Variant report

Variant	nsv1000584
Chromosome Location	chr3:102358773-102923378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1946)
CpG islands
(count:366)
Chromatin interactive
region (count:42)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1946 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:102389996-102390294	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:102392377-102392677	HepG2	liver:	n/a	n/a
3	ATF2	chr3:102846504-102846873	GM12878	blood:	n/a	n/a
4	ATF2	chr3:102406889-102407383	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:102407030-102407386	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr3:102433789-102434329	GM12878	blood:	n/a	n/a
7	ATF2	chr3:102846474-102847000	GM12878	blood:	n/a	n/a
8	BACH1	chr3:102648843-102648847	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr3:102652328-102652528	GM12878	blood:	n/a	n/a
10	BATF	chr3:102846641-102846881	GM12878	blood:	n/a	n/a
11	BATF	chr3:102433856-102434213	GM12878	blood:	n/a	chr3:102434009-102434020
12	BATF	chr3:102433864-102434252	GM12878	blood:	n/a	chr3:102434009-102434020
13	BCL11A	chr3:102846636-102846904	GM12878	blood:	n/a	chr3:102846753-102846762
14	BCL11A	chr3:102407054-102407384	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr3:102407072-102407277	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr3:102433900-102434146	GM12878	blood:	n/a	chr3:102434012-102434021
17	BCL3	chr3:102698808-102699149	A549	lung:	n/a	n/a
18	BCLAF1	chr3:102392360-102392720	GM12878	blood:	n/a	chr3:102392461-102392470
19	BCLAF1	chr3:102392318-102392743	GM12878	blood:	n/a	chr3:102392461-102392470
20	BHLHE40	chr3:102892955-102893330	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:102804471-102804525	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:102889471-102889774	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:102422725-102422866	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:102392374-102392692	GM12878	blood:	n/a	n/a
25	BRCA1	chr3:102392547-102392568	HepG2	liver:	n/a	n/a
26	BRCA1	chr3:102698938-102699119	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr3:102706022-102706061	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:102392399-102392703	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr3:102771085-102771792	HCT-116	colon:	n/a	n/a
30	CBX3	chr3:102767058-102767701	HCT-116	colon:	n/a	n/a
31	CBX3	chr3:102766422-102766858	HCT-116	colon:	n/a	n/a
32	CBX3	chr3:102645276-102645646	HCT-116	colon:	n/a	n/a
33	CBX3	chr3:102433895-102434298	HCT-116	colon:	n/a	n/a
34	CCNT2	chr3:102592280-102592455	K562	blood:	n/a	n/a
35	CCNT2	chr3:102882271-102882471	K562	blood:	n/a	n/a
36	CEBPB	chr3:102475613-102475945	Hela-S3	cervix:	n/a	chr3:102475781-102475792
37	CEBPB	chr3:102453031-102453389	IMR90	lung:	n/a	chr3:102453202-102453213
38	CEBPB	chr3:102428627-102428945	HepG2	liver:	n/a	chr3:102428795-102428808 chr3:102428795-102428806
39	CEBPB	chr3:102476691-102477111	A549	lung:	n/a	chr3:102476939-102476950
40	CEBPB	chr3:102452970-102453402	ECC-1	luminal epithelium:	n/a	chr3:102453202-102453213
41	CEBPB	chr3:102865958-102866305	Hela-S3	cervix:	n/a	chr3:102866124-102866135
42	CEBPB	chr3:102491824-102492038	A549	lung:	n/a	n/a
43	CEBPB	chr3:102899975-102900407	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr3:102570410-102570681	Hela-S3	cervix:	n/a	chr3:102570542-102570553
45	CEBPB	chr3:102570456-102570693	HepG2	liver:	n/a	chr3:102570542-102570553
46	CEBPB	chr3:102369586-102369668	A549	lung:	n/a	n/a
47	CEBPB	chr3:102546992-102547331	HepG2	liver:	n/a	chr3:102547136-102547147 chr3:102547150-102547161
48	CEBPB	chr3:102614513-102614802	HepG2	liver:	n/a	chr3:102614668-102614681 chr3:102614669-102614680
49	CEBPB	chr3:102666021-102666266	HepG2	liver:	n/a	n/a
50	CEBPB	chr3:102452955-102453352	A549	lung:	n/a	chr3:102453202-102453213

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:102399370-102399420	HepG2	liver:	n/a
