Variant report

Variant	nsv890833
Chromosome Location	chr8:39405337-39664696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:692)
CpG islands
(count:429)
Chromatin interactive
region (count:21)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39661584-39661750	K562	blood:	n/a	n/a
2	ARID3A	chr8:39547188-39547606	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:39599175-39599222	K562	blood:	n/a	n/a
4	ARID3A	chr8:39424300-39424895	HepG2	liver:	n/a	chr8:39424646-39424662
5	ARID3A	chr8:39621219-39621517	HepG2	liver:	n/a	n/a
6	ATF1	chr8:39552789-39552868	K562	blood:	n/a	n/a
7	ATF1	chr8:39574502-39574589	K562	blood:	n/a	n/a
8	ATF2	chr8:39542169-39542470	GM12878	blood:	n/a	n/a
9	BACH1	chr8:39661591-39661665	K562	blood:	n/a	n/a
10	BACH1	chr8:39601076-39601099	K562	blood:	n/a	n/a
11	BACH1	chr8:39601010-39601037	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr8:39637507-39637695	GM12878	blood:	n/a	n/a
13	BATF	chr8:39542251-39542689	GM12878	blood:	n/a	n/a
14	BATF	chr8:39538369-39538590	GM12878	blood:	n/a	chr8:39538508-39538519
15	BATF	chr8:39542225-39542523	GM12878	blood:	n/a	n/a
16	BATF	chr8:39637507-39637697	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:39542248-39542605	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:39542183-39542620	GM12878	blood:	n/a	n/a
19	BCLAF1	chr8:39542279-39542596	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:39540522-39540568	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:39439456-39439600	K562	blood:	n/a	n/a
22	BHLHE40	chr8:39542060-39542776	GM12878	blood:	n/a	n/a
23	CBX3	chr8:39498734-39499015	HCT-116	colon:	n/a	n/a
24	CBX3	chr8:39471220-39471427	K562	blood:	n/a	n/a
25	CBX3	chr8:39436347-39436562	K562	blood:	n/a	n/a
26	CCNT2	chr8:39613824-39613995	K562	blood:	n/a	n/a
27	CCNT2	chr8:39550530-39550861	K562	blood:	n/a	n/a
28	CEBPB	chr8:39621750-39622030	HepG2	liver:	n/a	chr8:39621879-39621890
29	CEBPB	chr8:39425240-39425556	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr8:39589146-39589277	A549	lung:	n/a	chr8:39589190-39589201
31	CEBPB	chr8:39550893-39551144	K562	blood:	n/a	chr8:39551018-39551029
32	CEBPB	chr8:39589214-39589269	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:39545791-39545917	A549	lung:	n/a	n/a
34	CEBPB	chr8:39444289-39444489	IMR90	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
35	CEBPB	chr8:39444323-39444503	A549	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
36	CEBPB	chr8:39610912-39610941	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:39417741-39418065	HepG2	liver:	n/a	chr8:39417873-39417884 chr8:39417830-39417841
38	CEBPB	chr8:39610769-39611092	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:39562647-39562945	A549	lung:	n/a	n/a
40	CEBPB	chr8:39458160-39458460	A549	lung:	n/a	chr8:39458289-39458300
41	CEBPB	chr8:39550934-39551155	IMR90	lung:	n/a	chr8:39551018-39551029
42	CEBPB	chr8:39417758-39418058	IMR90	lung:	n/a	chr8:39417873-39417884 chr8:39417830-39417841
43	CEBPB	chr8:39635155-39635197	A549	lung:	n/a	n/a
44	CEBPB	chr8:39584624-39585155	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:39562615-39562959	IMR90	lung:	n/a	n/a
46	CEBPB	chr8:39417791-39417944	K562	blood:	n/a	chr8:39417873-39417884 chr8:39417830-39417841
47	CEBPB	chr8:39458127-39458460	HepG2	liver:	n/a	chr8:39458289-39458300
48	CEBPB	chr8:39550875-39551134	HepG2	liver:	n/a	chr8:39551018-39551029
49	CEBPB	chr8:39562626-39562905	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:39647716-39648001	IMR90	lung:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39441975-39442025	SK-N-SH_RA	brain:	n/a
2	chr8:39442080-39442130	HRPEpiC	eye:	n/a
3	chr8:39441975-39442025	SK-N-SH_RA	brain:	n/a
4	chr8:39442080-39442130	HRPEpiC	eye:	n/a
5	chr8:39442078-39442128	NH-A	brain:	n/a
6	chr8:39441473-39441523	K562	blood:	n/a
7	chr8:39441968-39442018	SK-N-SH_RA	brain:	n/a
8	chr8:39442080-39442130	AG09319	gingival:	n/a
9	chr8:39442347-39442397	GM12891	blood:	n/a
10	chr8:39442089-39442139	HL-60	blood:	n/a
11	chr8:39441975-39442025	IMR90	lung:	fetal
12	chr8:39441975-39442025	Hepatocyte	liver:	n/a
13	chr8:39442089-39442139	GM12878	blood:	n/a
14	chr8:39441975-39442025	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:39441968-39442018	NB4	blood:	n/a
16	chr8:39441473-39441523	BE2_C	brain:	n/a
17	chr8:39441968-39442018	AG04449	skin:	fetal
18	chr8:39441975-39442025	H1-hESC	embryonic stem cell:	embryo
19	chr8:39441975-39442025	HL-60	blood:	n/a
