Variant report

Variant	nsv1015399
Chromosome Location	chr7:48321542-48544359
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	chr7:48338313-48338712	GM12878	blood:	n/a	n/a
4	ATF2	chr7:48338249-48338768	GM12878	blood:	n/a	n/a
5	BATF	chr7:48483391-48483642	GM12878	blood:	n/a	n/a
6	BATF	chr7:48338311-48338717	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:48338302-48338688	GM12878	blood:	n/a	n/a
8	BCL3	chr7:48338337-48338739	GM12878	blood:	n/a	n/a
9	BCL3	chr7:48400193-48400497	GM12878	blood:	n/a	n/a
10	BCL3	chr7:48400134-48400508	GM12878	blood:	n/a	n/a
11	BCL3	chr7:48537205-48537464	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:48495321-48495335	K562	blood:	n/a	n/a
13	BHLHE40	chr7:48430530-48430791	GM12878	blood:	n/a	n/a
14	BRCA1	chr7:48354292-48354447	GM12878	blood:	n/a	n/a
15	CCNT2	chr7:48470894-48471088	K562	blood:	n/a	n/a
16	CCNT2	chr7:48494647-48495097	K562	blood:	n/a	n/a
17	CEBPB	chr7:48498646-48499135	MCF-7	breast:	n/a	chr7:48498891-48498904
18	CEBPB	chr7:48498754-48499043	Hela-S3	cervix:	n/a	chr7:48498891-48498904
19	CEBPB	chr7:48325066-48325403	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:48473078-48473360	HepG2	liver:	n/a	chr7:48473193-48473204
21	CEBPB	chr7:48500485-48500804	HepG2	liver:	n/a	chr7:48500623-48500634
22	CEBPB	chr7:48500568-48500665	A549	lung:	n/a	chr7:48500623-48500634
23	CEBPB	chr7:48531253-48531488	HepG2	liver:	n/a	chr7:48531357-48531368 chr7:48531357-48531370
24	CEBPB	chr7:48473031-48473381	IMR90	lung:	n/a	chr7:48473193-48473204
25	CEBPB	chr7:48456901-48457130	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr7:48498813-48499028	HepG2	liver:	n/a	chr7:48498891-48498904
27	CEBPB	chr7:48338242-48338875	IMR90	lung:	n/a	chr7:48338420-48338431 chr7:48338420-48338431 chr7:48338418-48338431 chr7:48338415-48338432
28	CEBPB	chr7:48351809-48352083	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:48456467-48456702	HepG2	liver:	n/a	chr7:48456564-48456577 chr7:48456564-48456575
30	CEBPB	chr7:48429541-48429870	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:48350481-48350752	MCF-7	breast:	n/a	chr7:48350667-48350680 chr7:48350667-48350678
32	CEBPB	chr7:48510500-48510740	A549	lung:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
33	CEBPB	chr7:48473100-48473293	K562	blood:	n/a	chr7:48473193-48473204
34	CEBPB	chr7:48473131-48473331	Hela-S3	cervix:	n/a	chr7:48473193-48473204
35	CEBPB	chr7:48473077-48473360	A549	lung:	n/a	chr7:48473193-48473204
36	CEBPB	chr7:48340830-48341054	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:48510520-48510805	HepG2	liver:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
38	CEBPB	chr7:48498727-48499141	MCF-7	breast:	n/a	chr7:48498891-48498904
39	CEBPB	chr7:48350426-48350947	MCF-7	breast:	n/a	chr7:48350667-48350680 chr7:48350667-48350678
40	CEBPB	chr7:48510492-48510812	K562	blood:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
41	CEBPB	chr7:48350535-48350812	HepG2	liver:	n/a	chr7:48350667-48350680 chr7:48350667-48350678
42	CEBPB	chr7:48498776-48499010	A549	lung:	n/a	chr7:48498891-48498904
43	CEBPB	chr7:48429446-48429963	MCF-7	breast:	n/a	n/a
44	CEBPB	chr7:48510603-48510792	H1-hESC	embryonic stem cell:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
45	CEBPB	chr7:48542623-48542856	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:48466497-48466781	MCF-7	breast:	n/a	chr7:48466632-48466643
47	CEBPB	chr7:48501342-48501446	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:48429601-48429900	MCF-7	breast:	n/a	n/a
49	CEBPB	chr7:48428785-48428793	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:48392408-48392683	HepG2	liver:	n/a	chr7:48392560-48392569 chr7:48392558-48392569

