Variant report

Variant	nsv1020240
Chromosome Location	chr7:110971833-111132710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1141)
CpG islands
(count:183)
Chromatin interactive
region (count:120)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1141 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
2	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
4	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
6	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
7	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
8	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
9	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
10	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
11	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
12	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
14	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
15	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
16	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
17	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
18	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
19	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
20	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
22	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
23	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
24	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:111117429-111117846	K562	blood:	n/a	n/a
27	BHLHE40	chr7:111116668-111117082	K562	blood:	n/a	n/a
28	BHLHE40	chr7:111078559-111079458	K562	blood:	n/a	n/a
29	BHLHE40	chr7:111114414-111114577	K562	blood:	n/a	n/a
30	BHLHE40	chr7:111125938-111126377	K562	blood:	n/a	n/a
31	BHLHE40	chr7:111115170-111115607	K562	blood:	n/a	n/a
32	BHLHE40	chr7:111126597-111126935	K562	blood:	n/a	n/a
33	CBX3	chr7:111078458-111079603	K562	blood:	n/a	n/a
34	CBX3	chr7:111076674-111077685	K562	blood:	n/a	n/a
35	CBX3	chr7:111074271-111074726	K562	blood:	n/a	n/a
36	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
37	CBX3	chr7:111079900-111081343	K562	blood:	n/a	n/a
38	CBX3	chr7:111113468-111114389	K562	blood:	n/a	n/a
39	CBX3	chr7:111090809-111091116	K562	blood:	n/a	n/a
40	CBX3	chr7:111117217-111118801	K562	blood:	n/a	n/a
41	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
42	CBX3	chr7:111117495-111118260	K562	blood:	n/a	n/a
43	CBX3	chr7:111073025-111074149	K562	blood:	n/a	n/a
44	CBX3	chr7:111115072-111115643	K562	blood:	n/a	n/a
45	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
46	CCNT2	chr7:111125915-111126220	K562	blood:	n/a	n/a
47	CCNT2	chr7:111078445-111079337	K562	blood:	n/a	n/a
48	CCNT2	chr7:111115046-111115592	K562	blood:	n/a	chr7:111115405-111115425
49	CCNT2	chr7:111117578-111117780	K562	blood:	n/a	n/a
50	CEBPB	chr7:111116031-111116388	Hela-S3	cervix:	n/a	chr7:111116185-111116196

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111086055-111086105	U87	brain:	n/a
2	chr7:111033064-111033114	PFSK-1	brain:	n/a
3	chr7:111086055-111086105	HMEC	breast:	n/a
4	chr7:111033064-111033114	H1-hESC	embryonic stem cell:	embryo
5	chr7:111079100-111079150	AG09309	skin:	n/a
6	chr7:111079100-111079150	PFSK-1	brain:	n/a
7	chr7:111086055-111086105	HCM	heart:	n/a
8	chr7:111079100-111079150	GM19239	blood:	n/a
9	chr7:111033064-111033114	AG10803	skin:	n/a
10	chr7:111033064-111033114	HCPEpiC	choroid plexus:	n/a
11	chr7:111086055-111086105	BJ	skin:	n/a
12	chr7:111033064-111033114	GM06990	blood:	n/a
13	chr7:111033064-111033114	HNPCEpiC	eye:	n/a
14	chr7:111079100-111079150	HAEpiC	amniotic membrane:	n/a
15	chr7:111079100-111079150	NHBE	bronchial:	n/a
16	chr7:111086055-111086105	GM06990	blood:	n/a
17	chr7:111033064-111033114	AG04450	lung:	fetal
18	chr7:111033064-111033114	HepG2	liver:	n/a
19	chr7:111033064-111033114	HRE	kidney:	n/a
20	chr7:111033064-111033114	T-47D	breast:	n/a
21	chr7:111033064-111033114	GM19239	blood:	n/a
22	chr7:111079100-111079150	PrEC	prostate:	n/a
23	chr7:111086055-111086105	MCF10A-Er-Src	breast:	n/a
24	chr7:111033064-111033114	GM12891	blood:	n/a
25	chr7:111079100-111079150	HIPEpiC	eye:	n/a
26	chr7:111079100-111079150	AG04449	skin:	fetal
27	chr7:111079100-111079150	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:111033064-111033114	HEK293	kidney:	embryo
29	chr7:111079100-111079150	SKMC	muscle:	n/a
30	chr7:111086055-111086105	ECC-1	luminal epithelium:	n/a
31	chr7:111079100-111079150	SAEC	small airway:	n/a
32	chr7:111033064-111033114	PrEC	prostate:	n/a
33	chr7:111086055-111086105	MCF-7	breast:	n/a
34	chr7:111086055-111086105	T-47D	breast:	n/a
35	chr7:111079100-111079150	HCPEpiC	choroid plexus:	n/a
36	chr7:111086055-111086105	Jurkat	blood:	n/a
37	chr7:111079100-111079150	NH-A	brain:	n/a
38	chr7:111086055-111086105	IMR90	lung:	fetal
39	chr7:111086055-111086105	HepG2	liver:	n/a
40	chr7:111079100-111079150	HUVEC	blood vessel:	n/a
41	chr7:111079100-111079150	K562	blood:	n/a
42	chr7:111086055-111086105	GM19239	blood:	n/a
43	chr7:111033064-111033114	U87	brain:	n/a
44	chr7:111079100-111079150	PANC-1	pancreas:	n/a
45	chr7:111086055-111086105	HCF	heart:	n/a
46	chr7:111033064-111033114	Hepatocyte	liver:	n/a
47	chr7:111033064-111033114	AG04449	skin:	fetal
48	chr7:111033064-111033114	HMEC	breast:	n/a
49	chr7:111086055-111086105	AG10803	skin:	n/a
50	chr7:111079100-111079150	GM12892	blood:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
2	chr7:110946954..110949529-chr7:111129446..111130953,2	MCF-7	breast:
3	chr7:111030397..111032923-chr7:111067377..111070241,2	K562	blood:
4	chr7:111126340..111126902-chr7:111381753..111382269,2	K562	blood:
5	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
6	chr7:111008511..111011324-chr7:111012744..111015031,2	K562	blood:
7	chr7:111049337..111051671-chr7:111077981..111080558,2	K562	blood:
8	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
9	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
10	chr12:108200986..108203742-chr7:111052172..111055145,3	MCF-7	breast:
11	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
12	chr7:111031028..111033164-chr7:111033658..111035591,2	K562	blood:
13	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:
14	chr7:111111427..111114620-chr7:111124257..111128153,3	K562	blood:
15	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
16	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
17	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
18	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
19	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
20	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
21	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
22	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
23	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
24	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
25	chr7:111114124..111115929-chr7:111199099..111201690,2	K562	blood:
26	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
27	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
28	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
29	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
30	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
31	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
32	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
33	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
34	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
35	chr7:111030301..111032703-chr7:111035909..111038064,2	K562	blood:
36	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
37	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
38	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
39	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
40	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
41	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
42	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
43	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
44	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
45	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
46	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
47	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
48	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
49	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
50	chr7:110977304..110981066-chr7:110982767..110987604,6	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
ENSG00000184903	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000227948	chromatin interactions

