Variant report

Variant	nsv1017196
Chromosome Location	chr7:8307760-8406277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1114)
CpG islands
(count:245)
Chromatin interactive
region (count:94)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:8364734-8364927	K562	blood:	n/a	n/a
2	ARID3A	chr7:8317118-8317430	K562	blood:	n/a	n/a
3	ARID3A	chr7:8343584-8343742	K562	blood:	n/a	n/a
4	ARID3A	chr7:8335663-8336040	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:8335603-8336008	K562	blood:	n/a	n/a
6	ATF1	chr7:8335718-8336040	K562	blood:	n/a	n/a
7	ATF1	chr7:8330353-8330861	K562	blood:	n/a	n/a
8	ATF3	chr7:8343611-8343854	K562	blood:	n/a	n/a
9	ATF3	chr7:8330598-8330811	K562	blood:	n/a	n/a
10	BACH1	chr7:8336305-8336447	K562	blood:	n/a	n/a
11	BACH1	chr7:8364354-8364374	K562	blood:	n/a	n/a
12	BCL11A	chr7:8405176-8405398	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr7:8330795-8330896	K562	blood:	n/a	n/a
14	BHLHE40	chr7:8382172-8382211	K562	blood:	n/a	n/a
15	BHLHE40	chr7:8400273-8400390	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:8343540-8344243	K562	blood:	n/a	n/a
17	BRCA1	chr7:8365789-8365829	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:8335623-8335701	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:8405240-8405325	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:8335519-8336094	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr7:8343517-8344202	K562	blood:	n/a	n/a
22	CBX3	chr7:8359075-8359483	K562	blood:	n/a	n/a
23	CBX3	chr7:8335671-8336151	K562	blood:	n/a	n/a
24	CBX3	chr7:8352681-8353082	K562	blood:	n/a	n/a
25	CBX3	chr7:8335575-8336223	HCT-116	colon:	n/a	n/a
26	CCNT2	chr7:8343548-8344028	K562	blood:	n/a	n/a
27	CEBPB	chr7:8330606-8330901	K562	blood:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760
28	CEBPB	chr7:8403357-8403534	K562	blood:	n/a	n/a
29	CEBPB	chr7:8330601-8331017	ECC-1	luminal epithelium:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760
30	CEBPB	chr7:8389152-8389379	HepG2	liver:	n/a	chr7:8389236-8389244
31	CEBPB	chr7:8330611-8331009	Hela-S3	cervix:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760
32	CEBPB	chr7:8330385-8331260	MCF-7	breast:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760
33	CEBPB	chr7:8335635-8336048	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:8343462-8344101	K562	blood:	n/a	n/a
35	CEBPB	chr7:8336267-8336332	K562	blood:	n/a	n/a
36	CEBPB	chr7:8390322-8390522	IMR90	lung:	n/a	chr7:8390387-8390398
37	CEBPB	chr7:8343476-8343602	K562	blood:	n/a	n/a
38	CEBPB	chr7:8330520-8330920	K562	blood:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760
39	CEBPB	chr7:8343428-8344106	K562	blood:	n/a	n/a
40	CEBPB	chr7:8322385-8322690	HepG2	liver:	n/a	chr7:8322529-8322540
41	CEBPB	chr7:8330584-8330903	H1-hESC	embryonic stem cell:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760
42	CEBPB	chr7:8359885-8360053	K562	blood:	n/a	n/a
43	CEBPB	chr7:8390227-8390577	K562	blood:	n/a	chr7:8390314-8390325 chr7:8390387-8390398 chr7:8390312-8390325 chr7:8390314-8390325
44	CEBPB	chr7:8390294-8390426	A549	lung:	n/a	chr7:8390314-8390325 chr7:8390387-8390398 chr7:8390312-8390325 chr7:8390314-8390325
45	CEBPB	chr7:8390226-8390559	HepG2	liver:	n/a	chr7:8390314-8390325 chr7:8390387-8390398 chr7:8390312-8390325 chr7:8390314-8390325
46	CEBPB	chr7:8402366-8402882	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr7:8380396-8380678	HepG2	liver:	n/a	chr7:8380542-8380555 chr7:8380542-8380555 chr7:8380542-8380553 chr7:8380544-8380555
48	CEBPB	chr7:8330561-8331101	K562	blood:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760
49	CEBPB	chr7:8313800-8313929	A549	lung:	n/a	n/a
