Variant report

Variant	esv1797140
Chromosome Location	chr1:70604106-70724622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2148)
CpG islands
(count:1958)
Chromatin interactive
region (count:119)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:2148 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70687392-70687436	K562	blood:	n/a	n/a
2	ARID3A	chr1:70622219-70622512	K562	blood:	n/a	n/a
3	ARID3A	chr1:70671150-70671813	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:70670385-70670530	K562	blood:	n/a	n/a
5	ARID3A	chr1:70606204-70606214	K562	blood:	n/a	n/a
6	ARID3A	chr1:70685713-70686118	K562	blood:	n/a	n/a
7	ARID3A	chr1:70686778-70687628	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:70671280-70671917	K562	blood:	n/a	n/a
9	ATF1	chr1:70686896-70687222	K562	blood:	n/a	n/a
10	ATF1	chr1:70685744-70686062	K562	blood:	n/a	n/a
11	ATF1	chr1:70607942-70608040	K562	blood:	n/a	n/a
12	ATF1	chr1:70622256-70622578	K562	blood:	n/a	n/a
13	ATF1	chr1:70670789-70671821	K562	blood:	n/a	chr1:70671371-70671385
14	ATF2	chr1:70671030-70671771	GM12878	blood:	n/a	chr1:70671371-70671385
15	ATF2	chr1:70671068-70671594	H1-hESC	embryonic stem cell:	n/a	chr1:70671371-70671385
16	ATF2	chr1:70670980-70671719	GM12878	blood:	n/a	chr1:70671371-70671385
17	ATF2	chr1:70687416-70687795	GM12878	blood:	n/a	n/a
18	ATF2	chr1:70687385-70687790	GM12878	blood:	n/a	n/a
19	ATF2	chr1:70686740-70687470	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr1:70686837-70687147	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr1:70686755-70687325	GM12878	blood:	n/a	n/a
22	ATF3	chr1:70671086-70671520	HepG2	liver:	n/a	n/a
23	ATF3	chr1:70671078-70671489	K562	blood:	n/a	n/a
24	ATF3	chr1:70671000-70671590	HepG2	liver:	n/a	n/a
25	ATF3	chr1:70671051-70671587	A549	lung:	n/a	n/a
26	ATF3	chr1:70671031-70671659	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr1:70671037-70671604	K562	blood:	n/a	n/a
28	ATF3	chr1:70671040-70671604	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF3	chr1:70671015-70671489	K562	blood:	n/a	n/a
30	ATF3	chr1:70686879-70687149	K562	blood:	n/a	n/a
31	ATF3	chr1:70671202-70671457	GM12878	blood:	n/a	n/a
32	ATF3	chr1:70671046-70671594	GM12878	blood:	n/a	n/a
33	BACH1	chr1:70697205-70697461	K562	blood:	n/a	n/a
34	BACH1	chr1:70629532-70629602	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr1:70668015-70668084	K562	blood:	n/a	n/a
36	BACH1	chr1:70686894-70687290	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr1:70611113-70611144	K562	blood:	n/a	n/a
38	BACH1	chr1:70671146-70671582	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr1:70680392-70680405	K562	blood:	n/a	n/a
40	BATF	chr1:70668095-70668337	GM12878	blood:	n/a	n/a
41	BCL11A	chr1:70671170-70671559	GM12878	blood:	n/a	n/a
42	BCL3	chr1:70686713-70687297	A549	lung:	n/a	n/a
43	BCL3	chr1:70686837-70687516	GM12878	blood:	n/a	n/a
44	BCLAF1	chr1:70686739-70687982	GM12878	blood:	n/a	n/a
45	BCLAF1	chr1:70671018-70671950	K562	blood:	n/a	n/a
46	BCLAF1	chr1:70670947-70671765	GM12878	blood:	n/a	n/a
47	BCLAF1	chr1:70670972-70671697	GM12878	blood:	n/a	n/a
48	BCLAF1	chr1:70686816-70687458	GM12878	blood:	n/a	n/a
49	BHLHE40	chr1:70670886-70671703	K562	blood:	n/a	n/a
50	BHLHE40	chr1:70686401-70686402	K562	blood:	n/a	n/a

(count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70671216-70671266	PrEC	prostate:	n/a
2	chr1:70710389-70710439	Hepatocyte	liver:	n/a
3	chr1:70687506-70687556	AoSMC	blood vessel:	n/a
4	chr1:70687559-70687609	U87	brain:	n/a
5	chr1:70671146-70671196	GM12878	blood:	n/a
6	chr1:70687106-70687156	GM12892	blood:	n/a
7	chr1:70671216-70671266	PrEC	prostate:	n/a
8	chr1:70710389-70710439	Hepatocyte	liver:	n/a
9	chr1:70687506-70687556	AoSMC	blood vessel:	n/a
10	chr1:70687559-70687609	U87	brain:	n/a
