Variant report

Variant	nsv912823
Chromosome Location	chr20:23756139-23847009
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	ATF1	chr20:23781355-23781508	K562	blood:	n/a	n/a
2	BACH1	chr20:23832673-23832794	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr20:23828408-23828598	A549	lung:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
4	CEBPB	chr20:23828412-23828599	HepG2	liver:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
5	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
6	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
7	CTCF	chr20:23763120-23763270	K562	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
8	CTCF	chr20:23780360-23780510	GM12864	blood:	n/a	n/a
9	CTCF	chr20:23763131-23763294	Medullo	brain:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
10	CTCF	chr20:23762620-23762770	GM12873	blood:	n/a	n/a
11	CTCF	chr20:23763116-23763277	SK-N-SH_RA	brain:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
12	CTCF	chr20:23779900-23780050	NHDF-neo	bronchial:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
13	CTCF	chr20:23779878-23780430	HUVEC	blood vessel:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
14	CTCF	chr20:23779685-23780308	SK-N-SH	brain:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
15	CTCF	chr20:23779880-23780030	GM12865	blood:	n/a	n/a
16	CTCF	chr20:23780260-23780410	MCF-7	breast:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
17	CTCF	chr20:23763019-23763350	IMR90	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
18	CTCF	chr20:23763048-23763361	GM12878	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
19	CTCF	chr20:23763120-23763270	HCPEpiC	choroid plexus:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
20	CTCF	chr20:23763100-23763250	HFF	foreskin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
21	CTCF	chr20:23780240-23780390	GM12874	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
22	CTCF	chr20:23779888-23780347	NHEK	skin:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
23	CTCF	chr20:23779880-23780030	BJ	skin:	n/a	n/a
24	CTCF	chr20:23779809-23780177	H1-hESC	embryonic stem cell:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
25	CTCF	chr20:23763160-23763310	HCT-116	colon:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
26	CTCF	chr20:23780280-23780430	HUVEC	blood vessel:	n/a	chr20:23780320-23780329
27	CTCF	chr20:23763022-23763742	MCF-7	breast:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
28	CTCF	chr20:23763120-23763270	GM12865	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
29	CTCF	chr20:23780000-23780150	HCM	heart:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
30	CTCF	chr20:23779893-23780376	GM12891	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
31	CTCF	chr20:23762740-23762890	AG09319	gingival:	n/a	n/a
32	CTCF	chr20:23779899-23780423	H1-hESC	embryonic stem cell:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
33	CTCF	chr20:23756700-23756850	AG04449	skin:	n/a	chr20:23756767-23756780
34	CTCF	chr20:23779880-23780030	GM12874	blood:	n/a	n/a
35	CTCF	chr20:23763120-23763270	SAEC	small airway:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
36	CTCF	chr20:23826175-23826396	Gliobla	brain:	n/a	n/a
37	CTCF	chr20:23826220-23826370	HEK293	kidney:	n/a	n/a
38	CTCF	chr20:23779960-23780110	AG04450	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
39	CTCF	chr20:23805840-23805990	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr20:23779796-23780180	H1-hESC	embryonic stem cell:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
41	CTCF	chr20:23763040-23763190	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr20:23779980-23780130	GM12869	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
43	CTCF	chr20:23763084-23763290	Spleen_OC	spleen:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
44	CTCF	chr20:23779880-23780030	HepG2	liver:	n/a	n/a
45	CTCF	chr20:23805758-23806140	K562	blood:	n/a	n/a
46	CTCF	chr20:23779960-23780110	K562	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
47	CTCF	chr20:23763324-23763334	HepG2	liver:	n/a	n/a
48	CTCF	chr20:23822953-23822998	GM10266	blood:	n/a	n/a
49	CTCF	chr20:23762977-23763623	H1-hESC	embryonic stem cell:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
50	CTCF	chr20:23763387-23763527	LNCaP	prostate:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763449-23763465

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23807306-23807356	ovcar-3	ovarian:	n/a
2	chr20:23807778-23807828	HCF	heart:	n/a
3	chr20:23807359-23807409	AG10803	skin:	n/a
4	chr20:23807778-23807828	HAEpiC	amniotic membrane:	n/a
5	chr20:23807778-23807828	Hela-S3	cervix:	n/a
6	chr20:23807359-23807409	ovcar-3	ovarian:	n/a
7	chr20:23807736-23807786	HCM	heart:	n/a
8	chr20:23807359-23807409	GM12892	blood:	n/a
9	chr20:23807778-23807828	HEK293	kidney:	embryo
10	chr20:23807736-23807786	SKMC	muscle:	n/a
11	chr20:23807306-23807356	GM19239	blood:	n/a
12	chr20:23807778-23807828	CMK	blood:	n/a
13	chr20:23807778-23807828	HUVEC	blood vessel:	n/a
14	chr20:23807778-23807828	Hepatocyte	liver:	n/a
15	chr20:23807306-23807356	HRE	kidney:	n/a
16	chr20:23807306-23807356	GM12892	blood:	n/a
17	chr20:23807736-23807786	NB4	blood:	n/a
18	chr20:23806999-23807049	NH-A	brain:	n/a
19	chr20:23807306-23807356	Jurkat	blood:	n/a
20	chr20:23806999-23807049	PANC-1	pancreas:	n/a
