Variant report

Variant	nsv470382
Chromosome Location	chr7:102375663-102538515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2239)
CpG islands
(count:1221)
Chromatin interactive
region (count:71)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2239 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102478846-102479241	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102386072-102386189	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:102386048-102386259	K562	blood:	n/a	n/a
4	ARID3A	chr7:102389084-102389458	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:102514028-102514887	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:102509524-102509951	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:102500720-102501319	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:102516155-102516615	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:102452449-102452773	HepG2	liver:	n/a	n/a
10	ATF1	chr7:102389031-102389497	K562	blood:	n/a	n/a
11	ATF1	chr7:102533184-102533443	K562	blood:	n/a	n/a
12	ATF1	chr7:102531030-102531406	K562	blood:	n/a	n/a
13	ATF1	chr7:102516353-102516642	K562	blood:	n/a	n/a
14	ATF2	chr7:102475368-102475893	GM12878	blood:	n/a	n/a
15	ATF2	chr7:102484177-102484790	GM12878	blood:	n/a	n/a
16	ATF2	chr7:102389081-102389544	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr7:102475399-102475848	GM12878	blood:	n/a	n/a
18	ATF2	chr7:102481620-102482163	GM12878	blood:	n/a	n/a
19	ATF2	chr7:102389108-102389584	GM12878	blood:	n/a	n/a
20	ATF2	chr7:102484200-102484713	GM12878	blood:	n/a	n/a
21	ATF3	chr7:102516058-102516843	HCT-116	colon:	n/a	n/a
22	ATF3	chr7:102516084-102516739	A549	lung:	n/a	n/a
23	ATF3	chr7:102516248-102516624	K562	blood:	n/a	n/a
24	ATF3	chr7:102515996-102516786	A549	lung:	n/a	n/a
25	ATF3	chr7:102515979-102516734	HCT-116	colon:	n/a	n/a
26	BATF	chr7:102484252-102484610	GM12878	blood:	n/a	n/a
27	BATF	chr7:102410945-102411178	GM12878	blood:	n/a	n/a
28	BATF	chr7:102514586-102514859	GM12878	blood:	n/a	n/a
29	BATF	chr7:102475426-102475852	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
30	BATF	chr7:102484259-102484624	GM12878	blood:	n/a	n/a
31	BATF	chr7:102481731-102482084	GM12878	blood:	n/a	n/a
32	BATF	chr7:102400501-102400644	GM12878	blood:	n/a	n/a
33	BATF	chr7:102481751-102482055	GM12878	blood:	n/a	n/a
34	BATF	chr7:102382888-102383234	GM12878	blood:	n/a	n/a
35	BATF	chr7:102475444-102475777	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
36	BATF	chr7:102400487-102400681	GM12878	blood:	n/a	n/a
37	BATF	chr7:102514509-102514873	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:102484332-102484641	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:102481679-102482030	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:102475497-102475744	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:102475417-102475810	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:102410971-102411150	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:102484258-102484654	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:102514598-102514832	GM12878	blood:	n/a	chr7:102514741-102514750
45	BCL11A	chr7:102382918-102383177	GM12878	blood:	n/a	n/a
46	BCL3	chr7:102484358-102484686	GM12878	blood:	n/a	n/a
47	BCL3	chr7:102454575-102454898	GM12878	blood:	n/a	n/a
48	BCL3	chr7:102515964-102516936	A549	lung:	n/a	n/a
49	BCL3	chr7:102515891-102516752	A549	lung:	n/a	chr7:102515915-102515924
50	BCLAF1	chr7:102481611-102482122	GM12878	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102506387-102506437	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:102506387-102506437	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:102385712-102385762	HCT-116	colon:	n/a
4	chr7:102385712-102385762	PrEC	prostate:	n/a
5	chr7:102389239-102389289	ovcar-3	ovarian:	n/a
6	chr7:102389892-102389942	HAEpiC	amniotic membrane:	n/a
7	chr7:102506387-102506437	BJ	skin:	n/a
8	chr7:102389275-102389325	HIPEpiC	eye:	n/a
9	chr7:102388500-102388550	SK-N-SH	brain:	n/a
10	chr7:102389239-102389289	AoSMC	blood vessel:	n/a
11	chr7:102449340-102449390	HAEpiC	amniotic membrane:	n/a
12	chr7:102389327-102389377	U87	brain:	n/a
13	chr7:102453328-102453378	K562	blood:	n/a
14	chr7:102389239-102389289	GM12892	blood:	n/a
15	chr7:102389275-102389325	HNPCEpiC	eye:	n/a
16	chr7:102477205-102477255	HCM	heart:	n/a
17	chr7:102500111-102500161	H1-hESC	embryonic stem cell:	embryo
18	chr7:102470281-102470331	HMEC	breast:	n/a
19	chr7:102531568-102531618	K562	blood:	n/a
20	chr7:102389275-102389325	ProgFib	skin:	n/a
21	chr7:102389315-102389365	HL-60	blood:	n/a
22	chr7:102390529-102390579	HRE	kidney:	n/a
