src	breast:	n/a	chr7:109607627-109607636 chr7:109607627-109607634
49	FOS	chr7:109607485-109607740	MCF10A-Er-Src	breast:	n/a	chr7:109607627-109607636 chr7:109607627-109607634
50	FOS	chr7:109603960-109604049	MCF10A-Er-Src	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:109600399-109600449	HEEpiC	esophagus:	n/a
2	chr7:109599644-109599694	HAEpiC	amniotic membrane:	n/a
3	chr7:109570287-109570337	GM12878	blood:	n/a
4	chr7:109600733-109600783	SK-N-SH_RA	brain:	n/a
5	chr7:109570287-109570337	NT2-D1	testis:	n/a
6	chr7:109596752-109596802	HCM	heart:	n/a
7	chr7:109585055-109585105	SK-N-SH_RA	brain:	n/a
8	chr7:109599644-109599694	ProgFib	skin:	n/a
9	chr7:109600733-109600783	HEK293	kidney:	embryo
10	chr7:109600591-109600641	AG09309	skin:	n/a
11	chr7:109600591-109600641	ovcar-3	ovarian:	n/a
12	chr7:109600399-109600449	HAEpiC	amniotic membrane:	n/a
13	chr7:109600399-109600449	Hepatocyte	liver:	n/a
14	chr7:109596752-109596802	LNCaP	prostate:	n/a
15	chr7:109570287-109570337	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:109596752-109596802	NHDF-neo	bronchial:	n/a
17	chr7:109600591-109600641	NHBE	bronchial:	n/a
18	chr7:109600399-109600449	MCF10A-Er-Src	breast:	n/a
19	chr7:109570287-109570337	SAEC	small airway:	n/a
20	chr7:109570287-109570337	NB4	blood:	n/a
21	chr7:109596752-109596802	ovcar-3	ovarian:	n/a
22	chr7:109600425-109600475	MCF-7	breast:	n/a
23	chr7:109585055-109585105	HEK293	kidney:	embryo
24	chr7:109570287-109570337	Jurkat	blood:	n/a
25	chr7:109600399-109600449	Hela-S3	cervix:	n/a
26	chr7:109599644-109599694	HCF	heart:	n/a
27	chr7:109570287-109570337	SK-N-SH	brain:	n/a
28	chr7:109599644-109599694	HRE	kidney:	n/a
29	chr7:109599644-109599694	BJ	skin:	n/a
30	chr7:109585055-109585105	H1-hESC	embryonic stem cell:	embryo
31	chr7:109600399-109600449	GM06990	blood:	n/a
32	chr7:109570287-109570337	T-47D	breast:	n/a
33	chr7:109600591-109600641	AG04450	lung:	fetal
34	chr7:109585055-109585105	U87	brain:	n/a
35	chr7:109600591-109600641	HNPCEpiC	eye:	n/a
36	chr7:109585055-109585105	HRCEpiC	kidney:	n/a
37	chr7:109599644-109599694	CMK	blood:	n/a
38	chr7:109600591-109600641	SKMC	muscle:	n/a
39	chr7:109585055-109585105	GM19239	blood:	n/a
40	chr7:109600399-109600449	AoSMC	blood vessel:	n/a
41	chr7:109600425-109600475	AG04449	skin:	fetal
42	chr7:109600591-109600641	HMEC	breast:	n/a
43	chr7:109570287-109570337	PFSK-1	brain:	n/a
44	chr7:109599644-109599694	AG10803	skin:	n/a
45	chr7:109599644-109599694	BE2_C	brain:	n/a
46	chr7:109600591-109600641	HCPEpiC	choroid plexus:	n/a
47	chr7:109600399-109600449	NHBE	bronchial:	n/a
48	chr7:109600733-109600783	Hepatocyte	liver:	n/a
49	chr7:109570287-109570337	HMEC	breast:	n/a
50	chr7:109600733-109600783	K562	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:109537859..109540413-chr7:109543120..109545714,2	K562	blood:
2	chr12:7073001..7074519-chr7:109591479..109593234,2	MCF-7	breast:
3	chr7:109617231..109619713-chr7:109622419..109624214,3	K562	blood:
4	chr7:109621845..109625177-chr7:109626649..109628866,3	K562	blood:
5	chr7:109568885..109571688-chr7:109572507..109574918,2	K562	blood:
6	chr7:109595389..109597303-chr7:109602363..109605295,2	K562	blood:
7	chr7:109617231..109619713-chr7:109622419..109624214,3	K562	blood:
8	chr7:109595389..109597303-chr7:109602363..109605295,2	K562	blood:
9	chr7:109621845..109625177-chr7:109626649..109628866,3	K562	blood:
10	chr7:109568885..109571688-chr7:109572507..109574918,2	K562	blood:
11	chr7:109538440..109540413-chr7:109541881..109544620,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMMP2L-8	chr7:109599284-109600270	NR_003024
2	lnc-IMMP2L-7	chr7:109638491-109639681	NONHSAT122757