2	chr3:102452667-102452717	NHBE	bronchial:	n/a
3	chr3:102745783-102745833	AG04449	skin:	fetal
4	chr3:102775449-102775499	HCM	heart:	n/a
5	chr3:102745783-102745833	SK-N-SH	brain:	n/a
6	chr3:102452667-102452717	HUVEC	blood vessel:	n/a
7	chr3:102745783-102745833	AG10803	skin:	n/a
8	chr3:102392777-102392827	AG04450	lung:	fetal
9	chr3:102775449-102775499	SK-N-SH	brain:	n/a
10	chr3:102392777-102392827	AG10803	skin:	n/a
11	chr3:102392777-102392827	AG09309	skin:	n/a
12	chr3:102399370-102399420	Hepatocyte	liver:	n/a
13	chr3:102452667-102452717	HCT-116	colon:	n/a
14	chr3:102745783-102745833	K562	blood:	n/a
15	chr3:102745783-102745833	ovcar-3	ovarian:	n/a
16	chr3:102452667-102452717	SK-N-MC	brain:	n/a
17	chr3:102775941-102775991	HIPEpiC	eye:	n/a
18	chr3:102392777-102392827	K562	blood:	n/a
19	chr3:102775941-102775991	HUVEC	blood vessel:	n/a
20	chr3:102392777-102392827	HMEC	breast:	n/a
21	chr3:102392777-102392827	SAEC	small airway:	n/a
22	chr3:102399370-102399420	HCT-116	colon:	n/a
23	chr3:102775449-102775499	A549	lung:	n/a
24	chr3:102399370-102399420	A549	lung:	n/a
25	chr3:102399370-102399420	CMK	blood:	n/a
26	chr3:102392777-102392827	CMK	blood:	n/a
27	chr3:102745783-102745833	MCF10A-Er-Src	breast:	n/a
28	chr3:102745783-102745833	HEK293	kidney:	embryo
29	chr3:102452667-102452717	HCF	heart:	n/a
30	chr3:102392777-102392827	U87	brain:	n/a
31	chr3:102775941-102775991	BJ	skin:	n/a
32	chr3:102399370-102399420	HL-60	blood:	n/a
33	chr3:102775449-102775499	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:102775941-102775991	RPTEC	kidney:	n/a
35	chr3:102775941-102775991	NHBE	bronchial:	n/a
36	chr3:102399370-102399420	AG09309	skin:	n/a
37	chr3:102399370-102399420	ProgFib	skin:	n/a
38	chr3:102745783-102745833	H1-hESC	embryonic stem cell:	embryo
39	chr3:102775941-102775991	HL-60	blood:	n/a
40	chr3:102392777-102392827	PFSK-1	brain:	n/a
41	chr3:102775941-102775991	AoSMC	blood vessel:	n/a
42	chr3:102452667-102452717	AG04449	skin:	fetal
43	chr3:102399370-102399420	Caco-2	colon:	n/a
44	chr3:102775941-102775991	HMEC	breast:	n/a
45	chr3:102452667-102452717	HRPEpiC	eye:	n/a
46	chr3:102452667-102452717	Hepatocyte	liver:	n/a
47	chr3:102745783-102745833	NHDF-neo	bronchial:	n/a
48	chr3:102399370-102399420	HNPCEpiC	eye:	n/a
49	chr3:102392777-102392827	SK-N-SH_RA	brain:	n/a
50	chr3:102775449-102775499	HIPEpiC	eye:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:102605564..102608047-chr3:102611373..102613671,2	MCF-7	breast:
2	chr3:102879980..102881764-chr3:102891406..102893851,2	K562	blood:
3	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
4	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
5	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:
6	chr3:102390233..102392000-chr3:102397005..102399673,2	K562	blood:
7	chr3:102464455..102465347-chr3:103014445..103015094,2	MCF-7	breast:
8	chr10:6242657..6245501-chr3:102426733..102428233,2	MCF-7	breast:
9	chr12:122459732..122460381-chr3:102427713..102428233,2	MCF-7	breast:
10	chr3:101954215..101955159-chr3:102459734..102460417,3	MCF-7	breast:
11	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
12	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
13	chr3:102614501..102616425-chr3:102617335..102619639,2	K562	blood:
14	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
15	chr17:57914812..57915374-chr3:102427713..102428233,2	MCF-7	breast:
16	chr3:102391655..102393123-chr3:102459418..102460722,10	MCF-7	breast:
17	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
18	chr3:102391603..102393690-chr3:102431669..102434137,2	MCF-7	breast:
19	chr3:102189575..102190143-chr3:102459670..102460629,2	MCF-7	breast:
20	chr3:102392117..102393057-chr3:102459325..102460566,3	MCF-7	breast:
21	chr11:118778943..118781778-chr3:102426713..102428213,2	MCF-7	breast:
22	chr3:102605564..102608047-chr3:102611373..102613671,2	MCF-7	breast:
23	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
