Variant report

Variant	nsv831042
Chromosome Location	chr7:79984079-80122312
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1325)
CpG islands
(count:305)
Chromatin interactive
region (count:18)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1325 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:80033298-80033367	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:79991513-79991691	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:80083067-80083355	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:80014872-80015255	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:80023166-80023490	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:80021678-80021888	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:80080320-80080515	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:80117772-80117988	HepG2	liver:	n/a	n/a
9	BACH1	chr7:80107995-80108383	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:80104300-80104503	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:80080099-80080214	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:80110643-80110676	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:80057826-80058059	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:80018626-80018740	K562	blood:	n/a	n/a
15	BCL3	chr7:80112328-80112532	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:80001849-80001951	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:80034127-80034181	K562	blood:	n/a	n/a
18	BHLHE40	chr7:80023115-80023487	HepG2	liver:	n/a	n/a
19	BHLHE40	chr7:80084395-80084463	HepG2	liver:	n/a	n/a
20	BHLHE40	chr7:80023136-80023390	HepG2	liver:	n/a	n/a
21	BRCA1	chr7:80083095-80083366	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr7:80110448-80110844	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr7:80096014-80096932	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr7:80057803-80058045	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr7:80108002-80108365	HCT-116	colon:	n/a	n/a
26	CBX3	chr7:80040409-80040730	HCT-116	colon:	n/a	n/a
27	CBX3	chr7:80069805-80070205	HCT-116	colon:	n/a	n/a
28	CCNT2	chr7:80097910-80098110	K562	blood:	n/a	n/a
29	CEBPB	chr7:80014860-80015197	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:80014882-80015098	A549	lung:	n/a	n/a
31	CEBPB	chr7:80069610-80070141	A549	lung:	n/a	chr7:80069846-80069857
32	CEBPB	chr7:80014769-80015338	A549	lung:	n/a	n/a
33	CEBPB	chr7:80112375-80112643	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:80115162-80115578	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:80088237-80088390	HepG2	liver:	n/a	chr7:80088284-80088295 chr7:80088284-80088295 chr7:80088282-80088293
36	CEBPB	chr7:80079259-80079471	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:80061609-80061896	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:80051432-80051498	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:79986804-79987270	ECC-1	luminal epithelium:	n/a	chr7:79987061-79987072
40	CEBPB	chr7:80112355-80112659	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:80014878-80015267	A549	lung:	n/a	n/a
42	CEBPB	chr7:80033196-80033503	HepG2	liver:	n/a	chr7:80033325-80033336
43	CEBPB	chr7:79986939-79987216	A549	lung:	n/a	chr7:79987061-79987072
44	CEBPB	chr7:80033201-80033438	IMR90	lung:	n/a	chr7:80033325-80033336
45	CEBPB	chr7:80095945-80096970	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:80028373-80028422	A549	lung:	n/a	n/a
47	CEBPB	chr7:80014928-80015126	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:80074785-80075117	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:80102216-80102549	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:80069700-80070160	IMR90	lung:	n/a	chr7:80069846-80069857

