Variant report

Variant	nsv888992
Chromosome Location	chr7:110935979-111108260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1078)
CpG islands
(count:183)
Chromatin interactive
region (count:132)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1078 , 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	chr7:110997534-110997571	K562	blood:	n/a	n/a
2	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
3	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
4	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
5	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
6	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
8	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
9	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
10	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
11	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
13	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
14	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
15	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
16	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
17	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
18	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
19	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
21	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
22	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
23	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:111078559-111079458	K562	blood:	n/a	n/a
26	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
27	CBX3	chr7:111076674-111077685	K562	blood:	n/a	n/a
28	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
29	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
30	CBX3	chr7:111074271-111074726	K562	blood:	n/a	n/a
31	CBX3	chr7:111090809-111091116	K562	blood:	n/a	n/a
32	CBX3	chr7:111073025-111074149	K562	blood:	n/a	n/a
33	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
34	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
35	CBX3	chr7:111078458-111079603	K562	blood:	n/a	n/a
36	CBX3	chr7:111079900-111081343	K562	blood:	n/a	n/a
37	CCNT2	chr7:110953302-110953502	K562	blood:	n/a	n/a
38	CCNT2	chr7:110941498-110941584	K562	blood:	n/a	n/a
39	CCNT2	chr7:111078445-111079337	K562	blood:	n/a	n/a
40	CEBPB	chr7:111051675-111051855	HepG2	liver:	n/a	chr7:111051705-111051716
41	CEBPB	chr7:111033024-111033260	K562	blood:	n/a	n/a
42	CEBPB	chr7:110952902-110953344	A549	lung:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
43	CEBPB	chr7:111019342-111019579	HepG2	liver:	n/a	chr7:111019423-111019434 chr7:111019422-111019435 chr7:111019501-111019512 chr7:111019422-111019435 chr7:111019513-111019526 chr7:111019422-111019435
44	CEBPB	chr7:111099789-111100152	K562	blood:	n/a	n/a
45	CEBPB	chr7:110952998-110953331	HepG2	liver:	n/a	chr7:110953149-110953162 chr7:110953149-110953160
46	CEBPB	chr7:111051577-111051787	K562	blood:	n/a	chr7:111051705-111051716
47	CEBPB	chr7:111078668-111079235	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:111002722-111002977	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:111078455-111079282	K562	blood:	n/a	n/a
50	CEBPB	chr7:111004463-111004919	HCT-116	colon:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111079100-111079150	ProgFib	skin:	n/a
2	chr7:111079100-111079150	Jurkat	blood:	n/a
3	chr7:111079100-111079150	GM12892	blood:	n/a
4	chr7:111079100-111079150	LNCaP	prostate:	n/a
5	chr7:111086055-111086105	GM06990	blood:	n/a
6	chr7:111079100-111079150	AoSMC	blood vessel:	n/a
7	chr7:111086055-111086105	K562	blood:	n/a
8	chr7:111033064-111033114	SAEC	small airway:	n/a
9	chr7:111086055-111086105	PANC-1	pancreas:	n/a
10	chr7:111079100-111079150	HMEC	breast:	n/a
11	chr7:111086055-111086105	HCT-116	colon:	n/a
12	chr7:111079100-111079150	SK-N-SH	brain:	n/a
13	chr7:111086055-111086105	H1-hESC	embryonic stem cell:	embryo
14	chr7:111033064-111033114	LNCaP	prostate:	n/a
15	chr7:111079100-111079150	BE2_C	brain:	n/a
16	chr7:111079100-111079150	PFSK-1	brain:	n/a
17	chr7:111086055-111086105	HRPEpiC	eye:	n/a
18	chr7:111033064-111033114	U87	brain:	n/a
19	chr7:111086055-111086105	Hela-S3	cervix:	n/a
20	chr7:111033064-111033114	AG09309	skin:	n/a
21	chr7:111033064-111033114	T-47D	breast:	n/a
22	chr7:111086055-111086105	HCM	heart:	n/a
23	chr7:111033064-111033114	AoSMC	blood vessel:	n/a
24	chr7:111086055-111086105	Hepatocyte	liver:	n/a
25	chr7:111086055-111086105	MCF10A-Er-Src	breast:	n/a
26	chr7:111079100-111079150	HCM	heart:	n/a
27	chr7:111079100-111079150	T-47D	breast:	n/a
28	chr7:111079100-111079150	Hela-S3	cervix:	n/a
29	chr7:111033064-111033114	ProgFib	skin:	n/a
30	chr7:111033064-111033114	NHBE	bronchial:	n/a
31	chr7:111033064-111033114	AG04450	lung:	fetal
32	chr7:111033064-111033114	ECC-1	luminal epithelium:	n/a
33	chr7:111086055-111086105	NT2-D1	testis:	n/a
34	chr7:111079100-111079150	AG09309	skin:	n/a
35	chr7:111086055-111086105	NHDF-neo	bronchial:	n/a
36	chr7:111086055-111086105	PFSK-1	brain:	n/a
37	chr7:111079100-111079150	GM06990	blood:	n/a
38	chr7:111033064-111033114	MCF-7	breast:	n/a
39	chr7:111086055-111086105	ProgFib	skin:	n/a
40	chr7:111079100-111079150	HNPCEpiC	eye:	n/a
41	chr7:111033064-111033114	IMR90	lung:	fetal
42	chr7:111033064-111033114	GM12892	blood:	n/a
43	chr7:111079100-111079150	A549	lung:	n/a
44	chr7:111086055-111086105	HEK293	kidney:	embryo
45	chr7:111033064-111033114	PFSK-1	brain:	n/a
46	chr7:111079100-111079150	Hepatocyte	liver:	n/a
47	chr7:111079100-111079150	AG04450	lung:	fetal
48	chr7:111086055-111086105	HMEC	breast:	n/a
49	chr7:111086055-111086105	ECC-1	luminal epithelium:	n/a
50	chr7:111079100-111079150	GM19239	blood:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
2	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
3	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
4	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
5	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
6	chr7:111050830..111052648-chr7:111066245..111068187,2	K562	blood:
7	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
8	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
9	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
10	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
11	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
12	chr7:110955341..110956918-chr7:110957234..110959729,2	K562	blood:
13	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
14	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
15	chr7:110946494..110948605-chr7:110949688..110952299,2	K562	blood:
16	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
17	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
18	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
19	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
20	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
21	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
22	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
23	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
24	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
25	chr7:110964713..110967341-chr7:110967524..110969143,2	K562	blood:
26	chr7:111027546..111029195-chr7:111032815..111035330,2	K562	blood:
27	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
28	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
29	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
30	chr7:110929795..110932437-chr7:110933207..110936083,3	K562	blood:
31	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
32	chr7:110964713..110967341-chr7:110967524..110969143,2	K562	blood:
33	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
34	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
35	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
36	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
37	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
38	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
39	chr7:111031028..111033164-chr7:111033658..111035591,2	K562	blood:
40	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
41	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
42	chr7:110955341..110956918-chr7:110957234..110959729,2	K562	blood:
43	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
44	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
45	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
46	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
47	chr7:110963413..110966213-chr7:110967085..110969024,2	K562	blood:
48	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
49	chr7:111033619..111035253-chr7:111039961..111041629,2	K562	blood:
50	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:

No data

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

Extended variants
information (count: 5786 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5786 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11534045	chr7:110935979-110935980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564367553	chr7:110936015-110936016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200840227	chr7:110936042-110936043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200001219	chr7:110936044-110936045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200843112	chr7:110936045-110936046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs58082345	chr7:110936055-110936056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188654563	chr7:110936098-110936099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547293527	chr7:110936101-110936102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372394026	chr7:110936116-110936117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539030737	chr7:110936164-110936165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557755957	chr7:110936210-110936211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76833707	chr7:110936235-110936236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149088449	chr7:110936253-110936254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74339075	chr7:110936265-110936266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532910834	chr7:110936296-110936297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555083672	chr7:110936312-110936313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573496053	chr7:110936323-110936324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551021214	chr7:110936373-110936374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181186834	chr7:110936379-110936380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187129862	chr7:110936396-110936397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552830626	chr7:110936399-110936400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563176210	chr7:110936410-110936411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530421957	chr7:110936414-110936415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377177520	chr7:110936474-110936475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370106398	chr7:110936475-110936476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs253372	chr7:110936498-110936499	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs201949020	chr7:110936562-110936563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143154405	chr7:110936585-110936586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563714020	chr7:110936648-110936649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575592611	chr7:110936650-110936651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191399730	chr7:110936660-110936661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368277116	chr7:110936759-110936760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116613776	chr7:110936805-110936806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528681775	chr7:110936816-110936817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184132335	chr7:110936881-110936882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112223831	chr7:110936883-110936884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140305157	chr7:110936886-110936887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377406740	chr7:110936895-110936896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370469354	chr7:110936965-110936966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529467534	chr7:110937038-110937039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547613928	chr7:110937047-110937048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145223558	chr7:110937050-110937051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187054008	chr7:110937059-110937060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536691184	chr7:110937061-110937062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs137890404	chr7:110937113-110937114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143029801	chr7:110937116-110937117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs207468415	chr7:110937207-110937208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114109034	chr7:110937276-110937277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs253373	chr7:110937319-110937320	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs577821551	chr7:110937320-110937321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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

Chromatin state (count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110931400-110938200	Weak transcription	Psoas Muscle	Psoas
2	chr7:110932600-110936400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:110932800-110936800	Weak transcription	Adipose Nuclei	Adipose
4	chr7:110933000-110938200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr7:110936400-110938200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:110936800-110938400	Enhancers	Adipose Nuclei	Adipose
7	chr7:110938200-110938800	Enhancers	Psoas Muscle	Psoas
8	chr7:110938200-110939400	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr7:110938200-110940400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:110939000-110939400	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr7:110943600-110945400	Enhancers	Dnd41	blood
12	chr7:110945000-110945400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:110951400-110952200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:110952800-110954200	Enhancers	K562	blood
15	chr7:110953000-110953200	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:110953000-110953400	Enhancers	Fetal Thymus	thymus
17	chr7:110953000-110953400	Enhancers	Psoas Muscle	Psoas
18	chr7:110953000-110954000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:110953200-110953600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:110953200-110954000	Enhancers	Dnd41	blood
21	chr7:110953200-110955200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr7:110953600-110953800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:110953800-110954200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:110954000-110955200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:110954200-110955000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:110955000-110956200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:110955200-110955800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:110955200-110955800	Enhancers	HUVEC	blood vessel
29	chr7:110955200-110956000	Enhancers	Primary hematopoietic stem cells	blood
30	chr7:110955400-110955800	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr7:110955600-110956000	Weak transcription	K562	blood
32	chr7:110955800-110956400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:110956000-110960200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr7:110956200-110958200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:110956400-110958000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:110958000-110961800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:110958200-110961000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:110959000-110959400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:110960000-110983400	Weak transcription	Left Ventricle	heart
40	chr7:110960200-110960400	Enhancers	Primary hematopoietic stem cells	blood
41	chr7:110960200-110961000	Enhancers	GM12878-XiMat	blood
42	chr7:110960200-110961000	Enhancers	K562	blood
43	chr7:110960800-110961000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:110961000-110961800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr7:110961000-110964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:110961800-110962400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:110961800-110962400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:110962400-110962600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:110962400-110962800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:110962600-110967200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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