Variant report

Variant	nsv888639
Chromosome Location	chr7:84158180-84344258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1559)
CpG islands
(count:367)
Chromatin interactive
region (count:56)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1559 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:84332343-84332393	K562	blood:	n/a	n/a
2	ARID3A	chr7:84302368-84302402	K562	blood:	n/a	n/a
3	ARID3A	chr7:84287580-84287954	K562	blood:	n/a	n/a
4	ARID3A	chr7:84305107-84305335	K562	blood:	n/a	n/a
5	ATF1	chr7:84305022-84305312	K562	blood:	n/a	n/a
6	ATF1	chr7:84323619-84323645	K562	blood:	n/a	n/a
7	ATF1	chr7:84259630-84259842	K562	blood:	n/a	n/a
8	ATF1	chr7:84331188-84331414	K562	blood:	n/a	n/a
9	ATF1	chr7:84292651-84292819	K562	blood:	n/a	n/a
10	ATF1	chr7:84298510-84298929	K562	blood:	n/a	n/a
11	ATF3	chr7:84165333-84165902	A549	lung:	n/a	n/a
12	ATF3	chr7:84158579-84159198	A549	lung:	n/a	n/a
13	ATF3	chr7:84331078-84331730	A549	lung:	n/a	n/a
14	ATF3	chr7:84165356-84165961	A549	lung:	n/a	n/a
15	BACH1	chr7:84314329-84314388	K562	blood:	n/a	n/a
16	BATF	chr7:84305070-84305360	GM12878	blood:	n/a	n/a
17	BATF	chr7:84305143-84305369	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:84177692-84177958	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr7:84158630-84159471	A549	lung:	n/a	n/a
20	BCL3	chr7:84165334-84165953	A549	lung:	n/a	n/a
21	BCL3	chr7:84158463-84159465	A549	lung:	n/a	n/a
22	BCL3	chr7:84330997-84331738	A549	lung:	n/a	n/a
23	BCL3	chr7:84165165-84166072	A549	lung:	n/a	n/a
24	BHLHE40	chr7:84305313-84305318	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:84244524-84244740	K562	blood:	n/a	n/a
26	BRCA1	chr7:84304850-84305429	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr7:84330839-84331723	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:84158325-84159418	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr7:84302255-84302599	GM12878	blood:	n/a	n/a
30	CBX3	chr7:84232979-84233116	K562	blood:	n/a	n/a
31	CBX3	chr7:84261530-84261866	K562	blood:	n/a	n/a
32	CBX3	chr7:84331137-84331706	HCT-116	colon:	n/a	n/a
33	CBX3	chr7:84330750-84331792	HCT-116	colon:	n/a	n/a
34	CCNT2	chr7:84305040-84305328	K562	blood:	n/a	n/a
35	CCNT2	chr7:84298566-84298780	K562	blood:	n/a	n/a
36	CCNT2	chr7:84255504-84255628	K562	blood:	n/a	n/a
37	CEBPB	chr7:84314384-84314753	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:84304860-84305527	MCF-7	breast:	n/a	n/a
39	CEBPB	chr7:84311894-84312252	K562	blood:	n/a	chr7:84312067-84312080 chr7:84312068-84312079 chr7:84312006-84312018 chr7:84312067-84312078 chr7:84312067-84312080
40	CEBPB	chr7:84326810-84327248	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:84330785-84331659	IMR90	lung:	n/a	chr7:84331108-84331125 chr7:84331045-84331058 chr7:84331109-84331122
42	CEBPB	chr7:84306501-84306751	K562	blood:	n/a	chr7:84306589-84306600
43	CEBPB	chr7:84158620-84159258	MCF-7	breast:	n/a	n/a
44	CEBPB	chr7:84178742-84179124	IMR90	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
45	CEBPB	chr7:84329881-84330244	A549	lung:	n/a	n/a
46	CEBPB	chr7:84230169-84230320	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:84341618-84342466	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr7:84178130-84178390	HepG2	liver:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
49	CEBPB	chr7:84317981-84318406	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:84330740-84331782	A549	lung:	n/a	chr7:84331108-84331125 chr7:84331045-84331058 chr7:84331109-84331122

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84267140-84267190	T-47D	breast:	n/a
2	chr7:84267140-84267190	T-47D	breast:	n/a
3	chr7:84177905-84177955	AG09309	skin:	n/a
4	chr7:84161420-84161470	HRE	kidney:	n/a
5	chr7:84177905-84177955	H1-hESC	embryonic stem cell:	embryo
6	chr7:84177905-84177955	GM12891	blood:	n/a
7	chr7:84177905-84177955	NH-A	brain:	n/a
8	chr7:84277775-84277825	NHDF-neo	bronchial:	n/a
9	chr7:84177905-84177955	HEK293	kidney:	embryo
10	chr7:84177905-84177955	HCPEpiC	choroid plexus:	n/a
11	chr7:84267140-84267190	Jurkat	blood:	n/a
12	chr7:84267140-84267190	GM12878	blood:	n/a
13	chr7:84330779-84330829	AG04449	skin:	fetal
14	chr7:84277775-84277825	IMR90	lung:	fetal
15	chr7:84267140-84267190	HL-60	blood:	n/a
16	chr7:84177905-84177955	GM06990	blood:	n/a
17	chr7:84277775-84277825	U87	brain:	n/a
18	chr7:84161420-84161470	U87	brain:	n/a
19	chr7:84161222-84161272	MCF10A-Er-Src	breast:	n/a
20	chr7:84277775-84277825	NT2-D1	testis:	n/a
21	chr7:84161420-84161470	Caco-2	colon:	n/a
