Variant report

Variant	nsv889001
Chromosome Location	chr7:110959881-111108260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:893)
CpG islands
(count:183)
Chromatin interactive
region (count:111)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
4	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
5	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
6	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
7	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
8	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
9	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
10	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
11	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
12	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
13	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
14	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
15	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
16	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
17	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
19	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
20	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
21	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:111078559-111079458	K562	blood:	n/a	n/a
24	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
25	CBX3	chr7:111074271-111074726	K562	blood:	n/a	n/a
26	CBX3	chr7:111079900-111081343	K562	blood:	n/a	n/a
27	CBX3	chr7:111090809-111091116	K562	blood:	n/a	n/a
28	CBX3	chr7:111076674-111077685	K562	blood:	n/a	n/a
29	CBX3	chr7:111078458-111079603	K562	blood:	n/a	n/a
30	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
31	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
32	CBX3	chr7:111073025-111074149	K562	blood:	n/a	n/a
33	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
34	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
35	CCNT2	chr7:111078445-111079337	K562	blood:	n/a	n/a
36	CEBPB	chr7:111033008-111033349	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:111033024-111033260	K562	blood:	n/a	n/a
38	CEBPB	chr7:111099789-111100152	K562	blood:	n/a	n/a
39	CEBPB	chr7:111000057-111000344	A549	lung:	n/a	n/a
40	CEBPB	chr7:111099844-111100042	A549	lung:	n/a	n/a
41	CEBPB	chr7:111004390-111004910	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:111078668-111079235	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:111059906-111060145	K562	blood:	n/a	n/a
44	CEBPB	chr7:111004492-111004784	A549	lung:	n/a	n/a
45	CEBPB	chr7:111004475-111004941	HCT-116	colon:	n/a	n/a
46	CEBPB	chr7:111051675-111051855	HepG2	liver:	n/a	chr7:111051705-111051716
47	CEBPB	chr7:111000171-111000608	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:111003647-111003648	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr7:111053686-111053711	A549	lung:	n/a	n/a
50	CEBPB	chr7:111078944-111079144	A549	lung:	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	HIPEpiC	eye:	n/a
2	chr7:111033064-111033114	AoSMC	blood vessel:	n/a
3	chr7:111033064-111033114	GM19239	blood:	n/a
4	chr7:111079100-111079150	NH-A	brain:	n/a
5	chr7:111079100-111079150	IMR90	lung:	fetal
6	chr7:111086055-111086105	H1-hESC	embryonic stem cell:	embryo
7	chr7:111086055-111086105	GM19239	blood:	n/a
8	chr7:111033064-111033114	HCF	heart:	n/a
9	chr7:111079100-111079150	AG04449	skin:	fetal
10	chr7:111086055-111086105	GM06990	blood:	n/a
11	chr7:111079100-111079150	HCT-116	colon:	n/a
12	chr7:111033064-111033114	ECC-1	luminal epithelium:	n/a
13	chr7:111079100-111079150	PANC-1	pancreas:	n/a
14	chr7:111033064-111033114	A549	lung:	n/a
15	chr7:111033064-111033114	SKMC	muscle:	n/a
16	chr7:111033064-111033114	NHBE	bronchial:	n/a
17	chr7:111086055-111086105	HIPEpiC	eye:	n/a
18	chr7:111079100-111079150	BE2_C	brain:	n/a
19	chr7:111079100-111079150	HRPEpiC	eye:	n/a
20	chr7:111079100-111079150	NB4	blood:	n/a
21	chr7:111086055-111086105	CMK	blood:	n/a
22	chr7:111033064-111033114	LNCaP	prostate:	n/a
23	chr7:111033064-111033114	HCT-116	colon:	n/a
24	chr7:111086055-111086105	AG10803	skin:	n/a
25	chr7:111033064-111033114	HEEpiC	esophagus:	n/a
26	chr7:111086055-111086105	A549	lung:	n/a
27	chr7:111033064-111033114	SK-N-MC	brain:	n/a
28	chr7:111079100-111079150	HEK293	kidney:	embryo
29	chr7:111033064-111033114	BE2_C	brain:	n/a
30	chr7:111086055-111086105	SK-N-SH_RA	brain:	n/a
31	chr7:111086055-111086105	SAEC	small airway:	n/a
32	chr7:111033064-111033114	SAEC	small airway:	n/a
33	chr7:111086055-111086105	ECC-1	luminal epithelium:	n/a
34	chr7:111086055-111086105	PFSK-1	brain:	n/a
35	chr7:111086055-111086105	HRCEpiC	kidney:	n/a
36	chr7:111033064-111033114	NT2-D1	testis:	n/a
37	chr7:111033064-111033114	Hepatocyte	liver:	n/a
38	chr7:111079100-111079150	AoSMC	blood vessel:	n/a
39	chr7:111079100-111079150	Jurkat	blood:	n/a
40	chr7:111033064-111033114	H1-hESC	embryonic stem cell:	embryo
41	chr7:111086055-111086105	SK-N-SH	brain:	n/a
42	chr7:111033064-111033114	HAEpiC	amniotic membrane:	n/a
43	chr7:111033064-111033114	BJ	skin:	n/a
44	chr7:111033064-111033114	NB4	blood:	n/a
45	chr7:111079100-111079150	HL-60	blood:	n/a
46	chr7:111079100-111079150	HCF	heart:	n/a
47	chr7:111086055-111086105	U87	brain:	n/a
48	chr7:111079100-111079150	HepG2	liver:	n/a
49	chr7:111086055-111086105	AG04449	skin:	fetal
50	chr7:111079100-111079150	ProgFib	skin:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
2	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
3	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
4	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:
5	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
6	chr7:111030397..111032923-chr7:111067377..111070241,2	K562	blood:
7	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
8	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
9	chr7:110959334..110960882-chr7:110965813..110967484,2	K562	blood:
10	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
11	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
12	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
13	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
14	chr7:110975357..110976070-chr7:111125914..111126817,2	K562	blood:
15	chr7:111033110..111035570-chr7:111037254..111039437,2	K562	blood:
16	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
17	chr7:111049337..111051671-chr7:111077981..111080558,2	K562	blood:
18	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
19	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
20	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
21	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
22	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
23	chr7:111031028..111033164-chr7:111033658..111035591,2	K562	blood:
24	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
25	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
26	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
27	chr7:111050830..111052648-chr7:111066245..111068187,2	K562	blood:
28	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
29	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
30	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
31	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
32	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
33	chr7:111008511..111011324-chr7:111012744..111015031,2	K562	blood:
34	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
35	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
36	chr7:111008511..111011324-chr7:111012744..111015031,2	K562	blood:
37	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
38	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
39	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
40	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
41	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
42	chr7:110963413..110966213-chr7:110967085..110969024,2	K562	blood:
43	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
44	chr7:110963413..110966213-chr7:110967085..110969024,2	K562	blood:
45	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
46	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
47	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
