Variant report

Variant	nsv889511
Chromosome Location	chr7:153076838-153201572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1126)
CpG islands
(count:553)
Chromatin interactive
region (count:166)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1126 , 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	chr7:153143735-153143934	K562	blood:	n/a	n/a
2	ARID3A	chr7:153108540-153108589	K562	blood:	n/a	n/a
3	ARID3A	chr7:153103753-153104234	K562	blood:	n/a	n/a
4	ARID3A	chr7:153078807-153079063	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:153103307-153103458	K562	blood:	n/a	n/a
6	ARID3A	chr7:153109096-153109296	K562	blood:	n/a	n/a
7	ARID3A	chr7:153082623-153082873	K562	blood:	n/a	n/a
8	ARID3A	chr7:153104655-153106258	K562	blood:	n/a	n/a
9	ARID3A	chr7:153109739-153110062	K562	blood:	n/a	n/a
10	ARID3A	chr7:153130385-153130583	K562	blood:	n/a	n/a
11	ARID3A	chr7:153110322-153112174	K562	blood:	n/a	n/a
12	ATF1	chr7:153130251-153130554	K562	blood:	n/a	n/a
13	ATF1	chr7:153154941-153155221	K562	blood:	n/a	n/a
14	ATF1	chr7:153104526-153104952	K562	blood:	n/a	n/a
15	ATF1	chr7:153119688-153120319	K562	blood:	n/a	n/a
16	ATF1	chr7:153112718-153113068	K562	blood:	n/a	n/a
17	ATF1	chr7:153110923-153111307	K562	blood:	n/a	n/a
18	ATF3	chr7:153119989-153120275	K562	blood:	n/a	n/a
19	BACH1	chr7:153100843-153101026	K562	blood:	n/a	n/a
20	BACH1	chr7:153200611-153200865	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:153133123-153133319	K562	blood:	n/a	n/a
22	BACH1	chr7:153113244-153113564	K562	blood:	n/a	n/a
23	BACH1	chr7:153109751-153110110	K562	blood:	n/a	n/a
24	BACH1	chr7:153110739-153112141	K562	blood:	n/a	n/a
25	BACH1	chr7:153099558-153099965	K562	blood:	n/a	n/a
26	BACH1	chr7:153108498-153108636	K562	blood:	n/a	n/a
27	BACH1	chr7:153097892-153097911	K562	blood:	n/a	n/a
28	BACH1	chr7:153111122-153111267	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL3	chr7:153103242-153103537	K562	blood:	n/a	n/a
30	BCL3	chr7:153104489-153105071	K562	blood:	n/a	n/a
31	BCL3	chr7:153109499-153110250	K562	blood:	n/a	n/a
32	BCL3	chr7:153101811-153102227	K562	blood:	n/a	n/a
33	BCL3	chr7:153105524-153106503	K562	blood:	n/a	n/a
34	BCLAF1	chr7:153107687-153111130	K562	blood:	n/a	n/a
35	BCLAF1	chr7:153104261-153105189	K562	blood:	n/a	n/a
36	BCLAF1	chr7:153105443-153107677	K562	blood:	n/a	n/a
37	BCLAF1	chr7:153110402-153111174	K562	blood:	n/a	n/a
38	BHLHE40	chr7:153110425-153112117	K562	blood:	n/a	n/a
39	BHLHE40	chr7:153129078-153129498	K562	blood:	n/a	n/a
40	BHLHE40	chr7:153097843-153098018	K562	blood:	n/a	n/a
41	BHLHE40	chr7:153119270-153119662	K562	blood:	n/a	n/a
42	BHLHE40	chr7:153167374-153167638	K562	blood:	n/a	n/a
43	BHLHE40	chr7:153103811-153104266	K562	blood:	n/a	n/a
44	BHLHE40	chr7:153128439-153128484	K562	blood:	n/a	n/a
45	BHLHE40	chr7:153086025-153086031	K562	blood:	n/a	n/a
46	BHLHE40	chr7:153151428-153151430	K562	blood:	n/a	n/a
47	BHLHE40	chr7:153105622-153106329	K562	blood:	n/a	n/a
48	BHLHE40	chr7:153143758-153143944	K562	blood:	n/a	n/a
49	BHLHE40	chr7:153101789-153102645	K562	blood:	n/a	n/a
50	BHLHE40	chr7:153131156-153131336	K562	blood:	n/a	n/a

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153109375-153109425	HAEpiC	amniotic membrane:	n/a
2	chr7:153108684-153108734	BJ	skin:	n/a
3	chr7:153110492-153110542	GM12878	blood:	n/a
4	chr7:153109538-153109588	NT2-D1	testis:	n/a
5	chr7:153109375-153109425	HAEpiC	amniotic membrane:	n/a
6	chr7:153108684-153108734	BJ	skin:	n/a
7	chr7:153110492-153110542	GM12878	blood:	n/a
8	chr7:153109538-153109588	NT2-D1	testis:	n/a
9	chr7:153110994-153111044	NHDF-neo	bronchial:	n/a
10	chr7:153108726-153108776	SK-N-SH_RA	brain:	n/a
11	chr7:153108642-153108692	HEEpiC	esophagus:	n/a
12	chr7:153109538-153109588	SKMC	muscle:	n/a
13	chr7:153110492-153110542	LNCaP	prostate:	n/a
14	chr7:153109538-153109588	GM12891	blood:	n/a
15	chr7:153078797-153078847	U87	brain:	n/a
16	chr7:153110492-153110542	PANC-1	pancreas:	n/a
17	chr7:153110762-153110812	HUVEC	blood vessel:	n/a
18	chr7:153078797-153078847	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:153109538-153109588	IMR90	lung:	fetal
20	chr7:153108726-153108776	H1-hESC	embryonic stem cell:	embryo
21	chr7:153109538-153109588	RPTEC	kidney:	n/a
22	chr7:153078797-153078847	AG04450	lung:	fetal
23	chr7:153109538-153109588	SK-N-MC	brain:	n/a
24	chr7:153108726-153108776	A549	lung:	n/a
25	chr7:153078797-153078847	SK-N-SH	brain:	n/a
26	chr7:153110762-153110812	T-47D	breast:	n/a
27	chr7:153110492-153110542	T-47D	breast:	n/a
28	chr7:153110994-153111044	ProgFib	skin:	n/a
29	chr7:153110762-153110812	SAEC	small airway:	n/a
30	chr7:153078797-153078847	HepG2	liver:	n/a
31	chr7:153109538-153109588	PANC-1	pancreas:	n/a
32	chr7:153108642-153108692	GM19239	blood:	n/a
