Variant report

Variant	nsv1016708
Chromosome Location	chr7:110956248-111122293
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1061)
CpG islands
(count:185)
Chromatin interactive
region (count:124)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
2	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
3	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
4	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
5	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
6	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
7	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
8	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
9	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
10	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
12	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
13	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
14	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
16	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
17	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
18	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
19	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
20	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
21	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
22	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
24	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
25	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
26	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
27	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:111114414-111114577	K562	blood:	n/a	n/a
30	BHLHE40	chr7:111115170-111115607	K562	blood:	n/a	n/a
31	BHLHE40	chr7:111078559-111079458	K562	blood:	n/a	n/a
32	BHLHE40	chr7:111116668-111117082	K562	blood:	n/a	n/a
33	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:111117429-111117846	K562	blood:	n/a	n/a
35	CBX3	chr7:111079900-111081343	K562	blood:	n/a	n/a
36	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
37	CBX3	chr7:111078458-111079603	K562	blood:	n/a	n/a
38	CBX3	chr7:111113468-111114389	K562	blood:	n/a	n/a
39	CBX3	chr7:111117495-111118260	K562	blood:	n/a	n/a
40	CBX3	chr7:111117217-111118801	K562	blood:	n/a	n/a
41	CBX3	chr7:111090809-111091116	K562	blood:	n/a	n/a
42	CBX3	chr7:111115072-111115643	K562	blood:	n/a	n/a
43	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
44	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
45	CBX3	chr7:111073025-111074149	K562	blood:	n/a	n/a
46	CBX3	chr7:111076674-111077685	K562	blood:	n/a	n/a
47	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
48	CBX3	chr7:111074271-111074726	K562	blood:	n/a	n/a
49	CCNT2	chr7:111115046-111115592	K562	blood:	n/a	chr7:111115405-111115425
50	CCNT2	chr7:111078445-111079337	K562	blood:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111079100-111079150	HCT-116	colon:	n/a
2	chr7:111086055-111086105	SKMC	muscle:	n/a
3	chr7:111079100-111079150	HCT-116	colon:	n/a
4	chr7:111086055-111086105	SKMC	muscle:	n/a
5	chr7:111079100-111079150	BJ	skin:	n/a
6	chr7:111086055-111086105	AoSMC	blood vessel:	n/a
7	chr7:111086055-111086105	ECC-1	luminal epithelium:	n/a
8	chr7:111086055-111086105	GM19239	blood:	n/a
9	chr7:111086055-111086105	T-47D	breast:	n/a
10	chr7:111086055-111086105	PrEC	prostate:	n/a
11	chr7:111079100-111079150	MCF10A-Er-Src	breast:	n/a
12	chr7:111086055-111086105	GM12878	blood:	n/a
13	chr7:111086055-111086105	AG09319	gingival:	n/a
14	chr7:111033064-111033114	HepG2	liver:	n/a
15	chr7:111086055-111086105	MCF10A-Er-Src	breast:	n/a
16	chr7:111033064-111033114	K562	blood:	n/a
17	chr7:111086055-111086105	RPTEC	kidney:	n/a
18	chr7:111086055-111086105	CMK	blood:	n/a
19	chr7:111079100-111079150	HUVEC	blood vessel:	n/a
20	chr7:111079100-111079150	RPTEC	kidney:	n/a
21	chr7:111079100-111079150	AoSMC	blood vessel:	n/a
22	chr7:111033064-111033114	HL-60	blood:	n/a
23	chr7:111033064-111033114	HNPCEpiC	eye:	n/a
24	chr7:111086055-111086105	HL-60	blood:	n/a
25	chr7:111086055-111086105	MCF-7	breast:	n/a
26	chr7:111033064-111033114	U87	brain:	n/a
27	chr7:111033064-111033114	AG04450	lung:	fetal
28	chr7:111079100-111079150	HepG2	liver:	n/a
29	chr7:111079100-111079150	PANC-1	pancreas:	n/a
30	chr7:111086055-111086105	HAEpiC	amniotic membrane:	n/a
31	chr7:111079100-111079150	HAEpiC	amniotic membrane:	n/a
32	chr7:111033064-111033114	GM19239	blood:	n/a
33	chr7:111079100-111079150	HNPCEpiC	eye:	n/a
34	chr7:111079100-111079150	MCF-7	breast:	n/a
35	chr7:111079100-111079150	SKMC	muscle:	n/a
36	chr7:111079100-111079150	AG10803	skin:	n/a
37	chr7:111086055-111086105	Hepatocyte	liver:	n/a
38	chr7:111033064-111033114	NHDF-neo	bronchial:	n/a
39	chr7:111033064-111033114	AoSMC	blood vessel:	n/a
40	chr7:111086055-111086105	HCF	heart:	n/a
41	chr7:111079100-111079150	GM19239	blood:	n/a
42	chr7:111033064-111033114	HCF	heart:	n/a
43	chr7:111033064-111033114	HEEpiC	esophagus:	n/a
44	chr7:111033064-111033114	ovcar-3	ovarian:	n/a
45	chr7:111086055-111086105	HNPCEpiC	eye:	n/a
46	chr7:111086055-111086105	BE2_C	brain:	n/a
47	chr7:111079100-111079150	PrEC	prostate:	n/a
48	chr7:111079100-111079150	Caco-2	colon:	n/a
49	chr7:111079100-111079150	HEK293	kidney:	embryo
50	chr7:111079100-111079150	A549	lung:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:110969503..110970311-chr7:111375483..111376413,3	K562	blood:
2	chr7:110919663..110921773-chr7:111080756..111083394,2	K562	blood:
3	chr7:111050830..111052648-chr7:111066245..111068187,2	K562	blood:
4	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
5	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
6	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
7	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
8	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
9	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
10	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
11	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
12	chr7:110964713..110967341-chr7:110967524..110969143,2	K562	blood:
13	chr5:125812513..125813255-chr7:110998210..110998982,2	MCF-7	breast:
14	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
15	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
16	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
17	chr7:111049337..111051671-chr7:111077981..111080558,2	K562	blood:
18	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
19	chr7:111051033..111052648-chr7:111065834..111068187,2	K562	blood:
20	chr7:111115638..111117204-chr7:111120968..111123964,2	K562	blood:
21	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
22	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
23	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
24	chr7:110963413..110966213-chr7:110967085..110969024,2	K562	blood:
25	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
26	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
27	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
28	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
29	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
30	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
31	chr12:108202177..108204461-chr7:111052206..111055078,3	MCF-7	breast:
32	chr7:110911704..110914495-chr7:111113882..111116767,2	K562	blood:
33	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
34	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
35	chr7:111050112..111052168-chr7:111053965..111056674,3	K562	blood:
36	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
37	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
38	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
39	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
40	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
41	chr7:111027546..111029195-chr7:111032815..111035330,2	K562	blood:
42	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
43	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
44	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:
45	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
46	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
47	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
48	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
49	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
50	chr7:110977304..110981066-chr7:110982767..110987604,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
ENSG00000243621	TF binding region
IMMP2L	TF binding region
ENSG00000227948	CpG island
ENSG00000243621	CpG island
IMMP2L	CpG island
ENSG00000188825	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000243621	chromatin interactions

