Variant report

Variant	nsv1025873
Chromosome Location	chr7:124591433-124668423
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:405)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:124656923-124656953	K562	blood:	n/a	n/a
2	ARID3A	chr7:124637007-124637167	K562	blood:	n/a	n/a
3	ARID3A	chr7:124632397-124633404	K562	blood:	n/a	n/a
4	ATF1	chr7:124632844-124633185	K562	blood:	n/a	n/a
5	ATF3	chr7:124632775-124633232	K562	blood:	n/a	n/a
6	BACH1	chr7:124632210-124632237	K562	blood:	n/a	n/a
7	BACH1	chr7:124632839-124633414	K562	blood:	n/a	n/a
8	BHLHE40	chr7:124632911-124633233	K562	blood:	n/a	n/a
9	BHLHE40	chr7:124644549-124644599	K562	blood:	n/a	n/a
10	CBX3	chr7:124598035-124598565	K562	blood:	n/a	n/a
11	CBX3	chr7:124598035-124598354	K562	blood:	n/a	n/a
12	CBX3	chr7:124632774-124633230	K562	blood:	n/a	n/a
13	CCNT2	chr7:124632875-124633179	K562	blood:	n/a	n/a
14	CEBPB	chr7:124632813-124633472	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:124632741-124633509	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr7:124632819-124633342	MCF-7	breast:	n/a	n/a
17	CEBPB	chr7:124632938-124633193	K562	blood:	n/a	n/a
18	CEBPB	chr7:124641115-124641235	K562	blood:	n/a	n/a
19	CEBPB	chr7:124665488-124665855	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:124663957-124664143	K562	blood:	n/a	n/a
21	CEBPB	chr7:124606210-124606293	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:124632786-124633289	K562	blood:	n/a	n/a
23	CEBPB	chr7:124632731-124633255	MCF-7	breast:	n/a	n/a
24	CEBPB	chr7:124632893-124633288	K562	blood:	n/a	n/a
25	CHD2	chr7:124632838-124633185	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr7:124637080-124637230	K562	blood:	n/a	n/a
27	CTCF	chr7:124637007-124637196	A549	lung:	n/a	n/a
28	CTCF	chr7:124636960-124637110	A549	lung:	n/a	n/a
29	CTCF	chr7:124637040-124637190	AG04450	lung:	n/a	n/a
30	CTCF	chr7:124637060-124637210	AG04449	skin:	n/a	n/a
31	CTCF	chr7:124637048-124637194	GM20000	blood:	n/a	n/a
32	CTCF	chr7:124637100-124637250	HCFaa	heart:	n/a	n/a
33	CTCF	chr7:124636987-124637212	K562	blood:	n/a	n/a
34	CTCF	chr7:124637083-124637174	GM19239	blood:	n/a	n/a
35	CTCF	chr7:124637040-124637190	AG04449	skin:	n/a	n/a
36	CTCF	chr7:124637017-124637229	LNCaP	prostate:	n/a	n/a
37	CTCF	chr7:124637040-124637190	GM12871	blood:	n/a	n/a
38	CTCF	chr7:124637000-124637150	GM12872	blood:	n/a	n/a
39	CTCF	chr7:124636960-124637110	GM12865	blood:	n/a	n/a
40	CTCF	chr7:124637061-124637225	A549	lung:	n/a	n/a
41	CTCF	chr7:124637040-124637190	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr7:124637060-124637210	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr7:124636926-124637319	GM12878	blood:	n/a	n/a
44	CTCF	chr7:124636980-124637247	K562	blood:	n/a	n/a
45	CTCF	chr7:124662680-124662830	GM12864	blood:	n/a	n/a
