Variant report

Variant	nsv8197
Chromosome Location	chr7:105160920-105166965
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:856)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 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	chr7:105162532-105162842	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:105162675-105163137	K562	blood:	n/a	n/a
3	ATF2	chr7:105162441-105162701	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr7:105162419-105162922	K562	blood:	n/a	chr7:105162516-105162525
5	ATF3	chr7:105162479-105162756	A549	lung:	n/a	chr7:105162516-105162525
6	BACH1	chr7:105161884-105162223	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:105162629-105162935	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr7:105162453-105163079	A549	lung:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
9	BCLAF1	chr7:105162157-105163019	K562	blood:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
10	BHLHE40	chr7:105162519-105162872	HepG2	liver:	n/a	n/a
11	BHLHE40	chr7:105162517-105162823	A549	lung:	n/a	n/a
12	BHLHE40	chr7:105161948-105162953	HepG2	liver:	n/a	n/a
13	BHLHE40	chr7:105161582-105163259	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:105161610-105163105	K562	blood:	n/a	n/a
15	BRCA1	chr7:105161980-105162068	HepG2	liver:	n/a	n/a
16	BRCA1	chr7:105162680-105163061	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr7:105161716-105162247	K562	blood:	n/a	n/a
18	CBX3	chr7:105161068-105162276	K562	blood:	n/a	n/a
19	CBX3	chr7:105162379-105163324	K562	blood:	n/a	n/a
20	CCNT2	chr7:105161929-105162925	K562	blood:	n/a	n/a
21	CEBPB	chr7:105161176-105161715	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:105162864-105163023	K562	blood:	n/a	n/a
23	CEBPB	chr7:105162902-105163102	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:105162520-105163052	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:105161508-105161638	K562	blood:	n/a	n/a
26	CEBPD	chr7:105162390-105162874	HepG2	liver:	n/a	n/a
27	CEBPD	chr7:105162498-105162799	HepG2	liver:	n/a	n/a
28	CEBPD	chr7:105161796-105162088	HepG2	liver:	n/a	n/a
29	CEBPD	chr7:105161926-105162999	K562	blood:	n/a	n/a
30	CHD1	chr7:105162764-105163049	GM12878	blood:	n/a	n/a
31	CHD1	chr7:105161539-105162631	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr7:105161623-105162050	GM12878	blood:	n/a	n/a
33	CHD2	chr7:105161918-105163033	K562	blood:	n/a	n/a
34	CHD2	chr7:105161632-105162268	GM12878	blood:	n/a	n/a
35	CHD2	chr7:105162556-105163139	GM12878	blood:	n/a	n/a
36	CHD2	chr7:105161777-105161979	HepG2	liver:	n/a	n/a
37	CHD2	chr7:105161819-105162990	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr7:105162343-105162950	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr7:105162369-105162482	HepG2	liver:	n/a	n/a
40	CREB1	chr7:105161625-105163171	HepG2	liver:	n/a	n/a
41	CREB1	chr7:105161701-105163437	K562	blood:	n/a	n/a
42	CREB1	chr7:105162133-105162928	A549	lung:	n/a	n/a
43	CREB1	chr7:105162584-105162825	A549	lung:	n/a	n/a
44	CTCF	chr7:105162760-105162910	AG04449	skin:	n/a	n/a
45	CTCF	chr7:105161900-105162050	GM12869	blood:	n/a	n/a
46	CTCF	chr7:105161835-105161909	K562	blood:	n/a	n/a
47	CTCF	chr7:105162780-105162930	AG09319	gingival:	n/a	n/a
48	CTCF	chr7:105162800-105162950	Caco-2	colon:	n/a	n/a
49	CTCF	chr7:105162340-105162490	GM12866	blood:	n/a	n/a
50	CTCF	chr7:105162040-105162190	SK-N-SH_RA	brain:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105162878-105162928	SK-N-MC	brain:	n/a
2	chr7:105162941-105162991	AG04449	skin:	fetal
3	chr7:105162878-105162928	SK-N-MC	brain:	n/a
4	chr7:105162941-105162991	AG04449	skin:	fetal
5	chr7:105162600-105162650	HIPEpiC	eye:	n/a
6	chr7:105162878-105162928	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:105165592-105165642	HNPCEpiC	eye:	n/a
8	chr7:105162941-105162991	LNCaP	prostate:	n/a
9	chr7:105162814-105162864	GM06990	blood:	n/a
10	chr7:105162941-105162991	BJ	skin:	n/a
11	chr7:105162859-105162909	BJ	skin:	n/a
12	chr7:105162600-105162650	H1-hESC	embryonic stem cell:	embryo
13	chr7:105162735-105162785	GM12892	blood:	n/a
14	chr7:105162761-105162811	CMK	blood:	n/a
15	chr7:105162888-105162938	HRE	kidney:	n/a
16	chr7:105162735-105162785	BE2_C	brain:	n/a
17	chr7:105162878-105162928	AG04450	lung:	fetal
18	chr7:105162941-105162991	BE2_C	brain:	n/a
19	chr7:105162600-105162650	GM12892	blood:	n/a
20	chr7:105162814-105162864	AoSMC	blood vessel:	n/a
21	chr7:105162878-105162928	Hela-S3	cervix:	n/a
