Variant report

Variant	nsv591190
Chromosome Location	chr3:102345638-102946216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2078)
CpG islands
(count:366)
Chromatin interactive
region (count:43)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

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	chr3:102406889-102407383	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr3:102433789-102434329	GM12878	blood:	n/a	n/a
5	ATF2	chr3:102846474-102847000	GM12878	blood:	n/a	n/a
6	ATF2	chr3:102936818-102937806	GM12878	blood:	n/a	n/a
7	ATF2	chr3:102936808-102937519	GM12878	blood:	n/a	n/a
8	ATF2	chr3:102407030-102407386	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:102846504-102846873	GM12878	blood:	n/a	n/a
10	BACH1	chr3:102648843-102648847	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:102936907-102937418	GM12878	blood:	n/a	n/a
12	BATF	chr3:102936937-102937408	GM12878	blood:	n/a	n/a
13	BATF	chr3:102846641-102846881	GM12878	blood:	n/a	n/a
14	BATF	chr3:102433864-102434252	GM12878	blood:	n/a	chr3:102434009-102434020
15	BATF	chr3:102433856-102434213	GM12878	blood:	n/a	chr3:102434009-102434020
16	BATF	chr3:102652328-102652528	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:102846636-102846904	GM12878	blood:	n/a	chr3:102846753-102846762
18	BCL11A	chr3:102407072-102407277	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr3:102936945-102937388	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:102407054-102407384	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr3:102936940-102937450	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:102433900-102434146	GM12878	blood:	n/a	chr3:102434012-102434021
23	BCL3	chr3:102698808-102699149	A549	lung:	n/a	n/a
24	BCL3	chr3:102936869-102937427	GM12878	blood:	n/a	n/a
25	BCL3	chr3:102936961-102937363	GM12878	blood:	n/a	n/a
26	BCLAF1	chr3:102392318-102392743	GM12878	blood:	n/a	chr3:102392461-102392470
27	BCLAF1	chr3:102936803-102937523	GM12878	blood:	n/a	n/a
28	BCLAF1	chr3:102392360-102392720	GM12878	blood:	n/a	chr3:102392461-102392470
29	BCLAF1	chr3:102936936-102937419	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:102892955-102893330	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:102804471-102804525	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:102422725-102422866	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:102936950-102937419	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:102889471-102889774	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:102392374-102392692	GM12878	blood:	n/a	n/a
36	BRCA1	chr3:102392399-102392703	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr3:102392547-102392568	HepG2	liver:	n/a	n/a
38	BRCA1	chr3:102698938-102699119	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr3:102706022-102706061	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr3:102767058-102767701	HCT-116	colon:	n/a	n/a
41	CBX3	chr3:102645276-102645646	HCT-116	colon:	n/a	n/a
42	CBX3	chr3:102766422-102766858	HCT-116	colon:	n/a	n/a
43	CBX3	chr3:102771085-102771792	HCT-116	colon:	n/a	n/a
44	CBX3	chr3:102433895-102434298	HCT-116	colon:	n/a	n/a
45	CCNT2	chr3:102882271-102882471	K562	blood:	n/a	n/a
46	CCNT2	chr3:102592280-102592455	K562	blood:	n/a	n/a
47	CEBPB	chr3:102369586-102369668	A549	lung:	n/a	n/a
48	CEBPB	chr3:102452678-102453419	Hela-S3	cervix:	n/a	chr3:102453202-102453213
49	CEBPB	chr3:102580890-102581090	A549	lung:	n/a	n/a
50	CEBPB	chr3:102604626-102604906	HepG2	liver:	n/a	chr3:102604766-102604777

