Variant report

Variant	nsv610290
Chromosome Location	chr8:11391650-11430485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2098)
CpG islands
(count:977)
Chromatin interactive
region (count:40)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2098 , 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	ATF2	chr8:11396380-11397039	GM12878	blood:	n/a	n/a
2	ATF2	chr8:11402856-11404232	GM12878	blood:	n/a	n/a
3	ATF2	chr8:11395042-11395933	GM12878	blood:	n/a	n/a
4	ATF2	chr8:11421987-11422609	GM12878	blood:	n/a	n/a
5	ATF2	chr8:11416020-11416567	GM12878	blood:	n/a	n/a
6	ATF2	chr8:11411156-11411616	GM12878	blood:	n/a	n/a
7	ATF2	chr8:11411191-11411587	GM12878	blood:	n/a	n/a
8	ATF2	chr8:11418701-11418997	GM12878	blood:	n/a	n/a
9	ATF2	chr8:11396080-11397110	GM12878	blood:	n/a	n/a
10	ATF2	chr8:11390126-11391878	GM12878	blood:	n/a	n/a
11	ATF2	chr8:11421419-11423115	GM12878	blood:	n/a	n/a
12	ATF2	chr8:11394202-11396059	GM12878	blood:	n/a	n/a
13	ATF2	chr8:11416028-11417072	GM12878	blood:	n/a	n/a
14	ATF2	chr8:11402957-11404256	GM12878	blood:	n/a	n/a
15	ATF2	chr8:11391138-11391757	GM12878	blood:	n/a	n/a
16	BACH1	chr8:11421479-11422408	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:11422005-11422013	K562	blood:	n/a	n/a
18	BACH1	chr8:11411316-11411548	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr8:11396541-11396828	GM12878	blood:	n/a	n/a
20	BATF	chr8:11416168-11416454	GM12878	blood:	n/a	n/a
21	BATF	chr8:11395253-11395756	GM12878	blood:	n/a	n/a
22	BATF	chr8:11403782-11404243	GM12878	blood:	n/a	n/a
23	BATF	chr8:11403808-11404213	GM12878	blood:	n/a	n/a
24	BATF	chr8:11403194-11403693	GM12878	blood:	n/a	n/a
25	BATF	chr8:11403094-11403686	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:11403784-11404237	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:11403188-11403628	GM12878	blood:	n/a	chr8:11403287-11403296
28	BCL11A	chr8:11395105-11395737	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:11403087-11403748	GM12878	blood:	n/a	chr8:11403287-11403296
30	BCL11A	chr8:11403843-11404135	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:11416159-11416609	GM12878	blood:	n/a	n/a
32	BCL3	chr8:11403839-11404194	GM12878	blood:	n/a	n/a
33	BCL3	chr8:11423267-11423719	GM12878	blood:	n/a	n/a
34	BCL3	chr8:11416115-11417171	GM12878	blood:	n/a	n/a
35	BCL3	chr8:11395141-11395868	GM12878	blood:	n/a	chr8:11395756-11395769
36	BCL3	chr8:11421305-11422586	GM12878	blood:	n/a	chr8:11422235-11422243
37	BCL3	chr8:11421867-11422432	GM12878	blood:	n/a	chr8:11422235-11422243
38	BCL3	chr8:11396535-11396917	GM12878	blood:	n/a	n/a
39	BCL3	chr8:11403124-11403747	GM12878	blood:	n/a	chr8:11403287-11403296
40	BCL3	chr8:11418521-11418953	GM12878	blood:	n/a	chr8:11418702-11418710
41	BCL3	chr8:11421891-11422340	A549	lung:	n/a	chr8:11422235-11422243
42	BCL3	chr8:11403089-11403697	GM12878	blood:	n/a	chr8:11403287-11403296
43	BCL3	chr8:11422664-11423817	GM12878	blood:	n/a	n/a
44	BCL3	chr8:11395245-11395778	GM12878	blood:	n/a	chr8:11395756-11395769
45	BCLAF1	chr8:11423452-11423876	GM12878	blood:	n/a	n/a
46	BCLAF1	chr8:11421273-11422842	GM12878	blood:	n/a	chr8:11422235-11422243
47	BCLAF1	chr8:11396449-11396920	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:11418072-11419043	GM12878	blood:	n/a	chr8:11418397-11418405 chr8:11418702-11418710
49	BCLAF1	chr8:11415996-11417235	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:11403801-11404210	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11421337-11421387	Caco-2	colon:	n/a
2	chr8:11421337-11421387	Caco-2	colon:	n/a
3	chr8:11402219-11402269	NHDF-neo	bronchial:	n/a
4	chr8:11421594-11421644	SK-N-SH_RA	brain:	n/a
5	chr8:11424789-11424839	HCM	heart:	n/a
6	chr8:11418058-11418108	SKMC	muscle:	n/a
7	chr8:11421337-11421387	AG09319	gingival:	n/a
8	chr8:11419707-11419757	SKMC	muscle:	n/a
9	chr8:11418058-11418108	IMR90	lung:	fetal
10	chr8:11416365-11416415	BE2_C	brain:	n/a
11	chr8:11421594-11421644	Hepatocyte	liver:	n/a
12	chr8:11417517-11417567	GM12891	blood:	n/a
13	chr8:11413186-11413236	ECC-1	luminal epithelium:	n/a
14	chr8:11422433-11422483	HCT-116	colon:	n/a
15	chr8:11421594-11421644	HRE	kidney:	n/a
16	chr8:11411487-11411537	GM19239	blood:	n/a
17	chr8:11416365-11416415	HAEpiC	amniotic membrane:	n/a
18	chr8:11417517-11417567	AG09319	gingival:	n/a
19	chr8:11422167-11422217	A549	lung:	n/a
20	chr8:11402219-11402269	HepG2	liver:	n/a
21	chr8:11418058-11418108	HIPEpiC	eye:	n/a
22	chr8:11402219-11402269	GM12892	blood:	n/a
23	chr8:11416365-11416415	HL-60	blood:	n/a