Extended variants
information (count: 5898 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5898 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545701448	chr7:110956257-110956258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371988991	chr7:110956363-110956364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113805557	chr7:110956383-110956384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558917353	chr7:110956416-110956417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111434880	chr7:110956427-110956428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549520647	chr7:110956450-110956451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568088242	chr7:110956462-110956463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531925236	chr7:110956463-110956464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528975636	chr7:110956484-110956485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368814079	chr7:110956566-110956567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145860296	chr7:110956575-110956576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539263205	chr7:110956576-110956577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557600242	chr7:110956611-110956612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568444323	chr7:110956657-110956658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569851927	chr7:110956674-110956675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148597494	chr7:110956690-110956691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555470274	chr7:110956768-110956769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187998690	chr7:110956781-110956782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535101846	chr7:110956782-110956783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7795479	chr7:110956791-110956792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs376686479	chr7:110956811-110956812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs80028306	chr7:110956832-110956833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181222100	chr7:110956879-110956880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143756985	chr7:110956901-110956902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186411677	chr7:110956933-110956934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563925332	chr7:110956941-110956942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575838737	chr7:110956946-110956947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142911444	chr7:110956955-110956956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561504425	chr7:110956992-110956993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190058134	chr7:110957034-110957035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111640256	chr7:110957064-110957065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182112196	chr7:110957090-110957091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532483048	chr7:110957095-110957096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186651537	chr7:110957140-110957141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1981712	chr7:110957151-110957152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs141279895	chr7:110957184-110957185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145066085	chr7:110957198-110957199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369316601	chr7:110957202-110957203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146774566	chr7:110957224-110957225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs207468416	chr7:110957258-110957259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1981713	chr7:110957294-110957295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs535033431	chr7:110957305-110957306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572278975	chr7:110957361-110957362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553475485	chr7:110957394-110957395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140500849	chr7:110957396-110957397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191205226	chr7:110957406-110957407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183329914	chr7:110957435-110957436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554528793	chr7:110957483-110957484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185348053	chr7:110957507-110957508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61208673	chr7:110957510-110957511	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:93)

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
Melanoma	17363583	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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD

Chromatin state (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110955800-110956400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:110956000-110960200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:110956200-110958200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:110956400-110958000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:110958000-110961800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:110958200-110961000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:110959000-110959400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:110960000-110983400	Weak transcription	Left Ventricle	heart
9	chr7:110960200-110960400	Enhancers	Primary hematopoietic stem cells	blood
10	chr7:110960200-110961000	Enhancers	GM12878-XiMat	blood
11	chr7:110960200-110961000	Enhancers	K562	blood
12	chr7:110960800-110961000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:110961000-110961800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:110961000-110964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:110961800-110962400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:110961800-110962400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:110962400-110962600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:110962400-110962800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:110962600-110967200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:110964200-110964600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:110964200-110964600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr7:110964600-110967200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:110964600-110969000	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr7:110966400-110966600	Active TSS	K562	blood
25	chr7:110966600-110966800	Flanking Active TSS	K562	blood
26	chr7:110966800-110967000	Active TSS	K562	blood
27	chr7:110967000-110967400	Flanking Active TSS	K562	blood
28	chr7:110967200-110968800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:110967200-110969000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:110967400-110969400	Active TSS	K562	blood
31	chr7:110968400-110973000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:110968600-110968800	Enhancers	GM12878-XiMat	blood
33	chr7:110968800-110969200	Flanking Active TSS	GM12878-XiMat	blood
34	chr7:110968800-110969800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:110969000-110969600	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr7:110969000-110969800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr7:110969200-110969600	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr7:110969200-110970400	Enhancers	GM12878-XiMat	blood
39	chr7:110969400-110970000	Flanking Active TSS	K562	blood
40	chr7:110971200-110971400	Enhancers	Adipose Nuclei	Adipose
41	chr7:110971400-110978800	Weak transcription	Adipose Nuclei	Adipose
42	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:110973000-110973600	Enhancers	HMEC	breast
45	chr7:110973000-110973800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:110973000-110973800	Enhancers	NHEK	skin
47	chr7:110973600-110979800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:110973800-110983400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:110978000-110978200	Enhancers	Psoas Muscle	Psoas
50	chr7:110978800-110979200	Enhancers	Adipose Nuclei	Adipose

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