Variant report

Variant	esv1826570
Chromosome Location	chr3:19579860-20077414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3426)
CpG islands
(count:2138)
Chromatin interactive
region (count:194)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:13)

(count:3426 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:19970496-19970602	K562	blood:	n/a	n/a
2	ARID3A	chr3:19838885-19838997	K562	blood:	n/a	n/a
3	ARID3A	chr3:20063992-20065045	K562	blood:	n/a	n/a
4	ARID3A	chr3:19972705-19973731	K562	blood:	n/a	n/a
5	ARID3A	chr3:19853257-19853541	K562	blood:	n/a	n/a
6	ARID3A	chr3:19974779-19974812	K562	blood:	n/a	n/a
7	ARID3A	chr3:19930083-19930989	K562	blood:	n/a	n/a
8	ARID3A	chr3:19978769-19979488	K562	blood:	n/a	n/a
9	ARID3A	chr3:20002338-20002581	K562	blood:	n/a	n/a
10	ARID3A	chr3:19987115-19987639	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:20008657-20009619	K562	blood:	n/a	n/a
12	ARID3A	chr3:19999473-19999541	K562	blood:	n/a	n/a
13	ARID3A	chr3:19975714-19975914	K562	blood:	n/a	n/a
14	ARID3A	chr3:20057080-20057584	K562	blood:	n/a	n/a
15	ARID3A	chr3:20043611-20043819	K562	blood:	n/a	n/a
16	ARID3A	chr3:19942947-19943100	K562	blood:	n/a	n/a
17	ARID3A	chr3:19988281-19988728	HepG2	liver:	n/a	n/a
18	ARID3A	chr3:19940290-19940486	HepG2	liver:	n/a	n/a
19	ARID3A	chr3:19971710-19971731	K562	blood:	n/a	n/a
20	ARID3A	chr3:19926931-19927205	K562	blood:	n/a	n/a
21	ARID3A	chr3:20056175-20056432	K562	blood:	n/a	n/a
22	ARID3A	chr3:19979685-19979859	HepG2	liver:	n/a	n/a
23	ARID3A	chr3:19999876-19999936	K562	blood:	n/a	n/a
24	ARID3A	chr3:19989243-19989553	HepG2	liver:	n/a	n/a
25	ARID3A	chr3:19988883-19988922	K562	blood:	n/a	n/a
26	ARID3A	chr3:19986723-19988668	K562	blood:	n/a	n/a
27	ARID3A	chr3:20065245-20065546	K562	blood:	n/a	n/a
28	ARID3A	chr3:19908154-19908565	K562	blood:	n/a	n/a
29	ATF1	chr3:19972653-19973054	K562	blood:	n/a	n/a
30	ATF1	chr3:19973259-19973741	K562	blood:	n/a	n/a
31	ATF1	chr3:20064360-20065076	K562	blood:	n/a	n/a
32	ATF1	chr3:19785640-19785860	K562	blood:	n/a	n/a
33	ATF1	chr3:19930581-19931040	K562	blood:	n/a	n/a
34	ATF1	chr3:20057033-20057364	K562	blood:	n/a	n/a
35	ATF1	chr3:19978931-19979563	K562	blood:	n/a	n/a
36	ATF1	chr3:19987645-19988784	K562	blood:	n/a	n/a
37	ATF2	chr3:19972720-19973301	GM12878	blood:	n/a	n/a
38	ATF2	chr3:19987825-19988939	GM12878	blood:	n/a	n/a
39	ATF2	chr3:19686507-19687102	GM12878	blood:	n/a	n/a
40	ATF2	chr3:19972636-19973243	GM12878	blood:	n/a	n/a
41	ATF2	chr3:19581327-19581963	GM12878	blood:	n/a	n/a
42	ATF2	chr3:19987979-19988412	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr3:19601108-19601992	GM12878	blood:	n/a	n/a
44	ATF2	chr3:19640324-19640769	GM12878	blood:	n/a	n/a
45	ATF2	chr3:19686532-19687019	GM12878	blood:	n/a	n/a
46	ATF2	chr3:19580877-19582458	GM12878	blood:	n/a	n/a
47	ATF2	chr3:19601146-19601590	GM12878	blood:	n/a	n/a
48	ATF2	chr3:19584169-19584688	GM12878	blood:	n/a	n/a
49	ATF2	chr3:19640384-19640732	GM12878	blood:	n/a	n/a
50	ATF2	chr3:19988400-19988707	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19987528-19987578	GM19239	blood:	n/a
2	chr3:20026603-20026653	SKMC	muscle:	n/a
3	chr3:19988243-19988293	PrEC	prostate:	n/a
4	chr3:19987528-19987578	GM19239	blood:	n/a
5	chr3:20026603-20026653	SKMC	muscle:	n/a
6	chr3:19988243-19988293	PrEC	prostate:	n/a
7	chr3:19818187-19818237	AG10803	skin:	n/a
8	chr3:19988340-19988390	AG09309	skin:	n/a
9	chr3:19975514-19975564	SKMC	muscle:	n/a
10	chr3:19985031-19985081	HNPCEpiC	eye:	n/a
11	chr3:20053940-20053990	HEK293	kidney:	embryo
12	chr3:19988243-19988293	RPTEC	kidney:	n/a
13	chr3:19987665-19987715	K562	blood:	n/a
14	chr3:19987665-19987715	AG04449	skin:	fetal
15	chr3:19850542-19850592	GM06990	blood:	n/a
16	chr3:20049638-20049688	GM12892	blood:	n/a
17	chr3:19818187-19818237	ovcar-3	ovarian:	n/a
