Variant report

Variant	nsv464371
Chromosome Location	chr7:12371801-12434771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:639)
CpG islands
(count:184)
Chromatin interactive
region (count:55)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12424775-12425636	K562	blood:	n/a	n/a
2	ARID3A	chr7:12428736-12429092	K562	blood:	n/a	n/a
3	ARID3A	chr7:12425885-12425929	K562	blood:	n/a	n/a
4	ATF1	chr7:12424857-12425489	K562	blood:	n/a	n/a
5	ATF1	chr7:12391517-12391830	K562	blood:	n/a	n/a
6	ATF2	chr7:12397170-12397485	GM12878	blood:	n/a	n/a
7	BACH1	chr7:12409290-12409383	K562	blood:	n/a	n/a
8	BCL3	chr7:12397240-12397520	GM12878	blood:	n/a	n/a
9	BCLAF1	chr7:12424838-12425482	K562	blood:	n/a	n/a
10	BHLHE40	chr7:12391626-12391783	K562	blood:	n/a	n/a
11	BHLHE40	chr7:12412689-12412834	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:12431674-12431880	K562	blood:	n/a	n/a
13	CBX3	chr7:12424861-12425408	K562	blood:	n/a	n/a
14	CCNT2	chr7:12432707-12432774	K562	blood:	n/a	n/a
15	CCNT2	chr7:12422140-12422303	K562	blood:	n/a	n/a
16	CCNT2	chr7:12391547-12391847	K562	blood:	n/a	n/a
17	CCNT2	chr7:12418952-12419019	K562	blood:	n/a	n/a
18	CCNT2	chr7:12403056-12403099	K562	blood:	n/a	n/a
19	CCNT2	chr7:12383002-12383143	K562	blood:	n/a	n/a
20	CCNT2	chr7:12405891-12406052	K562	blood:	n/a	n/a
21	CCNT2	chr7:12424779-12425447	K562	blood:	n/a	n/a
22	CCNT2	chr7:12430237-12430378	K562	blood:	n/a	n/a
23	CEBPB	chr7:12413201-12413548	ECC-1	luminal epithelium:	n/a	chr7:12413407-12413418
24	CEBPB	chr7:12428747-12429052	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr7:12427349-12427455	A549	lung:	n/a	chr7:12427390-12427401
26	CEBPB	chr7:12427336-12427485	Hela-S3	cervix:	n/a	chr7:12427390-12427401
27	CEBPB	chr7:12428774-12429020	K562	blood:	n/a	n/a
28	CEBPB	chr7:12428603-12429086	K562	blood:	n/a	n/a
29	CEBPB	chr7:12413170-12413593	A549	lung:	n/a	chr7:12413407-12413418
30	CEBPB	chr7:12413265-12413569	H1-hESC	embryonic stem cell:	n/a	chr7:12413407-12413418
31	CEBPB	chr7:12427225-12427566	K562	blood:	n/a	chr7:12427390-12427401
32	CEBPB	chr7:12428743-12429125	MCF-7	breast:	n/a	n/a
33	CEBPB	chr7:12413221-12413469	K562	blood:	n/a	chr7:12413407-12413418
34	CEBPB	chr7:12428717-12429071	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:12424780-12425422	K562	blood:	n/a	n/a
36	CEBPB	chr7:12430755-12430776	HepG2	liver:	n/a	chr7:12430766-12430775 chr7:12430766-12430775 chr7:12430765-12430776
37	CEBPB	chr7:12430682-12430949	K562	blood:	n/a	chr7:12430766-12430775 chr7:12430766-12430775 chr7:12430765-12430776
38	CEBPB	chr7:12413219-12413802	K562	blood:	n/a	chr7:12413407-12413418
39	CEBPB	chr7:12376796-12377033	K562	blood:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
40	CEBPB	chr7:12428702-12429072	K562	blood:	n/a	n/a
41	CEBPB	chr7:12413230-12413569	A549	lung:	n/a	chr7:12413407-12413418
42	CEBPB	chr7:12413251-12413595	IMR90	lung:	n/a	chr7:12413407-12413418
43	CEBPB	chr7:12428724-12429042	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr7:12397108-12397677	GM12878	blood:	n/a	n/a
45	CEBPB	chr7:12418167-12418474	K562	blood:	n/a	chr7:12418334-12418345 chr7:12418333-12418346 chr7:12418333-12418344
46	CEBPB	chr7:12430777-12430888	A549	lung:	n/a	n/a
47	CEBPB	chr7:12376804-12377018	IMR90	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
48	CEBPB	chr7:12376790-12377114	A549	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
49	CEBPB	chr7:12413202-12413543	A549	lung:	n/a	chr7:12413407-12413418
50	CEBPB	chr7:12422917-12423570	Hela-S3	cervix:	n/a	chr7:12422959-12422970