24	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
25	chr3:102426713..102428233-chr9:94668915..94670633,2	K562	blood:
26	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
27	chr3:101954266..101954823-chr3:102459665..102460276,2	MCF-7	breast:
28	chr20:56269510..56272225-chr3:102426713..102428233,3	MCF-7	breast:
29	chr3:102426713..102428233-chr3:161131598..161134258,2	MCF-7	breast:
30	chr3:102879980..102881764-chr3:102891406..102893851,2	K562	blood:
31	chr17:56708753..56709302-chr3:102427713..102428213,2	MCF-7	breast:
32	chr17:58677371..58678089-chr3:102427713..102428213,2	MCF-7	breast:
33	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
34	chr17:57917124..57920044-chr3:102426713..102428447,2	MCF-7	breast:
35	chr20:61600485..61601062-chr3:102727370..102728350,2	NB4	blood:
36	chr12:56546032..56548424-chr3:102426713..102428233,2	MCF-7	breast:
37	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:
38	chr14:50456042..50458929-chr3:102668264..102669764,2	MCF-7	breast:
39	chr11:74967205..74967954-chr3:102761303..102762194,2	MCF-7	breast:
40	chr10:44756642..44757448-chr3:102730464..102731003,2	MCF-7	breast:
41	chr3:102390233..102392000-chr3:102397005..102399673,2	K562	blood:
42	chr3:102614501..102616425-chr3:102617335..102619639,2	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL24-2	chr3:102382007-102382267	XLOC_003194
2	lnc-ZPLD1-6	chr3:102888748-102888923	l_2419_chr3:102888747-102894491_prostate
3	lnc-ZPLD1-2	chr3:102863471-102863517	XLOC_002743
4	lnc-RPL24-2	chr3:102382143-102382168	XLOC_003194
5	lnc-RPL24-2	chr3:102386026-102386119	XLOC_003194
6	lnc-ZPLD1-2	chr3:102636251-102636282	XLOC_002743
7	lnc-ZPLD1-2	chr3:102865617-102865744	XLOC_002743
8	lnc-ZPLD1-5	chr3:102775889-102776094	expReg_chr3_7071_+
9	lnc-ZPLD1-1	chr3:102429679-102429722	NONHSAT090932
10	lnc-RPL24-2	chr3:102392598-102392850	XLOC_003194
11	lnc-RPL24-2	chr3:102383382-102384456	XLOC_003194
12	lnc-RPL24-2	chr3:102392598-102392757	XLOC_003194
13	lnc-RPL24-2	chr3:102392598-102392802	XLOC_003194
14	lnc-ZPLD1-1	chr3:102444626-102444901	NONHSAT090932
15	lnc-ZPLD1-1	chr3:102444624-102444901	NONHSAT090933
16	lnc-ZPLD1-2	chr3:102859657-102859798	XLOC_002743
17	lnc-ZPLD1-2	chr3:102817066-102817185	XLOC_002743
18	lnc-ZPLD1-1	chr3:102446238-102446423	NONHSAT090932
19	lnc-ZPLD1-4	chr3:102651432-102651473	FPKM1_group_21624_transcript_1
20	lnc-RPL24-2	chr3:102387891-102388106	XLOC_003194
21	lnc-ZPLD1-4	chr3:102644557-102644725	NONHSAT090938
22	lnc-ZPLD1-1	chr3:102446237-102446410	NONHSAT090933
23	lnc-ZPLD1-6	chr3:102894427-102894491	l_2419_chr3:102888747-102894491_prostate
24	lnc-ZPLD1-2	chr3:102868713-102868835	XLOC_002743
25	lnc-RPL24-2	chr3:102379501-102379812	XLOC_003194
26	lnc-ZPLD1-2	chr3:102871138-102871281	XLOC_002743
27	lnc-ZPLD1-1	chr3:102444625-102444901	XLOC_002742
28	lnc-ZPLD1-4	chr3:102644557-102644725	FPKM1_group_21624_transcript_1
29	lnc-RPL24-2	chr3:102386026-102386119	XLOC_003194
30	lnc-ZPLD1-1	chr3:102446238-102446410	XLOC_002742
31	lnc-ZPLD1-4	chr3:102651432-102651851	NONHSAT090938

No data

Variant related genes	Relation type
RNU6-461P	TF binding region
ENSG00000241754	TF binding region
RNU1-43P	TF binding region
RNU6-461P	CpG island
ENSG00000241754	CpG island
RNU1-43P	CpG island
ENSG00000186174	chromatin interactions
ENSG00000170525	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000110987	chromatin interactions
ENSG00000241754	chromatin interactions
ENSG00000196465	chromatin interactions
ENSG00000237590	chromatin interactions
ENSG00000213994	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000264211	chromatin interactions
ARHGAP12	miRNA target sites
FAM122A	miRNA target sites
SLC7A11	miRNA target sites
HOXA9	miRNA target sites
FAM122B	miRNA target sites
BTG3	miRNA target sites

Extended variants
