Variant report

Variant	nsv1024270
Chromosome Location	chr7:124900057-124945551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:124912339-124912344	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:124927356-124927377	K562	blood:	n/a	n/a
3	CCNT2	chr7:124924974-124925020	K562	blood:	n/a	n/a
4	CEBPB	chr7:124906409-124906530	HepG2	liver:	n/a	chr7:124906481-124906492 chr7:124906480-124906493
5	CEBPB	chr7:124918367-124918608	K562	blood:	n/a	chr7:124918485-124918496 chr7:124918485-124918498 chr7:124918487-124918498 chr7:124918485-124918498
6	CEBPB	chr7:124918411-124918602	HepG2	liver:	n/a	chr7:124918485-124918496 chr7:124918485-124918498 chr7:124918487-124918498 chr7:124918485-124918498
7	CHD2	chr7:124927361-124927542	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr7:124910466-124910527	Lung_OC	lung:	n/a	n/a
9	CTCF	chr7:124904672-124904690	LNCaP	prostate:	n/a	n/a
10	E2F4	chr7:124937513-124937704	MCF10A-Er-Src	breast:	n/a	n/a
11	ELK1	chr7:124927222-124927254	K562	blood:	n/a	n/a
12	EP300	chr7:124942960-124943399	SK-N-SH_RA	brain:	n/a	n/a
13	GATA3	chr7:124942587-124942686	SH-SY5Y	brain:	n/a	chr7:124942608-124942618
14	GATA3	chr7:124927531-124927664	SH-SY5Y	brain:	n/a	n/a
15	GATA3	chr7:124916378-124916493	SH-SY5Y	brain:	n/a	chr7:124916409-124916418 chr7:124916402-124916423
16	IRF1	chr7:124919806-124919823	K562	blood:	n/a	n/a
17	JUN	chr7:124943690-124943740	K562	blood:	n/a	n/a
18	JUND	chr7:124926693-124926895	HepG2	liver:	n/a	n/a
19	KAP1	chr7:124926447-124926933	K562	blood:	n/a	n/a
20	MAFF	chr7:124914904-124915137	K562	blood:	n/a	chr7:124914983-124915001
21	MAFF	chr7:124914813-124915168	HepG2	liver:	n/a	chr7:124914983-124915001
22	MAFK	chr7:124914909-124915143	HepG2	liver:	n/a	chr7:124914960-124914975
23	MAFK	chr7:124914802-124915173	IMR90	lung:	n/a	chr7:124914960-124914975
24	MAFK	chr7:124914893-124915108	K562	blood:	n/a	chr7:124914960-124914975
25	MAFK	chr7:124914805-124915171	HepG2	liver:	n/a	chr7:124914960-124914975
26	MAFK	chr7:124914964-124915023	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAZ	chr7:124911755-124911757	HepG2	liver:	n/a	n/a
28	MYC	chr7:124904535-124904694	H1-hESC	embryonic stem cell:	n/a	n/a
29	MYC	chr7:124938330-124938359	GM12878	blood:	n/a	n/a
30	NFYA	chr7:124924430-124924521	GM12878	blood:	n/a	n/a
31	NFYA	chr7:124914714-124914923	K562	blood:	n/a	chr7:124914891-124914909
32	NFYB	chr7:124939066-124939453	K562	blood:	n/a	n/a
33	NFYB	chr7:124914773-124915324	K562	blood:	n/a	chr7:124915086-124915101 chr7:124915044-124915059
34	NFYB	chr7:124914975-124915174	Hela-S3	cervix:	n/a	chr7:124915086-124915101 chr7:124915044-124915059
35	NFYB	chr7:124914799-124915292	GM12878	blood:	n/a	chr7:124915086-124915101 chr7:124915044-124915059
36	NFYB	chr7:124939097-124939428	GM12878	blood:	n/a	n/a
37	POLR2A	chr7:124924738-124925088	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr7:124903523-124903681	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr7:124935584-124935652	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr7:124904485-124904772	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr7:124920820-124920976	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr7:124904538-124904725	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr7:124919772-124919820	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr7:124913686-124913884	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr7:124923573-124923772	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr7:124918043-124918134	GM12878	blood:	n/a	n/a
47	POLR2A	chr7:124901230-124901368	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr7:124902088-124902223	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr7:124906032-124906113	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr7:124914934-124915031	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124904981-124905031	HIPEpiC	eye:	n/a
2	chr7:124904981-124905031	AG09309	skin:	n/a
3	chr7:124904981-124905031	AoSMC	blood vessel:	n/a
4	chr7:124904981-124905031	HepG2	liver:	n/a
5	chr7:124904981-124905031	MCF-7	breast:	n/a
6	chr7:124904981-124905031	HEK293	kidney:	embryo
7	chr7:124904981-124905031	Caco-2	colon:	n/a
8	chr7:124904981-124905031	AG04450	lung:	fetal
9	chr7:124904981-124905031	HMEC	breast:	n/a
10	chr7:124904981-124905031	NHDF-neo	bronchial:	n/a
11	chr7:124904981-124905031	HAEpiC	amniotic membrane:	n/a
12	chr7:124904981-124905031	ovcar-3	ovarian:	n/a
13	chr7:124904981-124905031	ECC-1	luminal epithelium:	n/a
14	chr7:124904981-124905031	AG10803	skin:	n/a
15	chr7:124904981-124905031	SK-N-MC	brain:	n/a
16	chr7:124904981-124905031	PFSK-1	brain:	n/a
17	chr7:124904981-124905031	HL-60	blood:	n/a
18	chr7:124904981-124905031	NB4	blood:	n/a
19	chr7:124904981-124905031	SK-N-SH_RA	brain:	n/a
20	chr7:124904981-124905031	GM19239	blood:	n/a
21	chr7:124904981-124905031	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:124904981-124905031	HNPCEpiC	eye:	n/a
23	chr7:124904981-124905031	HCF	heart:	n/a
24	chr7:124904981-124905031	HRE	kidney:	n/a
25	chr7:124904981-124905031	GM12892	blood:	n/a
26	chr7:124904981-124905031	H1-hESC	embryonic stem cell:	embryo
27	chr7:124904981-124905031	HUVEC	blood vessel:	n/a
28	chr7:124904981-124905031	NHBE	bronchial:	n/a
