Variant report

Variant	nsv888953
Chromosome Location	chr7:109534349-109648212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:294)
CpG islands
(count:491)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:109643522-109643630	K562	blood:	n/a	n/a
2	ATF1	chr7:109645029-109645204	K562	blood:	n/a	n/a
3	BACH1	chr7:109590985-109591005	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:109574018-109574056	K562	blood:	n/a	n/a
5	BATF	chr7:109647396-109647762	GM12878	blood:	n/a	n/a
6	BCL3	chr7:109647406-109647703	GM12878	blood:	n/a	n/a
7	CEBPB	chr7:109624910-109625197	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr7:109541285-109542360	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr7:109600727-109601032	IMR90	lung:	n/a	chr7:109600899-109600910
10	CEBPB	chr7:109595794-109595902	A549	lung:	n/a	n/a
11	CEBPB	chr7:109569274-109569479	HepG2	liver:	n/a	chr7:109569324-109569333 chr7:109569324-109569333 chr7:109569324-109569333
12	CEBPB	chr7:109596973-109597531	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr7:109611846-109612084	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:109611851-109612073	A549	lung:	n/a	n/a
15	CEBPB	chr7:109569232-109569428	A549	lung:	n/a	chr7:109569324-109569333 chr7:109569324-109569333 chr7:109569324-109569333
16	CEBPB	chr7:109600731-109601037	K562	blood:	n/a	chr7:109600899-109600910
17	CEBPB	chr7:109600756-109601006	HepG2	liver:	n/a	chr7:109600899-109600910
18	CEBPB	chr7:109611839-109612086	HepG2	liver:	n/a	n/a
19	CTCF	chr7:109643982-109644132	LNCaP	prostate:	n/a	n/a
20	CTCF	chr7:109644013-109644117	Medullo	brain:	n/a	n/a
21	CTCF	chr7:109644000-109644167	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:109643841-109644251	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:109580110-109580146	GM20000	blood:	n/a	n/a
24	CTCF	chr7:109644022-109644114	GM12878	blood:	n/a	n/a
25	CTCF	chr7:109644001-109644116	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr7:109644000-109644150	NHEK	skin:	n/a	n/a
27	CTCF	chr7:109641840-109641990	BE2_C	brain:	n/a	n/a
28	CTCF	chr7:109644060-109644210	HMEC	breast:	n/a	n/a
29	CTCF	chr7:109644011-109644161	LNCaP	prostate:	n/a	n/a
30	CTCF	chr7:109644032-109644133	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:109551945-109552024	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:109643940-109644090	Caco-2	colon:	n/a	n/a
33	CTCF	chr7:109644060-109644210	Caco-2	colon:	n/a	n/a
34	CTCF	chr7:109643824-109644298	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:109606520-109606670	NB4	blood:	n/a	n/a
36	CTCF	chr7:109579179-109579265	Lung_OC	lung:	n/a	n/a
37	CTCF	chr7:109643980-109644130	HPF	lung:	n/a	n/a
38	CTCF	chr7:109643881-109644247	GM12878	blood:	n/a	n/a
39	CTCF	chr7:109644013-109644133	HepG2	liver:	n/a	n/a
40	CTCF	chr7:109643980-109644130	GM06990	blood:	n/a	n/a
41	CTCF	chr7:109643920-109644070	HRE	kidney:	n/a	n/a
42	CTCF	chr7:109644000-109644150	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:109643980-109644130	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr7:109643960-109644110	BE2_C	brain:	n/a	n/a
45	CTCF	chr7:109644000-109644150	HMEC	breast:	n/a	n/a
46	CTCF	chr7:109604771-109604794	ProgFib	skin:	n/a	n/a
47	CTCF	chr7:109643978-109644161	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr7:109643980-109644130	SAEC	small airway:	n/a	n/a
49	CTCF	chr7:109644020-109644090	GM13977	blood:	n/a	n/a
50	CTCF	chr7:109644200-109644350	NHEK	skin:	n/a	n/a

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:109570287-109570337	AoSMC	blood vessel:	n/a
2	chr7:109596752-109596802	GM19239	blood:	n/a
3	chr7:109600733-109600783	HNPCEpiC	eye:	n/a
4	chr7:109570287-109570337	AoSMC	blood vessel:	n/a
5	chr7:109596752-109596802	GM19239	blood:	n/a
6	chr7:109600733-109600783	HNPCEpiC	eye:	n/a
7	chr7:109600591-109600641	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:109585055-109585105	PrEC	prostate:	n/a
9	chr7:109600733-109600783	SK-N-MC	brain:	n/a
10	chr7:109570287-109570337	NT2-D1	testis:	n/a
11	chr7:109596752-109596802	HL-60	blood:	n/a
12	chr7:109599644-109599694	HMEC	breast:	n/a
13	chr7:109600733-109600783	HL-60	blood:	n/a
14	chr7:109600733-109600783	Hepatocyte	liver:	n/a
15	chr7:109600399-109600449	K562	blood:	n/a
16	chr7:109600425-109600475	RPTEC	kidney:	n/a
17	chr7:109600399-109600449	HMEC	breast:	n/a
18	chr7:109600399-109600449	GM06990	blood:	n/a
19	chr7:109599644-109599694	H1-hESC	embryonic stem cell:	embryo
20	chr7:109585055-109585105	NHBE	bronchial:	n/a
21	chr7:109600425-109600475	SKMC	muscle:	n/a
22	chr7:109600733-109600783	GM19239	blood:	n/a
23	chr7:109570287-109570337	PrEC	prostate:	n/a
24	chr7:109600425-109600475	PANC-1	pancreas:	n/a
25	chr7:109600425-109600475	CMK	blood:	n/a
26	chr7:109596752-109596802	HRPEpiC	eye:	n/a
27	chr7:109570287-109570337	HCF	heart:	n/a
28	chr7:109600425-109600475	ovcar-3	ovarian:	n/a
29	chr7:109570287-109570337	CMK	blood:	n/a
30	chr7:109600591-109600641	SKMC	muscle:	n/a
31	chr7:109600733-109600783	GM12891	blood:	n/a