24	chr8:11413234-11413284	HMEC	breast:	n/a
25	chr8:11416365-11416415	GM06990	blood:	n/a
26	chr8:11421934-11421984	Jurkat	blood:	n/a
27	chr8:11422167-11422217	SK-N-SH_RA	brain:	n/a
28	chr8:11419707-11419757	BE2_C	brain:	n/a
29	chr8:11417517-11417567	HRPEpiC	eye:	n/a
30	chr8:11419707-11419757	HepG2	liver:	n/a
31	chr8:11413043-11413093	SK-N-SH	brain:	n/a
32	chr8:11411487-11411537	ProgFib	skin:	n/a
33	chr8:11421934-11421984	H1-hESC	embryonic stem cell:	embryo
34	chr8:11419707-11419757	NH-A	brain:	n/a
35	chr8:11416365-11416415	BJ	skin:	n/a
36	chr8:11422167-11422217	BJ	skin:	n/a
37	chr8:11411487-11411537	IMR90	lung:	fetal
38	chr8:11413186-11413236	HIPEpiC	eye:	n/a
39	chr8:11421594-11421644	HNPCEpiC	eye:	n/a
40	chr8:11421594-11421644	CMK	blood:	n/a
41	chr8:11413234-11413284	HUVEC	blood vessel:	n/a
42	chr8:11402219-11402269	HRCEpiC	kidney:	n/a
43	chr8:11422167-11422217	HIPEpiC	eye:	n/a
44	chr8:11419707-11419757	RPTEC	kidney:	n/a
45	chr8:11413043-11413093	AG09319	gingival:	n/a
46	chr8:11413234-11413284	MCF-7	breast:	n/a
47	chr8:11413234-11413284	SK-N-SH	brain:	n/a
48	chr8:11402219-11402269	SK-N-SH	brain:	n/a
49	chr8:11421594-11421644	AG10803	skin:	n/a
50	chr8:11421594-11421644	HRCEpiC	kidney:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11411028..11411558-chr8:11446874..11447601,2	K562	blood:
2	chr8:11390853..11393388-chr8:11395895..11397560,2	K562	blood:
3	chr8:11421707..11422824-chr8:11816126..11817083,9	K562	blood:
4	chr8:11422237..11424811-chr8:11602615..11604781,2	MCF-7	breast:
5	chr8:11421842..11422772-chr8:11603355..11604431,7	MCF-7	breast:
6	chr8:11379820..11382247-chr8:11420170..11422972,2	MCF-7	breast:
7	chr8:11422289..11424857-chr8:11598109..11600598,2	MCF-7	breast:
8	chr8:11421778..11422656-chr8:11816114..11817045,3	MCF-7	breast:
9	chr8:11424324..11425489-chr8:11573800..11574792,3	MCF-7	breast:
10	chr8:11389216..11391992-chr8:11394333..11396573,2	MCF-7	breast:
11	chr8:11426984..11428613-chr8:11595138..11596810,2	K562	blood:
12	chr8:11390853..11393388-chr8:11395895..11397560,2	K562	blood:
13	chr8:11420542..11422083-chr8:11608840..11610442,2	MCF-7	breast:
14	chr8:11394487..11397060-chr8:11401001..11403258,2	K562	blood:
15	chr8:11331911..11334130-chr8:11408479..11410507,2	MCF-7	breast:
16	chr8:11421685..11422256-chr8:11800840..11801381,2	K562	blood:
17	chr8:11410226..11416148-chr8:11417699..11422629,5	K562	blood:
18	chr8:11430122..11430693-chr8:11587796..11588653,2	MCF-7	breast:
19	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
20	chr8:11421781..11422781-chr8:11603539..11604516,9	K562	blood:
21	chr8:11424667..11425261-chr8:11603180..11604185,3	MCF-7	breast:
22	chr8:11410226..11416148-chr8:11417699..11422629,5	K562	blood:
23	chr8:11286965..11287640-chr8:11410754..11411417,2	MCF-7	breast:
24	chr8:11409226..11411204-chr8:11413317..11416179,2	K562	blood:
25	chr8:11429172..11431915-chr8:11433216..11435875,2	MCF-7	breast:
26	chr8:11271149..11271854-chr8:11412541..11413131,2	MCF-7	breast:
27	chr8:11428917..11429796-chr8:11587902..11588451,3	MCF-7	breast:
28	chr8:11266732..11267234-chr8:11421696..11422273,2	K562	blood:
29	chr8:11430194..11430977-chr8:11603626..11604340,2	MCF-7	breast:
30	chr8:11399538..11402795-chr8:11403672..11407842,3	K562	blood:
31	chr8:11422187..11423813-chr8:11429710..11432078,2	MCF-7	breast:
32	chr8:11409226..11411204-chr8:11413317..11416179,2	K562	blood:
33	chr8:11421719..11422643-chr8:11446645..11447610,4	K562	blood:
34	chr8:11389216..11391992-chr8:11394333..11396573,2	MCF-7	breast:
35	chr8:11418474..11420140-chr8:11572245..11574135,2	K562	blood:
36	chr8:11270794..11271511-chr8:11421638..11422402,4	MCF-7	breast:
37	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
38	chr8:11422187..11423813-chr8:11429710..11432078,2	MCF-7	breast:
39	chr8:11430263..11432062-chr8:11433287..11435276,2	K562	blood:
40	chr8:11429899..11432844-chr8:11444265..11445875,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-148O21.2.1-1	chr8:11417293-11417529	ENSG00000255354.1
2	lnc-RP11-148O21.2.1-2	chr8:11415399-11415531	ENSG00000255518.1
3	lnc-RP11-148O21.3.1-1	chr8:11410733-11411089	ENSG00000254774.1
4	lnc-RP11-148O21.2.1-1	chr8:11415975-11416256	ENSG00000255354.1
5	lnc-RP11-148O21.2.1-2	chr8:11413760-11414170	ENSG00000255518.1
6	lnc-RP11-148O21.3.1-1	chr8:11411639-11411716	ENSG00000254774.1
7	lnc-RP11-148O21.3.1-2	chr8:11409997-11410500	ENSG00000269954.1
8	lnc-RP11-148O21.2.1-1	chr8:11416421-11416495	ENSG00000255354.1

No data

