Variant report

Variant	nsv889150
Chromosome Location	chr7:125232034-125716635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1201)
CpG islands
(count:0)
Chromatin interactive
region (count:79)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1201 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:125245371-125245822	K562	blood:	n/a	n/a
2	ARID3A	chr7:125235405-125235419	K562	blood:	n/a	n/a
3	ARID3A	chr7:125238528-125238531	K562	blood:	n/a	n/a
4	ATF1	chr7:125304902-125304935	K562	blood:	n/a	n/a
5	ATF2	chr7:125292085-125292579	GM12878	blood:	n/a	n/a
6	ATF2	chr7:125606321-125606646	GM12878	blood:	n/a	n/a
7	ATF3	chr7:125245272-125245589	K562	blood:	n/a	n/a
8	BACH1	chr7:125250853-125250856	K562	blood:	n/a	n/a
9	BACH1	chr7:125432709-125432803	K562	blood:	n/a	n/a
10	BACH1	chr7:125245462-125245548	H1-hESC	embryonic stem cell:	n/a	chr7:125245471-125245485
11	BATF	chr7:125463611-125463967	GM12878	blood:	n/a	n/a
12	BATF	chr7:125656888-125657086	GM12878	blood:	n/a	chr7:125657018-125657029 chr7:125657002-125657013
13	BATF	chr7:125444374-125444778	GM12878	blood:	n/a	n/a
14	BATF	chr7:125400561-125400782	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:125444389-125444708	GM12878	blood:	n/a	n/a
16	BCL3	chr7:125292138-125292574	GM12878	blood:	n/a	n/a
17	BCL3	chr7:125460885-125461181	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:125375284-125375348	K562	blood:	n/a	n/a
19	BHLHE40	chr7:125315765-125315880	K562	blood:	n/a	n/a
20	BHLHE40	chr7:125242283-125242313	K562	blood:	n/a	n/a
21	BHLHE40	chr7:125301808-125302109	K562	blood:	n/a	n/a
22	BRCA1	chr7:125311175-125311315	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr7:125661964-125662015	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr7:125377833-125378215	K562	blood:	n/a	n/a
25	CBX3	chr7:125377948-125378165	K562	blood:	n/a	n/a
26	CBX3	chr7:125301630-125302099	K562	blood:	n/a	n/a
27	CBX3	chr7:125574542-125575099	HCT-116	colon:	n/a	n/a
28	CBX3	chr7:125574517-125575153	HCT-116	colon:	n/a	n/a
29	CCNT2	chr7:125507517-125507664	K562	blood:	n/a	n/a
30	CCNT2	chr7:125245371-125245832	K562	blood:	n/a	n/a
31	CCNT2	chr7:125301701-125301994	K562	blood:	n/a	n/a
32	CCNT2	chr7:125569775-125569946	K562	blood:	n/a	n/a
33	CEBPB	chr7:125578941-125579239	IMR90	lung:	n/a	chr7:125579076-125579087
34	CEBPB	chr7:125251714-125251994	A549	lung:	n/a	chr7:125251843-125251854
35	CEBPB	chr7:125654844-125655083	H1-hESC	embryonic stem cell:	n/a	chr7:125654981-125654994 chr7:125654881-125654892 chr7:125654881-125654892
36	CEBPB	chr7:125235170-125235356	A549	lung:	n/a	n/a
37	CEBPB	chr7:125577494-125577627	HepG2	liver:	n/a	chr7:125577588-125577599 chr7:125577589-125577598 chr7:125577589-125577598 chr7:125577587-125577600 chr7:125577587-125577600 chr7:125577589-125577598 chr7:125577587-125577598 chr7:125577589-125577598
38	CEBPB	chr7:125628636-125628960	HepG2	liver:	n/a	chr7:125628800-125628811 chr7:125628802-125628811
39	CEBPB	chr7:125654834-125655110	IMR90	lung:	n/a	chr7:125654981-125654994 chr7:125654881-125654892 chr7:125654881-125654892
40	CEBPB	chr7:125301811-125301972	K562	blood:	n/a	n/a
41	CEBPB	chr7:125459486-125459721	HepG2	liver:	n/a	chr7:125459654-125459665 chr7:125459653-125459666
42	CEBPB	chr7:125332503-125332772	A549	lung:	n/a	n/a
43	CEBPB	chr7:125700034-125700243	HepG2	liver:	n/a	chr7:125700115-125700126 chr7:125700113-125700126 chr7:125700115-125700126 chr7:125700113-125700124 chr7:125700113-125700126
44	CEBPB	chr7:125628748-125628924	A549	lung:	n/a	chr7:125628800-125628811 chr7:125628802-125628811
45	CEBPB	chr7:125603406-125603606	IMR90	lung:	n/a	chr7:125603411-125603422
46	CEBPB	chr7:125416308-125416463	A549	lung:	n/a	n/a
47	CEBPB	chr7:125539818-125539959	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:125517391-125517767	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:125251813-125251964	H1-hESC	embryonic stem cell:	n/a	chr7:125251843-125251854
50	CEBPB	chr7:125579018-125579149	K562	blood:	n/a	chr7:125579076-125579087