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12376625-12376675	GM12892	blood:	n/a
2	chr7:12376625-12376675	GM12892	blood:	n/a
3	chr7:12376625-12376675	HCPEpiC	choroid plexus:	n/a
4	chr7:12411370-12411420	K562	blood:	n/a
5	chr7:12411370-12411420	GM19239	blood:	n/a
6	chr7:12411370-12411420	HCM	heart:	n/a
7	chr7:12376625-12376675	IMR90	lung:	fetal
8	chr7:12376625-12376675	SAEC	small airway:	n/a
9	chr7:12411370-12411420	AG10803	skin:	n/a
10	chr7:12376625-12376675	SK-N-SH	brain:	n/a
11	chr7:12376625-12376675	HMEC	breast:	n/a
12	chr7:12411370-12411420	HEEpiC	esophagus:	n/a
13	chr7:12411370-12411420	MCF-7	breast:	n/a
14	chr7:12411370-12411420	AG09309	skin:	n/a
15	chr7:12376625-12376675	CMK	blood:	n/a
16	chr7:12410026-12410076	NB4	blood:	n/a
17	chr7:12411370-12411420	HRCEpiC	kidney:	n/a
18	chr7:12410026-12410076	HMEC	breast:	n/a
19	chr7:12376625-12376675	ECC-1	luminal epithelium:	n/a
20	chr7:12410026-12410076	HCF	heart:	n/a
21	chr7:12411370-12411420	SKMC	muscle:	n/a
22	chr7:12411370-12411420	HMEC	breast:	n/a
23	chr7:12376625-12376675	HL-60	blood:	n/a
24	chr7:12410026-12410076	BE2_C	brain:	n/a
25	chr7:12376625-12376675	SKMC	muscle:	n/a
26	chr7:12376625-12376675	GM12891	blood:	n/a
27	chr7:12410026-12410076	SKMC	muscle:	n/a
28	chr7:12410026-12410076	SK-N-MC	brain:	n/a
29	chr7:12376625-12376675	Caco-2	colon:	n/a
30	chr7:12376625-12376675	AG04449	skin:	fetal
31	chr7:12410026-12410076	IMR90	lung:	fetal
32	chr7:12376625-12376675	ProgFib	skin:	n/a
33	chr7:12376625-12376675	NHBE	bronchial:	n/a
34	chr7:12411370-12411420	PrEC	prostate:	n/a
35	chr7:12410026-12410076	GM12891	blood:	n/a
36	chr7:12410026-12410076	HepG2	liver:	n/a
37	chr7:12411370-12411420	BJ	skin:	n/a
38	chr7:12376625-12376675	U87	brain:	n/a
39	chr7:12410026-12410076	T-47D	breast:	n/a
40	chr7:12411370-12411420	MCF10A-Er-Src	breast:	n/a
41	chr7:12410026-12410076	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:12376625-12376675	HRPEpiC	eye:	n/a
43	chr7:12411370-12411420	NHDF-neo	bronchial:	n/a
44	chr7:12410026-12410076	AG09319	gingival:	n/a
45	chr7:12410026-12410076	Jurkat	blood:	n/a
46	chr7:12376625-12376675	MCF10A-Er-Src	breast:	n/a
47	chr7:12411370-12411420	PFSK-1	brain:	n/a
48	chr7:12411370-12411420	BE2_C	brain:	n/a
49	chr7:12410026-12410076	ProgFib	skin:	n/a
50	chr7:12410026-12410076	AG04449	skin:	fetal

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:12426277..12428963-chr7:12530535..12533181,2	K562	blood:
2	chr7:12423183..12428504-chr7:12441656..12445145,7	K562	blood:
3	chr7:12414352..12417133-chr7:12443944..12445537,2	K562	blood:
4	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
5	chr7:12408674..12410212-chr7:12426957..12428907,2	K562	blood:
6	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
7	chr7:12398772..12400728-chr7:12416119..12417972,2	K562	blood:
8	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
9	chr7:12380686..12382573-chr7:12386582..12389339,2	K562	blood:
10	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
11	chr7:12402068..12405586-chr7:12406959..12410606,5	K562	blood:
12	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
13	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
14	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
15	chr7:12401550..12404872-chr7:12410854..12415444,4	K562	blood:
16	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
17	chr7:12391134..12392692-chr7:12402911..12404517,2	K562	blood:
18	chr7:12356830..12359604-chr7:12404989..12406571,2	K562	blood:
19	chr7:12428351..12429175-chr7:12529458..12530800,4	MCF-7	breast:
20	chr7:12408799..12410708-chr7:12417249..12418833,2	K562	blood:
21	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
22	chr7:12401893..12405448-chr7:12416442..12419735,3	K562	blood:
23	chr7:12401893..12405448-chr7:12416442..12419735,3	K562	blood:
24	chr7:12401550..12404872-chr7:12410854..12415444,4	K562	blood:
25	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
26	chr7:12391914..12394742-chr7:12414391..12416688,2	K562	blood:
27	chr7:12408674..12410212-chr7:12426957..12428907,2	K562	blood:
28	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
29	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
30	chr7:12391914..12394742-chr7:12414391..12416688,2	K562	blood:
31	chr4:173623488..173624406-chr7:12420850..12421512,2	MCF-7	breast:
32	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
33	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
34	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
35	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
36	chr7:12408799..12410708-chr7:12417249..12418833,2	K562	blood:
37	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
38	chr7:12362078..12365720-chr7:12370304..12373327,3	K562	blood:
39	chr7:12376678..12378667-chr7:12443118..12444758,2	K562	blood:
40	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
41	chr7:12421246..12422799-chr7:12438154..12440817,2	K562	blood:
42	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
43	chr7:12428677..12429434-chr7:12476625..12477415,2	K562	blood:
44	chr7:12380686..12382573-chr7:12386582..12389339,2	K562	blood:
45	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
46	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
47	chr7:12391134..12392692-chr7:12402911..12404517,2	K562	blood:
48	chr7:12408712..12411098-chr7:12427407..12429029,2	K562	blood:
49	chr7:12408712..12411098-chr7:12427407..12429029,2	K562	blood:
50	chr7:12402068..12405586-chr7:12406959..12410606,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THSD7A-8	chr7:12381149-12381601	expReg_chr7_1130_-
2	lnc-THSD7A-4	chr7:12373091-12373352	NONHSAT119227
3	lnc-THSD7A-5	chr7:12376785-12377015	expReg_chr7_1125_-
4	lnc-THSD7A-6	chr7:12378965-12379591	expReg_chr7_1128_-
5	lnc-THSD7A-7	chr7:12380807-12381047	expReg_chr7_1129_-