No data

Variant related genes	Relation type
RPL3P8	TF binding region
EIF3IP1	TF binding region
RPL3P8	CpG island
EIF3IP1	CpG island
ENSG00000271969	chromatin interactions
ENSG00000207708	chromatin interactions

Extended variants
information (count: 1459 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4552825	chr7:109542198-109542199	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533668932	chr7:109542203-109542204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370284465	chr7:109542220-109542221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186460018	chr7:109542222-109542223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78568649	chr7:109542235-109542236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191051372	chr7:109542250-109542251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183363927	chr7:109542254-109542255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549298017	chr7:109542370-109542371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187351979	chr7:109542395-109542396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534860292	chr7:109542399-109542400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542428844	chr7:109542404-109542405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555735334	chr7:109542439-109542440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575901925	chr7:109542496-109542497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371712836	chr7:109542509-109542510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544279333	chr7:109542514-109542515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192182179	chr7:109542560-109542561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183328637	chr7:109542593-109542594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540700192	chr7:109542598-109542599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7795321	chr7:109542609-109542610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188065177	chr7:109542635-109542636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192644025	chr7:109542639-109542640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549172013	chr7:109542641-109542642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184486874	chr7:109542658-109542659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531677246	chr7:109542665-109542666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189515577	chr7:109542669-109542670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570945166	chr7:109542672-109542673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192604382	chr7:109542697-109542698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560876585	chr7:109542708-109542709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547058690	chr7:109542722-109542723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567356361	chr7:109542741-109542742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536506438	chr7:109565005-109565006	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs556479163	chr7:109565015-109565016	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs576024213	chr7:109565016-109565017	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs139411675	chr7:109565033-109565034	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs112339832	chr7:109565034-109565035	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs193203079	chr7:109565042-109565043	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs569830635	chr7:109565065-109565066	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs185480142	chr7:109565077-109565078	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs386716778	chr7:109565090-109565091	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs74548764	chr7:109565091-109565092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs144806195	chr7:109565107-109565108	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs551850748	chr7:109565108-109565109	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs190783876	chr7:109565117-109565118	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs528125202	chr7:109565118-109565119	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs145799701	chr7:109565124-109565125	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs567510289	chr7:109565125-109565126	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs149008439	chr7:109565133-109565134	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs371079769	chr7:109565151-109565152	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs550039295	chr7:109565154-109565155	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs570049062	chr7:109565160-109565161	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109541400-109542400	Enhancers	Hela-S3	cervix
2	chr7:109541600-109542200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:109541600-109542800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:109541600-109542800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:109541600-109542800	Enhancers	NHDF-Ad	bronchial
6	chr7:109541800-109542400	Enhancers	NHEK	skin
7	chr7:109565000-109566000	ZNF genes & repeats	Dnd41	blood
8	chr7:109565200-109566000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr7:109565200-109566200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:109566000-109567200	Weak transcription	Dnd41	blood
11	chr7:109569800-109570400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:109570000-109570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:109570000-109570600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr7:109570000-109570600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr7:109573000-109573200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:109578200-109578400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr7:109578200-109580000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
18	chr7:109578600-109579600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr7:109578800-109579400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:109579000-109579400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:109579000-109579600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:109579200-109580000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:109579400-109580200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:109579600-109584400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:109580200-109580400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:109580400-109585200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:109584800-109585600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr7:109585000-109585600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:109585000-109585800	Enhancers	Dnd41	blood
30	chr7:109585200-109585400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:109585200-109585600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:109585200-109585600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:109585800-109587000	Flanking Active TSS	Dnd41	blood
34	chr7:109587000-109587800	Enhancers	Dnd41	blood
35	chr7:109590000-109590400	Enhancers	A549	lung
36	chr7:109590200-109590800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:109590400-109591200	Flanking Active TSS	A549	lung
38	chr7:109590400-109591400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:109590800-109596600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr7:109591200-109591400	Enhancers	A549	lung
41	chr7:109594200-109594800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:109595400-109596800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr7:109595400-109596800	Enhancers	Fetal Lung	lung
44	chr7:109596200-109596400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:109596400-109597400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:109596600-109597000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:109596600-109597600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:109596600-109597600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr7:109596800-109597000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:109596800-109597400	Enhancers	HUES48 Cell Line	embryonic stem cell

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