Variant report

Variant	nsv1022980
Chromosome Location	chr7:48243227-48567060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1680)
CpG islands
(count:1039)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1680 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:48454339-48454412	K562	blood:	n/a	n/a
2	ATF1	chr7:48464645-48464750	K562	blood:	n/a	n/a
3	ATF2	chr7:48291310-48291832	GM12878	blood:	n/a	n/a
4	ATF2	chr7:48338249-48338768	GM12878	blood:	n/a	n/a
5	ATF2	chr7:48285619-48286161	GM12878	blood:	n/a	n/a
6	ATF2	chr7:48294644-48295012	GM12878	blood:	n/a	n/a
7	ATF2	chr7:48338313-48338712	GM12878	blood:	n/a	n/a
8	ATF2	chr7:48291293-48291808	GM12878	blood:	n/a	n/a
9	BACH1	chr7:48271579-48271852	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:48285668-48286127	GM12878	blood:	n/a	n/a
11	BATF	chr7:48294726-48294922	GM12878	blood:	n/a	n/a
12	BATF	chr7:48483391-48483642	GM12878	blood:	n/a	n/a
13	BATF	chr7:48294654-48294978	GM12878	blood:	n/a	n/a
14	BATF	chr7:48291362-48291801	GM12878	blood:	n/a	n/a
15	BATF	chr7:48291306-48291870	GM12878	blood:	n/a	n/a
16	BATF	chr7:48285785-48286103	GM12878	blood:	n/a	n/a
17	BATF	chr7:48338311-48338717	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:48285709-48286092	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:48294690-48294938	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:48338302-48338688	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:48291390-48291765	GM12878	blood:	n/a	n/a
22	BCL3	chr7:48400134-48400508	GM12878	blood:	n/a	n/a
23	BCL3	chr7:48537205-48537464	GM12878	blood:	n/a	n/a
24	BCL3	chr7:48291391-48291682	GM12878	blood:	n/a	n/a
25	BCL3	chr7:48294619-48294966	GM12878	blood:	n/a	n/a
26	BCL3	chr7:48400193-48400497	GM12878	blood:	n/a	n/a
27	BCL3	chr7:48285640-48286075	GM12878	blood:	n/a	n/a
28	BCL3	chr7:48338337-48338739	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:48291285-48291674	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:48291414-48291704	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:48298658-48298686	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:48430530-48430791	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:48294391-48294424	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:48495321-48495335	K562	blood:	n/a	n/a
35	BRCA1	chr7:48354292-48354447	GM12878	blood:	n/a	n/a
36	CCNT2	chr7:48494647-48495097	K562	blood:	n/a	n/a
37	CCNT2	chr7:48470894-48471088	K562	blood:	n/a	n/a
38	CEBPB	chr7:48392408-48392683	HepG2	liver:	n/a	chr7:48392560-48392569 chr7:48392558-48392569
39	CEBPB	chr7:48546971-48547149	HepG2	liver:	n/a	chr7:48547003-48547014 chr7:48547001-48547012 chr7:48547003-48547014 chr7:48547001-48547014
40	CEBPB	chr7:48531253-48531488	HepG2	liver:	n/a	chr7:48531357-48531368 chr7:48531357-48531370
41	CEBPB	chr7:48350592-48350791	IMR90	lung:	n/a	chr7:48350667-48350680 chr7:48350667-48350678
42	CEBPB	chr7:48473077-48473360	A549	lung:	n/a	chr7:48473193-48473204
43	CEBPB	chr7:48251984-48252302	IMR90	lung:	n/a	chr7:48252125-48252136
44	CEBPB	chr7:48351809-48352083	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:48456901-48457130	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:48473131-48473331	Hela-S3	cervix:	n/a	chr7:48473193-48473204
47	CEBPB	chr7:48338242-48338875	IMR90	lung:	n/a	chr7:48338420-48338431 chr7:48338420-48338431 chr7:48338418-48338431 chr7:48338415-48338432
48	CEBPB	chr7:48252757-48252966	A549	lung:	n/a	n/a
49	CEBPB	chr7:48456467-48456702	HepG2	liver:	n/a	chr7:48456564-48456577 chr7:48456564-48456575
50	CEBPB	chr7:48293034-48293220	HepG2	liver:	n/a	chr7:48293139-48293150 chr7:48293057-48293068