46	CTCF	chr7:124637000-124637150	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr7:124637060-124637210	BJ	skin:	n/a	n/a
48	CTCF	chr7:124637040-124637190	BE2_C	brain:	n/a	n/a
49	CTCF	chr7:124637031-124637234	LNCaP	prostate:	n/a	n/a
50	CTCF	chr7:124637023-124637298	H1-hESC	embryonic stem cell:	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	AG09319	gingival:	n/a
2	chr7:124625362-124625412	Hepatocyte	liver:	n/a
3	chr7:124633001-124633051	GM06990	blood:	n/a
4	chr7:124633001-124633051	AG09309	skin:	n/a
5	chr7:124633001-124633051	BJ	skin:	n/a
6	chr7:124625362-124625412	HL-60	blood:	n/a
7	chr7:124633001-124633051	K562	blood:	n/a
8	chr7:124625362-124625412	NHBE	bronchial:	n/a
9	chr7:124625362-124625412	BJ	skin:	n/a
10	chr7:124633001-124633051	AG10803	skin:	n/a
11	chr7:124633001-124633051	MCF-7	breast:	n/a
12	chr7:124625362-124625412	PrEC	prostate:	n/a
13	chr7:124625362-124625412	HepG2	liver:	n/a
14	chr7:124633001-124633051	HCT-116	colon:	n/a
15	chr7:124625362-124625412	AG10803	skin:	n/a
16	chr7:124625362-124625412	SK-N-SH_RA	brain:	n/a
17	chr7:124625362-124625412	Hela-S3	cervix:	n/a
18	chr7:124633001-124633051	HEK293	kidney:	embryo
19	chr7:124633001-124633051	NH-A	brain:	n/a
20	chr7:124633001-124633051	HMEC	breast:	n/a
21	chr7:124633001-124633051	Hela-S3	cervix:	n/a
22	chr7:124625362-124625412	BE2_C	brain:	n/a
23	chr7:124625362-124625412	HMEC	breast:	n/a
24	chr7:124633001-124633051	U87	brain:	n/a
25	chr7:124625362-124625412	MCF10A-Er-Src	breast:	n/a
26	chr7:124625362-124625412	HCM	heart:	n/a
27	chr7:124633001-124633051	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:124633001-124633051	HAEpiC	amniotic membrane:	n/a
29	chr7:124633001-124633051	A549	lung:	n/a
30	chr7:124633001-124633051	HUVEC	blood vessel:	n/a
31	chr7:124633001-124633051	SKMC	muscle:	n/a
32	chr7:124633001-124633051	ovcar-3	ovarian:	n/a
33	chr7:124633001-124633051	AG04449	skin:	fetal
34	chr7:124633001-124633051	HCPEpiC	choroid plexus:	n/a
35	chr7:124625362-124625412	NHDF-neo	bronchial:	n/a
36	chr7:124625362-124625412	GM06990	blood:	n/a
37	chr7:124625362-124625412	SK-N-MC	brain:	n/a
38	chr7:124625362-124625412	Jurkat	blood:	n/a
39	chr7:124625362-124625412	AoSMC	blood vessel:	n/a
40	chr7:124633001-124633051	HCM	heart:	n/a
41	chr7:124625362-124625412	IMR90	lung:	fetal
42	chr7:124625362-124625412	ProgFib	skin:	n/a
43	chr7:124633001-124633051	NHBE	bronchial:	n/a
44	chr7:124625362-124625412	PFSK-1	brain:	n/a
45	chr7:124633001-124633051	PFSK-1	brain:	n/a
46	chr7:124625362-124625412	HEEpiC	esophagus:	n/a
47	chr7:124625362-124625412	U87	brain:	n/a
48	chr7:124625362-124625412	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:124633001-124633051	PANC-1	pancreas:	n/a
50	chr7:124625362-124625412	HNPCEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

