Variant report

Variant	nsv562644
Chromosome Location	chr13:90429193-90886078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2381)
CpG islands
(count:185)
Chromatin interactive
region (count:231)
LncRNA
region (count:33)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90682174-90682341	K562	blood:	n/a	n/a
2	ARID3A	chr13:90625281-90625544	K562	blood:	n/a	n/a
3	ARID3A	chr13:90497424-90497670	K562	blood:	n/a	n/a
4	ARID3A	chr13:90462884-90462897	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:90798775-90798825	K562	blood:	n/a	n/a
6	ARID3A	chr13:90783636-90783652	K562	blood:	n/a	n/a
7	ARID3A	chr13:90764747-90764925	K562	blood:	n/a	n/a
8	ARID3A	chr13:90720372-90720449	K562	blood:	n/a	n/a
9	ARID3A	chr13:90551614-90552641	HepG2	liver:	n/a	n/a
10	ARID3A	chr13:90520785-90520820	K562	blood:	n/a	n/a
11	ARID3A	chr13:90733837-90733909	K562	blood:	n/a	n/a
12	ARID3A	chr13:90749033-90749172	K562	blood:	n/a	n/a
13	ARID3A	chr13:90577420-90577637	HepG2	liver:	n/a	n/a
14	ARID3A	chr13:90585014-90585385	HepG2	liver:	n/a	n/a
15	ARID3A	chr13:90585018-90585218	K562	blood:	n/a	n/a
16	ARID3A	chr13:90644313-90644329	K562	blood:	n/a	n/a
17	ARID3A	chr13:90512718-90512791	K562	blood:	n/a	n/a
18	ARID3A	chr13:90723185-90723815	HepG2	liver:	n/a	n/a
19	ATF1	chr13:90458876-90459006	K562	blood:	n/a	n/a
20	ATF1	chr13:90563357-90563940	K562	blood:	n/a	n/a
21	ATF1	chr13:90746006-90746518	K562	blood:	n/a	n/a
22	ATF1	chr13:90628499-90628699	K562	blood:	n/a	n/a
23	ATF1	chr13:90510751-90511105	K562	blood:	n/a	n/a
24	ATF1	chr13:90729840-90730040	K562	blood:	n/a	n/a
25	ATF1	chr13:90666607-90666981	K562	blood:	n/a	n/a
26	ATF1	chr13:90562006-90562368	K562	blood:	n/a	n/a
27	ATF1	chr13:90774717-90774782	K562	blood:	n/a	n/a
28	ATF1	chr13:90452879-90452924	K562	blood:	n/a	n/a
29	ATF1	chr13:90446074-90446297	K562	blood:	n/a	n/a
30	ATF1	chr13:90786453-90786660	K562	blood:	n/a	n/a
31	ATF1	chr13:90639555-90640158	K562	blood:	n/a	n/a
32	ATF1	chr13:90536949-90537223	K562	blood:	n/a	n/a
33	ATF1	chr13:90709492-90709697	K562	blood:	n/a	n/a
34	ATF1	chr13:90778489-90779075	K562	blood:	n/a	n/a
35	ATF1	chr13:90448578-90448855	K562	blood:	n/a	n/a
36	ATF1	chr13:90816261-90816303	K562	blood:	n/a	n/a
37	ATF1	chr13:90707883-90708575	K562	blood:	n/a	n/a
38	ATF1	chr13:90560976-90561171	K562	blood:	n/a	n/a
39	ATF1	chr13:90839349-90840283	K562	blood:	n/a	n/a
40	ATF1	chr13:90817824-90817836	K562	blood:	n/a	n/a
41	ATF1	chr13:90803934-90804073	K562	blood:	n/a	n/a
42	ATF1	chr13:90459939-90460250	K562	blood:	n/a	n/a
43	ATF1	chr13:90718299-90718552	K562	blood:	n/a	n/a
44	ATF1	chr13:90483482-90484025	K562	blood:	n/a	n/a
45	ATF1	chr13:90838752-90838825	K562	blood:	n/a	n/a
46	ATF1	chr13:90504797-90505152	K562	blood:	n/a	n/a
47	ATF1	chr13:90811429-90811540	K562	blood:	n/a	n/a
48	ATF1	chr13:90825472-90825641	K562	blood:	n/a	n/a
49	ATF1	chr13:90530348-90530819	K562	blood:	n/a	n/a
50	ATF1	chr13:90777427-90777622	K562	blood:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90536270-90536320	HCT-116	colon:	n/a
2	chr13:90661319-90661369	ECC-1	luminal epithelium:	n/a
3	chr13:90536270-90536320	HCT-116	colon:	n/a
4	chr13:90661319-90661369	ECC-1	luminal epithelium:	n/a
5	chr13:90536270-90536320	RPTEC	kidney:	n/a
6	chr13:90536270-90536320	PFSK-1	brain:	n/a
7	chr13:90536270-90536320	AG04449	skin:	fetal
8	chr13:90557520-90557570	BE2_C	brain:	n/a
9	chr13:90661319-90661369	GM12878	blood:	n/a
10	chr13:90661319-90661369	IMR90	lung:	fetal
11	chr13:90661319-90661369	HUVEC	blood vessel:	n/a
12	chr13:90661319-90661369	HNPCEpiC	eye:	n/a
13	chr13:90661319-90661369	HCF	heart:	n/a
14	chr13:90661319-90661369	HEEpiC	esophagus:	n/a
15	chr13:90536270-90536320	HRE	kidney:	n/a
16	chr13:90557520-90557570	SAEC	small airway:	n/a
17	chr13:90557520-90557570	Jurkat	blood:	n/a
18	chr13:90536270-90536320	A549	lung:	n/a
19	chr13:90661319-90661369	SK-N-SH	brain:	n/a
20	chr13:90557520-90557570	HAEpiC	amniotic membrane:	n/a