32	chr7:109570287-109570337	AG10803	skin:	n/a
33	chr7:109600399-109600449	H1-hESC	embryonic stem cell:	embryo
34	chr7:109596752-109596802	MCF10A-Er-Src	breast:	n/a
35	chr7:109600733-109600783	GM06990	blood:	n/a
36	chr7:109600399-109600449	AG10803	skin:	n/a
37	chr7:109596752-109596802	AoSMC	blood vessel:	n/a
38	chr7:109570287-109570337	GM12891	blood:	n/a
39	chr7:109600399-109600449	SAEC	small airway:	n/a
40	chr7:109585055-109585105	HCT-116	colon:	n/a
41	chr7:109570287-109570337	HL-60	blood:	n/a
42	chr7:109600591-109600641	Hela-S3	cervix:	n/a
43	chr7:109600733-109600783	NB4	blood:	n/a
44	chr7:109600733-109600783	RPTEC	kidney:	n/a
45	chr7:109600591-109600641	HIPEpiC	eye:	n/a
46	chr7:109596752-109596802	SKMC	muscle:	n/a
47	chr7:109596752-109596802	HCF	heart:	n/a
48	chr7:109600591-109600641	LNCaP	prostate:	n/a
49	chr7:109600425-109600475	Jurkat	blood:	n/a
50	chr7:109599644-109599694	SK-N-SH	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:109524189..109525857-chr7:109531930..109534908,2	K562	blood:
2	chr12:7073001..7074519-chr7:109591479..109593234,2	MCF-7	breast:
3	chr7:109538440..109540413-chr7:109541881..109544620,2	K562	blood:
4	chr7:109617231..109619713-chr7:109622419..109624214,3	K562	blood:
5	chr7:109537859..109540413-chr7:109543120..109545714,2	K562	blood:
6	chr7:109568885..109571688-chr7:109572507..109574918,2	K562	blood:
7	chr7:109595389..109597303-chr7:109602363..109605295,2	K562	blood:
8	chr7:109621845..109625177-chr7:109626649..109628866,3	K562	blood:
9	chr7:109595389..109597303-chr7:109602363..109605295,2	K562	blood:
10	chr7:109617231..109619713-chr7:109622419..109624214,3	K562	blood:
11	chr7:109643549..109644198-chr7:110082097..110083094,2	MCF-7	breast:
12	chr7:109568885..109571688-chr7:109572507..109574918,2	K562	blood:
13	chr7:109537859..109540413-chr7:109543120..109545714,2	K562	blood:
14	chr7:109621845..109625177-chr7:109626649..109628866,3	K562	blood:
15	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: 1777 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537809086	chr7:109535213-109535214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191571270	chr7:109535245-109535246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577664201	chr7:109535258-109535259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184787207	chr7:109535277-109535278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559504362	chr7:109535308-109535309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147145196	chr7:109535356-109535357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188503234	chr7:109535361-109535362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542038890	chr7:109535407-109535408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34479019	chr7:109535411-109535412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192983966	chr7:109535413-109535414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531117889	chr7:109535438-109535439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566790195	chr7:109535455-109535456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74352250	chr7:109535511-109535512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185687604	chr7:109535520-109535521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565026728	chr7:109535541-109535542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564353717	chr7:109535542-109535543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534819625	chr7:109535548-109535549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77822602	chr7:109535551-109535552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547083254	chr7:109535566-109535567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566995301	chr7:109535592-109535593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567330504	chr7:109535678-109535679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62478797	chr7:109535693-109535694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549209561	chr7:109535724-109535725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569123765	chr7:109535730-109535731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537797973	chr7:109535737-109535738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557713432	chr7:109535768-109535769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571188679	chr7:109535780-109535781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533557937	chr7:109535787-109535788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546615717	chr7:109535801-109535802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140246037	chr7:109535903-109535904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573402775	chr7:109535942-109535943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144352392	chr7:109535961-109535962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370334675	chr7:109535963-109535964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147378221	chr7:109535998-109535999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561968482	