33	chr7:153109375-153109425	AG04450	lung:	fetal
34	chr7:153078797-153078847	SK-N-MC	brain:	n/a
35	chr7:153110492-153110542	PFSK-1	brain:	n/a
36	chr7:153078797-153078847	GM12891	blood:	n/a
37	chr7:153110492-153110542	HUVEC	blood vessel:	n/a
38	chr7:153110492-153110542	GM12891	blood:	n/a
39	chr7:153108684-153108734	SK-N-MC	brain:	n/a
40	chr7:153108726-153108776	HEEpiC	esophagus:	n/a
41	chr7:153109375-153109425	H1-hESC	embryonic stem cell:	embryo
42	chr7:153110994-153111044	SK-N-SH	brain:	n/a
43	chr7:153108642-153108692	HRCEpiC	kidney:	n/a
44	chr7:153110994-153111044	PFSK-1	brain:	n/a
45	chr7:153108642-153108692	HCT-116	colon:	n/a
46	chr7:153109375-153109425	AG10803	skin:	n/a
47	chr7:153108726-153108776	BJ	skin:	n/a
48	chr7:153108726-153108776	HCM	heart:	n/a
49	chr7:153078797-153078847	Hepatocyte	liver:	n/a
50	chr7:153110994-153111044	SAEC	small airway:	n/a

(count:166 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:153168007..153170058-chr7:153173069..153175885,2	K562	blood:
2	chr7:152981185..152983494-chr7:153101027..153103155,2	K562	blood:
3	chr7:153095496..153100083-chr7:153227240..153231404,4	K562	blood:
4	chr7:153077622..153081135-chr7:153081678..153084143,4	K562	blood:
5	chr7:153037739..153042014-chr7:153077281..153081479,4	K562	blood:
6	chr7:153064116..153066468-chr7:153081031..153083301,2	K562	blood:
7	chr7:152947748..152949504-chr7:153104988..153107669,2	K562	blood:
8	chr7:153128567..153130736-chr7:153131262..153133294,2	K562	blood:
9	chr7:153078567..153079314-chr7:153528933..153530177,7	MCF-7	breast:
10	chr7:153100739..153103301-chr7:153343816..153346301,2	K562	blood:
11	chr7:153101996..153103872-chr7:153373674..153376458,2	K562	blood:
12	chr7:64297147..64300763-chr7:153106859..153112373,8	K562	blood:
13	chr7:153104280..153106430-chr7:153200479..153202606,2	K562	blood:
14	chr7:153130431..153132961-chr7:153133375..153135450,3	K562	blood:
15	chr7:152941333..152942973-chr7:153102433..153104894,2	K562	blood:
16	chr7:153098213..153100977-chr7:153153610..153156518,2	K562	blood:
17	chr7:153101066..153103741-chr7:153151385..153153304,3	K562	blood:
18	chr7:152890212..152890787-chr7:153078742..153079279,2	MCF-7	breast:
19	chr7:153138484..153140700-chr7:153144186..153146870,3	K562	blood:
20	chr7:153100488..153103412-chr7:153303424..153305965,2	K562	blood:
21	chr7:153145961..153147522-chr7:153147556..153149926,2	K562	blood:
22	chr7:153094292..153096861-chr7:153257977..153260330,2	K562	blood:
23	chr7:153021290..153023389-chr7:153093979..153096811,2	K562	blood:
24	chr7:153103747..153106321-chr7:153180376..153182318,2	K562	blood:
25	chr7:153119320..153121928-chr7:153170985..153172845,2	K562	blood:
26	chr7:152630894..152632696-chr7:153103935..153106331,2	K562	blood:
27	chr7:153104593..153107356-chr7:153151532..153153946,4	K562	blood:
28	chr7:153105650..153108822-chr7:153162776..153165855,3	K562	blood:
29	chr7:153033881..153035423-chr7:153075669..153078546,2	K562	blood:
30	chr7:153106936..153109083-chr7:153612449..153615319,2	K562	blood:
31	chr7:153055542..153057416-chr7:153103974..153105838,2	K562	blood:
32	chr7:153104305..153105912-chr7:153250061..153252295,2	K562	blood:
33	chr7:153078806..153081206-chr7:153081350..153083333,2	K562	blood:
34	chr11:5956902..5959925-chr7:153104319..153108206,5	K562	blood:
35	chr7:153102450..153104761-chr7:153532927..153535675,2	K562	blood:
36	chr7:153054222..153056316-chr7:153099590..153102499,2	K562	blood:
37	chr7:153104593..153107356-chr7:153151532..153153946,4	K562	blood:
38	chr7:153098583..153101313-chr7:153228583..153231539,3	K562	blood:
39	chr7:153098213..153100977-chr7:153153610..153156518,2	K562	blood:
40	chr7:153137391..153141168-chr7:153141506..153146066,7	K562	blood:
41	chr7:153103747..153106321-chr7:153180376..153182318,2	K562	blood:
42	chr7:153104280..153106430-chr7:153200479..153202606,2	K562	blood:
43	chr7:152975810..152978367-chr7:153090771..153092970,2	K562	blood:
44	chr7:153102748..153104810-chr7:153194160..153196266,2	K562	blood:
45	chr7:153077274..153079986-chr7:153084409..153086483,3	K562	blood:
46	chr7:153018926..153020911-chr7:153105135..153106975,2	K562	blood:
47	chr7:152788621..152790562-chr7:153104603..153106199,2	K562	blood:
48	chr7:153119320..153121928-chr7:153170985..153172845,2	K562	blood:
49	chr7:153179767..153181427-chr7:153183794..153186407,2	K562	blood:
50	chr7:153077274..153079986-chr7:153084409..153086483,3	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XRCC2-1	chr7:153104041-153104169	ENSG00000234722.3
2	lnc-DPP6-7	chr7:153146514-153146960	NONHSAT124301
3	lnc-XRCC2-2	chr7:153125396-153125424	XLOC_006657
4	lnc-XRCC2-1	chr7:153104041-153104171	ENSG00000234722
5	lnc-XRCC2-1	chr7:153109176-153109319	ENSG00000234722.3
6	lnc-XRCC2-2	chr7:153120803-153121101	XLOC_006657