22	chr7:105163736-105163786	SAEC	small airway:	n/a
23	chr7:105162888-105162938	SAEC	small airway:	n/a
24	chr7:105162888-105162938	Hela-S3	cervix:	n/a
25	chr7:105165592-105165642	GM12878	blood:	n/a
26	chr7:105162855-105162905	NB4	blood:	n/a
27	chr7:105162470-105162520	Caco-2	colon:	n/a
28	chr7:105162600-105162650	SK-N-SH_RA	brain:	n/a
29	chr7:105162878-105162928	HCF	heart:	n/a
30	chr7:105162470-105162520	HNPCEpiC	eye:	n/a
31	chr7:105162888-105162938	CMK	blood:	n/a
32	chr7:105162855-105162905	K562	blood:	n/a
33	chr7:105162941-105162991	GM12891	blood:	n/a
34	chr7:105162577-105162627	HCT-116	colon:	n/a
35	chr7:105162941-105162991	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:105162878-105162928	GM12878	blood:	n/a
37	chr7:105162859-105162909	BE2_C	brain:	n/a
38	chr7:105162855-105162905	HRPEpiC	eye:	n/a
39	chr7:105162814-105162864	HL-60	blood:	n/a
40	chr7:105162859-105162909	PrEC	prostate:	n/a
41	chr7:105162577-105162627	CMK	blood:	n/a
42	chr7:105162855-105162905	PrEC	prostate:	n/a
43	chr7:105162470-105162520	GM12891	blood:	n/a
44	chr7:105162470-105162520	SKMC	muscle:	n/a
45	chr7:105162878-105162928	T-47D	breast:	n/a
46	chr7:105162941-105162991	SK-N-SH_RA	brain:	n/a
47	chr7:105162761-105162811	HIPEpiC	eye:	n/a
48	chr7:105162878-105162928	PANC-1	pancreas:	n/a
49	chr7:105165592-105165642	NHDF-neo	bronchial:	n/a
50	chr7:105165592-105165642	AG09319	gingival:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:33914164..33914765-chr7:105161584..105162384,2	Hela-S3	cervix:
2	chr17:19551197..19552117-chr7:105161941..105162797,2	Hela-S3	cervix:
3	chr7:104653054..104655993-chr7:105161169..105164095,3	MCF-7	breast:
4	chr7:105083591..105086006-chr7:105160365..105162043,2	K562	blood:
5	chr7:105165463..105169628-chr7:105170973..105174351,5	MCF-7	breast:
6	chr7:105160846..105164326-chr7:105166102..105168555,5	MCF-7	breast:
7	chr7:105148185..105149870-chr7:105160014..105161672,2	K562	blood:
8	chr7:105162283..105162894-chr7:105172462..105173034,2	NB4	blood:
9	chr7:104653151..104655503-chr7:105160083..105164345,7	K562	blood:
10	chr7:105160261..105165362-chr7:105168599..105174293,22	MCF-7	breast:
11	chr5:148110184..148110980-chr7:105164824..105165344,2	MCF-7	breast:
12	chr5:10249794..10250737-chr7:105161803..105162758,2	Hela-S3	cervix:
13	chr7:105161082..105163079-chr7:105240360..105242686,2	K562	blood:
14	chr7:105161098..105164204-chr7:105164483..105168107,5	MCF-7	breast:
15	chr17:56708735..56709467-chr7:105162240..105162879,2	MCF-7	breast:
16	chr17:41465807..41466363-chr7:105162224..105162878,2	NB4	blood:
17	chr7:105143860..105147794-chr7:105158802..105162576,5	K562	blood:
18	chr7:105162077..105162858-chr7:105172193..105173344,3	MCF-7	breast:
19	chr7:105160926..105162522-chr7:105329627..105332211,2	K562	blood:
20	chr7:104772977..104775390-chr7:105160456..105162601,2	K562	blood:
21	chr19:55628556..55629065-chr7:105162615..105163265,2	Hela-S3	cervix:
22	chr7:105158727..105165017-chr7:105166972..105176993,56	K562	blood:
23	chr6:96969151..96969942-chr7:105161938..105162970,3	Hela-S3	cervix:
24	chr7:105027746..105030082-chr7:105160759..105163665,5	MCF-7	breast:
25	chr7:105160687..105164718-chr7:105170642..105174239,14	MCF-7	breast:
26	chr7:105026529..105029377-chr7:105162488..105165118,2	MCF-7	breast:
27	chr7:105161102..105162655-chr7:105181498..105183213,2	K562	blood:
28	chr19:1261170..1262083-chr7:105162048..105162685,2	Hela-S3	cervix:
29	chr7:105165151..105169952-chr7:105171142..105174252,8	MCF-7	breast:
30	chr7:105159598..105163989-chr7:105219696..105223115,7	MCF-7	breast:
31	chr7:105162459..105163197-chr7:105172183..105173025,3	MCF-7	breast:
32	chr7:104652163..104655972-chr7:105160292..105163807,4	MCF-7	breast:
33	chr7:105164878..105167399-chrX:150160313..150162804,2	MCF-7	breast:
34	chr7:65958424..65959012-chr7:105162357..105162865,2	NB4	blood:
35	chr1:209957159..209957989-chr7:105162027..105162579,2	Hela-S3	cervix:
36	chr7:105162231..105163027-chr7:105172004..105172750,2	K562	blood:
37	chr7:105160711..105163604-chr7:105655467..105658687,3	K562	blood:
38	chr1:156698268..156698938-chr7:105162358..105162859,2	Hela-S3	cervix:
39	chr7:105148472..105150405-chr7:105160556..105162918,2	MCF-7	breast:
40	chr7:104653151..104655346-chr7:105160083..105164134,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223886	TF binding region
PUS7	TF binding region
ENSG00000223886	CpG island
PUS7	CpG island