50	CEBPB	chr7:8330379-8331245	MCF-7	breast:	n/a	chr7:8330748-8330761 chr7:8330748-8330759 chr7:8330749-8330760

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:8343477-8343527	SK-N-SH	brain:	n/a
2	chr7:8343477-8343527	SK-N-SH	brain:	n/a
3	chr7:8383356-8383406	ECC-1	luminal epithelium:	n/a
4	chr7:8402871-8402921	HAEpiC	amniotic membrane:	n/a
5	chr7:8343477-8343527	HRPEpiC	eye:	n/a
6	chr7:8402871-8402921	ovcar-3	ovarian:	n/a
7	chr7:8343477-8343527	HCF	heart:	n/a
8	chr7:8383356-8383406	NB4	blood:	n/a
9	chr7:8383356-8383406	NHDF-neo	bronchial:	n/a
10	chr7:8343477-8343527	HRE	kidney:	n/a
11	chr7:8343477-8343527	BE2_C	brain:	n/a
12	chr7:8343477-8343527	LNCaP	prostate:	n/a
13	chr7:8402871-8402921	MCF10A-Er-Src	breast:	n/a
14	chr7:8383356-8383406	HRCEpiC	kidney:	n/a
15	chr7:8343477-8343527	SAEC	small airway:	n/a
16	chr7:8383869-8383919	SK-N-SH_RA	brain:	n/a
17	chr7:8383869-8383919	BE2_C	brain:	n/a
18	chr7:8383869-8383919	HAEpiC	amniotic membrane:	n/a
19	chr7:8383869-8383919	PFSK-1	brain:	n/a
20	chr7:8383356-8383406	H1-hESC	embryonic stem cell:	embryo
21	chr7:8402871-8402921	AG09309	skin:	n/a
22	chr7:8383869-8383919	T-47D	breast:	n/a
23	chr7:8402871-8402921	HNPCEpiC	eye:	n/a
24	chr7:8383356-8383406	A549	lung:	n/a
25	chr7:8383356-8383406	PANC-1	pancreas:	n/a
26	chr7:8383356-8383406	HRE	kidney:	n/a
27	chr7:8402871-8402921	MCF-7	breast:	n/a
28	chr7:8383869-8383919	BJ	skin:	n/a
29	chr7:8343477-8343527	SKMC	muscle:	n/a
30	chr7:8383356-8383406	AG04450	lung:	fetal
31	chr7:8343477-8343527	HepG2	liver:	n/a
32	chr7:8402871-8402921	GM06990	blood:	n/a
33	chr7:8383356-8383406	HCT-116	colon:	n/a
34	chr7:8383356-8383406	SKMC	muscle:	n/a
35	chr7:8383869-8383919	Hepatocyte	liver:	n/a
36	chr7:8402871-8402921	SKMC	muscle:	n/a
37	chr7:8402871-8402921	HUVEC	blood vessel:	n/a
38	chr7:8383356-8383406	GM06990	blood:	n/a
39	chr7:8343477-8343527	PANC-1	pancreas:	n/a
40	chr7:8402871-8402921	HIPEpiC	eye:	n/a
41	chr7:8402871-8402921	NHBE	bronchial:	n/a
42	chr7:8402871-8402921	A549	lung:	n/a
43	chr7:8343477-8343527	AG04449	skin:	fetal
44	chr7:8402871-8402921	HCF	heart:	n/a
45	chr7:8343477-8343527	HNPCEpiC	eye:	n/a
46	chr7:8402871-8402921	AG10803	skin:	n/a
47	chr7:8383356-8383406	ovcar-3	ovarian:	n/a
48	chr7:8402871-8402921	BE2_C	brain:	n/a
49	chr7:8402871-8402921	CMK	blood:	n/a
50	chr7:8402871-8402921	HEEpiC	esophagus:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:8300758..8303193-chr7:8315845..8318781,2	K562	blood:
2	chr7:8372140..8374996-chr7:8377219..8379253,2	MCF-7	breast:
3	chr7:8372140..8374996-chr7:8377219..8379253,2	MCF-7	breast:
4	chr7:8257240..8257766-chr7:8404862..8405637,2	MCF-7	breast:
5	chr7:7635151..7635721-chr7:8335409..8336300,2	K562	blood:
6	chr7:8321368..8324364-chr7:8332631..8334637,2	K562	blood:
7	chr7:8317034..8317682-chr7:8332241..8332845,2	MCF-7	breast:
8	chr7:8316765..8317280-chr7:8335499..8336119,2	K562	blood:
9	chr7:8404670..8406317-chr7:8430221..8432474,2	K562	blood:
10	chr7:8375674..8377816-chr7:8381555..8383560,2	K562	blood:
11	chr7:8354820..8356467-chr7:8360272..8362117,2	K562	blood:
12	chr7:8316804..8317671-chr7:8404378..8405905,6	MCF-7	breast:
13	chr7:8314601..8320359-chr7:8321544..8326844,6	K562	blood:
14	chr7:8353412..8355160-chr7:8364967..8367694,2	MCF-7	breast:
15	chr7:8342220..8345291-chr7:8349412..8353003,4	K562	blood:
16	chr7:8298365..8304526-chr7:8319374..8323828,6	K562	blood:
17	chr7:8381608..8383646-chr7:8392163..8393993,2	K562	blood:
18	chr7:8343127..8345217-chr7:8371849..8373432,2	MCF-7	breast:
19	chr7:8365461..8367052-chr7:8371679..8374090,2	MCF-7	breast:
20	chr7:8300256..8302518-chr7:8311230..8313576,2	MCF-7	breast:
21	chr7:8299901..8303974-chr7:8313052..8315434,4	K562	blood:
22	chr7:8316765..8317280-chr7:8335499..8336119,2	K562	blood:
23	chr7:7958467..7959967-chr7:8328195..8331123,2	K562	blood:
24	chr7:8298365..8300507-chr7:8320944..8323781,2	K562	blood:
25	chr7:8257061..8257622-chr7:8334918..8335755,2	MCF-7	breast:
26	chr7:8314102..8315802-chr7:8320914..8322938,2	MCF-7	breast:
27	chr7:8266864..8269021-chr7:8312151..8314215,2	MCF-7	breast:
28	chr7:8394059..8396898-chr7:8397727..8400702,2	K562	blood:
29	chr7:8307037..8309369-chr7:8314305..8316085,2	K562	blood:
30	chr7:8343821..8345598-chr7:8381541..8384525,2	K562	blood:
31	chr7:8335652..8336362-chr7:8404897..8405424,2	MCF-7	breast:
32	chr7:8316930..8317631-chr7:8335419..8336132,2	MCF-7	breast:
33	chr7:8322139..8324176-chr7:8327086..8329541,2	K562	blood:
34	chr7:8346660..8349456-chr7:8350822..8352856,2	K562	blood:
35	chr7:8354820..8356467-chr7:8360272..8362117,2	K562	blood:
36	chr7:8375674..8377816-chr7:8381555..8383560,2	K562	blood:
37	chr7:8335652..8336362-chr7:8404897..8405424,2	MCF-7	breast:
38	chr7:8299685..8303451-chr7:8328516..8331674,6	MCF-7	breast:
39	chr7:8397672..8399753-chr7:8401656..8404422,2	MCF-7	breast:
40	chr7:8322139..8324176-chr7:8327086..8329541,2	K562	blood:
41	chr7:8316930..8317631-chr7:8335419..8336132,2	MCF-7	breast:
42	chr7:8314601..8320359-chr7:8321544..8326844,6	K562	blood:
43	chr7:8283296..8285798-chr7:8310323..8312776,2	K562	blood:
44	chr6:18239538..18240523-chr7:8309954..8310661,2	MCF-7	breast:
45	chr7:8317034..8317682-chr7:8332241..8332845,2	MCF-7	breast:
46	chr7:8363447..8366490-chr7:8366907..8369516,4	K562	blood:
47	chr7:8354641..8357967-chr7:8360617..8365260,4	K562	blood:
48	chr7:8305496..8307351-chr7:8315240..8317891,2	K562	blood:
49	chr7:8322298..8327046-chr7:8329175..8332951,4	MCF-7	breast:
50	chr7:8300371..8302802-chr7:8361359..8363095,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NXPH1-4	chr7:8349280-8349445	ucscGeneNc_uc003srt_1
2	lnc-ICA1-4	chr7:8383337-8384124	NONHSAT119157
3	lnc-GLCCI1-2	chr7:8382755-8382920	ENSG00000229970
4	lnc-GLCCI1-2	chr7:8343371-8343426	ENSG00000229970
5	lnc-GLCCI1-2	chr7:8380647-8380973	ENSG00000229970
6	lnc-NXPH1-4	chr7:8346538-8346711	ucscGeneNc_uc003srt_1
7	lnc-GLCCI1-2	chr7:8383337-8384146	ENSG00000229970
8	lnc-NXPH1-4	chr7:8349862-8350671	ucscGeneNc_uc003srt_1
9	lnc-ICA1-4	chr7:8382797-8382916	NONHSAT119157
10	lnc-NXPH1-4	chr7:8347172-8347381	ucscGeneNc_uc003srt_1
11	lnc-GLCCI1-2	chr7:8380013-8380186	ENSG00000229970
12	lnc-ICA1-4	chr7:8393976-8394033	NONHSAT119157
13	lnc-GLCCI1-2	chr7:8380647-8380856	ENSG00000229970
14	lnc-GLCCI1-2	chr7:8380013-8380186	ENSG00000229970
15	lnc-NXPH1-2	chr7:8384553-8387652	NONHSAT119158

No data

Variant related genes	Relation type
ENSG00000272328	TF binding region
ENSG00000272328	CpG island
ENSG00000153363	chromatin interactions
ENSG00000229970	chromatin interactions
ENSG00000106415	chromatin interactions
ENSG00000272328	chromatin interactions
ENSG00000003147	chromatin interactions
ENSG00000233108	chromatin interactions
ENSG00000244239	chromatin interactions
SMARCC1	miRNA target sites
SSFA2	miRNA target sites
ERBB2IP	miRNA target sites
NVL	miRNA target sites
ZSCAN12	miRNA target sites

Extended variants