18	chr3:19791356-19791406	H1-hESC	embryonic stem cell:	embryo
19	chr3:19987665-19987715	HL-60	blood:	n/a
20	chr3:19990693-19990743	PFSK-1	brain:	n/a
21	chr3:19850542-19850592	T-47D	breast:	n/a
22	chr3:19989128-19989178	GM12891	blood:	n/a
23	chr3:19976136-19976186	AG10803	skin:	n/a
24	chr3:19752610-19752660	HEK293	kidney:	embryo
25	chr3:19990693-19990743	HepG2	liver:	n/a
26	chr3:19791356-19791406	AG09319	gingival:	n/a
27	chr3:19976136-19976186	SK-N-SH	brain:	n/a
28	chr3:19988460-19988510	T-47D	breast:	n/a
29	chr3:19987815-19987865	AoSMC	blood vessel:	n/a
30	chr3:19791304-19791354	PANC-1	pancreas:	n/a
31	chr3:19988243-19988293	GM12892	blood:	n/a
32	chr3:19791456-19791506	GM12878	blood:	n/a
33	chr3:19975738-19975788	ovcar-3	ovarian:	n/a
34	chr3:20049624-20049674	HMEC	breast:	n/a
35	chr3:19988243-19988293	BE2_C	brain:	n/a
36	chr3:19975483-19975533	A549	lung:	n/a
37	chr3:19975514-19975564	HCM	heart:	n/a
38	chr3:19992400-19992450	RPTEC	kidney:	n/a
39	chr3:19791356-19791406	RPTEC	kidney:	n/a
40	chr3:19987815-19987865	SK-N-SH_RA	brain:	n/a
41	chr3:20049624-20049674	AG10803	skin:	n/a
42	chr3:19752610-19752660	AG09309	skin:	n/a
43	chr3:19976136-19976186	GM12878	blood:	n/a
44	chr3:19988340-19988390	AG04449	skin:	fetal
45	chr3:19988132-19988182	PrEC	prostate:	n/a
46	chr3:19988396-19988446	AG04449	skin:	fetal
47	chr3:19975514-19975564	U87	brain:	n/a
48	chr3:19988340-19988390	Caco-2	colon:	n/a
49	chr3:19988340-19988390	NB4	blood:	n/a
50	chr3:19992400-19992450	AG10803	skin:	n/a

(count:194 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:19960840..19962756-chr3:19987285..19989171,2	K562	blood:
2	chr3:19960921..19963148-chr3:19974147..19975728,2	K562	blood:
3	chr3:19919756..19921311-chr3:20094992..20097825,2	K562	blood:
4	chr3:19679630..19681949-chr3:19683459..19685004,2	K562	blood:
5	chr3:19926588..19927515-chr3:19942549..19943117,5	MCF-7	breast:
6	chr3:20005781..20007385-chr3:20012300..20014395,2	K562	blood:
7	chr3:19976162..19983592-chr3:19985528..19991017,8	MCF-7	breast:
8	chr3:19987480..19989660-chr3:19996323..19998191,2	MCF-7	breast:
9	chr3:17936078..17936595-chr3:19908226..19908883,2	K562	blood:
10	chr17:33895021..33895646-chr3:19988844..19989353,2	Hela-S3	cervix:
11	chr3:20063707..20066137-chr3:20066791..20068854,2	K562	blood:
12	chr3:19975611..19979082-chr3:19987774..19990681,3	MCF-7	breast:
13	chr3:19961356..19963032-chr3:19986738..19988921,2	MCF-7	breast:
14	chr3:20063707..20066137-chr3:20066791..20068854,2	K562	blood:
15	chr3:19996748..19999658-chr3:20007262..20009565,3	K562	blood:
16	chr3:19963296..19965363-chr3:19967428..19970296,2	K562	blood:
17	chr3:19390558..19391094-chr3:19584541..19585367,2	MCF-7	breast:
18	chr3:19866393..19868702-chr3:19871331..19874203,2	K562	blood:
19	chr3:19961648..19963180-chr3:19974228..19975746,2	K562	blood:
20	chr3:20002226..20004591-chr3:20006312..20009350,3	MCF-7	breast:
21	chr3:20058205..20061001-chr3:20066769..20068692,2	K562	blood:
22	chr3:20035142..20037256-chr3:20064733..20066737,2	K562	blood:
23	chr3:19930446..19931966-chr3:19932163..19933731,2	MCF-7	breast:
24	chr3:20010598..20012211-chr3:20015468..20017013,2	K562	blood:
25	chr3:19958393..19961139-chr3:19961701..19963581,2	K562	blood:
26	chr3:19745768..19748356-chr3:19750935..19754447,3	K562	blood:
27	chr3:20063995..20066056-chr3:20077383..20080079,2	K562	blood:
28	chr3:19963049..19965826-chr3:19970318..19972819,2	MCF-7	breast:
29	chr3:19936727..19938285-chr3:19942132..19944334,2	K562	blood:
30	chr3:20058205..20061001-chr3:20066769..20068692,2	K562	blood:
31	chr3:19908798..19910478-chr3:19922117..19924794,2	K562	blood:
32	chr3:19986647..19989004-chr3:20010739..20012359,2	K562	blood:
33	chr3:19987782..19990680-chr3:20013275..20017779,4	K562	blood:
34	chr3:19936510..19939152-chr3:19987860..19990168,2	MCF-7	breast:
35	chr3:19922897..19926980-chr3:19987408..19989481,3	MCF-7	breast:
36	chr3:19990601..19993160-chr3:20063251..20065483,2	K562	blood:
37	chr3:20005781..20007385-chr3:20012300..20014395,2	K562	blood:
38	chr3:19926567..19927530-chr3:21592329..21593167,2	MCF-7	breast:
39	chr3:19988030..19989664-chr3:20003556..20005607,2	MCF-7	breast:
40	chr3:19991471..19993830-chr3:20005089..20007556,2	MCF-7	breast:
41	chr3:19863239..19864953-chr3:20226349..20229139,2	K562	blood:
42	chr3:20026329..20028709-chr3:20079789..20082702,2	K562	blood:
43	chr3:19930617..19933383-chr3:19987388..19990668,4	MCF-7	breast:
44	chr3:20067539..20069733-chr3:20073671..20076293,2	K562	blood:
45	chr3:19967166..19969606-chr3:20013917..20016357,2	MCF-7	breast:
46	chr3:19926188..19928582-chr3:19987242..19988957,2	MCF-7	breast:
47	chr3:19106302..19107287-chr3:19907999..19908895,3	MCF-7	breast:
48	chr3:20022682..20025378-chr3:20026127..20028940,2	MCF-7	breast:
49	chr3:19390433..19391079-chr3:19907967..19908843,4	MCF-7	breast:
50	chr3:20061429..20064668-chr3:20080168..20082891,4	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFHB-1	chr3:19729726-19729972	XLOC_003064
2	lnc-EFHB-3	chr3:20049344-20049739	NONHSAT088609
3	lnc-EFHB-1	chr3:19717560-19717598	XLOC_003064
4	lnc-EFHB-2	chr3:19988411-19988517	NONHSAT088605
5	lnc-EFHB-4	chr3:20042522-20043588	NR_027694
6	lnc-EFHB-4	chr3:20053542-20053765	NR_027694
7	lnc-EFHB-4	chr3:20021453-20021666	NR_027694
8	lnc-EFHB-2	chr3:19987406-19987746	NONHSAT088605
9	lnc-EFHB-4	chr3:20053542-20053749	NONHSAT088608
10	lnc-EFHB-4	chr3:20025686-20025788	NR_027694
11	lnc-EFHB-4	chr3:20042467-20043588	NONHSAT088608

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	RAB5A	hsa-miR-101-3p	chr3:20025772-20025793
2	RAB5A	hsa-miR-130b-3p	chr3:20026129-20026150
3	RAB5A	hsa-miR-130a-3p	chr3:20026128-20026150
4	RAB5A	hsa-miR-130a-3p	chr3:20026477-20026484
5	RAB5A	hsa-miR-101-3p	chr3:20026199-20026206
6	RAB5A	hsa-miR-18a-5p	chr3:20025965-20025987
7	RAB5A	hsa-miR-33a-5p	chr3:20026571-20026591
8	RAB5A	hsa-miR-130a-3p	chr3:20026463-20026484
9	RAB5A	hsa-miR-130b-3p	chr3:20026477-20026484
10	RAB5A	hsa-miR-101-3p	chr3:20026272-20026293
11	RAB5A	hsa-miR-33a-5p	chr3:20026130-20026148
12	RAB5A	hsa-miR-130b-3p	chr3:20026461-20026484
13	RAB5A	hsa-miR-101-3p	chr3:20026185-20026206

Variant related genes	Relation type
KAT2B	TF binding region
ENSG00000229468	TF binding region
RNU4-85P	TF binding region
EFHB	TF binding region
RAB5A	TF binding region
PP2D1	TF binding region
ENSG00000230697	TF binding region
HSPA8P18	TF binding region
KAT2B	CpG island
ENSG00000229468	CpG island
RNU4-85P	CpG island
EFHB	CpG island
RAB5A	CpG island
PP2D1	CpG island
ENSG00000230697	CpG island
HSPA8P18	CpG island
ENSG00000169241	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000100441	chromatin interactions
ENSG00000162607	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000235194	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000229468	chromatin interactions
ENSG00000163576	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000230697	chromatin interactions
ENSG00000183960	chromatin interactions
ENSG00000267321	chromatin interactions
ENSG00000183977	chromatin interactions
ESYT1	miRNA target sites

Extended variants
information (count: 10326 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10326 , 50 per page) page: 1 2 3 4 5 6 7 ... 207