information (count: 7689 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7689 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537516879	chr3:102367439-102367440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150865985	chr3:102367515-102367516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182111750	chr3:102367518-102367519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531574814	chr3:102367520-102367521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534699907	chr3:102367529-102367530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148996263	chr3:102367537-102367538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557417840	chr3:102367550-102367551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571961791	chr3:102367680-102367681	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs542434554	chr3:102367718-102367719	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs560713928	chr3:102367732-102367733	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs575815139	chr3:102367738-102367739	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs187771029	chr3:102367748-102367749	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs139364863	chr3:102367771-102367772	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs532177159	chr3:102367781-102367782	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs143053873	chr3:102367782-102367783	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs560095050	chr3:102367855-102367856	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs575598759	chr3:102367906-102367907	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs546134751	chr3:102367915-102367916	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs1464116	chr3:102367926-102367927	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548817493	chr3:102368024-102368025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73863965	chr3:102368049-102368050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532415938	chr3:102368057-102368058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139072636	chr3:102368068-102368069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192340358	chr3:102368069-102368070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570816933	chr3:102368101-102368102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374407268	chr3:102368122-102368123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80249453	chr3:102368139-102368140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144007917	chr3:102368164-102368165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536173080	chr3:102368209-102368210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554419201	chr3:102368293-102368294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576230718	chr3:102368314-102368315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35848274	chr3:102368328-102368329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397775723	chr3:102368338-102368339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs71798770	chr3:102368339-102368340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200368148	chr3:102368340-102368341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115947237	chr3:102368366-102368367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72946922	chr3:102368410-102368411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs57757391	chr3:102368455-102368456	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs56163111	chr3:102368500-102368501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183209073	chr3:102368504-102368505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529699085	chr3:102368530-102368531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548927631	chr3:102368536-102368537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563968342	chr3:102368538-102368539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531143775	chr3:102368557-102368558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368333817	