Variant report

Variant	nsv1020911
Chromosome Location	chr7:112581515-112615249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:112591210-112591392	K562	blood:	n/a	n/a
2	ATF1	chr7:112599838-112599896	K562	blood:	n/a	n/a
3	ATF1	chr7:112610852-112610969	K562	blood:	n/a	n/a
4	CCNT2	chr7:112614259-112614408	K562	blood:	n/a	n/a
5	CEBPB	chr7:112607913-112608165	K562	blood:	n/a	n/a
6	CEBPB	chr7:112607411-112607467	K562	blood:	n/a	n/a
7	CEBPB	chr7:112613927-112614080	Hela-S3	cervix:	n/a	chr7:112614062-112614075 chr7:112614063-112614074
8	CEBPB	chr7:112613922-112614193	HepG2	liver:	n/a	chr7:112614062-112614075 chr7:112614063-112614074
9	CEBPB	chr7:112613905-112614205	IMR90	lung:	n/a	chr7:112614062-112614075 chr7:112614185-112614198 chr7:112614063-112614074
10	CEBPB	chr7:112607909-112608293	K562	blood:	n/a	n/a
11	CEBPB	chr7:112581584-112581784	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:112607905-112608244	K562	blood:	n/a	n/a
13	CEBPB	chr7:112598065-112598107	HepG2	liver:	n/a	n/a
14	CTCF	chr7:112611000-112611150	HEEpiC	esophagus:	n/a	n/a
15	CTCF	chr7:112610999-112611068	ProgFib	skin:	n/a	n/a
16	CTCF	chr7:112610943-112611094	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:112610960-112611110	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr7:112610940-112611090	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr7:112610980-112611130	GM12865	blood:	n/a	n/a
20	CTCF	chr7:112610980-112611130	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr7:112610940-112611090	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr7:112610940-112611090	NB4	blood:	n/a	n/a
23	CTCF	chr7:112610973-112611049	GM12878	blood:	n/a	n/a
24	CTCF	chr7:112610960-112611110	HEK293	kidney:	n/a	n/a
25	CTCF	chr7:112611020-112611170	GM06990	blood:	n/a	n/a
26	CTCF	chr7:112610940-112611090	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr7:112610920-112611070	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr7:112610973-112611097	GM12878	blood:	n/a	n/a
29	CTCF	chr7:112610940-112611090	BE2_C	brain:	n/a	n/a
30	CTCF	chr7:112610884-112611188	K562	blood:	n/a	n/a
31	CTCF	chr7:112610940-112611090	GM12872	blood:	n/a	n/a
32	CTCF	chr7:112610940-112611090	HVMF	connective:	n/a	n/a
33	CTCF	chr7:112610980-112611250	GM12868	blood:	n/a	n/a
34	CTCF	chr7:112610973-112611101	Gliobla	brain:	n/a	n/a
35	CTCF	chr7:112611020-112611170	HMF	breast:	n/a	n/a
36	CTCF	chr7:112610860-112611010	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr7:112610900-112611050	HMF	breast:	n/a	n/a
38	CTCF	chr7:112611020-112611170	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr7:112610940-112611170	AG09319	gingival:	n/a	n/a
40	CTCF	chr7:112610920-112611070	Caco-2	colon:	n/a	n/a
41	CTCF	chr7:112610920-112611070	HCT-116	colon:	n/a	n/a
42	CTCF	chr7:112610994-112611058	HepG2	liver:	n/a	n/a
43	CTCF	chr7:112610900-112611050	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:112610920-112611070	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr7:112611000-112611150	A549	lung:	n/a	n/a
46	CTCF	chr7:112610940-112611090	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr7:112610900-112611050	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr7:112610963-112611098	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:112610960-112611110	GM12872	blood:	n/a	n/a
50	CTCF	chr7:112611040-112611190	GM12869	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112582716-112582766	SKMC	muscle:	n/a
2	chr7:112582716-112582766	NB4	blood:	n/a
3	chr7:112582716-112582766	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:112582716-112582766	GM12878	blood:	n/a
5	chr7:112582716-112582766	A549	lung:	n/a
6	chr7:112582716-112582766	ProgFib	skin:	n/a
7	chr7:112582716-112582766	NH-A	brain:	n/a
8	chr7:112582716-112582766	CMK	blood:	n/a
9	chr7:112582716-112582766	BJ	skin:	n/a
10	chr7:112582716-112582766	H1-hESC	embryonic stem cell:	embryo
11	chr7:112582716-112582766	AG09309	skin:	n/a
12	chr7:112582716-112582766	BE2_C	brain:	n/a
13	chr7:112582716-112582766	HNPCEpiC	eye:	n/a
14	chr7:112582716-112582766	RPTEC	kidney:	n/a
15	chr7:112582716-112582766	HCM	heart:	n/a
16	chr7:112582716-112582766	T-47D	breast:	n/a
17	chr7:112582716-112582766	HCF	heart:	n/a
18	chr7:112582716-112582766	HCT-116	colon:	n/a
19	chr7:112582716-112582766	LNCaP	prostate:	n/a
20	chr7:112582716-112582766	K562	blood:	n/a
21	chr7:112582716-112582766	GM12891	blood:	n/a
22	chr7:112582716-112582766	Hepatocyte	liver:	n/a
23	chr7:112582716-112582766	HUVEC	blood vessel:	n/a
24	chr7:112582716-112582766	Caco-2	colon:	n/a
25	chr7:112582716-112582766	NT2-D1	testis:	n/a
26	chr7:112582716-112582766	Jurkat	blood:	n/a
27	chr7:112582716-112582766	HRE	kidney:	n/a
28	chr7:112582716-112582766	PFSK-1	brain:	n/a
29	chr7:112582716-112582766	HepG2	liver:	n/a
30	chr7:112582716-112582766	PANC-1	pancreas:	n/a
31	chr7:112582716-112582766	AG04450	lung:	fetal
32	chr7:112582716-112582766	NHBE	bronchial:	n/a
33	chr7:112582716-112582766	AG04449	skin:	fetal
34	chr7:112582716-112582766	HRPEpiC	eye:	n/a
35	chr7:112582716-112582766	PrEC	prostate:	n/a
36	chr7:112582716-112582766	ECC-1	luminal epithelium:	n/a
37	chr7:112582716-112582766	AoSMC	blood vessel:	n/a
38	chr7:112582716-112582766	GM06990	blood:	n/a
39	chr7:112582716-112582766	HCPEpiC	choroid plexus:	n/a
40	chr7:112582716-112582766	SK-N-SH_RA	brain:	n/a
41	chr7:112582716-112582766	HEK293	kidney:	embryo
42	chr7:112582716-112582766	GM19239	blood:	n/a
43	chr7:112582716-112582766	HIPEpiC	eye:	n/a
44	chr7:112582716-112582766	MCF10A-Er-Src	breast:	n/a
45	chr7:112582716-112582766	HEEpiC	esophagus:	n/a
46	chr7:112582716-112582766	AG10803	skin:	n/a
47	chr7:112582716-112582766	Hela-S3	cervix:	n/a
48	chr7:112582716-112582766	HMEC	breast:	n/a