21	chr13:90536270-90536320	AG09309	skin:	n/a
22	chr13:90536270-90536320	NB4	blood:	n/a
23	chr13:90661319-90661369	ProgFib	skin:	n/a
24	chr13:90536270-90536320	AoSMC	blood vessel:	n/a
25	chr13:90536270-90536320	ProgFib	skin:	n/a
26	chr13:90661319-90661369	AG04450	lung:	fetal
27	chr13:90557520-90557570	HEEpiC	esophagus:	n/a
28	chr13:90536270-90536320	HMEC	breast:	n/a
29	chr13:90661319-90661369	K562	blood:	n/a
30	chr13:90661319-90661369	NHDF-neo	bronchial:	n/a
31	chr13:90661319-90661369	HAEpiC	amniotic membrane:	n/a
32	chr13:90536270-90536320	HRPEpiC	eye:	n/a
33	chr13:90536270-90536320	NHDF-neo	bronchial:	n/a
34	chr13:90536270-90536320	SK-N-SH	brain:	n/a
35	chr13:90536270-90536320	AG04450	lung:	fetal
36	chr13:90661319-90661369	HCM	heart:	n/a
37	chr13:90536270-90536320	HEK293	kidney:	embryo
38	chr13:90661319-90661369	Jurkat	blood:	n/a
39	chr13:90661319-90661369	T-47D	breast:	n/a
40	chr13:90557520-90557570	H1-hESC	embryonic stem cell:	embryo
41	chr13:90557520-90557570	PrEC	prostate:	n/a
42	chr13:90557520-90557570	NT2-D1	testis:	n/a
43	chr13:90661319-90661369	BE2_C	brain:	n/a
44	chr13:90661319-90661369	HepG2	liver:	n/a
45	chr13:90661319-90661369	AoSMC	blood vessel:	n/a
46	chr13:90557520-90557570	HPAEpiC	pulmonary alveolar:	n/a
47	chr13:90661319-90661369	HCT-116	colon:	n/a
48	chr13:90557520-90557570	NHDF-neo	bronchial:	n/a
49	chr13:90661319-90661369	PFSK-1	brain:	n/a
50	chr13:90557520-90557570	K562	blood:	n/a

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr13:90848833..90851236-chr13:90855883..90857949,2	K562	blood:
2	chr13:90583708..90585215-chr2:205937243..205938743,2	K562	blood:
3	chr13:90583688..90585209-chr3:73158523..73160592,3	MCF-7	breast:
4	chr13:90535683..90539242-chr13:90544865..90546775,3	K562	blood:
5	chr13:90583692..90586688-chrX:77930321..77933319,2	K562	blood:
6	chr13:90760228..90761976-chr13:90768337..90770152,2	K562	blood:
7	chr10:103123126..103126131-chr13:90583690..90586710,7	MCF-7	breast:
8	chr13:90590871..90593494-chr13:90596073..90598011,2	K562	blood:
9	chr10:103124610..103126130-chr13:90583687..90585216,5	K562	blood:
10	chr13:90814292..90817053-chr13:90817881..90820195,2	K562	blood:
11	chr11:62609126..62609718-chr13:90584688..90585208,7	MCF-7	breast:
12	chr13:90497518..90499702-chr13:90509556..90511719,2	K562	blood:
13	chr13:90451578..90453716-chr13:90460021..90462776,2	K562	blood:
14	chr13:90848833..90851236-chr13:90855883..90857949,2	K562	blood:
15	chr13:90539319..90541574-chr13:91998332..92001318,2	K562	blood:
16	chr13:90767500..90771414-chr13:90771603..90775646,3	K562	blood:
17	chr13:90862129..90863023-chr5:145846043..145846583,2	MCF-7	breast:
18	chr13:90583692..90586688-chr19:17578817..17580337,4	K562	blood:
19	chr13:90497518..90499702-chr13:90509556..90511719,2	K562	blood:
20	chr13:81108572..81110898-chr13:90437772..90440257,3	K562	blood:
21	chr13:90461092..90463944-chr13:90499339..90502245,2	K562	blood:
22	chr13:90829561..90831370-chr13:90833603..90835132,2	K562	blood:
23	chr13:90720137..90722598-chr13:90723221..90725922,2	K562	blood:
24	chr13:90513066..90514981-chr13:90520544..90522949,2	K562	blood:
25	chr13:90840334..90842479-chr13:90849460..90851751,2	K562	blood:
26	chr13:90576287..90578487-chr13:90579534..90581109,2	K562	blood:
27	chr13:90759395..90761976-chr13:90768337..90771167,3	K562	blood:
28	chr11:62608617..62609723-chr13:90584689..90585209,9	Hela-S3	cervix:
29	chr13:90680961..90684661-chr13:90686168..90687885,3	K562	blood:
30	chr13:90750086..90752997-chr13:90754100..90756762,5	K562	blood:
31	chr13:90517201..90517899-chr4:180957059..180957638,2	MCF-7	breast:
32	chr13:90686920..90689377-chr13:90707957..90709473,2	K562	blood:
33	chr1:160082466..160083968-chr13:90583692..90585197,2	K562	blood:
34	chr13:90585210..90586713-chr17:41438934..41440457,2	MCF-7	breast:
35	chr13:90438180..90442021-chr13:90442191..90444686,4	K562	blood:
36	chr13:90585208..90586716-chr17:41380446..41383729,6	MCF-7	breast:
37	chr13:90820278..90822167-chr13:90827317..90829782,2	K562	blood:
38	chr13:90767832..90770164-chr13:90776166..90779331,3	K562	blood:
39	chr13:90820278..90822167-chr13:90827317..90829782,2	K562	blood:
40	chr13:90583696..90585208-chr17:41444061..41445603,2	K562	blood:
41	chr13:90613653..90615299-chr13:90617771..90620491,2	K562	blood:
42	chr13:90544412..90546341-chr13:90551514..90554190,2	K562	blood:
43	chr13:90583696..90585208-chr2:153036711..153038231,2	MCF-7	breast:
44	chr13:90520551..90523101-chr13:90523541..90526179,2	K562	blood:
45	chr13:90585195..90585712-chr17:41465633..41466487,2	HCT-116	colon:
46	chr13:90583688..90585209-chr6:29527999..29529519,2	K562	blood:
47	chr13:90829561..90831370-chr13:90833603..90835132,2	K562	blood:
48	chr13:90613653..90615299-chr13:90617771..90620491,2	K562	blood:
49	chr13:90628839..90630474-chr13:90638003..90640039,2	K562	blood:
50	chr13:90585188..90585713-chr17:41465840..41466365,3	NB4	blood:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-27	chr13:90537509-90537789	NONHSAT034637
2	lnc-SLITRK6-28	chr13:90580934-90581047	l_900_chr13:90577875-90581583_kidney
3	lnc-SLITRK6-27	chr13:90539777-90539848	NONHSAT034637
4	lnc-DCT-10	chr13:90758189-90758456	NONHSAT034643
5	lnc-DCT-10	chr13:90771027-90771973	ENSG00000261446.1
6	lnc-DCT-10	chr13:90760108-90760794	NONHSAT034643
7	lnc-DCT-10	chr13:90731381-90731516	NONHSAT034642
8	lnc-SLITRK6-28	chr13:90581478-90581583	l_900_chr13:90577875-90581583_kidney
9	lnc-DCT-10	chr13:90712506-90712866	ENSG00000261446.1
10	lnc-SLITRK6-28	chr13:90577876-90578113	l_900_chr13:90577875-90581583_kidney
11	lnc-SLITRK6-28	chr13:90577907-90578113	NONHSAT034639
12	lnc-GPC5-10	chr13:90798075-90798214	NONHSAT034645
13	lnc-DCT-10	chr13:90758837-90760915	ENSG00000261446.1
14	lnc-DCT-10	chr13:90758201-90758456	NONHSAT034642
15	lnc-DCT-10	chr13:90712501-90712866	NONHSAT034642
16	lnc-DCT-10	chr13:90718982-90719064	NONHSAT034642
17	lnc-DCT-10	chr13:90758837-90760915	NONHSAT034642
18	lnc-DCT-10	chr13:90718982-90719064	ENSG00000261446.1
19	lnc-DCT-10	chr13:90771027-90771971	NONHSAT034642
20	lnc-SLITRK6-28	chr13:90580934-90581047	NONHSAT034639
21	lnc-DCT-10	chr13:90731381-90731516	ENSG00000261446.1
22	lnc-GPC5-10	chr13:90804188-90804830	ucscGeneNc_uc001vlq_1
23	lnc-SLITRK6-28	chr13:90581478-90581662	NONHSAT034638
24	lnc-GPC5-10	chr13:90798075-90798214	ucscGeneNc_uc001vlq_1
25	lnc-GPC5-10	chr13:90799953-90800025	ucscGeneNc_uc001vlq_1
26	lnc-SLITRK6-28	chr13:90581478-90581620	NONHSAT034639
27	lnc-GPC5-10	chr13:90800411-90800481	NONHSAT034645
28	lnc-GPC5-10	chr13:90799953-90800025	NONHSAT034645
29	lnc-GPC5-9	chr13:90823120-90824053	NONHSAT034646
30	lnc-DCT-10	chr13:90758201-90758456	ENSG00000261446.1
31	lnc-SLITRK6-28	chr13:90577868-90578113	NONHSAT034638
32	lnc-GPC5-10	chr13:90804188-90804834	NONHSAT034645
33	lnc-GPC5-10	chr13:90800411-90800481	ucscGeneNc_uc001vlq_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-622	chr13:90883496-90883516	MIMAT0003291

No data

Variant related genes	Relation type
KRT18P27	TF binding region
RPL7L1P1	TF binding region
ENSG00000200733	TF binding region
PEX12P1	TF binding region
MIR622	TF binding region
LINC00559	TF binding region
FAR1P1	TF binding region
RNA5SP34	TF binding region
KRT18P27	CpG island
RPL7L1P1	CpG island
ENSG00000200733	CpG island
PEX12P1	CpG island
MIR622	CpG island
LINC00559	CpG island
FAR1P1	CpG island
RNA5SP34	CpG island
ENSG00000261446	chromatin interactions
ENSG00000215417	chromatin interactions
ENSG00000148308	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000067596	chromatin interactions
ENSG00000236905	chromatin interactions
ENSG00000130304	chromatin interactions
ENSG00000225936	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000111057	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000200733	chromatin interactions
ENSG00000234227	chromatin interactions
KRAS	Mature miRNA region

Extended variants