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17513072	chr3:19579860-19579861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568723487	chr3:19579933-19579934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547760031	chr3:19579940-19579941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193103467	chr3:19579963-19579964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575011361	chr3:19579966-19579967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146535340	chr3:19579997-19579998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542734895	chr3:19580045-19580046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6764770	chr3:19580108-19580109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573901564	chr3:19580142-19580143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73034053	chr3:19580147-19580148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368242974	chr3:19580155-19580156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184356488	chr3:19580177-19580178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144880682	chr3:19580273-19580274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11719031	chr3:19580303-19580304	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs572531047	chr3:19580308-19580309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543243238	chr3:19580310-19580311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189221616	chr3:19580327-19580328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564912792	chr3:19580377-19580378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77597796	chr3:19580394-19580395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527563586	chr3:19580404-19580405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567555908	chr3:19580420-19580421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374093392	chr3:19580449-19580450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138714997	chr3:19580450-19580451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565571573	chr3:19580497-19580498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140283433	chr3:19580499-19580500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34338687	chr3:19580529-19580530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150331804	chr3:19580533-19580534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548796096	chr3:19580647-19580648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs908216	chr3:19580707-19580708	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs529881029	chr3:19580836-19580837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548782941	chr3:19580838-19580839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567384657	chr3:19580856-19580857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538021762	chr3:19580906-19580907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191551680	chr3:19580920-19580921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370617405	chr3:19580922-19580923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184075504	chr3:19580923-19580924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs137994859	chr3:19580943-19580944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116048016	chr3:19581038-19581039	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs572590495	chr3:19581086-19581087	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs188853198	chr3:19581092-19581093	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs555029321	chr3:19581133-19581134	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs576609187	chr3:19581163-19581164	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs543988089	chr3:19581266-19581267	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116329910	chr3:19581282-19581283	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181558379	chr3:19581324-19581325	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186790025	chr3:19581334-19581335	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566049710	chr3:19581501-19581502	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559684998	chr3:19581570-19581571	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539730484	chr3:19581598-19581599	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190443751	chr3:19581608-19581609	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	19363497	CNVD