ENSG00000072210	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000233797	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000014123	chromatin interactions
ENSG00000185055	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000223886	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000230508	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000239569	chromatin interactions

Extended variants
information (count: 280 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202165929	chr7:105160927-105160928	Weak transcription Strong transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs372341473	chr7:105160946-105160947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs186708689	chr7:105160951-105160952	Weak transcription Strong transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs61131839	chr7:105160966-105160967	Weak transcription Strong transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs147942711	chr7:105160967-105160968	Weak transcription Strong transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs575552967	chr7:105160976-105160977	Weak transcription Strong transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs143327743	chr7:105161012-105161013	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs534450634	chr7:105161015-105161016	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs191611749	chr7:105161062-105161063	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs141620955	chr7:105161117-105161118	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs577538575	chr7:105161127-105161128	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs62486983	chr7:105161146-105161147	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564983941	chr7:105161163-105161164	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs148453677	chr7:105161190-105161191	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs527236498	chr7:105161201-105161202	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs73190172	chr7:105161210-105161211	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73190174	chr7:105161216-105161217	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529927559	chr7:105161221-105161222	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs118134111	chr7:105161229-105161230	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs569484910	chr7:105161236-105161237	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs532190929	chr7:105161270-105161271	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs552210787	chr7:105161277-105161278	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs138643172	chr7:105161333-105161334	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs535162386	chr7:105161390-105161391	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs184888184	chr7:105161412-105161413	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs551496989	chr7:105161447-105161448	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs377423767	chr7:105161472-105161473	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs560958499	chr7:105161493-105161494	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs536192105	chr7:105161499-105161500	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs370554206	chr7:105161554-105161555	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs568470137	chr7:105161647-105161648	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs528265854	chr7:105161661-105161662	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs190484642	chr7:105161666-105161667	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs577475061	chr7:105161681-105161682	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs546425367	chr7:105161683-105161684	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs138185775	chr7:105161685-105161686	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs141802752	chr7:105161722-105161723	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs73190175	chr7:105161735-105161736	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs711427	chr7:105161755-105161756	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs73190178	chr7:105161839-105161840	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs148152188	chr7:105161846-105161847	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