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:102775449-102775499	CMK	blood:	n/a
2	chr3:102775449-102775499	T-47D	breast:	n/a
3	chr3:102775941-102775991	A549	lung:	n/a
4	chr3:102745783-102745833	GM12892	blood:	n/a
5	chr3:102392777-102392827	K562	blood:	n/a
6	chr3:102775941-102775991	HCT-116	colon:	n/a
7	chr3:102392777-102392827	SK-N-MC	brain:	n/a
8	chr3:102399370-102399420	PrEC	prostate:	n/a
9	chr3:102745783-102745833	GM12878	blood:	n/a
10	chr3:102452667-102452717	LNCaP	prostate:	n/a
11	chr3:102775941-102775991	IMR90	lung:	fetal
12	chr3:102745783-102745833	CMK	blood:	n/a
13	chr3:102392777-102392827	HCPEpiC	choroid plexus:	n/a
14	chr3:102452667-102452717	HEK293	kidney:	embryo
15	chr3:102452667-102452717	H1-hESC	embryonic stem cell:	embryo
16	chr3:102399370-102399420	RPTEC	kidney:	n/a
17	chr3:102399370-102399420	T-47D	breast:	n/a
18	chr3:102392777-102392827	HEEpiC	esophagus:	n/a
19	chr3:102775449-102775499	HIPEpiC	eye:	n/a
20	chr3:102775449-102775499	HCPEpiC	choroid plexus:	n/a
21	chr3:102452667-102452717	RPTEC	kidney:	n/a
22	chr3:102399370-102399420	PANC-1	pancreas:	n/a
23	chr3:102452667-102452717	ovcar-3	ovarian:	n/a
24	chr3:102775449-102775499	NHBE	bronchial:	n/a
25	chr3:102775941-102775991	BJ	skin:	n/a
26	chr3:102745783-102745833	NHBE	bronchial:	n/a
27	chr3:102399370-102399420	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:102775449-102775499	HCM	heart:	n/a
29	chr3:102452667-102452717	HAEpiC	amniotic membrane:	n/a
30	chr3:102399370-102399420	NT2-D1	testis:	n/a
31	chr3:102745783-102745833	HepG2	liver:	n/a
32	chr3:102775941-102775991	H1-hESC	embryonic stem cell:	embryo
33	chr3:102399370-102399420	AG09309	skin:	n/a
34	chr3:102399370-102399420	AG10803	skin:	n/a
35	chr3:102392777-102392827	AG09319	gingival:	n/a
36	chr3:102392777-102392827	NHBE	bronchial:	n/a
37	chr3:102745783-102745833	Hela-S3	cervix:	n/a
38	chr3:102399370-102399420	BE2_C	brain:	n/a
39	chr3:102745783-102745833	GM19239	blood:	n/a
40	chr3:102399370-102399420	GM12891	blood:	n/a
41	chr3:102399370-102399420	PFSK-1	brain:	n/a
42	chr3:102452667-102452717	ProgFib	skin:	n/a
43	chr3:102775449-102775499	MCF-7	breast:	n/a
44	chr3:102775941-102775991	HRPEpiC	eye:	n/a
45	chr3:102399370-102399420	IMR90	lung:	fetal
46	chr3:102392777-102392827	SK-N-SH	brain:	n/a
47	chr3:102452667-102452717	K562	blood:	n/a
48	chr3:102745783-102745833	HCF	heart:	n/a
49	chr3:102775941-102775991	LNCaP	prostate:	n/a
50	chr3:102745783-102745833	BJ	skin:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56546032..56548424-chr3:102426713..102428233,2	MCF-7	breast:
2	chr1:188479024..188479715-chr3:102939006..102939691,2	MCF-7	breast:
3	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:
4	chr3:101954266..101954823-chr3:102459665..102460276,2	MCF-7	breast:
5	chr17:57914812..57915374-chr3:102427713..102428233,2	MCF-7	breast:
6	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
7	chr3:102189575..102190143-chr3:102459670..102460629,2	MCF-7	breast:
8	chr3:102388490..102390464-chr3:102393522..102395423,2	K562	blood:
9	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
10	chr3:102605564..102608047-chr3:102611373..102613671,2	MCF-7	breast:
11	chr3:102390233..102392000-chr3:102397005..102399673,2	K562	blood:
12	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
13	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
14	chr11:118778943..118781778-chr3:102426713..102428213,2	MCF-7	breast:
15	chr3:102614501..102616425-chr3:102617335..102619639,2	K562	blood:
16	chr10:6242657..6245501-chr3:102426733..102428233,2	MCF-7	breast:
17	chr3:101954215..101955159-chr3:102459734..102460417,3	MCF-7	breast:
18	chr3:102390944..102392108-chr3:102459462..102460176,3	MCF-7	breast:
19	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:
20	chr3:102426713..102428233-chr3:161131598..161134258,2	MCF-7	breast:
21	chr14:50456042..50458929-chr3:102668264..102669764,2	MCF-7	breast:
22	chr3:102605564..102608047-chr3:102611373..102613671,2	MCF-7	breast:
23	chr3:102464455..102465347-chr3:103014445..103015094,2	MCF-7	breast:
24	chr17:58677371..58678089-chr3:102427713..102428213,2	MCF-7	breast:
25	chr3:102879980..102881764-chr3:102891406..102893851,2	K562	blood:
26	chr20:56269510..56272225-chr3:102426713..102428233,3	MCF-7	breast:
27	chr11:74967205..74967954-chr3:102761303..102762194,2	MCF-7	breast:
28	chr3:102614501..102616425-chr3:102617335..102619639,2	K562	blood:
29	chr17:56708753..56709302-chr3:102427713..102428213,2	MCF-7	breast:
30	chr12:122459732..122460381-chr3:102427713..102428233,2	MCF-7	breast:
31	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
32	chr3:102879980..102881764-chr3:102891406..102893851,2	K562	blood:
33	chr10:44756642..44757448-chr3:102730464..102731003,2	MCF-7	breast:
34	chr3:102476779..102479193-chr3:102480269..102482631,2	K562	blood:
35	chr3:102482837..102485158-chr3:102486260..102488498,2	MCF-7	breast:
36	chr3:102391603..102393690-chr3:102431669..102434137,2	MCF-7	breast:
37	chr20:61600485..61601062-chr3:102727370..102728350,2	NB4	blood:
38	chr3:102392117..102393057-chr3:102459325..102460566,3	MCF-7	breast:
39	chr17:57917124..57920044-chr3:102426713..102428447,2	MCF-7	breast:
40	chr3:102426713..102428233-chr9:94668915..94670633,2	K562	blood:
41	chr3:102388308..102390464-chr3:102393036..102395423,2	K562	blood:
42	chr3:102391655..102393123-chr3:102459418..102460722,10	MCF-7	breast:
43	chr3:102390233..102392000-chr3:102397005..102399673,2	K562	blood:

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

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

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
ENSG00000062716	chromatin interactions
ENSG00000186174	chromatin interactions
ENSG00000264211	chromatin interactions
ENSG00000170525	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000241754	chromatin interactions
ENSG00000237590	chromatin interactions
ENSG00000110987	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000213994	chromatin interactions
ENSG00000196465	chromatin interactions
FAM122B	miRNA target sites
SLC7A11	miRNA target sites
HOXA9	miRNA target sites
ARHGAP12	miRNA target sites
FAM122A	miRNA target sites
BTG3	miRNA target sites

Extended variants
information (count: 8043 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:8043 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1356106	chr3:102345638-102345639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs137908818	chr3:102345667-102345668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13071126	chr3:102345683-102345684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs528153965	chr3:102345784-102345785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs58984852	chr3:102345890-102345891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555366416	chr3:102345914-102345915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573667295	chr3:102345917-102345918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544186816	chr3:102345956-102345957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201357204	chr3:102345971-102345972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187738234	chr3:102345985-102345986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570849182	chr3:102346005-102346006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546211337	chr3:102346093-102346094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564266993	chr3:102346116-102346117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528197275	chr3:102346124-102346125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1399765	chr3:102346138-102346139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567747464	chr3:102346157-102346158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191257990	chr3:102346216-102346217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114890629	chr3:102346251-102346252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528844187	chr3:102346252-102346253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141071157	chr3:102346256-102346257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7619933	chr3:102346262-102346263	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs150266145	chr3:102346281-102346282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183370621	chr3:102346311-102346312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567029484	chr3:102346366-102346367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74825639	chr3:102346377-102346378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527890917	chr3:102346385-102346386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540033623	chr3:102350406-102350407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545917326	chr3:102350409-102350410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4264709	chr3:102350444-102350445	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs573360393	chr3:102350452-102350453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549343021	chr3:102350499-102350500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9833063	chr3:102350504-102350505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs543820078	chr3:102350531-102350532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187775431	chr3:102350583-102350584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192342510	chr3:102350599-102350600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184025280	chr3:102350602-102350603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147374167	chr3:102350662-102350663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188574847	chr3:102350674-102350675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80230357	chr3:102350708-102350709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551891190	chr3:102350728-102350729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78829619	chr3:102350819-102350820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535355144	chr3:102350830-102350831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547353777	chr3:102350880-102350881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193066475	chr3:102350976-102350977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370803236	chr3:102350985-102350986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557520032	chr3:102350990-102350991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569261220	chr3:102351004-102351005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs137964805	chr3:102351055-102351056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562966181	chr3:102351102-102351103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77051249	chr3:102351104-102351105	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:625 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102344800-102346200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:102345600-102346200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:102346200-102346400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:102346200-102346400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr3:102350400-102352400	Weak transcription	Pancreas	Pancrea
6	chr3:102367400-102367600	Enhancers	Stomach Mucosa	stomach
7	chr3:102367600-102368000	Active TSS	Stomach Mucosa	stomach
8	chr3:102368000-102369000	Weak transcription	Stomach Mucosa	stomach
9	chr3:102369000-102369400	Enhancers	Stomach Mucosa	stomach
10	chr3:102374600-102375600	Enhancers	Stomach Mucosa	stomach
11	chr3:102379400-102383400	Enhancers	Liver	Liver
12	chr3:102381200-102381400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr3:102383400-102389000	Weak transcription	Liver	Liver
14	chr3:102385800-102387400	Enhancers	Stomach Mucosa	stomach
15	chr3:102387200-102387600	Enhancers	Fetal Muscle Leg	muscle
16	chr3:102387400-102389400	Weak transcription	Stomach Mucosa	stomach
17	chr3:102389000-102392200	Enhancers	Liver	Liver
18	chr3:102389400-102390000	Enhancers	Stomach Mucosa	stomach
19	chr3:102389600-102390400	Enhancers	Fetal Intestine Small	intestine
20	chr3:102389800-102390400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:102389800-102390400	Enhancers	HepG2	liver
22	chr3:102389800-102392000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr3:102390000-102392200	Weak transcription	Stomach Mucosa	stomach
24	chr3:102390400-102392600	Weak transcription	HepG2	liver
25	chr3:102390800-102391000	Enhancers	Brain Anterior Caudate	brain
26	chr3:102391000-102392600	Weak transcription	Brain Anterior Caudate	brain
27	chr3:102391200-102391400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:102391200-102394800	Enhancers	Fetal Heart	heart
29	chr3:102392000-102392200	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr3:102392200-102392400	Enhancers	Fetal Lung	lung
31	chr3:102392200-102392400	Enhancers	Stomach Mucosa	stomach
32	chr3:102392200-102392600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:102392200-102392800	Flanking Active TSS	Liver	Liver
34	chr3:102392200-102392800	Active TSS	Right Atrium	heart
35	chr3:102392200-102393000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr3:102392200-102393000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr3:102392200-102393000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:102392200-102393000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr3:102392200-102393000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr3:102392200-102393000	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr3:102392200-102393000	Enhancers	Fetal Stomach	stomach
42	chr3:102392400-102392600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr3:102392400-102392600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr3:102392400-102392600	Enhancers	Brain Germinal Matrix	brain
45	chr3:102392400-102392600	Enhancers	Fetal Kidney	kidney
46	chr3:102392400-102392600	Active TSS	Ovary	ovary
47	chr3:102392400-102392600	Active TSS	NH-A	brain
48	chr3:102392400-102392800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
49	chr3:102392400-102392800	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr3:102392400-102392800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood

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