11	chr1:70671146-70671196	GM12878	blood:	n/a
12	chr1:70687106-70687156	GM12892	blood:	n/a
13	chr1:70667229-70667279	HRPEpiC	eye:	n/a
14	chr1:70671216-70671266	U87	brain:	n/a
15	chr1:70687506-70687556	IMR90	lung:	fetal
16	chr1:70671119-70671169	HL-60	blood:	n/a
17	chr1:70671645-70671695	NH-A	brain:	n/a
18	chr1:70606906-70606956	HCPEpiC	choroid plexus:	n/a
19	chr1:70687415-70687465	GM12892	blood:	n/a
20	chr1:70671364-70671414	AG10803	skin:	n/a
21	chr1:70671639-70671689	HNPCEpiC	eye:	n/a
22	chr1:70670919-70670969	NB4	blood:	n/a
23	chr1:70710389-70710439	SK-N-SH_RA	brain:	n/a
24	chr1:70675418-70675468	GM12878	blood:	n/a
25	chr1:70671309-70671359	BJ	skin:	n/a
26	chr1:70710422-70710472	PFSK-1	brain:	n/a
27	chr1:70671186-70671236	HMEC	breast:	n/a
28	chr1:70671378-70671428	IMR90	lung:	fetal
29	chr1:70671441-70671491	NHBE	bronchial:	n/a
30	chr1:70687415-70687465	AG04449	skin:	fetal
31	chr1:70671186-70671236	NHDF-neo	bronchial:	n/a
32	chr1:70671186-70671236	GM12891	blood:	n/a
33	chr1:70671639-70671689	NT2-D1	testis:	n/a
34	chr1:70715648-70715698	HRE	kidney:	n/a
35	chr1:70671639-70671689	AG10803	skin:	n/a
36	chr1:70671639-70671689	ECC-1	luminal epithelium:	n/a
37	chr1:70606906-70606956	AG10803	skin:	n/a
38	chr1:70687124-70687174	T-47D	breast:	n/a
39	chr1:70671645-70671695	HAEpiC	amniotic membrane:	n/a
40	chr1:70684371-70684421	HEK293	kidney:	embryo
41	chr1:70710422-70710472	HAEpiC	amniotic membrane:	n/a
42	chr1:70684371-70684421	GM12878	blood:	n/a
43	chr1:70687415-70687465	RPTEC	kidney:	n/a
44	chr1:70710422-70710472	HCT-116	colon:	n/a
45	chr1:70671186-70671236	HRE	kidney:	n/a
46	chr1:70687506-70687556	HRPEpiC	eye:	n/a
47	chr1:70687301-70687351	ProgFib	skin:	n/a
48	chr1:70671441-70671491	MCF-7	breast:	n/a
49	chr1:70671260-70671310	SK-N-SH	brain:	n/a
50	chr1:70671762-70671812	HL-60	blood:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:70499914..70500706-chr1:70608453..70608981,2	MCF-7	breast:
2	chr1:70625805..70628227-chr1:70630477..70632879,2	K562	blood:
3	chr1:70670145..70673365-chr1:70675136..70679229,4	K562	blood:
4	chr1:70685799..70687948-chr1:70819964..70821804,2	MCF-7	breast:
5	chr1:70674179..70677274-chr1:70677921..70681026,3	K562	blood:
6	chr1:70671247..70672785-chr1:70672964..70674754,3	K562	blood:
7	chr1:70610824..70612517-chr1:70634874..70637196,2	K562	blood:
8	chr1:70608921..70611354-chr1:70613745..70615584,2	K562	blood:
9	chr1:70686774..70687532-chr11:76091229..76092168,2	HCT-116	colon:
10	chr1:70634010..70636931-chr1:70644146..70645771,2	K562	blood:
11	chr1:70637171..70639889-chr1:70665455..70667033,2	K562	blood:
12	chr1:70643607..70646837-chr1:70686224..70688710,3	K562	blood:
13	chr1:70669434..70671203-chr1:70686815..70688649,2	MCF-7	breast:
14	chr1:70607998..70610574-chr1:70685135..70686722,2	K562	blood:
15	chr1:70670478..70672427-chr1:70697851..70699860,2	K562	blood:
16	chr1:70686750..70687728-chr17:48784876..48785472,2	Hela-S3	cervix:
17	chr1:70669751..70673129-chr1:70685079..70688457,4	MCF-7	breast:
18	chr1:70680332..70681916-chr1:70685597..70687772,2	MCF-7	breast:
19	chr1:70687235..70688815-chr1:70690103..70691870,2	MCF-7	breast:
20	chr1:70687323..70689346-chr1:70692516..70694332,3	MCF-7	breast:
21	chr1:70714127..70716625-chr1:70718344..70722644,5	K562	blood:
22	chr1:70611242..70612910-chr1:70616232..70618034,2	K562	blood:
23	chr1:70661362..70665473-chr1:70669237..70671298,4	K562	blood:
24	chr1:70648453..70649982-chr1:70670347..70672343,2	K562	blood:
25	chr1:70687323..70689346-chr1:70692516..70694332,3	MCF-7	breast:
26	chr1:70613655..70616182-chr1:70616886..70621035,4	K562	blood:
27	chr1:70622913..70625686-chr1:70626879..70630763,3	K562	blood:
28	chr1:70675754..70677274-chr1:70677363..70679421,2	K562	blood:
29	chr1:70632648..70635188-chr1:70637548..70640122,2	K562	blood:
30	chr1:70686799..70689606-chr1:70818481..70820974,3	K562	blood:
31	chr1:70694395..70695957-chr1:70712165..70714538,2	K562	blood:
32	chr1:70645372..70647137-chr1:70649997..70652208,2	K562	blood:
33	chr1:70671253..70671885-chr3:57582557..57583363,2	Hela-S3	cervix:
34	chr1:70677362..70679072-chr1:70694969..70697768,2	K562	blood:
35	chr1:70684364..70687178-chr1:70692446..70695041,2	MCF-7	breast:
36	chr1:70694395..70695957-chr1:70712165..70714538,2	K562	blood:
37	chr1:70652911..70655573-chr1:70665415..70667122,3	K562	blood:
38	chr1:70652911..70655573-chr1:70665415..70667122,3	K562	blood:
39	chr1:70709756..70712647-chr1:71546604..71549117,2	MCF-7	breast:
40	chr1:70606579..70609498-chr1:70685222..70687844,2	K562	blood:
41	chr1:70685268..70690578-chr1:70702989..70707451,6	MCF-7	breast:
42	chr1:70690194..70693110-chr1:70772753..70775116,2	K562	blood:
43	chr1:70632648..70635188-chr1:70637548..70640122,2	K562	blood:
44	chr1:70675754..70677274-chr1:70677363..70679421,2	K562	blood:
45	chr1:70622913..70625686-chr1:70626879..70630763,3	K562	blood:
46	chr1:70686741..70687626-chr16:29827433..29828123,2	Hela-S3	cervix:
47	chr1:70684364..70687178-chr1:70692446..70695041,2	MCF-7	breast:
48	chr1:70635318..70637973-chr1:70641469..70643129,2	K562	blood:
49	chr1:70671321..70673336-chr1:70700811..70702610,2	K562	blood:
50	chr1:70692896..70695423-chr1:70718003..70720357,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC7-2	chr1:70612804-70612878	ENSG00000231835.1
2	lnc-LRRC7-2	chr1:70613572-70613688	ENSG00000231835.1
3	lnc-LRRC40-1	chr1:70686506-70686706	ENSG00000228988.1
4	lnc-LRRC40-1	chr1:70684272-70684527	ENSG00000228988.1
5	lnc-ANKRD13C-2	chr1:70645829-70646123	NONHSAT003845
6	lnc-LRRC7-5	chr1:70695747-70696301	NONHSAT003849
7	lnc-LRRC7-1	chr1:70607065-70610047	ENSG00000261223.1
8	lnc-LRRC7-2	chr1:70617431-70617628	ENSG00000231835.1
9	lnc-LRRC7-5	chr1:70696778-70696957	NONHSAT003849

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	LRRC40	hsa-miR-155-5p	chr1:70610660-70610683
2	SFRS11	hsa-miR-376a-3p	chr1:70716778-70716802
3	LRRC40	hsa-miR-26b-5p	chr1:70610727-70610747
4	LRRC40	hsa-miR-26b-5p	chr1:70611043-70611063
5	LRRC40	hsa-miR-26b-5p	chr1:70610788-70610810
6	LRRC40	hsa-miR-34a-5p	chr1:70611318-70611311
7	LRRC40	hsa-miR-34a-5p	chr1:70611312-70611336

Variant related genes	Relation type
LRRC7	TF binding region
SRSF11	TF binding region
LRRC40	TF binding region
RN7SL242P	TF binding region
ENSG00000228988	TF binding region
LRRC7	CpG island
SRSF11	CpG island
LRRC40	CpG island
RN7SL242P	CpG island
ENSG00000228988	CpG island
ENSG00000116761	chromatin interactions
ENSG00000228988	chromatin interactions
ENSG00000244389	chromatin interactions
ENSG00000168374	chromatin interactions
ENSG00000033122	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000263136	chromatin interactions
ENSG00000260083	chromatin interactions
ENSG00000132485	chromatin interactions
ENSG00000143476	chromatin interactions
ENSG00000154945	chromatin interactions
ENSG00000137492	chromatin interactions
ENSG00000229956	chromatin interactions
ENSG00000143493	chromatin interactions
ENSG00000066557	chromatin interactions
ENSG00000197568	chromatin interactions
ENSG00000116754	chromatin interactions
ENSG00000265991	chromatin interactions

Extended variants
