Variant report

Variant	nsv1026624
Chromosome Location	chr7:12963907-13123408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1505)
CpG islands
(count:367)
Chromatin interactive
region (count:121)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1505 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:13059660-13059769	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:13061158-13061756	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:13055750-13055895	K562	blood:	n/a	n/a
4	ARID3A	chr7:13024945-13025261	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:13090328-13090658	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:13090394-13090680	K562	blood:	n/a	n/a
7	ARID3A	chr7:12969174-12969445	K562	blood:	n/a	n/a
8	ARID3A	chr7:12970216-12970508	K562	blood:	n/a	n/a
9	ARID3A	chr7:12991036-12991529	K562	blood:	n/a	n/a
10	ARID3A	chr7:13106506-13106882	K562	blood:	n/a	n/a
11	ARID3A	chr7:13072169-13072296	K562	blood:	n/a	n/a
12	ARID3A	chr7:13018928-13019159	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:13022325-13022364	K562	blood:	n/a	n/a
14	ARID3A	chr7:12989044-12989290	K562	blood:	n/a	n/a
15	ARID3A	chr7:13006650-13007009	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:12997018-12997501	K562	blood:	n/a	n/a
17	ARID3A	chr7:12981059-12982720	HepG2	liver:	n/a	n/a
18	ARID3A	chr7:12988970-12989555	HepG2	liver:	n/a	n/a
19	ARID3A	chr7:13001266-13002208	K562	blood:	n/a	n/a
20	ARID3A	chr7:13056390-13057663	HepG2	liver:	n/a	n/a
21	ARID3A	chr7:13097011-13097123	K562	blood:	n/a	n/a
22	ARID3A	chr7:13082250-13082693	HepG2	liver:	n/a	n/a
23	ARID3A	chr7:13017865-13018065	K562	blood:	n/a	n/a
24	ATF1	chr7:13001613-13001873	K562	blood:	n/a	n/a
25	ATF1	chr7:13084011-13084211	K562	blood:	n/a	n/a
26	ATF1	chr7:12991175-12991494	K562	blood:	n/a	n/a
27	ATF1	chr7:13074981-13075168	K562	blood:	n/a	n/a
28	ATF1	chr7:13090455-13090529	K562	blood:	n/a	n/a
29	ATF1	chr7:12969223-12969475	K562	blood:	n/a	n/a
30	ATF2	chr7:13097270-13097686	GM12878	blood:	n/a	n/a
31	ATF3	chr7:12991180-12991513	K562	blood:	n/a	n/a
32	ATF3	chr7:12963613-12964030	HCT-116	colon:	n/a	chr7:12963836-12963847 chr7:12963836-12963847
33	BACH1	chr7:13057721-13057814	K562	blood:	n/a	n/a
34	BACH1	chr7:13112061-13112090	K562	blood:	n/a	n/a
35	BACH1	chr7:13090371-13090647	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr7:13089906-13090689	K562	blood:	n/a	n/a
37	BACH1	chr7:13094079-13094100	K562	blood:	n/a	n/a
38	BCL3	chr7:13056919-13057542	A549	lung:	n/a	n/a
39	BCL3	chr7:13070944-13071546	A549	lung:	n/a	chr7:13071258-13071267 chr7:13071259-13071268
40	BCL3	chr7:13056780-13057654	A549	lung:	n/a	n/a
41	BHLHE40	chr7:13097430-13097605	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:13056643-13057473	HepG2	liver:	n/a	n/a
43	BHLHE40	chr7:12981186-12981510	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:12991253-12991526	K562	blood:	n/a	n/a
45	BHLHE40	chr7:13055716-13055735	K562	blood:	n/a	n/a
46	BHLHE40	chr7:12997109-12997456	K562	blood:	n/a	n/a
47	BHLHE40	chr7:13034316-13034323	K562	blood:	n/a	n/a
48	BHLHE40	chr7:13085367-13085422	K562	blood:	n/a	n/a
49	BRCA1	chr7:13057093-13057357	HepG2	liver:	n/a	n/a
50	BRCA1	chr7:12991188-12991474	Hela-S3	cervix:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13055962-13056012	U87	brain:	n/a
2	chr7:13055962-13056012	U87	brain:	n/a
3	chr7:13072314-13072364	HNPCEpiC	eye:	n/a
4	chr7:12971260-12971310	SKMC	muscle:	n/a
5	chr7:12971260-12971310	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:12971332-12971382	Caco-2	colon:	n/a
7	chr7:13055962-13056012	IMR90	lung:	fetal
8	chr7:12971332-12971382	K562	blood:	n/a
9	chr7:13055962-13056012	NHDF-neo	bronchial:	n/a
10	chr7:13055962-13056012	AG09319	gingival:	n/a
11	chr7:13072314-13072364	ECC-1	luminal epithelium:	n/a
12	chr7:12971260-12971310	GM12878	blood:	n/a
13	chr7:13072314-13072364	MCF-7	breast:	n/a
14	chr7:13025242-13025292	HCF	heart:	n/a
15	chr7:12971332-12971382	U87	brain:	n/a
16	chr7:13055962-13056012	SK-N-SH_RA	brain:	n/a
17	chr7:13072314-13072364	HIPEpiC	eye:	n/a
18	chr7:12971260-12971310	Jurkat	blood:	n/a
19	chr7:13057352-13057402	H1-hESC	embryonic stem cell:	embryo
20	chr7:13057352-13057402	PrEC	prostate:	n/a
21	chr7:13055962-13056012	BE2_C	brain:	n/a
22	chr7:12971332-12971382	HNPCEpiC	eye:	n/a
23	chr7:12971260-12971310	NT2-D1	testis:	n/a