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48352531-48352581	SAEC	small airway:	n/a
2	chr7:48352531-48352581	SAEC	small airway:	n/a
3	chr7:48495215-48495265	HIPEpiC	eye:	n/a
4	chr7:48351895-48351945	T-47D	breast:	n/a
5	chr7:48493792-48493842	AG04449	skin:	fetal
6	chr7:48494608-48494658	SK-N-SH_RA	brain:	n/a
7	chr7:48494734-48494784	K562	blood:	n/a
8	chr7:48495333-48495383	GM06990	blood:	n/a
9	chr7:48494579-48494629	NB4	blood:	n/a
10	chr7:48495333-48495383	HMEC	breast:	n/a
11	chr7:48494579-48494629	SK-N-MC	brain:	n/a
12	chr7:48493792-48493842	IMR90	lung:	fetal
13	chr7:48493792-48493842	PANC-1	pancreas:	n/a
14	chr7:48495215-48495265	GM06990	blood:	n/a
15	chr7:48352531-48352581	Hepatocyte	liver:	n/a
16	chr7:48351495-48351545	AG04449	skin:	fetal
17	chr7:48352531-48352581	HCF	heart:	n/a
18	chr7:48495157-48495207	U87	brain:	n/a
19	chr7:48494519-48494569	NT2-D1	testis:	n/a
20	chr7:48494362-48494412	HNPCEpiC	eye:	n/a
21	chr7:48494734-48494784	Caco-2	colon:	n/a
22	chr7:48495072-48495122	Jurkat	blood:	n/a
23	chr7:48494362-48494412	RPTEC	kidney:	n/a
24	chr7:48494608-48494658	GM12891	blood:	n/a
25	chr7:48351495-48351545	U87	brain:	n/a
26	chr7:48351495-48351545	NB4	blood:	n/a
27	chr7:48495215-48495265	HL-60	blood:	n/a
28	chr7:48494362-48494412	AG04450	lung:	fetal
29	chr7:48493792-48493842	AoSMC	blood vessel:	n/a
30	chr7:48495215-48495265	PFSK-1	brain:	n/a
31	chr7:48494156-48494206	AG09309	skin:	n/a
32	chr7:48494362-48494412	CMK	blood:	n/a
33	chr7:48494579-48494629	AG09319	gingival:	n/a
34	chr7:48351495-48351545	GM19239	blood:	n/a
35	chr7:48495215-48495265	A549	lung:	n/a
36	chr7:48494156-48494206	HCPEpiC	choroid plexus:	n/a
37	chr7:48493792-48493842	SAEC	small airway:	n/a
38	chr7:48494579-48494629	SK-N-SH	brain:	n/a
39	chr7:48494608-48494658	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:48351495-48351545	PFSK-1	brain:	n/a
41	chr7:48352531-48352581	BE2_C	brain:	n/a
42	chr7:48351495-48351545	PrEC	prostate:	n/a
43	chr7:48495072-48495122	PFSK-1	brain:	n/a
44	chr7:48495333-48495383	HRCEpiC	kidney:	n/a
45	chr7:48495072-48495122	PANC-1	pancreas:	n/a
46	chr7:48494156-48494206	Jurkat	blood:	n/a
47	chr7:48351895-48351945	HCM	heart:	n/a
48	chr7:48494519-48494569	GM06990	blood:	n/a
49	chr7:48494519-48494569	AG10803	skin:	n/a
50	chr7:48494519-48494569	CMK	blood:	n/a