21	chr20:23807359-23807409	IMR90	lung:	fetal
22	chr20:23806999-23807049	BJ	skin:	n/a
23	chr20:23807778-23807828	HRE	kidney:	n/a
24	chr20:23807778-23807828	HPAEpiC	pulmonary alveolar:	n/a
25	chr20:23806999-23807049	HepG2	liver:	n/a
26	chr20:23807736-23807786	SK-N-SH_RA	brain:	n/a
27	chr20:23807736-23807786	HAEpiC	amniotic membrane:	n/a
28	chr20:23807778-23807828	MCF-7	breast:	n/a
29	chr20:23807359-23807409	NT2-D1	testis:	n/a
30	chr20:23807778-23807828	PANC-1	pancreas:	n/a
31	chr20:23807359-23807409	H1-hESC	embryonic stem cell:	embryo
32	chr20:23807778-23807828	NH-A	brain:	n/a
33	chr20:23807359-23807409	K562	blood:	n/a
34	chr20:23807359-23807409	ProgFib	skin:	n/a
35	chr20:23807306-23807356	GM06990	blood:	n/a
36	chr20:23806999-23807049	HEK293	kidney:	embryo
37	chr20:23807736-23807786	PrEC	prostate:	n/a
38	chr20:23807778-23807828	HCT-116	colon:	n/a
39	chr20:23807306-23807356	A549	lung:	n/a
40	chr20:23807778-23807828	A549	lung:	n/a
41	chr20:23807306-23807356	HCT-116	colon:	n/a
42	chr20:23807736-23807786	Hepatocyte	liver:	n/a
43	chr20:23807736-23807786	SK-N-MC	brain:	n/a
44	chr20:23807778-23807828	AG04449	skin:	fetal
45	chr20:23807778-23807828	PFSK-1	brain:	n/a
46	chr20:23807736-23807786	U87	brain:	n/a
47	chr20:23807359-23807409	HAEpiC	amniotic membrane:	n/a
48	chr20:23807306-23807356	SK-N-MC	brain:	n/a
49	chr20:23807306-23807356	MCF-7	breast:	n/a
50	chr20:23807306-23807356	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23648665..23649293-chr20:23837547..23838405,2	MCF-7	breast:
2	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
3	chr20:23779854..23780390-chr20:23870001..23870554,2	MCF-7	breast:
4	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
5	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
6	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
7	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
8	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
9	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
10	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
11	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-3	chr20:23785871-23786300	XLOC_013494
2	lnc-CST8-3	chr20:23778778-23778924	XLOC_013494
3	lnc-CST8-3	chr20:23784376-23784473	XLOC_013494
4	lnc-CST8-3	chr20:23785160-23785281	XLOC_013494

Variant related genes	Relation type
ENSG00000230908	TF binding region
CST2	TF binding region
ENSG00000230908	CpG island
CST2	CpG island
XIAP	miRNA target sites
WWP2	miRNA target sites
WWC2	miRNA target sites

Extended variants
information (count: 2632 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2632 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6138072	chr20:23756139-23756140	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572239412	chr20:23756155-23756156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4309635	chr20:23756170-23756171	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs142841478	chr20:23756179-23756180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577765615	chr20:23756192-23756193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73902176	chr20:23756196-23756197	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371036142	chr20:23756243-23756244	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6049100	chr20:23756265-23756266	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377483389	chr20:23756266-23756267	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373665575	chr20:23756294-23756295	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563105180	chr20:23756323-23756324	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574405878	chr20:23756342-23756343	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543330656	chr20:23756390-23756391	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559777891	chr20:23756418-23756419	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs528734033	chr20:23756429-23756430	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs545227327	chr20:23756433-23756434	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs142021936	chr20:23756444-23756445	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs565050803	chr20:23756457-23756458	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs376861921	chr20:23756497-23756498	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs530881257	chr20:23756525-23756526	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs6049101	chr20:23756529-23756530	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567351571	chr20:23756552-23756553	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs530028004	chr20:23756573-23756574	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs549300715	chr20:23756576-23756577	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs565832926	chr20:23756583-23756584	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs561672464	chr20:23756595-23756596	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs557943047	chr20:23756599-23756600	Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs4325826	chr20:23756608-23756609	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs4640452	chr20:23756613-23756614	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs557069194	chr20:23756628-23756629	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs78912444	chr20:23756670-23756671	