29	chr7:124904981-124905031	GM06990	blood:	n/a
30	chr7:124904981-124905031	MCF10A-Er-Src	breast:	n/a
31	chr7:124904981-124905031	SK-N-SH	brain:	n/a
32	chr7:124904981-124905031	AG09319	gingival:	n/a
33	chr7:124904981-124905031	NT2-D1	testis:	n/a
34	chr7:124904981-124905031	SAEC	small airway:	n/a
35	chr7:124904981-124905031	Hela-S3	cervix:	n/a
36	chr7:124904981-124905031	HEEpiC	esophagus:	n/a
37	chr7:124904981-124905031	Hepatocyte	liver:	n/a
38	chr7:124904981-124905031	Jurkat	blood:	n/a
39	chr7:124904981-124905031	HCM	heart:	n/a
40	chr7:124904981-124905031	U87	brain:	n/a
41	chr7:124904981-124905031	CMK	blood:	n/a
42	chr7:124904981-124905031	HRCEpiC	kidney:	n/a
43	chr7:124904981-124905031	LNCaP	prostate:	n/a
44	chr7:124904981-124905031	T-47D	breast:	n/a
45	chr7:124904981-124905031	HRPEpiC	eye:	n/a
46	chr7:124904981-124905031	PrEC	prostate:	n/a
47	chr7:124904981-124905031	BJ	skin:	n/a
48	chr7:124904981-124905031	PANC-1	pancreas:	n/a
49	chr7:124904981-124905031	ProgFib	skin:	n/a
50	chr7:124904981-124905031	AG04449	skin:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124816634..124819440-chr7:124929772..124932344,2	K562	blood:
2	chr7:124855825..124857755-chr7:124906299..124909207,2	MCF-7	breast:
3	chr7:124904732..124906870-chr7:124909560..124912125,2	K562	blood:
4	chr7:124904732..124906870-chr7:124909560..124912125,2	K562	blood:
5	chr7:124914060..124916364-chr7:124917880..124920305,2	K562	blood:
6	chr7:124914060..124916364-chr7:124917880..124920305,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POT1-2	chr7:124904097-124904328	NONHSAT123104
2	lnc-POT1-5	chr7:124940558-124940932	NONHSAT123105
3	lnc-POT1-2	chr7:124904097-124904345	ENSG00000219445
4	lnc-POT1-2	chr7:124904097-124904345	NR_110183

No data

Variant related genes	Relation type
ENSG00000213291	TF binding region
ENSG00000219445	TF binding region
ENSG00000213291	CpG island
ENSG00000219445	CpG island
PHF10	miRNA target sites

Extended variants
information (count: 1089 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532244344	chr7:124900072-124900073	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552244536	chr7:124900074-124900075	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62477088	chr7:124900079-124900080	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs370009479	chr7:124900177-124900178	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373189330	chr7:124900202-124900203	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145545618	chr7:124900216-124900217	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376298433	chr7:124900218-124900219	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138164024	chr7:124900221-124900222	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372980383	chr7:124900285-124900286	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536480868	chr7:124900295-124900296	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553509219	chr7:124900345-124900346	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573047936	chr7:124900361-124900362	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375952773	chr7:124900393-124900394	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558536315	chr7:124900412-124900413	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575193698	chr7:124900433-124900434	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34557803	chr7:124900454-124900455	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs374102958	chr7:124900501-124900502	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12539596	chr7:124900509-124900510	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540105019	chr7:124900525-124900526	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560287958	chr7:124900553-124900554	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563419751	chr7:124900559-124900560	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532256497	chr7:124900573-124900574	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552256692	chr7:124900574-124900575	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568893378	chr7:124900584-124900585	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183414125	chr7:124900594-124900595	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148248293	chr7:124900684-124900685	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567893024	chr7:124900705-124900706	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188760245	chr7:124900791-124900792	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546918423	chr7:124900823-124900824	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201704746	chr7:124900836-124900837	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538747996	chr7:124900853-124900854	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558596158	chr7:124900893-124900894	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575250989	chr7:124900918-124900919	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537883817	chr7:124900932-124900933	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374771145	chr7:124900944-124900945	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574686027	chr7:124900976-124900977	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10275923	