Variant report

Variant	nsv889159
Chromosome Location	chr7:125418926-125927493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:961)
CpG islands
(count:0)
Chromatin interactive
region (count:46)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:125606321-125606646	GM12878	blood:	n/a	n/a
2	BACH1	chr7:125432709-125432803	K562	blood:	n/a	n/a
3	BACH1	chr7:125817876-125818052	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:125897717-125897800	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:125863211-125863507	GM12878	blood:	n/a	n/a
6	BATF	chr7:125444374-125444778	GM12878	blood:	n/a	n/a
7	BATF	chr7:125850801-125851102	GM12878	blood:	n/a	n/a
8	BATF	chr7:125463611-125463967	GM12878	blood:	n/a	n/a
9	BATF	chr7:125656888-125657086	GM12878	blood:	n/a	chr7:125657018-125657029 chr7:125657002-125657013
10	BATF	chr7:125850778-125851091	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:125444389-125444708	GM12878	blood:	n/a	n/a
12	BCL3	chr7:125460885-125461181	GM12878	blood:	n/a	n/a
13	BCL3	chr7:125863562-125864018	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:125720305-125720422	GM12878	blood:	n/a	n/a
15	BRCA1	chr7:125661964-125662015	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr7:125763163-125763299	GM12878	blood:	n/a	n/a
17	CBX3	chr7:125574517-125575153	HCT-116	colon:	n/a	n/a
18	CBX3	chr7:125574542-125575099	HCT-116	colon:	n/a	n/a
19	CCNT2	chr7:125507517-125507664	K562	blood:	n/a	n/a
20	CCNT2	chr7:125569775-125569946	K562	blood:	n/a	n/a
21	CEBPB	chr7:125843366-125843555	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:125901758-125901932	HepG2	liver:	n/a	chr7:125901796-125901807
23	CEBPB	chr7:125878477-125878525	A549	lung:	n/a	chr7:125878483-125878494
24	CEBPB	chr7:125487686-125487951	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:125719752-125720054	IMR90	lung:	n/a	chr7:125719898-125719909 chr7:125719900-125719911 chr7:125719898-125719911
26	CEBPB	chr7:125603329-125603585	HepG2	liver:	n/a	chr7:125603411-125603422
27	CEBPB	chr7:125539818-125539959	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr7:125469475-125469633	H1-hESC	embryonic stem cell:	n/a	chr7:125469586-125469597
29	CEBPB	chr7:125578941-125579239	IMR90	lung:	n/a	chr7:125579076-125579087
30	CEBPB	chr7:125883270-125883603	HepG2	liver:	n/a	chr7:125883426-125883437
31	CEBPB	chr7:125431406-125431521	K562	blood:	n/a	n/a
32	CEBPB	chr7:125700034-125700243	HepG2	liver:	n/a	chr7:125700115-125700126 chr7:125700113-125700126 chr7:125700115-125700126 chr7:125700113-125700124 chr7:125700113-125700126
33	CEBPB	chr7:125603367-125603565	K562	blood:	n/a	chr7:125603411-125603422
34	CEBPB	chr7:125579018-125579149	K562	blood:	n/a	chr7:125579076-125579087
35	CEBPB	chr7:125677488-125677754	HepG2	liver:	n/a	chr7:125677605-125677616
36	CEBPB	chr7:125883394-125883501	A549	lung:	n/a	chr7:125883426-125883437
37	CEBPB	chr7:125553556-125553759	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:125654905-125655125	HepG2	liver:	n/a	chr7:125654981-125654994
39	CEBPB	chr7:125641111-125641392	HepG2	liver:	n/a	chr7:125641225-125641236
40	CEBPB	chr7:125586220-125586477	A549	lung:	n/a	chr7:125586287-125586298 chr7:125586287-125586296
41	CEBPB	chr7:125654834-125655110	IMR90	lung:	n/a	chr7:125654981-125654994 chr7:125654881-125654892 chr7:125654881-125654892
42	CEBPB	chr7:125654878-125655143	Hela-S3	cervix:	n/a	chr7:125654981-125654994 chr7:125654881-125654892 chr7:125654881-125654892
43	CEBPB	chr7:125459574-125459591	A549	lung:	n/a	n/a
44	CEBPB	chr7:125497039-125497286	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:125608121-125608318	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:125518695-125519476	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:125459486-125459721	HepG2	liver:	n/a	chr7:125459654-125459665 chr7:125459653-125459666
48	CEBPB	chr7:125628636-125628960	HepG2	liver:	n/a	chr7:125628800-125628811 chr7:125628802-125628811
49	CEBPB	chr7:125828396-125828716	HepG2	liver:	n/a	chr7:125828560-125828571
50	CEBPB	chr7:125719721-125720047	H1-hESC	embryonic stem cell:	n/a	chr7:125719898-125719909 chr7:125719900-125719911 chr7:125719898-125719911