49	chr7:112582716-112582766	ovcar-3	ovarian:	n/a
50	chr7:112582716-112582766	GM12892	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:112578476..112580812-chr7:112583356..112586040,2	MCF-7	breast:
2	chr7:112605934..112608716-chr7:112610889..112612705,2	K562	blood:
3	chr7:112580392..112582093-chr7:112599898..112601408,2	MCF-7	breast:
4	chr7:112602086..112604534-chr7:112611738..112613298,2	K562	blood:
5	chr7:112569158..112571513-chr7:112600317..112602732,2	MCF-7	breast:
6	chr7:112608892..112612012-chr7:112612504..112614943,3	MCF-7	breast:
7	chr7:112583353..112585564-chr7:112597999..112600804,2	MCF-7	breast:
8	chr7:112430077..112432189-chr7:112593600..112595306,2	MCF-7	breast:
9	chr7:112580392..112582093-chr7:112599898..112601408,2	MCF-7	breast:
10	chr7:112608892..112612012-chr7:112612504..112614943,3	MCF-7	breast:
11	chr7:112602086..112604534-chr7:112611738..112613298,2	K562	blood:
12	chr7:112578925..112581917-chr7:112594123..112596440,2	MCF-7	breast:
13	chr7:112579425..112581874-chr7:112585299..112587492,4	K562	blood:
14	chr7:112577667..112580375-chr7:112582881..112584475,2	MCF-7	breast:
15	chr7:112583353..112585564-chr7:112597999..112600804,2	MCF-7	breast:
16	chr7:112605934..112608716-chr7:112610889..112612705,2	K562	blood:
17	chr7:112428924..112430644-chr7:112579193..112581843,2	K562	blood:
18	chr7:112578366..112581242-chr7:112590311..112591816,2	MCF-7	breast:
19	chr7:112601365..112604036-chr7:112606772..112610926,4	K562	blood:
20	chr7:112477234..112479370-chr7:112580510..112582070,2	K562	blood:
21	chr7:112601365..112604036-chr7:112606772..112610926,4	K562	blood:
22	chr7:112609190..112612964-chr7:112622640..112627113,4	K562	blood:
23	chr7:112579376..112581874-chr7:112583714..112588388,6	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf60-1	chr7:112594690-112594823	NR_110162
2	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122806
3	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122805
4	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122803
5	lnc-C7orf60-1	chr7:112613674-112613727	ENSG00000234520
6	lnc-C7orf60-1	chr7:112613660-112613727	NONHSAT122804
7	lnc-C7orf60-1	chr7:112594718-112594823	NONHSAT122808
8	lnc-C7orf60-1	chr7:112596577-112596757	ENSG00000234520
9	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122806
10	lnc-C7orf60-1	chr7:112596577-112596757	NONHSAT122803
11	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122804
12	lnc-C7orf60-1	chr7:112613660-112613727	NR_110162
13	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122803
14	lnc-C7orf60-1	chr7:112596577-112596768	NONHSAT122808
15	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122805
16	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122805
17	lnc-C7orf60-1	chr7:112594701-112594823	ENSG00000234520
18	lnc-C7orf60-1	chr7:112613660-112613727	ENSG00000234520
19	lnc-C7orf60-1	chr7:112596577-112596757	NR_110162
20	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122806
21	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122804
22	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122804

No data

Variant related genes	Relation type
C7orf60	TF binding region
C7orf60	CpG island
ENSG00000146802	chromatin interactions
ENSG00000164603	chromatin interactions

Extended variants
information (count: 1087 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1087 , 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	rs78981809	chr7:112581516-112581517	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370439202	chr7:112581519-112581520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187647543	chr7:112581582-112581583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs554293660	chr7:112581595-112581596	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs535412578	chr7:112581613-112581614	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs548079880	chr7:112581628-112581629	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs150330350	chr7:112581644-112581645	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs571000079	chr7:112581651-112581652	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs558046700	chr7:112581662-112581663	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs111984269	chr7:112581705-112581706	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs576904898	chr7:112581745-112581746	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs537929078	chr7:112581774-112581775	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375768107	chr7:112581795-112581796	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs190654193	chr7:112581834-112581835	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs547457914	chr7:112581860-112581861	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs144889732	chr7:112581916-112581917	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs368243987	chr7:112581938-112581939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574486854	chr7:112581946-112581947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532793315	chr7:112581963-112581964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139565424	chr7:112581984-112581985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540034307	chr7:112582001-112582002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182889947	chr7:112582073-112582074	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs560409847	chr7:112582082-112582083	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs556795995	chr7:112582129-112582130	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149023075	chr7:112582149-112582150	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs7798366	chr7:112582173-112582174	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs114392483	