20	chr8:39441473-39441523	GM12891	blood:	n/a
21	chr8:39441968-39442018	CMK	blood:	n/a
22	chr8:39441968-39442018	NHBE	bronchial:	n/a
23	chr8:39442089-39442139	ECC-1	luminal epithelium:	n/a
24	chr8:39441975-39442025	Caco-2	colon:	n/a
25	chr8:39441968-39442018	GM12892	blood:	n/a
26	chr8:39442078-39442128	Hela-S3	cervix:	n/a
27	chr8:39441968-39442018	HNPCEpiC	eye:	n/a
28	chr8:39442089-39442139	NHBE	bronchial:	n/a
29	chr8:39441975-39442025	HMEC	breast:	n/a
30	chr8:39442347-39442397	CMK	blood:	n/a
31	chr8:39442089-39442139	HepG2	liver:	n/a
32	chr8:39441473-39441523	NH-A	brain:	n/a
33	chr8:39442078-39442128	HIPEpiC	eye:	n/a
34	chr8:39441968-39442018	ProgFib	skin:	n/a
35	chr8:39442078-39442128	AG10803	skin:	n/a
36	chr8:39441968-39442018	HMEC	breast:	n/a
37	chr8:39441473-39441523	PrEC	prostate:	n/a
38	chr8:39441968-39442018	Jurkat	blood:	n/a
39	chr8:39442080-39442130	PFSK-1	brain:	n/a
40	chr8:39441975-39442025	HNPCEpiC	eye:	n/a
41	chr8:39442078-39442128	LNCaP	prostate:	n/a
42	chr8:39442089-39442139	HCPEpiC	choroid plexus:	n/a
43	chr8:39441473-39441523	IMR90	lung:	fetal
44	chr8:39442089-39442139	HEEpiC	esophagus:	n/a
45	chr8:39442347-39442397	SK-N-MC	brain:	n/a
46	chr8:39441975-39442025	AG10803	skin:	n/a
47	chr8:39442080-39442130	RPTEC	kidney:	n/a
48	chr8:39441975-39442025	K562	blood:	n/a
49	chr8:39441473-39441523	SAEC	small airway:	n/a
50	chr8:39442078-39442128	Jurkat	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39629924..39632128-chr8:39633892..39635911,2	MCF-7	breast:
2	chr8:39602749..39604278-chr8:39604368..39606576,2	K562	blood:
3	chr8:39410685..39412216-chr8:39708899..39710030,6	MCF-7	breast:
4	chr8:39629008..39630969-chr8:39633550..39635113,2	K562	blood:
5	chr8:39602749..39604278-chr8:39604368..39606576,2	K562	blood:
6	chr8:39629924..39632128-chr8:39633892..39635911,2	MCF-7	breast:
7	chr8:39629008..39630969-chr8:39633550..39635113,2	K562	blood:
8	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
9	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
10	chr8:39410966..39411938-chr8:39709121..39709647,2	MCF-7	breast:
11	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
12	chr8:39610203..39611775-chr8:39614895..39616496,2	K562	blood:
13	chr8:39622412..39624554-chr8:39628340..39630731,2	MCF-7	breast:
14	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
15	chr8:39622412..39624554-chr8:39628340..39630731,2	MCF-7	breast:
16	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
17	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
18	chr8:39610203..39611775-chr8:39614895..39616496,2	K562	blood:
19	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
20	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
21	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM18-1	chr8:39437484-39437653	NONHSAT126174
2	lnc-IDO1-4	chr8:39467004-39467080	NONHSAT126178
3	lnc-ADAM18-1	chr8:39430763-39430927	NONHSAT126174
4	lnc-IDO1-2	chr8:39549919-39550084	l_3583_chr8:39549918-39556807_testes
5	lnc-ADAM18-1	chr8:39424224-39424336	ENSG00000254082
6	lnc-ADAM18-2	chr8:39412110-39413320	NONHSAT126172
7	lnc-ADAM18-1	chr8:39420631-39420645	NONHSAT126174
8	lnc-IDO1-4	chr8:39462146-39462255	NONHSAT126178
9	lnc-IDO1-3	chr8:39564309-39564423	NONHSAT126180
10	lnc-IDO1-4	chr8:39466561-39466639	NONHSAT126178
11	lnc-ADAM18-1	chr8:39435933-39435990	NONHSAT126175
12	lnc-ADAM18-2	chr8:39415865-39416173	NONHSAT126172
13	lnc-ADAM18-1	chr8:39430763-39430927	NONHSAT126175
14	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126179
15	lnc-IDO1-4	chr8:39463826-39463881	NONHSAT126178
16	lnc-ADAM18-1	chr8:39424224-39424336	NONHSAT126175
17	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126180
18	lnc-ADAM18-2	chr8:39415511-39415698	NONHSAT126172
19	lnc-IDO1-3	chr8:39581267-39581477	NONHSAT126180
20	lnc-IDO1-3	chr8:39564309-39564423	NONHSAT126179
21	lnc-IDO1-3	chr8:39542693-39542931	NONHSAT126180
22	lnc-ADAM18-1	chr8:39435933-39435990	ENSG00000254082
23	lnc-IDO1-3	chr8:39542649-39542931	NONHSAT126179
24	lnc-ADAM18-1	chr8:39433100-39433160	NONHSAT126175
25	lnc-ADAM18-1	chr8:39437484-39437653	NONHSAT126175
26	lnc-IDO1-2	chr8:39556641-39556699	l_3583_chr8:39549918-39556807_testes
27	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
28	lnc-IDO1-2	chr8:39552257-39552314	l_3583_chr8:39549918-39556807_testes
29	lnc-ADAM18-1	chr8:39430763-39430927	ENSG00000254082
30	lnc-IDO1-2	chr8:39556704-39556807	l_3583_chr8:39549918-39556807_testes