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80096608-80096658	CMK	blood:	n/a
2	chr7:79998779-79998829	K562	blood:	n/a
3	chr7:79998779-79998829	HL-60	blood:	n/a
4	chr7:80096608-80096658	AG09319	gingival:	n/a
5	chr7:79998795-79998845	HEEpiC	esophagus:	n/a
6	chr7:80096608-80096658	H1-hESC	embryonic stem cell:	embryo
7	chr7:79997911-79997961	H1-hESC	embryonic stem cell:	embryo
8	chr7:79998779-79998829	SKMC	muscle:	n/a
9	chr7:80096608-80096658	HepG2	liver:	n/a
10	chr7:79997911-79997961	HIPEpiC	eye:	n/a
11	chr7:80096608-80096658	Hela-S3	cervix:	n/a
12	chr7:80080213-80080263	GM12878	blood:	n/a
13	chr7:80096608-80096658	GM12892	blood:	n/a
14	chr7:79998795-79998845	ovcar-3	ovarian:	n/a
15	chr7:79998779-79998829	SK-N-SH_RA	brain:	n/a
16	chr7:79998795-79998845	H1-hESC	embryonic stem cell:	embryo
17	chr7:80096608-80096658	HNPCEpiC	eye:	n/a
18	chr7:79998795-79998845	AG09309	skin:	n/a
19	chr7:79998779-79998829	Hepatocyte	liver:	n/a
20	chr7:80080213-80080263	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:79998795-79998845	PFSK-1	brain:	n/a
22	chr7:80080213-80080263	AG04450	lung:	fetal
23	chr7:80096608-80096658	HRE	kidney:	n/a
24	chr7:80096608-80096658	NHBE	bronchial:	n/a
25	chr7:80096608-80096658	BJ	skin:	n/a
26	chr7:79998779-79998829	HUVEC	blood vessel:	n/a
27	chr7:79998779-79998829	NHDF-neo	bronchial:	n/a
28	chr7:80096608-80096658	GM12891	blood:	n/a
29	chr7:79997911-79997961	Hepatocyte	liver:	n/a
30	chr7:79997911-79997961	HCT-116	colon:	n/a
31	chr7:79998795-79998845	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:80080213-80080263	AoSMC	blood vessel:	n/a
33	chr7:79998779-79998829	GM12892	blood:	n/a
34	chr7:79998795-79998845	AG04450	lung:	fetal
35	chr7:79997911-79997961	GM06990	blood:	n/a
36	chr7:80080213-80080263	GM12891	blood:	n/a
37	chr7:79997911-79997961	CMK	blood:	n/a
38	chr7:80080213-80080263	SKMC	muscle:	n/a
39	chr7:79997911-79997961	MCF10A-Er-Src	breast:	n/a
40	chr7:79998779-79998829	AG09319	gingival:	n/a
41	chr7:79998779-79998829	IMR90	lung:	fetal
42	chr7:79998779-79998829	GM19239	blood:	n/a
43	chr7:79998795-79998845	U87	brain:	n/a
44	chr7:79998795-79998845	AoSMC	blood vessel:	n/a
45	chr7:80096608-80096658	GM06990	blood:	n/a
46	chr7:80096608-80096658	HCPEpiC	choroid plexus:	n/a
47	chr7:80080213-80080263	BE2_C	brain:	n/a
48	chr7:79998795-79998845	BE2_C	brain:	n/a
49	chr7:79998795-79998845	HRE	kidney:	n/a
50	chr7:79997911-79997961	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:80057471..80058066-chr7:80288234..80289022,3	MCF-7	breast:
2	chr7:80057501..80059024-chr7:80309987..80311233,7	MCF-7	breast:
3	chr7:80096464..80097970-chr7:80098984..80101525,2	K562	blood:
4	chr7:79763755..79764439-chr7:80021328..80022232,2	MCF-7	breast:
5	chr7:79689284..79689874-chr7:80021349..80022344,3	MCF-7	breast:
6	chr7:79689612..79690202-chr7:80082690..80083447,3	MCF-7	breast:
7	chr7:80096464..80097970-chr7:80098984..80101525,2	K562	blood:
8	chr7:79724626..79725468-chr7:80021262..80022262,4	MCF-7	breast:
9	chr7:80102854..80105069-chr7:80112565..80115333,2	K562	blood:
10	chr7:79982868..79985812-chr7:79986232..79988708,2	MCF-7	breast:
11	chr7:80096594..80099585-chr7:80101660..80104577,2	MCF-7	breast:
12	chr7:79724662..79725555-chr7:80021287..80022137,2	MCF-7	breast:
13	chr7:79982868..79985812-chr7:79986232..79988708,2	MCF-7	breast:
14	chr7:80096594..80099585-chr7:80101660..80104577,2	MCF-7	breast:
15	chr7:80057613..80058392-chr7:80288390..80289288,3	MCF-7	breast:
16	chr7:80102854..80105069-chr7:80112565..80115333,2	K562	blood:
17	chr7:80057560..80058347-chr7:80243745..80244716,2	MCF-7	breast:
18	chr7:79971854..79974583-chr7:79981836..79984361,2	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAT3-1	chr7:80003128-80003306	NONHSAT121743
2	lnc-GNAT3-1	chr7:80003657-80003755	ENSG00000232667
3	lnc-GNAT3-1	chr7:80003657-80003755	NONHSAT121740
4	lnc-GNAT3-1	chr7:80003657-80003757	NONHSAT121741
5	lnc-GNAT3-1	chr7:80000517-80000893	NONHSAT121741
6	lnc-GNAT3-1	chr7:80001443-80001610	ENSG00000232667
7	lnc-GNAT3-1	chr7:80009611-80009791	NONHSAT121743
8	lnc-GNAT3-1	chr7:80001443-80001610	ENSG00000232667.5
9	lnc-GNAT3-1	chr7:80000833-80000893	ENSG00000232667
10	lnc-GNAT3-1	chr7:80003132-80003306	NONHSAT121741
11	lnc-GNAT3-1	chr7:80001237-80001610	ENSG00000232667.5
12	lnc-GNAT3-1	chr7:80000502-80000893	NONHSAT121740
13	lnc-GNAT3-1	chr7:80009611-80009790	ENSG00000232667.5
14	lnc-GNAT3-1	chr7:80003132-80003203	ENSG00000232667.5
15	lnc-GNAT3-1	chr7:80001443-80001610	NONHSAT121741
16	lnc-GNAT3-1	chr7:80001448-80001610	NONHSAT121743
17	lnc-GNAT3-1	chr7:80001443-80001610	NONHSAT121740
18	lnc-GNAT3-1	chr7:80003128-80003306	ENSG00000232667
19	lnc-GNAT3-1	chr7:79984323-79984462	ENSG00000232667.5
20	lnc-GNAT3-1	chr7:80003128-80003306	ENSG00000232667.5
21	lnc-GNAT3-3	chr7:80006870-80007151	NONHSAT121744
22	lnc-GNAT3-1	chr7:80003128-80003306	ENSG00000232667.5
23	lnc-GNAT3-1	chr7:80001443-80001545	ENSG00000232667.5
24	lnc-GNAT3-1	chr7:80001443-80001610	ENSG00000232667.5
25	lnc-GNAT3-1	chr7:80013219-80013440	ENSG00000232667.5
26	lnc-GNAT3-1	chr7:79991431-79991540	ENSG00000232667.5
27	lnc-GNAT3-1	chr7:80003657-80003785	ENSG00000232667.5
28	lnc-GNAT3-1	chr7:80003657-80003776	NONHSAT121743
29	lnc-GNAT3-1	chr7:80000502-80000893	ENSG00000232667.5
30	lnc-GNAT3-1	chr7:80014165-80014295	ENSG00000232667.5
31	lnc-GNAT3-1	chr7:80003128-80003306	NONHSAT121740
32	lnc-GNAT3-1	chr7:79984323-79984462	ENSG00000232667.5