information (count: 4198 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4198 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1571161	chr1:70604106-70604107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572785897	chr1:70604151-70604152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550470644	chr1:70604154-70604155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142859334	chr1:70604162-70604163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150409316	chr1:70604209-70604210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565828009	chr1:70604293-70604294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371107528	chr1:70604300-70604301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535623299	chr1:70604338-70604339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548042911	chr1:70604351-70604352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138166985	chr1:70604383-70604384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182238657	chr1:70604445-70604446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371140856	chr1:70604506-70604507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140172216	chr1:70604512-70604513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576004316	chr1:70604594-70604595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538690700	chr1:70604623-70604624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17464136	chr1:70604633-70604634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1454578	chr1:70604680-70604681	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574358702	chr1:70604693-70604694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188380480	chr1:70604707-70604708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192701633	chr1:70604778-70604779	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs574992869	chr1:70604780-70604781	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs185446585	chr1:70604784-70604785	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs76853344	chr1:70604793-70604794	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs189822851	chr1:70604849-70604850	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs61784320	chr1:70604891-70604892	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs559401309	chr1:70604896-70604897	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs144307845	chr1:70604904-70604905	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs192505476	chr1:70604906-70604907	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572907018	chr1:70604943-70604944	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs140076531	chr1:70604966-70604967	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs11209591	chr1:70604967-70604968	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544969121	chr1:70605031-70605032	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs115298898	chr1:70605048-70605049	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs55634563	chr1:70605061-70605062	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142146702	chr1:70605065-70605066	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs565757983	chr1:70605072-70605073	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs376685418	chr1:70605093-70605094	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs200477365	chr1:70605175-70605176	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs555079059	chr1:70605229-70605230	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs574914683	chr1:70605247-70605248	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs146350782	chr1:70605324-70605325	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs114195602	chr1:70605347-70605348	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs184597151	chr1:70605438-70605439	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs546525500	chr1:70605444-70605445	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs199885574	chr1:70605451-70605452	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs559365190	chr1:70605524-70605525	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528111888	chr1:70605525-70605526	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs541546762	chr1:70605548-70605549	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs17131225	chr1:70605578-70605579	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142989948	chr1:70605603-70605604	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3263 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70596800-70609200	Weak transcription	Liver	Liver