31	lnc-ADAM18-2	chr8:39413665-39413968	NONHSAT126172
32	lnc-IDO1-4	chr8:39468048-39468263	NONHSAT126178
33	lnc-ADAM18-1	chr8:39424225-39424336	NONHSAT126174
34	lnc-ADAM18-1	chr8:39433100-39433157	NONHSAT126174
35	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
36	lnc-IDO1-3	chr8:39581267-39581426	NONHSAT126179
37	lnc-ADAM18-1	chr8:39433100-39433157	ENSG00000254082
38	lnc-IDO1-3	chr8:39587417-39587581	NONHSAT126179
39	lnc-ADAM18-1	chr8:39433113-39433157	ENSG00000254082

No data

Variant related genes	Relation type
ADAM2	TF binding region
ENSG00000221018	TF binding region
ENSG00000252176	TF binding region
ADAM18	TF binding region
ENSG00000254067	TF binding region
ENSG00000254082	TF binding region
ADAM2	CpG island
ENSG00000221018	CpG island
ENSG00000252176	CpG island
ADAM18	CpG island
ENSG00000254067	CpG island
ENSG00000254082	CpG island

Extended variants
information (count: 5624 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:5624 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6474156	chr8:39405337-39405338	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547120757	chr8:39405342-39405343	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs375336295	chr8:39405361-39405362	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs567009945	chr8:39405368-39405369	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs56192265	chr8:39405398-39405399	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs76142926	chr8:39405399-39405400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs564923074	chr8:39405463-39405464	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs532139216	chr8:39405494-39405495	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs569856075	chr8:39405496-39405497	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs149145773	chr8:39405507-39405508	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs142264670	chr8:39405512-39405513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs117341060	chr8:39405518-39405519	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs552141969	chr8:39405523-39405524	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs186802571	chr8:39405524-39405525	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs190456064	chr8:39405555-39405556	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs112433447	chr8:39405585-39405586	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs77351456	chr8:39405621-39405622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557480881	chr8:39405634-39405635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577358906	chr8:39405648-39405649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76418218	chr8:39405670-39405671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559600441	chr8:39405676-39405677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374997757	chr8:39405687-39405688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527325272	chr8:39405710-39405711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146829463	chr8:39405715-39405716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531127410	chr8:39405716-39405717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560671377	chr8:39405740-39405741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115735759	chr8:39405749-39405750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549720758	chr8:39405768-39405769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76440652	chr8:39405819-39405820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569871851	chr8:39405835-39405836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7838204	chr8:39405858-39405859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs7819481	chr8:39405882-39405883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565964106	chr8:39405889-39405890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535029351	chr8:39405897-39405898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554971146	chr8:39405903-39405904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535155462	chr8:39405954-39405955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112735535	chr8:39405955-39405956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140609447	chr8:39405991-39405992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558152937	chr8:39406022-39406023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201481387	chr8:39406037-39406038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557173961	