Variant report

Variant	nsv1016655
Chromosome Location	chr7:124575684-124684279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:124637007-124637167	K562	blood:	n/a	n/a
2	ARID3A	chr7:124656923-124656953	K562	blood:	n/a	n/a
3	ARID3A	chr7:124632397-124633404	K562	blood:	n/a	n/a
4	ATF1	chr7:124581503-124581757	K562	blood:	n/a	n/a
5	ATF1	chr7:124632844-124633185	K562	blood:	n/a	n/a
6	ATF3	chr7:124632775-124633232	K562	blood:	n/a	n/a
7	BACH1	chr7:124632839-124633414	K562	blood:	n/a	n/a
8	BACH1	chr7:124632210-124632237	K562	blood:	n/a	n/a
9	BHLHE40	chr7:124632911-124633233	K562	blood:	n/a	n/a
10	BHLHE40	chr7:124644549-124644599	K562	blood:	n/a	n/a
11	CBX3	chr7:124598035-124598354	K562	blood:	n/a	n/a
12	CBX3	chr7:124598035-124598565	K562	blood:	n/a	n/a
13	CBX3	chr7:124632774-124633230	K562	blood:	n/a	n/a
14	CBX3	chr7:124581318-124581885	K562	blood:	n/a	n/a
15	CCNT2	chr7:124632875-124633179	K562	blood:	n/a	n/a
16	CEBPB	chr7:124665488-124665855	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:124632893-124633288	K562	blood:	n/a	n/a
18	CEBPB	chr7:124632731-124633255	MCF-7	breast:	n/a	n/a
19	CEBPB	chr7:124663957-124664143	K562	blood:	n/a	n/a
20	CEBPB	chr7:124632938-124633193	K562	blood:	n/a	n/a
21	CEBPB	chr7:124632786-124633289	K562	blood:	n/a	n/a
22	CEBPB	chr7:124632819-124633342	MCF-7	breast:	n/a	n/a
23	CEBPB	chr7:124641115-124641235	K562	blood:	n/a	n/a
24	CEBPB	chr7:124632813-124633472	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:124606210-124606293	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:124632741-124633509	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr7:124632838-124633185	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr7:124586008-124586014	K562	blood:	n/a	n/a
29	CTCF	chr7:124673706-124673889	LNCaP	prostate:	n/a	n/a
30	CTCF	chr7:124632873-124632894	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr7:124669000-124669150	HVMF	connective:	n/a	n/a
32	CTCF	chr7:124673600-124673750	HCT-116	colon:	n/a	n/a
33	CTCF	chr7:124637016-124637208	Medullo	brain:	n/a	n/a
34	CTCF	chr7:124636976-124637208	A549	lung:	n/a	n/a
35	CTCF	chr7:124637060-124637210	GM12865	blood:	n/a	n/a
36	CTCF	chr7:124637020-124637170	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr7:124673660-124673810	NB4	blood:	n/a	n/a
38	CTCF	chr7:124636980-124637247	K562	blood:	n/a	n/a
39	CTCF	chr7:124673598-124674008	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:124636940-124637090	NHLF	lung:	n/a	n/a
41	CTCF	chr7:124637060-124637210	HL-60	blood:	n/a	n/a
42	CTCF	chr7:124637060-124637210	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:124673669-124673922	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:124637000-124637150	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr7:124673728-124673844	GM19239	blood:	n/a	n/a
46	CTCF	chr7:124671020-124671170	GM12866	blood:	n/a	n/a
47	CTCF	chr7:124673638-124673903	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr7:124637060-124637210	AG04449	skin:	n/a	n/a
49	CTCF	chr7:124673698-124673861	A549	lung:	n/a	n/a
50	CTCF	chr7:124637040-124637205	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124633001-124633051	ovcar-3	ovarian:	n/a
2	chr7:124625362-124625412	NHDF-neo	bronchial:	n/a
3	chr7:124625362-124625412	SK-N-MC	brain:	n/a
4	chr7:124625362-124625412	AG09309	skin:	n/a
5	chr7:124633001-124633051	ECC-1	luminal epithelium:	n/a
6	chr7:124633001-124633051	HEK293	kidney:	embryo
7	chr7:124625362-124625412	NH-A	brain:	n/a
8	chr7:124633001-124633051	MCF10A-Er-Src	breast:	n/a
9	chr7:124633001-124633051	HRPEpiC	eye:	n/a
10	chr7:124633001-124633051	SK-N-SH_RA	brain:	n/a
11	chr7:124625362-124625412	HRCEpiC	kidney:	n/a
12	chr7:124625362-124625412	HUVEC	blood vessel:	n/a
13	chr7:124625362-124625412	U87	brain:	n/a
14	chr7:124625362-124625412	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:124625362-124625412	T-47D	breast:	n/a
16	chr7:124625362-124625412	SK-N-SH	brain:	n/a
17	chr7:124625362-124625412	HCF	heart:	n/a
18	chr7:124625362-124625412	AG09319	gingival:	n/a
19	chr7:124633001-124633051	HAEpiC	amniotic membrane:	n/a
20	chr7:124625362-124625412	CMK	blood:	n/a
21	chr7:124625362-124625412	LNCaP	prostate:	n/a
22	chr7:124625362-124625412	SAEC	small airway:	n/a
23	chr7:124625362-124625412	MCF10A-Er-Src	breast:	n/a