22	chr7:84267140-84267190	NHDF-neo	bronchial:	n/a
23	chr7:84161420-84161470	SK-N-MC	brain:	n/a
24	chr7:84267140-84267190	ECC-1	luminal epithelium:	n/a
25	chr7:84277775-84277825	SAEC	small airway:	n/a
26	chr7:84277775-84277825	HCT-116	colon:	n/a
27	chr7:84161222-84161272	GM12878	blood:	n/a
28	chr7:84161420-84161470	HEK293	kidney:	embryo
29	chr7:84161222-84161272	PrEC	prostate:	n/a
30	chr7:84277775-84277825	HIPEpiC	eye:	n/a
31	chr7:84330779-84330829	HRCEpiC	kidney:	n/a
32	chr7:84267140-84267190	BJ	skin:	n/a
33	chr7:84161420-84161470	HAEpiC	amniotic membrane:	n/a
34	chr7:84161420-84161470	SK-N-SH_RA	brain:	n/a
35	chr7:84267140-84267190	SK-N-SH_RA	brain:	n/a
36	chr7:84330779-84330829	GM12892	blood:	n/a
37	chr7:84330779-84330829	SKMC	muscle:	n/a
38	chr7:84177905-84177955	Hela-S3	cervix:	n/a
39	chr7:84330779-84330829	SAEC	small airway:	n/a
40	chr7:84161420-84161470	HIPEpiC	eye:	n/a
41	chr7:84277775-84277825	HUVEC	blood vessel:	n/a
42	chr7:84177905-84177955	A549	lung:	n/a
43	chr7:84267140-84267190	HIPEpiC	eye:	n/a
44	chr7:84161420-84161470	HEEpiC	esophagus:	n/a
45	chr7:84177905-84177955	Jurkat	blood:	n/a
46	chr7:84267140-84267190	AG04449	skin:	fetal
47	chr7:84330779-84330829	AG09309	skin:	n/a
48	chr7:84267140-84267190	NHBE	bronchial:	n/a
49	chr7:84177905-84177955	AG04450	lung:	fetal
50	chr7:84267140-84267190	HepG2	liver:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
2	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
3	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
4	chr7:84231197..84234055-chr7:84234117..84236974,2	K562	blood:
5	chr3:161089345..161090957-chr7:84248345..84250491,2	MCF-7	breast:
6	chr7:84250435..84252517-chr7:84252923..84255018,2	K562	blood:
7	chr7:84325930..84329136-chr7:84329688..84332999,3	K562	blood:
8	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
9	chr1:149857245..149858849-chr7:84173495..84175226,2	MCF-7	breast:
10	chr7:84158432..84159047-chr7:84499527..84500086,2	MCF-7	breast:
11	chr7:84244149..84244717-chr7:84651890..84652789,2	MCF-7	breast:
12	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
13	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
14	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
15	chr7:84312169..84314896-chr7:84317846..84320190,3	K562	blood:
16	chr7:84311385..84314153-chr7:84316076..84317631,2	K562	blood:
17	chr7:84312169..84314896-chr7:84317846..84320190,3	K562	blood:
18	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
19	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
20	chr17:56736359..56736893-chr7:84265214..84266196,2	MCF-7	breast:
21	chr7:84316486..84318065-chr7:84325058..84327513,2	K562	blood:
22	chr7:84319553..84321871-chr7:84324252..84327875,3	K562	blood:
23	chr7:84231197..84234055-chr7:84234117..84236974,2	K562	blood:
24	chr7:83904428..83905120-chr7:84165177..84165677,2	MCF-7	breast:
25	chr7:84215550..84219199-chr7:84222001..84225003,3	K562	blood:
26	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
27	chr7:84325930..84329136-chr7:84329688..84332999,3	K562	blood:
28	chr7:84275439..84277976-chr7:84279778..84282553,2	K562	blood:
29	chr7:84297350..84299961-chr7:84307072..84309162,3	K562	blood:
30	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
31	chr7:84158367..84158951-chr7:84240610..84241382,2	MCF-7	breast:
32	chr7:84158595..84159433-chr7:84240484..84241224,2	MCF-7	breast:
33	chr7:84311385..84314153-chr7:84316076..84317631,2	K562	blood:
34	chr7:84158367..84158951-chr7:84240610..84241382,2	MCF-7	breast:
35	chr7:84315326..84318065-chr7:84325058..84327523,3	K562	blood:
36	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:
37	chr7:84316486..84318065-chr7:84325058..84327513,2	K562	blood:
38	chr7:84172414..84174090-chr7:84421942..84424878,2	K562	blood:
39	chr7:84250435..84252517-chr7:84252923..84255018,2	K562	blood:
40	chr7:84275439..84277976-chr7:84279778..84282553,2	K562	blood:
41	chr7:84165588..84166207-chr7:84499370..84499987,2	MCF-7	breast:
42	chr7:84297350..84299961-chr7:84307072..84309162,3	K562	blood:
43	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
44	chr7:84215550..84219199-chr7:84222001..84225003,3	K562	blood:
45	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
46	chr7:84165204..84166004-chr7:84499385..84500020,2	MCF-7	breast:
47	chr7:84165149..84165684-chr7:84582450..84583007,2	MCF-7	breast:
48	chr7:84165144..84166088-chr7:84499191..84500054,5	MCF-7	breast:
49	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