42	rs6954598	chr7:105161894-105161895	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs537380098	chr7:105161969-105161970	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs543278702	chr7:105162145-105162146	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
45	rs549632193	chr7:105162149-105162150	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
46	rs4730094	chr7:105162183-105162184	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
47	rs532320146	chr7:105162212-105162213	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
48	rs62486984	chr7:105162249-105162250	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs200474347	chr7:105162267-105162268	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
50	rs559534582	chr7:105162273-105162274	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105080000-105161200	Weak transcription	Pancreas	Pancrea
2	chr7:105124400-105161800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr7:105128600-105161200	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:105128600-105161600	Weak transcription	Brain Substantia Nigra	brain
5	chr7:105128800-105161200	Weak transcription	Brain Angular Gyrus	brain
6	chr7:105134400-105161200	Weak transcription	Brain Anterior Caudate	brain
7	chr7:105134800-105161600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:105137800-105161200	Weak transcription	NHDF-Ad	bronchial
9	chr7:105137800-105161200	Weak transcription	NHLF	lung
10	chr7:105141000-105161800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr7:105141400-105161200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr7:105141400-105161200	Weak transcription	Fetal Brain Male	brain
13	chr7:105141400-105161400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr7:105141600-105161200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr7:105141600-105161400	Weak transcription	Primary B cells from cord blood	blood
16	chr7:105143000-105161200	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr7:105143000-105161200	Weak transcription	Esophagus	oesophagus
18	chr7:105143000-105161200	Weak transcription	Placenta	Placenta
19	chr7:105143000-105161200	Weak transcription	Ovary	ovary
20	chr7:105143000-105161200	Weak transcription	Spleen	Spleen
21	chr7:105143000-105161600	Weak transcription	Aorta	Aorta
22	chr7:105143000-105161800	Weak transcription	Thymus	Thymus
23	chr7:105143400-105161400	Weak transcription	Fetal Brain Female	brain
24	chr7:105143800-105161200	Weak transcription	Lung	lung
25	chr7:105143800-105161400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr7:105144200-105161200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr7:105145400-105161200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr7:105146200-105161400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:105146200-105161400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr7:105146200-105161600	Weak transcription	Fetal Intestine Large	intestine
31	chr7:105146200-105161800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:105146600-105161200	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr7:105146800-105161200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:105146800-105161200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:105146800-105161200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr7:105147200-105161200	Weak transcription	HSMMtube	muscle
37	chr7:105147400-105161600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr7:105148800-105161200	Weak transcription	Fetal Muscle Trunk	muscle
39	chr7:105149000-105161200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr7:105149000-105161200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr7:105149000-105161200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr7:105149000-105161200	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr7:105149000-105161200	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr7:105149000-105161200	Weak transcription	HSMM	muscle
45	chr7:105149000-105161400	Weak transcription	Primary B cells from peripheral blood	blood
46	chr7:105149000-105161400	Weak transcription	Primary T cells from cord blood	blood
47	chr7:105149000-105161400	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr7:105149000-105161400	Weak transcription	Adipose Nuclei	Adipose
49	chr7:105149000-105161600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr7:105149200-105161200	Weak transcription	Liver	Liver

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