chr7:109541419-109541420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561049184	chr7:109541448-109541449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531015487	chr7:109541482-109541483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550760865	chr7:109541495-109541496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570977569	chr7:109541500-109541501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573104822	chr7:109541573-109541574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115396986	chr7:109541574-109541575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546858506	chr7:109541603-109541604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566771150	chr7:109541618-109541619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535414181	chr7:109541630-109541631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555330033	chr7:109541657-109541658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568725555	chr7:109541672-109541673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111464528	chr7:109541756-109541757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191016721	chr7:109541820-109541821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377645928	chr7:109541834-109541835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545976042	chr7:109541838-109541839	Enhancers	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:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109535200-109535400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:109535200-109536000	Enhancers	Pancreas	Pancrea
3	chr7:109535600-109536000	Enhancers	Gastric	stomach
4	chr7:109541400-109542400	Enhancers	Hela-S3	cervix
5	chr7:109541600-109542200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:109541600-109542800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:109541600-109542800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:109541600-109542800	Enhancers	NHDF-Ad	bronchial
9	chr7:109541800-109542400	Enhancers	NHEK	skin
10	chr7:109565000-109566000	ZNF genes & repeats	Dnd41	blood
11	chr7:109565200-109566000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
12	chr7:109565200-109566200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:109566000-109567200	Weak transcription	Dnd41	blood
14	chr7:109569800-109570400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:109570000-109570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:109570000-109570600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:109570000-109570600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:109573000-109573200	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr7:109578200-109578400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr7:109578200-109580000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr7:109578600-109579600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
22	chr7:109578800-109579400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:109579000-109579400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:109579000-109579600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:109579200-109580000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:109579400-109580200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:109579600-109584400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:109580200-109580400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:109580400-109585200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:109584800-109585600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:109585000-109585600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:109585000-109585800	Enhancers	Dnd41	blood
33	chr7:109585200-109585400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:109585200-109585600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:109585200-109585600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr7:109585800-109587000	Flanking Active TSS	Dnd41	blood
37	chr7:109587000-109587800	Enhancers	Dnd41	blood
38	chr7:109590000-109590400	Enhancers	A549	lung
39	chr7:109590200-109590800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr7:109590400-109591200	Flanking Active TSS	A549	lung
41	chr7:109590400-109591400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:109590800-109596600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr7:109591200-109591400	Enhancers	A549	lung
44	chr7:109594200-109594800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:109595400-109596800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr7:109595400-109596800	Enhancers	Fetal Lung	lung
47	chr7:109596200-109596400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:109596400-109597400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:109596600-109597000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr7:109596600-109597600	Enhancers	H9 Cell Line	embryonic stem cell

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