Variant report

Variant	nsv608060
Chromosome Location	chr7:102486254-102624192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1929)
CpG islands
(count:1406)
Chromatin interactive
region (count:91)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102618784-102618922	K562	blood:	n/a	n/a
2	ARID3A	chr7:102613385-102614106	K562	blood:	n/a	n/a
3	ARID3A	chr7:102500720-102501319	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:102566747-102567026	K562	blood:	n/a	n/a
5	ARID3A	chr7:102509524-102509951	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:102615512-102615697	K562	blood:	n/a	n/a
7	ARID3A	chr7:102516155-102516615	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:102623549-102623551	K562	blood:	n/a	n/a
9	ARID3A	chr7:102514028-102514887	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:102622029-102622173	K562	blood:	n/a	n/a
11	ARID3A	chr7:102624128-102624420	K562	blood:	n/a	n/a
12	ATF1	chr7:102615471-102615652	K562	blood:	n/a	n/a
13	ATF1	chr7:102516353-102516642	K562	blood:	n/a	n/a
14	ATF1	chr7:102613562-102614182	K562	blood:	n/a	n/a
15	ATF1	chr7:102624155-102624485	K562	blood:	n/a	n/a
16	ATF1	chr7:102618759-102618993	K562	blood:	n/a	n/a
17	ATF1	chr7:102531030-102531406	K562	blood:	n/a	n/a
18	ATF1	chr7:102575929-102576170	K562	blood:	n/a	n/a
19	ATF1	chr7:102533184-102533443	K562	blood:	n/a	n/a
20	ATF3	chr7:102515996-102516786	A549	lung:	n/a	n/a
21	ATF3	chr7:102515979-102516734	HCT-116	colon:	n/a	n/a
22	ATF3	chr7:102613482-102614149	K562	blood:	n/a	n/a
23	ATF3	chr7:102516248-102516624	K562	blood:	n/a	n/a
24	ATF3	chr7:102516084-102516739	A549	lung:	n/a	n/a
25	ATF3	chr7:102516058-102516843	HCT-116	colon:	n/a	n/a
26	BACH1	chr7:102613561-102613930	K562	blood:	n/a	n/a
27	BACH1	chr7:102613704-102613707	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:102619511-102619519	K562	blood:	n/a	n/a
29	BATF	chr7:102514509-102514873	GM12878	blood:	n/a	n/a
30	BATF	chr7:102514586-102514859	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:102514598-102514832	GM12878	blood:	n/a	chr7:102514741-102514750
32	BCL3	chr7:102515891-102516752	A549	lung:	n/a	chr7:102515915-102515924
33	BCL3	chr7:102515964-102516936	A549	lung:	n/a	n/a
34	BCLAF1	chr7:102613400-102614259	K562	blood:	n/a	n/a
35	BHLHE40	chr7:102575929-102576160	K562	blood:	n/a	n/a
36	BHLHE40	chr7:102516444-102516605	K562	blood:	n/a	n/a
37	BHLHE40	chr7:102624110-102624467	K562	blood:	n/a	n/a
38	BHLHE40	chr7:102622117-102622125	K562	blood:	n/a	n/a
39	BHLHE40	chr7:102613578-102614258	K562	blood:	n/a	n/a
40	BHLHE40	chr7:102622878-102622930	K562	blood:	n/a	n/a
41	BHLHE40	chr7:102615498-102615614	K562	blood:	n/a	n/a
42	BRCA1	chr7:102531852-102531897	GM12878	blood:	n/a	n/a
43	BRCA1	chr7:102516256-102516827	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr7:102618851-102619385	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:102582702-102582789	H1-hESC	embryonic stem cell:	n/a	n/a
46	CBX3	chr7:102514418-102515075	HCT-116	colon:	n/a	n/a
47	CBX3	chr7:102596525-102596838	K562	blood:	n/a	n/a
48	CBX3	chr7:102613428-102614115	K562	blood:	n/a	n/a
49	CBX3	chr7:102548441-102548837	K562	blood:	n/a	n/a
50	CBX3	chr7:102516236-102516555	K562	blood:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102566723-102566773	GM12892	blood:	n/a
2	chr7:102585030-102585080	H1-hESC	embryonic stem cell:	embryo
3	chr7:102553045-102553095	NH-A	brain:	n/a
4	chr7:102566723-102566773	GM12892	blood:	n/a
5	chr7:102585030-102585080	H1-hESC	embryonic stem cell:	embryo
6	chr7:102553045-102553095	NH-A	brain:	n/a
7	chr7:102553369-102553419	LNCaP	prostate:	n/a
8	chr7:102585030-102585080	ProgFib	skin:	n/a
9	chr7:102531568-102531618	HCT-116	colon:	n/a
10	chr7:102614121-102614171	AG09309	skin:	n/a
11	chr7:102500111-102500161	HRPEpiC	eye:	n/a
12	chr7:102558323-102558373	HCF	heart:	n/a
13	chr7:102553045-102553095	HCM	heart:	n/a
14	chr7:102574445-102574495	GM19239	blood:	n/a
15	chr7:102574105-102574155	Jurkat	blood:	n/a
16	chr7:102553437-102553487	LNCaP	prostate:	n/a
17	chr7:102574475-102574525	BE2_C	brain:	n/a
18	chr7:102531568-102531618	HEEpiC	esophagus:	n/a
19	chr7:102566723-102566773	MCF-7	breast:	n/a
20	chr7:102552239-102552289	GM12878	blood:	n/a
21	chr7:102500111-102500161	HCM	heart:	n/a
22	chr7:102553432-102553482	Hela-S3	cervix:	n/a
23	chr7:102576358-102576408	NH-A	brain:	n/a
24	chr7:102574504-102574554	GM12878	blood:	n/a
25	chr7:102574504-102574554	HCM	heart:	n/a
26	chr7:102614121-102614171	BE2_C	brain:	n/a
27	chr7:102506387-102506437	HIPEpiC	eye:	n/a
