Variant report

Variant	nsv890725
Chromosome Location	chr8:39212435-39587864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:946)
CpG islands
(count:734)
Chromatin interactive
region (count:23)
LncRNA
region (count:242)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39424300-39424895	HepG2	liver:	n/a	chr8:39424646-39424662
2	ARID3A	chr8:39391480-39391748	K562	blood:	n/a	n/a
3	ARID3A	chr8:39393079-39393534	K562	blood:	n/a	n/a
4	ARID3A	chr8:39268778-39268961	K562	blood:	n/a	n/a
5	ARID3A	chr8:39547188-39547606	HepG2	liver:	n/a	n/a
6	ATF1	chr8:39393057-39393338	K562	blood:	n/a	n/a
7	ATF1	chr8:39552789-39552868	K562	blood:	n/a	n/a
8	ATF1	chr8:39574502-39574589	K562	blood:	n/a	n/a
9	ATF2	chr8:39542169-39542470	GM12878	blood:	n/a	n/a
10	ATF3	chr8:39390540-39390824	K562	blood:	n/a	n/a
11	BACH1	chr8:39338192-39338414	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr8:39542225-39542523	GM12878	blood:	n/a	n/a
13	BATF	chr8:39538369-39538590	GM12878	blood:	n/a	chr8:39538508-39538519
14	BATF	chr8:39542251-39542689	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:39542183-39542620	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:39338201-39338396	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:39215071-39215373	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:39542248-39542605	GM12878	blood:	n/a	n/a
19	BCL11A	chr8:39215146-39215389	GM12878	blood:	n/a	n/a
20	BCLAF1	chr8:39338104-39338425	GM12878	blood:	n/a	n/a
21	BCLAF1	chr8:39542279-39542596	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:39368980-39370112	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:39540522-39540568	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:39379884-39380110	K562	blood:	n/a	n/a
26	BHLHE40	chr8:39393076-39393265	K562	blood:	n/a	n/a
27	BHLHE40	chr8:39542060-39542776	GM12878	blood:	n/a	n/a
28	BHLHE40	chr8:39439456-39439600	K562	blood:	n/a	n/a
29	CBX3	chr8:39436347-39436562	K562	blood:	n/a	n/a
30	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
31	CBX3	chr8:39241402-39241706	K562	blood:	n/a	n/a
32	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
33	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
34	CBX3	chr8:39498734-39499015	HCT-116	colon:	n/a	n/a
35	CBX3	chr8:39471220-39471427	K562	blood:	n/a	n/a
36	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
37	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
38	CCNT2	chr8:39550530-39550861	K562	blood:	n/a	n/a
39	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
40	CEBPB	chr8:39545791-39545917	A549	lung:	n/a	n/a
41	CEBPB	chr8:39562647-39562945	A549	lung:	n/a	n/a
42	CEBPB	chr8:39391429-39391709	HepG2	liver:	n/a	chr8:39391593-39391604
43	CEBPB	chr8:39550893-39551144	K562	blood:	n/a	chr8:39551018-39551029
44	CEBPB	chr8:39444323-39444503	A549	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
45	CEBPB	chr8:39390600-39390943	K562	blood:	n/a	n/a
46	CEBPB	chr8:39444289-39444489	IMR90	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
47	CEBPB	chr8:39373729-39373930	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr8:39393043-39393343	K562	blood:	n/a	n/a
49	CEBPB	chr8:39373801-39373927	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:39550934-39551155	IMR90	lung:	n/a	chr8:39551018-39551029