24	chr7:124625362-124625412	HAEpiC	amniotic membrane:	n/a
25	chr7:124633001-124633051	SK-N-SH	brain:	n/a
26	chr7:124625362-124625412	GM12878	blood:	n/a
27	chr7:124625362-124625412	GM12892	blood:	n/a
28	chr7:124625362-124625412	HRPEpiC	eye:	n/a
29	chr7:124633001-124633051	HEEpiC	esophagus:	n/a
30	chr7:124625362-124625412	AG04450	lung:	fetal
31	chr7:124625362-124625412	HIPEpiC	eye:	n/a
32	chr7:124633001-124633051	SK-N-MC	brain:	n/a
33	chr7:124633001-124633051	K562	blood:	n/a
34	chr7:124625362-124625412	GM19239	blood:	n/a
35	chr7:124633001-124633051	Hepatocyte	liver:	n/a
36	chr7:124633001-124633051	HepG2	liver:	n/a
37	chr7:124633001-124633051	ProgFib	skin:	n/a
38	chr7:124625362-124625412	PANC-1	pancreas:	n/a
39	chr7:124625362-124625412	PFSK-1	brain:	n/a
40	chr7:124633001-124633051	AG09309	skin:	n/a
41	chr7:124633001-124633051	AG04449	skin:	fetal
42	chr7:124633001-124633051	NHBE	bronchial:	n/a
43	chr7:124625362-124625412	HL-60	blood:	n/a
44	chr7:124625362-124625412	HRE	kidney:	n/a
45	chr7:124625362-124625412	K562	blood:	n/a
46	chr7:124633001-124633051	GM12891	blood:	n/a
47	chr7:124633001-124633051	Hela-S3	cervix:	n/a
48	chr7:124633001-124633051	SAEC	small airway:	n/a
49	chr7:124633001-124633051	SKMC	muscle:	n/a
50	chr7:124633001-124633051	GM06990	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124652094..124654102-chr7:124655952..124659375,3	K562	blood:
2	chr7:124570010..124572071-chr7:124632097..124634842,3	MCF-7	breast:
3	chr7:124656588..124658906-chr7:124962987..124965229,2	K562	blood:
4	chr7:124568419..124570704-chr7:124629136..124631296,2	MCF-7	breast:
5	chr7:124495485..124496005-chr7:124636684..124637532,2	MCF-7	breast:
6	chr7:124570250..124573246-chr7:124575640..124577419,2	K562	blood:
7	chr7:124666403..124669373-chr7:124671418..124674369,2	MCF-7	breast:
8	chr7:124625632..124627676-chr7:124628734..124631039,2	MCF-7	breast:
9	chr7:124584280..124585909-chr7:124591798..124594072,2	K562	blood:
10	chr7:124610367..124612617-chr7:124646921..124649703,2	K562	blood:
11	chr7:124641428..124646399-chr7:124650390..124654210,4	K562	blood:
12	chr7:124682680..124683208-chr7:124956334..124957073,2	MCF-7	breast:
13	chr7:124606875..124608614-chr7:124609059..124611420,2	MCF-7	breast:
14	chr7:124674442..124676696-chr7:124676789..124679518,2	MCF-7	breast:
15	chr7:124625632..124627676-chr7:124628734..124631039,2	MCF-7	breast:
16	chr7:124610367..124612617-chr7:124646921..124649703,2	K562	blood:
17	chr7:124674442..124676696-chr7:124676789..124679518,2	MCF-7	breast:
18	chr7:124559307..124561381-chr7:124633111..124635066,2	MCF-7	breast:
19	chr7:124641428..124646399-chr7:124650390..124654210,4	K562	blood:
20	chr7:124651129..124654102-chr7:124654805..124659375,5	K562	blood:
21	chr7:124584280..124585909-chr7:124591798..124594072,2	K562	blood:
22	chr7:124611698..124614462-chr7:124706318..124708451,2	K562	blood:
23	chr7:124606875..124608614-chr7:124609059..124611420,2	MCF-7	breast:
24	chr7:124651129..124654102-chr7:124654805..124659375,5	K562	blood:
25	chr7:124652094..124654102-chr7:124655952..124659375,3	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
2	lnc-POT1-3	chr7:124673634-124673820	ucscGeneNc_uc010lky_1
3	lnc-SPAM1-7	chr7:124627790-124627842	NONHSAT123095
4	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
5	lnc-POT1-3	chr7:124675591-124675731	ucscGeneNc_uc010lky_1
6	lnc-SPAM1-7	chr7:124631917-124632152	NONHSAT123095
7	lnc-POT1-3	chr7:124656869-124658131	ucscGeneNc_uc010lky_1
8	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
9	lnc-SPAM1-4	chr7:124580334-124580439	NONHSAT123092
10	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
11	lnc-SPAM1-4	chr7:124638324-124638458	XLOC_006231
12	lnc-POT1-3	chr7:124677270-124677347	ucscGeneNc_uc010lky_1
13	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
14	lnc-SPAM1-4	chr7:124640736-124641066	ENSG00000224897
15	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
16	lnc-SPAM1-4	chr7:124640736-124641124	XLOC_006231
17	lnc-SPAM1-4	chr7:124660387-124660535	NONHSAT123092
18	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
19	lnc-SPAM1-4	chr7:124580334-124580439	ENSG00000224897
20	lnc-SPAM1-4	chr7:124633062-124633253	ENSG00000224897
21	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897

No data

Variant related genes	Relation type
