Variant report

Variant	nsv829876
Chromosome Location	chr4:20638736-20835621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:20775077-20775342	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:20692322-20692456	K562	blood:	n/a	n/a
3	ARID3A	chr4:20700015-20700842	K562	blood:	n/a	n/a
4	ARID3A	chr4:20701592-20701812	K562	blood:	n/a	n/a
5	ARID3A	chr4:20701873-20702300	HepG2	liver:	n/a	n/a
6	ATF1	chr4:20701653-20702260	K562	blood:	n/a	chr4:20702025-20702039
7	ATF1	chr4:20700407-20700806	K562	blood:	n/a	n/a
8	ATF2	chr4:20701648-20702230	H1-hESC	embryonic stem cell:	n/a	chr4:20702025-20702039
9	ATF3	chr4:20701728-20702041	A549	lung:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
10	ATF3	chr4:20700358-20700813	K562	blood:	n/a	n/a
11	ATF3	chr4:20701812-20702063	GM12878	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
12	ATF3	chr4:20701755-20702123	H1-hESC	embryonic stem cell:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
13	ATF3	chr4:20701701-20702121	K562	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
14	ATF3	chr4:20701711-20702195	HepG2	liver:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
15	ATF3	chr4:20701697-20702170	H1-hESC	embryonic stem cell:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
16	ATF3	chr4:20701739-20702217	K562	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
17	ATF3	chr4:20701734-20702174	GM12878	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
18	BACH1	chr4:20817391-20817392	H1-hESC	embryonic stem cell:	n/a	n/a
19	BHLHE40	chr4:20700392-20700749	K562	blood:	n/a	n/a
20	BHLHE40	chr4:20811465-20811810	HepG2	liver:	n/a	n/a
21	BHLHE40	chr4:20775048-20775386	HepG2	liver:	n/a	n/a
22	BHLHE40	chr4:20701625-20702344	K562	blood:	n/a	n/a
23	BHLHE40	chr4:20686889-20687054	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:20701479-20702280	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:20688384-20688430	K562	blood:	n/a	n/a
26	BHLHE40	chr4:20726709-20727073	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:20701761-20702364	HepG2	liver:	n/a	n/a
28	BRCA1	chr4:20701819-20702207	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr4:20686884-20687072	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr4:20701812-20702075	HepG2	liver:	n/a	n/a
31	CBX3	chr4:20701588-20702105	K562	blood:	n/a	n/a
32	CCNT2	chr4:20701740-20702316	K562	blood:	n/a	n/a
33	CCNT2	chr4:20700385-20700870	K562	blood:	n/a	n/a
34	CEBPB	chr4:20700057-20700382	A549	lung:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
35	CEBPB	chr4:20701891-20702151	K562	blood:	n/a	n/a
36	CEBPB	chr4:20700058-20700392	Hela-S3	cervix:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
37	CEBPB	chr4:20691553-20691591	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:20741677-20741914	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:20798521-20798728	HepG2	liver:	n/a	chr4:20798642-20798653
40	CEBPB	chr4:20699992-20700456	MCF-7	breast:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
41	CEBPB	chr4:20814036-20814312	IMR90	lung:	n/a	chr4:20814155-20814166
42	CEBPB	chr4:20699982-20700715	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
43	CEBPB	chr4:20702839-20703100	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:20699967-20700805	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
45	CEBPB	chr4:20700088-20700367	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
46	CEBPB	chr4:20733786-20734123	H1-hESC	embryonic stem cell:	n/a	chr4:20733957-20733968
47	CEBPB	chr4:20797177-20797386	A549	lung:	n/a	chr4:20797259-20797272 chr4:20797259-20797270
48	CEBPB	chr4:20741665-20741893	K562	blood:	n/a	n/a
49	CEBPB	chr4:20700053-20700351	H1-hESC	embryonic stem cell:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
50	CEBPB	chr4:20699983-20700439	MCF-7	breast:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20701889-20701939	ECC-1	luminal epithelium:	n/a
2	chr4:20701889-20701939	ECC-1	luminal epithelium:	n/a
3	chr4:20701990-20702040	HRPEpiC	eye:	n/a
4	chr4:20706485-20706535	HCF	heart:	n/a
5	chr4:20701691-20701741	HCT-116	colon:	n/a
6	chr4:20811042-20811092	HRPEpiC	eye:	n/a
7	chr4:20706485-20706535	GM06990	blood:	n/a
8	chr4:20811042-20811092	HCPEpiC	choroid plexus:	n/a
9	chr4:20660098-20660148	SK-N-MC	brain:	n/a
10	chr4:20706485-20706535	HRCEpiC	kidney:	n/a
11	chr4:20702045-20702095	HUVEC	blood vessel:	n/a
12	chr4:20702182-20702232	PrEC	prostate:	n/a
13	chr4:20701889-20701939	HMEC	breast:	n/a
14	chr4:20701925-20701975	MCF10A-Er-Src	breast:	n/a
15	chr4:20701925-20701975	HAEpiC	amniotic membrane:	n/a