23	chr7:102389892-102389942	HUVEC	blood vessel:	n/a
24	chr7:102389205-102389255	CMK	blood:	n/a
25	chr7:102453328-102453378	HUVEC	blood vessel:	n/a
26	chr7:102389790-102389840	HL-60	blood:	n/a
27	chr7:102389239-102389289	LNCaP	prostate:	n/a
28	chr7:102389239-102389289	CMK	blood:	n/a
29	chr7:102477205-102477255	ECC-1	luminal epithelium:	n/a
30	chr7:102506387-102506437	HMEC	breast:	n/a
31	chr7:102531568-102531618	PANC-1	pancreas:	n/a
32	chr7:102477205-102477255	HNPCEpiC	eye:	n/a
33	chr7:102389481-102389531	PANC-1	pancreas:	n/a
34	chr7:102500111-102500161	Caco-2	colon:	n/a
35	chr7:102389205-102389255	AoSMC	blood vessel:	n/a
36	chr7:102389481-102389531	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:102389239-102389289	HCF	heart:	n/a
38	chr7:102500111-102500161	HCM	heart:	n/a
39	chr7:102389275-102389325	HCF	heart:	n/a
40	chr7:102389892-102389942	Hela-S3	cervix:	n/a
41	chr7:102389275-102389325	GM12891	blood:	n/a
42	chr7:102389275-102389325	GM12878	blood:	n/a
43	chr7:102389327-102389377	GM12891	blood:	n/a
44	chr7:102453328-102453378	HL-60	blood:	n/a
45	chr7:102390529-102390579	HUVEC	blood vessel:	n/a
46	chr7:102477205-102477255	AoSMC	blood vessel:	n/a
47	chr7:102389315-102389365	HRCEpiC	kidney:	n/a
48	chr7:102389315-102389365	HEK293	kidney:	embryo
49	chr7:102389327-102389377	Hela-S3	cervix:	n/a
50	chr7:102389191-102389241	HRE	kidney:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:102504642..102507106-chr7:102507263..102511653,3	K562	blood:
2	chr7:102473443..102475589-chr7:102480022..102482918,2	K562	blood:
3	chr7:102527046..102528879-chr7:102528977..102531238,2	MCF-7	breast:
4	chr7:102517778..102519381-chr7:102714945..102717591,2	MCF-7	breast:
5	chr7:102501610..102503166-chr7:102508637..102510523,2	K562	blood:
6	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:
7	chr7:102483542..102485503-chr7:102492215..102494195,2	K562	blood:
8	chr7:102452440..102454909-chr7:102615064..102617723,2	K562	blood:
9	chr7:102497060..102498758-chr7:102613043..102615053,2	K562	blood:
10	chr7:102451931..102453738-chr7:102614138..102615717,2	K562	blood:
11	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:
12	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
13	chr7:102510827..102513027-chr7:102515036..102518141,3	K562	blood:
14	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:
15	chr7:102516404..102517929-chr7:102714703..102716697,2	MCF-7	breast:
16	chr7:102389047..102390959-chr7:102788572..102791008,2	K562	blood:
17	chr7:102489665..102492498-chr7:102495300..102497224,2	K562	blood:
18	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
19	chr7:102445308..102447740-chr7:102490751..102492572,2	K562	blood:
20	chr7:102517307..102518855-chr7:102521320..102524235,2	MCF-7	breast:
21	chr7:102458375..102460773-chr7:102462398..102464575,2	K562	blood:
22	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:
23	chr7:102522158..102525265-chr7:102531503..102535074,3	K562	blood:
24	chr7:102513883..102516664-chr7:102520756..102522395,2	K562	blood:
25	chr7:102526206..102528003-chr7:102535680..102538379,2	MCF-7	breast:
26	chr7:76751236..76752770-chr7:102389322..102390934,2	MCF-7	breast:
27	chr7:102513883..102516664-chr7:102520756..102522395,2	K562	blood:
28	chr7:102474929..102477472-chr7:102495351..102498066,2	K562	blood:
29	chr7:102459925..102462268-chr7:102466191..102467871,2	K562	blood:
30	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:
31	chr7:76751236..76751872-chr7:102389110..102389768,2	MCF-7	breast:
32	chr7:102458375..102460773-chr7:102462398..102464575,2	K562	blood:
33	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:
34	chr7:76750772..76751740-chr7:102389401..102390157,2	HCT-116	colon:
35	chr7:102499316..102501151-chr7:102502125..102504544,2	K562	blood:
36	chr7:102513072..102513724-chr9:129702545..129703389,2	MCF-7	breast:
37	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
38	chr7:102459530..102461153-chr7:102484743..102487140,2	K562	blood:
39	chr7:102501221..102503373-chr7:102515985..102518701,2	MCF-7	breast:
40	chr7:102529179..102531129-chr7:102713390..102716151,2	MCF-7	breast:
41	chr7:102459925..102462268-chr7:102466191..102467871,2	K562	blood:
42	chr7:102483542..102485503-chr7:102492215..102494195,2	K562	blood:
43	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
44	chr7:102497049..102499033-chr7:102503041..102505939,2	K562	blood:
45	chr7:102387955..102390990-chr7:102714406..102717094,4	MCF-7	breast:
46	chr7:102466773..102468562-chr7:102472761..102475356,2	MCF-7	breast:
47	chr20:52596990..52599653-chr7:102503790..102506770,2	MCF-7	breast:
48	chr7:102522158..102525265-chr7:102531503..102535074,3	K562	blood:
49	chr7:102473090..102475084-chr7:102477070..102479073,2	K562	blood:
50	chr7:102510827..102513027-chr7:102515036..102518141,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM185A-1	chr7:102497897-102498202	NONHSAT122525
2	lnc-AC105052.1-2	chr7:102456637-102456718	NONHSAT122523
3	lnc-AC105052.1-2	chr7:102454781-102454863	NONHSAT122523
4	lnc-AC105052.1-2	chr7:102453685-102453978	NONHSAT122523

No data

Variant related genes	Relation type
RNU6-1136P	TF binding region
RN7SKP198	TF binding region
ENSG00000213385	TF binding region
FBXL13	TF binding region
FAM185A	TF binding region
RNU6-1136P	CpG island
RN7SKP198	CpG island
ENSG00000213385	CpG island
FBXL13	CpG island
FAM185A	CpG island
ENSG00000230257	chromatin interactions
ENSG00000214439	chromatin interactions
ENSG00000135205	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000238324	chromatin interactions
ENSG00000128606	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000161048	chromatin interactions
ENSG00000252643	chromatin interactions

Extended variants
information (count: 5132 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5132 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542085717	chr7:102381419-102381420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563904251	chr7:102381425-102381426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530666351	chr7:102381469-102381470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375360705	chr7:102381470-102381471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184930881	chr7:102381478-102381479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552264643	chr7:102381513-102381514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553873248	chr7:102381520-102381521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564076351	chr7:102381529-102381530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528065971	chr7:102381550-102381551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71570337	chr7:102381575-102381576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189550412	chr7:102381578-102381579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568296068	chr7:102381580-102381581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147501377	chr7:102381618-102381619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576490978	chr7:102381634-102381635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182081295	chr7:102381674-102381675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34289735	chr7:102381676-102381677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186677588	chr7:102381743-102381744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377156106	chr7:102381765-102381766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71570338	chr7:102381808-102381809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537157543	chr7:102381809-102381810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71570339	chr7:102381854-102381855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71570340	chr7:102381858-102381859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190353832	chr7:102381904-102381905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142743827	chr7:102381906-102381907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181949572	chr7:102381919-102381920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71570341	chr7:102381922-102381923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186073160	chr7:102381931-102381932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189743882	chr7:102381992-102381993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113114546	chr7:102382033-102382034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575864150	chr7:102382064-102382065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545938143	chr7:102382080-102382081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71106693	chr7:102382094-102382095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71296556	chr7:102382095-102382096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144509814	chr7:102382128-102382129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528176841	chr7:102382149-102382150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539873276	chr7:102382194-102382195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2537484	chr7:102382209-102382210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112958233	chr7:102382214-102382215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142532491	