48	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
49	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
50	chr7:110958175..110962470-chr7:110967524..110970471,4	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
ENSG00000227948	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 5253 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5253 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6466376	chr7:110959881-110959882	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530077479	chr7:110959931-110959932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146814768	chr7:110959945-110959946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560237312	chr7:110960010-110960011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553913249	chr7:110960071-110960072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188907876	chr7:110960073-110960074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563406841	chr7:110960076-110960077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs56306737	chr7:110960083-110960084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181930619	chr7:110960150-110960151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186340783	chr7:110960155-110960156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538529371	chr7:110960163-110960164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140626412	chr7:110960187-110960188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370646458	chr7:110960222-110960223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142780947	chr7:110960291-110960292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151041145	chr7:110960314-110960315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554657773	chr7:110960315-110960316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572982152	chr7:110960342-110960343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116325598	chr7:110960380-110960381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558779620	chr7:110960392-110960393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576993758	chr7:110960394-110960395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189904286	chr7:110960421-110960422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139463005	chr7:110960424-110960425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115615082	chr7:110960474-110960475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574751152	chr7:110960538-110960539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541824741	chr7:110960549-110960550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569726636	chr7:110960567-110960568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560172696	chr7:110960580-110960581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527771223	chr7:110960615-110960616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572401545	chr7:110960635-110960636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374243496	chr7:110960642-110960643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545782201	chr7:110960664-110960665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545940726	chr7:110960692-110960693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564686174	chr7:110960778-110960779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181012679	chr7:110960813-110960814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369041063	chr7:110960829-110960830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140375706	chr7:110960837-110960838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568662353	chr7:110960857-110960858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150377821	chr7:110960867-110960868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558041789	chr7:110960875-110960876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370819506	chr7:110960876-110960877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576319370	chr7:110960877-110960878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185947440	chr7:110960889-110960890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566518136	chr7:110960895-110960896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533847912	chr7:110960961-110960962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558722236	chr7:110960966-110960967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570593673	chr7:110961005-110961006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117502636	chr7:110961105-110961106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116153189	chr7:110961108-110961109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561841516	chr7:110961134-110961135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570655625	chr7:110961142-110961143	Weak transcription Enhancers	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:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110956000-110960200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:110958000-110961800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:110958200-110961000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:110960000-110983400	Weak transcription	Left Ventricle	heart
5	chr7:110960200-110960400	Enhancers	Primary hematopoietic stem cells	blood
6	chr7:110960200-110961000	Enhancers	GM12878-XiMat	blood
7	chr7:110960200-110961000	Enhancers	K562	blood
8	chr7:110960800-110961000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:110961000-110961800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:110961000-110964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:110961800-110962400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:110961800-110962400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:110962400-110962600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:110962400-110962800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:110962600-110967200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:110964200-110964600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:110964200-110964600	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr7:110964600-110967200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr7:110964600-110969000	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr7:110966400-110966600	Active TSS	K562	blood
21	chr7:110966600-110966800	Flanking Active TSS	K562	blood
22	chr7:110966800-110967000	Active TSS	K562	blood
23	chr7:110967000-110967400	Flanking Active TSS	K562	blood
24	chr7:110967200-110968800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:110967200-110969000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:110967400-110969400	Active TSS	K562	blood
27	chr7:110968400-110973000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:110968600-110968800	Enhancers	GM12878-XiMat	blood
29	chr7:110968800-110969200	Flanking Active TSS	GM12878-XiMat	blood
30	chr7:110968800-110969800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:110969000-110969600	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr7:110969000-110969800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:110969200-110969600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr7:110969200-110970400	Enhancers	GM12878-XiMat	blood
35	chr7:110969400-110970000	Flanking Active TSS	K562	blood
36	chr7:110971200-110971400	Enhancers	Adipose Nuclei	Adipose
37	chr7:110971400-110978800	Weak transcription	Adipose Nuclei	Adipose
38	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:110973000-110973600	Enhancers	HMEC	breast
41	chr7:110973000-110973800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:110973000-110973800	Enhancers	NHEK	skin
43	chr7:110973600-110979800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:110973800-110983400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:110978000-110978200	Enhancers	Psoas Muscle	Psoas
46	chr7:110978800-110979200	Enhancers	Adipose Nuclei	Adipose
47	chr7:110978800-110979400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:110978800-110979800	Enhancers	Pancreatic Islets	Pancreatic Islet

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