POT1-AS1	TF binding region
EEF1GP1	TF binding region
POT1-AS1	CpG island
EEF1GP1	CpG island
ENSG00000186676	chromatin interactions
ENSG00000128513	chromatin interactions
ENSG00000224897	chromatin interactions
BAHCC1	miRNA target sites
FGL2	miRNA target sites
SPRY2	miRNA target sites
IL1RAP	miRNA target sites
IMPA1	miRNA target sites
RRBP1	miRNA target sites
SACM1L	miRNA target sites
AXL	miRNA target sites
CKAP5	miRNA target sites
ZNHIT1	miRNA target sites
CA2	miRNA target sites

Extended variants
information (count: 1644 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1644 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7799518	chr7:124575684-124575685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527774206	chr7:124575686-124575687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547943556	chr7:124575748-124575749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570882277	chr7:124575753-124575754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556237719	chr7:124575774-124575775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577772086	chr7:124575795-124575796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539789583	chr7:124575796-124575797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7780541	chr7:124575825-124575826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs543521531	chr7:124575873-124575874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569886170	chr7:124575901-124575902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193223778	chr7:124575915-124575916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555133202	chr7:124575941-124575942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10081336	chr7:124575945-124575946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs35146319	chr7:124575949-124575950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs543036748	chr7:124575957-124575958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10709318	chr7:124575993-124575994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527625382	chr7:124576000-124576001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397729835	chr7:124576001-124576002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201796081	chr7:124576003-124576004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528280460	chr7:124576008-124576009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201980706	chr7:124576009-124576010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56228925	chr7:124576010-124576011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397736170	chr7:124576017-124576018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577679268	chr7:124576068-124576069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7780893	chr7:124576099-124576100	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185606579	chr7:124576150-124576151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564276115	chr7:124576156-124576157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538926660	chr7:124576215-124576216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533118590	chr7:124576217-124576218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10255638	chr7:124576255-124576256	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs17147723	chr7:124576298-124576299	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs535177363	chr7:124576303-124576304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562248203	chr7:124576358-124576359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10243479	chr7:124576414-124576415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs190069644	chr7:124576425-124576426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148138034	chr7:124576447-124576448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181731302	chr7:124576491-124576492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370059808	chr7:124576556-124576557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550146316	chr7:124576571-124576572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569993429	chr7:124576576-124576577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529135933	chr7:124576594-124576595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548895076	chr7:124576608-124576609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534992203	