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39223182-39223232	CMK	blood:	n/a
2	chr8:39380341-39380391	SKMC	muscle:	n/a
3	chr8:39223182-39223232	CMK	blood:	n/a
4	chr8:39380341-39380391	SKMC	muscle:	n/a
5	chr8:39223182-39223232	HCM	heart:	n/a
6	chr8:39441473-39441523	AG09309	skin:	n/a
7	chr8:39380341-39380391	NHDF-neo	bronchial:	n/a
8	chr8:39442080-39442130	Hela-S3	cervix:	n/a
9	chr8:39380592-39380642	NHDF-neo	bronchial:	n/a
10	chr8:39223182-39223232	HIPEpiC	eye:	n/a
11	chr8:39328433-39328483	NHDF-neo	bronchial:	n/a
12	chr8:39441968-39442018	HCPEpiC	choroid plexus:	n/a
13	chr8:39380435-39380485	AG04450	lung:	fetal
14	chr8:39380341-39380391	GM19239	blood:	n/a
15	chr8:39441975-39442025	NHBE	bronchial:	n/a
16	chr8:39328433-39328483	GM12891	blood:	n/a
17	chr8:39441968-39442018	RPTEC	kidney:	n/a
18	chr8:39441968-39442018	SK-N-MC	brain:	n/a
19	chr8:39441975-39442025	SAEC	small airway:	n/a
20	chr8:39442089-39442139	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:39380592-39380642	HCPEpiC	choroid plexus:	n/a
22	chr8:39328433-39328483	PFSK-1	brain:	n/a
23	chr8:39442078-39442128	HAEpiC	amniotic membrane:	n/a
24	chr8:39380435-39380485	BJ	skin:	n/a
25	chr8:39328433-39328483	NB4	blood:	n/a
26	chr8:39380341-39380391	CMK	blood:	n/a
27	chr8:39380341-39380391	HEK293	kidney:	embryo
28	chr8:39442347-39442397	HCT-116	colon:	n/a
29	chr8:39380592-39380642	LNCaP	prostate:	n/a
30	chr8:39442078-39442128	AG04449	skin:	fetal
31	chr8:39380592-39380642	Hela-S3	cervix:	n/a
32	chr8:39442078-39442128	CMK	blood:	n/a
33	chr8:39441975-39442025	HUVEC	blood vessel:	n/a
34	chr8:39441968-39442018	H1-hESC	embryonic stem cell:	embryo
35	chr8:39442078-39442128	HRCEpiC	kidney:	n/a
36	chr8:39442347-39442397	GM12892	blood:	n/a
37	chr8:39442089-39442139	U87	brain:	n/a
38	chr8:39380592-39380642	HNPCEpiC	eye:	n/a
39	chr8:39442080-39442130	HIPEpiC	eye:	n/a
40	chr8:39380435-39380485	Hela-S3	cervix:	n/a
41	chr8:39328433-39328483	AoSMC	blood vessel:	n/a
42	chr8:39442080-39442130	T-47D	breast:	n/a
43	chr8:39380341-39380391	HNPCEpiC	eye:	n/a
44	chr8:39442347-39442397	SK-N-MC	brain:	n/a
45	chr8:39441968-39442018	HRE	kidney:	n/a
46	chr8:39442078-39442128	NHBE	bronchial:	n/a
47	chr8:39442347-39442397	HepG2	liver:	n/a
48	chr8:39380435-39380485	GM19239	blood:	n/a
49	chr8:39441975-39442025	U87	brain:	n/a
50	chr8:39223182-39223232	HEK293	kidney:	embryo

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
2	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
3	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
4	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
5	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
6	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
7	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
8	chr8:39410966..39411938-chr8:39709121..39709647,2	MCF-7	breast:
9	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
10	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
11	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
12	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
13	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
14	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
15	chr8:39179668..39181798-chr8:39380661..39383115,2	K562	blood:
16	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
17	chr8:39410685..39412216-chr8:39708899..39710030,6	MCF-7	breast:
18	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
19	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
20	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
21	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
22	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
23	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:

(count:242 , 50 per page) page: 1 2 3 4 5

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126153
2	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126163
3	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126160
4	lnc-ADAM18-1	chr8:39424224-39424336	NONHSAT126175
5	lnc-ADAM32-1	chr8:39250093-39250179	NONHSAT126152
6	lnc-IDO1-2	chr8:39556641-39556699	l_3583_chr8:39549918-39556807_testes
7	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126168
8	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126169
9	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126165
10	lnc-ADAM2-6	chr8:39308564-39308680	NONHSAT126166
11	lnc-ADAM32-1	chr8:39274733-39274745	NONHSAT126160
12	lnc-ADAM2-4	chr8:39274731-39274897	XLOC_007062
13	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126169
14	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126163
15	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126163
16	lnc-ADAM2-6	chr8:39335215-39335462	NONHSAT126166
17	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT147629
18	lnc-ADAM2-6	chr8:39335215-39335365	NONHSAT126163
19	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126164
20	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126151
21	lnc-ADAM18-1	chr8:39435933-39435990	NONHSAT126175
22	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126165
23	lnc-IDO1-3	chr8:39581267-39581426	NONHSAT126179
24	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126166
25	lnc-ADAM32-1	chr8:39250093-39250179	NONHSAT126155
26	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126171
27	lnc-ADAM18-1	chr8:39424225-39424336	NONHSAT126174
28	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126167
29	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126166
30	lnc-ADAM2-4	chr8:39274730-39274897	NONHSAT126161
31	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126163
32	lnc-ADAM32-1	chr8:39274733-39274897	NONHSAT126148
33	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126155
34	lnc-ADAM18-1	chr8:39433100-39433157	ENSG00000254082
35	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126164
36	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT147628
37	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT147628
38	lnc-ADAM32-1	chr8:39238308-39238347	NONHSAT147629
39	lnc-ADAM32-1	chr8:39239036-39239254	NONHSAT126160
40	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126168
41	lnc-ADAM32-1	chr8:39274733-39274897	NONHSAT126150
42	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126150
43	lnc-ADAM18-2	chr8:39415865-39416173	NONHSAT126172
44	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126163
45	lnc-IDO1-3	chr8:39564309-39564423	NONHSAT126179
46	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126166
47	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126155
48	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126164
49	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
50	lnc-ADAM32-1	chr8:39274733-39274745	NONHSAT126153