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48494156-48494206	NHBE	bronchial:	n/a
2	chr7:48493792-48493842	K562	blood:	n/a
3	chr7:48494156-48494206	NHBE	bronchial:	n/a
4	chr7:48493792-48493842	K562	blood:	n/a
5	chr7:48495333-48495383	HUVEC	blood vessel:	n/a
6	chr7:48494156-48494206	HIPEpiC	eye:	n/a
7	chr7:48491590-48491640	SK-N-SH	brain:	n/a
8	chr7:48352531-48352581	NT2-D1	testis:	n/a
9	chr7:48319696-48319746	HCM	heart:	n/a
10	chr7:48495333-48495383	SKMC	muscle:	n/a
11	chr7:48351895-48351945	MCF10A-Er-Src	breast:	n/a
12	chr7:48351495-48351545	HCF	heart:	n/a
13	chr7:48494519-48494569	SKMC	muscle:	n/a
14	chr7:48495072-48495122	NHDF-neo	bronchial:	n/a
15	chr7:48494519-48494569	SAEC	small airway:	n/a
16	chr7:48494362-48494412	Caco-2	colon:	n/a
17	chr7:48494156-48494206	NB4	blood:	n/a
18	chr7:48494734-48494784	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:48494579-48494629	ProgFib	skin:	n/a
20	chr7:48495215-48495265	T-47D	breast:	n/a
21	chr7:48494734-48494784	HAEpiC	amniotic membrane:	n/a
22	chr7:48494608-48494658	ProgFib	skin:	n/a
23	chr7:48494156-48494206	HRE	kidney:	n/a
24	chr7:48494362-48494412	RPTEC	kidney:	n/a
25	chr7:48351895-48351945	HCT-116	colon:	n/a
26	chr7:48351495-48351545	Jurkat	blood:	n/a
27	chr7:48494519-48494569	SK-N-SH	brain:	n/a
28	chr7:48494519-48494569	K562	blood:	n/a
29	chr7:48491590-48491640	GM19239	blood:	n/a
30	chr7:48494734-48494784	NH-A	brain:	n/a
31	chr7:48319696-48319746	SK-N-SH_RA	brain:	n/a
32	chr7:48494519-48494569	MCF-7	breast:	n/a
33	chr7:48351895-48351945	AG04450	lung:	fetal
34	chr7:48494579-48494629	AG09309	skin:	n/a
35	chr7:48493792-48493842	RPTEC	kidney:	n/a
36	chr7:48352531-48352581	AG04449	skin:	fetal
37	chr7:48319696-48319746	HRE	kidney:	n/a
38	chr7:48491590-48491640	NHBE	bronchial:	n/a
39	chr7:48495072-48495122	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:48351895-48351945	NH-A	brain:	n/a
41	chr7:48494734-48494784	SK-N-SH_RA	brain:	n/a
42	chr7:48495072-48495122	HAEpiC	amniotic membrane:	n/a
43	chr7:48494519-48494569	CMK	blood:	n/a
44	chr7:48493792-48493842	GM19239	blood:	n/a
45	chr7:48494579-48494629	SK-N-MC	brain:	n/a
46	chr7:48552817-48552867	HCPEpiC	choroid plexus:	n/a
47	chr7:48494608-48494658	PrEC	prostate:	n/a
48	chr7:48351895-48351945	HL-60	blood:	n/a
49	chr7:48494362-48494412	NHBE	bronchial:	n/a
50	chr7:48552817-48552867	HMEC	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:48464162..48465007-chr7:49040934..49041504,2	MCF-7	breast:
2	chr7:48546224..48548443-chr7:48555422..48558329,2	MCF-7	breast:
3	chr7:48339343..48339865-chr7:49892019..49892834,2	K562	blood:
4	chr7:48376419..48377077-chr7:49891980..49892898,2	MCF-7	breast:
5	chr7:48464147..48465026-chr7:48914660..48915807,4	MCF-7	breast:
6	chr7:48279225..48282090-chr7:48283159..48287155,3	K562	blood:
7	chr7:48464131..48464720-chr7:49830437..49831304,2	MCF-7	breast:
8	chr7:48464066..48464994-chr7:48914675..48915561,3	MCF-7	breast:
9	chr7:48338977..48339698-chr7:48914621..48915709,3	MCF-7	breast:
10	chr7:48376280..48377237-chrX:150918854..150919433,2	MCF-7	breast:
11	chr7:48339292..48339820-chr7:49892008..49892873,2	MCF-7	breast:
12	chr7:48513865..48515812-chr7:49402658..49405453,2	K562	blood:
13	chr7:48350873..48351428-chr7:48826215..48827185,2	MCF-7	breast:
14	chr7:48279225..48282090-chr7:48283159..48287155,3	K562	blood:
15	chr7:48375884..48377251-chr7:48914594..48915844,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUN3-5	chr7:48491789-48495224	NONHSAT120528