No data

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
2	chr7:125449848..125452738-chr7:125466258..125468115,2	K562	blood:
3	chr7:125243932..125247685-chr7:125249366..125252787,4	K562	blood:
4	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
5	chr7:125458557..125461124-chr7:125464853..125467696,3	K562	blood:
6	chr7:125369632..125371193-chr7:125372789..125375510,2	K562	blood:
7	chr7:125384743..125387377-chr7:125395816..125398229,2	K562	blood:
8	chr7:125391124..125394118-chr7:125397604..125400061,2	K562	blood:
9	chr7:124699671..124700472-chr7:125310284..125311293,4	MCF-7	breast:
10	chr7:125384743..125387377-chr7:125395816..125398229,2	K562	blood:
11	chr7:125235978..125238946-chr7:125246634..125248463,2	K562	blood:
12	chr7:125234853..125237677-chr7:125237685..125240938,4	K562	blood:
13	chr3:189159456..189161667-chr7:125457789..125460538,2	MCF-7	breast:
14	chr7:125598344..125601168-chr7:125601374..125603496,2	K562	blood:
15	chr7:125503485..125505838-chr7:125510638..125513517,2	K562	blood:
16	chr7:125234853..125237677-chr7:125237685..125240938,4	K562	blood:
17	chr7:125243932..125247685-chr7:125249366..125252787,4	K562	blood:
18	chr7:125414524..125416692-chr7:125417841..125420169,2	K562	blood:
19	chr7:125271199..125273030-chr7:125279444..125281182,2	K562	blood:
20	chr7:125598344..125601168-chr7:125601374..125603496,2	K562	blood:
21	chr7:125392984..125395323-chr7:125485232..125486912,2	K562	blood:
22	chr7:125385463..125387105-chr7:125388625..125390168,2	K562	blood:
23	chr7:125458557..125461124-chr7:125464853..125467696,3	K562	blood:
24	chr7:125241383..125243841-chr7:125245305..125247119,2	K562	blood:
25	chr7:125620692..125622990-chr7:125623881..125626292,2	K562	blood:
26	chr7:125435373..125437398-chr7:125441806..125444028,2	K562	blood:
27	chr7:125458557..125461124-chr7:125464853..125467696,2	K562	blood:
28	chr7:125385463..125387105-chr7:125388625..125390168,2	K562	blood:
29	chr7:125606198..125608530-chr7:125608776..125611774,2	K562	blood:
30	chr7:125298032..125299556-chr7:125301749..125304185,2	K562	blood:
31	chr7:125266350..125268456-chr7:125268990..125271512,2	K562	blood:
32	chr7:125414524..125416692-chr7:125417841..125420169,2	K562	blood:
33	chr7:125269070..125270794-chr7:125275616..125278202,2	K562	blood:
34	chr1:11968074..11970490-chr7:125663203..125664731,2	MCF-7	breast:
35	chr7:125531353..125533872-chr7:125536141..125538542,2	K562	blood:
36	chr7:125251686..125253446-chr7:125261235..125263882,2	K562	blood:
37	chr7:125435373..125437398-chr7:125441806..125444028,2	K562	blood:
38	chr7:125385605..125387936-chr7:125388625..125390972,2	K562	blood:
39	chr7:125241383..125243591-chr7:125245619..125247438,2	K562	blood:
40	chr7:125480828..125483147-chr7:125484662..125486648,3	K562	blood:
41	chr7:125338629..125340672-chr7:125343129..125344648,2	K562	blood:
42	chr7:125266350..125268456-chr7:125268990..125271512,2	K562	blood:
43	chr7:125425665..125427173-chr7:125429693..125431589,2	K562	blood:
44	chr7:125458557..125461124-chr7:125464853..125467696,2	K562	blood:
45	chr7:125241383..125243841-chr7:125245305..125247119,2	K562	blood:
46	chr7:125338629..125340672-chr7:125343129..125344648,2	K562	blood:
47	chr7:125280203..125282931-chr7:125290069..125292178,2	K562	blood:
48	chr7:125503485..125505838-chr7:125510638..125513517,2	K562	blood:
49	chr7:125271199..125273030-chr7:125279444..125281182,2	K562	blood:
50	chr7:125023517..125024026-chr7:125310752..125311652,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-6	chr7:125557925-125558172	XLOC_006234
2	lnc-ARF5-6	chr7:125560111-125560207	XLOC_006234
3	lnc-ARF5-6	chr7:125573828-125573886	XLOC_006234
4	lnc-ARF5-6	chr7:125564266-125564441	XLOC_006234
5	lnc-ARF5-6	chr7:125563748-125564004	XLOC_006234