information (count: 6902 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6902 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563967334	chr13:90431632-90431633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528006171	chr13:90431657-90431658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376200582	chr13:90431662-90431663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564546176	chr13:90431723-90431724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531709868	chr13:90431736-90431737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550256495	chr13:90431786-90431787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12862882	chr13:90431794-90431795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs148298037	chr13:90431806-90431807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547638506	chr13:90431836-90431837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9588754	chr13:90431837-90431838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532482875	chr13:90431851-90431852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539784484	chr13:90431891-90431892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557464192	chr13:90431910-90431911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34165945	chr13:90431934-90431935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569635160	chr13:90431939-90431940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536707554	chr13:90431951-90431952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148870183	chr13:90431968-90431969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74998353	chr13:90432012-90432013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574664476	chr13:90432043-90432044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546403971	chr13:90432054-90432055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562915348	chr13:90432074-90432075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541998062	chr13:90432075-90432076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553982336	chr13:90432087-90432088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572398346	chr13:90432166-90432167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546137780	chr13:90432176-90432177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564277968	chr13:90432196-90432197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559631554	chr13:90432205-90432206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543521163	chr13:90432207-90432208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562186533	chr13:90432281-90432282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9588755	chr13:90432287-90432288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551830798	chr13:90432337-90432338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs80287876	chr13:90432338-90432339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376529044	chr13:90432381-90432382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533214617	chr13:90432389-90432390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141415867	chr13:90432390-90432391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9588756	chr13:90432458-90432459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532061368	chr13:90432576-90432577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs386773207	chr13:90432582-90432583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9522703	chr13:90432585-90432586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs115713574	chr13:90432618-90432619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9515626	chr13:90432619-90432620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs9522704	chr13:90432676-90432677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs74241648	chr13:90432685-90432686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150846665	chr13:90432687-90432688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566596881	