16	chr4:20701914-20701964	SKMC	muscle:	n/a
17	chr4:20811042-20811092	NT2-D1	testis:	n/a
18	chr4:20660098-20660148	ovcar-3	ovarian:	n/a
19	chr4:20702329-20702379	HEK293	kidney:	embryo
20	chr4:20701950-20702000	IMR90	lung:	fetal
21	chr4:20701691-20701741	AG10803	skin:	n/a
22	chr4:20702329-20702379	SK-N-MC	brain:	n/a
23	chr4:20702182-20702232	ProgFib	skin:	n/a
24	chr4:20701914-20701964	Hepatocyte	liver:	n/a
25	chr4:20701914-20701964	CMK	blood:	n/a
26	chr4:20702045-20702095	HEEpiC	esophagus:	n/a
27	chr4:20702182-20702232	ovcar-3	ovarian:	n/a
28	chr4:20702045-20702095	HMEC	breast:	n/a
29	chr4:20706485-20706535	HNPCEpiC	eye:	n/a
30	chr4:20701691-20701741	GM12892	blood:	n/a
31	chr4:20701925-20701975	AG10803	skin:	n/a
32	chr4:20702377-20702427	ovcar-3	ovarian:	n/a
33	chr4:20660098-20660148	GM19239	blood:	n/a
34	chr4:20701925-20701975	HUVEC	blood vessel:	n/a
35	chr4:20704940-20704990	K562	blood:	n/a
36	chr4:20701691-20701741	Caco-2	colon:	n/a
37	chr4:20701990-20702040	AG09309	skin:	n/a
38	chr4:20701990-20702040	T-47D	breast:	n/a
39	chr4:20701575-20701625	AG09309	skin:	n/a
40	chr4:20701914-20701964	HRPEpiC	eye:	n/a
41	chr4:20698772-20698822	AG04449	skin:	fetal
42	chr4:20729211-20729261	IMR90	lung:	fetal
43	chr4:20702377-20702427	BJ	skin:	n/a
44	chr4:20701914-20701964	Hela-S3	cervix:	n/a
45	chr4:20729211-20729261	AG04449	skin:	fetal
46	chr4:20701990-20702040	HMEC	breast:	n/a
47	chr4:20729211-20729261	GM12891	blood:	n/a
48	chr4:20660098-20660148	BJ	skin:	n/a
49	chr4:20701914-20701964	MCF10A-Er-Src	breast:	n/a
50	chr4:20702377-20702427	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20702290..20703806-chr4:20728599..20731005,2	K562	blood:
2	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
3	chr4:20647329..20649016-chr4:20649617..20652093,2	K562	blood:
4	chr4:20678463..20679308-chr6:4856088..4856696,2	MCF-7	breast:
5	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
6	chr4:20736248..20737799-chr4:20738056..20739802,2	MCF-7	breast:
7	chr4:20699912..20701731-chr4:20714831..20716673,2	K562	blood:
8	chr4:20776494..20778419-chr4:20785252..20787706,2	K562	blood:
9	chr4:20759824..20762284-chr4:20763447..20765411,2	K562	blood:
10	chr4:20774749..20775678-chr4:21136384..21137379,5	MCF-7	breast:
11	chr4:20650338..20652484-chr4:20652879..20655131,2	K562	blood:
12	chr4:20701257..20703146-chr4:20703451..20705273,2	MCF-7	breast:
13	chr4:20736248..20737799-chr4:20738056..20739802,2	MCF-7	breast:
14	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
15	chr4:20774939..20775520-chr4:21136553..21137202,2	MCF-7	breast:
16	chr4:20700439..20703043-chr4:20709421..20711457,2	MCF-7	breast:
17	chr4:20650338..20652484-chr4:20652879..20655131,2	K562	blood:
18	chr4:20701536..20702331-chr9:91933301..91933855,2	Hela-S3	cervix:
19	chr4:20774692..20775734-chr4:21470776..21471557,3	MCF-7	breast:
20	chr4:20736150..20738048-chr4:20747130..20748840,2	K562	blood:
21	chr4:20702290..20703806-chr4:20728599..20731005,2	K562	blood:
22	chr4:20733613..20735469-chr4:20737753..20739786,2	K562	blood:
23	chr4:20733613..20735469-chr4:20737753..20739786,2	K562	blood:
24	chr4:20424367..20425209-chr4:20686856..20687583,2	MCF-7	breast:
25	chr4:20700439..20703043-chr4:20709421..20711457,2	MCF-7	breast:
26	chr4:20701205..20703695-chr4:20723209..20725454,2	MCF-7	breast:
27	chr4:20736150..20738048-chr4:20747130..20748840,2	K562	blood:
28	chr4:20702272..20703966-chr4:20709575..20711144,2	MCF-7	breast:
29	chr4:20673472..20675496-chr4:20701529..20703125,2	K562	blood:
30	chr4:20647329..20649016-chr4:20649617..20652093,2	K562	blood:
31	chr4:20693086..20698959-chr4:20699230..20704175,9	K562	blood:
32	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
33	chr4:20700229..20702940-chr4:20728046..20730028,2	MCF-7	breast:
34	chr4:20705332..20707768-chr4:20710083..20712545,3	K562	blood:
35	chr4:20702272..20703966-chr4:20709575..20711144,2	MCF-7	breast:
36	chr4:20699912..20701731-chr4:20714831..20716673,2	K562	blood:
37	chr4:20700788..20703573-chr4:20723140..20724857,2	MCF-7	breast:
38	chr4:20700245..20702604-chr4:20707211..20709448,2	MCF-7	breast:
39	chr4:20420524..20421239-chr4:20686532..20687103,2	K562	blood:
40	chr4:20702888..20705883-chr4:20707634..20710929,3	K562	blood:
41	chr4:20700245..20702604-chr4:20707211..20709448,2	MCF-7	breast:
42	chr4:20693086..20698959-chr4:20699230..20704175,9	K562	blood:
43	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
44	chr4:20702290..20704847-chr4:20728043..20731005,3	K562	blood:
45	chr4:20756151..20758021-chr4:20765219..20767901,2	K562	blood:
46	chr4:20705332..20707768-chr4:20710083..20712545,3	K562	blood:
47	chr4:20702290..20704847-chr4:20728043..20731005,3	K562	blood:
48	chr4:20759824..20762284-chr4:20763447..20765411,2	K562	blood:
49	chr4:20756151..20758021-chr4:20765219..20767901,2	K562	blood:
50	chr4:20423749..20424719-chr4:20686427..20687473,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLIT2-3	chr4:20731428-20733259	NONHSAT095738
2	lnc-SLIT2-2	chr4:20703381-20703507	NONHSAT095736
3	lnc-SLIT2-3	chr4:20733323-20734177	NONHSAT095738
4	lnc-PACRGL-6	chr4:20768431-20768995	ENSG00000272995.1
5	lnc-SLIT2-2	chr4:20704298-20704317	NONHSAT095736
6	lnc-SLIT2-2	chr4:20703764-20703844	NONHSAT095736
7	lnc-SLIT2-2	chr4:20702061-20702329	NONHSAT095736

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PACRGL	hsa-miR-373-3p	chr4:20754297-20754319

Variant related genes	Relation type
ENSG00000272995	TF binding region
PACRGL	TF binding region
ENSG00000272995	CpG island
PACRGL	CpG island
ENSG00000187742	chromatin interactions
ENSG00000163138	chromatin interactions

Extended variants
information (count: 7170 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:7170 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4697174	chr4:20638770-20638771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563651132	chr4:20638783-20638784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530924089	chr4:20638818-20638819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550138659	chr4:20638835-20638836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147467565	chr4:20638864-20638865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529127744	chr4:20638868-20638869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138379355	chr4:20638893-20638894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191931696	chr4:20638944-20638945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539473795	chr4:20638982-20638983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551184221	chr4:20638985-20638986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116294700	chr4:20639033-20639034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536636516	chr4:20639059-20639060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555670029	chr4:20639060-20639061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573969417	chr4:20639070-20639071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372825718	chr4:20639088-20639089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534901857	chr4:20639150-20639151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553488810	chr4:20639172-20639173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553166787	chr4:20639209-20639210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183667066	chr4:20639250-20639251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545528303	chr4:20639258-20639259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143928019	chr4:20639314-20639315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575742673	chr4:20639315-20639316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79163930	chr4:20639361-20639362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187902485	chr4:20639364-20639365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111878047	chr4:20639454-20639455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139842662	chr4:20639460-20639461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556134898	chr4:20639461-20639462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149405912	chr4:20639466-20639467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576003786	chr4:20639506-20639507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559546976	chr4:20639571-20639572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532975225	chr4:20639587-20639588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116496135	chr4:20639598-20639599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569392746	chr4:20639630-20639631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544529236	chr4:20639668-20639669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377647948	chr4:20639684-20639685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144813782	chr4:20639715-20639716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548533934	chr4:20639726-20639727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567627375	chr4:20639911-20639912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564710422	