Chromatin state (count:2884 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19576800-19580200	Weak transcription	Primary B cells from cord blood	blood
2	chr3:19577600-19580600	Weak transcription	Adipose Nuclei	Adipose
3	chr3:19577800-19581000	Weak transcription	Fetal Brain Female	brain
4	chr3:19578000-19585600	Enhancers	Primary B cells from peripheral blood	blood
5	chr3:19579400-19581000	Enhancers	GM12878-XiMat	blood
6	chr3:19580200-19581200	Enhancers	Primary B cells from cord blood	blood
7	chr3:19580600-19582200	Enhancers	Adipose Nuclei	Adipose
8	chr3:19580600-19582200	Enhancers	Fetal Intestine Large	intestine
9	chr3:19580800-19581600	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr3:19580800-19582200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr3:19580800-19582600	Enhancers	Primary hematopoietic stem cells	blood
12	chr3:19581000-19581200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:19581000-19581400	Enhancers	Aorta	Aorta
14	chr3:19581000-19581600	Enhancers	Primary T cells from cord blood	blood
15	chr3:19581000-19581600	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr3:19581000-19582400	Flanking Active TSS	GM12878-XiMat	blood
17	chr3:19581200-19581400	Enhancers	Fetal Brain Female	brain
18	chr3:19581200-19581400	Enhancers	Fetal Intestine Small	intestine
19	chr3:19581200-19581400	Enhancers	Left Ventricle	heart
20	chr3:19581200-19581600	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr3:19581200-19581600	Enhancers	Fetal Thymus	thymus
22	chr3:19581200-19581600	Enhancers	Thymus	Thymus
23	chr3:19581200-19581600	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr3:19581200-19581800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:19581200-19582000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr3:19581200-19582400	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr3:19581200-19582400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr3:19581600-19581800	Enhancers	Primary B cells from cord blood	blood
29	chr3:19581600-19582000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr3:19581800-19582000	Flanking Active TSS	Primary B cells from cord blood	blood
31	chr3:19581800-19582200	Bivalent Enhancer	Fetal Brain Male	brain
32	chr3:19581800-19582400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr3:19582000-19582200	Enhancers	Fetal Intestine Small	intestine
34	chr3:19582000-19582600	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr3:19582000-19584200	Enhancers	Primary B cells from cord blood	blood
36	chr3:19582200-19584200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr3:19582400-19582800	Enhancers	GM12878-XiMat	blood
38	chr3:19582400-19584200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:19582400-19584400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:19582400-19584600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr3:19582600-19583400	Weak transcription	Primary hematopoietic stem cells	blood
42	chr3:19582800-19583200	Flanking Active TSS	GM12878-XiMat	blood
43	chr3:19583200-19586000	Enhancers	GM12878-XiMat	blood
44	chr3:19583400-19585000	Enhancers	Primary hematopoietic stem cells	blood
45	chr3:19584200-19584400	Flanking Active TSS	Primary B cells from cord blood	blood
46	chr3:19584200-19584800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr3:19584200-19584800	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr3:19584200-19585000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:19584400-19584600	Enhancers	Primary B cells from cord blood	blood
50	chr3:19584400-19585000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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