chr8:39406041-39406042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577397590	chr8:39406085-39406086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546068779	chr8:39406114-39406115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182334317	chr8:39406147-39406148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573173702	chr8:39406153-39406154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145456832	chr8:39406183-39406184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77821705	chr8:39406190-39406191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147501114	chr8:39406202-39406203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185050978	chr8:39406209-39406210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529650192	chr8:39406214-39406215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Cancer	21249187	CNVD
Autism	19287141	CNVD
Rett syndrome	21593744	CNVD
Recurrent pregnancy loss	19789632	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39404800-39405600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:39405600-39412400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:39412400-39412600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:39412400-39413200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
5	chr8:39412600-39417200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:39416400-39418200	Enhancers	Fetal Intestine Large	intestine
7	chr8:39416600-39417000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:39417000-39417200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr8:39417000-39417600	Enhancers	Placenta	Placenta
10	chr8:39417200-39417400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:39419000-39419200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:39419200-39419400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:39424200-39425000	Enhancers	HepG2	liver
14	chr8:39425000-39425800	Weak transcription	HepG2	liver
15	chr8:39425800-39426000	Enhancers	Placenta	Placenta
16	chr8:39425800-39426000	Enhancers	HepG2	liver
17	chr8:39426000-39434200	Weak transcription	Placenta	Placenta
18	chr8:39427800-39428000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:39428000-39434000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:39434000-39434400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:39434000-39435800	Enhancers	Placenta Amnion	Placenta Amnion
22	chr8:39434200-39434800	Enhancers	Placenta	Placenta
23	chr8:39434400-39435600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr8:39434400-39437800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:39434600-39435800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr8:39434800-39435200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr8:39434800-39435400	Weak transcription	Placenta	Placenta
28	chr8:39435000-39435600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr8:39435200-39435400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:39435200-39435400	Enhancers	HepG2	liver
31	chr8:39435400-39436200	Weak transcription	HepG2	liver
32	chr8:39435400-39436400	Enhancers	Placenta	Placenta
33	chr8:39435400-39438200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr8:39435600-39436400	Enhancers	Primary hematopoietic stem cells	blood
35	chr8:39435800-39436800	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr8:39436200-39437000	Enhancers	HepG2	liver
37	chr8:39436400-39437600	Weak transcription	Placenta	Placenta
38	chr8:39436800-39438200	Enhancers	Fetal Heart	heart
39	chr8:39436800-39438200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr8:39437000-39438400	Weak transcription	HepG2	liver
41	chr8:39437000-39439200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:39437600-39439600	Enhancers	Placenta	Placenta
43	chr8:39437800-39439000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:39438200-39438600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr8:39438200-39438600	Active TSS	Fetal Heart	heart
46	chr8:39438200-39439000	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr8:39438600-39439200	Flanking Active TSS	Fetal Heart	heart
48	chr8:39438600-39439400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
49	chr8:39438800-39439200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
50	chr8:39438800-39440800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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