Extended variants
information (count: 5701 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5701 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539165185	chr7:110971864-110971865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113656655	chr7:110971918-110971919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs37637	chr7:110971919-110971920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs554920113	chr7:110972010-110972011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201045013	chr7:110972053-110972054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187042011	chr7:110972058-110972059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559158389	chr7:110972063-110972064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534680085	chr7:110972069-110972070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115507846	chr7:110972071-110972072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577721578	chr7:110972106-110972107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73424007	chr7:110972150-110972151	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563515986	chr7:110972179-110972180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147449608	chr7:110972192-110972193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561286982	chr7:110972264-110972265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79226506	chr7:110972297-110972298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75039309	chr7:110972298-110972299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192222364	chr7:110972310-110972311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561322515	chr7:110972327-110972328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375127101	chr7:110972383-110972384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35127245	chr7:110972391-110972392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139875041	chr7:110972409-110972410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540674545	chr7:110972452-110972453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530436679	chr7:110972458-110972459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565241083	chr7:110972510-110972511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532677966	chr7:110972512-110972513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550759107	chr7:110972560-110972561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569136778	chr7:110972568-110972569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557896844	chr7:110972573-110972574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375040448	chr7:110972620-110972621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144473610	chr7:110972705-110972706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56938422	chr7:110972720-110972721	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182395612	chr7:110972725-110972726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35294175	chr7:110972787-110972788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573062099	chr7:110972920-110972921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368028906	chr7:110972935-110972936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147847793	chr7:110972936-110972937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139215233	chr7:110972957-110972958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571245450	chr7:110972983-110972984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186759387	chr7:110972984-110972985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557173617	chr7:110973020-110973021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149926769	chr7:110973095-110973096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542910988	chr7:110973098-110973099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191815707	chr7:110973145-110973146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544386739	chr7:110973215-110973216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182511946	chr7:110973248-110973249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540253295	chr7:110973252-110973253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7787829	chr7:110973256-110973257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs578228271	chr7:110973257-110973258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188750233	chr7:110973268-110973269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192839245	chr7:110973312-110973313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	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:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110960000-110983400	Weak transcription	Left Ventricle	heart
2	chr7:110968400-110973000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:110971400-110978800	Weak transcription	Adipose Nuclei	Adipose
4	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:110973000-110973600	Enhancers	HMEC	breast
7	chr7:110973000-110973800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:110973000-110973800	Enhancers	NHEK	skin
9	chr7:110973600-110979800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:110973800-110983400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:110978000-110978200	Enhancers	Psoas Muscle	Psoas
12	chr7:110978800-110979200	Enhancers	Adipose Nuclei	Adipose
13	chr7:110978800-110979400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:110978800-110979800	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr7:110979400-110981600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:110979800-110980800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:110980400-110981000	Enhancers	NHEK	skin
20	chr7:110980800-110983200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:110981600-110982000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:110983200-110983600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:110983400-110983600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:110983400-110983600	ZNF genes & repeats	Left Ventricle	heart
25	chr7:110983400-110983800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
26	chr7:110983600-110984200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:110984000-110985600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:110987000-110987800	Enhancers	Psoas Muscle	Psoas
29	chr7:110987400-111002800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:110987800-110989600	Weak transcription	Psoas Muscle	Psoas
31	chr7:110989600-110989800	Enhancers	Psoas Muscle	Psoas
32	chr7:110996800-110997400	Enhancers	K562	blood
33	chr7:110997000-110997200	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr7:110997000-110997200	Enhancers	HSMMtube	muscle
35	chr7:110997000-110997800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr7:110997000-110998200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr7:110997000-110998400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:110997000-110998600	Enhancers	A549	lung
39	chr7:110997000-110998800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:110997000-110999000	Enhancers	HMEC	breast
41	chr7:110997000-110999200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:110997000-110999200	Enhancers	Hela-S3	cervix
43	chr7:110997000-110999400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:110997000-110999800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr7:110997200-110997400	Enhancers	NH-A	brain
46	chr7:110997200-110998000	Weak transcription	HSMMtube	muscle
47	chr7:110997200-110998200	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr7:110997200-110998200	Enhancers	Osteobl	bone
49	chr7:110997200-110998400	Enhancers	HSMM	muscle
50	chr7:110997200-110998600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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