No data

Variant related genes	Relation type
ABCA13	TF binding region
ABCA13	CpG island
ENSG00000179869	chromatin interactions

Extended variants
information (count: 12274 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:12274 , 50 per page) page: 1 2 3 4 5 6 7 ... 246

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555219747	chr7:48243231-48243232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371944467	chr7:48243233-48243234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576456832	chr7:48243316-48243317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150954987	chr7:48243324-48243325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559192633	chr7:48243356-48243357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78614041	chr7:48243378-48243379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs67466763	chr7:48243403-48243404	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530245408	chr7:48243511-48243512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569749851	chr7:48243574-48243575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553461805	chr7:48243614-48243615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368658335	chr7:48243686-48243687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183321009	chr7:48243687-48243688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531199186	chr7:48243704-48243705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558697409	chr7:48243709-48243710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34262924	chr7:48243724-48243725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574490658	chr7:48243732-48243733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140799992	chr7:48243795-48243796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10227268	chr7:48243849-48243850	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs188725898	chr7:48243892-48243893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34950764	chr7:48243925-48243926	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs531061919	chr7:48243933-48243934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371206370	chr7:48243983-48243984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546110622	chr7:48243999-48244000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141390203	chr7:48244008-48244009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192564835	chr7:48244033-48244034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539017017	chr7:48244040-48244041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34978094	chr7:48244045-48244046	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs201608444	chr7:48244054-48244055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35586320	chr7:48244069-48244070	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs149407256	chr7:48244088-48244089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555252473	chr7:48244100-48244101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144807951	chr7:48244113-48244114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543650458	chr7:48244116-48244117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs36010716	chr7:48244137-48244138	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575759708	chr7:48244138-48244139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545113296	chr7:48244163-48244164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564693932	chr7:48244175-48244176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568191988	chr7:48244204-48244205	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560112222	chr7:48244205-48244206	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184001558	chr7:48244236-48244237	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148112919	chr7:48244248-48244249	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529904200	chr7:48244250-48244251	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550032666	chr7:48244301-48244302	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28588066	chr7:48244392-48244393	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs6583476	chr7:48244414-48244415	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs552654738	chr7:48244416-48244417	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564235314	chr7:48244444-48244445	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565893324	chr7:48244541-48244542	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143928949	chr7:48244588-48244589	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147241714	chr7:48244621-48244622	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Abnormal phenotypes	18644119	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48230600-48246200	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr7:48240200-48244200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:48244200-48244600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:48246200-48247200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:48246400-48247400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:48247200-48248600	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr7:48248600-48250600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr7:48248600-48251200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:48250600-48251000	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr7:48251000-48252000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:48251200-48252000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:48252000-48253000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:48252000-48253400	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr7:48253000-48253400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:48253000-48253400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:48253400-48278200	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr7:48256800-48257200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:48257200-48257600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:48274000-48274200	Bivalent Enhancer	Aorta	Aorta
20	chr7:48275400-48278000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr7:48277600-48290400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:48278200-48278600	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr7:48278600-48279000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr7:48278800-48279200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr7:48279000-48279800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
26	chr7:48279200-48279400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:48279400-48280400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:48279800-48289200	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr7:48280400-48280800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:48280400-48280800	Enhancers	Lung	lung
31	chr7:48280400-48281800	Enhancers	Primary hematopoietic stem cells	blood
32	chr7:48280400-48281800	Enhancers	HUVEC	blood vessel
33	chr7:48280400-48282000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:48280600-48280800	Enhancers	Fetal Lung	lung
35	chr7:48280600-48281800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr7:48280800-48281000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:48280800-48281200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr7:48280800-48284600	Weak transcription	Fetal Lung	lung
39	chr7:48281000-48281200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr7:48281200-48281400	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr7:48281200-48281400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:48281200-48284000	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr7:48281400-48282000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:48281800-48283600	Weak transcription	Primary hematopoietic stem cells	blood
45	chr7:48281800-48283800	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr7:48281800-48284000	Weak transcription	HUVEC	blood vessel
47	chr7:48282000-48283000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:48282000-48283400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:48283000-48284200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:48283000-48286000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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