No data

Variant related genes	Relation type
VWDE	TF binding region
VWDE	CpG island
ENSG00000106460	chromatin interactions
ENSG00000146530	chromatin interactions
ENSG00000203523	chromatin interactions

Extended variants
information (count: 2880 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2880 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3815528	chr7:12371801-12371802	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74924922	chr7:12371816-12371817	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141322863	chr7:12371821-12371822	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532060346	chr7:12371822-12371823	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75969152	chr7:12371824-12371825	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs33933665	chr7:12371825-12371826	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552141566	chr7:12371838-12371839	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529490494	chr7:12371851-12371852	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181511421	chr7:12371853-12371854	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371119851	chr7:12371859-12371860	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531840369	chr7:12371907-12371908	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73680913	chr7:12371908-12371909	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs3815527	chr7:12371949-12371950	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs534105083	chr7:12371952-12371953	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs386710413	chr7:12372023-12372024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114875258	chr7:12372025-12372026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3815525	chr7:12372029-12372030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs114118277	chr7:12372033-12372034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138313853	chr7:12372044-12372045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575468805	chr7:12372047-12372048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75018073	chr7:12372085-12372086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187042811	chr7:12372086-12372087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73290474	chr7:12372092-12372093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs540426189	chr7:12372123-12372124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10265056	chr7:12372159-12372160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532195547	chr7:12372211-12372212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545487691	chr7:12372275-12372276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77752763	chr7:12372276-12372277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567846842	chr7:12372295-12372296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76595131	chr7:12372301-12372302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370266055	chr7:12372309-12372310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17165862	chr7:12372317-12372318	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs527917369	chr7:12372327-12372328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189473450	chr7:12372332-12372333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532915924	chr7:12372338-12372339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112697705	chr7:12372371-12372372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs80002987	chr7:12372381-12372382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549921753	chr7:12372383-12372384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386710414	chr7:12372410-12372411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116662981	chr7:12372412-12372413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114440810	chr7:12372414-12372415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74769068	chr7:12372421-12372422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533990627	chr7:12372444-12372445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538762203	chr7:12372469-12372470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181527277	chr7:12372551-12372552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568897756	chr7:12372569-12372570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368271495	chr7:12372580-12372581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199835074	chr7:12372589-12372590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs5882354	chr7:12372591-12372592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35648886	chr7:12372592-12372593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12354400-12405000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:12363800-12392800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:12367000-12372000	Strong transcription	K562	blood
4	chr7:12367400-12372000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr7:12367600-12372000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr7:12368200-12433200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:12368800-12376600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:12369400-12372000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:12369800-12372000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:12369800-12372000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:12370000-12372000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr7:12370400-12376200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:12370400-12384800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr7:12370600-12372000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:12370600-12379000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr7:12371400-12372000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr7:12371800-12376200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:12372000-12373000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:12372000-12375800	Weak transcription	K562	blood
20	chr7:12372000-12376200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:12372000-12376400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr7:12372000-12376600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:12372000-12376600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:12372000-12376600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:12372000-12379800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:12373000-12373400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:12373400-12375800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:12374200-12374400	Enhancers	Gastric	stomach
29	chr7:12375800-12377000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:12375800-12387200	Strong transcription	K562	blood
31	chr7:12376200-12376800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:12376200-12377000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr7:12376200-12377200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:12376400-12385800	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr7:12376600-12377000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:12376600-12377000	Genic enhancers	H9 Cell Line	embryonic stem cell
37	chr7:12376600-12377000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:12376600-12377200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:12376800-12385800	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr7:12377000-12378400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr7:12377000-12379000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:12377000-12379400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:12377000-12385000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr7:12377000-12408000	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr7:12377200-12378400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr7:12377200-12380400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr7:12378400-12380600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr7:12378400-12385600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr7:12379000-12382800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr7:12379000-12386000	Strong transcription	HUES6 Cell Line	embryonic stem cell

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