7	lnc-DPP6-3	chr7:153092527-153092639	XLOC_006297
8	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722.3
9	lnc-DPP6-2	chr7:153120526-153120601	XLOC_006298
10	lnc-DPP6-3	chr7:153092498-153092703	XLOC_006297
11	lnc-DPP6-3	chr7:153093149-153093207	XLOC_006297
12	lnc-DPP6-3	chr7:153086676-153086815	XLOC_006297
13	lnc-XRCC2-1	chr7:153109178-153109319	ENSG00000234722
14	lnc-DPP6-2	chr7:153119376-153119626	XLOC_006298
15	lnc-XRCC2-1	chr7:153102578-153102683	ENSG00000234722
16	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722
17	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722
18	lnc-XRCC2-1	chr7:153110698-153111021	ENSG00000234722
19	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722.3

No data

Variant related genes	Relation type
ENSG00000233489	TF binding region
ENSG00000234722	TF binding region
ENSG00000233489	CpG island
ENSG00000234722	CpG island
ENSG00000197774	chromatin interactions
ENSG00000234722	chromatin interactions
ENSG00000234338	chromatin interactions
ENSG00000171222	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000233489	chromatin interactions
ENSG00000236198	chromatin interactions
ENSG00000223700	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000261455	chromatin interactions
CCT2	miRNA target sites
DHX57	miRNA target sites
LRRC1	miRNA target sites
APAF1	miRNA target sites

Extended variants
information (count: 3522 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3522 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1444455	chr7:153076838-153076839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527807473	chr7:153076850-153076851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79266031	chr7:153076916-153076917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11771851	chr7:153076980-153076981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs140849708	chr7:153076986-153076987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150108753	chr7:153077036-153077037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375882340	chr7:153077051-153077052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559506410	chr7:153077069-153077070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550202117	chr7:153077118-153077119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571946055	chr7:153077188-153077189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186834567	chr7:153077190-153077191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548495410	chr7:153077298-153077299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563605558	chr7:153077326-153077327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141116083	chr7:153077346-153077347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77104050	chr7:153077406-153077407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190470227	chr7:153077426-153077427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375098772	chr7:153077446-153077447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555079940	chr7:153077447-153077448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573280486	chr7:153077454-153077455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544243031	chr7:153077468-153077469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562631996	chr7:153077473-153077474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530432851	chr7:153077474-153077475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577879681	chr7:153077487-153077488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182201480	chr7:153077492-153077493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7811033	chr7:153077502-153077503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs527516025	chr7:153077515-153077516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543121095	chr7:153077516-153077517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561411172	chr7:153077520-153077521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531596291	chr7:153077542-153077543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138511548	chr7:153077547-153077548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570500317	chr7:153077560-153077561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571799696	chr7:153077565-153077566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376779539	chr7:153077605-153077606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12534742	chr7:153077616-153077617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs185342094	chr7:153077642-153077643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547644603	chr7:153077668-153077669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529826500	