No data

Variant related genes	Relation type
ENSG00000221418	TF binding region
ENSG00000197462	TF binding region
ENSG00000201801	chromatin interactions
ENSG00000107281	chromatin interactions
ENSG00000199347	chromatin interactions

Extended variants
information (count: 9823 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:9823 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142170795	chr7:125245202-125245203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114478064	chr7:125245213-125245214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573242434	chr7:125245263-125245264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577974452	chr7:125245364-125245365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1419702	chr7:125245398-125245399	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs1419703	chr7:125245418-125245419	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs151183035	chr7:125245455-125245456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549580389	chr7:125245461-125245462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568439859	chr7:125245491-125245492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561349692	chr7:125245542-125245543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532001667	chr7:125245544-125245545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73722010	chr7:125245565-125245566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs568793528	chr7:125245588-125245589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142587092	chr7:125245621-125245622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184309004	chr7:125245630-125245631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536599503	chr7:125245682-125245683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546909493	chr7:125245701-125245702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189312155	chr7:125245707-125245708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566220729	chr7:125245719-125245720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199896057	chr7:125245738-125245739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182385469	chr7:125245745-125245746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566721356	chr7:125245797-125245798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538111933	chr7:125245818-125245819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556194988	chr7:125245853-125245854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10269413	chr7:125245865-125245866	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs140291265	chr7:125245876-125245877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538460529	chr7:125245896-125245897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560503882	chr7:125245897-125245898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558691880	chr7:125245942-125245943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184844454	chr7:125245950-125245951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543163405	chr7:125245975-125245976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76761396	chr7:125245998-125245999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150229403	chr7:125246075-125246076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189357095	chr7:125246083-125246084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181369654	chr7:125246125-125246126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532708005	chr7:125246173-125246174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555867392	chr7:125246184-125246185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550947328	chr7:125246205-125246206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371659723	chr7:125246232-125246233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62914760	chr7:125246233-125246234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146810614	chr7:125246253-125246254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527359462	chr7:125246262-125246263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548822428	chr7:125246336-125246337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs757316	chr7:125246445-125246446	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs537650409	chr7:125246447-125246448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185944658	chr7:125246453-125246454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571559151	chr7:125246473-125246474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200264532	chr7:125246505-125246506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111273625	chr7:125246508-125246509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs66699515	chr7:125246509-125246510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	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
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20858243	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	19246517	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:125245200-125245600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr7:125245200-125245800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:125245200-125245800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:125245200-125246000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:125245800-125249800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:125249800-125250600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:125252800-125253400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:125253400-125258200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:125258200-125258400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:125258400-125259000	ZNF genes & repeats	Pancreas	Pancrea
11	chr7:125258600-125258800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr7:125258600-125259000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:125259000-125259600	Weak transcription	Pancreas	Pancrea
14	chr7:125261000-125263200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:125262400-125262800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:125262600-125263200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:125262800-125263200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:125262800-125263200	Active TSS	HMEC	breast
19	chr7:125263200-125263400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:125263200-125263400	Enhancers	HMEC	breast
21	chr7:125263200-125264000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:125268200-125269800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:125285200-125288200	Weak transcription	Pancreas	Pancrea
24	chr7:125288200-125288600	Enhancers	Pancreas	Pancrea
25	chr7:125288200-125289400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:125288800-125289000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:125289200-125289800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:125289400-125292000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr7:125291200-125291400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:125291400-125291600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:125291600-125292600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:125291800-125292400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:125292000-125292200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:125292000-125292400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:125292000-125292600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:125292600-125293400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:125293400-125294400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:125294400-125294600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:125299800-125300600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr7:125299800-125300600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:125299800-125302000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:125299800-125302000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:125300000-125300400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr7:125300000-125300400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:125300000-125300400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:125300000-125300400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:125300000-125300600	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:125300000-125300600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:125300200-125302600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr7:125300200-125302800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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