50	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-2	chr7:84178522-84178569	XLOC_006159
2	lnc-GRM3-2	chr7:84200294-84200423	NONHSAT121790
3	lnc-GRM3-2	chr7:84161792-84161923	XLOC_006159
4	lnc-GRM3-2	chr7:84178463-84178569	XLOC_006159
5	lnc-GRM3-2	chr7:84178463-84178569	NR_110080
6	lnc-GRM3-2	chr7:84200295-84204159	XLOC_006159
7	lnc-GRM3-2	chr7:84161792-84161923	NR_110080
8	lnc-GRM3-2	chr7:84213466-84213638	NONHSAT121790
9	lnc-GRM3-2	chr7:84213467-84213634	NR_110080
10	lnc-GRM3-2	chr7:84178521-84178569	NONHSAT121790
11	lnc-GRM3-2	chr7:84200295-84200423	XLOC_006159
12	lnc-GRM3-2	chr7:84213467-84213638	XLOC_006159
13	lnc-GRM3-2	chr7:84200295-84200423	NR_110080

No data

Variant related genes	Relation type
ENSG00000235139	TF binding region
RPL7P30	TF binding region
ENSG00000265050	TF binding region
ENSG00000235139	CpG island
RPL7P30	CpG island
ENSG00000265050	CpG island
ENSG00000184260	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000196542	chromatin interactions
ENSG00000202077	chromatin interactions
ARFGEF1	miRNA target sites
ARHGAP1	miRNA target sites
ARFIP1	miRNA target sites

Extended variants
information (count: 4772 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4772 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2715048	chr7:84158180-84158181	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142907540	chr7:84158213-84158214	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs184626715	chr7:84158243-84158244	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs137874798	chr7:84158245-84158246	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs149453623	chr7:84158310-84158311	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs554003192	chr7:84158323-84158324	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs576968973	chr7:84158344-84158345	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs544046655	chr7:84158346-84158347	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs78075950	chr7:84158451-84158452	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs529919622	chr7:84158535-84158536	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs147151237	chr7:84158541-84158542	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs560107145	chr7:84158570-84158571	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs1014498	chr7:84158588-84158589	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552644462	chr7:84158603-84158604	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs570831294	chr7:84158604-84158605	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs74553959	chr7:84158616-84158617	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs34768110	chr7:84158639-84158640	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs140399886	chr7:84158680-84158681	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs116246232	chr7:84158767-84158768	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs543204743	chr7:84158775-84158776	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs536152077	chr7:84158782-84158783	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs142754955	chr7:84158849-84158850	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs554645283	chr7:84158857-84158858	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs572885036	chr7:84158865-84158866	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs187050931	chr7:84158911-84158912	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs558639431	chr7:84158969-84158970	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs576827321	chr7:84158986-84158987	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs191897326	chr7:84159022-84159023	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs184235329	chr7:84159044-84159045	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs574435052	chr7:84159059-84159060	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs557192213	chr7:84159063-84159064	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs541732578	chr7:84159075-84159076	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs147288780	chr7:84159152-84159153	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs527708422	chr7:84159173-84159174	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs80078150	chr7:84159315-84159316	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs565129678	chr7:84159370-84159371	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs577227291	chr7:84159415-84159416	