chr7:124901006-124901007	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs376054260	chr7:124901007-124901008	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560394612	chr7:124901033-124901034	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10260252	chr7:124901039-124901040	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184028396	chr7:124901051-124901052	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562606325	chr7:124901056-124901057	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531412848	chr7:124901062-124901063	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547922962	chr7:124901112-124901113	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368345644	chr7:124901120-124901121	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561714223	chr7:124901124-124901125	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372376755	chr7:124901147-124901148	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530336516	chr7:124901148-124901149	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547223372	chr7:124901173-124901174	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187250218	chr7:124901227-124901228	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Myelodysplastic syndrome	21251322	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
Chordoma	21215367	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124898600-124901200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:124898800-124902000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:124899200-124901200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:124899800-124901600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:124900000-124901200	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr7:124900000-124901200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:124900000-124901200	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr7:124900000-124901200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:124900000-124901200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:124900000-124901800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:124900000-124904800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr7:124901200-124901600	Active TSS	H1 Cell Line	embryonic stem cell
13	chr7:124901200-124901600	Transcr. at gene 5' and 3'	H9 Cell Line	embryonic stem cell
14	chr7:124901200-124901600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr7:124901200-124902200	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
16	chr7:124901200-124902400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
17	chr7:124901200-124904400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:124901200-124904800	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr7:124901200-124906400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:124901600-124902200	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr7:124901600-124903800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:124901600-124904800	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr7:124901600-124905000	Active TSS	H9 Cell Line	embryonic stem cell
24	chr7:124901800-124904800	Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr7:124902200-124903600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr7:124902200-124904800	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr7:124902400-124904800	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr7:124903600-124905200	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr7:124903800-124904400	Active TSS	H1 Cell Line	embryonic stem cell
30	chr7:124904000-124905200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr7:124904400-124904800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:124904800-124905000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr7:124904800-124905000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr7:124904800-124905200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:124904800-124905200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr7:124904800-124905400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr7:124904800-124906000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr7:124905000-124905200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:124905000-124905800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr7:124905200-124905400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr7:124905200-124908400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr7:124905400-124905800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr7:124905400-124906200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:124905800-124908600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr7:124906000-124908600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr7:124906200-124907000	Enhancers	Fetal Lung	lung
47	chr7:124906200-124908600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr7:124906400-124912200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:124908400-124909000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr7:124908600-124909000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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