2	chr1:70599000-70606000	Weak transcription	Osteobl	bone
3	chr1:70599000-70606600	Weak transcription	K562	blood
4	chr1:70599000-70609600	Weak transcription	GM12878-XiMat	blood
5	chr1:70600200-70605600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:70600200-70606000	Weak transcription	Aorta	Aorta
7	chr1:70600400-70604600	Weak transcription	Fetal Brain Female	brain
8	chr1:70600400-70605200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr1:70600400-70605600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:70600400-70605800	Weak transcription	NHDF-Ad	bronchial
11	chr1:70600600-70605200	Weak transcription	Brain Germinal Matrix	brain
12	chr1:70600600-70605200	Weak transcription	Fetal Heart	heart
13	chr1:70601000-70615400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:70601000-70643200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr1:70601200-70605400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:70601200-70606000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr1:70601200-70606200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr1:70601200-70652000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:70601800-70605200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr1:70603000-70605200	Weak transcription	Psoas Muscle	Psoas
21	chr1:70603000-70614800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:70603400-70605000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr1:70603400-70648800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:70603600-70604800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:70603600-70605200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr1:70604400-70605000	Enhancers	Fetal Brain Male	brain
27	chr1:70604600-70605600	Enhancers	Fetal Brain Female	brain
28	chr1:70604600-70608600	Enhancers	Fetal Lung	lung
29	chr1:70604800-70605800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:70604800-70606400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:70605000-70605200	Active TSS	Primary B cells from cord blood	blood
32	chr1:70605000-70605200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr1:70605000-70605200	Flanking Active TSS	Fetal Brain Male	brain
34	chr1:70605000-70605200	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr1:70605200-70605400	Enhancers	Brain Anterior Caudate	brain
36	chr1:70605200-70605400	Enhancers	Fetal Brain Male	brain
37	chr1:70605200-70605400	Enhancers	Psoas Muscle	Psoas
38	chr1:70605200-70605400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr1:70605200-70605600	Enhancers	Fetal Heart	heart
40	chr1:70605200-70606200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr1:70605200-70606200	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr1:70605200-70607000	Enhancers	Brain Germinal Matrix	brain
43	chr1:70605200-70607000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr1:70605200-70607000	Enhancers	Ovary	ovary
45	chr1:70605200-70607200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr1:70605200-70612200	Weak transcription	Primary B cells from cord blood	blood
47	chr1:70605400-70605600	Flanking Active TSS	Fetal Brain Male	brain
48	chr1:70605400-70605800	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr1:70605400-70606200	Weak transcription	Psoas Muscle	Psoas
50	chr1:70605400-70606600	Enhancers	Brain Inferior Temporal Lobe	brain

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