chr4:20639934-20639935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs5856572	chr4:20640009-20640010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199636155	chr4:20640010-20640011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3074577	chr4:20640022-20640023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578085099	chr4:20640028-20640029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191211867	chr4:20640139-20640140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578154069	chr4:20640155-20640156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538842565	chr4:20640156-20640157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557454692	chr4:20640180-20640181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575779111	chr4:20640202-20640203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545906129	chr4:20640249-20640250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56237079	chr4:20640285-20640286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20636800-20641800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:20640600-20642000	Enhancers	Liver	Liver
3	chr4:20641800-20642200	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr4:20642000-20647400	Weak transcription	Liver	Liver
5	chr4:20643200-20644000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr4:20643200-20644600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr4:20644000-20645200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr4:20644600-20645000	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr4:20645000-20645400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr4:20645200-20645400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:20645200-20645400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr4:20645200-20647000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:20645600-20646600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:20645800-20646400	Enhancers	Placenta Amnion	Placenta Amnion
15	chr4:20646600-20647600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:20647000-20647200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:20647000-20648600	Enhancers	Adipose Nuclei	Adipose
18	chr4:20647200-20647600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:20647400-20648600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:20647400-20649000	Enhancers	Liver	Liver
21	chr4:20647600-20648600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:20648600-20649400	Weak transcription	Adipose Nuclei	Adipose
23	chr4:20648600-20651200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:20649400-20650800	Enhancers	Adipose Nuclei	Adipose
25	chr4:20651000-20651600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:20651600-20654000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:20652600-20653000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:20653600-20653800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:20653600-20654200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr4:20653600-20654400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:20653600-20654600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:20653800-20654400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:20654000-20654600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr4:20654400-20654600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:20654400-20659600	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:20654600-20673800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr4:20659400-20660400	Enhancers	Placenta Amnion	Placenta Amnion
38	chr4:20659600-20660000	Enhancers	H9 Cell Line	embryonic stem cell
39	chr4:20659600-20660200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:20659600-20660600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:20659600-20660800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr4:20659600-20661200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr4:20659600-20661400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr4:20659600-20661400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:20659600-20661400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:20659800-20660000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:20659800-20660400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:20659800-20660400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr4:20659800-20660600	Enhancers	NHEK	skin
50	chr4:20659800-20660800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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