24	chr7:12971260-12971310	SK-N-MC	brain:	n/a
25	chr7:13025242-13025292	HCT-116	colon:	n/a
26	chr7:13057352-13057402	GM12878	blood:	n/a
27	chr7:13055962-13056012	HEK293	kidney:	embryo
28	chr7:13072314-13072364	NT2-D1	testis:	n/a
29	chr7:12971260-12971310	CMK	blood:	n/a
30	chr7:13055962-13056012	HNPCEpiC	eye:	n/a
31	chr7:13025242-13025292	AG04449	skin:	fetal
32	chr7:12971260-12971310	HCPEpiC	choroid plexus:	n/a
33	chr7:13055962-13056012	SK-N-MC	brain:	n/a
34	chr7:13072314-13072364	AG10803	skin:	n/a
35	chr7:12971332-12971382	PANC-1	pancreas:	n/a
36	chr7:13055962-13056012	GM19239	blood:	n/a
37	chr7:13057352-13057402	Hepatocyte	liver:	n/a
38	chr7:13025242-13025292	AG09319	gingival:	n/a
39	chr7:13057352-13057402	BE2_C	brain:	n/a
40	chr7:12971260-12971310	SK-N-SH_RA	brain:	n/a
41	chr7:13055962-13056012	HL-60	blood:	n/a
42	chr7:13072314-13072364	SKMC	muscle:	n/a
43	chr7:13025242-13025292	T-47D	breast:	n/a
44	chr7:13072314-13072364	Jurkat	blood:	n/a
45	chr7:12971260-12971310	PANC-1	pancreas:	n/a
46	chr7:12971260-12971310	HCM	heart:	n/a
47	chr7:13072314-13072364	GM12878	blood:	n/a
48	chr7:12971332-12971382	PFSK-1	brain:	n/a
49	chr7:13055962-13056012	SAEC	small airway:	n/a
50	chr7:13057352-13057402	HepG2	liver:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:12725420..12727462-chr7:12966302..12969517,3	MCF-7	breast:
2	chr7:12980961..12983258-chr7:13154370..13156023,2	MCF-7	breast:
3	chr7:13091634..13094570-chr7:13095004..13097471,2	K562	blood:
4	chr7:12726504..12729722-chr7:13092003..13095862,3	K562	blood:
5	chr7:13056069..13058196-chr7:13060337..13062403,2	MCF-7	breast:
6	chr7:13021586..13023198-chr7:13026408..13028122,2	K562	blood:
7	chr7:13111805..13113325-chr7:13115222..13117599,2	K562	blood:
8	chr7:13005159..13006862-chr7:13012261..13014568,2	K562	blood:
9	chr7:12989951..12991980-chr7:12999639..13002112,2	K562	blood:
10	chr7:12730382..12732328-chr7:13069192..13071887,3	K562	blood:
11	chr7:13088931..13090663-chr7:13093892..13095543,2	K562	blood:
12	chr7:13056096..13059019-chr7:13091108..13093835,2	K562	blood:
13	chr7:13094404..13096720-chr7:13097474..13099748,2	K562	blood:
14	chr7:13100363..13102009-chr7:13102221..13104284,2	K562	blood:
15	chr7:12776917..12778957-chr7:13100732..13103715,2	MCF-7	breast:
16	chr7:13007791..13010494-chr7:13016088..13018337,2	K562	blood:
17	chr7:12907138..12909951-chr7:12999390..13002085,2	K562	blood:
18	chr7:13067871..13070074-chr7:13070910..13073106,2	K562	blood:
19	chr7:13005159..13006862-chr7:13012261..13014568,2	K562	blood:
20	chr7:13023717..13025887-chr7:13027646..13029322,2	K562	blood:
21	chr7:12996184..12998633-chr7:12999943..13002751,2	K562	blood:
22	chr7:13105294..13107639-chr7:13110167..13112332,4	K562	blood:
23	chr7:13044871..13047028-chr7:13047401..13048917,2	K562	blood:
24	chr7:12726106..12728466-chr7:13017401..13019789,2	MCF-7	breast:
25	chr7:13023717..13025887-chr7:13027646..13029322,2	K562	blood:
26	chr7:13081390..13084291-chr7:13084595..13087584,2	K562	blood:
27	chr7:12970290..12973079-chr7:13097205..13098974,2	K562	blood:
28	chr7:13067871..13070074-chr7:13070910..13073106,2	K562	blood:
29	chr7:12730592..12732679-chr7:13123373..13125180,2	K562	blood:
30	chr7:13000222..13002006-chr7:13022745..13025584,2	K562	blood:
31	chr7:13091224..13092839-chr7:13093299..13095856,2	K562	blood:
32	chr7:12988128..12991573-chr7:12991577..12994524,4	K562	blood:
33	chr7:13080083..13082250-chr7:13086917..13089071,2	K562	blood:
34	chr7:13095947..13098043-chr7:13101119..13103304,2	MCF-7	breast:
35	chr7:13061821..13064035-chr7:13076250..13077788,2	MCF-7	breast:
36	chr7:13094404..13096720-chr7:13097474..13099748,2	K562	blood:
37	chr7:12725676..12727718-chr7:12981615..12985353,4	MCF-7	breast:
38	chr7:12998941..13001719-chr7:13004251..13006120,2	MCF-7	breast:
39	chr7:13000222..13002006-chr7:13022745..13025584,2	K562	blood:
40	chr7:13085851..13087402-chr7:13106082..13107771,2	K562	blood:
41	chr7:13093779..13096148-chr7:13099334..13101239,2	K562	blood:
42	chr7:12726944..12729146-chr7:13085985..13088167,2	K562	blood:
43	chr7:12982252..12985209-chr7:12989086..12991470,2	MCF-7	breast:
44	chr7:12687097..12689372-chr7:13046142..13048475,2	K562	blood:
45	chr7:13081390..13084291-chr7:13084595..13087584,2	K562	blood:
46	chr7:13056069..13058196-chr7:13060337..13062403,2	MCF-7	breast:
47	chr7:13011583..13014531-chr7:13023994..13025631,2	MCF-7	breast:
48	chr7:13003252..13004931-chr7:13007196..13009928,2	K562	blood:
49	chr7:13015931..13018099-chr7:13026528..13028162,2	K562	blood:
50	chr7:13088931..13090663-chr7:13093892..13095543,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL4A-6	chr7:13006732-13006797	NONHSAT119246
2	lnc-ARL4A-7	chr7:13108158-13108539	NONHSAT119247
3	lnc-ARL4A-7	chr7:13107541-13107733	NONHSAT119247
4	lnc-ARL4A-7	chr7:13107622-13107733	NONHSAT119248
5	lnc-ARL4A-6	chr7:13006471-13006612	NONHSAT119246

No data

Variant related genes	Relation type
RBMX2P4	TF binding region
RBMX2P4	CpG island
ENSG00000271253	chromatin interactions
ENSG00000222974	chromatin interactions
ENSG00000122644	chromatin interactions
ENSG00000230879	chromatin interactions

Extended variants
information (count: 6929 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6929 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs991088	chr7:12963907-12963908	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs74189109	chr7:12963910-12963911	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs58498024	chr7:12963930-12963931	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs148560207	chr7:12963963-12963964	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs181258811	chr7:12963964-12963965	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs77675220	chr7:12963965-12963966	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs142947053	chr7:12963970-12963971	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs78083833	chr7:12963986-12963987	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs9986893	chr7:12964005-12964006	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs115991756	chr7:12964012-12964013	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs577896133	chr7:12964021-12964022	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs991087	chr7:12964022-12964023	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562908963	chr7:12964063-12964064	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs553452102	chr7:12964065-12964066	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs374454888	chr7:12964105-12964106	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528999058	chr7:12964151-12964152	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs186075655	chr7:12964175-12964176	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs386710469	chr7:12964191-12964192	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs115564870	chr7:12964192-12964193	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs151113584	chr7:12964211-12964212	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs62448194	chr7:12964213-12964214	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs191024746	chr7:12964227-12964228	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs530808690	chr7:12964239-12964240	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs550222383	chr7:12964276-12964277	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs7804406	chr7:12964294-12964295	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs184071993	chr7:12964340-12964341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141115586	chr7:12964386-12964387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566038580	chr7:12964394-12964395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534916540	chr7:12964396-12964397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57768185	chr7:12964399-12964400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545985916	chr7:12964404-12964405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143977377	chr7:12964412-12964413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376356095	chr7:12964430-12964431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187561150	chr7:12964440-12964441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576263458	chr7:12964451-12964452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556685958	chr7:12964469-12964470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190503936	chr7:12964560-12964561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs62448211	chr7:12964563-12964564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559442875	chr7:12964618-12964619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528170786	