No data

Variant related genes	Relation type
ADAM5	TF binding region
ENSG00000254067	TF binding region
ENSG00000254082	TF binding region
ADAM3A	TF binding region
ENSG00000252176	TF binding region
ADAM18	TF binding region
ADAM5	CpG island
ENSG00000254067	CpG island
ENSG00000254082	CpG island
ADAM3A	CpG island
ENSG00000252176	CpG island
ADAM18	CpG island
ENSG00000196115	chromatin interactions

Extended variants
information (count: 6126 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:6126 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202077787	chr8:39215041-39215042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529604488	chr8:39215062-39215063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540932990	chr8:39215106-39215107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183643601	chr8:39215149-39215150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548159683	chr8:39215158-39215159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561306830	chr8:39215165-39215166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369957065	chr8:39215167-39215168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142944861	chr8:39215168-39215169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530425578	chr8:39215173-39215174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146998561	chr8:39215187-39215188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs199758802	chr8:39215222-39215223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570226752	chr8:39215248-39215249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559255965	chr8:39215264-39215265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79661786	chr8:39215278-39215279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74792039	chr8:39215324-39215325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs137919721	chr8:39215399-39215400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557203103	chr8:39221024-39221025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558666441	chr8:39221051-39221052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4236761	chr8:39221085-39221086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536090914	chr8:39221094-39221095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553132055	chr8:39221171-39221172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553926295	chr8:39221195-39221196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73610581	chr8:39221197-39221198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140658703	chr8:39221279-39221280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572239789	chr8:39221316-39221317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147895098	chr8:39221438-39221439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562181031	chr8:39221440-39221441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367941434	chr8:39221486-39221487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141353772	chr8:39221600-39221601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371849740	chr8:39221636-39221637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192835471	chr8:39221666-39221667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564798131	chr8:39221734-39221735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533499126	chr8:39221765-39221766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370999851	chr8:39221776-39221777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185196366	chr8:39221798-39221799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145258919	chr8:39221828-39221829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528095982	chr8:39221841-39221842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77844446	chr8:39221844-39221845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76212174	chr8:39221867-39221868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536825842	chr8:39221913-39221914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550549159	chr8:39221917-39221918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570715752	chr8:39221960-39221961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562056434	chr8:39221962-39221963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150979143	chr8:39221973-39221974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190468651	chr8:39233210-39233211	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs181998274	chr8:39233221-39233222	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs185243607	chr8:39233358-39233359	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs201882137	chr8:39233365-39233366	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs531776240	chr8:39238312-39238313	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs140081159	chr8:39238341-39238342	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Chordoma	21215367	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Medulloblastoma	21163964	CNVD
Cancer	21249187	CNVD
Autism	19287141	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Rett syndrome	21593744	CNVD
Recurrent pregnancy loss	19789632	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39215000-39215400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:39221000-39222000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:39238600-39241200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:39241200-39241400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:39241400-39241600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:39250000-39250200	Active TSS	Fetal Lung	lung
7	chr8:39250200-39254400	Weak transcription	Fetal Lung	lung
8	chr8:39254400-39256800	Enhancers	Fetal Lung	lung
9	chr8:39254600-39254800	Enhancers	Colon Smooth Muscle	Colon
10	chr8:39256800-39258000	Weak transcription	Fetal Lung	lung
11	chr8:39261200-39262400	Weak transcription	Fetal Lung	lung
12	chr8:39262400-39263600	Enhancers	Fetal Lung	lung
13	chr8:39268800-39269200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:39269000-39269800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr8:39269400-39270200	Enhancers	Placenta Amnion	Placenta Amnion
16	chr8:39272400-39272800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
17	chr8:39272400-39273000	Active TSS	K562	blood
18	chr8:39272600-39272800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:39272800-39273200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:39273200-39273400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:39283800-39285200	Enhancers	Fetal Lung	lung
22	chr8:39296800-39297000	Active TSS	HSMM	muscle
23	chr8:39297000-39297200	Flanking Active TSS	HSMM	muscle
24	chr8:39298800-39300000	Enhancers	Fetal Lung	lung
25	chr8:39300000-39301000	Weak transcription	Fetal Lung	lung
26	chr8:39301000-39301200	Enhancers	Fetal Lung	lung
27	chr8:39301200-39302200	Weak transcription	Fetal Lung	lung
28	chr8:39302000-39302400	Enhancers	Spleen	Spleen
29	chr8:39302200-39302400	Enhancers	Fetal Lung	lung
30	chr8:39305400-39306400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:39317600-39318000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr8:39328200-39328600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:39328400-39328800	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:39328400-39329200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:39328400-39329400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr8:39328600-39329000	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr8:39328600-39329000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:39328600-39329200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:39328600-39329400	Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr8:39328600-39334800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:39328800-39329200	Active TSS	H1 Cell Line	embryonic stem cell
42	chr8:39328800-39329200	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr8:39329200-39329400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr8:39329200-39329400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:39334800-39335000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:39335000-39335800	Enhancers	Fetal Lung	lung
47	chr8:39335000-39340400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:39335400-39336400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr8:39335600-39337200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr8:39335800-39336400	Flanking Active TSS	Fetal Lung	lung

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