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs17231124	chr7:84159432-84159433	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553329154	chr7:84159434-84159435	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs550396535	chr7:84159436-84159437	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs572842555	chr7:84159458-84159459	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs78512839	chr7:84159488-84159489	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs529468019	chr7:84159578-84159579	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs548110758	chr7:84159589-84159590	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs189646764	chr7:84159639-84159640	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs148775482	chr7:84159644-84159645	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs561574560	chr7:84159667-84159668	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs558249282	chr7:84159700-84159701	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs182066616	chr7:84159703-84159704	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs537538577	chr7:84159712-84159713	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84153200-84158800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:84154800-84158200	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:84155000-84158400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:84155000-84158400	Weak transcription	HSMM	muscle
5	chr7:84155000-84158400	Weak transcription	HUVEC	blood vessel
6	chr7:84155000-84158400	Weak transcription	NHLF	lung
7	chr7:84155000-84158400	Weak transcription	Osteobl	bone
8	chr7:84155000-84158600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:84155000-84158600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr7:84155000-84158800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:84155000-84158800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:84155200-84158200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr7:84155200-84158400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:84156600-84158200	Enhancers	A549	lung
15	chr7:84157400-84160800	Enhancers	Hela-S3	cervix
16	chr7:84157600-84158600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:84157600-84159600	Enhancers	Fetal Intestine Large	intestine
18	chr7:84157600-84162400	Enhancers	Fetal Intestine Small	intestine
19	chr7:84157800-84158400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:84158000-84158200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:84158000-84158600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr7:84158000-84159200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:84158000-84160000	Enhancers	NHEK	skin
24	chr7:84158000-84160800	Enhancers	NHDF-Ad	bronchial
25	chr7:84158200-84158600	Flanking Active TSS	A549	lung
26	chr7:84158200-84159400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:84158200-84159400	Enhancers	Colon Smooth Muscle	Colon
28	chr7:84158200-84159600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr7:84158200-84161000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:84158400-84159600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:84158400-84159600	Enhancers	HSMM	muscle
32	chr7:84158400-84159600	Enhancers	HUVEC	blood vessel
33	chr7:84158400-84159600	Enhancers	NHLF	lung
34	chr7:84158400-84159600	Enhancers	Osteobl	bone
35	chr7:84158400-84160000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:84158400-84162600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:84158600-84159000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr7:84158600-84159000	Enhancers	A549	lung
39	chr7:84158600-84159200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:84158600-84160000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:84158600-84160600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr7:84158600-84161200	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:84158800-84159200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:84158800-84159200	Enhancers	Fetal Lung	lung
45	chr7:84158800-84159400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:84158800-84159400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:84158800-84159400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:84158800-84159400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr7:84158800-84159600	Enhancers	Stomach Mucosa	stomach
50	chr7:84158800-84159600	Enhancers	HMEC	breast

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