chr7:12964629-12964630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545255502	chr7:12964635-12964636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs554875301	chr7:12964685-12964686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112303623	chr7:12964697-12964698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530831746	chr7:12964779-12964780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555591835	chr7:12964811-12964812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs117848844	chr7:12964837-12964838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs13236466	chr7:12964850-12964851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs573130854	chr7:12964851-12964852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376437603	chr7:12964882-12964883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549086000	chr7:12964904-12964905	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:900 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12961400-12964400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:12961400-12964400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:12962000-12967000	Weak transcription	Stomach Mucosa	stomach
4	chr7:12962000-12967400	Weak transcription	Fetal Intestine Large	intestine
5	chr7:12962000-12970200	Weak transcription	HUVEC	blood vessel
6	chr7:12962200-12967200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr7:12962600-12966000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:12962800-12964400	Enhancers	HMEC	breast
9	chr7:12963000-12964400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr7:12963400-12964200	Enhancers	Liver	Liver
11	chr7:12963600-12964000	Enhancers	Muscle Satellite Cultured Cells	--
12	chr7:12963800-12964000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:12963800-12964000	Enhancers	NHEK	skin
14	chr7:12964000-12964200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:12964000-12964200	Flanking Active TSS	NHEK	skin
16	chr7:12964200-12964800	Enhancers	NHEK	skin
17	chr7:12964200-12965200	Weak transcription	Liver	Liver
18	chr7:12964400-12965600	Weak transcription	HMEC	breast
19	chr7:12964400-12967200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:12964400-12969200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:12964800-12965800	Weak transcription	NHEK	skin
22	chr7:12965200-12965600	Enhancers	Liver	Liver
23	chr7:12965200-12966600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:12965200-12966800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:12965200-12968200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:12965400-12966600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:12965400-12968400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:12965600-12966200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:12965800-12966000	Enhancers	HMEC	breast
30	chr7:12965800-12966200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr7:12965800-12966200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:12965800-12966200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:12965800-12966200	Enhancers	NHEK	skin
34	chr7:12965800-12966400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr7:12965800-12966400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:12966000-12966200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:12966000-12966200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:12966200-12967600	Weak transcription	NHEK	skin
39	chr7:12966200-12969200	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr7:12966400-12966800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr7:12966400-12967600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:12966400-12969200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr7:12966600-12967000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:12966600-12969200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:12966800-12968000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr7:12967000-12967400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:12967000-12969600	Enhancers	Stomach Mucosa	stomach
48	chr7:12967200-12967400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr7:12967200-12968200	Enhancers	Ovary	ovary
50	chr7:12967200-12968200	Enhancers	Rectal Mucosa Donor 31	rectum

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