information (count: 4343 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4343 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6961662	chr7:8307760-8307761	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76013181	chr7:8307847-8307848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6965830	chr7:8307886-8307887	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs79269794	chr7:8307917-8307918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138872027	chr7:8307926-8307927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187068527	chr7:8307931-8307932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570547994	chr7:8307952-8307953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550441324	chr7:8307954-8307955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568607725	chr7:8307985-8307986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111652365	chr7:8308021-8308022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192554466	chr7:8308032-8308033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149298305	chr7:8308041-8308042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565407640	chr7:8308071-8308072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35277265	chr7:8308081-8308082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141727468	chr7:8308082-8308083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144525868	chr7:8308110-8308111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557289527	chr7:8308129-8308130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185294112	chr7:8308135-8308136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73061660	chr7:8308139-8308140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188563533	chr7:8308166-8308167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73238408	chr7:8308208-8308209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148064142	chr7:8308219-8308220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541188632	chr7:8308220-8308221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193084571	chr7:8308227-8308228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527743134	chr7:8308242-8308243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546231319	chr7:8308247-8308248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185037665	chr7:8308302-8308303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531729175	chr7:8308307-8308308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12531556	chr7:8308310-8308311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550236910	chr7:8308312-8308313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553520991	chr7:8308319-8308320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35618108	chr7:8308338-8308339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532413490	chr7:8308350-8308351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529484371	chr7:8308369-8308370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547537513	chr7:8308389-8308390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79654183	chr7:8308390-8308391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539187781	chr7:8308424-8308425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557424941	chr7:8308476-8308477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371954712	chr7:8308516-8308517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569336156	chr7:8308527-8308528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77201601	chr7:8308546-8308547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375280857	chr7:8308547-8308548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555388410	chr7:8308645-8308646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117968387	chr7:8308672-8308673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141771824	chr7:8308693-8308694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553165244	chr7:8308716-8308717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10273651	chr7:8308769-8308770	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546366318	chr7:8308781-8308782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111339502	chr7:8308783-8308784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs367577157	chr7:8308807-8308808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	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
