Variant report

Variant	nsv608473
Chromosome Location	chr7:139491967-139539218
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:484)
CpG islands
(count:366)
Chromatin interactive
region (count:45)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:139529332-139529539	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:139506942-139507136	HepG2	liver:	n/a	n/a
3	ATF1	chr7:139528842-139529018	K562	blood:	n/a	n/a
4	ATF1	chr7:139521164-139521470	K562	blood:	n/a	n/a
5	ATF1	chr7:139525757-139525957	K562	blood:	n/a	n/a
6	ATF2	chr7:139498019-139498463	GM12878	blood:	n/a	n/a
7	ATF2	chr7:139529350-139529976	GM12878	blood:	n/a	n/a
8	ATF2	chr7:139497982-139498502	GM12878	blood:	n/a	n/a
9	ATF3	chr7:139525712-139526032	K562	blood:	n/a	n/a
10	BACH1	chr7:139521611-139521616	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr7:139499407-139499842	GM12878	blood:	n/a	n/a
12	BATF	chr7:139528827-139529129	GM12878	blood:	n/a	chr7:139528966-139528977
13	BATF	chr7:139529459-139529881	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:139525825-139526025	K562	blood:	n/a	n/a
15	BHLHE40	chr7:139517046-139517225	K562	blood:	n/a	n/a
16	BHLHE40	chr7:139528886-139529147	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:139529261-139529262	K562	blood:	n/a	n/a
18	BHLHE40	chr7:139498276-139498379	GM12878	blood:	n/a	n/a
19	CBX3	chr7:139503195-139503639	K562	blood:	n/a	n/a
20	CBX3	chr7:139515703-139516078	K562	blood:	n/a	n/a
21	CBX3	chr7:139503244-139503621	K562	blood:	n/a	n/a
22	CCNT2	chr7:139517146-139517451	K562	blood:	n/a	n/a
23	CEBPB	chr7:139524920-139525218	K562	blood:	n/a	chr7:139525049-139525060
24	CEBPB	chr7:139524934-139525210	A549	lung:	n/a	chr7:139525049-139525060
25	CEBPB	chr7:139525003-139525162	Hela-S3	cervix:	n/a	chr7:139525049-139525060
26	CEBPB	chr7:139503152-139503418	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:139515553-139515800	IMR90	lung:	n/a	chr7:139515636-139515647
28	CEBPB	chr7:139530127-139530415	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:139524901-139525233	IMR90	lung:	n/a	chr7:139525049-139525060
30	CEBPB	chr7:139503200-139503358	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:139524919-139525198	HepG2	liver:	n/a	chr7:139525049-139525060
32	CEBPB	chr7:139515320-139515787	HepG2	liver:	n/a	chr7:139515636-139515647
33	CEBPB	chr7:139510544-139511142	IMR90	lung:	n/a	n/a
34	CEBPD	chr7:139517039-139517533	K562	blood:	n/a	n/a
35	CEBPD	chr7:139508797-139509322	K562	blood:	n/a	n/a
36	CEBPD	chr7:139517030-139517546	K562	blood:	n/a	n/a
37	CHD1	chr7:139523515-139524772	IMR90	lung:	n/a	n/a
38	CHD1	chr7:139529680-139530168	GM12878	blood:	n/a	n/a
39	CHD2	chr7:139529002-139529013	GM12878	blood:	n/a	n/a
40	CTCF	chr7:139526960-139527110	SAEC	small airway:	n/a	n/a
41	CTCF	chr7:139519660-139519810	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr7:139498928-139498972	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:139526940-139527090	GM12870	blood:	n/a	n/a
44	CTCF	chr7:139529020-139529170	GM12873	blood:	n/a	n/a
45	CTCF	chr7:139527020-139527175	GM13977	blood:	n/a	n/a
46	CTCF	chr7:139526960-139527110	GM12865	blood:	n/a	n/a
47	CTCF	chr7:139526977-139527155	GM19240	blood:	n/a	n/a
48	CTCF	chr7:139526848-139527345	HCT-116	colon:	n/a	n/a
49	CTCF	chr7:139526940-139527090	HMEC	breast:	n/a	n/a
50	CTCF	chr7:139527020-139527170	GM06990	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:139498041-139498091	GM12878	blood:	n/a
2	chr7:139528673-139528723	BJ	skin:	n/a
3	chr7:139528673-139528723	K562	blood:	n/a
4	chr7:139498041-139498091	AG09309	skin:	n/a
5	chr7:139529130-139529180	HIPEpiC	eye:	n/a
6	chr7:139510502-139510552	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:139529130-139529180	GM12878	blood:	n/a
8	chr7:139510502-139510552	GM06990	blood:	n/a
9	chr7:139522635-139522685	MCF10A-Er-Src	breast:	n/a
10	chr7:139528855-139528905	T-47D	breast:	n/a
11	chr7:139528855-139528905	ProgFib	skin:	n/a
12	chr7:139529130-139529180	MCF10A-Er-Src	breast:	n/a
13	chr7:139510502-139510552	IMR90	lung:	fetal
14	chr7:139510502-139510552	PFSK-1	brain:	n/a
15	chr7:139522635-139522685	HNPCEpiC	eye:	n/a
16	chr7:139528673-139528723	ECC-1	luminal epithelium:	n/a
17	chr7:139510502-139510552	HMEC	breast:	n/a
18	chr7:139528855-139528905	AG09319	gingival:	n/a
19	chr7:139510502-139510552	K562	blood:	n/a
20	chr7:139528855-139528905	HAEpiC	amniotic membrane:	n/a