No data

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:125760007..125761516-chr7:125765341..125767216,2	K562	blood:
2	chr7:125842751..125845029-chr7:125853403..125855723,2	K562	blood:
3	chr7:125782315..125785004-chr7:125785020..125787237,2	MCF-7	breast:
4	chr7:125779581..125782022-chr7:125791583..125793511,2	K562	blood:
5	chr7:125606198..125608530-chr7:125608776..125611774,2	K562	blood:
6	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
7	chr7:125606198..125608530-chr7:125608776..125611774,2	K562	blood:
8	chr7:125392984..125395323-chr7:125485232..125486912,2	K562	blood:
9	chr7:125620692..125622990-chr7:125623881..125626292,2	K562	blood:
10	chr3:189159456..189161667-chr7:125457789..125460538,2	MCF-7	breast:
11	chr7:125779581..125782022-chr7:125791583..125793511,2	K562	blood:
12	chr7:125760007..125761516-chr7:125765341..125767216,2	K562	blood:
13	chr7:125620692..125622990-chr7:125623881..125626292,2	K562	blood:
14	chr7:125717773..125720293-chr7:125877157..125879096,2	K562	blood:
15	chr7:125425665..125427173-chr7:125429693..125431589,2	K562	blood:
16	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
17	chr7:125717773..125720293-chr7:125877157..125879096,2	K562	blood:
18	chr7:125480828..125483147-chr7:125484662..125486648,3	K562	blood:
19	chr7:125435373..125437398-chr7:125441806..125444028,2	K562	blood:
20	chr7:125458557..125461124-chr7:125464853..125467696,2	K562	blood:
21	chr7:125870675..125872321-chr7:125874700..125877650,2	K562	blood:
22	chr7:125458557..125461124-chr7:125464853..125467696,3	K562	blood:
23	chr7:125449848..125452738-chr7:125466258..125468115,2	K562	blood:
24	chr7:125459178..125461778-chr7:125471242..125473065,2	K562	blood:
25	chr7:125598344..125601168-chr7:125601374..125603496,2	K562	blood:
26	chr1:11968074..11970490-chr7:125663203..125664731,2	MCF-7	breast:
27	chr7:125449848..125452738-chr7:125466258..125468115,2	K562	blood:
28	chr7:125531353..125533872-chr7:125536141..125538542,2	K562	blood:
29	chr7:125458557..125461124-chr7:125464853..125467696,3	K562	blood:
30	chr7:125782315..125785004-chr7:125785020..125787237,2	MCF-7	breast:
31	chr7:125466756..125469484-chr9:139938867..139941802,2	MCF-7	breast:
32	chr7:125503485..125505838-chr7:125510638..125513517,2	K562	blood:
33	chr7:125531353..125533872-chr7:125536141..125538542,2	K562	blood:
34	chr7:125842751..125845029-chr7:125853403..125855723,2	K562	blood:
35	chr7:125683918..125686254-chr7:125689679..125692270,2	K562	blood:
36	chr7:125683918..125686254-chr7:125689679..125692270,2	K562	blood:
37	chr7:125480828..125483147-chr7:125484662..125486648,3	K562	blood:
38	chr7:125425665..125427173-chr7:125429693..125431589,2	K562	blood:
39	chr3:64659748..64660652-chr7:125742703..125743269,2	MCF-7	breast:
40	chr7:125598344..125601168-chr7:125601374..125603496,2	K562	blood:
41	chr7:125458557..125461124-chr7:125464853..125467696,2	K562	blood:
42	chr7:125414524..125416692-chr7:125417841..125420169,2	K562	blood:
43	chr7:125870675..125872321-chr7:125874700..125877650,2	K562	blood:
44	chr7:125435373..125437398-chr7:125441806..125444028,2	K562	blood:
45	chr7:125459178..125461778-chr7:125471242..125473065,2	K562	blood:
46	chr7:125503485..125505838-chr7:125510638..125513517,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-5	chr7:125873591-125873666	XLOC_006235
2	lnc-ARF5-6	chr7:125573828-125573886	XLOC_006234
3	lnc-ARF5-5	chr7:125924175-125924312	XLOC_006235
4	lnc-ARF5-5	chr7:125873591-125873666	XLOC_006235
5	lnc-ARF5-5	chr7:125886687-125886768	NONHSAT123116
6	lnc-ARF5-6	chr7:125557925-125558172	XLOC_006234
7	lnc-ARF5-5	chr7:125886687-125886785	XLOC_006235
8	lnc-ARF5-5	chr7:125873713-125873937	NONHSAT123116
9	lnc-ARF5-5	chr7:125886687-125886768	XLOC_006235
10	lnc-ARF5-5	chr7:125870287-125870467	XLOC_006235
11	lnc-ARF5-5	chr7:125891205-125891250	NONHSAT123116
12	lnc-ARF5-6	chr7:125564266-125564441	XLOC_006234
13	lnc-ARF5-5	chr7:125870287-125870467	XLOC_006235
14	lnc-ARF5-5	chr7:125870287-125870467	XLOC_006235
15	lnc-ARF5-5	chr7:125873591-125873666	XLOC_006235
16	lnc-ARF5-5	chr7:125924175-125924216	XLOC_006235
17	lnc-ARF5-6	chr7:125563748-125564004	XLOC_006234
18	lnc-ARF5-6	chr7:125560111-125560207	XLOC_006234