28	chr7:102574445-102574495	AG09309	skin:	n/a
29	chr7:102558323-102558373	Jurkat	blood:	n/a
30	chr7:102608657-102608707	SK-N-SH_RA	brain:	n/a
31	chr7:102500111-102500161	BJ	skin:	n/a
32	chr7:102574105-102574155	AG04449	skin:	fetal
33	chr7:102553457-102553507	Hela-S3	cervix:	n/a
34	chr7:102574445-102574495	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:102574504-102574554	SK-N-MC	brain:	n/a
36	chr7:102583144-102583194	AG04450	lung:	fetal
37	chr7:102553045-102553095	SK-N-SH	brain:	n/a
38	chr7:102553457-102553507	ovcar-3	ovarian:	n/a
39	chr7:102613822-102613872	HEEpiC	esophagus:	n/a
40	chr7:102608657-102608707	HIPEpiC	eye:	n/a
41	chr7:102585030-102585080	HNPCEpiC	eye:	n/a
42	chr7:102608657-102608707	MCF-7	breast:	n/a
43	chr7:102553437-102553487	HRE	kidney:	n/a
44	chr7:102553437-102553487	NHDF-neo	bronchial:	n/a
45	chr7:102531568-102531618	ovcar-3	ovarian:	n/a
46	chr7:102553369-102553419	GM12878	blood:	n/a
47	chr7:102558323-102558373	ovcar-3	ovarian:	n/a
48	chr7:102608657-102608707	HCT-116	colon:	n/a
49	chr7:102574504-102574554	AG04449	skin:	fetal
50	chr7:102583144-102583194	ProgFib	skin:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:102619656..102622103-chr7:102669784..102672550,2	K562	blood:
2	chr7:102597515..102601300-chr7:102603866..102605931,3	K562	blood:
3	chr7:102582192..102585117-chr7:102714444..102717261,2	K562	blood:
4	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:
5	chr7:102497049..102499033-chr7:102503041..102505939,2	K562	blood:
6	chr7:102562952..102565366-chr7:102565830..102568184,3	MCF-7	breast:
7	chr7:102459530..102461153-chr7:102484743..102487140,2	K562	blood:
8	chr7:102497060..102498758-chr7:102613043..102615053,2	K562	blood:
9	chr7:102537736..102539276-chr7:102622119..102624837,2	MCF-7	breast:
10	chr7:102583093..102586318-chr7:102605440..102608597,3	K562	blood:
11	chr7:102586835..102589764-chr7:102713384..102716042,2	K562	blood:
12	chr7:102597515..102601300-chr7:102603866..102605931,3	K562	blood:
13	chr7:102556611..102558865-chr7:102559053..102561670,2	K562	blood:
14	chr7:102489665..102492498-chr7:102495300..102497224,2	K562	blood:
15	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:
16	chr7:102529179..102531129-chr7:102713390..102716151,2	MCF-7	breast:
17	chr7:102589644..102592537-chr7:102602943..102605917,2	K562	blood:
18	chr7:102583146..102586073-chr7:102591265..102594000,2	K562	blood:
19	chr7:102451931..102453738-chr7:102614138..102615717,2	K562	blood:
20	chr7:102513883..102516664-chr7:102520756..102522395,2	K562	blood:
21	chr7:102501610..102503166-chr7:102508637..102510523,2	K562	blood:
22	chr7:102501221..102503373-chr7:102515985..102518701,2	MCF-7	breast:
23	chr7:102499316..102501151-chr7:102502125..102504544,2	K562	blood:
24	chr7:102504642..102507106-chr7:102507263..102511653,3	K562	blood:
25	chr7:102594911..102596485-chr7:102613650..102615584,2	K562	blood:
26	chr7:102445308..102447740-chr7:102490751..102492572,2	K562	blood:
27	chr20:52596990..52599653-chr7:102503790..102506770,2	MCF-7	breast:
28	chr7:102527046..102528879-chr7:102528977..102531238,2	MCF-7	breast:
29	chr7:102516404..102517929-chr7:102714703..102716697,2	MCF-7	breast:
30	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:
31	chr7:102611388..102613212-chr7:102692044..102694457,2	K562	blood:
32	chr7:102597576..102599200-chr7:102609739..102612061,2	K562	blood:
33	chr7:102583035..102585728-chr7:102590103..102592728,2	K562	blood:
34	chr7:102497060..102498758-chr7:102613043..102615053,2	K562	blood:
35	chr7:102576586..102579076-chr7:102580024..102585100,6	K562	blood:
36	chr7:102569147..102571411-chr7:102714127..102716965,2	K562	blood:
37	chr7:102618985..102623059-chr7:102696660..102699924,3	K562	blood:
38	chr7:102573625..102578360-chr7:102582596..102585243,4	K562	blood:
39	chr7:102586889..102588859-chr7:102610741..102612720,2	K562	blood:
40	chr7:102513072..102513724-chr9:129702545..129703389,2	MCF-7	breast:
41	chr7:102597576..102599200-chr7:102609739..102612061,2	K562	blood:
42	chr7:102583146..102586073-chr7:102591265..102594000,2	K562	blood:
43	chr7:102574165..102576650-chr7:102576864..102579530,2	K562	blood:
44	chr7:102556325..102558865-chr7:102559053..102562636,3	K562	blood:
45	chr7:102526206..102528003-chr7:102535680..102538379,2	MCF-7	breast:
46	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
47	chr7:102589644..102592537-chr7:102602943..102605917,2	K562	blood:
48	chr7:102499316..102501151-chr7:102502125..102504544,2	K562	blood:
49	chr7:102616176..102618073-chr7:103034545..103036072,2	K562	blood:
50	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC17-1	chr7:102613969-102614218	ENSG00000230257
2	lnc-LRRC17-1	chr7:102618828-102618967	ENSG00000230257
3	lnc-FAM185A-2	chr7:102553447-102553592	NONHSAT122526
4	lnc-FAM185A-1	chr7:102497897-102498202	NONHSAT122525
5	lnc-FAM185A-2	chr7:102573506-102573897	NONHSAT122526

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRC17	hsa-miR-26b-5p	chr7:102584899-102584922
2	LRRC17	hsa-miR-181a-5p	chr7:102584970-102584992

Variant related genes	Relation type
RN7SKP198	TF binding region
FBXL13	TF binding region
LRRC17	TF binding region
NFE4	TF binding region
RN7SKP198	CpG island
FBXL13	CpG island
LRRC17	CpG island
NFE4	CpG island
ENSG00000170632	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000252643	chromatin interactions
ENSG00000128606	chromatin interactions
ENSG00000230257	chromatin interactions
ENSG00000236226	chromatin interactions
ENSG00000238324	chromatin interactions

Extended variants
information (count: 4885 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4885 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11496066	chr7:102486254-102486255	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140489006	chr7:102486304-102486305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556045354	chr7:102486316-102486317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184274249	chr7:102486317-102486318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375863610	chr7:102486322-102486323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71570402	chr7:102486328-102486329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544337699	chr7:102486333-102486334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs17136100	chr7:102486354-102486355	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs548877034	chr7:102486357-102486358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577642330	chr7:102486358-102486359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545021909	chr7:102486360-102486361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181875140	chr7:102486361-102486362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562401928	chr7:102486406-102486407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527630977	chr7:102486472-102486473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542511117	chr7:102486507-102486508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560758583	chr7:102486516-102486517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531369412	chr7:102486518-102486519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs71572203	chr7:102486523-102486524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573774064	chr7:102486581-102486582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374417529	chr7:102486590-102486591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540894764	chr7:102486592-102486593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577699215	chr7:102486613-102486614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150439394	chr7:102486712-102486713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146545171	chr7:102486745-102486746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533254606	chr7:102486750-102486751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186992633	chr7:102486805-102486806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566752918	chr7:102486861-102486862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs377152561	chr7:102486862-102486863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141169459	chr7:102486878-102486879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556059365	chr7:102486948-102486949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567878038	chr7:102486952-102486953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143808143	chr7:102486991-102486992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369272119	chr7:102486992-102486993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74359232	chr7:102486996-102486997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538467250	chr7:102487008-102487009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144996085	chr7:102487018-102487019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116241630	chr7:102487037-102487038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373450638	chr7:102487063-102487064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150236922	