chr3:102368594-102368595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570946159	chr3:102368597-102368598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188839752	chr3:102368638-102368639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546672113	chr3:102368650-102368651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148625357	chr3:102368737-102368738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535451761	chr3:102368775-102368776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102367400-102367600	Enhancers	Stomach Mucosa	stomach
2	chr3:102367600-102368000	Active TSS	Stomach Mucosa	stomach
3	chr3:102368000-102369000	Weak transcription	Stomach Mucosa	stomach
4	chr3:102369000-102369400	Enhancers	Stomach Mucosa	stomach
5	chr3:102374600-102375600	Enhancers	Stomach Mucosa	stomach
6	chr3:102379400-102383400	Enhancers	Liver	Liver
7	chr3:102381200-102381400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr3:102383400-102389000	Weak transcription	Liver	Liver
9	chr3:102385800-102387400	Enhancers	Stomach Mucosa	stomach
10	chr3:102387200-102387600	Enhancers	Fetal Muscle Leg	muscle
11	chr3:102387400-102389400	Weak transcription	Stomach Mucosa	stomach
12	chr3:102389000-102392200	Enhancers	Liver	Liver
13	chr3:102389400-102390000	Enhancers	Stomach Mucosa	stomach
14	chr3:102389600-102390400	Enhancers	Fetal Intestine Small	intestine
15	chr3:102389800-102390400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:102389800-102390400	Enhancers	HepG2	liver
17	chr3:102389800-102392000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr3:102390000-102392200	Weak transcription	Stomach Mucosa	stomach
19	chr3:102390400-102392600	Weak transcription	HepG2	liver
20	chr3:102390800-102391000	Enhancers	Brain Anterior Caudate	brain
21	chr3:102391000-102392600	Weak transcription	Brain Anterior Caudate	brain
22	chr3:102391200-102391400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:102391200-102394800	Enhancers	Fetal Heart	heart
24	chr3:102392000-102392200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr3:102392200-102392400	Enhancers	Fetal Lung	lung
26	chr3:102392200-102392400	Enhancers	Stomach Mucosa	stomach
27	chr3:102392200-102392600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:102392200-102392800	Flanking Active TSS	Liver	Liver
29	chr3:102392200-102392800	Active TSS	Right Atrium	heart
30	chr3:102392200-102393000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:102392200-102393000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:102392200-102393000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:102392200-102393000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr3:102392200-102393000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr3:102392200-102393000	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr3:102392200-102393000	Enhancers	Fetal Stomach	stomach
37	chr3:102392400-102392600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr3:102392400-102392600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr3:102392400-102392600	Enhancers	Brain Germinal Matrix	brain
40	chr3:102392400-102392600	Enhancers	Fetal Kidney	kidney
41	chr3:102392400-102392600	Active TSS	Ovary	ovary
42	chr3:102392400-102392600	Active TSS	NH-A	brain
43	chr3:102392400-102392800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr3:102392400-102392800	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr3:102392400-102392800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
46	chr3:102392400-102392800	Flanking Active TSS	Fetal Lung	lung
47	chr3:102392400-102392800	Active TSS	Fetal Muscle Trunk	muscle
48	chr3:102392400-102392800	Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr3:102392400-102392800	Active TSS	Stomach Mucosa	stomach
50	chr3:102392400-102392800	Active TSS	Hela-S3	cervix

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