Variant related genes	Relation type
ENSG00000255518	TF binding region
LINC00208	TF binding region
ENSG00000269954	TF binding region
BLK	TF binding region
ENSG00000255354	TF binding region
ENSG00000254774	TF binding region
ENSG00000255518	CpG island
LINC00208	CpG island
ENSG00000269954	CpG island
BLK	CpG island
ENSG00000255354	CpG island
ENSG00000254774	CpG island
ENSG00000254774	chromatin interactions
ENSG00000154319	chromatin interactions
ENSG00000255518	chromatin interactions
ENSG00000170983	chromatin interactions
ENSG00000269954	chromatin interactions
ENSG00000136573	chromatin interactions

Extended variants
information (count: 2471 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:2471 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2248932	chr8:11391650-11391651	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566020576	chr8:11391651-11391652	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536789468	chr8:11391656-11391657	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554509285	chr8:11391659-11391660	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74994552	chr8:11391674-11391675	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139839868	chr8:11391700-11391701	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558834415	chr8:11391719-11391720	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542437879	chr8:11391748-11391749	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541244326	chr8:11391798-11391799	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77196636	chr8:11391825-11391826	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs572009480	chr8:11391849-11391850	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs193088900	chr8:11391851-11391852	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs141632296	chr8:11391905-11391906	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs531339394	chr8:11391913-11391914	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs199515747	chr8:11391917-11391918	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs566323186	chr8:11391999-11392000	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs74491406	chr8:11392004-11392005	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73541732	chr8:11392013-11392014	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565884151	chr8:11392020-11392021	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530106876	chr8:11392042-11392043	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139287670	chr8:11392058-11392059	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569675027	chr8:11392087-11392088	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149963231	chr8:11392092-11392093	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2248909	chr8:11392093-11392094	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs184112175	chr8:11392147-11392148	Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188460480	chr8:11392214-11392215	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553260787	chr8:11392220-11392221	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574978643	chr8:11392226-11392227	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79563211	chr8:11392256-11392257	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145056329	chr8:11392283-11392284	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550634465	chr8:11392299-11392300	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570615440	chr8:11392323-11392324	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181094874	chr8:11392328-11392329	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543424251	chr8:11392365-11392366	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564931414	chr8:11392411-11392412	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148720014	chr8:11392419-11392420	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541341080	chr8:11392442-11392443	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559238184	chr8:11392494-11392495	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529848702	chr8:11392495-11392496	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548022058	chr8:11392496-11392497	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77358795	chr8:11392510-11392511	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530945955	chr8:11392521-11392522	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372923162	chr8:11392523-11392524	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75867350	chr8:11392537-11392538	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570846533	chr8:11392543-11392544	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114757908	chr8:11392546-11392547	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547279733	chr8:11392552-11392553	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183671090	chr8:11392557-11392558	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536049816	chr8:11392558-11392559	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187994276	chr8:11392564-11392565	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	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