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs529643446	chr20:23756672-23756673	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs145875185	chr20:23756693-23756694	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs553635227	chr20:23756702-23756703	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs573420516	chr20:23756707-23756708	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs545214167	chr20:23756737-23756738	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs565109453	chr20:23756738-23756739	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs530988753	chr20:23756740-23756741	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs544335816	chr20:23756768-23756769	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs6138073	chr20:23756772-23756773	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs79763794	chr20:23756799-23756800	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs147402900	chr20:23756800-23756801	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs565974223	chr20:23756803-23756804	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs138227739	chr20:23756826-23756827	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs7261342	chr20:23756827-23756828	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7261217	chr20:23756855-23756856	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs34942145	chr20:23756862-23756863	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs7261302	chr20:23756911-23756912	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs557130604	chr20:23756913-23756914	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs567205556	chr20:23756919-23756920	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23747600-23756200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr20:23756000-23756800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:23756000-23757400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr20:23756200-23756400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr20:23756200-23756600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
6	chr20:23756200-23757000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr20:23756400-23756800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
8	chr20:23756400-23756800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr20:23756400-23757200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr20:23756400-23757400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr20:23756400-23757600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr20:23756600-23756800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr20:23756600-23756800	Bivalent Enhancer	Fetal Stomach	stomach
14	chr20:23756600-23757000	Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr20:23756600-23757600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr20:23756600-23757800	Enhancers	Fetal Kidney	kidney
17	chr20:23756800-23757000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr20:23756800-23757400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr20:23757000-23757400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr20:23757200-23757400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr20:23757200-23757400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr20:23757200-23757400	Enhancers	Fetal Intestine Large	intestine
23	chr20:23757200-23757600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr20:23757200-23757600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:23757200-23757600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr20:23757200-23757600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr20:23757200-23757600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr20:23757200-23757800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr20:23757200-23758000	Enhancers	Osteobl	bone
30	chr20:23757200-23758200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr20:23757400-23757600	Enhancers	H9 Cell Line	embryonic stem cell
32	chr20:23757400-23757600	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr20:23757400-23757600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr20:23757600-23759000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr20:23757600-23759000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr20:23757800-23759000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr20:23758200-23759000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr20:23758800-23760000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr20:23759000-23759800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr20:23759000-23759800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr20:23759000-23759800	Enhancers	NHDF-Ad	bronchial
42	chr20:23759000-23760000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr20:23759000-23760000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr20:23759200-23759400	Flanking Active TSS	Osteobl	bone
45	chr20:23759200-23760000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr20:23759400-23760000	Enhancers	Osteobl	bone
47	chr20:23759800-23760000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr20:23762200-23763600	Enhancers	Dnd41	blood
49	chr20:23775400-23776600	Enhancers	Placenta Amnion	Placenta Amnion
50	chr20:23776200-23776600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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