chr7:102487185-102487186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149719881	chr7:102487195-102487196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs66505768	chr7:102487196-102487197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs61387388	chr7:102487203-102487204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200157454	chr7:102487204-102487205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371844037	chr7:102487205-102487206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375303061	chr7:102487234-102487235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527852503	chr7:102487338-102487339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553731489	chr7:102487342-102487343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74938172	chr7:102487343-102487344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547990753	chr7:102487346-102487347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542528779	chr7:102487376-102487377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1765 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102470000-102490200	Weak transcription	Gastric	stomach
2	chr7:102470000-102516400	Weak transcription	Pancreas	Pancrea
3	chr7:102470800-102493200	Weak transcription	Primary T cells from cord blood	blood
4	chr7:102471800-102500000	Weak transcription	Left Ventricle	heart
5	chr7:102477800-102500800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:102478000-102489200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:102478200-102500000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:102478200-102500000	Weak transcription	Ovary	ovary
9	chr7:102478800-102489600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr7:102478800-102492600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr7:102482800-102499600	Weak transcription	Fetal Lung	lung
12	chr7:102482800-102500200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:102483000-102491200	Weak transcription	Fetal Stomach	stomach
14	chr7:102483400-102487000	Weak transcription	HepG2	liver
15	chr7:102483400-102499600	Weak transcription	K562	blood
16	chr7:102486200-102487400	Enhancers	NHEK	skin
17	chr7:102487000-102487400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:102487000-102487800	Enhancers	HepG2	liver
19	chr7:102489200-102491600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:102489200-102492400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:102489400-102490400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:102489600-102489800	Enhancers	Aorta	Aorta
23	chr7:102489600-102490000	Enhancers	Placenta Amnion	Placenta Amnion
24	chr7:102489800-102490400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:102490000-102490400	Enhancers	HMEC	breast
26	chr7:102490000-102490400	Enhancers	NHDF-Ad	bronchial
27	chr7:102490000-102499600	Weak transcription	Aorta	Aorta
28	chr7:102490200-102490400	Enhancers	Gastric	stomach
29	chr7:102490400-102491200	Weak transcription	Gastric	stomach
30	chr7:102490400-102500000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:102490400-102500000	Weak transcription	NHDF-Ad	bronchial
32	chr7:102491200-102491400	Enhancers	Fetal Stomach	stomach
33	chr7:102491400-102491800	Enhancers	Osteobl	bone
34	chr7:102491400-102495000	Weak transcription	Fetal Stomach	stomach
35	chr7:102492400-102496400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:102492600-102493400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr7:102492800-102493000	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr7:102493000-102493400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
39	chr7:102493400-102499800	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:102496400-102497000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:102497000-102499000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:102497600-102499200	Weak transcription	Fetal Stomach	stomach
43	chr7:102498800-102501200	Enhancers	HSMM	muscle
44	chr7:102499000-102499400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr7:102499000-102501400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:102499200-102499800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:102499200-102500600	Enhancers	Colon Smooth Muscle	Colon
48	chr7:102499200-102501200	Enhancers	Fetal Stomach	stomach
49	chr7:102499200-102501200	Enhancers	NHLF	lung
50	chr7:102499400-102499600	Weak transcription	Muscle Satellite Cultured Cells	--

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