No data

Variant related genes	Relation type
ENSG00000221418	TF binding region
ENSG00000197462	TF binding region
ENSG00000107281	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000201801	chromatin interactions
FBXO8	miRNA target sites
SLC33A1	miRNA target sites
SLC31A2	miRNA target sites
SLC30A7	miRNA target sites
FBXO34	miRNA target sites
FBXW7	miRNA target sites

Extended variants
information (count: 9331 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:9331 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7782610	chr7:125418926-125418927	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs553355450	chr7:125418934-125418935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554208461	chr7:125418973-125418974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77873649	chr7:125419017-125419018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535575631	chr7:125419050-125419051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557141309	chr7:125419120-125419121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144961270	chr7:125419196-125419197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531292234	chr7:125419245-125419246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543142025	chr7:125419279-125419280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs57033334	chr7:125419290-125419291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147527597	chr7:125419297-125419298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569432075	chr7:125419333-125419334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185473123	chr7:125419340-125419341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559340667	chr7:125419341-125419342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189591234	chr7:125419379-125419380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180934498	chr7:125419406-125419407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572290713	chr7:125419412-125419413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375740993	chr7:125419420-125419421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145914697	chr7:125419421-125419422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186178394	chr7:125419455-125419456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527658354	chr7:125419469-125419470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537519597	chr7:125419484-125419485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552674657	chr7:125419494-125419495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570938317	chr7:125419554-125419555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79660316	chr7:125419555-125419556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369303818	chr7:125419558-125419559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115331313	chr7:125419569-125419570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192452557	chr7:125419601-125419602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575024428	chr7:125419734-125419735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183401390	chr7:125419758-125419759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188845772	chr7:125419838-125419839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575607026	chr7:125419876-125419877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191594844	chr7:125419881-125419882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140106363	chr7:125419905-125419906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576876784	chr7:125419907-125419908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145504010	chr7:125419935-125419936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144951676	chr7:125419979-125419980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529929386	chr7:125419991-125419992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182527011	chr7:125420000-125420001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575798228	chr7:125420033-125420034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563595714	chr7:125420034-125420035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs118025170	chr7:125420047-125420048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149069892	chr7:125420069-125420070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543402523	chr7:125420086-125420087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570809130	chr7:125420087-125420088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142112186	chr7:125420088-125420089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112444774	chr7:125420099-125420100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532385745	chr7:125420123-125420124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568667741	chr7:125420160-125420161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535676450	chr7:125420164-125420165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	19246517	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:125413800-125421400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:125421400-125421600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:125452800-125454600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr7:125454200-125454800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:125454800-125455200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:125455200-125456000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:125456000-125459600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:125459600-125459800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:125459800-125460200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:125460200-125460800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:125472600-125481800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:125474000-125474800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:125481800-125482000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:125486400-125486600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr7:125486800-125489400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:125487000-125487600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
17	chr7:125487400-125487600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr7:125487400-125487800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
19	chr7:125487400-125488400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr7:125487600-125488000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr7:125487600-125488200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr7:125487600-125488200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:125487600-125488400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:125487600-125488600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:125487600-125488600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:125487800-125488200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr7:125488000-125488200	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr7:125488000-125488400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:125488200-125488400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr7:125488200-125488400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:125488200-125488600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr7:125488200-125488800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:125488400-125488600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:125488400-125488600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:125488400-125488800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr7:125488400-125488800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:125488400-125491400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:125488800-125489000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr7:125488800-125490200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr7:125490200-125490600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:125490400-125490600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr7:125493400-125493600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:125515400-125515800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:125516000-125516600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
45	chr7:125516400-125518400	Enhancers	Hela-S3	cervix
46	chr7:125518400-125518800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:125518400-125518800	Flanking Active TSS	Hela-S3	cervix
48	chr7:125518800-125519200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:125518800-125519200	Active TSS	Hela-S3	cervix
50	chr7:125519200-125519600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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