chr7:102382225-102382226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370242387	chr7:102382273-102382274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568714773	chr7:102382298-102382299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150512462	chr7:102382381-102382382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139597682	chr7:102382402-102382403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549200779	chr7:102382437-102382438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143507344	chr7:102382543-102382544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201347055	chr7:102382584-102382585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535116906	chr7:102382755-102382756	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs71570346	chr7:102382760-102382761	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs71570347	chr7:102382770-102382771	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs553134028	chr7:102382795-102382796	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2071 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102381400-102381600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:102381600-102388800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:102382400-102382600	Enhancers	GM12878-XiMat	blood
4	chr7:102382400-102383000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:102382400-102383000	Enhancers	K562	blood
6	chr7:102382600-102382800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:102382600-102382800	Enhancers	Brain Substantia Nigra	brain
8	chr7:102382600-102383000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr7:102382600-102383000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:102382600-102383000	Enhancers	Brain Angular Gyrus	brain
11	chr7:102382600-102383000	Enhancers	Brain Cingulate Gyrus	brain
12	chr7:102382600-102383000	Flanking Active TSS	GM12878-XiMat	blood
13	chr7:102382600-102383200	Enhancers	Brain Hippocampus Middle	brain
14	chr7:102382800-102383000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:102382800-102383000	Enhancers	Brain Anterior Caudate	brain
16	chr7:102382800-102383000	Flanking Active TSS	HSMMtube	muscle
17	chr7:102382800-102383000	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr7:102382800-102383800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:102382800-102383800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:102382800-102388800	Weak transcription	Brain Substantia Nigra	brain
21	chr7:102383000-102383200	Enhancers	GM12878-XiMat	blood
22	chr7:102383000-102383800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:102383000-102384400	Weak transcription	Brain Angular Gyrus	brain
24	chr7:102383000-102388600	Weak transcription	Brain Anterior Caudate	brain
25	chr7:102383000-102388600	Weak transcription	K562	blood
26	chr7:102383000-102388800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:102383000-102388800	Weak transcription	Brain Cingulate Gyrus	brain
28	chr7:102383000-102388800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr7:102383000-102388800	Weak transcription	HSMMtube	muscle
30	chr7:102383200-102383600	Weak transcription	GM12878-XiMat	blood
31	chr7:102383200-102383800	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:102383400-102384000	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr7:102383600-102384600	Enhancers	GM12878-XiMat	blood
34	chr7:102383800-102384000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:102383800-102384200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:102383800-102385000	Enhancers	Brain Hippocampus Middle	brain
37	chr7:102383800-102388800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:102384000-102388600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:102384000-102388800	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr7:102384200-102388600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:102384400-102384600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr7:102384400-102385000	Enhancers	Brain Angular Gyrus	brain
43	chr7:102384400-102385000	Active TSS	HepG2	liver
44	chr7:102384600-102385000	Enhancers	Fetal Muscle Trunk	muscle
45	chr7:102384600-102385200	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr7:102384600-102388600	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr7:102384600-102388600	Weak transcription	GM12878-XiMat	blood
48	chr7:102384800-102385200	Enhancers	Ovary	ovary
49	chr7:102385000-102385200	Enhancers	HepG2	liver
50	chr7:102385000-102388600	Weak transcription	Brain Angular Gyrus	brain

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