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

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

Variant related genes	Relation type
ABCA13	TF binding region
ABCA13	CpG island

Extended variants
information (count: 8458 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:8458 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113168979	chr7:48321598-48321599	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs59328053	chr7:48321717-48321718	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs569658610	chr7:48321798-48321799	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538443307	chr7:48321814-48321815	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146047537	chr7:48321918-48321919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572487539	chr7:48321928-48321929	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112261717	chr7:48321967-48321968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555048462	chr7:48321970-48321971	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114832744	chr7:48321995-48321996	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543877655	chr7:48321998-48321999	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563966040	chr7:48322054-48322055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577637863	chr7:48322067-48322068	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112049743	chr7:48322091-48322092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78077760	chr7:48322107-48322108	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141013064	chr7:48322156-48322157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372212573	chr7:48322158-48322159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184982303	chr7:48322223-48322224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547133137	chr7:48322224-48322225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560661175	chr7:48322277-48322278	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138709771	chr7:48322283-48322284	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116535166	chr7:48322296-48322297	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569594066	chr7:48322365-48322366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538591056	chr7:48322382-48322383	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552462807	chr7:48322448-48322449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs386712986	chr7:48322451-48322452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6973602	chr7:48322452-48322453	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555091454	chr7:48322569-48322570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575034184	chr7:48322570-48322571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537417194	chr7:48322613-48322614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555480800	chr7:48322629-48322630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557422470	chr7:48322634-48322635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11983293	chr7:48322637-48322638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577322856	chr7:48322652-48322653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546150603	chr7:48322662-48322663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10499676	chr7:48322665-48322666	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs573318850	chr7:48322675-48322676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537403807	chr7:48322676-48322677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73323705	chr7:48322694-48322695	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs529767477	chr7:48322702-48322703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549351041	chr7:48322752-48322753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562911047	chr7:48322766-48322767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141263028	chr7:48322791-48322792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552144904	chr7:48322799-48322800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566004905	chr7:48322820-48322821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10278121	chr7:48322821-48322822	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs574890016	chr7:48322902-48322903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73323707	chr7:48322958-48322959	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs77518994	chr7:48323007-48323008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9691909	chr7:48323030-48323031	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs557510259	chr7:48323033-48323034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

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
Autism	22495309	CNVD

Chromatin state (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48318800-48322000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:48319000-48322000	Enhancers	Primary hematopoietic stem cells	blood
3	chr7:48319000-48322000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:48319200-48322200	Enhancers	Thymus	Thymus
5	chr7:48319800-48322400	Enhancers	Fetal Thymus	thymus
6	chr7:48319800-48382200	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:48320000-48321600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr7:48320400-48325000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:48320600-48324800	Weak transcription	HMEC	breast
10	chr7:48320600-48338000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:48321400-48324600	Weak transcription	NHLF	lung
12	chr7:48321600-48324800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:48322000-48324800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:48322000-48325000	Weak transcription	Primary hematopoietic stem cells	blood
15	chr7:48322000-48325000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:48322600-48333800	Weak transcription	Spleen	Spleen
17	chr7:48324600-48325200	Enhancers	NHLF	lung
18	chr7:48324800-48325200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:48324800-48325200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:48324800-48325400	Enhancers	HMEC	breast
21	chr7:48324800-48326600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:48325000-48325400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:48325000-48326600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:48325000-48329800	Enhancers	Primary hematopoietic stem cells	blood
25	chr7:48325200-48327000	Weak transcription	NHLF	lung
26	chr7:48326400-48329400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:48326600-48327000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:48326600-48327200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:48327000-48327200	Enhancers	NHLF	lung
30	chr7:48327000-48329600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:48327200-48327800	Weak transcription	NHLF	lung
32	chr7:48327200-48328600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:48327400-48327600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:48327800-48328000	Enhancers	NHLF	lung
35	chr7:48328400-48329800	Enhancers	Fetal Heart	heart
36	chr7:48328600-48328800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:48328600-48328800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:48328800-48329200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:48328800-48332200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr7:48329200-48329600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:48329200-48330200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:48329600-48330000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:48329800-48330200	Flanking Active TSS	Fetal Heart	heart
44	chr7:48329800-48330600	Flanking Active TSS	Primary hematopoietic stem cells	blood
45	chr7:48330000-48333600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:48330200-48330800	Enhancers	Fetal Heart	heart
47	chr7:48330200-48332000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:48330600-48333600	Enhancers	Primary hematopoietic stem cells	blood
49	chr7:48331000-48331400	ZNF genes & repeats	Lung	lung
50	chr7:48332000-48332200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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