chr7:112582174-112582175	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs189118270	chr7:112582186-112582187	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs549868191	chr7:112582203-112582204	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs10268162	chr7:112582247-112582248	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs193045861	chr7:112582315-112582316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547447096	chr7:112582372-112582373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566391835	chr7:112582374-112582375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539729212	chr7:112582385-112582386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372640439	chr7:112582411-112582412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373520656	chr7:112582412-112582413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554521756	chr7:112582507-112582508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143030864	chr7:112582523-112582524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537593003	chr7:112582528-112582529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556301963	chr7:112582562-112582563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35548417	chr7:112582625-112582626	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs554619638	chr7:112582633-112582634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142263980	chr7:112582636-112582637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10228144	chr7:112582640-112582641	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548552399	chr7:112582647-112582648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182972688	chr7:112582663-112582664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545778055	chr7:112582665-112582666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564361127	chr7:112582698-112582699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138439514	chr7:112582712-112582713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543180988	chr7:112582713-112582714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Acute myeloid leukemia	16864856	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112580800-112583600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:112581000-112581800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr7:112581000-112583600	Weak transcription	Placenta	Placenta
4	chr7:112581000-112584000	Weak transcription	Fetal Brain Male	brain
5	chr7:112581000-112585200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr7:112581000-112585200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr7:112581000-112593800	Weak transcription	Left Ventricle	heart
8	chr7:112581400-112584600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr7:112583600-112583800	Enhancers	Placenta	Placenta
10	chr7:112583600-112583800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr7:112585200-112585600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr7:112585200-112585800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr7:112593800-112594200	ZNF genes & repeats	Left Ventricle	heart
14	chr7:112594200-112630400	Weak transcription	Left Ventricle	heart
15	chr7:112599000-112600000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr7:112599600-112600000	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr7:112603200-112603600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:112603400-112603600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr7:112603400-112605200	Enhancers	Fetal Heart	heart
20	chr7:112603600-112614200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:112605000-112605400	Enhancers	Placenta Amnion	Placenta Amnion
22	chr7:112605600-112606400	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr7:112605600-112606600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:112605800-112606600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:112605800-112607600	Active TSS	Right Atrium	heart
26	chr7:112606400-112606600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr7:112606600-112607000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:112606600-112607000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:112607600-112614200	Weak transcription	Right Atrium	heart
30	chr7:112608000-112608400	Enhancers	HepG2	liver
31	chr7:112608000-112608400	Active TSS	K562	blood
32	chr7:112609200-112609600	Enhancers	Right Ventricle	heart
33	chr7:112609600-112613000	Weak transcription	Right Ventricle	heart
34	chr7:112613000-112613600	Active TSS	Right Ventricle	heart
35	chr7:112613400-112614200	Enhancers	Placenta Amnion	Placenta Amnion
36	chr7:112613800-112614000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:112613800-112614000	Enhancers	Osteobl	bone
38	chr7:112614000-112614200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:112614000-112614400	Flanking Active TSS	Osteobl	bone
40	chr7:112614000-112614600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:112614000-112614600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:112614200-112614400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:112614200-112614600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:112614200-112614600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:112614200-112614600	Active TSS	Right Atrium	heart
46	chr7:112614200-112615200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr7:112614200-112615400	Enhancers	Fetal Heart	heart
48	chr7:112614400-112614800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:112614400-112615400	Enhancers	Osteobl	bone
50	chr7:112614600-112615400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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