21	chr7:139529130-139529180	HAEpiC	amniotic membrane:	n/a
22	chr7:139529130-139529180	HRE	kidney:	n/a
23	chr7:139528673-139528723	SK-N-SH_RA	brain:	n/a
24	chr7:139529130-139529180	Hela-S3	cervix:	n/a
25	chr7:139498041-139498091	AG09319	gingival:	n/a
26	chr7:139528855-139528905	H1-hESC	embryonic stem cell:	embryo
27	chr7:139528855-139528905	HCF	heart:	n/a
28	chr7:139528855-139528905	SK-N-SH_RA	brain:	n/a
29	chr7:139498041-139498091	GM19239	blood:	n/a
30	chr7:139498041-139498091	NH-A	brain:	n/a
31	chr7:139510502-139510552	CMK	blood:	n/a
32	chr7:139510502-139510552	GM12891	blood:	n/a
33	chr7:139528855-139528905	HEK293	kidney:	embryo
34	chr7:139522635-139522685	BE2_C	brain:	n/a
35	chr7:139529130-139529180	AG04449	skin:	fetal
36	chr7:139528855-139528905	HEEpiC	esophagus:	n/a
37	chr7:139498041-139498091	PrEC	prostate:	n/a
38	chr7:139529130-139529180	AoSMC	blood vessel:	n/a
39	chr7:139529130-139529180	HEK293	kidney:	embryo
40	chr7:139528855-139528905	HCPEpiC	choroid plexus:	n/a
41	chr7:139529130-139529180	NT2-D1	testis:	n/a
42	chr7:139528855-139528905	NHBE	bronchial:	n/a
43	chr7:139528673-139528723	RPTEC	kidney:	n/a
44	chr7:139510502-139510552	GM19239	blood:	n/a
45	chr7:139528673-139528723	AG04450	lung:	fetal
46	chr7:139528855-139528905	HNPCEpiC	eye:	n/a
47	chr7:139498041-139498091	LNCaP	prostate:	n/a
48	chr7:139522635-139522685	AG09319	gingival:	n/a
49	chr7:139522635-139522685	ovcar-3	ovarian:	n/a
50	chr7:139529130-139529180	HepG2	liver:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:139513511..139516788-chr7:139520742..139523420,3	MCF-7	breast:
2	chr7:139517510..139519171-chr7:139675166..139676811,2	K562	blood:
3	chr7:139517568..139521373-chr7:139521587..139526613,5	K562	blood:
4	chr7:139490500..139493379-chr7:139496695..139499079,2	K562	blood:
5	chr7:139490458..139492000-chr7:139496695..139498330,2	K562	blood:
6	chr7:139476377..139478702-chr7:139512997..139515322,2	K562	blood:
7	chr7:139509619..139511685-chr7:139672736..139675273,2	K562	blood:
8	chr7:139485125..139487946-chr7:139498173..139499742,2	K562	blood:
9	chr7:139510717..139512298-chr7:139514084..139516330,2	K562	blood:
10	chr7:139517568..139521373-chr7:139521587..139526613,5	K562	blood:
11	chr7:139476835..139480662-chr7:139509680..139512004,3	K562	blood:
12	chr7:139490458..139492000-chr7:139496695..139498330,2	K562	blood:
13	chr7:139501134..139503476-chr7:139509112..139512787,3	K562	blood:
14	chr7:139479210..139481182-chr7:139491846..139493959,3	K562	blood:
15	chr7:139496148..139499029-chr7:139499477..139502002,2	K562	blood:
16	chr7:139520918..139522874-chr7:139551760..139554613,2	K562	blood:
17	chr7:139496148..139499029-chr7:139499477..139502002,2	K562	blood:
18	chr7:139529269..139531920-chr7:139536482..139539397,2	MCF-7	breast:
19	chr7:139538171..139540494-chr7:139550630..139553046,2	K562	blood:
20	chr7:139485093..139487934-chr7:139493683..139497739,3	K562	blood:
21	chr7:139525637..139527393-chr7:139527540..139529526,2	K562	blood:
22	chr7:139476813..139479584-chr7:139529025..139531896,2	MCF-7	breast:
23	chr7:139477083..139479483-chr7:139538319..139540657,2	K562	blood:
24	chr7:139482695..139484256-chr7:139496292..139498797,2	K562	blood:
25	chr7:139485450..139487997-chr7:139490287..139492572,3	K562	blood:
26	chr7:139022629..139025216-chr7:139516939..139518610,2	K562	blood:
27	chr7:139521931..139523978-chr7:139621670..139623337,2	K562	blood:
28	chr7:139512207..139514973-chr7:139519326..139521466,2	K562	blood:
29	chr7:139495484..139499018-chr7:139500374..139502989,3	K562	blood:
30	chr7:139524710..139527393-chr7:139527540..139530071,3	K562	blood:
31	chr7:139512207..139514973-chr7:139519326..139521466,2	K562	blood:
32	chr7:139507010..139509196-chr7:139510108..139512774,2	K562	blood:
33	chr7:139513511..139516788-chr7:139520742..139523420,3	MCF-7	breast:
34	chr7:139520823..139523874-chr7:139528601..139531758,3	K562	blood:
35	chr7:139532720..139535197-chr7:139540862..139542480,2	K562	blood:
36	chr7:139512986..139515006-chr7:139515072..139518035,2	MCF-7	breast:
37	chr7:139510717..139512298-chr7:139514084..139516330,2	K562	blood:
38	chr7:139486823..139488377-chr7:139490221..139491972,2	MCF-7	breast:
39	chr7:139501134..139503476-chr7:139509112..139512787,3	K562	blood:
40	chr7:139529269..139531920-chr7:139536482..139539397,2	MCF-7	breast:
41	chr7:139488642..139491637-chr7:139494794..139496351,2	K562	blood:
42	chr7:139495484..139499018-chr7:139500374..139502989,3	K562	blood:
43	chr7:139512986..139515006-chr7:139515072..139518035,2	MCF-7	breast:
44	chr7:139507010..139509196-chr7:139510108..139512774,2	K562	blood:
45	chr7:139490500..139493379-chr7:139496695..139499079,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBXAS1-3	chr7:139497009-139497283	NONHSAT123651
2	lnc-CLEC2L-2	chr7:139523530-139525908	l_3489_NR_024451
3	lnc-TBXAS1-3	chr7:139497009-139497283	NONHSAT123653
4	lnc-TBXAS1-3	chr7:139497009-139497282	NONHSAT123654

No data

Variant related genes	Relation type
TBXAS1	TF binding region
TBXAS1	CpG island
ENSG00000059377	chromatin interactions
ENSG00000164898	chromatin interactions
ENSG00000064393	chromatin interactions
ENSG00000146963	chromatin interactions

Extended variants
information (count: 1683 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1683 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17177953	chr7:139491967-139491968	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149450385	chr7:139492049-139492050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541797736	chr7:139492063-139492064	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76824302	chr7:139492099-139492100	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541129435	chr7:139492103-139492104	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17161128	chr7:139492104-139492105	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs532981618	chr7:139492143-139492144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143861032	chr7:139492193-139492194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563121335	chr7:139492216-139492217	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148620762	chr7:139492332-139492333	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548998432	chr7:139492372-139492373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567663064	chr7:139492400-139492401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528430989	chr7:139492414-139492415	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs58216762	chr7:139492438-139492439	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1074978	chr7:139492513-139492514	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs73475971	chr7:139492524-139492525	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs114959712	chr7:139492532-139492533	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569468298	chr7:139492543-139492544	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536990990	chr7:139492555-139492556	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554922974	chr7:139492615-139492616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113475654	chr7:139492632-139492633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187510993	chr7:139492638-139492639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1074977	chr7:139492647-139492648	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs73475976	chr7:139492663-139492664	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs192746904	chr7:139492666-139492667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76710956	chr7:139492678-139492679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575308127	chr7:139492695-139492696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559158705	chr7:139492697-139492698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58632561	chr7:139492698-139492699	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184493718	chr7:139492748-139492749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188464424	chr7:139492754-139492755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547048891	chr7:139492812-139492813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151182326	chr7:139492830-139492831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34467392	chr7:139492917-139492918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532698986	chr7:139492929-139492930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541807719	chr7:139492945-139492946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376335929	chr7:139493002-139493003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200386389	chr7:139493014-139493015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563689483	chr7:139493075-139493076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530768230	chr7:139493082-139493083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139618272	