chr7:124576609-124576610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80317755	chr7:124576614-124576615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534476140	chr7:124576638-124576639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10272889	chr7:124576641-124576642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs141924099	chr7:124576675-124576676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188702195	chr7:124576698-124576699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180777770	chr7:124576710-124576711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184975398	chr7:124576711-124576712	Weak transcription	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124570200-124585400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:124575400-124580200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:124577200-124577400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:124577400-124581200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:124578200-124579200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:124580200-124580400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:124580200-124581000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:124580400-124580800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:124580800-124585400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr7:124581000-124581200	Enhancers	K562	blood
11	chr7:124581200-124581400	Flanking Active TSS	K562	blood
12	chr7:124581200-124582400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:124581400-124581600	Enhancers	K562	blood
14	chr7:124581600-124582000	Flanking Active TSS	K562	blood
15	chr7:124582000-124582800	Enhancers	K562	blood
16	chr7:124585200-124585600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:124585200-124585600	ZNF genes & repeats	Lung	lung
18	chr7:124585400-124585600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:124585400-124585600	Enhancers	Gastric	stomach
20	chr7:124588200-124588800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr7:124591600-124594800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:124592400-124592600	Flanking Active TSS	Left Ventricle	heart
23	chr7:124592600-124592800	ZNF genes & repeats	Left Ventricle	heart
24	chr7:124592600-124597800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr7:124594800-124595200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:124596000-124596800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:124596200-124596600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr7:124596400-124596800	Enhancers	Placenta Amnion	Placenta Amnion
29	chr7:124597600-124600400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:124598400-124599400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:124599400-124600400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:124599400-124601000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:124599800-124600200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr7:124600000-124600600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:124600000-124600600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:124600400-124602400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:124601000-124601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:124602400-124602600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:124604800-124605400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:124612400-124612800	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr7:124629600-124632600	Weak transcription	Stomach Mucosa	stomach
42	chr7:124629800-124630400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:124630000-124630400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:124630200-124630400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:124630200-124630400	Enhancers	Hela-S3	cervix
46	chr7:124630200-124630600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:124630200-124630600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:124630200-124630600	Enhancers	NH-A	brain
49	chr7:124630400-124632800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:124630400-124633200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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