chr13:90432692-90432693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9522705	chr13:90432721-90432722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs576690049	chr13:90432811-90432812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185160486	chr13:90432825-90432826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138427042	chr13:90432866-90432867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529403426	chr13:90432873-90432874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90431600-90438600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:90433800-90434200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr13:90435600-90435800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr13:90435600-90435800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr13:90435600-90436000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr13:90435800-90437000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr13:90436000-90436400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr13:90436400-90436800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr13:90436600-90437000	Active TSS	Gastric	stomach
10	chr13:90443400-90443800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr13:90443600-90444000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr13:90460000-90460400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr13:90464400-90466000	Enhancers	HUVEC	blood vessel
14	chr13:90465200-90465800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr13:90465800-90466000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
16	chr13:90468200-90468600	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr13:90474600-90475000	Enhancers	Brain Cingulate Gyrus	brain
18	chr13:90474600-90475200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:90474800-90475000	Enhancers	A549	lung
20	chr13:90475000-90479800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr13:90475200-90479800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:90479400-90480000	Enhancers	Brain Angular Gyrus	brain
23	chr13:90479400-90480400	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr13:90479800-90480000	Active TSS	Brain Anterior Caudate	brain
25	chr13:90479800-90480200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr13:90479800-90480200	Enhancers	Brain Cingulate Gyrus	brain
27	chr13:90479800-90480200	Enhancers	Brain Hippocampus Middle	brain
28	chr13:90479800-90480400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:90479800-90480400	Enhancers	Brain Substantia Nigra	brain
30	chr13:90479800-90481600	Enhancers	Adipose Nuclei	Adipose
31	chr13:90480000-90480200	Flanking Active TSS	Brain Angular Gyrus	brain
32	chr13:90480000-90480200	Flanking Active TSS	Brain Anterior Caudate	brain
33	chr13:90480000-90480400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:90480000-90480400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr13:90480000-90480400	Enhancers	Fetal Lung	lung
36	chr13:90480200-90484600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:90480400-90482600	Weak transcription	Fetal Lung	lung
38	chr13:90480400-90484600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:90482600-90483200	Enhancers	Fetal Lung	lung
40	chr13:90483200-90485200	Weak transcription	Fetal Lung	lung
41	chr13:90483800-90484000	Enhancers	A549	lung
42	chr13:90484000-90485000	Weak transcription	A549	lung
43	chr13:90484600-90485200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr13:90484600-90485400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:90485000-90485400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr13:90485000-90486000	Enhancers	A549	lung
47	chr13:90485200-90485600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr13:90485200-90485800	Enhancers	Fetal Lung	lung
49	chr13:90492000-90492400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr13:90492000-90492400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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