chr7:139493088-139493089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191874661	chr7:139493103-139493104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73475978	chr7:139493116-139493117	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548885348	chr7:139493122-139493123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184305219	chr7:139493128-139493129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145246434	chr7:139493191-139493192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528611186	chr7:139493216-139493217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374676463	chr7:139493226-139493227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147631834	chr7:139493261-139493262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577210683	chr7:139493311-139493312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139479000-139497400	Weak transcription	NH-A	brain
2	chr7:139483400-139497600	Weak transcription	Fetal Kidney	kidney
3	chr7:139483600-139492000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr7:139484800-139499000	Weak transcription	A549	lung
5	chr7:139485000-139497800	Weak transcription	NHEK	skin
6	chr7:139485000-139498000	Weak transcription	HMEC	breast
7	chr7:139485000-139502200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:139485600-139495400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:139485800-139499600	Weak transcription	Aorta	Aorta
10	chr7:139487200-139493600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:139488600-139498000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:139488800-139498400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:139489400-139498000	Weak transcription	Esophagus	oesophagus
14	chr7:139489400-139502600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:139491200-139492000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr7:139491200-139492600	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr7:139492000-139492800	Strong transcription	Muscle Satellite Cultured Cells	--
18	chr7:139492000-139498000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr7:139492600-139496200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr7:139492800-139497400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr7:139493600-139497000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:139495600-139495800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:139495800-139497000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:139497000-139498000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:139497000-139498200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:139497000-139498400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:139497200-139497600	Enhancers	Osteobl	bone
28	chr7:139497200-139497800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:139497200-139498400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:139497400-139497600	Enhancers	Muscle Satellite Cultured Cells	--
31	chr7:139497400-139497600	Enhancers	Fetal Stomach	stomach
32	chr7:139497400-139497600	Enhancers	Left Ventricle	heart
33	chr7:139497400-139497800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr7:139497400-139497800	Enhancers	NH-A	brain
35	chr7:139497400-139498200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:139497400-139498400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:139497400-139498400	Enhancers	HSMMtube	muscle
38	chr7:139497600-139498600	Enhancers	Fetal Kidney	kidney
39	chr7:139497600-139499800	Weak transcription	Left Ventricle	heart
40	chr7:139497600-139503400	Weak transcription	Fetal Stomach	stomach
41	chr7:139497800-139498000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:139497800-139498000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr7:139497800-139498000	Enhancers	GM12878-XiMat	blood
44	chr7:139497800-139498400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr7:139497800-139498800	Enhancers	Brain Substantia Nigra	brain
46	chr7:139497800-139498800	Enhancers	Fetal Thymus	thymus
47	chr7:139497800-139498800	Enhancers	NHEK	skin
48	chr7:139497800-139500200	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr7:139498000-139498200	Enhancers	Adipose Nuclei	Adipose
50	chr7:139498000-139498200	Flanking Active TSS	Duodenum Mucosa	Duodenum

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