No data

Variant related genes	Relation type
ENSG00000232667	TF binding region
CD36	TF binding region
SNRPBP1	TF binding region
ENSG00000232667	CpG island
CD36	CpG island
SNRPBP1	CpG island
ENSG00000127955	chromatin interactions

Extended variants
information (count: 5073 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:5073 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374092225	chr7:79984081-79984082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567433492	chr7:79984100-79984101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs202128330	chr7:79984124-79984125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112064635	chr7:79984146-79984147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs304755	chr7:79984147-79984148	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549766495	chr7:79984215-79984216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113631364	chr7:79984228-79984229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186956727	chr7:79984296-79984297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17153753	chr7:79984309-79984310	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs535075948	chr7:79984348-79984349	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs571449495	chr7:79984349-79984350	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs191198586	chr7:79984401-79984402	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs183325666	chr7:79984425-79984426	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs77745205	chr7:79984433-79984434	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs186912372	chr7:79984446-79984447	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs189744419	chr7:79984468-79984469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556206538	chr7:79984477-79984478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183339468	chr7:79984622-79984623	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545710102	chr7:79984624-79984625	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187788535	chr7:79984633-79984634	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572662333	chr7:79984675-79984676	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192903607	chr7:79984676-79984677	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561098444	chr7:79984681-79984682	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530143501	chr7:79984689-79984690	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200799045	chr7:79984760-79984761	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71555064	chr7:79984770-79984771	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374349654	chr7:79984842-79984843	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537513972	chr7:79984847-79984848	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1818432	chr7:79984902-79984903	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185317931	chr7:79984903-79984904	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551690198	chr7:79984908-79984909	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527355488	chr7:79984930-79984931	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571466723	chr7:79984937-79984938	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571039100	chr7:79984968-79984969	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534066904	chr7:79985034-79985035	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547101978	chr7:79985056-79985057	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547619292	chr7:79985080-79985081	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188588618	chr7:79985140-79985141	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5885172	chr7:79985167-79985168	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116904322	chr7:79985227-79985228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4410853	chr7:79985250-79985251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556292104	chr7:79985252-79985253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576020926	chr7:79985265-79985266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538269935	chr7:79985306-79985307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9655865	chr7:79985310-79985311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs192616777	chr7:79985394-79985395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184597439	chr7:79985398-79985399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561186431	chr7:79985453-79985454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77036995	chr7:79985469-79985470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543537733	chr7:79985499-79985500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79978400-79984600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:79984600-79985200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:79985200-79985600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:79985600-79986200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:79986200-79995400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:79986600-79987000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:79986800-79987200	Enhancers	Osteobl	bone
8	chr7:79986800-79987600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:79987000-79991400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:79987200-79992000	Weak transcription	Osteobl	bone
11	chr7:79987600-79991800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:79988200-79989400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:79991400-79992400	Enhancers	Hela-S3	cervix
14	chr7:79991400-79992400	Enhancers	HSMM	muscle
15	chr7:79991400-79992600	Enhancers	NHDF-Ad	bronchial
16	chr7:79991400-79992800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr7:79991400-79993000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr7:79991600-79992000	Enhancers	NHLF	lung
19	chr7:79991600-79992600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:79991600-79992800	Enhancers	A549	lung
21	chr7:79991800-79992400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:79991800-79992600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:79992000-79992600	Enhancers	Osteobl	bone
24	chr7:79998600-79999400	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr7:79998600-80000400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:79998800-79999000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:79998800-79999200	Enhancers	HUVEC	blood vessel
28	chr7:79998800-79999600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr7:79999000-79999800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:79999400-79999600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr7:79999600-79999800	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr7:79999800-80000200	Enhancers	Brain Germinal Matrix	brain
33	chr7:79999800-80000200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr7:79999800-80000400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:80000200-80000400	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr7:80000400-80000600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:80000400-80003000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:80000400-80008000	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr7:80000600-80000800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:80000800-80001400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:80001200-80001600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:80001200-80001800	Enhancers	HSMMtube	muscle
43	chr7:80001200-80001800	Enhancers	NHLF	lung
44	chr7:80001200-80002800	Enhancers	HSMM	muscle
45	chr7:80001200-80003200	Enhancers	A549	lung
46	chr7:80001400-80002200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:80001400-80002600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr7:80001600-80001800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr7:80001600-80001800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:80001600-80001800	Enhancers	Liver	Liver

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