chr7:153077726-153077727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536477692	chr7:153077746-153077747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189801362	chr7:153077754-153077755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567063954	chr7:153077765-153077766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537404302	chr7:153077771-153077772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556144828	chr7:153077778-153077779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111263950	chr7:153077784-153077785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556461248	chr7:153077805-153077806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568003906	chr7:153077838-153077839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149645852	chr7:153077840-153077841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375058211	chr7:153077844-153077845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35272147	chr7:153077856-153077857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554136138	chr7:153077907-153077908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116890557	chr7:153077918-153077919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153067600-153082400	Weak transcription	K562	blood
2	chr7:153078000-153078800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr7:153078200-153078800	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr7:153078400-153078600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr7:153078400-153078600	Enhancers	Brain Anterior Caudate	brain
6	chr7:153078400-153078600	Active TSS	Duodenum Smooth Muscle	Duodenum
7	chr7:153078400-153078600	Enhancers	Fetal Kidney	kidney
8	chr7:153078400-153078600	Enhancers	Fetal Stomach	stomach
9	chr7:153078400-153078800	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr7:153078400-153078800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr7:153078400-153078800	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr7:153078400-153078800	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr7:153078400-153078800	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr7:153078400-153078800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
15	chr7:153078400-153078800	Enhancers	Brain Hippocampus Middle	brain
16	chr7:153078400-153079000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr7:153078400-153079000	Enhancers	Rectal Smooth Muscle	rectum
18	chr7:153078400-153079000	Active TSS	Stomach Smooth Muscle	stomach
19	chr7:153078400-153082000	Enhancers	Colon Smooth Muscle	Colon
20	chr7:153078600-153078800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr7:153078600-153078800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:153078600-153078800	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr7:153078600-153078800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr7:153078600-153079000	Flanking Active TSS	Fetal Kidney	kidney
25	chr7:153078600-153079000	Enhancers	Fetal Muscle Trunk	muscle
26	chr7:153078600-153079800	Enhancers	Fetal Muscle Leg	muscle
27	chr7:153078600-153082000	Enhancers	Adipose Nuclei	Adipose
28	chr7:153078800-153079000	Active TSS	Brain Anterior Caudate	brain
29	chr7:153078800-153079600	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr7:153078800-153083200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr7:153079000-153079200	Enhancers	Fetal Kidney	kidney
32	chr7:153079000-153079200	Flanking Active TSS	Rectal Smooth Muscle	rectum
33	chr7:153079000-153079200	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr7:153079200-153081800	Enhancers	Rectal Smooth Muscle	rectum
35	chr7:153079200-153083200	Enhancers	Stomach Smooth Muscle	stomach
36	chr7:153079600-153080800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr7:153080200-153081000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:153080600-153080800	Enhancers	Spleen	Spleen
39	chr7:153080800-153081600	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr7:153081600-153082600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr7:153081800-153082400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr7:153082000-153086000	Weak transcription	Colon Smooth Muscle	Colon
43	chr7:153082400-153082600	Enhancers	Rectal Smooth Muscle	rectum
44	chr7:153082400-153083800	Enhancers	K562	blood
45	chr7:153082600-153082800	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr7:153083200-153083800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:153083200-153085800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr7:153083800-153084400	Weak transcription	K562	blood
49	chr7:153084400-153089600	Strong transcription	K562	blood
50	chr7:153085600-153087000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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