Oral cancer	21386901	CNVD
Prostate cancer	21088497	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
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
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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Gastric cancer	22315472	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:838 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11383000-11407000	Weak transcription	Dnd41	blood
2	chr8:11390200-11392200	Flanking Active TSS	GM12878-XiMat	blood
3	chr8:11390400-11392200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:11390400-11392400	Enhancers	Fetal Thymus	thymus
5	chr8:11390800-11392400	Enhancers	Primary hematopoietic stem cells	blood
6	chr8:11390800-11392400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:11391000-11392000	Enhancers	Primary B cells from peripheral blood	blood
8	chr8:11391400-11391800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:11391400-11391800	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr8:11391400-11392400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr8:11391400-11395400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:11391600-11392200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr8:11391800-11394800	Genic enhancers	Primary B cells from cord blood	blood
14	chr8:11392000-11392200	Flanking Active TSS	Primary B cells from peripheral blood	blood
15	chr8:11392200-11392400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr8:11392200-11393000	Enhancers	GM12878-XiMat	blood
17	chr8:11392200-11395600	Genic enhancers	Primary B cells from peripheral blood	blood
18	chr8:11392200-11397200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:11392400-11394800	Weak transcription	Fetal Thymus	thymus
20	chr8:11392400-11396800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:11392400-11397200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr8:11392400-11403400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr8:11393000-11393200	Flanking Active TSS	GM12878-XiMat	blood
24	chr8:11393200-11393400	Enhancers	GM12878-XiMat	blood
25	chr8:11393400-11393600	Flanking Active TSS	GM12878-XiMat	blood
26	chr8:11393600-11394200	Enhancers	GM12878-XiMat	blood
27	chr8:11394200-11395200	Flanking Active TSS	GM12878-XiMat	blood
28	chr8:11394800-11395200	Enhancers	Primary B cells from cord blood	blood
29	chr8:11394800-11396000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:11394800-11396400	Enhancers	Fetal Thymus	thymus
31	chr8:11395000-11395600	Enhancers	Liver	Liver
32	chr8:11395000-11395800	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr8:11395000-11396400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:11395200-11395400	Enhancers	Fetal Kidney	kidney
35	chr8:11395200-11395600	Enhancers	GM12878-XiMat	blood
36	chr8:11395200-11395800	Bivalent Enhancer	Fetal Lung	lung
37	chr8:11395200-11397600	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr8:11395400-11395600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr8:11395400-11395800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr8:11395400-11395800	Enhancers	Lung	lung
41	chr8:11395600-11395800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr8:11395600-11395800	Active TSS	Spleen	Spleen
43	chr8:11395600-11396400	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
44	chr8:11395600-11398000	Flanking Active TSS	GM12878-XiMat	blood
45	chr8:11395800-11396000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr8:11395800-11396200	Weak transcription	Spleen	Spleen
47	chr8:11396200-11396400	Enhancers	Spleen	Spleen
48	chr8:11396400-11396800	Genic enhancers	Primary B cells from peripheral blood	blood
49	chr8:11396400-11400000	Weak transcription	Spleen	Spleen
50	chr8:11396600-11397600	Enhancers	Fetal Lung	lung

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