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

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
2	lnc-POT1-3	chr7:124656869-124658131	ucscGeneNc_uc010lky_1
3	lnc-SPAM1-4	chr7:124640736-124641124	XLOC_006231
4	lnc-SPAM1-4	chr7:124640736-124641066	ENSG00000224897
5	lnc-SPAM1-4	chr7:124638324-124638458	XLOC_006231
6	lnc-SPAM1-7	chr7:124631917-124632152	NONHSAT123095
7	lnc-SPAM1-4	chr7:124660387-124660535	NONHSAT123092
8	lnc-SPAM1-4	chr7:124633062-124633253	ENSG00000224897
9	lnc-SPAM1-7	chr7:124627790-124627842	NONHSAT123095
10	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
11	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
12	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
13	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897

No data

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

Extended variants
information (count: 1088 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1088 , 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	rs144364584	chr7:124591621-124591622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537194606	chr7:124591662-124591663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183920575	chr7:124591691-124591692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546956882	chr7:124591692-124591693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373354923	chr7:124591758-124591759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566844567	chr7:124591797-124591798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539050006	chr7:124591810-124591811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs67870530	chr7:124591878-124591879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs151098216	chr7:124591881-124591882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572245373	chr7:124592002-124592003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538043972	chr7:124592003-124592004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375643162	chr7:124592011-124592012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554510830	chr7:124592013-124592014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7799523	chr7:124592033-124592034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs187806111	chr7:124592034-124592035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539979689	chr7:124592053-124592054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7799535	chr7:124592060-124592061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs576393644	chr7:124592086-124592087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545403293	chr7:124592122-124592123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28712568	chr7:124592147-124592148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551693351	chr7:124592176-124592177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370687769	chr7:124592179-124592180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377322010	chr7:124592180-124592181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531155146	chr7:124592266-124592267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544781870	chr7:124592320-124592321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6971179	chr7:124592351-124592352	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs552628194	chr7:124592404-124592405	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530340078	chr7:124592409-124592410	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs547081299	chr7:124592467-124592468	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs185744189	chr7:124592474-124592475	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs189810459	chr7:124592485-124592486	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs552652256	chr7:124592563-124592564	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs552201831	chr7:124592574-124592575	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs569166414	chr7:124592587-124592588	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs375464491	chr7:124592597-124592598	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs369749809	chr7:124592598-124592599	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs397793068	chr7:124592604-124592605	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs193202244	chr7:124592623-124592624	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs548345542	chr7:124592633-124592634	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs140764345	chr7:124592634-124592635	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs183953430	chr7:124592642-124592643	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs6971413	chr7:124592668-124592669	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs553409320	chr7:124592682-124592683	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs548408304	chr7:124592685-124592686	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs539042240	chr7:124592693-124592694	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs150127204	chr7:124592700-124592701	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs6466970	chr7:124592755-124592756	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs544606734	chr7:124592836-124592837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188682043	chr7:124592864-124592865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570742647	chr7:124592955-124592956	Weak transcription	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
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

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124591600-124594800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:124592400-124592600	Flanking Active TSS	Left Ventricle	heart
3	chr7:124592600-124592800	ZNF genes & repeats	Left Ventricle	heart
4	chr7:124592600-124597800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:124594800-124595200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:124596000-124596800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:124596200-124596600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:124596400-124596800	Enhancers	Placenta Amnion	Placenta Amnion
9	chr7:124597600-124600400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:124598400-124599400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:124599400-124600400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr7:124599400-124601000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:124599800-124600200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr7:124600000-124600600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr7:124600000-124600600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:124600400-124602400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:124601000-124601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:124602400-124602600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:124604800-124605400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr7:124612400-124612800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr7:124629600-124632600	Weak transcription	Stomach Mucosa	stomach
22	chr7:124629800-124630400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:124630000-124630400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:124630200-124630400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:124630200-124630400	Enhancers	Hela-S3	cervix
26	chr7:124630200-124630600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:124630200-124630600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:124630200-124630600	Enhancers	NH-A	brain
29	chr7:124630400-124632800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:124630400-124633200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:124630600-124631000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:124630600-124631800	Weak transcription	Hela-S3	cervix
33	chr7:124630600-124632200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:124630600-124632400	Weak transcription	NH-A	brain
35	chr7:124631000-124631200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:124631000-124631200	Enhancers	Aorta	Aorta
37	chr7:124631200-124632800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr7:124631800-124632800	Enhancers	Hela-S3	cervix
39	chr7:124632200-124633200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:124632400-124632800	Enhancers	NH-A	brain
41	chr7:124632600-124633600	Enhancers	Stomach Mucosa	stomach
42	chr7:124632800-124633000	Flanking Active TSS	Hela-S3	cervix
43	chr7:124632800-124633000	Flanking Active TSS	K562	blood
44	chr7:124632800-124633000	Flanking Active TSS	NH-A	brain
45	chr7:124632800-124633200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:124632800-124633200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr7:124632800-124633200	Enhancers	Osteobl	bone
48	chr7:124632800-124633600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr7:124632800-124633800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:124632800-124633800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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