Depressive disorder	21152026	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:8302400-8320400	Weak transcription	Fetal Heart	heart
2	chr7:8303000-8317800	Weak transcription	Pancreas	Pancrea
3	chr7:8306200-8308000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr7:8307600-8308600	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr7:8307800-8308600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr7:8308000-8308400	Enhancers	Primary hematopoietic stem cells	blood
7	chr7:8308000-8308400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:8308000-8308400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:8308000-8308600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr7:8308600-8309000	Enhancers	Fetal Intestine Large	intestine
11	chr7:8308600-8313800	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr7:8308600-8313800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:8308600-8314000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr7:8313800-8314200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr7:8313800-8314800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr7:8314000-8314800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr7:8314400-8314800	Enhancers	Hela-S3	cervix
18	chr7:8317800-8318200	Enhancers	Pancreas	Pancrea
19	chr7:8318200-8322000	Weak transcription	Pancreas	Pancrea
20	chr7:8319200-8326600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr7:8320400-8320600	Enhancers	Fetal Heart	heart
22	chr7:8320600-8321600	Weak transcription	Fetal Heart	heart
23	chr7:8321600-8325400	Enhancers	Fetal Heart	heart
24	chr7:8321800-8322200	Enhancers	Left Ventricle	heart
25	chr7:8322000-8322400	Enhancers	Pancreas	Pancrea
26	chr7:8322200-8323200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr7:8322200-8326600	Weak transcription	Left Ventricle	heart
28	chr7:8322400-8330200	Weak transcription	Pancreas	Pancrea
29	chr7:8322800-8323400	Enhancers	Placenta	Placenta
30	chr7:8323200-8327200	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr7:8324200-8324600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:8324800-8325200	Enhancers	Stomach Mucosa	stomach
33	chr7:8325200-8330400	Weak transcription	Stomach Mucosa	stomach
34	chr7:8325400-8326400	Weak transcription	Fetal Heart	heart
35	chr7:8325600-8325800	Enhancers	H9 Cell Line	embryonic stem cell
36	chr7:8325800-8326600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr7:8326400-8327800	Enhancers	Fetal Heart	heart
38	chr7:8326600-8326800	Enhancers	Left Ventricle	heart
39	chr7:8326600-8327000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:8326600-8327400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr7:8326600-8327400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:8326600-8329200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:8326800-8327200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:8326800-8327200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr7:8326800-8327600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr7:8326800-8327600	Weak transcription	Left Ventricle	heart
47	chr7:8326800-8328000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr7:8326800-8328800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr7:8327000-8327800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr7:8327000-8329600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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